P92 Understanding the order of methylation and condensation in geminal-dimethyl producing polyketide synthase domains
Monday, January 12, 2015
California Ballroom C and Santa Fe Room
Sean Poust1, Ryan Phelan2, Kai Deng3, Christopher Petzold4, Leonard Katz4 and Jay Keasling4, (1)Department of Chemical and Biomolecular Engineering, University of California, Berkeley, Emeryville, CA, (2)Lawrence Berkeley National Laboratory, Joint BioEnergy Institute, Berkeley, CA, (3)Biological and Materials Science Center, Joint BioEnergy Institute, Emeryville, CA, (4)Joint BioEnergy Institute, Emeryville, CA
Methyl transfer in geminal-dimethyl producing type I polyketide synthases (PKS) has not been rigorously studied.  The methyl transfer reaction in type I polyketide synthases is presumed to occur after the extension reaction performed by the ketosynthase, but the reaction order has not been experimentally determined.  We sought to understand the order of extension and methylation in the yersiniabactin PKS and in module 8 of the epothilone PKS to develop a mechanistic understanding of PKS-catalyzed methylation. Tandem and high-resolution mass spectrometry techniques allowed us to examine acyl intermediates formed during the course of in vitro reactions with gem-dimethyl producing PKSs.