메뉴 건너뛰기




Volumn 93, Issue 1, 2006, Pages 48-55

Influence of secondary reactions on the synthetic efficiency of DHAP-aldolases

Author keywords

Aldolases; DHAP; Secondary reactions; Stereoselective synthesis

Indexed keywords

BIOCATALYSTS; CATALYSIS; REACTION KINETICS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

EID: 30944454261     PISSN: 00063592     EISSN: 10970290     Source Type: Journal    
DOI: 10.1002/bit.20690     Document Type: Article
Times cited : (18)

References (26)
  • 1
    • 3042767989 scopus 로고    scopus 로고
    • Studies on the expression of recombinant fuculose-1-phosphate aldolase in E.coli
    • Durany O, Caminal G, de Mas C, López-Santín J. 2004. Studies on the expression of recombinant fuculose-1-phosphate aldolase in E.coli. Process Biochem 39:1677-1684.
    • (2004) Process Biochem , vol.39 , pp. 1677-1684
    • Durany, O.1    Caminal, G.2    De Mas, C.3    López-Santín, J.4
  • 2
    • 7444235940 scopus 로고    scopus 로고
    • Fed-batch production of recombinant fuculose-1-phosphate aldolase in E. Coli
    • Durany O, de Mas C, López-Santín J. 2005. Fed-batch production of recombinant fuculose-1-phosphate aldolase in E. Coli. Process Biochem 40:707-716.
    • (2005) Process Biochem , vol.40 , pp. 707-716
    • Durany, O.1    De Mas, C.2    López-Santín, J.3
  • 3
    • 0142228971 scopus 로고    scopus 로고
    • Stereoselective aldol additions catalyzed by dihydroxyacetone phosphate dependent aldolases in emulsion systems: Preparation and structural characterization of linear and cyclic aminopolyols from aminoaldehydes
    • Espelt L, Parella T, Bujons J, Solans C, Joglar J, Delgado A, Clapés P. 2003a. Stereoselective aldol additions catalyzed by dihydroxyacetone phosphate dependent aldolases in emulsion systems: Preparation and structural characterization of linear and cyclic aminopolyols from aminoaldehydes. Chem Eur J 9:4887-4899.
    • (2003) Chem Eur J , vol.9 , pp. 4887-4899
    • Espelt, L.1    Parella, T.2    Bujons, J.3    Solans, C.4    Joglar, J.5    Delgado, A.6    Clapés, P.7
  • 4
    • 0037452629 scopus 로고    scopus 로고
    • Enzymatic Carbon-Carbon bond formation in water-in-oil highly concentrated emulsions (gel emulsions)
    • Espelt L, Clapes P, Esquena J, Manich A, Solans C. 2003b. Enzymatic Carbon-Carbon bond formation in water-in-oil highly concentrated emulsions (gel emulsions). Langmuir 19:1337-1346.
    • (2003) Langmuir , vol.19 , pp. 1337-1346
    • Espelt, L.1    Clapes, P.2    Esquena, J.3    Manich, A.4    Solans, C.5
  • 5
    • 14844302834 scopus 로고    scopus 로고
    • Aldol additions of dihydroxyacetone phosphate to N-Cbz-amino aldehydes catalyzed by L-Fuculose-1-Phosphate aldolase in emulsion systems: Inversion of stereoselectivity as a function of the acceptor aldehyde
    • Espelt L, Bujons J, Parella T, Calveras J, Joglar J, Delgado A, Clapes P. 2005. Aldol additions of dihydroxyacetone phosphate to N-Cbz-amino aldehydes catalyzed by L-Fuculose-1-Phosphate aldolase in emulsion systems: Inversion of stereoselectivity as a function of the acceptor aldehyde. Chem Eur J 11:1392-1401.
    • (2005) Chem Eur J , vol.11 , pp. 1392-1401
    • Espelt, L.1    Bujons, J.2    Parella, T.3    Calveras, J.4    Joglar, J.5    Delgado, A.6    Clapes, P.7
  • 6
    • 0028099491 scopus 로고
    • Higher-carbon sugars by enzymatic chain extension. Oxidative generation of aldol precursors in situ
    • Eyrisch O, Keller M, Fessner WD. 1994. Higher-carbon sugars by enzymatic chain extension. Oxidative generation of aldol precursors in situ. Tetrahedron Lett 35:9013-9016.
