-
1
-
-
84870774453
-
Enzymatic modification of 2, 6-dimethoxyphenol for the synthesis of dimers with high antioxidant capacity
-
COI: 1:CAS:528:DC%2BC38XhtVymsrvM
-
Adelakun OE, Kudanga T, Green IR, le Roes-Hill M, Burton SG (2012a) Enzymatic modification of 2, 6-dimethoxyphenol for the synthesis of dimers with high antioxidant capacity. Process Biochem 47:1926–1932. doi:10.1016/j.procbio.2012.06.027
-
(2012)
Process Biochem
, vol.47
, pp. 1926-1932
-
-
Adelakun, O.E.1
Kudanga, T.2
Green, I.R.3
le Roes-Hill, M.4
Burton, S.G.5
-
2
-
-
80054932959
-
Laccase-catalyzed dimerization of ferulic acid amplifies antioxidant activity
-
COI: 1:CAS:528:DC%2BC3MXhtlKhsrrP
-
Adelakun OE, Kudanga T, Parker A, Green IR, le Roes-Hill M, Burton SG (2012b) Laccase-catalyzed dimerization of ferulic acid amplifies antioxidant activity. J Mol Catal B Enzym 74:29–35. doi:10.1016/j.molcatb.2011.08.010
-
(2012)
J Mol Catal B Enzym
, vol.74
, pp. 29-35
-
-
Adelakun, O.E.1
Kudanga, T.2
Parker, A.3
Green, I.R.4
le Roes-Hill, M.5
Burton, S.G.6
-
3
-
-
0000040234
-
Synthesis of 2-O-α-d-glucopyranosyl L-ascorbic acidby cyclomaltodextrin glucanotransferase from Bacillus stearothermophilus
-
COI: 1:CAS:528:DyaK3MXlsFOjs7g%3D
-
Aga H, Yoneyama SS, Yamamoto I (1991) Synthesis of 2-O-α-d-glucopyranosyl L-ascorbic acidby cyclomaltodextrin glucanotransferase from Bacillus stearothermophilus. Agric Biol Chem 55:1751–1756. doi:10.1080/00021369.1991.10870856
-
(1991)
Agric Biol Chem
, vol.55
, pp. 1751-1756
-
-
Aga, H.1
Yoneyama, S.S.2
Yamamoto, I.3
-
4
-
-
84876388876
-
Enhancement of propyl gallate yield in nonaquous medium using novel cell associated tannase of Bacillus massiliensis
-
COI: 1:CAS:528:DC%2BC38XhvVamu7%2FK, PID: 23581780
-
Aithal M, Belur PD (2013) Enhancement of propyl gallate yield in nonaquous medium using novel cell associated tannase of Bacillus massiliensis. Prep Biochem Biotechnol 43:445–455. doi:10.1080/10826068.2012.745873
-
(2013)
Prep Biochem Biotechnol
, vol.43
, pp. 445-455
-
-
Aithal, M.1
Belur, P.D.2
-
5
-
-
0022979165
-
Retinyl esters synthesis by polyethylene glycol-modified lipase in benzene
-
COI: 1:CAS:528:DyaL28XlsFWmsrs%3D
-
Ajima A, Takahashi K, Matsushima A, Saito Y, Inada Y (1986) Retinyl esters synthesis by polyethylene glycol-modified lipase in benzene. Biotechnol Lett 8:547–552
-
(1986)
Biotechnol Lett
, vol.8
, pp. 547-552
-
-
Ajima, A.1
Takahashi, K.2
Matsushima, A.3
Saito, Y.4
Inada, Y.5
-
6
-
-
80054730685
-
Functionalization of chitosan by laccase-catalyzed oxidation of ferulic acid and ethyl ferulate under heterogeneous reaction conditions
-
COI: 1:CAS:528:DC%2BC3MXhtlemsL3K
-
Aljawish A, Chevalot I, Piffaut B, Rondeau-Mouro C, Girardin M, Jasniewski J, Schera J, Muniglia L (2012) Functionalization of chitosan by laccase-catalyzed oxidation of ferulic acid and ethyl ferulate under heterogeneous reaction conditions. Carbohydr Polym 87:537–544. doi:10.1016/j.carbpol.2011.08.016
-
(2012)
Carbohydr Polym
, vol.87
, pp. 537-544
-
-
Aljawish, A.1
Chevalot, I.2
Piffaut, B.3
Rondeau-Mouro, C.4
Girardin, M.5
Jasniewski, J.6
Schera, J.7
Muniglia, L.8
-
7
-
-
84860830934
-
Synthesis of naringin 6"-ricinoleate using immobilized lipase
-
COI: 1:CAS:528:DC%2BC38XpsVWmsbc%3D, PID: 22578215
-
Almeida VM, Branco CRC, Assis SA, Vieira IJC, Braz-Filho R, Branco A (2012) Synthesis of naringin 6"-ricinoleate using immobilized lipase. Chem Cent J 6:41. doi:10.1186/1752-153X-6-41
-
(2012)
Chem Cent J
, vol.6
, pp. 41
-
-
Almeida, V.M.1
Branco, C.R.C.2
Assis, S.A.3
Vieira, I.J.C.4
Braz-Filho, R.5
Branco, A.6
-
8
-
-
78650907842
-
Final amended safety assessment of hydroquinone as used in cosmetics
-
Andersen A, Bergfeld WF, Belsito DV, Hill RA, Klaassen CD, Liebler DC, Marks JG, Shank RC, Slaga TJ, Snyder PW (2010) Final amended safety assessment of hydroquinone as used in cosmetics. Int J Toxicol 29:2745–2875. doi:10.1177/1091581810385957
-
(2010)
Int J Toxicol
, vol.29
, pp. 2745-2875
-
-
Andersen, A.1
Bergfeld, W.F.2
Belsito, D.V.3
Hill, R.A.4
Klaassen, C.D.5
Liebler, D.C.6
Marks, J.G.7
Shank, R.C.8
Slaga, T.J.9
Snyder, P.W.10
-
9
-
-
0036956353
-
Final report on the safety assessment of tocopherol, tocopheryl acetate, tocopheryl linoleate, tocopheryl linoleate/oleate, tocopheryl nicotinate, tocopheryl succinate, dioleyl tocopheryl methylsilanol, potassium ascorbyl tocopherol phosphate, and tocophersolan
-
PID: 12537931
-
Zondlo Fiume M (2002) Final report on the safety assessment of tocopherol, tocopheryl acetate, tocopheryl linoleate, tocopheryl linoleate/oleate, tocopheryl nicotinate, tocopheryl succinate, dioleyl tocopheryl methylsilanol, potassium ascorbyl tocopherol phosphate, and tocophersolan. Int J Toxicol 21:51–116
-
(2002)
Int J Toxicol
, vol.21
, pp. 51-116
-
-
Zondlo Fiume, M.1
-
10
-
-
80052965048
-
Synthesis of epicatechin glucosides by a β-cyclodextrin glycosyltransfesrase
-
COI: 1:CAS:528:DC%2BC3MXhtFymu7rE
-
Aramsangtienchai P, Chavasiri W, Ito K, Pongsawasdi P (2011) Synthesis of epicatechin glucosides by a β-cyclodextrin glycosyltransfesrase. J Mol Catal B Enzym 73:27–34. doi:10.1016/j.molcatb.2011.07.013
-
(2011)
J Mol Catal B Enzym
, vol.73
, pp. 27-34
-
-
Aramsangtienchai, P.1
Chavasiri, W.2
Ito, K.3
Pongsawasdi, P.4
-
11
-
-
2442557246
-
Acylation of natural flavonoids using lipase of Candida antarctica as biocatalyst
-
COI: 1:CAS:528:DC%2BD2cXktVCrsrk%3D
-
Ardhaoui M, Falcimaigne A, Engasser JM, Moussou P, Pauly G, Ghoul M (2004b) Acylation of natural flavonoids using lipase of Candida antarctica as biocatalyst. J Mol Catal B Enzym 29:63–67. doi:10.1016/j.molcatb.2004.02.013
-
(2004)
J Mol Catal B Enzym
, vol.29
, pp. 63-67
-
-
Ardhaoui, M.1
Falcimaigne, A.2
Engasser, J.M.3
Moussou, P.4
Pauly, G.5
Ghoul, M.6
-
12
-
-
2442462158
-
Effect of acyl donor chain length and substitutions pattern on the enzymatic acylation of flavonoids
-
COI: 1:CAS:528:DC%2BD2cXkt1aks7g%3D, PID: 15163517
-
Ardhaoui M, Falcimaigne A, Ognier S, Engasser JM, Moussou P, Pauly G, Ghoul M (2004a) Effect of acyl donor chain length and substitutions pattern on the enzymatic acylation of flavonoids. J Biotechnol 110:265–271. doi:10.1016/j.jbiotec.2004.03.003
-
(2004)
J Biotechnol
, vol.110
, pp. 265-271
-
-
Ardhaoui, M.1
Falcimaigne, A.2
Ognier, S.3
Engasser, J.M.4
Moussou, P.5
Pauly, G.6
Ghoul, M.7
-
13
-
-
70349529574
-
Optimization of enzymatic synthesis of palm-based kojic acid ester using response surface methodology
-
COI: 1:CAS:528:DC%2BD1MXht1Srtb3P, PID: 19745577
-
Ashari SE, Mohamad R, Ariff A, Basir M, Salleh AB (2009) Optimization of enzymatic synthesis of palm-based kojic acid ester using response surface methodology. J Oleo Sci 58:503–510
-
(2009)
J Oleo Sci
, vol.58
, pp. 503-510
-
-
Ashari, S.E.1
Mohamad, R.2
Ariff, A.3
Basir, M.4
Salleh, A.B.5
-
14
-
-
37549025470
-
Hydrolysis of epigallocatechin gallate using a tannase from Paecilomyces variotii
-
COI: 1:CAS:528:DC%2BD1cXitVGisQ%3D%3D
-
Battestin V, Macedo GA, De Freitas VAP (2008) Hydrolysis of epigallocatechin gallate using a tannase from Paecilomyces variotii. Food Chem 108:228–233. doi:10.1016/j.foodchem.2007.10.068
-
(2008)
Food Chem
, vol.108
, pp. 228-233
-
-
Battestin, V.1
Macedo, G.A.2
De Freitas, V.A.P.3
-
15
-
-
79957529164
-
Propyl gallate synthesis using acidophilic tannase and simultaneous production of tannase and gallic acid by marine Aspergillus awamori BTMFW032
-
COI: 1:CAS:528:DC%2BC3MXmtlWrurc%3D, PID: 21279470
-
Beena PS, Basheer SM, Bhat SG, Bahkali AH, Chandrasekaran M (2011) Propyl gallate synthesis using acidophilic tannase and simultaneous production of tannase and gallic acid by marine Aspergillus awamori BTMFW032. Appl Biochem Biotechnol 164:612–628. doi:10.1007/s12010-011-9162-x
-
(2011)
Appl Biochem Biotechnol
, vol.164
, pp. 612-628
-
-
Beena, P.S.1
Basheer, S.M.2
Bhat, S.G.3
Bahkali, A.H.4
Chandrasekaran, M.5
-
16
-
-
78049253526
-
Enzymatic propyl gallate synthesis in solvent-free system: optimization by response surface methodology
-
COI: 1:CAS:528:DC%2BC3cXhtleqtLnN
-
Bouaziz A, Horchani H, Salem NB, Chaari A, Chaabouni M, Gargouri Y, Sayari A (2010) Enzymatic propyl gallate synthesis in solvent-free system: optimization by response surface methodology. J Mol Catal B Enzym 67:242–250. doi:10.1016/j.molcatb.2010.08.013
-
(2010)
J Mol Catal B Enzym
, vol.67
, pp. 242-250
-
-
Bouaziz, A.1
Horchani, H.2
Salem, N.B.3
Chaari, A.4
Chaabouni, M.5
Gargouri, Y.6
Sayari, A.7
-
17
-
-
0033585445
-
Enzymatic synthesis of α-butyl glycoside lactate: a new α-hydroxy acid derivative
-
COI: 1:CAS:528:DyaK1cXotFGjs7s%3D, PID: 10099533
-
Bousquet MP, Willemot RM, Monsan P, Boures E (1999) Enzymatic synthesis of α-butyl glycoside lactate: a new α-hydroxy acid derivative. Biotechnol Bioeng 62:225–234
-
(1999)
Biotechnol Bioeng
, vol.62
, pp. 225-234
-
-
Bousquet, M.P.1
Willemot, R.M.2
Monsan, P.3
Boures, E.4
-
18
-
-
84861023623
-
Laccase-mediated functionalization of chitosan by caffeic and gallic acids for modulating antioxidant and antimicrobial properties
-
Božič M, Gorgieva S, Kokol V (2012a) Laccase-mediated functionalization of chitosan by caffeic and gallic acids for modulating antioxidant and antimicrobial properties. Carbohydr Polym 87:2388–2398. doi:10.1016/j.carbpol.2011.11.006
-
(2012)
Carbohydr Polym
, vol.87
, pp. 2388-2398
-
-
Božič, M.1
Gorgieva, S.2
Kokol, V.3
-
19
-
-
84861627815
-
Homogeneous and heterogeneous methods for laccase-mediated functionalization of chitosan by tannic acid and quercetin
-
PID: 24750872
-
Božič M, Gorgieva S, Kokol V (2012b) Homogeneous and heterogeneous methods for laccase-mediated functionalization of chitosan by tannic acid and quercetin. Carbohydr Polym 89:854–864. doi:10.1016/j.carbpol.2012.04.021
-
(2012)
Carbohydr Polym
, vol.89
, pp. 854-864
-
-
Božič, M.1
Gorgieva, S.2
Kokol, V.3
-
20
-
-
0033225654
-
High yields of ascorbyl palmitate by thermostable lipase-mediated esterification
-
COI: 1:CAS:528:DyaK1MXnsV2ruro%3D
-
Bradoo S, Saxerna RK, Gupta R (1999) High yields of ascorbyl palmitate by thermostable lipase-mediated esterification. JAOCS 76:1291–1295
-
(1999)
JAOCS
, vol.76
, pp. 1291-1295
-
-
Bradoo, S.1
Saxerna, R.K.2
Gupta, R.3
-
21
-
-
80052979899
-
Cosmeceuticals: current trends and market analysis
-
Brandt FS, Cazzaniga A, Hann M (2011) Cosmeceuticals: current trends and market analysis. Semin Cut Med Surg 1:141–143. doi:10.1016/j.sder.2011.05.006
-
(2011)
Semin Cut Med Surg
, vol.1
, pp. 141-143
-
-
Brandt, F.S.1
Cazzaniga, A.2
Hann, M.3
-
22
-
-
63249085406
-
Enzymatic synthesis of palm-based ascorbyl esters
-
COI: 1:CAS:528:DC%2BD1MXkt1Sntrs%3D
-
Burham H, Rasheed RAGA, Noor NM, Badruddin S, Sidek H (2009) Enzymatic synthesis of palm-based ascorbyl esters. J Mol Catal B Enzym 58:153–157. doi:10.1016/j.molcatb.2008.12.012
-
(2009)
J Mol Catal B Enzym
, vol.58
, pp. 153-157
-
-
Burham, H.1
Rasheed, R.A.G.A.2
Noor, N.M.3
Badruddin, S.4
Sidek, H.5
-
23
-
-
1342345165
-
Preparation and purification of epigallocatechin by high-speed countercurrent chromatography (HSCC)
-
COI: 1:CAS:528:DC%2BD2cXlsFenug%3D%3D
-
Cao X, Ito Y (2004) Preparation and purification of epigallocatechin by high-speed countercurrent chromatography (HSCC). J Liq Chromatogr Relat Technol 27:145–152. doi:10.1081/JLC-120027091
-
(2004)
J Liq Chromatogr Relat Technol
, vol.27
, pp. 145-152
-
-
Cao, X.1
Ito, Y.2
-
24
-
-
84878749056
-
Enzymatic synthesis of butyl ferulate by silica-immobilized lipase in non-aqueous medium
-
COI: 1:CAS:528:DC%2BC38XlvFKjt7w%3D
-
Chandel C, Kumar A, Kanwar SS (2011) Enzymatic synthesis of butyl ferulate by silica-immobilized lipase in non-aqueous medium. J Biomed Nanotechnol 2:400–408. doi:10.4236/jbnb.2011.24049
-
(2011)
J Biomed Nanotechnol
, vol.2
, pp. 400-408
-
-
Chandel, C.1
Kumar, A.2
Kanwar, S.S.3
-
25
-
-
36749090008
-
Enzymatic acylation of flavonoids: effect of the nature of the substrate, origin of lipase and operating conditions on conversion yield and regioselectivity
-
COI: 1:CAS:528:DC%2BD2sXhtFKksLvL, PID: 17937478
-
Chebil L, Anthoni J, Humeau C, Gerardin C, Engasser JM, Ghoul M (2007) Enzymatic acylation of flavonoids: effect of the nature of the substrate, origin of lipase and operating conditions on conversion yield and regioselectivity. J Agric Food Chem 55:9496–9502. doi:10.1021/jf071943j
-
(2007)
J Agric Food Chem
, vol.55
, pp. 9496-9502
-
-
Chebil, L.1
Anthoni, J.2
Humeau, C.3
Gerardin, C.4
Engasser, J.M.5
Ghoul, M.6
-
26
-
-
79951738137
-
Lipase-catalyzed esterification of ferulic acid with oleyl alcohol in ionic liquid/isooctane binary systems
-
COI: 1:CAS:528:DC%2BC3MXnvVSksg%3D%3D, PID: 21250692
-
Chen B, Liu H, Guo Z, Huang J, Wang M, Xu X, Zheng L (2011b) Lipase-catalyzed esterification of ferulic acid with oleyl alcohol in ionic liquid/isooctane binary systems. J Agric Food Chem 59:1256–1263. doi:10.1021/jf104101z
-
(2011)
J Agric Food Chem
, vol.59
, pp. 1256-1263
-
-
Chen, B.1
Liu, H.2
Guo, Z.3
Huang, J.4
Wang, M.5
Xu, X.6
Zheng, L.7
-
27
-
-
0036568818
-
Optimization of kojic acid monolaurate synthesis with lipase PS from Pseudomonas cepacia
-
COI: 1:CAS:528:DC%2BD38XjtFKqtbs%3D
-
Chen CS, Liu KJ, Lou YH, Shieh CJ (2002) Optimization of kojic acid monolaurate synthesis with lipase PS from Pseudomonas cepacia. J Sci Food Agric 82:601–605. doi:10.1002/jsfa.1083
-
(2002)
J Sci Food Agric
, vol.82
, pp. 601-605
-
-
Chen, C.S.1
Liu, K.J.2
Lou, Y.H.3
Shieh, C.J.4
-
28
-
-
77956449174
-
Optimization of ultrasound-accelerated synthesis of enzymatic caffeic acid phenethyl ester by response surface methodology
-
COI: 1:CAS:528:DC%2BC3cXhtFGqsbnE, PID: 20797894
-
Chen HC, Chen JH, Chang C, Shieh CJ (2011a) Optimization of ultrasound-accelerated synthesis of enzymatic caffeic acid phenethyl ester by response surface methodology. Ultrason Sonochem 18:455–459. doi:10.1016/j.ultsonch.2010.07.018
-
(2011)
Ultrason Sonochem
, vol.18
, pp. 455-459
-
-
Chen, H.C.1
Chen, J.H.2
Chang, C.3
Shieh, C.J.4
-
29
-
-
77957244527
-
Optimized synthesis of lipase-catalyzed octyl caffeate by Novozym® 435
-
COI: 1:CAS:528:DC%2BC3cXht1ertL%2FJ
-
Chen HC, Twu YK, Chang CMJ, Liue YC, Shieh CJ (2010) Optimized synthesis of lipase-catalyzed octyl caffeate by Novozym® 435. Ind Crop Prod 32:522–526. doi:10.1016/j.indcrop.2010.06.028
