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Glucose 1-phosphate thymidylyltransferase in the synthesis of uridine 5′-diphosphate galactose and its application in the synthesis of N-acetyllactosamine
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Glucose 1-phosphate thymidylyltransferase in the synthesis of uridine 5′-diphosphate galactose and its application in the synthesis of N-acetyllactosamine

Wei-Ting Chien, Chien-Fu Liang, Ching-Ching Yu, Jian-Hong Lin, Haung-Ting WuChun-Cheng Lin
Advanced Synthesis and Catalysis, 卷.354(1), 頁碼.123-132
01/2012

摘要

Biosynthesis Carbohydrates Enzymes Galactosyltransferase Immobilization N-acetyllactosamine Uridine 5′-diphosphate galactose (UDP-Gal) Uridylyltransferase Catalysis Organic Chemistry
In this study, we describe the direct synthesis of uridine 5′-diphosphate galactose (UDP-Gal) by a wild-type bacterial thymidylyltransferase (RmlA), which is used to synthesize thymidine 5′-diphosphate glucose (TDP-glucose) in nature. By using magnesium (Mg <sup>2+</sup> ) as a cofactor and a reaction temperature of 55 8C, a one hundred milligram-scale synthesis of UDP-Gal was achieved by RmlA. In addition, RmlA was site-specifically and covalently immobilized on magnetic nanoparticles (MNPa) The resulting RmlA-MNP complex retained almost 95% of its activity after reuse in ten consecutive enzyme assays. Furthermore, β-1,4- galactosyltransferase (GalT) from Neisseria meningitides was successfully overexpressed and purified by using an intein-mediated protein expression system. GalT was relatively stable at 25 °C, and its activity was enhanced in the presence of DTT and BSA. Thus, it was feasible to synthesize N-acetyllactosamine (LacNAc) using RmlA and GalT in a sequential addition of enzyme and adjustment of thereaction temperature. These results demonstrate the potential applications of bacterial RmlA in carbohydrate synthesis. © 2012 Wiley-VCH Verlag GmbH&Co. KGaA, Weinheim.

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