메뉴 건너뛰기




Volumn 87, Issue 4, 2010, Pages 1281-1289

Biotechnological production and applications of N-acetyl-d-neuraminic acid: Current state and perspectives

Author keywords

Application; Biocatalysis; N Acetyl d neuraminic acid; Sialic acid

Indexed keywords

BIOCATALYSIS; BIOTECHNOLOGICAL PRODUCTION; GLYCANS; PHARMACEUTICAL INDUSTRY; POTENTIAL APPLICATIONS; SIALIC ACID; SIALIC ACIDS; TERMINAL POSITION;

EID: 77955552372     PISSN: 01757598     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00253-010-2700-6     Document Type: Short Survey
Times cited : (41)

References (70)
  • 1
    • 13044268636 scopus 로고
    • Preparation of a soluble bifunctional enzyme by gene fusion
    • 10.1038/nbt0985-821
    • L Bülow P Ljungcrantz K Mosbach 1985 Preparation of a soluble bifunctional enzyme by gene fusion Nat Biotechnol 3 821 823 10.1038/nbt0985-821
    • (1985) Nat Biotechnol , vol.3 , pp. 821-823
    • Bülow, L.1    Ljungcrantz, P.2    Mosbach, K.3
  • 2
    • 0032586151 scopus 로고    scopus 로고
    • Alkaline biocatalysis for the direct synthesis of N-acetyl-D-neuraminic acid (Neu5Ac) from N-Acetyl-D-glucosamine (GlcNAc)
    • DOI 10.1002/(SICI)1097-0290(1999)66:2<131::AID-BIT6>3.0.CO;2-X
    • S Blayer JM Woodley MJ Dawson MD Lilly 1999 Alkaline biocatalysis for the direct synthesis of N-acetyl-d-neuraminic acid (Neu5Ac) from N-acetyl-d-glucosamine (GlcNAc) Biotechnol Bioeng 66 131 136 10.1002/(SICI)1097-0290(1999)66:2<131::AID-BIT6>3.0.CO;2-X 1:CAS:528:DyaK1MXnvFylt7w%3D (Pubitemid 32262273)
    • (1999) Biotechnology and Bioengineering , vol.66 , Issue.2 , pp. 131-136
    • Blayer, S.1    Woodley, J.M.2    Dawson, M.J.3    Lilly, M.D.4
  • 3
    • 33847273107 scopus 로고    scopus 로고
    • Permeability issues in whole-cell bioprocesses and cellular membrane engineering
    • 10.1007/s00253-006-0811-x 1:CAS:528:DC%2BD2sXitVKjsL4%3D
    • RR Chen 2007 Permeability issues in whole-cell bioprocesses and cellular membrane engineering Appl Microbiol Biotechnol 74 730 738 10.1007/s00253-006- 0811-x 1:CAS:528:DC%2BD2sXitVKjsL4%3D
    • (2007) Appl Microbiol Biotechnol , vol.74 , pp. 730-738
    • Chen, R.R.1
  • 4
    • 77449115880 scopus 로고    scopus 로고
    • Advances in the biology and chemistry of sialic acids
    • 10.1021/cb900266r 1:CAS:528:DC%2BC3cXhs1yrsQ%3D%3D
    • X Chen A Varki 2010 Advances in the biology and chemistry of sialic acids ACS Chem Biol 5 163 176 10.1021/cb900266r 1:CAS:528:DC%2BC3cXhs1yrsQ%3D%3D
    • (2010) ACS Chem Biol , vol.5 , pp. 163-176
    • Chen, X.1    Varki, A.2
  • 5
    • 0001423041 scopus 로고
    • The sialic acids. I. The structure and enzymatic synthesis of N-acetylneuraminic acid
    • 1:CAS:528:DyaF3cXht12ksbs%3D
    • DG Comb S Roseman 1960 The sialic acids. I. The structure and enzymatic synthesis of N-acetylneuraminic acid J Biol Chem 235 2529 2537 1:CAS:528:DyaF3cXht12ksbs%3D
    • (1960) J Biol Chem , vol.235 , pp. 2529-2537
    • Comb, D.G.1    Roseman, S.2
  • 6
    • 70449200010 scopus 로고
    • The synthesis of N-acetylneuraminic acid
    • 1:CAS:528:DyaG1cXmtVyksg%3D%3D
    • JW Cornforth ME Firth A Gottschalk 1958 The synthesis of N-acetylneuraminic acid Biochem J 68 57 61 1:CAS:528:DyaG1cXmtVyksg%3D%3D
    • (1958) Biochem J , vol.68 , pp. 57-61
    • Cornforth, J.W.1    Firth, M.E.2    Gottschalk, A.3
  • 7
    • 0035962918 scopus 로고    scopus 로고
    • Stereoselective synthesis of (S)-(+)-Naproxen catalyzed by carboxyl esterase in a multicompartment electrolyzer
    • DOI 10.1016/S0165-022X(01)00158-0, PII S0165022X01001580
    • M Cretich M Chiari G Carrea 2001 Stereoselective synthesis of (S)-(+)-naproxen catalyzed by carboxyl esterase in a multicompartment electrolyzer J Biochem Biophys Meth 48 247 256 10.1016/S0165-022X(01)00158-0 1:CAS:528:DC%2BD3MXjvV2rs7c%3D (Pubitemid 32510982)
    • (2001) Journal of Biochemical and Biophysical Methods , vol.48 , Issue.3 , pp. 247-256
    • Cretich, M.1    Chiari, M.2    Carrea, G.3
  • 10
    • 0023889181 scopus 로고
    • Stereoselective total syntheses of the naturally occurring enantiomers of N-acetylneuraminic acid and 3-deoxy-d-manno-2-octulosonic acid: A new and atereospecific approach to sialo and 3-deoxy-d-manno-2-octulosonic acid conjugates