-
(2010)
Ind Crop Prod
, vol.32
, pp. 522-526
-
-
Chen, H.C.1
Twu, Y.K.2
Chang, C.M.J.3
Liue, Y.C.4
Shieh, C.J.5
-
30
-
-
58249085342
-
Lipase-catalysed synthesis of esters of ferulic acid with natural compounds and evaluation of their antioxidant properties
-
COI: 1:CAS:528:DC%2BD1MXntVKltQ%3D%3D
-
Chigorimbo-Murefu NTL, Riva S, Burton SG (2009) Lipase-catalysed synthesis of esters of ferulic acid with natural compounds and evaluation of their antioxidant properties. J Mol Cat: Enzym B 56:277–282. doi:10.1016/j.molcatb.2008.05.017
-
(2009)
J Mol Cat: Enzym B
, vol.56
, pp. 277-282
-
-
Chigorimbo-Murefu, N.T.L.1
Riva, S.2
Burton, S.G.3
-
31
-
-
79959910684
-
Biosynthesis of (+)-catechin glycosides using recombinant amylosucrase from Deinococcus geothermalis DSM 11300
-
COI: 1:CAS:528:DC%2BC3MXosFagtrk%3D
-
Cho HK, Kim HH, Seo DH, Jung JH, Park JH, Baek NI, Kim MJ, Yoo SH, Cha J, Kim YR, Park CS (2011) Biosynthesis of (+)-catechin glycosides using recombinant amylosucrase from Deinococcus geothermalis DSM 11300. Enzym Microb Technol 49:246–253. doi:10.1016/j.enzmictec.2011.05.007
-
(2011)
Enzym Microb Technol
, vol.49
, pp. 246-253
-
-
Cho, H.K.1
Kim, H.H.2
Seo, D.H.3
Jung, J.H.4
Park, J.H.5
Baek, N.I.6
Kim, M.J.7
Yoo, S.H.8
Cha, J.9
Kim, Y.R.10
Park, C.S.11
-
32
-
-
33750025050
-
Cosmeceuticals
-
COI: 1:CAS:528:DC%2BD2sXhvFCqsrY%3D, PID: 17055397
-
Choi CM, Berson DS (2006) Cosmeceuticals. Semin Cutan Med Surg 25:163–168
-
(2006)
Semin Cutan Med Surg
, vol.25
, pp. 163-168
-
-
Choi, C.M.1
Berson, D.S.2
-
33
-
-
84868226725
-
Enzymatic synthesis of phenolic lipids using flaxseed oil and ferulic acid in supercritical carbon dioxide media
-
COI: 1:CAS:528:DC%2BC38XhslOlurjO
-
Ciftci D, Saldana MDA (2012) Enzymatic synthesis of phenolic lipids using flaxseed oil and ferulic acid in supercritical carbon dioxide media. J Supercrit Fluids 72:255–262. doi:10.1016/j.supflu.2012.09.007
-
(2012)
J Supercrit Fluids
, vol.72
, pp. 255-262
-
-
Ciftci, D.1
Saldana, M.D.A.2
-
34
-
-
67349231801
-
1,3-Diferuloyl-sn-glycerol from the biocatalytic transesterification of ethyl-4-hydroxy-3-methoxy cinnamic acid (ethyl ferulate) and soybean oil
-
COI: 1:CAS:528:DC%2BD1MXmtVKgu7g%3D, PID: 19238329
-
Compton DL, Laszlo (2009) 1,3-Diferuloyl-sn-glycerol from the biocatalytic transesterification of ethyl-4-hydroxy-3-methoxy cinnamic acid (ethyl ferulate) and soybean oil. Biotechnol Lett 31:889–896
-
(2009)
Biotechnol Lett
, vol.31
, pp. 889-896
-
-
Compton, D.L.1
Laszlo2
-
35
-
-
0033732381
-
Lipase-catalyzed synthesis of ferulate esters
-
COI: 1:CAS:528:DC%2BD3cXjsVKgtL0%3D
-
Compton DL, Laszlo JA, Berhow MA (2000) Lipase-catalyzed synthesis of ferulate esters. JAOCS 77:513–519
-
(2000)
JAOCS
, vol.77
, pp. 513-519
-
-
Compton, D.L.1
Laszlo, J.A.2
Berhow, M.A.3
-
36
-
-
84973834057
-
Final report on the safety assessment of retinyl palmitate and retinol
-
Cosmetic Ingredient Review (1987) Final report on the safety assessment of retinyl palmitate and retinol. J Am Coll Toxicol 6:279–320. doi:10.3109/10915818709098562
-
(1987)
J Am Coll Toxicol
, vol.6
, pp. 279-320
-
-
-
37
-
-
37349085881
-
Final report on the amended safety assessment of propyl gallate
-
Cosmetic International Review (2007) Final report on the amended safety assessment of propyl gallate. Int J Toxicol 26:89–118. doi:10.1080/10915810701663176
-
(2007)
Int J Toxicol
, vol.26
, pp. 89-118
-
-
-
38
-
-
84895536154
-
Lipase catalyzed ascorbyl palmitate synthesis under microwave irradiation
-
COI: 1:CAS:528:DC%2BC2cXlvFelsLk%3D
-
Costa ICR, Sutili FK, da Silva GVV, Leite SGF, Miranda LSM, de Souza ROMA (2014) Lipase catalyzed ascorbyl palmitate synthesis under microwave irradiation. J Mol Catal B Enzym 102:127–131. doi:10.1016/j.molcatb.2014.02.002
-
(2014)
J Mol Catal B Enzym
, vol.102
, pp. 127-131
-
-
Costa, I.C.R.1
Sutili, F.K.2
da Silva, G.V.V.3
Leite, S.G.F.4
Miranda, L.S.M.5
de Souza, R.O.M.A.6
-
39
-
-
77954301071
-
Regioselective synthesis of feruloylated glycosides using the feruloyl esterase expressed in selected commercial multi-enzymatic preparations as biocatalysts
-
COI: 1:CAS:528:DC%2BC3cXotlSnt7c%3D
-
Couto J, Karboune S, Mathew R (2010) Regioselective synthesis of feruloylated glycosides using the feruloyl esterase expressed in selected commercial multi-enzymatic preparations as biocatalysts. Biocatal Biotransfor 28:235–244. doi:10.3109/10242422.2010.493209
-
(2010)
Biocatal Biotransfor
, vol.28
, pp. 235-244
-
-
Couto, J.1
Karboune, S.2
Mathew, R.3
-
40
-
-
80052965784
-
Optimization of feruloyl esterase-catalyzed synthesis of feruloylated oligosaccharides by response face methodology
-
COI: 1:CAS:528:DC%2BC3MXhtFymu7vO
-
Couto J, St-Louis R, Karboune S (2011) Optimization of feruloyl esterase-catalyzed synthesis of feruloylated oligosaccharides by response face methodology. J Mol Catal B Enzym 73:53–62. doi:10.1016/j.molcatb.2011.07.016
-
(2011)
J Mol Catal B Enzym
, vol.73
, pp. 53-62
-
-
Couto, J.1
St-Louis, R.2
Karboune, S.3
-
41
-
-
84889871013
-
Ultrasound-assisted lipase-catalyzed synthesis of D-isoascorbyl palmitate: process optimization and kinetic evaluation
-
PID: 24321598
-
Cui FJ, Zhao HX, Sun WJ, Wei Z, Yu SL, Zhou Q, Dong Y (2013) Ultrasound-assisted lipase-catalyzed synthesis of D-isoascorbyl palmitate: process optimization and kinetic evaluation. Chem Cent J 7:180. doi:10.1186/1752-153X-7-180
-
(2013)
Chem Cent J
, vol.7
, pp. 180
-
-
Cui, F.J.1
Zhao, H.X.2
Sun, W.J.3
Wei, Z.4
Yu, S.L.5
Zhou, Q.6
Dong, Y.7
-
42
-
-
70349424839
-
Skin penetration of epigallocatechin-3-gallate and quercetin from green tea and ginkgo biloba extracts vehiculated in cosmetic formulations
-
COI: 1:CAS:528:DC%2BD1MXhsVensLnJ, PID: 19786823
-
Dal Belo SE, Gaspar LR, Maia Campos PMBG, Marty JP (2009) Skin penetration of epigallocatechin-3-gallate and quercetin from green tea and ginkgo biloba extracts vehiculated in cosmetic formulations. Skin Pharmacol Physiol 22:299–304. doi:10.1159/000241299
-
(2009)
Skin Pharmacol Physiol
, vol.22
, pp. 299-304
-
-
Dal Belo, S.E.1
Gaspar, L.R.2
Maia Campos, P.M.B.G.3
Marty, J.P.4
-
43
-
-
80052203791
-
Optimized enzymatic synthesis of hesperidin fatty acid esters in a two-phase system containing ionic liquid
-
PID: 21862958
-
De Araujo MEMB, Contesini FJ, Franco YEM, Sawaya ACHF, Alberot TG, Dalfre N, Carvalho RO (2011) Optimized enzymatic synthesis of hesperidin fatty acid esters in a two-phase system containing ionic liquid. Molecules 16:7171–7182. doi:10.3390/molecules16087171
-
(2011)
Molecules
, vol.16
, pp. 7171-7182
-
-
De Araujo, M.E.M.B.1
Contesini, F.J.2
Franco, Y.E.M.3
Sawaya, A.C.H.F.4
Alberot, T.G.5
Dalfre, N.6
Carvalho, R.O.7
-
44
-
-
64649091106
-
A molecular modeling study to rationalize the regioselectivity in acylation of flavonoid glycosides catalyzed by Candida antarctica lipase B
-
De Oliveira EB, Humeau C, Chebil L, Maia ER, Dehez F, Maigret B, Ghoul M, Engasser JM (2009) A molecular modeling study to rationalize the regioselectivity in acylation of flavonoid glycosides catalyzed by Candida antarctica lipase B. J Mol Catal B Enzym 59:96–105. doi:10.1016/j.molcatb.2009.01.011
-
(2009)
J Mol Catal B Enzym
, vol.59
, pp. 96-105
-
-
De Oliveira, E.B.1
Humeau, C.2
Chebil, L.3
Maia, E.R.4
Dehez, F.5
Maigret, B.6
Ghoul, M.7
Engasser, J.M.8
-
45
-
-
33748551994
-
Effect of molecular sieves on lipase-catalyzed esterification of rutin with stearic acid
-
COI: 1:CAS:528:DC%2BD28XnsFemu7g%3D, PID: 16910711
-
Duan Y, Du Z, Yao Y, Li R, Wu D (2006) Effect of molecular sieves on lipase-catalyzed esterification of rutin with stearic acid. J Agric Food Chem 54:6219–6225
-
(2006)
J Agric Food Chem
, vol.54
, pp. 6219-6225
-
-
Duan, Y.1
Du, Z.2
Yao, Y.3
Li, R.4
Wu, D.5
-
46
-
-
84891833221
-
Solvent-free lipase-catalyzed synthesis of a novel hydroxyl-fatty acid derivative of kojic acid
-
COI: 1:CAS:528:DC%2BC3sXhvVKisbvJ
-
El-Boulifi N, Ashari SE, Serrano M, Aracil J, Martinez M (2014) Solvent-free lipase-catalyzed synthesis of a novel hydroxyl-fatty acid derivative of kojic acid. Enzym Microb Technol 55:128–132. doi:10.1016/j.enzmictec.2013.10.009
-
(2014)
Enzym Microb Technol
, vol.55
, pp. 128-132
-
-
El-Boulifi, N.1
Ashari, S.E.2
Serrano, M.3
Aracil, J.4
Martinez, M.5
-
47
-
-
0346095155
-
Enzymatic synthesis of new aromatic esters of phloridzin
-
COI: 1:CAS:528:DC%2BD2cXjtFersA%3D%3D
-
Enaud E, Humeau C, Piffaut B, Girardin M (2004) Enzymatic synthesis of new aromatic esters of phloridzin. J Mol Catal B Enzym 27:1–6. doi:10.1016/j.molcatb.2003.08.002
-
(2004)
J Mol Catal B Enzym
, vol.27
, pp. 1-6
-
-
Enaud, E.1
Humeau, C.2
Piffaut, B.3
Girardin, M.4
-
48
-
-
0032509428
-
Lipase catalyzed regio- and stereospecific hydrolysis: chemoenzymatic synthesis of both (R)- and (S)-enantiomers of a-lipoic acid
-
COI: 1:CAS:528:DyaK1MXkvF2qtw%3D%3D
-
Fadnavis NW, Babu RL, Vadivel SK, Deshpande AA, Bhalerao UT (1998) Lipase catalyzed regio- and stereospecific hydrolysis: chemoenzymatic synthesis of both (R)- and (S)-enantiomers of a-lipoic acid. Tetrahedron Asymmetry 9:4109–4112. doi:10.1016/S0957-4166(98)00447-9
-
(1998)
Tetrahedron Asymmetry
, vol.9
, pp. 4109-4112
-
-
Fadnavis, N.W.1
Babu, R.L.2
Vadivel, S.K.3
Deshpande, A.A.4
Bhalerao, U.T.5
-
49
-
-
79954420894
-
Synthesis of propyl gallate by transesterification of tannic acid in aqueous media catalyzed by immobilized derivatives of tannase from Lactobacillus plantarum
-
COI: 1:CAS:528:DC%2BC3MXksVChs7g%3D, PID: 25214351
-
Fernandez-Lorente G, Bolivar JM, Martin JR, Curiel JA, Munoz R, de las Rivas B, Carrascosa AV, Guisan JM (2011) Synthesis of propyl gallate by transesterification of tannic acid in aqueous media catalyzed by immobilized derivatives of tannase from Lactobacillus plantarum. Food Chem 128:214–217. doi:10.1016/j.foodchem.2011.02.057
-
(2011)
Food Chem
, vol.128
, pp. 214-217
-
-
Fernandez-Lorente, G.1
Bolivar, J.M.2
Martin, J.R.3
Curiel, J.A.4
Munoz, R.5
de las Rivas, B.6
Carrascosa, A.V.7
Guisan, J.M.8
-
51
-
-
84977141023
-
Cold-adapted proteases as an emerging class of therapeutics
-
PID: 25135820
-
Fornbacke M, Clarsund M (2013) Cold-adapted proteases as an emerging class of therapeutics. Infect Dis Ther 2:15–26. doi:10.1007/s40121-013-0002-x
-
(2013)
Infect Dis Ther
, vol.2
, pp. 15-26
-
-
Fornbacke, M.1
Clarsund, M.2
-
52
-
-
85004650810
-
Enzymatic synthesis of (+)catechin-a-glucoside and its effect on tyrosinase activity
-
COI: 1:CAS:528:DyaK2cXhtVShs7Y%3D
-
Funayama M, Nishino T, Hirota A, Murao S, Takenishi S, Nakano H (1993) Enzymatic synthesis of (+)catechin-a-glucoside and its effect on tyrosinase activity. Biosci Biotechnol Biochem 57:1666–1669. doi:10.1271/bbb.57.1666
-
(1993)
Biosci Biotechnol Biochem
, vol.57
, pp. 1666-1669
-
-
Funayama, M.1
Nishino, T.2
Hirota, A.3
Murao, S.4
Takenishi, S.5
Nakano, H.6
-
53
-
-
77956174741
-
Large-scale separation of silybin diastereoisomers using lipases
-
COI: 1:CAS:528:DC%2BC3cXhtV2gtLzF
-
Gazak R, Marhol P, Purchartova K, Monti D, Biedermann D, Riva S, Cvak L, Kren V (2010) Large-scale separation of silybin diastereoisomers using lipases. Process Biochem 45:1657–1663. doi:10.1016/j.procbio.2010.06.019
-
(2010)
Process Biochem
, vol.45
, pp. 1657-1663
-
-
Gazak, R.1
Marhol, P.2
Purchartova, K.3
Monti, D.4
Biedermann, D.5
Riva, S.6
Cvak, L.7
Kren, V.8
-
54
-
-
0000326191
-
Laccases: a useful group of oxidoreductive enzymes
-
COI: 1:CAS:528:DyaK1MXislChsLw%3D
-
Gianfreda L, Xu F, Bollag JM (1999) Laccases: a useful group of oxidoreductive enzymes. Biorem J 3:1–26. doi:10.1080/10889869991219163
-
(1999)
Biorem J
, vol.3
, pp. 1-26
-
-
Gianfreda, L.1
Xu, F.2
Bollag, J.M.3
-
55
-
-
0035101715
-
Synthesis of pentylferulate by a feruloyl esterase from Aspergillus niger using water-in-oil microemulsions
-
COI: 1:CAS:528:DC%2BD3MXhs1Sns7k%3D
-
Giuliani S, Piana C, Setti L, Hochkoeppler A, Pifferi PG, Williamson PG, Faulds CB (2001) Synthesis of pentylferulate by a feruloyl esterase from Aspergillus niger using water-in-oil microemulsions. Biotechnol Lett 23:325–330
-
(2001)
Biotechnol Lett
, vol.23
, pp. 325-330
-
-
Giuliani, S.1
Piana, C.2
Setti, L.3
Hochkoeppler, A.4
Pifferi, P.G.5
Williamson, P.G.6
Faulds, C.B.7
-
56
-
-
84874814840
-
Characterization of a tannase from Emericela nidulans immobilized on ionic and covalent supports for propyl gallate synthesis
-
COI: 1:CAS:528:DC%2BC3sXjsleju7s%3D, PID: 23242498
-
Goncalves HB, Jorge JA, Pessela BC, Fernanzed Lorente G, Guisan JM, Guimaraes LHS (2013) Characterization of a tannase from Emericela nidulans immobilized on ionic and covalent supports for propyl gallate synthesis. Biotechnol Lett 35:591–598. doi:10.1007/s10529-012-1111-4
-
(2013)
Biotechnol Lett
, vol.35
, pp. 591-598
-
-
Goncalves, H.B.1
Jorge, J.A.2
Pessela, B.C.3
Fernanzed Lorente, G.4
Guisan, J.M.5
Guimaraes, L.H.S.6
-
57
-
-
0032697910
-
Parametric optimisation of Aspergillus terreus lipase production and its potential in ester synthesis
-
Gulati R, Saxena RK, Gupta R, Yadav RP, Davidson S (1999) Parametric optimisation of Aspergillus terreus lipase production and its potential in ester synthesis. Process Biochem 35:459–464. doi:10.1016/S0032-9592(99)00090-4
-
(1999)
Process Biochem
, vol.35
, pp. 459-464
-
-
Gulati, R.1
Saxena, R.K.2
Gupta, R.3
Yadav, R.P.4
Davidson, S.5
-
58
-
-
84857451784
-
Effect of ionic liquids on enzymatic synthesis of caffeic acid phenethyl ester
-
COI: 1:CAS:528:DC%2BC38Xht1ygtg%3D%3D, PID: 21909673
-
Ha SH, Van Anh T, Lee SH, Koo M (2012) Effect of ionic liquids on enzymatic synthesis of caffeic acid phenethyl ester. Bioprocess Biosyst Eng 35:235–240. doi:10.1007/s00449-011-0601-4
-
(2012)
Bioprocess Biosyst Eng
, vol.35
, pp. 235-240
-
-
Ha, S.H.1
Van Anh, T.2
Lee, S.H.3
Koo, M.4
-
59
-
-
57149097683
-
Enzymatic esterification of lactic acid, utilizing the basicity of particular polar organic solvents to suppress acidity of lactic acid
-
COI: 1:CAS:528:DC%2BD1cXhtlWntLzO
-
Hasegawa S, Azuma M, Takahashi K (2008) Enzymatic esterification of lactic acid, utilizing the basicity of particular polar organic solvents to suppress acidity of lactic acid. J Chem Technol Biotechnol 83:1503–1510. doi:10.1002/jctb.1935
-
(2008)
J Chem Technol Biotechnol
, vol.83
, pp. 1503-1510
-
-
Hasegawa, S.1
