摘要

The antibiotic TA of Myxococcus xanthus is produced by a type-1 polyketide synthase mechanism. Previous Studies have indicated that TA genes are clustered within a 36-kb region. The chemical structure of TA indicates the need for several post-modification steps. which are introduced to form the final bioactive molecule. These include three C-methylations. an O-methylation and a specific hydroxylation, In this study, we describe the genetic analysis of taK, encoding a specific polyketide beta -ketoacyl:acyl carrier protein synthase, which contains an unusual beta -ketoacyl synthase and acyltransferase motifs and is likely to be involved in antibiotic TA post-modification. Functional analysis of this beta -ketoacyl:acyl carrier protein synthase by specific gene disruption suggests that it is essential for the production of an active TA molecule.

  • 出版日期2001-9-25

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