    • 10.1021/ja00220a035 1:CAS:528:DyaL1cXit1ajs7c%3D
    • SJ Danishefsky MP DeNinno SH Chen 1988 Stereoselective total syntheses of the naturally occurring enantiomers of N-acetylneuraminic acid and 3-deoxy-d-manno-2-octulosonic acid: a new and atereospecific approach to sialo and 3-deoxy-d-manno-2-octulosonic acid conjugates J Am Chem Soc 110 3929 3940 10.1021/ja00220a035 1:CAS:528:DyaL1cXit1ajs7c%3D
    • (1988) J Am Chem Soc , vol.110 , pp. 3929-3940
    • Danishefsky, S.J.1    Deninno, M.P.2    Chen, S.H.3
  • 11
    • 0025745022 scopus 로고
    • The synthesis and glycosidation of N-acetylneuraminic acid
    • 10.1055/s-1991-26522
    • MP Deninno 1991 The synthesis and glycosidation of N-acetylneuraminic acid Synthesis 8 583 593 10.1055/s-1991-26522
    • (1991) Synthesis , vol.8 , pp. 583-593
    • Deninno, M.P.1
  • 12
    • 0035286968 scopus 로고    scopus 로고
    • Zanamivir and oseltamivir: Two new options for the treatment and prevention of influenza
    • 10.1016/S0149-2918(01)80042-4 1:CAS:528:DC%2BD3MXjvVartr4%3D
    • WB Dreitlein J Maratos J Brocavich 2001 Zanamivir and oseltamivir: two new options for the treatment and prevention of influenza Clin Ther 23 327 355 10.1016/S0149-2918(01)80042-4 1:CAS:528:DC%2BD3MXjvVartr4%3D
    • (2001) Clin Ther , vol.23 , pp. 327-355
    • Dreitlein, W.B.1    Maratos, J.2    Brocavich, J.3
  • 14
    • 0027933103 scopus 로고
    • Parotid saliva composition during and after irradiation of head and neck cancer
    • DOI 10.1016/0964-1955(94)90002-7
    • U Funegard L Franzen T Ericson R Henriksson 1994 Parotid saliva composition during and after irradiation of head and neck cancer Eur J Cancer B Oral Oncol 30B 230 233 10.1016/0964-1955(94)90002-7 1:STN:280: DyaK2M%2FjvValsA%3D%3D (Pubitemid 24257731)
    • (1994) European Journal of Cancer Part B: Oral Oncology , vol.30 , Issue.4 , pp. 230-233
    • Funegard, U.1    Franzen, L.2    Ericson, T.3    Henriksson, R.4
  • 15
    • 3042744805 scopus 로고    scopus 로고
    • Chemistry of N-acetylneuraminic acid (Neu5Ac)
    • 1:CAS:528:DC%2BD2cXlsFCjtrY%3D
    • K Furuhata 2004 Chemistry of N-acetylneuraminic acid (Neu5Ac) Trends Glycosci Glycotechnol 16 143 169 1:CAS:528:DC%2BD2cXlsFCjtrY%3D
    • (2004) Trends Glycosci Glycotechnol , vol.16 , pp. 143-169
    • Furuhata, K.1
  • 16
    • 33748530708 scopus 로고    scopus 로고
    • Enantioselective reduction of ketones with "designer cells" at high substrate concentrations: Highly efficient access to functionalized optically active alcohols
    • DOI 10.1002/anie.200503394
    • H Gröger F Chamouleau N Orologas C Rollmann K Drauz W Hummel A Weckbecker O May 2006 Enantioselective reduction of ketones with "designer cells" at high substrate concentrations: highly efficient access to functionalized optically active alcohols Angew Chem 45 5677 5681 10.1002/anie.200503394 (Pubitemid 44366776)
    • (2006) Angewandte Chemie - International Edition , vol.45 , Issue.34 , pp. 5677-5681
    • Groger, H.1    Chamouleau, F.2    Orologas, N.3    Rollmann, C.4    Drauz, K.5    Hummel, W.6    Weckbecker, A.7    May, O.8
  • 17
    • 0031994280 scopus 로고    scopus 로고
    • Microbial transformations
    • 10.1016/S1367-5931(98)80039-2 1:CAS:528:DyaK1cXitFygtbg%3D
    • HL Holland 1998 Microbial transformations Curr Opin Chem Biol 2 77 84 10.1016/S1367-5931(98)80039-2 1:CAS:528:DyaK1cXitFygtbg%3D
    • (1998) Curr Opin Chem Biol , vol.2 , pp. 77-84
    • Holland, H.L.1
  • 19
    • 76649137965 scopus 로고    scopus 로고
    • Coupled bioconversion for preparation of N-acetyl-d: -neuraminic acid using immobilized N-acetyl-d: -glucosamine-2-epimerase and N-acetyl-d: -neuraminic acid lyase
    • 10.1007/s00253-009-2163-9 1:CAS:528:DC%2BC3cXmvVGmtw%3D%3D
    • S Hu J Chen Z Yang L Shao H Bai J Luo W Jiang Y Yang 2010 Coupled bioconversion for preparation of N-acetyl-d: -neuraminic acid using immobilized N-acetyl-d: -glucosamine-2-epimerase and N-acetyl-d: -neuraminic acid lyase Appl Microbiol Biotechnol 85 1383 1391 10.1007/s00253-009-2163-9 1:CAS:528:DC%2BC3cXmvVGmtw%3D%3D
    • (2010) Appl Microbiol Biotechnol , vol.85 , pp. 1383-1391
