2009
DOI: 10.1016/j.procbio.2008.10.010
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A novel transglycosylating β-galactosidase from Enterobacter cloacae B5

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Cited by 35 publications
(33 citation statements)
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“…b-Galactosidases have been also used to produce heterooligosaccharides (HeOSs); e.g., lactulose was enzymatically synthesized by a Sulfolobus solfataricus b-galactosidase from lactose and fructose (Kim, Park, & Oh, 2006), whereas Kluyveromyces lactis b-galactosidase galactosylated aromatic primary alcohols (Bridiau, Taboubi, Marzouki, Legoy, & Maugard, 2006). A wide range of sugar alcohols and mono-and disaccharides have been shown to act as an acceptor carbohydrate for a b-galactosidase of Enterobacter cloacae B5 (Lu, Xiao, Li, & Wang, 2009). The choice of acceptor carbohydrate and enzyme allows the formation of tailor-made HeOSs with potential application as food additives or therapeutics.…”
Section: Introductionmentioning
confidence: 99%
“…b-Galactosidases have been also used to produce heterooligosaccharides (HeOSs); e.g., lactulose was enzymatically synthesized by a Sulfolobus solfataricus b-galactosidase from lactose and fructose (Kim, Park, & Oh, 2006), whereas Kluyveromyces lactis b-galactosidase galactosylated aromatic primary alcohols (Bridiau, Taboubi, Marzouki, Legoy, & Maugard, 2006). A wide range of sugar alcohols and mono-and disaccharides have been shown to act as an acceptor carbohydrate for a b-galactosidase of Enterobacter cloacae B5 (Lu, Xiao, Li, & Wang, 2009). The choice of acceptor carbohydrate and enzyme allows the formation of tailor-made HeOSs with potential application as food additives or therapeutics.…”
Section: Introductionmentioning
confidence: 99%
“…32cB ␤-dgalactosidase catalyzed the synthesis of heterooligosaccharides, namely lactulose, galactosyl-xylose or galactosyl-arabinose, and glycosylated salicin. ␤-d-Galactosidases from Enetrobacter agglomerans B1 and E. cloacae B5 catalyze glycosyl transfer from ONPG to various acceptors such as hexoses (glucose, galactose, mannose, fructose, sorbose), pentoses (arabinose, xylose), disaccharides (cellobiose, sucrose, trehalose), hexahydroxyalcohols (mannitol, sorbitol), cyclitol (inositol) and aromatic glycoside (salicin) [33,34]. The enzymatic synthesis, by Aspergillus oryzae ␤-d-galactosidase, of galactosyl-xylose from ONPG and xylose as substrates has been also reported [35].…”
Section: Discussionmentioning
confidence: 99%
“…However, this process leads to the formation of a certain amount of by-products as a result of sugar degradation under harsh conditions, namely a pH 10.5-11.5 and temperatures of between 70 and 100 • C. The enzymatic synthesis of lactulose offers much milder conditions and can be conducted in crude lactose materials such as whey or whey permeate [32]. Heterologous galactosyl transfer catalyzed by ␤-d-galactosidase yields a virtually unlimited diversity of oligosaccharides [33][34][35][36][37][38][39]. However, none of cold-active ␤-d-galactosidases have yet been used for this purpose.…”
Section: Introductionmentioning
confidence: 99%
“…Recently novel β‐galactosidase capable of glycosyl transfer was purified from a strain of Enterobacter cloacae B5 isolated from soil. This strain synthesizes GOS with a high yield of 55% from 275 g/L lactose at 50 °C for 12 h. A gene encoding the enzyme was cloned in E. coli and the recombinant enzyme was found to have similar transglycosylation activity to the natural enzyme (Lu and others 2009). …”
Section: Biotechnological Methods For Enhanced Gos Productionmentioning
confidence: 99%