2005
DOI: 10.1016/j.carres.2005.08.019
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Convenient enzymatic synthesis of a p-nitrophenyl oligosaccharide series of sialyl N-acetyllactosamine, sialyl Lex and relevant compounds

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Cited by 19 publications
(11 citation statements)
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“…Although bgalactosidases from numerous microorganisms have been used to produce prebiotic GOS, few of them have been applied in synthesizing additional chemicals. Most synthetic work was focused on two microbial b-galactosidases: one from Bacillus circulans and the other from Aspergillus oryzae [11][12][13][14][15][16].…”
Section: Introductionmentioning
confidence: 99%
“…Although bgalactosidases from numerous microorganisms have been used to produce prebiotic GOS, few of them have been applied in synthesizing additional chemicals. Most synthetic work was focused on two microbial b-galactosidases: one from Bacillus circulans and the other from Aspergillus oryzae [11][12][13][14][15][16].…”
Section: Introductionmentioning
confidence: 99%
“…[10][11][12][13][14] A limited number of structures have been synthesized in small amounts using glycosyltransferases as an alternative approach to the chemical synthesis. [15][16][17][18] In this work, we developed an efficient enzymatic strategy to produce 24 pLN derivatives in gram-scale amounts to supply our glycan compound library (www.functionalglycomics.org). We have taken advantage of the relaxed substrate specificity of the recombinant bacterial enzymes b-(1!4)-galactosyltransferase (b4GalT; EC 2.4.1.38) and b-(1!3)-N-acetylglucosaminyltransferase (b3GlcNAcT; EC 2.4.1.149), which, by concerted action, generate repeating LN units.…”
Section: Introductionmentioning
confidence: 99%
“…4,5,12,13) In particular, -galactosidase-2 does not require high lactose concentrations to produce high yields of oligosaccharides, in contrast to most -galactosidases reported to date. 4) -Galactosidase-2 produces GOS at a yield of about 41% from a 4.56% solution of lactose at 40 C. Hence, during the past 20 years, the commercial enzyme Biolacta Ò has frequently been utilized to synthesize various functional galactosylated compounds [32][33][34][35][36][37][38][39][40][41][42] as well as GOS. 5,9,12,13,43,44) In a later study, Vetere et al 45) isolated a third enzyme, with a molecular mass of 86 kDa, from Biolacta Ò , but they did not study oligosaccharide production.…”
mentioning
confidence: 99%