Azuma, M.2
Takahashi, K.3
-
60
-
-
0000033399
-
Enzymatic synthesis of galactosylkojic acid with immobilized b-galactosidase from Bacillus circulans
-
COI: 1:CAS:528:DyaK2MXkvVeru7w%3D
-
Hassan MA, Ismail F, Yamamoto S, Yamada H, Nakanishi K (1995) Enzymatic synthesis of galactosylkojic acid with immobilized b-galactosidase from Bacillus circulans. Biosci Biotechnol Biochem 59:543–545. doi:10.1271/bbb.59.543
-
(1995)
Biosci Biotechnol Biochem
, vol.59
, pp. 543-545
-
-
Hassan, M.A.1
Ismail, F.2
Yamamoto, S.3
Yamada, H.4
Nakanishi, K.5
-
61
-
-
84856262342
-
Photoprotective effects of a formulation containing tannase-converted green tea extract against UVB-induced oxidative stress in hairless mice
-
COI: 1:CAS:528:DC%2BC38Xkt1WntQ%3D%3D, PID: 22068688
-
Hong YH, Jung EY, Shin KS, Kim TY, Yu KW, Chang UJ, Suh HJ (2012) Photoprotective effects of a formulation containing tannase-converted green tea extract against UVB-induced oxidative stress in hairless mice. Appl Biochem Biotechnol 166:165–175. doi:10.1007/s12010-011-9413-x
-
(2012)
Appl Biochem Biotechnol
, vol.166
, pp. 165-175
-
-
Hong, Y.H.1
Jung, E.Y.2
Shin, K.S.3
Kim, T.Y.4
Yu, K.W.5
Chang, U.J.6
Suh, H.J.7
-
62
-
-
84878668680
-
Tannase-converted green tea catechins and their anti-wrinkle activity in humans
-
PID: 23725307
-
Hong YH, Jung EY, Shin KS, Yu KW, Chang UJ, Suh HJ (2013) Tannase-converted green tea catechins and their anti-wrinkle activity in humans. J Cosmet Dermatol 12:137–143. doi:10.1111/jocd.12038
-
(2013)
J Cosmet Dermatol
, vol.12
, pp. 137-143
-
-
Hong, Y.H.1
Jung, E.Y.2
Shin, K.S.3
Yu, K.W.4
Chang, U.J.5
Suh, H.J.6
-
63
-
-
33748428180
-
Production of ascorbyl palmitate by surfactant-coated lipase in organic media
-
COI: 1:CAS:528:DC%2BD28XmvV2itrs%3D, PID: 16881677
-
Hsieh HJ, Nair GR, Wu WT (2006) Production of ascorbyl palmitate by surfactant-coated lipase in organic media. J Agric Food Chem 54:5777–5781
-
(2006)
J Agric Food Chem
, vol.54
, pp. 5777-5781
-
-
Hsieh, H.J.1
Nair, G.R.2
Wu, W.T.3
-
64
-
-
4544268983
-
Enzyme-catalyzed acylation of plant polyphenols for interpretation of their functions
-
Ishihara K, Nishimura Y, Kubo T, Okada C, Hamada H, Nakajima N (2002) Enzyme-catalyzed acylation of plant polyphenols for interpretation of their functions. Plant Biotechnology 19:211--214. doi:10.5511/plantbiotechnology.19.211
-
(2002)
Plant Biotechnology
, vol.19
, pp. 211-214
-
-
Ishihara, K.1
Nishimura, Y.2
Kubo, T.3
Okada, C.4
Hamada, H.5
Nakajima, N.6
-
65
-
-
77952102101
-
Enzymatic preparation of arbutin derivatives: lipase-catalyzed direct acylation without the need of vinyl ester as an acyl donor
-
COI: 1:CAS:528:DC%2BC3cXhtVCktb3M, PID: 20471593
-
Ishihara K, Katsube Y, Kumazawa N, Kuratani M, Masuoka N, Nakajima N (2010) Enzymatic preparation of arbutin derivatives: lipase-catalyzed direct acylation without the need of vinyl ester as an acyl donor. J Biosci Bioeng 109:554–556. doi:10.1016/j.jbiosc.2009.11.009
-
(2010)
J Biosci Bioeng
, vol.109
, pp. 554-556
-
-
Ishihara, K.1
Katsube, Y.2
Kumazawa, N.3
Kuratani, M.4
Masuoka, N.5
Nakajima, N.6
-
66
-
-
84881231766
-
Synthesis of aliphatic esters of cinnamic acid as potential lipophilic antioxidants catalyzed by lipase B from Candida antarctica
-
COI: 1:CAS:528:DC%2BC3sXhtF2ms7nK, PID: 23703579
-
Jakovetic SM, Jugovic BZ, Gvozdenovic MM, Bezbradica DJI, Antov MG, Mijin DZ, Knezevic-Jugovic ZD (2013) Synthesis of aliphatic esters of cinnamic acid as potential lipophilic antioxidants catalyzed by lipase B from Candida antarctica. Appl Biochem Biotechnol 170:1560–1573. doi:10.1007/s12010-013-0294-z
-
(2013)
Appl Biochem Biotechnol
, vol.170
, pp. 1560-1573
-
-
Jakovetic, S.M.1
Jugovic, B.Z.2
Gvozdenovic, M.M.3
Bezbradica, D.J.I.4
Antov, M.G.5
Mijin, D.Z.6
Knezevic-Jugovic, Z.D.7
-
67
-
-
84882793166
-
Synthesis of vitamin E succinate from Candida rugosa lipase in organic medium
-
COI: 1:CAS:528:DC%2BC3sXhtVGmu7%2FF
-
Jiang XJ, Hu Y, Jiang L, Gong JH, Huang H (2013) Synthesis of vitamin E succinate from Candida rugosa lipase in organic medium. Chem Res Chin Univ 29:223–226. doi:10.1007/s40242-013-2486-z
-
(2013)
Chem Res Chin Univ
, vol.29
, pp. 223-226
-
-
Jiang, X.J.1
Hu, Y.2
Jiang, L.3
Gong, J.H.4
Huang, H.5
-
68
-
-
43149123787
-
Inhibitory effects of arbutin-β-glycosides synthesized from enzymatic transglycosylation for melanogenesis
-
COI: 1:CAS:528:DC%2BD1cXitFKgtLw%3D, PID: 18040603
-
Jun SY, Park KM, Choi KW, Jang MK, Kang HY, Lee SH, Park KH, Cha J (2008) Inhibitory effects of arbutin-β-glycosides synthesized from enzymatic transglycosylation for melanogenesis. Biotechnol Lett 30:743–748. doi:10.1007/s10529-007-9605-1
-
(2008)
Biotechnol Lett
, vol.30
, pp. 743-748
-
-
Jun, S.Y.1
Park, K.M.2
Choi, K.W.3
Jang, M.K.4
Kang, H.Y.5
Lee, S.H.6
Park, K.H.7
Cha, J.8
-
69
-
-
84855676090
-
Bioorganic synthesis, characterization and antioxidant activity of esters of natural phenolics and α-lipoic acid
-
COI: 1:CAS:528:DC%2BC38XpsFagsg%3D%3D, PID: 22138637
-
Kaki SS, Grey C, Adlercreutz P (2012) Bioorganic synthesis, characterization and antioxidant activity of esters of natural phenolics and α-lipoic acid. J Biotechnol 157:344–349. doi:10.1016/j.jbiotec.2011.11.012
-
(2012)
J Biotechnol
, vol.157
, pp. 344-349
-
-
Kaki, S.S.1
Grey, C.2
Adlercreutz, P.3
-
70
-
-
67650711219
-
Synthesis and characterization of hydroquinone fructoside using Leuconostoc mesenteroides levansucrase
-
COI: 1:CAS:528:DC%2BD1MXotVGrtbs%3D, PID: 19294375
-
Kang J, Kim YM, Kim N, Kim DW, Nam SH, Kim D (2009) Synthesis and characterization of hydroquinone fructoside using Leuconostoc mesenteroides levansucrase. Appl Microbiol Biotechnol 83:1009–1016. doi:10.1007/s00253-009-1936-5
-
(2009)
Appl Microbiol Biotechnol
, vol.83
, pp. 1009-1016
-
-
Kang, J.1
Kim, Y.M.2
Kim, N.3
Kim, D.W.4
Nam, S.H.5
Kim, D.6
-
71
-
-
34547999034
-
Effect of different reaction parameters on the lipase-catalyzed selective acylation of polyhydroxylated natural compounds in ionic liquids
-
COI: 1:CAS:528:DC%2BD2sXpsFKjurk%3D
-
Katsoura MH, Polydera AC, Katapodis P, Kolisis FN, Stamatis H (2007) Effect of different reaction parameters on the lipase-catalyzed selective acylation of polyhydroxylated natural compounds in ionic liquids. Process Biochem 42:1326–1334. doi:10.1016/j.procbio.2007.07.004
-
(2007)
Process Biochem
, vol.42
, pp. 1326-1334
-
-
Katsoura, M.H.1
Polydera, A.C.2
Katapodis, P.3
Kolisis, F.N.4
Stamatis, H.5
-
72
-
-
33646500540
-
Use of ionic liquids as media for the biocatalytic preparation of flavonoid derivatives with antioxidant potency
-
COI: 1:CAS:528:DC%2BD28Xks1eltbo%3D, PID: 16457903
-
Katsoura MH, Polydera AC, Tsironis L, Tselepis AD, Stamatis H (2006) Use of ionic liquids as media for the biocatalytic preparation of flavonoid derivatives with antioxidant potency. J Biotechnol 123:491–503. doi:10.1016/j.jbiotec.2005.12.022
-
(2006)
J Biotechnol
, vol.123
, pp. 491-503
-
-
Katsoura, M.H.1
Polydera, A.C.2
Tsironis, L.3
Tselepis, A.D.4
Stamatis, H.5
-
73
-
-
70349547372
-
Enzymatic synthesis and characterization of palm-based kojic acid ester
-
COI: 1:CAS:528:DC%2BD1cXhtValt7%2FM
-
Khamaruddin NH, Basri M, Lian GEC, Salleh AB, Abdul-Rahman RNZR, Ariff A, Mohamad R, Awang R (2008) Enzymatic synthesis and characterization of palm-based kojic acid ester. J Oil Palm Res 20:461–469
-
(2008)
J Oil Palm Res
, vol.20
, pp. 461-469
-
-
Khamaruddin, N.H.1
Basri, M.2
Lian, G.E.C.3
Salleh, A.B.4
Abdul-Rahman, R.N.Z.R.5
Ariff, A.6
Mohamad, R.7
Awang, R.8
-
74
-
-
84946498102
-
Enzyme catalyzed synthesis of cosmetic esters and its intensification: a review
-
COI: 1:CAS:528:DC%2BC2MXhsVGnt73N
-
Khan NR, Rathod VK (2015) Enzyme catalyzed synthesis of cosmetic esters and its intensification: a review. Process Biochem 50:1793–1806. doi:10.1016/j.procbio.2015.07.014
-
(2015)
Process Biochem
, vol.50
, pp. 1793-1806
-
-
Khan, N.R.1
Rathod, V.K.2
-
75
-
-
0023783751
-
Detergentless microemulsions as media for enzymatic reactions
-
COI: 1:STN:280:DyaL1czivFSkug%3D%3D, PID: 3166425
-
Khmelnitsky YL, Hilhorst R, Veeger C (1988) Detergentless microemulsions as media for enzymatic reactions. Eur J Biochem 176:265–271
-
(1988)
Eur J Biochem
, vol.176
, pp. 265-271
-
-
Khmelnitsky, Y.L.1
Hilhorst, R.2
Veeger, C.3
-
76
-
-
61949141678
-
Green enzymatic synthesis of L-ascorbyl fatty acid ester: an antioxidant
-
COI: 1:CAS:528:DC%2BD1MXjsVWrt7o%3D
-
Kidwai M, Mothsra P, Gupta N, Jumar SS, Gupta R (2009) Green enzymatic synthesis of L-ascorbyl fatty acid ester: an antioxidant. Synth Commun 39:1143–1151. doi:10.1080/00397910802513045
-
(2009)
Synth Commun
, vol.39
, pp. 1143-1151
-
-
Kidwai, M.1
Mothsra, P.2
Gupta, N.3
Jumar, S.S.4
Gupta, R.5
-
77
-
-
84864610361
-
Synthesis of highly water-soluble feruloyl diglycerols by esterification of an Aspergillus niger feruloyl esterase
-
COI: 1:CAS:528:DC%2BC38XhtVegtbbM, PID: 22526804
-
Kikugawa M, Tsuchiyama M, Kai K, Sakamoto T (2012) Synthesis of highly water-soluble feruloyl diglycerols by esterification of an Aspergillus niger feruloyl esterase. Appl Microbiol Biotechnol 95:615–622. doi:10.1007/s00253-012-4056-6
-
(2012)
Appl Microbiol Biotechnol
, vol.95
, pp. 615-622
-
-
Kikugawa, M.1
Tsuchiyama, M.2
Kai, K.3
Sakamoto, T.4
-
78
-
-
82455209023
-
Glucosylation of the flavonoid, astragalin by Leuconostoc mesenteroides B-512FMCM dextransucrease acceptor reactions and characterization of the products
-
COI: 1:CAS:528:DC%2BC3MXhsFOhtbzI
-
Kim GE, Kang HK, Seo ES, Jung SH, Park JS, Kim DH, Kim DW, Ahn SA, Sunwoo C, Kim D (2012) Glucosylation of the flavonoid, astragalin by Leuconostoc mesenteroides B-512FMCM dextransucrease acceptor reactions and characterization of the products. Enzym Microb Technol 50:50–56. doi:10.1016/j.enzmictec
-
(2012)
Enzym Microb Technol
, vol.50
, pp. 50-56
-
-
Kim, G.E.1
Kang, H.K.2
Seo, E.S.3
Jung, S.H.4
Park, J.S.5
Kim, D.H.6
Kim, D.W.7
Ahn, S.A.8
Sunwoo, C.9
Kim, D.10
-
79
-
-
84978165741
-
Chapter 1. Cosmeceuticals from marine resources: prospects and commercial trends
-
Kim S-K, CRC Press, Taylor & Francis Group, New York 9781439860281
-
Kim SK, Wijesekara I (2012) Chapter 1. Cosmeceuticals from marine resources: prospects and commercial trends. In: Kim S-K (ed) Marine cosmeceuticals—trends and prospects. CRC Press, Taylor & Francis Group, New York ISBN 9781439860281
-
(2012)
Marine cosmeceuticals—trends and prospects
-
-
Kim, S.K.1
Wijesekara, I.2
-
80
-
-
0035805434
-
Lipase catalyzed synthesis of organic acid esters of lactic acid in non-aqueous media
-
COI: 1:CAS:528:DC%2BD3MXitF2ltbo%3D, PID: 11278035
-
Kiran KR, Divakar S (2001) Lipase catalyzed synthesis of organic acid esters of lactic acid in non-aqueous media. J Biotechnol 87:109–121. doi:10.1016/S0168-1656(01)00242-5
-
(2001)
J Biotechnol
, vol.87
, pp. 109-121
-
-
Kiran, K.R.1
Divakar, S.2
-
81
-
-
0032927533
-
Selective enzymatic preparation of vinyl sugar esters using DMSO as a denaturing co-solvent
-
COI: 1:CAS:528:DyaK1MXjs1Ols7k%3D
-
Kitagawa M, Fan H, Raku T, Shibatani S, Maekawa Y, Hiraguri Y, et al. (1999) Selective enzymatic preparation of vinyl sugar esters using DMSO as a denaturing co-solvent. Biotechnol Lett 21:355–359. doi:10.1023/A:1005451009804
-
(1999)
Biotechnol Lett
, vol.21
, pp. 355-359
-
-
Kitagawa, M.1
Fan, H.2
Raku, T.3
Shibatani, S.4
Maekawa, Y.5
Hiraguri, Y.6
-
82
-
-
0000630613
-
Enzymatic syntheses of two stable (−)-epigallocatechin gallate-glucosides by sucrose phosphorylase
-
COI: 1:CAS:528:DyaK2MXpslyhtrk%3D
-
Kitao S, Matsudo T, Saitoh M, Horiuchi T, Sekine H (1995) Enzymatic syntheses of two stable (−)-epigallocatechin gallate-glucosides by sucrose phosphorylase. Biosci Biotechnol Biochem 59:2167–2169. doi:10.1271/bbb.59.2167
-
(1995)
Biosci Biotechnol Biochem
, vol.59
, pp. 2167-2169
-
-
Kitao, S.1
Matsudo, T.2
Saitoh, M.3
Horiuchi, T.4
Sekine, H.5
-
83
-
-
0028095950
-
a-D-glycosyl transfer of phenolic compounds by sucrose phosphorylase from Leuconostoc mesenteroides and production of a-arbutin
-
COI: 1:CAS:528:DyaK2cXitFWhu70%3D, PID: 27315703
-
Kitao S, Sekine H (1994) a-D-glycosyl transfer of phenolic compounds by sucrose phosphorylase from Leuconostoc mesenteroides and production of a-arbutin. Biosci Biotechnol Biochem 58:38–42. doi:10.1271/bbb.58.38
-
(1994)
Biosci Biotechnol Biochem
, vol.58
, pp. 38-42
-
-
Kitao, S.1
Sekine, H.2
-
84
-
-
85008131320
-
Syntheses of two kojic acid glucosides with sucrose phosphorylase from Leuconostoc mesenteroides
-
COI: 1:CAS:528:DyaK2cXivFaks7w%3D
-
Kitao S, Serine H (1994) Syntheses of two kojic acid glucosides with sucrose phosphorylase from Leuconostoc mesenteroides. Biosci Biotechnol Biochem 58:419–420. doi:10.1271/bbb.58.419
-
(1994)
Biosci Biotechnol Biochem
, vol.58
, pp. 419-420
-
-
Kitao, S.1
Serine, H.2
-
85
-
-
0035174413
-
Semi-continuous production of lauroyl kojic acid through lipase-catalyzed condensation in acetonitrile
-
COI: 1:CAS:528:DC%2BD3MXot1OksLw%3D
-
Kobayashi T, Adachi S, Nakanishi K, Matsuno R (2001) Semi-continuous production of lauroyl kojic acid through lipase-catalyzed condensation in acetonitrile. J Biochem Eng 9:85–89. doi:10.1016/S1369-703X(01)00129-2
-
(2001)
J Biochem Eng
, vol.9
, pp. 85-89
-
-
Kobayashi, T.1
Adachi, S.2
Nakanishi, K.3
Matsuno, R.4
-
86
-
-
79551478887
-
Potential applications of laccase-mediated coupling and grafting reactions: a review
-
COI: 1:CAS:528:DC%2BC3MXhs1agtbk%3D
-
Kudanga T, Nyanhongo GS, Guebitz GM, Burton S (2011) Potential applications of laccase-mediated coupling and grafting reactions: a review. Enzym Microb Technol 48:195–208. doi:10.1016/j.enzmictec.2010.11.007
-
(2011)
Enzym Microb Technol
, vol.48
, pp. 195-208
-
-
Kudanga, T.1
Nyanhongo, G.S.2
Guebitz, G.M.3
Burton, S.4
-
87
-
-
79952444316
-
Synthesis of 3-cyclohexylpropyl caffeate from 5-caffeoylquinic acid with consecutive enzymatic conversions in ionic liquid
-
COI: 1:CAS:528:DC%2BC3MXjsFaitLc%3D
-
Kurata A, Takemoto S, Fujita T, Iwai K, Furusawa M, Kishimoto N (2011) Synthesis of 3-cyclohexylpropyl caffeate from 5-caffeoylquinic acid with consecutive enzymatic conversions in ionic liquid. J Mol Catal B Enzym 69:161–167. doi:10.1016/j.molcatb.2011.01.012
-
(2011)
J Mol Catal B Enzym
, vol.69
, pp. 161-167
-
-
Kurata, A.1