    • Hu, S.1    Chen, J.2    Yang, Z.3    Shao, L.4    Bai, H.5    Luo, J.6    Jiang, W.7    Yang, Y.8
  • 20
    • 16244376449 scopus 로고    scopus 로고
    • Whole organism biocatalysis
    • DOI 10.1016/j.cbpa.2005.02.001, Bioorganic Chemistry / Biocatalysis and Biotransformation
    • T Ishige K Honda S Shimizu 2005 Whole organism biocatalysis Curr Opin Chem Biol 9 174 180 10.1016/j.cbpa.2005.02.001 1:CAS:528:DC%2BD2MXivFSlsrk%3D (Pubitemid 40462487)
    • (2005) Current Opinion in Chemical Biology , vol.9 , Issue.2 , pp. 174-180
    • Ishige, T.1    Honda, K.2    Shimizu, S.3
  • 21
    • 0038625074 scopus 로고    scopus 로고
    • Mimicking natural evolution in vitro: An N-acetylneuraminate lyase mutant with an increased dihydrodipicolinate synthase activity
    • DOI 10.1073/pnas.0531477100
    • AC Joerger S Mayer AR Fersht 2003 Mimicking natural evolution in vitro: an N-acetylneuraminate lyase mutant with an increased dihydrodipicolinate synthase activity Proc Natl Acad Sci USA 100 5694 5699 10.1073/pnas.0531477100 1:CAS:528:DC%2BD3sXjvFOlsr0%3D (Pubitemid 36576870)
    • (2003) Proceedings of the National Academy of Sciences of the United States of America , vol.100 , Issue.10 , pp. 5694-5699
    • Joerger, A.C.1    Mayer, S.2    Fersht, A.R.3
  • 22
    • 0026186301 scopus 로고
    • Large-scale preparation of sialic acid from chalaza and egg-yolk membrane
    • 10.1016/S0008-6215(00)90540-8 1:CAS:528:DyaK3MXltlWiu7c%3D
    • LR Juneja M Koketsu K Nishimoto M Kim T Yamamoto T Itoh 1991 Large-scale preparation of sialic acid from chalaza and egg-yolk membrane Carbohydr Res 214 179 186 10.1016/S0008-6215(00)90540-8 1:CAS:528:DyaK3MXltlWiu7c%3D
    • (1991) Carbohydr Res , vol.214 , pp. 179-186
    • Juneja, L.R.1    Koketsu, M.2    Nishimoto, K.3    Kim, M.4    Yamamoto, T.5    Itoh, T.6
  • 23
    • 63649129432 scopus 로고    scopus 로고
    • Comparison of the effectiveness of zanamivir and oseltamivir against influenza A/H1N1, A/H3N2, and B
    • 10.1086/597360
    • N Kawai H Ikematsu N Iwaki T Maeda T Kawashima N Hirotsu S Kashiwagi 2009 Comparison of the effectiveness of zanamivir and oseltamivir against influenza A/H1N1, A/H3N2, and B Clin Infect Dis 48 996 997 10.1086/597360
    • (2009) Clin Infect Dis , vol.48 , pp. 996-997
    • Kawai, N.1    Ikematsu, H.2    Iwaki, N.3    Maeda, T.4    Kawashima, T.5    Hirotsu, N.6    Kashiwagi, S.7
  • 24
    • 0030792933 scopus 로고    scopus 로고
    • Sialic acids in molecular and cellular interactions
    • 10.1016/S0074-7696(08)62127-0 1:CAS:528:DyaK2sXlvFalu7g%3D
    • S Kelm R Schauer 1997 Sialic acids in molecular and cellular interactions Int Rev Cytol 175 137 240 10.1016/S0074-7696(08)62127-0 1:CAS:528: DyaK2sXlvFalu7g%3D
    • (1997) Int Rev Cytol , vol.175 , pp. 137-240
    • Kelm, S.1    Schauer, R.2
  • 25
    • 0029731590 scopus 로고    scopus 로고
    • The sialoadhesins-a family of sialic acid-dependent cellular recognition molecules within the immunoglobulin superfamily
    • 10.1007/BF01053186 1:CAS:528:DyaK2sXjvFyruw%3D%3D
    • S Kelm R Schauer PR Crocker 1996 The sialoadhesins-a family of sialic acid-dependent cellular recognition molecules within the immunoglobulin superfamily Glycoconj J 13 913 926 10.1007/BF01053186 1:CAS:528: DyaK2sXjvFyruw%3D%3D
    • (1996) Glycoconj J , vol.13 , pp. 913-926
    • Kelm, S.1    Schauer, R.2    Crocker, P.R.3
  • 26
    • 0022648953 scopus 로고
    • Inhibition of experimental pulmonary metastasis of mouse colon adenocarcinoma 26 sublines by a sialic acid:nucleoside conjugate having sialyltransferase inhibiting activity
    • 1:CAS:528:DyaL28Xht1Ontbw%3D
    • I Kijima-Suda Y Miyamoto S Toyoshima M Itoh T Osawa 1986 Inhibition of experimental pulmonary metastasis of mouse colon adenocarcinoma 26 sublines by a sialic acid:nucleoside conjugate having sialyltransferase inhibiting activity Cancer Res 46 858 862 1:CAS:528:DyaL28Xht1Ontbw%3D
    • (1986) Cancer Res , vol.46 , pp. 858-862
    • Kijima-Suda, I.1    Miyamoto, Y.2    Toyoshima, S.3    Itoh, M.4    Osawa, T.5
  • 27
    • 0023766995 scopus 로고