    • (1994) Tetrahedron Lett , vol.35 , pp. 9013-9016
    • Eyrisch, O.1    Keller, M.2    Fessner, W.D.3
  • 7
    • 2442762438 scopus 로고    scopus 로고
    • Chemical and chemo-enzymatic approaches to unnatural ketoses and glycosidase inhibitors with basic nitrogen in the sugar ring
    • Fechter MH, Stutz AE, Tauss A. 1999. Chemical and chemo-enzymatic approaches to unnatural ketoses and glycosidase inhibitors with basic nitrogen in the sugar ring. Curr Org Chem 3:269-285.
    • (1999) Curr Org Chem , vol.3 , pp. 269-285
    • Fechter, M.H.1    Stutz, A.E.2    Tauss, A.3
  • 8
    • 0035709383 scopus 로고    scopus 로고
    • Biocatalytic synthesis of hydroxylated natural products using aldolases and related enzymes
    • Fessner WD, Helaine V. 2001. Biocatalytic synthesis of hydroxylated natural products using aldolases and related enzymes. Curr Opin Biotech 12: 574-586.
    • (2001) Curr Opin Biotech , vol.12 , pp. 574-586
    • Fessner, W.D.1    Helaine, V.2
  • 9
    • 0002350948 scopus 로고    scopus 로고
    • Enzymatic C-C bond formation in asymmetric synthesis
    • Fessner WD, Walter C. 1996. Enzymatic C-C bond formation in asymmetric synthesis. Top Curr Chem 184:97-194.
    • (1996) Top Curr Chem , vol.184 , pp. 97-194
    • Fessner, W.D.1    Walter, C.2
  • 11
    • 28244468595 scopus 로고
    • 6-Deoxy-L-lyxo- and 6-deoxy-L arabino-hexulose 1-phosphates. Enzymic synthesis by antagonistic metabolic pathways
    • Fessner W, Schneider A, Eyrisch O, Sinerius G, Badia J. 1993. 6-Deoxy-L-lyxo- and 6-deoxy-L arabino-hexulose 1-phosphates. Enzymic synthesis by antagonistic metabolic pathways. Tetrehedron Asymm 41:781-790.
    • (1993) Tetrehedron Asymm , vol.41 , pp. 781-790
    • Fessner, W.1    Schneider, A.2    Eyrisch, O.3    Sinerius, G.4    Badia, J.5
  • 12
    • 0033546262 scopus 로고    scopus 로고
    • A user-friendly entry to 2-lodoxybenzoic Acid (IBX)
    • Frigerio M, Santagostino M, Sputore S. 1999. A user-friendly entry to 2-lodoxybenzoic Acid (IBX). J Org Chem 64:4537-4538.
    • (1999) J Org Chem , vol.64 , pp. 4537-4538
    • Frigerio, M.1    Santagostino, M.2    Sputore, S.3
  • 13
    • 3042819881 scopus 로고    scopus 로고
    • Enzymes in preparative mono- and oligo-saccharide synthesis
    • Hamilton CJ. 2004. Enzymes in preparative mono- and oligo-saccharide synthesis. Nat Prod Rep 21:365-385.
    • (2004) Nat Prod Rep , vol.21 , pp. 365-385
    • Hamilton, C.J.1
  • 15
    • 0033657768 scopus 로고    scopus 로고
    • Complex carbohydrate synthesis tools for glycobiologists: Enzyme-based approach and programmable one-pot strategies
    • Koeller KM, Wong CH. 2000. Complex carbohydrate synthesis tools for glycobiologists: Enzyme-based approach and programmable one-pot strategies. Glycobiology 10:1157-1169.
    • (2000) Glycobiology , vol.10 , pp. 1157-1169
    • Koeller, K.M.1    Wong, C.H.2
  • 16
    • 0034678591 scopus 로고    scopus 로고
    • The catalytic asymmetric aldol reaction
    • Machajewski TD, Wong CH. 2000. The catalytic asymmetric aldol reaction. Angew Chem Int Ed 39:1353-1374.
    • (2000) Angew Chem Int Ed , vol.39 , pp. 1353-1374
    • Machajewski, T.D.1    Wong, C.H.2
  • 17
    • 0027396022 scopus 로고
    • The formation of methylglyoxal from triose phosphates
    • Phillips S, Thornalley PJ. 1993. The formation of methylglyoxal from triose phosphates. Eur J Biochem 212:101-105.
    • (1993) Eur J Biochem , vol.212 , pp. 101-105
    • Phillips, S.1    Thornalley, P.J.2
  • 18
    • 0021471746 scopus 로고