Takemoto, S.2
Fujita, T.3
Iwai, K.4
Furusawa, M.5
Kishimoto, N.6
-
88
-
-
0347285469
-
Laccase-catalyzed synthesis and antioxidant property of poly (catechin)
-
COI: 1:CAS:528:DC%2BD2cXjvVOhsw%3D%3D
-
Kurisawa M, Chung J, Uyama H, Kobayashi S (2003a) Laccase-catalyzed synthesis and antioxidant property of poly (catechin). Macromol Biosci 3:758–764. doi:10.1002/mabi.200300038
-
(2003)
Macromol Biosci
, vol.3
, pp. 758-764
-
-
Kurisawa, M.1
Chung, J.2
Uyama, H.3
Kobayashi, S.4
-
89
-
-
0141615053
-
Enzymatic synthesis and antioxidant properties of poly (rutin)
-
COI: 1:CAS:528:DC%2BD3sXmt1eisrk%3D
-
Kurisawa M, Chung JE, Uyama H, Kobayashi S (2003b) Enzymatic synthesis and antioxidant properties of poly (rutin). Biomacromoles 4:1394–1399. doi:10.1021/bm034136b
-
(2003)
Biomacromoles
, vol.4
, pp. 1394-1399
-
-
Kurisawa, M.1
Chung, J.E.2
Uyama, H.3
Kobayashi, S.4
-
90
-
-
33847712180
-
Transglycosylation of ascorbic acid to ascorbic acid 2-glucoside by a recombinant sucrose phosphorylase feorm Bifidobacterium longum
-
COI: 1:CAS:528:DC%2BD2sXis1ekurg%3D, PID: 17216298
-
Kwon T, Kim CT, Lee JH (2007) Transglycosylation of ascorbic acid to ascorbic acid 2-glucoside by a recombinant sucrose phosphorylase feorm Bifidobacterium longum. Biotechnol Lett 29:611–615. doi:10.1007/s10529-006-9285-2
-
(2007)
Biotechnol Lett
, vol.29
, pp. 611-615
-
-
Kwon, T.1
Kim, C.T.2
Lee, J.H.3
-
91
-
-
84879685363
-
Enzymatic synthesis of kojic acid esters and their potential industrial applications
-
COI: 1:CAS:528:DC%2BC3sXkt1GrtrY%3D
-
Lajis AFB, Basir M, Mohamad R, Hamid M, Ashari SE, Ishak N, Zookiflie A, Ariff AB (2013) Enzymatic synthesis of kojic acid esters and their potential industrial applications. Chem Pap 67:573–585. doi:10.2478/s11696-013-0336-6
-
(2013)
Chem Pap
, vol.67
, pp. 573-585
-
-
Lajis, A.F.B.1
Basir, M.2
Mohamad, R.3
Hamid, M.4
Ashari, S.E.5
Ishak, N.6
Zookiflie, A.7
Ariff, A.B.8
-
92
-
-
84871836075
-
Depigmenting effect of kojic acid esters in hyperpigmented B16F1 melanoma cells
-
PID: 23091364
-
Lajis AFB, Hamid M, Ariff AB (2012) Depigmenting effect of kojic acid esters in hyperpigmented B16F1 melanoma cells. J Biomed Biotechnol 2012:952452. doi:10.1155/2012/952452
-
(2012)
J Biomed Biotechnol
, vol.2012
, pp. 952452
-
-
Lajis, A.F.B.1
Hamid, M.2
Ariff, A.B.3
-
93
-
-
0027420545
-
Enzyme mediated regioprotection-deprotection of hydroxyl groups in (+)-catechin
-
Lambusta D, Nicolosi G, Patty A, Piattelli M (1993) Enzyme mediated regioprotection-deprotection of hydroxyl groups in (+)-catechin. Synthesis 11:1155–1158. doi:10.1055/s-1993-26019
-
(1993)
Synthesis
, vol.11
, pp. 1155-1158
-
-
Lambusta, D.1
Nicolosi, G.2
Patty, A.3
Piattelli, M.4
-
94
-
-
33749856055
-
Enzymatic glycerolysis and transesterification of vegetable oil for enhanced production of feruloylated glycerols
-
COI: 1:CAS:528:DC%2BD28Xht12ht7zO
-
Laszlo JA, Compton DL (2006) Enzymatic glycerolysis and transesterification of vegetable oil for enhanced production of feruloylated glycerols. JAOCS 83:765–770
-
(2006)
JAOCS
, vol.83
, pp. 765-770
-
-
Laszlo, J.A.1
Compton, D.L.2
-
95
-
-
84865112001
-
Anti-inflammatory effects of arbutin in lipopolysaccharide-stimulated BV2 microglial cells
-
COI: 1:CAS:528:DC%2BC38XhtVelsb%2FI, PID: 22487852
-
Lee HJ, Kim JW (2012) Anti-inflammatory effects of arbutin in lipopolysaccharide-stimulated BV2 microglial cells. Inflamm Res 61:817–825. doi:10.1007/s00011-012-0474-02
-
(2012)
Inflamm Res
, vol.61
, pp. 817-825
-
-
Lee, H.J.1
Kim, J.W.2
-
96
-
-
84923571286
-
Highly efficient and regioselective synthesis of dihydromyricetinesters by immobilized lipase
-
COI: 1:CAS:528:DC%2BC2MXjtFGnu70%3D, PID: 25701177
-
Li W, Wu H, Liu B, Hou X, Wan D, Lou W, Zhao J (2015) Highly efficient and regioselective synthesis of dihydromyricetinesters by immobilized lipase. J Biotechnol 199:31–37. doi:10.1016/j.jbiotec.2015.02.012
-
(2015)
J Biotechnol
, vol.199
, pp. 31-37
-
-
Li, W.1
Wu, H.2
Liu, B.3
Hou, X.4
Wan, D.5
Lou, W.6
Zhao, J.7
-
97
-
-
0032202366
-
Lipase-catalyzed synthesis of kojic acid esters in organic solvents
-
COI: 1:CAS:528:DyaK1cXnvFOkt7o%3D
-
Liu KJ, Shaw JF (1998) Lipase-catalyzed synthesis of kojic acid esters in organic solvents. JAOCS 75:1507–1511
-
(1998)
JAOCS
, vol.75
, pp. 1507-1511
-
-
Liu, K.J.1
Shaw, J.F.2
-
98
-
-
84944158230
-
Lipase-catalyzed regioselective synthesis of flavone C-glucosides esters and high-efficiency oil-soluble antioxidant of bamboo leaves
-
COI: 1:CAS:528:DC%2BC2MXltFWksr0%3D
-
Liu L, Pang M, Zhang Y (2015) Lipase-catalyzed regioselective synthesis of flavone C-glucosides esters and high-efficiency oil-soluble antioxidant of bamboo leaves. Eur J Lipid Sci Technol 117:1636–1646. doi:10.1002/ejlt.201400541
-
(2015)
Eur J Lipid Sci Technol
, vol.117
, pp. 1636-1646
-
-
Liu, L.1
Pang, M.2
Zhang, Y.3
-
99
-
-
84863783401
-
Cloning, expression and characterization of a lipase gene from the Candida antarctica ZJB09193 and its application in biosynthesis of vitamin A esters
-
COI: 1:CAS:528:DC%2BC38XhtVShtLjI, PID: 22281522
-
Liu ZQ, Zheng XB, Zhang SP, Zheng YG (2012) Cloning, expression and characterization of a lipase gene from the Candida antarctica ZJB09193 and its application in biosynthesis of vitamin A esters. Microbiol Res 167:452–460. doi:10.1016/j.micres.2011.12.004
-
(2012)
Microbiol Res
, vol.167
, pp. 452-460
-
-
Liu, Z.Q.1
Zheng, X.B.2
Zhang, S.P.3
Zheng, Y.G.4
-
100
-
-
77954086889
-
Effect of room temperature ionic liquid structure on the enzymatic acylation of flavonoids
-
COI: 1:CAS:528:DC%2BC3cXosV2gsbo%3D
-
Lue BM, Guo Z, Xu X (2010) Effect of room temperature ionic liquid structure on the enzymatic acylation of flavonoids. Process Biochem 45:1375–1382. doi:10.1016/j.procbio.2010.05.024
-
(2010)
Process Biochem
, vol.45
, pp. 1375-1382
-
-
Lue, B.M.1
Guo, Z.2
Xu, X.3
-
101
-
-
84886055554
-
Controllable regioselective acylation of flavonoids catalyzed by lipase in microreactors
-
COI: 1:CAS:528:DC%2BC3sXhs1amurbF
-
Luo XP, Du LH, He F, Zhou CH (2013) Controllable regioselective acylation of flavonoids catalyzed by lipase in microreactors. J Carbohydr Chem 32:450–462. doi:10.1080/07328303.2013.843095
-
(2013)
J Carbohydr Chem
, vol.32
, pp. 450-462
-
-
Luo, X.P.1
Du, L.H.2
He, F.3
Zhou, C.H.4
-
102
-
-
39749155042
-
Study of lipase-catalysed synthesis of ascorbyl benzoate in cyclohexanone using response surface methodology
-
COI: 1:CAS:528:DC%2BD1cXivFekt7g%3D
-
Lv LX, Chen SY, Li YQ (2008) Study of lipase-catalysed synthesis of ascorbyl benzoate in cyclohexanone using response surface methodology. J Sci Food Agric 88:659–666. doi:10.1002/jsfa.3132
-
(2008)
J Sci Food Agric
, vol.88
, pp. 659-666
-
-
Lv, L.X.1
Chen, S.Y.2
Li, Y.Q.3
-
103
-
-
51449084024
-
Lipoic acid as an anti-inflammatory and neuroprotective treatment for Azheimer’s disease
-
COI: 1:CAS:528:DC%2BD1cXhtFWltbnF, PID: 18655815
-
Maczurek A, Hager K, Kenklies M, Sharman M, Martins R, Engel J, Carlson DA, Munch G (2008) Lipoic acid as an anti-inflammatory and neuroprotective treatment for Azheimer’s disease. Adv Drug Deliv Rev 60:1463–1470. doi:10.1016/j.addr.2008.04.015
-
(2008)
Adv Drug Deliv Rev
, vol.60
, pp. 1463-1470
-
-
Maczurek, A.1
Hager, K.2
Kenklies, M.3
Sharman, M.4
Martins, R.5
Engel, J.6
Carlson, D.A.7
Munch, G.8
-
104
-
-
84883331597
-
Regioselective glycosylation of hydroquinone to α-arbutin by cyclodextrin glucanotransferase from Thermoanaerobacter sp
-
COI: 1:CAS:528:DC%2BC3sXhsFOgurrN
-
Mathew S, Adlercreutz P (2013) Regioselective glycosylation of hydroquinone to α-arbutin by cyclodextrin glucanotransferase from Thermoanaerobacter sp. Biochem Eng J 79:187–193. doi:10.1016/j.bej.2013.08.001
-
(2013)
Biochem Eng J
, vol.79
, pp. 187-193
-
-
Mathew, S.1
Adlercreutz, P.2
-
105
-
-
45749115459
-
Continuous synthesis of glyceryl ferulate using immobilized Candida antarctica lipase
-
COI: 1:CAS:528:DC%2BD1cXotVelsrY%3D, PID: 18536506
-
Matsuo T, Kobayashi T, Kimura Y, Hosoda A, Taniguchi H, Adachi S (2008) Continuous synthesis of glyceryl ferulate using immobilized Candida antarctica lipase. J Oleo Sci 57:375–380
-
(2008)
J Oleo Sci
, vol.57
, pp. 375-380
-
-
Matsuo, T.1
Kobayashi, T.2
Kimura, Y.3
Hosoda, A.4
Taniguchi, H.5
Adachi, S.6
-
106
-
-
0034681557
-
Enzymatic synthesis of derivatives of vitamin A in organic media
-
COI: 1:CAS:528:DC%2BD3cXhsFGqsL0%3D
-
Maugard T, Legoy MD (2000) Enzymatic synthesis of derivatives of vitamin A in organic media. J Mol Catal B Enzym 8:275–280. doi:10.1016/S1381-1177(99)00078-8
-
(2000)
J Mol Catal B Enzym
, vol.8
, pp. 275-280
-
-
Maugard, T.1
Legoy, M.D.2
-
107
-
-
79960043851
-
Enzymatic synthesis of lipophilic rutin and vanillyl esters from fish byproducts
-
COI: 1:CAS:528:DC%2BC3MXntlOms70%3D, PID: 21630661
-
Mbatia B, Kaki SS, Mattiasson B, Mulla F, Adlercreutz P (2011) Enzymatic synthesis of lipophilic rutin and vanillyl esters from fish byproducts. J Agric Food Chem 59:7021–7027. doi:10.1021/jf200867r
-
(2011)
J Agric Food Chem
, vol.59
, pp. 7021-7027
-
-
Mbatia, B.1
Kaki, S.S.2
Mattiasson, B.3
Mulla, F.4
Adlercreutz, P.5
-
108
-
-
13544259806
-
Biocatalytic preparation of acylated derivatives of flavonoid glycosides enhances their antioxidant and antimicrobial activity
-
COI: 1:CAS:528:DC%2BD2MXhtFOntro%3D, PID: 15707690
-
Mellou F, Lazari D, Skaltsa H, Tselepis AD, Kolisis FN, Stamatis H (2005) Biocatalytic preparation of acylated derivatives of flavonoid glycosides enhances their antioxidant and antimicrobial activity. J Biotechnol 116:295–304
-
(2005)
J Biotechnol
, vol.116
, pp. 295-304
-
-
Mellou, F.1
Lazari, D.2
Skaltsa, H.3
Tselepis, A.D.4
Kolisis, F.N.5
Stamatis, H.6
-
109
-
-
33746558608
-
Enzymatic esterification of flavonoids with unsaturated fatty acids: effect of the novel esters on vascular endothelial growth factor release from K562 cells
-
COI: 1:CAS:528:DC%2BD28XnsFylsL8%3D
-
Mellou F, Loutrari H, Stamatis H, Roussos C, Kolisis FN (2006) Enzymatic esterification of flavonoids with unsaturated fatty acids: effect of the novel esters on vascular endothelial growth factor release from K562 cells. Process Biochem 41:2029–2034. doi:10.1016/j.procbio.2006.05.002
-
(2006)
Process Biochem
, vol.41
, pp. 2029-2034
-
-
Mellou, F.1
Loutrari, H.2
Stamatis, H.3
Roussos, C.4
Kolisis, F.N.5
-
110
-
-
61449194088
-
Fungal laccases as tools for the synthesis of new hybrid molecules and biomaterials
-
COI: 1:CAS:528:DC%2BD1MXisVWkurg%3D, PID: 19183983
-
Mikolasch A, Schauer F (2009) Fungal laccases as tools for the synthesis of new hybrid molecules and biomaterials. Appl Microbiol Biotechnol 82:605–624. doi:10.1007/s00253-009-1869-z
-
(2009)
Appl Microbiol Biotechnol
, vol.82
, pp. 605-624
-
-
Mikolasch, A.1
Schauer, F.2
-
111
-
-
84908565425
-
Lipase-catalyzed esterification of phloridzin: acyl donor effect on enzymatic affinity and antioxidant properties of esters
-
Milisavljecic A, Stojanovic M, Carevic M, Mihailovic M, Velickoviz D, Milosavic N, Bezbradica D (2014) Lipase-catalyzed esterification of phloridzin: acyl donor effect on enzymatic affinity and antioxidant properties of esters. Ind Eng Chem Res 53(43):16644–16651. doi:10.1021/ie5027259
-
(2014)
Ind Eng Chem Res
, vol.53
, Issue.43
, pp. 16644-16651
-
-
Milisavljecic, A.1
Stojanovic, M.2
Carevic, M.3
Mihailovic, M.4
Velickoviz, D.5
Milosavic, N.6
Bezbradica, D.7
-
112
-
-
34548409004
-
A simple and efficient one-step, regioselective, enzymatic glucosylation of arbutin by α-glucosidase
-
Milosavić NB, Prodanović RM, Jankov RM (2007) A simple and efficient one-step, regioselective, enzymatic glucosylation of arbutin by α-glucosidase. Tetrahedron Lett 48:7222–7224. doi:10.1016/j.tetlet.2007.07.152
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 7222-7224
-
-
Milosavić, N.B.1
Prodanović, R.M.2
Jankov, R.M.3
-
113
-
-
33644872994
-
Synthesis, structure analyses and characterization of novel epigallocatechin gallate (EGCG) glycosides using a glucansucrase from Leuconostoc mesenteroides B-129CB
-
COI: 1:CAS:528:DC%2BD28XmtF2ksQ%3D%3D, PID: 16478241
-
Moon YH, Lee JH, Ahn JS, Nam SH, Oh DK, Park DH, Chung HJ, Kang S, Day DF, Kim D (2006a) Synthesis, structure analyses and characterization of novel epigallocatechin gallate (EGCG) glycosides using a glucansucrase from Leuconostoc mesenteroides B-129CB. J Agric Food Chem 54:1230–1237. doi:10.1021/jf052359i
-
(2006)
J Agric Food Chem
, vol.54
, pp. 1230-1237
-
-
Moon, Y.H.1
Lee, J.H.2
Ahn, J.S.3
Nam, S.H.4
Oh, D.K.5
Park, D.H.6
Chung, H.J.7
Kang, S.8
Day, D.F.9
Kim, D.10
-
114
-
-
33847645045
-
Synthesis and characterization of novel quercetin-a-D-glucopyranosides using glucansucrase from Leuconostoc mesenteroides
-
COI: 1:CAS:528:DC%2BD2sXisl2ltbY%3D
-
Moon YH, Lee JH, Jhon DY, Jun WJ, Kang SS, Sim J, Choi H, Moon JH, Kim D (2007b) Synthesis and characterization of novel quercetin-a-D-glucopyranosides using glucansucrase from Leuconostoc mesenteroides. Enzym Microb Technol 40:1124–1129. doi:10.1016/j.enzmictec.2006.08.019
-
(2007)
Enzym Microb Technol
, vol.40
, pp. 1124-1129
-
-
Moon, Y.H.1
Lee, J.H.2
Jhon, D.Y.3
Jun, W.J.4
Kang, S.S.5
Sim, J.6
Choi, H.7
Moon, J.H.8
Kim, D.9
-
115
-
-
36248977079
-
Enzymatic synthesis and characterization of arbutin glucosides using glucansucrase from Leuconostoc mesenteroides B-1299CB
-
COI: 1:CAS:528:DC%2BD2sXht12ktL3L, PID: 17917726
-
Moon YM, Nam SH, Kang J, Kim YM, Lee JH, Kang HK, Breton V, Jun WJ, Park KD, Kimura A, Kim D (2007a) Enzymatic synthesis and characterization of arbutin glucosides using glucansucrase from Leuconostoc mesenteroides B-1299CB. Appl Microbiol Biotechnol 77:559–567. doi:10.1007/s00253-007-1202-7
-
(2007)
Appl Microbiol Biotechnol
, vol.77
, pp. 559-567
-
-
Moon, Y.M.1
Nam, S.H.2
Kang, J.3
Kim, Y.M.4
Lee, J.H.5
Kang, H.K.6
Breton, V.7
Jun, W.J.8
Park, K.D.9
Kimura, A.10
Kim, D.11
-
116
-
-
84881008449
-
Synthesis of ascrobyl oleate by transesterification of olive oil wih ascorbic acid in polar organic media catalyzed by immobilized lipases
-
COI: 1:CAS:528:DC%2BC3sXhsVWju7vF, PID: 23891831
-
Moreno-Perez S, Filice M, Guisan JM, Fernandez-Lorente G (2013) Synthesis of ascrobyl oleate by transesterification of olive oil wih ascorbic acid in polar organic media catalyzed by immobilized lipases. Chem Phys Lipids 174:48–54. doi:10.1016/j.chemphyslip.2013.06.003
