Journal
CHEMICAL COMMUNICATIONS
Volume 46, Issue 33, Pages 6066-6068Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c0cc01381a
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Funding
- NSF [CHE-0548235]
- NIH [R01GM076360, U01CA128442]
- NATIONAL CANCER INSTITUTE [U01CA128442] Funding Source: NIH RePORTER
- NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM076360] Funding Source: NIH RePORTER
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Two bacterial beta 1-4-galactosyltransferases, NmLgtB and Hp1-4GalT, exhibit promiscuous and complementary acceptor substrate specificity. They have been used in an efficient one-pot multienzyme system to synthesize LacNAc, lactose, and their derivatives including those containing negatively charged 6-O-sulfated GlcNAc and C2-substituted GlcNAc or Glc, from monosaccharide derivatives and inexpensive Glc-1-P.
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