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Isoprenoid-like alkylations in polyketide biosynthesis

期刊

NATURAL PRODUCT REPORTS
卷 25, 期 5, 页码 845-853

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ROYAL SOC CHEMISTRY
DOI: 10.1039/b807243d

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  1. NIH [GM081743]
  2. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [F32GM081743] Funding Source: NIH RePORTER

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Polyketides are secondary metabolites biosynthesized by the iterative Claisen condensation of malonate units. Despite utilizing only a small set of biochemical transformations, the polyketide biosynthetic machinery yields products Of Striking structural complexity and diversity. Recently, a new polyketicle alkylation pathway was characterized that allows access to beta-branched structures. This Highlight will describe this alkylation sequence, with special emphasis on its parallels to isoprenoid biosynthesis from primary metabolism and the scope of structures accessible via this pathway.

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