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- W2953358911 abstract "A series of deoxygenated uridine 5‘-diphosphogalactose (UDP-Gal) derivatives are evaluated as donors for three different retaining galactosyltransferases using capillary electrophoresis with laser-induced fluorescence detection. The enzymes investigated were calf thymus α(1→3) galactosyltransferase (E.C. 2.4.1.151), blood group B α(1→3) galactosyltransferase (E.C. 2.4.1.37) and Neisseria meningitidis α(1→4) galactosyltransferase. UDP-2-deoxy-Gal and UDP-6-deoxy-Gal were found to be active as donors for all three enzymes. Preparative syntheses utilizing these UDP-Gal derivatives were performed on mg scales, affording deoxygenated trisaccharide analogues in 5−100% yields." @default.
- W2953358911 created "2019-06-27" @default.
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- W2953358911 date "2000-02-01" @default.
- W2953358911 modified "2023-10-10" @default.
- W2953358911 title "Enzymatic Synthesis of Oligosaccharide Analogues: Evaluation of UDP-Gal Analogues as Donors for Three Retaining α-Galactosyltransferases" @default.
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- W2953358911 doi "https://doi.org/10.1021/ja990964u" @default.
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