-
(2013)
Chem Phys Lipids
, vol.174
, pp. 48-54
-
-
Moreno-Perez, S.1
Filice, M.2
Guisan, J.M.3
Fernandez-Lorente, G.4
-
117
-
-
0019870682
-
Regulation of collagen synthesis by ascorbic acid
-
COI: 1:CAS:528:DyaL3MXkt1Wqsrg%3D, PID: 6265920
-
Murad S, Grove D, Lindberg KA, Reynolds G, Sivarajah A, Pinnell SR (1981) Regulation of collagen synthesis by ascorbic acid. Proc Natl Acad Sci U S A 78:2879–2882
-
(1981)
Proc Natl Acad Sci U S A
, vol.78
, pp. 2879-2882
-
-
Murad, S.1
Grove, D.2
Lindberg, K.A.3
Reynolds, G.4
Sivarajah, A.5
Pinnell, S.R.6
-
118
-
-
0031963932
-
Antioxidant activity of a novel vitamin E derivative, 2-(α-L-glucopyranosyl) methyl-2, 5, 7, 8-tetramethylchroman-6-ol
-
COI: 1:CAS:528:DyaK2sXotVSjsLg%3D, PID: 9433895
-
Murase H, Moon JH, Yamauchi R, Kato K, Kunieda T, Yoshikawa T, Terao J (1998) Antioxidant activity of a novel vitamin E derivative, 2-(α-L-glucopyranosyl) methyl-2, 5, 7, 8-tetramethylchroman-6-ol. Free Radic Biol Med 24:217–225. doi:10.1016/S0891-5849(97)00221-9
-
(1998)
Free Radic Biol Med
, vol.24
, pp. 217-225
-
-
Murase, H.1
Moon, J.H.2
Yamauchi, R.3
Kato, K.4
Kunieda, T.5
Yoshikawa, T.6
Terao, J.7
-
119
-
-
72949091842
-
Synthesis of acyl arbutin by an immobilized lipase and its suppressive ability against lipid oxidation in a bulk system and O/W emulsion
-
COI: 1:CAS:528:DC%2BC3cXis1OgsQ%3D%3D, PID: 19897895
-
Nagai M, Watanabe Y, Nomura M (2009) Synthesis of acyl arbutin by an immobilized lipase and its suppressive ability against lipid oxidation in a bulk system and O/W emulsion. Biosci Biotechnol Biochem 73:2501–2505
-
(2009)
Biosci Biotechnol Biochem
, vol.73
, pp. 2501-2505
-
-
Nagai, M.1
Watanabe, Y.2
Nomura, M.3
-
120
-
-
0029018665
-
Glycosyltransferase from Streptococcus sobrinus catalyzes glycosylation of catechin
-
COI: 1:CAS:528:DyaK2MXms1GrsL8%3D, PID: 16535083
-
Nakahara K, Kontani M, Ono H, Kodama T, Tanaka T, Ooshima T, Hamada S (1995) Glycosyltransferase from Streptococcus sobrinus catalyzes glycosylation of catechin. Appl Environ Microbiol 61:2768–2770
-
(1995)
Appl Environ Microbiol
, vol.61
, pp. 2768-2770
-
-
Nakahara, K.1
Kontani, M.2
Ono, H.3
Kodama, T.4
Tanaka, T.5
Ooshima, T.6
Hamada, S.7
-
121
-
-
61649104375
-
Lipase-catalyzed regioselective protection/deprotection of hydroxyl groups of the isoflavone irilone isolated from Iris germanica
-
COI: 1:CAS:528:DC%2BD1MXjtVyitrg%3D
-
Nazir N, Koul S, Qurishi MA, Taneja SC, Qazi GN (2009) Lipase-catalyzed regioselective protection/deprotection of hydroxyl groups of the isoflavone irilone isolated from Iris germanica. Biocatal Biotransfor 27:118–123. doi:10.1080/10242420802583457
-
(2009)
Biocatal Biotransfor
, vol.27
, pp. 118-123
-
-
Nazir, N.1
Koul, S.2
Qurishi, M.A.3
Taneja, S.C.4
Qazi, G.N.5
-
122
-
-
33845929196
-
Oxidation of 8-hydroxyquinoline catalyzed by laccase from Trametes pubescens yields an antioxidant aromatic polymer
-
COI: 1:CAS:528:DC%2BD2sXisVGltg%3D%3D
-
Ncanana S, Burton S (2007) Oxidation of 8-hydroxyquinoline catalyzed by laccase from Trametes pubescens yields an antioxidant aromatic polymer. J Mol Catal B Enzym 44:66–71. doi:10.1016/j.molcatb.2006.09.005
-
(2007)
J Mol Catal B Enzym
, vol.44
, pp. 66-71
-
-
Ncanana, S.1
Burton, S.2
-
123
-
-
0024259723
-
Cosmetics: content and function
-
COI: 1:STN:280:DyaL1M7ntlGisw%3D%3D, PID: 2976745
-
Nelson FP, Rumsfield J (1988) Cosmetics: content and function. Int J Dermatol 27:665–672
-
(1988)
Int J Dermatol
, vol.27
, pp. 665-672
-
-
Nelson, F.P.1
Rumsfield, J.2
-
124
-
-
0346964455
-
Biotransformation of resveratrol: synthesis of trans-dehydrodimers catalyzed by laccases from Myceliophtora thermophyla and from Trametes pubescens
-
COI: 1:CAS:528:DC%2BD3sXhtVWgsrzI
-
Nicotra S, Cramarossa MR, Mucci A, Pagnoni UM, Riva S, Forti L (2004) Biotransformation of resveratrol: synthesis of trans-dehydrodimers catalyzed by laccases from Myceliophtora thermophyla and from Trametes pubescens. Tetrahedron 60:595–600. doi:10.1016/j.tet.2003.10.117
-
(2004)
Tetrahedron
, vol.60
, pp. 595-600
-
-
Nicotra, S.1
Cramarossa, M.R.2
Mucci, A.3
Pagnoni, U.M.4
Riva, S.5
Forti, L.6
-
125
-
-
84863513151
-
Synthesis of propyl gallate from tannic acid catalyzed by tannase from Aspergillus oryzae: process optimization of transesterification in anhydrous media
-
COI: 1:CAS:528:DC%2BC38XhtF2ht7rL
-
Nie G, Liu H, Chen Z, Wang P, Zhao G, Zheng Z (2012b) Synthesis of propyl gallate from tannic acid catalyzed by tannase from Aspergillus oryzae: process optimization of transesterification in anhydrous media. J Mol Catal B Enzym 82:102–108. doi:10.1016/j.molcatb.2012.06.003
-
(2012)
J Mol Catal B Enzym
, vol.82
, pp. 102-108
-
-
Nie, G.1
Liu, H.2
Chen, Z.3
Wang, P.4
Zhao, G.5
Zheng, Z.6
-
126
-
-
84862783744
-
Development of a tannase biocatalyst based on bio-imprinting for the production of propyl gallate by transesterification in organic media
-
COI: 1:CAS:528:DC%2BC38Xms12nsrg%3D
-
Nie G, Zheng Z, Jin W, Gong G, Wang L (2012a) Development of a tannase biocatalyst based on bio-imprinting for the production of propyl gallate by transesterification in organic media. J Mol Catal B Enzym 78:32–37. doi:10.1016/j.molcatb.2012.01.007
-
(2012)
J Mol Catal B Enzym
, vol.78
, pp. 32-37
-
-
Nie, G.1
Zheng, Z.2
Jin, W.3
Gong, G.4
Wang, L.5
-
127
-
-
84895067457
-
One-pot synthesis of propyl gallate by a novel whole-cell biocatalyst
-
COI: 1:CAS:528:DC%2BC3sXhvFOgtrzP
-
Nie G, Zheng Z, Yue W, Liu Y, Liu H, Wang P, Zhao G, Cai W, Xue Z (2014) One-pot synthesis of propyl gallate by a novel whole-cell biocatalyst. Process Biochem 49:277–282. doi:10.1016/j.procbio.2013.11.009
-
(2014)
Process Biochem
, vol.49
, pp. 277-282
-
-
Nie, G.1
Zheng, Z.2
Yue, W.3
Liu, Y.4
Liu, H.5
Wang, P.6
Zhao, G.7
Cai, W.8
Xue, Z.9
-
128
-
-
0027964863
-
Acceptor specificity in the glycosylation reaction of Bacillus subtilis X-23 α-amylase towards various phenolic compounds and the structure of kojic acid glucoside
-
COI: 1:CAS:528:DyaK2cXlvF2htro%3D
-
Nishimura T, Kometani T, Takii H, Terada Y, Okada S (1994) Acceptor specificity in the glycosylation reaction of Bacillus subtilis X-23 α-amylase towards various phenolic compounds and the structure of kojic acid glucoside. J Ferment Bioeng 78:37–41
-
(1994)
J Ferment Bioeng
, vol.78
, pp. 37-41
-
-
Nishimura, T.1
Kometani, T.2
Takii, H.3
Terada, Y.4
Okada, S.5
-
129
-
-
77949365784
-
Safety assessment of personal care products/cosmetics and their ingredients
-
COI: 1:CAS:528:DC%2BC3cXit1OgtL8%3D, PID: 20005888
-
Nohynek GI, Antignac E, Re T, Toutain H (2010) Safety assessment of personal care products/cosmetics and their ingredients. Toxicol Appl Pharmacol 243:239–259. doi:10.1016/j.taap.2009.12.001
-
(2010)
Toxicol Appl Pharmacol
, vol.243
, pp. 239-259
-
-
Nohynek, G.I.1
Antignac, E.2
Re, T.3
Toutain, H.4
-
130
-
-
84876320127
-
Enzymatic hybridization of α-lipoic acid with bioactive compounds in ionic solvents
-
COI: 1:CAS:528:DC%2BC3sXmvV2msbs%3D, PID: 23567667
-
Papadopoulou AA, Katsoura MH, Chatzikonstantinou A, Kyriakou E, Polydera A, Tzakos A, Stamatis H (2013) Enzymatic hybridization of α-lipoic acid with bioactive compounds in ionic solvents. Bioresour Technol 136:41–48. doi:10.1016/j.biortech.2013.02.067
-
(2013)
Bioresour Technol
, vol.136
, pp. 41-48
-
-
Papadopoulou, A.A.1
Katsoura, M.H.2
Chatzikonstantinou, A.3
Kyriakou, E.4
Polydera, A.5
Tzakos, A.6
Stamatis, H.7
-
131
-
-
0035210378
-
Lipase-catalysed synthesis of β-methylglucoside esters containing an α-hydroxy acid
-
COI: 1:CAS:528:DC%2BD38Xps1Cg
-
Park DW, Kim JS, Haam S, Kim HS, Kim WS (2001) Lipase-catalysed synthesis of β-methylglucoside esters containing an α-hydroxy acid. Biotechnol Lett 23:1947–1952
-
(2001)
Biotechnol Lett
, vol.23
, pp. 1947-1952
-
-
Park, D.W.1
Kim, J.S.2
Haam, S.3
Kim, H.S.4
Kim, W.S.5
-
132
-
-
0347720956
-
Vacuum-driven lipase-catalysed direct condensation of L-ascorbic acid and fatty acids in ionic liquids: synthesis of a natural surface active antioxidant
-
COI: 1:CAS:528:DC%2BD3sXpsFyms7k%3D
-
Park S, Viklund F, Hult K, Kazlauskas RJ (2003) Vacuum-driven lipase-catalysed direct condensation of L-ascorbic acid and fatty acids in ionic liquids: synthesis of a natural surface active antioxidant. Green Chem 5:715–719. doi:10.1039/B307715B
-
(2003)
Green Chem
, vol.5
, pp. 715-719
-
-
Park, S.1
Viklund, F.2
Hult, K.3
Kazlauskas, R.J.4
-
133
-
-
28444460239
-
Substrate specificity and transglycosylation catalyzed by a thermostable β-glucosidase from marine hyperthermophile Thermotoga neapolitana
-
COI: 1:CAS:528:DC%2BD2MXht1Gqu7jM, PID: 16082555
-
Park TH, Choi KW, Park CS, Lee SB, Kang HY, Shon KJ, Park JS, Cha J (2005) Substrate specificity and transglycosylation catalyzed by a thermostable β-glucosidase from marine hyperthermophile Thermotoga neapolitana. Appl Microbiol Biotechnol 69:411–422. doi:10.1007/s00253-005-0055-1
-
(2005)
Appl Microbiol Biotechnol
, vol.69
, pp. 411-422
-
-
Park, T.H.1
Choi, K.W.2
Park, C.S.3
Lee, S.B.4
Kang, H.Y.5
Shon, K.J.6
Park, J.S.7
Cha, J.8
-
134
-
-
3042728086
-
Regioselective acylation of flavonoids catalyzed by immobilized Candida antarctica lipase under reduced pressure
-
COI: 1:CAS:528:DC%2BD2cXltFWnu70%3D, PID: 15218382
-
Passicos E, Santarelli X, Coulon D (2004) Regioselective acylation of flavonoids catalyzed by immobilized Candida antarctica lipase under reduced pressure. Biotechnol Lett 26:1073–1076
-
(2004)
Biotechnol Lett
, vol.26
, pp. 1073-1076
-
-
Passicos, E.1
Santarelli, X.2
Coulon, D.3
-
135
-
-
0037157127
-
Efficient transesterification of sucrose catalysed by the metalloprotease thermolysin in dimethylsulfoxide
-
COI: 1:CAS:528:DC%2BD38XjvVSnu7g%3D, PID: 12023041
-
Pedersen NR, Halling PJ, Pedersen LH, Wimmer R, Matthiesen R, Veltman OR (2002) Efficient transesterification of sucrose catalysed by the metalloprotease thermolysin in dimethylsulfoxide. FEBS Lett 519:181–184. doi:10.1016/S0014-5793(02)02753-9
-
(2002)
FEBS Lett
, vol.519
, pp. 181-184
-
-
Pedersen, N.R.1
Halling, P.J.2
Pedersen, L.H.3
Wimmer, R.4
Matthiesen, R.5
Veltman, O.R.6
-
136
-
-
0037459153
-
Synthesis of sucrose laurate using a new alkaline protease
-
COI: 1:CAS:528:DC%2BD3sXhvV2gs7c%3D
-
Pedersen NR, Wimmer R, Matthiesen R, Pedersen LH, Gessesse A (2003) Synthesis of sucrose laurate using a new alkaline protease. Tetrahedron Asymmetry 14:667–673. doi:10.1016/S0957-4166(03)00086-7
-
(2003)
Tetrahedron Asymmetry
, vol.14
, pp. 667-673
-
-
Pedersen, N.R.1
Wimmer, R.2
Matthiesen, R.3
Pedersen, L.H.4
Gessesse, A.5
-
137
-
-
0347052802
-
Activity and stability of lipases in the synthesis of butyl lactate
-
COI: 1:CAS:528:DC%2BD2cXovFKk
-
Pirozzi D, Greco G Jr (2004) Activity and stability of lipases in the synthesis of butyl lactate. Enzym Microb Technol 34:94–100. doi:10.1016/j.enzmictec.2003.01.002
-
(2004)
Enzym Microb Technol
, vol.34
, pp. 94-100
-
-
Pirozzi, D.1
Greco, G.2
-
138
-
-
0032103791
-
Anatomy of lipase binding sites: the scissile fatty acid binding site
-
COI: 1:CAS:528:DyaK1cXks1Krurg%3D, PID: 9720251
-
Pleiss J, Fischer M, Schmid R (1998) Anatomy of lipase binding sites: the scissile fatty acid binding site. Chem Phys Lipids 93:67–80. doi:10.1016/S0009-3084(98)00030-9
-
(1998)
Chem Phys Lipids
, vol.93
, pp. 67-80
-
-
Pleiss, J.1
Fischer, M.2
Schmid, R.3
-
139
-
-
84880112930
-
Utilization of bahera fruits for production of tannase and gallic acid by Aspergillus heteromorphus MTCC 5466 and synthesis of propyl gallate thereof
-
COI: 1:CAS:528:DC%2BC3MXhtlCmt7%2FP
-
Prasad D, Grupt RK, Venkataratnam GS, Kamin NR, Gowthaman MK (2011) Utilization of bahera fruits for production of tannase and gallic acid by Aspergillus heteromorphus MTCC 5466 and synthesis of propyl gallate thereof. Global J Biotech Biochem 6:119–128
-
(2011)
Global J Biotech Biochem
, vol.6
, pp. 119-128
-
-
Prasad, D.1
Grupt, R.K.2
Venkataratnam, G.S.3
Kamin, N.R.4
Gowthaman, M.K.5
-
140
-
-
27644513775
-
Transglucosylation of hydroquinone catalysed by α-glucosidase from baker’s yeast
-
Prodanović R, Milosavić N, Sladić D, Zlatović M, Božić B, Veličković TĆ, Vujčić Z (2005) Transglucosylation of hydroquinone catalysed by α-glucosidase from baker’s yeast. J Mol Catal B Enzym 35:142–146. doi:10.1016/j.molcatb.2005.06.011
-
(2005)
J Mol Catal B Enzym
, vol.35
, pp. 142-146
-
-
Prodanović, R.1
Milosavić, N.2
Sladić, D.3
Zlatović, M.4
Božić, B.5
Veličković, T.Ć.6
Vujčić, Z.7
-
141
-
-
33845917513
-
Enzymatic galloylation of catechins in room temperature ionic liquids
-
COI: 1:CAS:528:DC%2BD2sXisVGlsA%3D%3D
-
Raab T, Bel-Rhid R, Williamson G, Hansen CE, Chaillot D (2007) Enzymatic galloylation of catechins in room temperature ionic liquids. J Mol Catal B Enzym 44:60–65. doi:10.1016/j.molcatb.2006.09.003
-
(2007)
J Mol Catal B Enzym
, vol.44
, pp. 60-65
-
-
Raab, T.1
Bel-Rhid, R.2
Williamson, G.3
Hansen, C.E.4
Chaillot, D.5
-
142
-
-
84978134494
-
Enzymatic synthesis of olive-based ferulate esters: optimization by response surface methodology
-
Radzi SM, Rahman NJA, Noor HM, Ariffin N (2014) Enzymatic synthesis of olive-based ferulate esters: optimization by response surface methodology. IJISR 8:762–765
-
(2014)
IJISR
, vol.8
, pp. 762-765
-
-
Radzi, S.M.1
Rahman, N.J.A.2
Noor, H.M.3
Ariffin, N.4
-
143
-
-
0038079920
-
Regioselective synthesis of kojic acid esters by Bacillus subtilis protease
-
COI: 1:CAS:528:DC%2BD3sXktlagurw%3D, PID: 12889833
-
Raku T, Tokiwa Y (2003) Regioselective synthesis of kojic acid esters by Bacillus subtilis protease. Biotechnol Lett 25:969–974. doi:10.1023/A:1024088303960
-
(2003)
Biotechnol Lett
, vol.25
, pp. 969-974
-
-
Raku, T.1
Tokiwa, Y.2
-
144
-
-
0037415313
-
Enzymatic procedures for the synthesis of water-soluble retinol derivatives in organic media
-
COI: 1:CAS:528:DC%2BD38XpvVaitLk%3D
-
Rejasse B, Maugard T, Legoy MD (2003) Enzymatic procedures for the synthesis of water-soluble retinol derivatives in organic media. Enzym Microb Technol 32:312–320. doi:10.1016/S0141-0229(02)00289-2
-
(2003)
Enzym Microb Technol
, vol.32
, pp. 312-320
-
-
Rejasse, B.1
Maugard, T.2
Legoy, M.D.3
-
145
-
-
79751535317
-
Synthesis and properties of ascorbyl esters catalyzed by lipozyme TL IM using triglycerides as acyl donors
