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Title: Biosynthesis of desosamine: construction of a new macrolide carrying a genetically designed sugar moiety. Author: Borisova SA, Zhao L, Sherman DH, Liu HW. Journal: Org Lett; 1999 Jul 15; 1(1):133-6. PubMed ID: 10822548. Abstract: [formula: see text] The appended sugars in macrolide antibiotics are indispensable to the biological activities of these important drugs. In an effort to generate a set of novel macrolide derivatives, we have created a new analogue of methymycin and neomethymycin, antibiotics produced by Streptomyces venezuelae. This analogue 15 carrying a different sugar, D-quinovose, instead of D-desosamine, was constructed by taking advantage of targeted gene deletion combined with a specific pathway-independent C-3 reduction capability of the wild type S. venezuelae.[Abstract] [Full Text] [Related] [New Search]