    • Enzymes in carbohydrate synthesis-N-acetylneuraminic acid aldolase catalyzed-reactions and preparation of N-acetyl-2-deoxy-d-neuraminic acid-derivatives
    • 10.1021/ja00227a031 1:CAS:528:DyaL1cXlt1Ggur8%3D
    • MJ Kim WJ Hennen HM Sweers CH Wong 1988 Enzymes in carbohydrate synthesis-N-acetylneuraminic acid aldolase catalyzed-reactions and preparation of N-acetyl-2-deoxy-d-neuraminic acid-derivatives J Am Chem Soc 110 6481 6486 10.1021/ja00227a031 1:CAS:528:DyaL1cXlt1Ggur8%3D
    • (1988) J Am Chem Soc , vol.110 , pp. 6481-6486
    • Kim, M.J.1    Hennen, W.J.2    Sweers, H.M.3    Wong, C.H.4
  • 28
    • 0026556267 scopus 로고
    • Preparation of N-acetylneuraminic acid from delipidated egg yolk
    • 10.1007/BF00731701 1:CAS:528:DyaK38XktVemsLc%3D
    • M Koketsu LR Juneja H Kawanami M Kim T Yamamoto 1992 Preparation of N-acetylneuraminic acid from delipidated egg yolk Glycoconj J 9 70 74 10.1007/BF00731701 1:CAS:528:DyaK38XktVemsLc%3D
    • (1992) Glycoconj J , vol.9 , pp. 70-74
    • Koketsu, M.1    Juneja, L.R.2    Kawanami, H.3    Kim, M.4    Yamamoto, T.5
  • 29
    • 0025850357 scopus 로고
    • Enzymatic 2-step synthesis of N-acetylneuraminic acid in the enzyme membrane reactor
    • 10.1002/anie.199108271
    • U Kragl D Gygax O Ghisalba C Wandrey 1991 Enzymatic 2-step synthesis of N-acetylneuraminic acid in the enzyme membrane reactor Angew Chem 30 827 828 10.1002/anie.199108271
    • (1991) Angew Chem , vol.30 , pp. 827-828
    • Kragl, U.1    Gygax, D.2    Ghisalba, O.3    Wandrey, C.4
  • 30
    • 3142536462 scopus 로고    scopus 로고
    • Production of N-acetylneuraminic acid from N-acetylglucosamine and pyruvate using recombinant human renin binding protein and sialic acid aldolase in one pot
    • DOI 10.1016/j.enzmictec.2003.10.020, PII S0141022904001255
    • JO Lee JK Yi SG Lee S Takahashi BG Kim 2004 Production of N-acetylneuraminic acid from N-acetylglucosamine and pyruvate using recombinant human renin binding protein and sialic acid aldolase in one pot Enzyme Microb Technol 35 121 125 10.1016/j.enzmictec.2003.10.020 1:CAS:528: DC%2BD2cXls1ehsrc%3D (Pubitemid 38900988)
    • (2004) Enzyme and Microbial Technology , vol.35 , Issue.2-3 , pp. 121-125
    • Lee, J.-O.1    Yi, J.-K.2    Lee, S.-G.3    Takahashi, S.4    Kim, B.-G.5
  • 31
    • 34147123274 scopus 로고    scopus 로고
    • Production of N-acetyl-d-neuraminic acid by recombinant whole cells expressing Anabaena sp. CH1 N-acetyl-d-glucosamine 2-epimerase and Escherichia coli N-acetyl-d-neuraminic acid lyase
    • DOI 10.1016/j.jbiotec.2007.01.027, PII S0168165607001083
    • YC Lee HC Chien WH Hsu 2007 Production of N-acetyl-d-neuraminic acid by recombinant whole cells expressing Anabaena sp. CH1 N-acetyl-d-glucosamine 2-epimerase and Escherichia coli N-acetyl-d-neuraminic acid lyase J Biotechnol 129 453 460 10.1016/j.jbiotec.2007.01.027 1:CAS:528:DC%2BD2sXktFyqtr0%3D (Pubitemid 46560167)
    • (2007) Journal of Biotechnology , vol.129 , Issue.3 , pp. 453-460
    • Lee, Y.-C.1    Chien, H.-C.R.2    Hsu, W.-H.3
  • 32
    • 0000792452 scopus 로고
    • Unusual stereoselectivity in sialic acid aldolase-catalyzed aldol condensations: Synthesis of both enantiomers of high-carbon monosaccharides
    • 10.1021/ja00052a008 1:CAS:528:DyaK3sXlvF2ksg%3D%3D
    • CH Lin T Sugai RL Halcomb Y Ichikawa CH Wong 1992 Unusual stereoselectivity in sialic acid aldolase-catalyzed aldol condensations: synthesis of both enantiomers of high-carbon monosaccharides J Am Chem Soc 114 10138 10145 10.1021/ja00052a008 1:CAS:528:DyaK3sXlvF2ksg%3D%3D
    • (1992) J Am Chem Soc , vol.114 , pp. 10138-10145
    • Lin, C.H.1    Sugai, T.2    Halcomb, R.L.3    Ichikawa, Y.4    Wong, C.H.5
  • 34
    • 0031874166 scopus 로고    scopus 로고
    • Simple and large-scale production of N-acetylneuraminic acid from N- acetyl-D-glucosamine and pyruvate using N-acyl-dglucosamine 2-epimerase and n-acetylneuraminate lyase
    • DOI 10.1016/S0008-6215(97)10106-9, PII S0008621597101069
    • I Maru J Ohnishi Y Ohta Y Tsukada 1998 Simple and large-scale production of N-acetylneuraminic acid from N-acetyl-d-glucosamine and pyruvate using N-acyl-d-glucosamine 2-epimerase and N-acetylneuraminate lyase Carbohydr Res 306 575 578 10.1016/S0008-6215(97)10106-9 1:CAS:528:DyaK1cXmt1ejtLc%3D (Pubitemid 28318110)