-
COI: 1:CAS:528:DC%2BC3MXnsVyrtw%3D%3D
-
Reyes-Duarte D, Lopez-Cortes N, Torres P, Comelles F, Parra JL, Pena S, Ugidos AV, Ballesteros A, Plou FJ (2011) Synthesis and properties of ascorbyl esters catalyzed by lipozyme TL IM using triglycerides as acyl donors. J Am Oil Chem Soc 88:57–64. doi:10.1007/s11746-010-1643-5
-
(2011)
J Am Oil Chem Soc
, vol.88
, pp. 57-64
-
-
Reyes-Duarte, D.1
Lopez-Cortes, N.2
Torres, P.3
Comelles, F.4
Parra, J.L.5
Pena, S.6
Ugidos, A.V.7
Ballesteros, A.8
Plou, F.J.9
-
146
-
-
0029998244
-
A two-step efficient chemoenzymatic synthesis of flavonoid glycoside malonates
-
COI: 1:CAS:528:DyaK28Xjt1elt7s%3D, PID: 8786368
-
Riva S (1996) A two-step efficient chemoenzymatic synthesis of flavonoid glycoside malonates. J Nat Prod 59:618–621. doi:10.1021/np960239m
-
(1996)
J Nat Prod
, vol.59
, pp. 618-621
-
-
Riva, S.1
-
147
-
-
33947390465
-
Lipase-catalyzed esterification of lactic acid with straight-chain alcohols
-
COI: 1:CAS:528:DC%2BD28XntVemtQ%3D%3D
-
Roenne TH, Xu X, Tan T (2005) Lipase-catalyzed esterification of lactic acid with straight-chain alcohols. JAOCS 82:881–885
-
(2005)
JAOCS
, vol.82
, pp. 881-885
-
-
Roenne, T.H.1
Xu, X.2
Tan, T.3
-
148
-
-
33645297655
-
Lipase-catalyzed transesterification of trilinolein or trilinolenin with selected phenolic acids
-
COI: 1:CAS:528:DC%2BD28XislKnsL0%3D
-
Sabally K, Karboune S, St-Louis R, Kermasha S (2006) Lipase-catalyzed transesterification of trilinolein or trilinolenin with selected phenolic acids. JAOCS 83:101–107
-
(2006)
JAOCS
, vol.83
, pp. 101-107
-
-
Sabally, K.1
Karboune, S.2
St-Louis, R.3
Kermasha, S.4
-
149
-
-
77957020511
-
Antifungal activity of natural and enzymatically-modified flavonoids isolated from citrus species
-
COI: 1:CAS:528:DC%2BC3cXht1Sns73O
-
Salas MP, Celiz G, Geronazzo H, Daz M, Resnik SL (2011) Antifungal activity of natural and enzymatically-modified flavonoids isolated from citrus species. Food Chem 124:1411–1415. doi:10.1016/j.foodchem.2010.07.100
-
(2011)
Food Chem
, vol.124
, pp. 1411-1415
-
-
Salas, M.P.1
Celiz, G.2
Geronazzo, H.3
Daz, M.4
Resnik, S.L.5
-
150
-
-
74449093003
-
Effect of acyl donor chain length on isoquercitrin acylation and biological activities of corresponding esters
-
COI: 1:CAS:528:DC%2BC3cXhtValsrs%3D
-
Salem JH, Humeau C, Chevalot I, Harscoat-Schiavo C, Vanderesse R, Blanchard F, Fick F (2010) Effect of acyl donor chain length on isoquercitrin acylation and biological activities of corresponding esters. Process Biochem 45:382–389. doi:10.1016/j.procbio.2009.10.012
-
(2010)
Process Biochem
, vol.45
, pp. 382-389
-
-
Salem, J.H.1
Humeau, C.2
Chevalot, I.3
Harscoat-Schiavo, C.4
Vanderesse, R.5
Blanchard, F.6
Fick, F.7
-
151
-
-
0034511884
-
Alpha-anomer-selective glucosylation of (+)-catechin by the crude enzyme, showing glucosyl transfer activity, of Xanthomonas campestris WU-9701
-
COI: 1:CAS:528:DC%2BD3MXhs12nurs%3D, PID: 16232922
-
Sato T, Nakagawa H, Kurosu J, Yoshida K, Tsugane T, Shimura S, Kirimura K, Kino K, Usami S (2000) Alpha-anomer-selective glucosylation of (+)-catechin by the crude enzyme, showing glucosyl transfer activity, of Xanthomonas campestris WU-9701. J Biosci Bioeng 90:625–630
-
(2000)
J Biosci Bioeng
, vol.90
, pp. 625-630
-
-
Sato, T.1
Nakagawa, H.2
Kurosu, J.3
Yoshida, K.4
Tsugane, T.5
Shimura, S.6
Kirimura, K.7
Kino, K.8
Usami, S.9
-
152
-
-
84863824499
-
High-yield enzymatic bioconversion of hydroquinone to α-arbutin, a powerful skin lightening agent, by amylosucrase
-
COI: 1:CAS:528:DC%2BC38XntVSmtbo%3D, PID: 22314516
-
Seo DH, Jung JH, Ha SJ, Cho HK, Jung DH, Kim TJ, Baek NI, Yoo SH, Part CS (2012b) High-yield enzymatic bioconversion of hydroquinone to α-arbutin, a powerful skin lightening agent, by amylosucrase. Appl Microbiol Biotechnol 94:1189–1197. doi:10.1007/s00253-012-3905-7
-
(2012)
Appl Microbiol Biotechnol
, vol.94
, pp. 1189-1197
-
-
Seo, D.H.1
Jung, J.H.2
Ha, S.J.3
Cho, H.K.4
Jung, D.H.5
Kim, T.J.6
Baek, N.I.7
Yoo, S.H.8
Part, C.S.9
-
153
-
-
84872010432
-
Biotechnological production of arbutins (α- and β-arbutins), skin-lightening agents, and their derivatives
-
COI: 1:CAS:528:DC%2BC38Xht1Ggs7zP, PID: 22843425
-
Seo DH, Jung JH, Lee JE, Jeon EJ, Kim W, Park CS (2012a) Biotechnological production of arbutins (α- and β-arbutins), skin-lightening agents, and their derivatives. Appl Microbiol Biotechnol 95:1417–1425. doi:10.1007/s00253-012-4297-4
-
(2012)
Appl Microbiol Biotechnol
, vol.95
, pp. 1417-1425
-
-
Seo, D.H.1
Jung, J.H.2
Lee, J.E.3
Jeon, E.J.4
Kim, W.5
Park, C.S.6
-
154
-
-
69749117730
-
Synthesis and characterization of hydroquinone glucoside using Leuconostoc mesenteroides dextransucrase
-
COI: 1:CAS:528:DC%2BD1MXhtFamsrnN
-
Seo ES, Kang J, Lee JH, Kim GE, Kim GJ, Kim D (2009) Synthesis and characterization of hydroquinone glucoside using Leuconostoc mesenteroides dextransucrase. Enzym Microb Technol 45:355–360. doi:10.1016/j.enzmictec.2009.07.011
-
(2009)
Enzym Microb Technol
, vol.45
, pp. 355-360
-
-
Seo, E.S.1
Kang, J.2
Lee, J.H.3
Kim, G.E.4
Kim, G.J.5
Kim, D.6
-
155
-
-
84555218104
-
Cosmeceuticals: regulatory scenario in the US, Europe and India
-
Sharma P (2011) Cosmeceuticals: regulatory scenario in the US, Europe and India. Int J Pharm Technol 3:1512–1535
-
(2011)
Int J Pharm Technol
, vol.3
, pp. 1512-1535
-
-
Sharma, P.1
-
156
-
-
0037330573
-
Synthesis of antioxidant propyl gallate using tannase from Aspergillus niger van Teighem in nonaqueous media
-
COI: 1:CAS:528:DC%2BD3sXptFanuw%3D%3D, PID: 12565937
-
Sharma S, Gupta MN (2003) Synthesis of antioxidant propyl gallate using tannase from Aspergillus niger van Teighem in nonaqueous media. Bioorg Med Chem Lett 13:395–397. doi:10.1016/S0960-894X(02)00977-0
-
(2003)
Bioorg Med Chem Lett
, vol.13
, pp. 395-397
-
-
Sharma, S.1
Gupta, M.N.2
-
157
-
-
84902241643
-
Evaluation of the versatility of the tannases produced from Aspergillus niger and Penicillium variable with respect to gallic acid production, gallate ester synthesis, animal feed improvement, tannery effluent degradation and tannin stain removal
-
Sharma S, Saxena RK (2012) Evaluation of the versatility of the tannases produced from Aspergillus niger and Penicillium variable with respect to gallic acid production, gallate ester synthesis, animal feed improvement, tannery effluent degradation and tannin stain removal. Res Biotechnol 3:9–20
-
(2012)
Res Biotechnol
, vol.3
, pp. 9-20
-
-
Sharma, S.1
Saxena, R.K.2
-
158
-
-
62249150863
-
Transglucosylation of caffeic acid by a recombinant sucrose phosphorylase in aqueous buffer and aqueous-supercritical CO2 media
-
COI: 1:CAS:528:DC%2BD1MXjsVeitb0%3D
-
Shin MH, Cheong NY, Lee JH, Kim KH (2009) Transglucosylation of caffeic acid by a recombinant sucrose phosphorylase in aqueous buffer and aqueous-supercritical CO2 media. Food Chem 115:1028–1033. doi:10.1016/j.foodchem.2009.01.013
-
(2009)
Food Chem
, vol.115
, pp. 1028-1033
-
-
Shin, M.H.1
Cheong, N.Y.2
Lee, J.H.3
Kim, K.H.4
-
159
-
-
84866843844
-
Preparation of starch–sodium lignosulfonate graft copolymers via laccase catalysis and characterization of antioxidant activity
-
COI: 1:CAS:528:DC%2BC38Xhs1aqt7%2FM, PID: 23121948
-
Shogren RL, Biswas A (2013) Preparation of starch–sodium lignosulfonate graft copolymers via laccase catalysis and characterization of antioxidant activity. Carbohydr Polym 91:581–585. doi:10.1016/j.carbpol.2012.08.079
-
(2013)
Carbohydr Polym
, vol.91
, pp. 581-585
-
-
Shogren, R.L.1
Biswas, A.2
-
160
-
-
33747605566
-
Direct acylation of flavonoid glycosides with phenolic acids catalysed by Candida antarctica lipase B (Novozym 435®)
-
COI: 1:CAS:528:DC%2BD28Xosl2rsbw%3D
-
Stevenson DE, Wibisono R, Jensen DJ, Stanley RA, Cooney JM (2006) Direct acylation of flavonoid glycosides with phenolic acids catalysed by Candida antarctica lipase B (Novozym 435®). Enzym Microb Technol 39:1236–1241. doi:10.1016/j.enzmictec.2006.03.006
-
(2006)
Enzym Microb Technol
, vol.39
, pp. 1236-1241
-
-
Stevenson, D.E.1
Wibisono, R.2
Jensen, D.J.3
Stanley, R.A.4
Cooney, J.M.5
-
161
-
-
1542576162
-
Synthesis of arbutin α-glucosides and a comparison of their inhibitory effects with those of α-arbutin and arbutin on human tyrosinase
-
COI: 1:CAS:528:DC%2BD3sXmsFWnsr4%3D, PID: 12843585
-
Sugimoto K, Nishimura T, Nomura K, Sugimoto K, Kuriki T (2003) Synthesis of arbutin α-glucosides and a comparison of their inhibitory effects with those of α-arbutin and arbutin on human tyrosinase. Chem Pharm Bull 51:798–801
-
(2003)
Chem Pharm Bull
, vol.51
, pp. 798-801
-
-
Sugimoto, K.1
Nishimura, T.2
Nomura, K.3
Sugimoto, K.4
Kuriki, T.5
-
162
-
-
17644420639
-
Synthesis of α-arbutin-α-glycosides and their inhibitory effects on human tyrosinase
-
COI: 1:CAS:528:DC%2BD2MXksVKnur8%3D, PID: 16233788
-
Sugimoto K, Nomura J, Nishimura T, Kiso T, Sugimoto K, Kuriki T (2005) Synthesis of α-arbutin-α-glycosides and their inhibitory effects on human tyrosinase. J Biosci Bioeng 99:272–276
-
(2005)
J Biosci Bioeng
, vol.99
, pp. 272-276
-
-
Sugimoto, K.1
Nomura, J.2
Nishimura, T.3
Kiso, T.4
Sugimoto, K.5
Kuriki, T.6
-
163
-
-
34547679566
-
Novel transglucosylating reaction of sucrose phosphorylase to carboxylic compounds such as benzoic acid
-
COI: 1:CAS:528:DC%2BD2sXhtVCmtrjK, PID: 17697979
-
Sugimoto K, Nomura K, Nishiura H, Ohdan K, Nishimura T, Hayashi H, Kuriki T (2007) Novel transglucosylating reaction of sucrose phosphorylase to carboxylic compounds such as benzoic acid. J Biosci Bioeng 104:22–29. doi:10.1263/jbb.104.22
-
(2007)
J Biosci Bioeng
, vol.104
, pp. 22-29
-
-
Sugimoto, K.1
Nomura, K.2
Nishiura, H.3
Ohdan, K.4
Nishimura, T.5
Hayashi, H.6
Kuriki, T.7
-
164
-
-
84881003451
-
Enhanced transesterification of ethyl ferulate with glycerolfor preparing glyceryl diferulate using a lipase in ionic liquids as reaction medium
-
COI: 1:CAS:528:DC%2BC3sXht1Srur7I, PID: 23690034
-
Sun S, Qin F, Bi Y, Chen J, Yang G, Liu W (2013b) Enhanced transesterification of ethyl ferulate with glycerolfor preparing glyceryl diferulate using a lipase in ionic liquids as reaction medium. Biotechnol Lett 35:1449–1454. doi:10.1007/s10529-013-1222-6
-
(2013)
Biotechnol Lett
, vol.35
, pp. 1449-1454
-
-
Sun, S.1
Qin, F.2
Bi, Y.3
Chen, J.4
Yang, G.5
Liu, W.6
-
165
-
-
35748942247
-
A novel, two consecutive enzyme synthesis of feruloylated monoacyl- and diacyl-glycerols in a solvent-free system
-
COI: 1:CAS:528:DC%2BD2sXht1ejtLjE, PID: 17657410
-
Sun S, Shan L, Liu Y, Jin Q, Wang X, Wang Z (2007) A novel, two consecutive enzyme synthesis of feruloylated monoacyl- and diacyl-glycerols in a solvent-free system. Biotechnol Lett 29:1947–1950. doi:10.1007/s10529-007-9486-3
-
(2007)
Biotechnol Lett
, vol.29
, pp. 1947-1950
-
-
Sun, S.1
Shan, L.2
Liu, Y.3
Jin, Q.4
Wang, X.5
Wang, Z.6
-
166
-
-
68649115813
-
Solvent-free enzymatic synthesis of feruloylated diacylglycerols and kinetic study
-
COI: 1:CAS:528:DC%2BD1MXisFagsrs%3D
-
Sun S, Shan L, Liu Y, Jin Y, Jin Q, Song Y, Wang X (2009) Solvent-free enzymatic synthesis of feruloylated diacylglycerols and kinetic study. J Mol Catal B Enzym 57:104–108. doi:10.1016/j.molcatb.2008.07.010
-
(2009)
J Mol Catal B Enzym
, vol.57
, pp. 104-108
-
-
Sun, S.1
Shan, L.2
Liu, Y.3
Jin, Y.4
Jin, Q.5
Song, Y.6
Wang, X.7
-
167
-
-
84875247161
-
Solvent-free enzymatic transesterification of ethyl ferulate and monostearin: optimized by response surface methodology
-
Sun S, Song F, Bi Y, Yang G, Liu W (2013a) Solvent-free enzymatic transesterification of ethyl ferulate and monostearin: optimized by response surface methodology. J Biotechnol 164:340–345. doi:10.1016/j.jbiotec.2013.01.013
-
(2013)
J Biotechnol
, vol.164
, pp. 340-345
-
-
Sun, S.1
Song, F.2
Bi, Y.3
Yang, G.4
Liu, W.5
-
168
-
-
84896447400
-
Solvent-free enzymatic synthesis of feruloylated structured lipids by the transesterification of ethyl ferulate with castor oil
-
Sun S, Zhu S, Bi Y (2014) Solvent-free enzymatic synthesis of feruloylated structured lipids by the transesterification of ethyl ferulate with castor oil. Food Chemistry 158:292--295. doi:10.1016/j.foodchem.2014.02.146
-
(2014)
Food Chemistry
, vol.158
, pp. 292-295
-
-
Sun, S.1
Zhu, S.2
Bi, Y.3
-
169
-
-
85008537101
-
Enzymatic synthesis of novel phosphatidylkojic acid and phosphatidylarbutin, and their inhibitory effects on tyrosinase activity
-
Takami M, Hidaka N, Miki S, Suzuki Y (1994) Enzymatic synthesis of novel phosphatidylkojic acid and phosphatidylarbutin, and their inhibitory effects on tyrosinase activity. Biosci Biotechnol Biochem 58:1716--1717. doi:10.1271/bbb.58.1716
-
(1994)
Biosci Biotechnol Biochem
, vol.58
, pp. 1716-1717
-
-
Takami, M.1
Hidaka, N.2
Miki, S.3
Suzuki, Y.4
-
170
-
-
83055196868
-
Chemoenzymatic synthesis of phytosteryl ferulates and evaluation of their antioxidant activity
-
COI: 1:CAS:528:DC%2BC3MXhtlGktrrK, PID: 22023159
-
Tan Z, Shahidi F (2011) Chemoenzymatic synthesis of phytosteryl ferulates and evaluation of their antioxidant activity. J Agric Food Chem 59:12375–12383. doi:10.1021/jf2034237
-
(2011)
J Agric Food Chem
, vol.59
, pp. 12375-12383
-
-
Tan, Z.1
Shahidi, F.2
-
171
-
-
84859791693
-
A novel chemoenzymatic synthesis of phytosteryl caffeates and assessment of their antioxidant activity
-
COI: 1:CAS:528:DC%2BC38Xjt1eqtLs%3D
-
Tan Z, Shahidi F (2012) A novel chemoenzymatic synthesis of phytosteryl caffeates and assessment of their antioxidant activity. Food Chem 133:1427–1434. doi:10.1016/j.foodchem.2012.02.030
-
(2012)
Food Chem
, vol.133
, pp. 1427-1434
-
-
Tan, Z.1
Shahidi, F.2
-
172
-
-
84873713746
-
Phytosteryl sinapates and vanillates: chemoenzymatic synthesis and antioxidant capacity assessment
-
COI: 1:CAS:528:DC%2BC3sXitlalsbc%3D, PID: 23411265
-
Tan Z, Shahidi F (2013) Phytosteryl sinapates and vanillates: chemoenzymatic synthesis and antioxidant capacity assessment. Food Chem 138:1438–1447. doi:10.1016/j.foodchem.2012.10.093
-
(2013)
Food Chem
, vol.138
, pp. 1438-1447
-
-
Tan, Z.1
Shahidi, F.2
-
173
-
-
68049137644
-
Enzymatic preparation of acylated derivatives of silybin in organic and ionic liquid media and evaluation of their antitumour proliferative activity
-
COI: 1:CAS:528:DC%2BD1MXltFChsbc%3D
-
