In vitro analysis of carboxyacyl substrate tolerance in the loading and first extension modules of borrelidin polyketide synthase

Biochemistry. 2014 Sep 30;53(38):5975-7. doi: 10.1021/bi500951c. Epub 2014 Sep 16.

Abstract

The borrelidin polyketide synthase (PKS) begins with a carboxylated substrate and, unlike typical decarboxylative loading PKSs, retains the carboxy group in the final product. The specificity and tolerance of incorporation of carboxyacyl substrate into type I PKSs have not been explored. Here, we show that the first extension module is promiscuous in its ability to extend both carboxyacyl and non-carboxyacyl substrates. However, the loading module has a requirement for substrates containing a carboxy moiety, which are not decarboxylated in situ. Thus, the loading module is the basis for the observed specific incorporation of carboxylated starter units by the borelidin PKS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Fatty Alcohols / chemistry
  • Fatty Alcohols / metabolism
  • Molecular Structure
  • Polyketide Synthases / genetics
  • Polyketide Synthases / metabolism*
  • Polyketides / chemistry
  • Polyketides / metabolism*
  • Substrate Specificity

Substances

  • Fatty Alcohols
  • Polyketides
  • borrelidin
  • Polyketide Synthases