    • (1998) Carbohydrate Research , vol.306 , Issue.4 , pp. 575-578
    • Maru, I.1    Ohnishi, J.2    Ohta, Y.3    Tsukada, Y.4
  • 35
    • 0036105953 scopus 로고    scopus 로고
    • Why is sialic acid attracting interest now? Complete enzymatic synthesis of sialic acid with N-acylglucosamine 2-epimerase
    • 10.1263/jbb.93.258 1:CAS:528:DC%2BD38Xjs1WgsLw%3D
    • I Maru J Ohnishi Y Ohta Y Tsukada 2002 Why is sialic acid attracting interest now? Complete enzymatic synthesis of sialic acid with N-acylglucosamine 2-epimerase J Biosci Bioeng 93 258 265 10.1263/jbb.93.258 1:CAS:528: DC%2BD38Xjs1WgsLw%3D
    • (2002) J Biosci Bioeng , vol.93 , pp. 258-265
    • Maru, I.1    Ohnishi, J.2    Ohta, Y.3    Tsukada, Y.4
  • 37
    • 25444501243 scopus 로고    scopus 로고
    • Neuraminidase inhibitors for influenza
    • DOI 10.1056/NEJMra050740
    • A Moscona 2005 Neuraminidase inhibitors for influenza New Engl J Med 353 1363 1373 10.1056/NEJMra050740 1:CAS:528:DC%2BD2MXhtVGmtL3L (Pubitemid 41362704)
    • (2005) New England Journal of Medicine , vol.353 , Issue.13 , pp. 1363-1373
    • Moscona, A.1
  • 38
    • 0142042801 scopus 로고    scopus 로고
    • Anti-adhesion therapy of bacterial diseases: Prospects and problems
    • DOI 10.1016/S0928-8244(03)00228-1
    • I Ofek DL Hasty N Sharon 2003 Anti-adhesion therapy of bacterial diseases: prospects and problems FEMS Immunol Med Microbiol 38 181 191 10.1016/S0928-8244(03)00228-1 1:CAS:528:DC%2BD3sXns12mu70%3D (Pubitemid 37289742)
    • (2003) FEMS Immunology and Medical Microbiology , vol.38 , Issue.3 , pp. 181-191
    • Ofek, I.1    Hasty, D.L.2    Sharon, N.3
  • 39
    • 0036809880 scopus 로고    scopus 로고
    • A bright future for anti-adhesion therapy of infectious diseases
    • 10.1007/PL00012494 1:CAS:528:DC%2BD38XovVOnur4%3D
    • I Ofek N Sharon 2002 A bright future for anti-adhesion therapy of infectious diseases Cell Mol Life Sci 59 1666 1667 10.1007/PL00012494 1:CAS:528:DC%2BD38XovVOnur4%3D
    • (2002) Cell Mol Life Sci , vol.59 , pp. 1666-1667
    • Ofek, I.1    Sharon, N.2
  • 40
    • 12844287005 scopus 로고    scopus 로고
    • The coenzyme specificity of Candida tenuis xylose reductase (AKR2B5) explored by site-directed mutagenesis and X-ray crystallography
    • DOI 10.1042/BJ20040363
    • B Petschacher S Leitgeb KL Kavanagh DK Wilson B Nidetzky 2005 The coenzyme specificity of Candida tenuis xylose reductase (AKR2B5) explored by site-directed mutagenesis and X-ray crystallography Biochem J 385 75 83 10.1042/BJ20040363 1:CAS:528:DC%2BD2cXhtVOht7bE (Pubitemid 40164025)
    • (2005) Biochemical Journal , vol.385 , Issue.1 , pp. 75-83
    • Petschacher, B.1    Leitgeb, S.2    Kavanagh, K.L.3    Wilson, D.K.4    Nidetzky, B.5
  • 41
    • 42449145157 scopus 로고    scopus 로고
    • Altering the coenzyme preference of xylose reductase to favor utilization of NADH enhances ethanol yield from xylose in a metabolically engineered strain of Saccharomyces cerevisiae
    • B Petschacher B Nidetzky 2008 Altering the coenzyme preference of xylose reductase to favor utilization of NADH enhances ethanol yield from xylose in a metabolically engineered strain of Saccharomyces cerevisiae Microb Cell Fact 7 9
    • (2008) Microb Cell Fact , vol.7 , pp. 9
    • Petschacher, B.1    Nidetzky, B.2
  • 42
    • 0025572709 scopus 로고
    • ELAM-1 mediates cell adhesion by recognition of a carbohydrate ligand, sialyl-lex
    • 10.1126/science.1701274 1:CAS:528:DyaK3MXnvFaisw%3D%3D
    • ML Phillips E Nudelman FC Gaeta M Perez AK Singhal S Hakomori JC Paulson 1990 ELAM-1 mediates cell adhesion by recognition of a carbohydrate ligand, sialyl-lex Science 250 1130 1132 10.1126/science.1701274 1:CAS:528: DyaK3MXnvFaisw%3D%3D
    • (1990) Science , vol.250 , pp. 1130-1132
    • Phillips, M.L.1    Nudelman, E.2    Gaeta, F.C.3    Perez, M.4    Singhal, A.K.5    Hakomori, S.6    Paulson, J.C.7
  • 43
    • 0032929297 scopus 로고    scopus 로고
    • Convergent pathways for utilization of the amino sugars N-acetylglucosamine, N-acetylmannosamine, and N-acetylneuraminic acid by Escherichia coli