Theodosiou E, Katsoura MH, Loutrari H, Purchartova K, Kren V, Kolisis FN, Stamatis H (2009) Enzymatic preparation of acylated derivatives of silybin in organic and ionic liquid media and evaluation of their antitumour proliferative activity. Biocatal Biotransfor 27:161–169. doi:10.1080/10242420902937777
-
(2009)
Biocatal Biotransfor
, vol.27
, pp. 161-169
-
-
Theodosiou, E.1
Katsoura, M.H.2
Loutrari, H.3
Purchartova, K.4
Kren, V.5
Kolisis, F.N.6
Stamatis, H.7
-
174
-
-
33847314304
-
Enzymatic synthesis of arbutin undecylenic acid ester and its inhibitory effect on mushroom tyrosinase
-
COI: 1:CAS:528:DC%2BD2sXhvVehsbc%3D, PID: 17195058
-
Tokiwa Y, Kitagawa M, Raku T (2007a) Enzymatic synthesis of arbutin undecylenic acid ester and its inhibitory effect on mushroom tyrosinase. Biotechnol Lett 29:481–486. doi:10.1007/s10529-006-9267-4
-
(2007)
Biotechnol Lett
, vol.29
, pp. 481-486
-
-
Tokiwa, Y.1
Kitagawa, M.2
Raku, T.3
-
175
-
-
34247850945
-
Enzymatic synthesis of arbutin undecylenic acid ester and its inhibitory effect on melanin synthesis
-
COI: 1:CAS:528:DC%2BD2sXlt1Kju7g%3D, PID: 17418566
-
Tokiwa Y, Kitagawa M, Raku T, Yanagitani S, Yoshino K (2007b) Enzymatic synthesis of arbutin undecylenic acid ester and its inhibitory effect on melanin synthesis. Bioorg Med Chem Lett 17:3105–3108. doi:10.1016/j.bmcl.2007.03.039
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 3105-3108
-
-
Tokiwa, Y.1
Kitagawa, M.2
Raku, T.3
Yanagitani, S.4
Yoshino, K.5
-
176
-
-
12244255095
-
Purification and characterization of a feruloyl esterase from Fusarium oxysporum catalyzing esterification of phenolic acids in ternary water-organic solvent mixtures
-
COI: 1:CAS:528:DC%2BD3sXisFSlsr8%3D, PID: 12668312
-
Topakas E, Stamatis H, Biely P, Kekos D, Macris BJ, Christakopoulos P (2003b) Purification and characterization of a feruloyl esterase from Fusarium oxysporum catalyzing esterification of phenolic acids in ternary water-organic solvent mixtures. J Biotechnol 102:33–44. doi:10.1016/S0168-1656(02)00363-2
-
(2003)
J Biotechnol
, vol.102
, pp. 33-44
-
-
Topakas, E.1
Stamatis, H.2
Biely, P.3
Kekos, D.4
Macris, B.J.5
Christakopoulos, P.6
-
177
-
-
1542359003
-
Purification and characterization of a type B feruloyl esterase (StFae-A) from the thermophilic fungus Sporotrichum thermophile
-
COI: 1:CAS:528:DC%2BD2cXhtleiurg%3D, PID: 14615854
-
Topakas E, Stamatis H, Biely P, Christakopoulos P (2004) Purification and characterization of a type B feruloyl esterase (StFae-A) from the thermophilic fungus Sporotrichum thermophile. Appl Microbiol Biotechnol 63:686–690
-
(2004)
Appl Microbiol Biotechnol
, vol.63
, pp. 686-690
-
-
Topakas, E.1
Stamatis, H.2
Biely, P.3
Christakopoulos, P.4
-
178
-
-
0042882381
-
Purification and characterization of a Fusarium oxysporum feruloyl esterase (FoFAE-I) catalysing transesterification of phenolic acid esters
-
COI: 1:CAS:528:DC%2BD3sXmvVyht7k%3D
-
Topakas E, Stamatis H, Mastihubova M, Biely P, Kekos D, Macris BJ, Christakopoulos P (2003a) Purification and characterization of a Fusarium oxysporum feruloyl esterase (FoFAE-I) catalysing transesterification of phenolic acid esters. Enzym Microb Technol 33:729–737. doi:10.1016/S0141-0229(03)00213-8
-
(2003)
Enzym Microb Technol
, vol.33
, pp. 729-737
-
-
Topakas, E.1
Stamatis, H.2
Mastihubova, M.3
Biely, P.4
Kekos, D.5
Macris, B.J.6
Christakopoulos, P.7
-
179
-
-
0033230284
-
Part I: enzymatic synthesis of lactate and glycolate esters of fatty alcohols
-
COI: 1:CAS:528:DyaK1MXntVCgtr8%3D
-
Torres C, Otero C (1999) Part I: enzymatic synthesis of lactate and glycolate esters of fatty alcohols. Enzym Microb Technol 25:745–752. doi:10.1016/S0141-0229(99)00117-9
-
(1999)
Enzym Microb Technol
, vol.25
, pp. 745-752
-
-
Torres, C.1
Otero, C.2
-
180
-
-
0035811961
-
Part III: direct enzymatic esterification of lactic acid with fatty acids
-
COI: 1:CAS:528:DC%2BD3MXks1Ols7s%3D
-
Torres C, Otero C (2001) Part III: direct enzymatic esterification of lactic acid with fatty acids. Enzym Microb Technol 29:3–12. doi:10.1016/S0141-0229(01)00344-1
-
(2001)
Enzym Microb Technol
, vol.29
, pp. 3-12
-
-
Torres, C.1
Otero, C.2
-
181
-
-
74849137796
-
Enzymatic modification of ascorbic acid and alpha-tocopherol to enhance their stability in food and nutritional applications
-
COI: 1:CAS:528:DC%2BD1cXlslensro%3D
-
Torres P, Kunamneni A, Ballesteros A, Plou FJ (2008a) Enzymatic modification of ascorbic acid and alpha-tocopherol to enhance their stability in food and nutritional applications. Open Food Sci J 2:1–9
-
(2008)
Open Food Sci J
, vol.2
, pp. 1-9
-
-
Torres, P.1
Kunamneni, A.2
Ballesteros, A.3
Plou, F.J.4
-
182
-
-
38049001011
-
Acetylation of vitamin E by Candida antarctica lipase B immobilized on different carries
-
COI: 1:CAS:528:DC%2BD1cXpt1Ogsg%3D%3D
-
Torres P, Reyes-Duarte D, Lopez-Cortes N, Ferrer M, Ballesteros A, Plou FJ (2008b) Acetylation of vitamin E by Candida antarctica lipase B immobilized on different carries. Process Biochem 43:145–153. doi:10.1016/j.procbio.2007.11.008
-
(2008)
Process Biochem
, vol.43
, pp. 145-153
-
-
Torres, P.1
Reyes-Duarte, D.2
Lopez-Cortes, N.3
Ferrer, M.4
Ballesteros, A.5
Plou, F.J.6
-
183
-
-
1942505809
-
The enzymatic synthesis of gallic acid derivatives
-
Toth G, Hensler D (1952) The enzymatic synthesis of gallic acid derivatives. Acta Chim II 10:209–212
-
(1952)
Acta Chim II
, vol.10
, pp. 209-212
-
-
Toth, G.1
Hensler, D.2
-
184
-
-
33744996040
-
Esterification of ferulic acid with polyols using a ferulic acid esterase from Aspergillus niger
-
Tsuchiyama M, Sakamoto T, Fujita T, Murata S, Kawasaki H (2006) Esterification of ferulic acid with polyols using a ferulic acid esterase from Aspergillus niger. Biochim Biophys Acta 7:1071–1079. doi:10.1016/j.bbagen.2006.03.022
-
(2006)
Biochim Biophys Acta
, vol.7
, pp. 1071-1079
-
-
Tsuchiyama, M.1
Sakamoto, T.2
Fujita, T.3
Murata, S.4
Kawasaki, H.5
-
185
-
-
36148962393
-
Enzymatic synthesis of hydroxycinnamic acid glycerol esters using type A feruloyl esterase from Aspergillus niger
-
COI: 1:CAS:528:DC%2BD2sXhtlShtL%2FN, PID: 17928681
-
Tsuchiyama M, Sakamoto T, Tanimori S, Murata S, Kawasaki H (2007) Enzymatic synthesis of hydroxycinnamic acid glycerol esters using type A feruloyl esterase from Aspergillus niger. Biosci Biotechnol Biochem 71:2606–2609
-
(2007)
Biosci Biotechnol Biochem
, vol.71
, pp. 2606-2609
-
-
Tsuchiyama, M.1
Sakamoto, T.2
Tanimori, S.3
Murata, S.4
Kawasaki, H.5
-
187
-
-
79954822317
-
Pycnoporus laccase-mediated bioconversion of rutin to oligomers suitable for biotechnology applications
-
COI: 1:CAS:528:DC%2BC3MXjtVKrtrs%3D, PID: 21210103
-
Uzan E, Portet B, Lubrano C, Milesi S, Favel A, Lesage-Meessen L, Lomascolo A (2011) Pycnoporus laccase-mediated bioconversion of rutin to oligomers suitable for biotechnology applications. Appl Microbiol Biotechnol 90:97–105. doi:10.1007/s00253-010-3075-4
-
(2011)
Appl Microbiol Biotechnol
, vol.90
, pp. 97-105
-
-
Uzan, E.1
Portet, B.2
Lubrano, C.3
Milesi, S.4
Favel, A.5
Lesage-Meessen, L.6
Lomascolo, A.7
-
188
-
-
34848820031
-
Chemoenzymatic synthesis of feruloyl-D-arabinose as a potential anti-mycobacterial agent
-
COI: 1:CAS:528:DC%2BD2sXhtV2mtr3F, PID: 17676274
-
Vafiadi C, Topakas E, Alderwick LJ, Besra GS, Christakopoulos P (2007a) Chemoenzymatic synthesis of feruloyl-D-arabinose as a potential anti-mycobacterial agent. Biotechnol Lett 29:1771–1774
-
(2007)
Biotechnol Lett
, vol.29
, pp. 1771-1774
-
-
Vafiadi, C.1
Topakas, E.2
Alderwick, L.J.3
Besra, G.S.4
Christakopoulos, P.5
-
189
-
-
38749131170
-
Enzymatic synthesis of butyl hydroxycinnamates and their inhibitory effect on LDL-oxidation
-
COI: 1:CAS:528:DC%2BD1cXhslygsr8%3D, PID: 18155313
-
Vafiadi C, Topakas E, Alissandratos A, Faulds CB, Christakopoulos P (2008b) Enzymatic synthesis of butyl hydroxycinnamates and their inhibitory effect on LDL-oxidation. J Biotechnol 133:497–504
-
(2008)
J Biotechnol
, vol.133
, pp. 497-504
-
-
Vafiadi, C.1
Topakas, E.2
Alissandratos, A.3
Faulds, C.B.4
Christakopoulos, P.5
-
190
-
-
34547623728
-
Structural characterization of ESI-MS of feruloylated arabino-oligosaccharides synthesized by chemoenzymatic esterification
-
COI: 1:CAS:528:DC%2BD2sXhtVSitLzM, PID: 17909492
-
Vafiadi C, Topakas E, Bakx EJ, Schols HA, Christakopoulos P (2007b) Structural characterization of ESI-MS of feruloylated arabino-oligosaccharides synthesized by chemoenzymatic esterification. Molecules 12:1367–1375
-
(2007)
Molecules
, vol.12
, pp. 1367-1375
-
-
Vafiadi, C.1
Topakas, E.2
Bakx, E.J.3
Schols, H.A.4
Christakopoulos, P.5
-
191
-
-
44649151272
-
Preparation of multipurpose cross-linked enzyme aggregates and their application to production of alkyl ferulates
-
COI: 1:CAS:528:DC%2BD1cXmvVKrtL4%3D
-
Vafiadi C, Topakas E, Christakopoulos P (2008a) Preparation of multipurpose cross-linked enzyme aggregates and their application to production of alkyl ferulates. J Mol Catal B Enzym 54:35–41. doi:10.1016/j.molcatb.2007.12.005
-
(2008)
J Mol Catal B Enzym
, vol.54
, pp. 35-41
-
-
Vafiadi, C.1
Topakas, E.2
Christakopoulos, P.3
-
192
-
-
33746919075
-
The feruloyl esterase system of Talaromyces stipitatus: determining the hydrolytic and synthetic specificity of TsFaeC
-
COI: 1:CAS:528:DC%2BD28Xot1Wkt7c%3D, PID: 16584797
-
Vafiadi C, Topakas E, Christakopoulos P, Faulds CB (2006) The feruloyl esterase system of Talaromyces stipitatus: determining the hydrolytic and synthetic specificity of TsFaeC. J Biotechnol 125:210–221
-
(2006)
J Biotechnol
, vol.125
, pp. 210-221
-
-
Vafiadi, C.1
Topakas, E.2
Christakopoulos, P.3
Faulds, C.B.4
-
193
-
-
12944324721
-
Mapping the hydrolytic and synthetic selectivity of a type C feruloyl esterase (StFaeC) from Sporotrichum thermophile using alkyl ferulates
-
COI: 1:CAS:528:DC%2BD2MXos1akuw%3D%3D
-
Vafiadi C, Topakas E, Wong KKY, Suckling ID, Christakopoulos P (2005) Mapping the hydrolytic and synthetic selectivity of a type C feruloyl esterase (StFaeC) from Sporotrichum thermophile using alkyl ferulates. Tetrahedron Asymmetry 16:373–379. doi:10.1016/j.tetasy.2004.11.037
-
(2005)
Tetrahedron Asymmetry
, vol.16
, pp. 373-379
-
-
Vafiadi, C.1
Topakas, E.2
Wong, K.K.Y.3
Suckling, I.D.4
Christakopoulos, P.5
-
194
-
-
57349092178
-
Feruloyl esterase-catalyzed synthesis of glycerol sinapate using ionic liquid mixtures
-
COI: 1:CAS:528:DC%2BD1cXhsV2ltr3K, PID: 18822324
-
Vafiadi C, Topakas E, Nahmias VR, Faulds CB, Christakopoulos P (2009) Feruloyl esterase-catalyzed synthesis of glycerol sinapate using ionic liquid mixtures. J Biotechnol 139:124–129. doi:10.1016/j.jbiotec.2008.08.008
-
(2009)
J Biotechnol
, vol.139
, pp. 124-129
-
-
Vafiadi, C.1
Topakas, E.2
Nahmias, V.R.3
Faulds, C.B.4
Christakopoulos, P.5
-
195
-
-
84899505952
-
Chemo-enzymatic synthesis of silybin and 2,3-dehydrosilybin dimers
-
PID: 24699152
-
Vavrikova E, Vacek J, Valentova K, Marchol P, Ulrichova J, Kuzma M, Kren V (2014) Chemo-enzymatic synthesis of silybin and 2,3-dehydrosilybin dimers. Molecules 19:4115–4134. doi:10.3390/molecules19044115
-
(2014)
Molecules
, vol.19
, pp. 4115-4134
-
-
Vavrikova, E.1
Vacek, J.2
Valentova, K.3
Marchol, P.4
Ulrichova, J.5
Kuzma, M.6
Kren, V.7
-
196
-
-
0042928514
-
Antioxidative properties and enzymatic synthesis of ascorbyl FA esters
-
COI: 1:CAS:528:DC%2BD3sXmvFGlsrs%3D
-
Viklund F, Alander J, Hult K (2003) Antioxidative properties and enzymatic synthesis of ascorbyl FA esters. JAOCS 80:795–799
-
(2003)
JAOCS
, vol.80
, pp. 795-799
-
-
Viklund, F.1
Alander, J.2
Hult, K.3
-
197
-
-
77952581454
-
Lipophilic rutin derivatives for antioxidant protection of oil-based foods
-
COI: 1:CAS:528:DC%2BC3cXms1eqtb4%3D
-
Viskupicova J, Danihelova M, Ondrejovic M, Liptaj T, Sturdik E (2010) Lipophilic rutin derivatives for antioxidant protection of oil-based foods. Food Chem 123:45–50. doi:10.1016/j.foodchem.2010.03.125
-
(2010)
Food Chem
, vol.123
, pp. 45-50
-
-
Viskupicova, J.1
Danihelova, M.2
Ondrejovic, M.3
Liptaj, T.4
Sturdik, E.5
-
198
-
-
84897654312
-
A novel continuous flow biosynthesis of caffeic acid phenethyl ester from alkyl caffeate and phenethanol in a packed bed microreactor
-
COI: 1:CAS:528:DC%2BC2cXmslWqsro%3D, PID: 24583213
-
Wang J, Gu SS, Cui HS, Wu XY, Wu FA (2014) A novel continuous flow biosynthesis of caffeic acid phenethyl ester from alkyl caffeate and phenethanol in a packed bed microreactor. Bioresour Technol 158:39–47. doi:10.1016/j.biortech.2014.01.145
-
(2014)
Bioresour Technol
, vol.158
, pp. 39-47
-
-
Wang, J.1
Gu, S.S.2
Cui, H.S.3
Wu, X.Y.4
Wu, F.A.5
-
199
-
-
84885448524
-
Rapid synthesis of propyl caffeate in ionic liquid using a packed bed enzyme microreactor under continuous-flow conditions
-
COI: 1:CAS:528:DC%2BC3sXhs12ltLbP, PID: 24128399
-
Wang J, Gu SS, Cui HS, Yang LQ, Wu XY (2013) Rapid synthesis of propyl caffeate in ionic liquid using a packed bed enzyme microreactor under continuous-flow conditions. Bioresour Technol 149:367–374. doi:10.1016/j.biortech.2013.09.098
-
(2013)
Bioresour Technol
, vol.149
, pp. 367-374
-
-
Wang, J.1
Gu, S.S.2
Cui, H.S.3
Yang, L.Q.4
Wu, X.Y.5
-
200
-
-
84920744649
-
Ultrasound irradiation accelerates the lipase-catalyzed synthesis of methyl caffeate in an ionic liquid
-
COI: 1:CAS:528:DC%2BC2cXhvF2mtr7M
-
Wang J, Wang S, Li Z, Gu S, Wu X, Wu F (2015) Ultrasound irradiation accelerates the lipase-catalyzed synthesis of methyl caffeate in an ionic liquid. J Mol Catal B Enzym 111:21–28. doi:10.1016/j.molcatb.2014.11.006
-
(2015)
J Mol Catal B Enzym
, vol.111
, pp. 21-28
-
-
Wang, J.1
Wang, S.2
Li, Z.3
Gu, S.4
Wu, X.5
Wu, F.6
-
201
-
-
0041302263
-
Production of saturated acyl-L-ascorbate by immobilized lipase using a continuous stirred tank reactor
-
COI: 1:CAS:528:DC%2BD3sXkvVGiu74%3D, PID: 14705888
-
Watanabe Y, Kuwabara K, Adachi S, Nakanishi K, Matsuno R (2003) Production of saturated acyl-L-ascorbate by immobilized lipase using a continuous stirred tank reactor. J Agric Food Chem 51:4628–4632
-
(2003)
J Agric Food Chem
, vol.51
, pp. 4628-4632
-
-
Watanabe, Y.1
Kuwabara, K.2
Adachi, S.3
Nakanishi, K.4
Matsuno, R.5
-
202
-
-
58349093116
-
Synthesis of lauroyl phenolic glycoside by immobilized lipase in organic solvent and its antioxidative activity
-
COI: 1:CAS:528:DC%2BD1MXhtVeisL0%3D
-
