4.7 Article

Highly efficient chemoenzymatic synthesis of beta 1-4-linked galactosides with promiscuous bacterial beta 1-4-galactosyltransferases

Journal

CHEMICAL COMMUNICATIONS
Volume 46, Issue 33, Pages 6066-6068

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c0cc01381a

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Funding

  1. NSF [CHE-0548235]
  2. NIH [R01GM076360, U01CA128442]
  3. NATIONAL CANCER INSTITUTE [U01CA128442] Funding Source: NIH RePORTER
  4. 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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