    • 1:CAS:528:DyaK1MXitFWhtA%3D%3D
    • J Plumbridge E Vimr 1999 Convergent pathways for utilization of the amino sugars N-acetylglucosamine, N-acetylmannosamine, and N-acetylneuraminic acid by Escherichia coli J Bacteriol 181 47 54 1:CAS:528:DyaK1MXitFWhtA%3D%3D
    • (1999) J Bacteriol , vol.181 , pp. 47-54
    • Plumbridge, J.1    Vimr, E.2
  • 44
    • 0029043814 scopus 로고
    • N-acetyl-d-neuraminic acid synthesis in Escherichia coli K1 occurs through condensation of N-acetyl-d-mannosamine and pyruvate
    • 1:CAS:528:DyaK2MXmtFersrY%3D
    • LB Rodriguez-Aparicio MA Ferrero A Reglero 1995 N-acetyl-d-neuraminic acid synthesis in Escherichia coli K1 occurs through condensation of N-acetyl-d-mannosamine and pyruvate Biochem J 308 Pt 2 501 505 1:CAS:528:DyaK2MXmtFersrY%3D
    • (1995) Biochem J , vol.308 , Issue.PART 2 , pp. 501-505
    • Rodriguez-Aparicio, L.B.1    Ferrero, M.A.2    Reglero, A.3
  • 45
    • 0034444960 scopus 로고    scopus 로고
    • Achievements and challenges of sialic acid research
    • DOI 10.1023/A:1011062223612
    • R Schauer 2000 Achievements and challenges of sialic acid research Glycoconj J 17 485 499 10.1023/A:1011062223612 1:CAS:528:DC%2BD3MXksVOgtL8%3D (Pubitemid 32480340)
    • (2000) Glycoconjugate Journal , vol.17 , Issue.7-9 , pp. 485-499
    • Schauer, R.1
  • 46
    • 0021453752 scopus 로고
    • The anti-recognition function of sialic acids: Studies with erythrocytes and macrophages
    • 10.1351/pac198456070907 1:CAS:528:DyaL2cXlsV2mtL8%3D
    • R Schauer AK Shukla C Schröder E Müller 1984 The anti-recognition function of sialic acids: studies with erythrocytes and macrophages Pure Appl Chem 56 907 921 10.1351/pac198456070907 1:CAS:528:DyaL2cXlsV2mtL8%3D
    • (1984) Pure Appl Chem , vol.56 , pp. 907-921
    • Schauer, R.1    Shukla, A.K.2    Schröder, C.3    Müller, E.4
  • 47
    • 0035843170 scopus 로고    scopus 로고
    • Industrial biocatalysis today and tomorrow
    • DOI 10.1038/35051736
    • A Schmid JS Dordick B Hauer A Kiener M Wubbolts B Witholt 2001 Industrial biocatalysis today and tomorrow Nature 409 258 268 10.1038/35051736 1:CAS:528:DC%2BD3MXlvFWhug%3D%3D (Pubitemid 32144296)
    • (2001) Nature , vol.409 , Issue.6817 , pp. 258-268
    • Schmid, A.1    Dordick, J.S.2    Hauer, B.3    Kiener, A.4    Wubbolts, M.5    Witholt, B.6
  • 48
    • 84988126671 scopus 로고
    • Nitriles as solvents in glycosylation reactions: Highly selective β-glycoside synthesis
    • 10.1055/s-1990-21214
    • RR Schmidt M Behrendt A Toepfer 1990 Nitriles as solvents in glycosylation reactions: highly selective β-glycoside synthesis Synlett 11 694 696 10.1055/s-1990-21214
    • (1990) Synlett , vol.11 , pp. 694-696
    • Schmidt, R.R.1    Behrendt, M.2    Toepfer, A.3
  • 49
    • 0037436563 scopus 로고    scopus 로고
    • Dispelling the myths - Biocatalysis in industrial synthesis
    • DOI 10.1126/science.1079237
    • HE Schoemaker D Mink MG Wubbolts 2003 Dispelling the myths-biocatalysis in industrial synthesis Science 299 1694 1697 10.1126/science.1079237 1:CAS:528:DC%2BD3sXitVSjtLk%3D (Pubitemid 36337188)
    • (2003) Science , vol.299 , Issue.5613 , pp. 1694-1697
    • Schoemaker, H.E.1    Mink, D.2    WubboLts, M.G.3
  • 50
    • 33646103431 scopus 로고    scopus 로고
    • Carbohydrates as future anti-adhesion drugs for infectious diseases
    • 1:CAS:528:DC%2BD28Xjsl2msb0%3D
    • N Sharon 2006 Carbohydrates as future anti-adhesion drugs for infectious diseases Biochim Biophys Acta 1760 527 537 1:CAS:528:DC%2BD28Xjsl2msb0%3D
    • (2006) Biochim Biophys Acta , vol.1760 , pp. 527-537
    • Sharon, N.1
  • 51
    • 0034441393 scopus 로고    scopus 로고
    • Safe as mother's milk: Carbohydrates as future anti-adhesion drugs for bacterial diseases
    • DOI 10.1023/A:1011091029973
    • N Sharon I Ofek 2000 Safe as mother's milk: carbohydrates as future anti-adhesion drugs for bacterial diseases Glycoconj J 17 659 664 10.1023/A:1011091029973 1:CAS:528:DC%2BD3MXksVOgtb0%3D (Pubitemid 32480351)
    • (2000) Glycoconjugate Journal , vol.17 , Issue.7-9 , pp. 659-664
    • Sharon, N.1    Ofek, I.2
  • 53
    • 0031037910 scopus 로고    scopus 로고
