Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Enzymatic Sulfation of isoamyl Gallate and (-)-Epigallocatechin Gallate by Bacterial Arylsulfotransferase
Motoaki KOIZUMITeruaki AKAOLisa IMAMURAKeiji DOHITakashi YOSHIDATakuo OKUDAKyoichi KOBASHI
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1992 Volume 40 Issue 7 Pages 1864-1867

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Abstract

A novel type of arylsulfotransferase which was obtained from a human intestinal bacterium catalyzes the sulfation of polyphenols related to tannins. Isoamyl gallate and (-)-epigallocatechin gallate were found to be sulfated rapidly using p-nitrophenylsulfate as a donor substrate. In the case of isoamyl gallate, two sulfated products, 3-monosulfate and 4-monosulfate, were isolated when an equimolar amount of p-nitrophenylsulfate was incubated with isoamyl gallate. In the case of (-)-epigallocatechin gallate. 4'-monosulfate was isolated at an equimolar incubation of donor and acceptor. Thus, arylsulfotransferase was useful for the convenient preparation of sulfate esters of these polyphenols.

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© The Pharmaceutical Society of Japan
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