    • Acid-base catalysis for the elimination and isomerization reactions of triose phosphates
    • Richard JP. 1984. Acid-base catalysis for the elimination and isomerization reactions of triose phosphates. J Am Chem Soc 106:4926-4936.
    • (1984) J Am Chem Soc , vol.106 , pp. 4926-4936
    • Richard, J.P.1
  • 19
    • 0027286747 scopus 로고
    • Mechanism for the formation of methylglyoxal from triosephosphates
    • Richard JP. 1993. Mechanism for the formation of methylglyoxal from triosephosphates. Biochem Soc Trans 21:549-553.
    • (1993) Biochem Soc Trans , vol.21 , pp. 549-553
    • Richard, J.P.1
  • 20
    • 0030792812 scopus 로고    scopus 로고
    • Microbial aldolases and transketolases: New biocatalytic approaches to simple and complex sugars
    • Takayama S, McGarvey GJ, Wong CH. 1997. Microbial aldolases and transketolases: New biocatalytic approaches to simple and complex sugars. Annu Rev Microbiol 51:285-310.
    • (1997) Annu Rev Microbiol , vol.51 , pp. 285-310
    • Takayama, S.1    McGarvey, G.J.2    Wong, C.H.3
  • 21
    • 0021859376 scopus 로고
    • High-performance liquid chromatographie determination of glucose 1-phosphate and glucuronic acid 1-phosphate
    • Tjioe TT, Van der Wiel JP, Stickkelman RM, Straathof AJ, Van Rantwijk F. 1985. High-performance liquid chromatographie determination of glucose 1-phosphate and glucuronic acid 1-phosphate. J Chromatogr 330:412-414.
    • (1985) J Chromatogr , vol.330 , pp. 412-414
    • Tjioe, T.T.1    Van Der Wiel, J.P.2    Stickkelman, R.M.3    Straathof, A.J.4    Van Rantwijk, F.5
  • 22
    • 0142027677 scopus 로고    scopus 로고
    • High level production of recombinant His-tagged rhamnulose-1-phosphate aldolase in Escherichia coli
    • Vidal L, Durany O, Suau T, Ferrer P, Benaiges MD, Caminal G. 2003. High level production of recombinant His-tagged rhamnulose-1-phosphate aldolase in Escherichia coli. J Chem Technol Biotechnol 78:1171-1179.
    • (2003) J Chem Technol Biotechnol , vol.78 , pp. 1171-1179
    • Vidal, L.1    Durany, O.2    Suau, T.3    Ferrer, P.4    Benaiges, M.D.5    Caminal, G.6
  • 23
    • 0024337552 scopus 로고
    • Use of a recombinant bacterial fructose-1,6-diphosphate aldolase in aldol reactions: Preparative syntheses of 1-deoxynojirimycin, 1-deoxymannojirimycin, 1,4-dideoxy-1,4-imino-D-arabinitol, and fagomine
    • von der Osten CH, Sinskey AJ, Barbas CF III, Pederson RL, Wang YF, Wong CH. 1989. Use of a recombinant bacterial fructose-1,6-diphosphate aldolase in aldol reactions: Preparative syntheses of 1-deoxynojirimycin, 1-deoxymannojirimycin, 1,4-dideoxy-1,4-imino-D-arabinitol, and fagomine. J Am Chem Soc 111:3924-3927.
    • (1989) J Am Chem Soc , vol.111 , pp. 3924-3927
    • Von Der Osten, C.H.1    Sinskey, A.J.2    Barbas III, C.F.3    Pederson, R.L.4    Wang, Y.F.5    Wong, C.H.6
  • 25
    • 0033964068 scopus 로고    scopus 로고
    • Enzyme-catalyzed synthesis of carbohydrates
    • Wymer M, Toone EJ. 2000. Enzyme-catalyzed synthesis of carbohydrates. Curr Opin Chem Biol 4:110-119.
    • (2000) Curr Opin Chem Biol , vol.4 , pp. 110-119
    • Wymer, M.1    Toone, E.J.2
  • 26
    • 0014010844 scopus 로고    scopus 로고
    • The stereo-chemistry of the conversion of D and L 1,2-propanediols to propionaldehyde
    • Zagalak B, Frey P, Karabatsos GL, Abeles R. 1996. The stereo-chemistry of the conversion of D and L 1,2-propanediols to propionaldehyde. J Biol Chem 241:3028-3035.
    • (1996) J Biol Chem , vol.241 , pp. 3028-3035
    • Zagalak, B.1    Frey, P.2    Karabatsos, G.L.3    Abeles, R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.