    • Inhibition of Helicobacter pylori binding to gastrointestinal epithelial cells by sialic acid-containing oligosaccharides
    • 1:CAS:528:DyaK2sXpvVSlsg%3D%3D
    • PM Simon PL Goode A Mobasseri D Zopf 1997 Inhibition of Helicobacter pylori binding to gastrointestinal epithelial cells by sialic acid-containing oligosaccharides Infect Immun 65 750 757 1:CAS:528:DyaK2sXpvVSlsg%3D%3D
    • (1997) Infect Immun , vol.65 , pp. 750-757
    • Simon, P.M.1    Goode, P.L.2    Mobasseri, A.3    Zopf, D.4
  • 55
    • 0001047463 scopus 로고
    • Preparation of N-acetyl-d-mannosamine (2-acetamido-2-deoxy-d-mannose) and d-mannosamine hydrochloride (2-amino-2-deoxy-d-mannose)
    • 10.1021/ja01519a031 1:CAS:528:DyaG1MXht1Wms7w%3D
    • CT Spivak S Roseman 1959 Preparation of N-acetyl-d-mannosamine (2-acetamido-2-deoxy-d-mannose) and d-mannosamine hydrochloride (2-amino-2-deoxy-d-mannose) J Am Chem Soc 81 2403 2404 10.1021/ja01519a031 1:CAS:528:DyaG1MXht1Wms7w%3D
    • (1959) J Am Chem Soc , vol.81 , pp. 2403-2404
    • Spivak, C.T.1    Roseman, S.2
  • 56
    • 0036900263 scopus 로고    scopus 로고
    • The production of fine chemicals by biotransformations
    • DOI 10.1016/S0958-1669(02)00360-9
    • AJ Straathof S Panke A Schmid 2002 The production of fine chemicals by biotransformations Curr Opin Biotechnol 13 548 556 10.1016/S0958-1669(02)00360-9 1:CAS:528:DC%2BD38XptlWlsLk%3D (Pubitemid 35448055)
    • (2002) Current Opinion in Biotechnology , vol.13 , Issue.6 , pp. 548-556
    • Straathof, A.J.J.1    Panke, S.2    Schmid, A.3
  • 57
    • 0029620465 scopus 로고
    • Improved enzymatic procedure for a preparative-scale synthesis of sialic acid and KDN
    • DOI 10.1246/bcsj.68.3581
    • T Sugai A Kuboki S Hiramatsu H Okazaki H Ohta 1995 Improved enzymatic procedure for a preparative-scale synthesis of sialic acid and KDN Bull Chem Soc Jpn 68 3581 3589 10.1246/bcsj.68.3581 1:CAS:528:DyaK28XpvFCr (Pubitemid 26022493)
    • (1995) Bulletin of the Chemical Society of Japan , vol.68 , Issue.12 , pp. 3581-3589
    • Sugai, T.1    Kuboki, A.2    Hiramatsu, S.3    Okazaki, H.4    Ohta, H.5
  • 58
    • 0037070491 scopus 로고    scopus 로고
    • Production of N-acetyl-D-neuraminic acid by coupling bacteria expressing N-acetyl-D-glucosamine 2-epimerase and N-acetyl-D-neuraminic acid synthetase
    • DOI 10.1016/S0141-0229(01)00515-4, PII S0141022901005154
    • K Tabata S Koizumi T Endo A Ozaki 2002 Production of N-acetyl-d- neuraminic acid by coupling bacteria expressing N-acetyl-d-glucosamine 2-epimerase and N-acetyl-d-neuraminic acid synthetase Enzyme Microb Technol 30 327 333 10.1016/S0141-0229(01)00515-4 1:CAS:528:DC%2BD38XhslWhu74%3D (Pubitemid 34203842)
    • (2002) Enzyme and Microbial Technology , vol.30 , Issue.3 , pp. 327-333
    • Tabata, K.1    Koizumi, S.2    Endo, T.3    Ozaki, A.4
  • 59
    • 0032443144 scopus 로고    scopus 로고
    • Structure, function and metabolism of sialic acids
    • DOI 10.1007/s000180050258
    • C Traving R Schauer 1998 Structure, function and metabolism of sialic acids Cell Mol Life Sci 54 1330 1349 10.1007/s000180050258 1:CAS:528: DyaK1MXitlGltg%3D%3D (Pubitemid 29015295)
    • (1998) Cellular and Molecular Life Sciences , vol.54 , Issue.12 , pp. 1330-1349
    • Traving, C.1    Schauer, R.2
  • 60
    • 0023933272 scopus 로고
    • Synthetic sialyl compounds as well as natural gangliosides induce neuritogenesis in a mouse neuroblastoma cell line (Neuro2a)
    • 10.1111/j.1471-4159.1988.tb02928.x 1:CAS:528:DyaL1cXhs1ars7s%3D
    • S Tsuji T Yamashita M Tanaka Y Nagai 1988 Synthetic sialyl compounds as well as natural gangliosides induce neuritogenesis in a mouse neuroblastoma cell line (Neuro2a) J Neurochem 50 414 423 10.1111/j.1471-4159.1988.tb02928.x 1:CAS:528:DyaL1cXhs1ars7s%3D
    • (1988) J Neurochem , vol.50 , pp. 414-423
    • Tsuji, S.1    Yamashita, T.2    Tanaka, M.3    Nagai, Y.4
  • 61
    • 34547929295 scopus 로고    scopus 로고
    • Diversity in cell surface sialic acid presentations: Implications for biology and disease
    • DOI 10.1038/labinvest.3700656, PII 3700656
    • NM Varki A Varki 2007 Diversity in cell surface sialic acid presentations: implications for biology and disease Lab Invest 87 851 857 10.1038/labinvest.3700656 1:CAS:528:DC%2BD2sXptFensbg%3D (Pubitemid 47267816)