Watanabe Y, Nagai M, Yamanaka K, Jose K, Nomura M (2009) Synthesis of lauroyl phenolic glycoside by immobilized lipase in organic solvent and its antioxidative activity. J Biochem Eng 43:261–265. doi:10.1016/j.bej.2008.10.008
-
(2009)
J Biochem Eng
, vol.43
, pp. 261-265
-
-
Watanabe, Y.1
Nagai, M.2
Yamanaka, K.3
Jose, K.4
Nomura, M.5
-
203
-
-
43849109673
-
Enzymatic synthesis of conjugated linoleoyl ascorbate in acetone
-
Watanabe Y, Sawahara Y, Nosaka H, Yamanaka K, Adachi S (2008) Enzymatic synthesis of conjugated linoleoyl ascorbate in acetone. Biochem Eng J 40:268–372. doi:10.1016/j.bej.2008.01.007
-
(2008)
Biochem Eng J
, vol.40
, pp. 268-372
-
-
Watanabe, Y.1
Sawahara, Y.2
Nosaka, H.3
Yamanaka, K.4
Adachi, S.5
-
204
-
-
0021885724
-
Enzymatic synthesis of gallic acid esters
-
Weetall HH (1985) Enzymatic synthesis of gallic acid esters. Appl Biochem Biotechnol 11
-
(1985)
Appl Biochem Biotechnol
, pp. 11
-
-
Weetall, H.H.1
-
205
-
-
0041429214
-
Enzymatic esterification for glycoside lactate synthesis in organic solvent
-
COI: 1:CAS:528:DC%2BD3sXms12is78%3D
-
Wei D, Gu C, Song Q, Su W (2003) Enzymatic esterification for glycoside lactate synthesis in organic solvent. Enzym Microb Technol 33:508–512. doi:10.1016/S0141-0229(03)00156-X
-
(2003)
Enzym Microb Technol
, vol.33
, pp. 508-512
-
-
Wei, D.1
Gu, C.2
Song, Q.3
Su, W.4
-
206
-
-
0037164163
-
Enzymatic synthesis of ethyl glucoside lactate in non-aqueous system
-
COI: 1:CAS:528:DC%2BD38XnsVaitLY%3D
-
Wei DZ, Zou P, Tu MB, Zheng H (2002) Enzymatic synthesis of ethyl glucoside lactate in non-aqueous system. J Mol Catal B Enzym 18:273–278. doi:10.1016/S1381-1177(02)00106-6
-
(2002)
J Mol Catal B Enzym
, vol.18
, pp. 273-278
-
-
Wei, D.Z.1
Zou, P.2
Tu, M.B.3
Zheng, H.4
-
207
-
-
56949085849
-
Enzymatic synthesis of caffeic acid phenethyl ester
-
COI: 1:CAS:528:DC%2BD1cXhtFKqurfO
-
Widjaja A, Yeh TH, Ju YH (2008) Enzymatic synthesis of caffeic acid phenethyl ester. J Chin Inst Chem Eng 39:413–418. doi:10.1016/j.jcice.2008.05.003
-
(2008)
J Chin Inst Chem Eng
, vol.39
, pp. 413-418
-
-
Widjaja, A.1
Yeh, T.H.2
Ju, Y.H.3
-
208
-
-
84867190867
-
Synthesis and characterization of ampelopsin glucosides using dextransucrase from Leuconostoc mesenteroides B-1299CB4: glucosylation enhancing physicochemical properties
-
COI: 1:CAS:528:DC%2BC38XhtFKmtrrM
-
Woo HJ, Kang HK, Nguyen TTH, Kim GE, Kim YM, Park JS, Kim D, Cha J, Moon YH, Nam SH, Xia YM, Kimura A, Kim D (2012) Synthesis and characterization of ampelopsin glucosides using dextransucrase from Leuconostoc mesenteroides B-1299CB4: glucosylation enhancing physicochemical properties. Enzym Microb Technol 51:311–318. doi:10.1016/j.enzmictec.2012.07.014
-
(2012)
Enzym Microb Technol
, vol.51
, pp. 311-318
-
-
Woo, H.J.1
Kang, H.K.2
Nguyen, T.T.H.3
Kim, G.E.4
Kim, Y.M.5
Park, J.S.6
Kim, D.7
Cha, J.8
Moon, Y.H.9
Nam, S.H.10
Xia, Y.M.11
Kimura, A.12
Kim, D.13
-
209
-
-
77956429695
-
Ultrasound-promoted enzymatic synthesis of troxerutin esters in nonaqueous solvents
-
COI: 1:CAS:528:DC%2BC3cXhtFGqsbvN, PID: 20637677
-
Xiao Y, Yang L, Mao P, Zhao Z, Lin X (2011) Ultrasound-promoted enzymatic synthesis of troxerutin esters in nonaqueous solvents. Ultrason Sonochem 18:303–309. doi:10.1016/j.ultsonch.2010.06.010
-
(2011)
Ultrason Sonochem
, vol.18
, pp. 303-309
-
-
Xiao, Y.1
Yang, L.2
Mao, P.3
Zhao, Z.4
Lin, X.5
-
210
-
-
27144492920
-
Controllable regioselective acylation of rutin catalyzed by enzymes in non-aqueous solvents
-
COI: 1:CAS:528:DC%2BD2MXhtFersLvF, PID: 16245179
-
Xiao YM, Wu Q, Wu WB, Zhang QY, Lin XF (2005) Controllable regioselective acylation of rutin catalyzed by enzymes in non-aqueous solvents. Biotechnol Lett 27:1591–1595. doi:10.1007/s10529-005-2513-3
-
(2005)
Biotechnol Lett
, vol.27
, pp. 1591-1595
-
-
Xiao, Y.M.1
Wu, Q.2
Wu, W.B.3
Zhang, Q.Y.4
Lin, X.F.5
-
211
-
-
79751493110
-
Lipase-catalyzed synthesis of a-tocopheryl ferulate
-
COI: 1:CAS:528:DC%2BC3MXhslGgsbY%3D
-
Xin JY, Chen LI, Zhang YX, Wen RR, Zhao DM, Xia CG (2011) Lipase-catalyzed synthesis of a-tocopheryl ferulate. Food Biotechnol 25:43–57. doi:10.1080/08905436.2011.547116
-
(2011)
Food Biotechnol
, vol.25
, pp. 43-57
-
-
Xin, J.Y.1
Chen, L.I.2
Zhang, Y.X.3
Wen, R.R.4
Zhao, D.M.5
Xia, C.G.6
-
212
-
-
49249104856
-
Lipase-catalyzed synthesis of feruloyl oleins in solvent-free medium
-
COI: 1:CAS:528:DC%2BD1cXpvVKlsbc%3D
-
Xin JY, Zhang L, Chem LL, Zheng Y, Wu XM, Xia CG (2009) Lipase-catalyzed synthesis of feruloyl oleins in solvent-free medium. Food Chem 112:640–645. doi:10.1016/j.foodchem.2008.06.024
-
(2009)
Food Chem
, vol.112
, pp. 640-645
-
-
Xin, J.Y.1
Zhang, L.2
Chem, L.L.3
Zheng, Y.4
Wu, X.M.5
Xia, C.G.6
-
213
-
-
67349241910
-
Kinetic resolution of α-lipoic acid via enzymatic differentiation of a remote stereocenter
-
Yan H, Wang Z, Chen L (2009) Kinetic resolution of α-lipoic acid via enzymatic differentiation of a remote stereocenter. J Ind Microbiol Biotechnol 36:643–648. doi:10.1007/s10295-009-0531-1
-
(2009)
J Ind Microbiol Biotechnol
, vol.36
, pp. 643-648
-
-
Yan, H.1
Wang, Z.2
Chen, L.3
-
214
-
-
84880182687
-
Enzymatic synthesis of feruloylated lysophospholipid in a selected organic solvent medium
-
COI: 1:CAS:528:DC%2BC3sXhtlGksrzF, PID: 23993487
-
Yang H, Mu Y, Chen H, Xiu Z, Yang T (2013) Enzymatic synthesis of feruloylated lysophospholipid in a selected organic solvent medium. Food Chem 141:3317–3322. doi:10.1016/j.foodchem.2013.06.012
-
(2013)
Food Chem
, vol.141
, pp. 3317-3322
-
-
Yang, H.1
Mu, Y.2
Chen, H.3
Xiu, Z.4
Yang, T.5
-
215
-
-
67349241910
-
Kinetic resolution of a-lipoic acid via enzymatic differentiation of a remote sterocenter
-
Yang HD, Wang Z, Chen LJ (2009) Kinetic resolution of a-lipoic acid via enzymatic differentiation of a remote sterocenter. J Ind Microbiol Biotechnol 36:643–648. doi:10.1007/s10295-009-0531-1
-
(2009)
J Ind Microbiol Biotechnol
, vol.36
, pp. 643-648
-
-
Yang, H.D.1
Wang, Z.2
Chen, L.J.3
-
216
-
-
70249110360
-
A highly regioselective route to arbutin esters by immobilized lipase from Penicillium expansum
-
COI: 1:CAS:528:DC%2BD1MXhtFGltrjN, PID: 19695875
-
Yang RL, Li N, Li RF, Smith TJ, Zong MH (2010a) A highly regioselective route to arbutin esters by immobilized lipase from Penicillium expansum. Bioresour Technol 101:1–5. doi:10.1016/j.biortech.2009.07.067
-
(2010)
Bioresour Technol
, vol.101
, pp. 1-5
-
-
Yang, R.L.1
Li, N.2
Li, R.F.3
Smith, T.J.4
Zong, M.H.5
-
217
-
-
77956924031
-
Highly regioselective synthesis of novel aromatic esters of arbutin catalyzed by immobilized lipase from Penicillium expansum
-
COI: 1:CAS:528:DC%2BC3cXhtFygtbjO
-
Yang RL, Li N, Ye M, Zong MH (2010b) Highly regioselective synthesis of novel aromatic esters of arbutin catalyzed by immobilized lipase from Penicillium expansum. J Mol Catal B Enzym 67:41–44. doi:10.1016/j.molcatb.2010.07.003
-
(2010)
J Mol Catal B Enzym
, vol.67
, pp. 41-44
-
-
Yang, R.L.1
Li, N.2
Ye, M.3
Zong, M.H.4
-
218
-
-
84861938811
-
Enzymatic transesterification of ethyl ferulate with fish oil and reaction optimization by response surface methodology
-
COI: 1:CAS:528:DC%2BC38XmvFarsrg%3D
-
Yang Z, Glasius M, Xu X (2012) Enzymatic transesterification of ethyl ferulate with fish oil and reaction optimization by response surface methodology. Food Technol Biotechnol 50:88–97
-
(2012)
Food Technol Biotechnol
, vol.50
, pp. 88-97
-
-
Yang, Z.1
Glasius, M.2
Xu, X.3
-
219
-
-
33646130825
-
Synthesis of vitamin A esters by immobilized Candida sp. lipase in organic media
-
COI: 1:CAS:528:DC%2BD28Xis1Cgtbs%3D
-
Yin C, Liu T, Tan T (2006) Synthesis of vitamin A esters by immobilized Candida sp. lipase in organic media. Chin J Chem Eng 14:81–86. doi:10.1016/S1004-9541(06)60041-4
-
(2006)
Chin J Chem Eng
, vol.14
, pp. 81-86
-
-
Yin, C.1
Liu, T.2
Tan, T.3
-
220
-
-
79952501566
-
Enzyme-catalyzed synthesis of vitamin E succinate using a chemically modified Novozym-435
-
COI: 1:CAS:528:DC%2BC3MXjt1als7g%3D
-
Yin C, Zhang C, Gao M (2011) Enzyme-catalyzed synthesis of vitamin E succinate using a chemically modified Novozym-435. Chin J Chem Eng 19:135–139. doi:10.1016/S1004-9541(09)60189-0
-
(2011)
Chin J Chem Eng
, vol.19
, pp. 135-139
-
-
Yin, C.1
Zhang, C.2
Gao, M.3
-
221
-
-
24344466975
-
Microencapsulated mycelium-bound tannase from Aspergillus niger an efficient catalyst for esterification of propyl gallate in organic solvents
-
COI: 1:CAS:528:DC%2BD2MXhtVOqsb7M, PID: 16148363
-
Yu XW, Li YQ (2005) Microencapsulated mycelium-bound tannase from Aspergillus niger an efficient catalyst for esterification of propyl gallate in organic solvents. Appl Biochem Biotechnol 126:177–187
-
(2005)
Appl Biochem Biotechnol
, vol.126
, pp. 177-187
-
-
Yu, X.W.1
Li, Y.Q.2
-
222
-
-
44449087549
-
Expression of Aspergillus oryzae tannase in Pichia pastoris and its application in the synthesis of propyl gallate in organic solvent
-
COI: 1:CAS:528:DC%2BD1cXlvVGqurw%3D
-
Yu XW, Li YQ (2008) Expression of Aspergillus oryzae tannase in Pichia pastoris and its application in the synthesis of propyl gallate in organic solvent. Food Technol Biotechnol 46:80–85
-
(2008)
Food Technol Biotechnol
, vol.46
, pp. 80-85
-
-
Yu, X.W.1
Li, Y.Q.2
-
223
-
-
34547128586
-
Synthesis of propyl gallate by mycelium-bound tannase from Aspergillus niger in organic solvent
-
COI: 1:CAS:528:DC%2BD2sXotFWqtb0%3D
-
Yu XW, Li YQ, Zhou SH, Zheng YY (2007) Synthesis of propyl gallate by mycelium-bound tannase from Aspergillus niger in organic solvent. World J Microbiol Biotechnol 23:1091–1098. doi:10.1007/s11274-006-9338-7
-
(2007)
World J Microbiol Biotechnol
, vol.23
, pp. 1091-1098
-
-
Yu, X.W.1
Li, Y.Q.2
Zhou, S.H.3
Zheng, Y.Y.4
-
224
-
-
78650628885
-
Enzymatic synthesis of feruloylated lipids: comparison of the efficiency of vinyl ferulate and ethyl ferulate as substrates
-
COI: 1:CAS:528:DC%2BC3cXhsVKkt77F
-
Yu Y, Zheng Y, Quan J, Wu CY, Wang YJ, Brandford-White C, Zhu LM (2010) Enzymatic synthesis of feruloylated lipids: comparison of the efficiency of vinyl ferulate and ethyl ferulate as substrates. J Am Oil Chem Soc J 87:1443–1449. doi:10.1007/s11746-010-1636-4
-
(2010)
J Am Oil Chem Soc J
, vol.87
, pp. 1443-1449
-
-
Yu, Y.1
Zheng, Y.2
Quan, J.3
Wu, C.Y.4
Wang, Y.J.5
Brandford-White, C.6
Zhu, L.M.7
-
225
-
-
79958845258
-
Dependency of the hydrogen bonding capacity of the solvent anion on the thermal stability of feruloyl esterases in ionic liquid systems
-
COI: 1:CAS:528:DC%2BC3MXntV2murw%3D
-
Zeuner B, Ståhlberg T, van Buu ON, Kunov-Kruse AJ, Riisager A, Meyer AS (2011) Dependency of the hydrogen bonding capacity of the solvent anion on the thermal stability of feruloyl esterases in ionic liquid systems. Green Chem 13:1550–1557. doi:10.1039/C1GC15115K
-
(2011)
Green Chem
, vol.13
, pp. 1550-1557
-
-
Zeuner, B.1
Ståhlberg, T.2
van Buu, O.N.3
Kunov-Kruse, A.J.4
Riisager, A.5
Meyer, A.S.6
-
226
-
-
84861062973
-
Kinetics of enzymatic synthesis of L-ascorbyl acetate by lipozyme TLIM and Novozym 435
-
Zhang DH, Li YQ, Li C, Lv YQ, Yv-Qin L, Yang L (2012) Kinetics of enzymatic synthesis of L-ascorbyl acetate by lipozyme TLIM and Novozym 435. Biotechnol Bioprocess Eng 17:60–66. doi:10.1007/s12257-011-0249-6
-
(2012)
Biotechnol Bioprocess Eng
, vol.17
, pp. 60-66
-
-
Zhang, D.H.1
Li, Y.Q.2
Li, C.3
Lv, Y.Q.4
Yv-Qin, L.5
Yang, L.6
-
227
-
-
84964284107
-
Novel trends for use of microbial tannases
-
COI: 1:CAS:528:DC%2BC2cXhsFagsbjJ, PID: 24679165
-
Zhang S (2015) Novel trends for use of microbial tannases. Prep Biochem Biotechnol 45:221–232. doi:10.1080/10826068.2014.907182
-
(2015)
Prep Biochem Biotechnol
, vol.45
, pp. 221-232
-
-
Zhang, S.1
-
228
-
-
84894249432
-
Enzymatic synthesis of lard-based ascorbyl esters in a packed-bed reactor: optimization by response surface methodology and evaluation of antioxidant properties
-
COI: 1:CAS:528:DC%2BC2cXhtFWhsLs%3D
-
Zhao H, Liu J, Lv F, Ye R, Bie X, Zhang C, Lu Z (2014) Enzymatic synthesis of lard-based ascorbyl esters in a packed-bed reactor: optimization by response surface methodology and evaluation of antioxidant properties. LWT Food Sci Technol 57:393–399. doi:10.1016/j.lwt.2013.12.015
-
(2014)
LWT Food Sci Technol
, vol.57
, pp. 393-399
-
-
Zhao, H.1
Liu, J.2
Lv, F.3
Ye, R.4
Bie, X.5
Zhang, C.6
Lu, Z.7
-
229
-
-
84879489446
-
Ultrasound irradiation promoted lipase-catalyzed synthesis of flavonoid esters with unsaturated fatty acids
-
COI: 1:CAS:528:DC%2BC3sXhtFWrsr7N
-
Zheng MM, Wang L, Huang FH, Guo PM, Wei F, Deng QC, Zheng C, Wan CY (2013) Ultrasound irradiation promoted lipase-catalyzed synthesis of flavonoid esters with unsaturated fatty acids. J Mol Catal B Enzym 95:82–88. doi:10.1016/j.molcatb.2013.05.028
-
(2013)
J Mol Catal B Enzym
, vol.95
, pp. 82-88
-
-
Zheng, M.M.1
Wang, L.2
Huang, F.H.3
Guo, P.M.4
Wei, F.5
Deng, Q.C.6
Zheng, C.7
Wan, C.Y.8
-
230
-
-
45849135234
-
Optimization of selective lipase-catalyzed feruloylated monoacylglycerols by response surface methodology
-
COI: 1:CAS:528:DC%2BD1cXntVaht78%3D
-
Zheng Y, Quan J, Zhu LM, Jiang B, Nie HL (2008) Optimization of selective lipase-catalyzed feruloylated monoacylglycerols by response surface methodology. J Am Oil Chem Soc 85:635–639. doi:10.1007/s11746-008-1248-4
-
(2008)
J Am Oil Chem Soc
, vol.85
, pp. 635-639
-
-
Zheng, Y.1
Quan, J.2
Zhu, L.M.3
Jiang, B.4
Nie, H.L.5
-
231
-
-
84893667908
-
Lipase-catalyzed synthesis of acetylated EGCG and antioxidant properties of the acetylated derivatives
-
COI: 1:CAS:528:DC%2BC3sXhvVagtrnJ
-
Zhu S, Li Y, Li Z, Ma C, Lou Z, Yokoyama W, Wang H (2014) Lipase-catalyzed synthesis of acetylated EGCG and antioxidant properties of the acetylated derivatives. Food Res Int 56:279–286. doi:10.1016/j.foodres.2013.10.026
-
(2014)
Food Res Int
, vol.56
, pp. 279-286
-
-
Zhu, S.1
Li, Y.2
Li, Z.3
Ma, C.4
Lou, Z.5
Yokoyama, W.6
Wang, H.7
-
232
-
-
84874945816
-
An efficient microwave-assisted enzyme-catalyzed regioselective synthesis of long chain acylated derivatives of flavonoid glycosides
-
COI: 1:CAS:528:DC%2BC3sXjtlalu7g%3D
-
Ziaullah HPVR (2013) An efficient microwave-assisted enzyme-catalyzed regioselective synthesis of long chain acylated derivatives of flavonoid glycosides. Tetrahedron Lett 54:1933–1937. doi:10.1016/j.tetlet.2013.01.103
-
(2013)
Tetrahedron Lett
, vol.54
, pp. 1933-1937
-
-
Ziaullah, H.P.V.R.1
|