    • (2007) Laboratory Investigation , vol.87 , Issue.9 , pp. 851-857
    • Varki, N.M.1    Varki, A.2
  • 62
    • 36749056771 scopus 로고    scopus 로고
    • The war against influenza: Discovery and development of sialidase inhibitors
    • DOI 10.1038/nrd2400, PII NRD2400
    • M von Itzstein 2007 The war against influenza: discovery and development of sialidase inhibitors Nat Rev Drug Discov 6 967 974 10.1038/nrd2400 (Pubitemid 350201787)
    • (2007) Nature Reviews Drug Discovery , vol.6 , Issue.12 , pp. 967-974
    • Von Itzstein, M.1
  • 64
    • 68849112214 scopus 로고    scopus 로고
    • Production of N-acetyl-d-neuraminic acid using two sequential enzymes overexpressed as double-tagged fusion proteins
    • 10.1186/1472-6750-9-63 1:CAS:528:DC%2BC3cXltVyjsLg%3D
    • TH Wang YY Chen HH Pan FP Wang CH Cheng WC Lee 2009 Production of N-acetyl-d-neuraminic acid using two sequential enzymes overexpressed as double-tagged fusion proteins BMC Biotechnol 9 63 10.1186/1472-6750-9-63 1:CAS:528:DC%2BC3cXltVyjsLg%3D
    • (2009) BMC Biotechnol , vol.9 , pp. 63
    • Wang, T.H.1    Chen, Y.Y.2    Pan, H.H.3    Wang, F.P.4    Cheng, C.H.5    Lee, W.C.6
  • 65
    • 0028804946 scopus 로고
    • Cell-contact mediated modulation of the sialylation of contactinhibin
    • 10.1007/BF00731264 1:CAS:528:DyaK2MXovVemsrk%3D
    • RJ Wieser CE Baumann F Oesch 1995 Cell-contact mediated modulation of the sialylation of contactinhibin Glycoconj J 12 672 679 10.1007/BF00731264 1:CAS:528:DyaK2MXovVemsrk%3D
    • (1995) Glycoconj J , vol.12 , pp. 672-679
    • Wieser, R.J.1    Baumann, C.E.2    Oesch, F.3
  • 67
    • 34547211296 scopus 로고    scopus 로고
    • Efficient whole-cell biocatalytic synthesis of N-acetyl-d-neuraminic acid
    • 10.1002/adsc.200700094 1:CAS:528:DC%2BD2sXos1Cquro%3D
    • P Xu JH Qiu YN Zhang J Chen PG Wang B Yan J Song RM Xi ZX Deng CQ Ma 2007 Efficient whole-cell biocatalytic synthesis of N-acetyl-d-neuraminic acid Adv Synth Catal 349 1614 1618 10.1002/adsc.200700094 1:CAS:528:DC%2BD2sXos1Cquro%3D
    • (2007) Adv Synth Catal , vol.349 , pp. 1614-1618
    • Xu, P.1    Qiu, J.H.2    Zhang, Y.N.3    Chen, J.4    Wang, P.G.5    Yan, B.6    Song, J.7    Xi, R.M.8    Deng, Z.X.9    Ma, C.Q.10
  • 68
    • 0014669636 scopus 로고
    • Configuration of the ketosidic bond of sialic acid
    • 1:CAS:528:DyaF1MXmsVChuw%3D%3D
    • RK Yu R Ledeen 1969 Configuration of the ketosidic bond of sialic acid J Biol Chem 244 1306 1313 1:CAS:528:DyaF1MXmsVChuw%3D%3D
    • (1969) J Biol Chem , vol.244 , pp. 1306-1313
    • Yu, R.K.1    Ledeen, R.2
  • 69
    • 77249100713 scopus 로고    scopus 로고
    • An efficient method for N-acetyl-d-neuraminic acid production using coupled bacterial cells with a safe temperature-induced system
    • 10.1007/s00253-009-2302-3 1:CAS:528:DC%2BC3cXit1amsLo%3D
    • Y Zhang F Tao M Du C Ma J Qiu L Gu X He P Xu 2010 An efficient method for N-acetyl-d-neuraminic acid production using coupled bacterial cells with a safe temperature-induced system Appl Microbiol Biotechnol 86 481 489 10.1007/s00253-009-2302-3 1:CAS:528:DC%2BC3cXit1amsLo%3D
    • (2010) Appl Microbiol Biotechnol , vol.86 , pp. 481-489
    • Zhang, Y.1    Tao, F.2    Du, M.3    Ma, C.4    Qiu, J.5    Gu, L.6    He, X.7    Xu, P.8
  • 70
    • 34548017156 scopus 로고    scopus 로고
    • Modelling the reaction course of N-acetylneuraminic acid synthesis from N-acetyl-D-glucosamine - New strategies for the optimisation of neuraminic acid synthesis
    • DOI 10.1007/s00253-007-1033-6
    • V Zimmermann HG Hennemann T Daussmann U Kragl 2007 Modelling the reaction course of N-acetylneuraminic acid synthesis from N-acetyl-d-glucosamine-new strategies for the optimisation of neuraminic acid synthesis Appl Microbiol Biotechnol 76 597 605 10.1007/s00253-007-1033-6 1:CAS:528:DC%2BD2sXpt1ahtrs%3D (Pubitemid 47283110)
    • (2007) Applied Microbiology and Biotechnology , vol.76 , Issue.3 , pp. 597-605
    • Zimmermann, V.1    Hennemann, H.-G.2    Daussmann, T.3    Kragl, U.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.