posted on 2015-12-17, 06:31authored byYi Zou, Wei Xu, Yuta Tsunematsu, Mancheng Tang, Kenji Watanabe, Yi Tang
Biochemical studies of purified and
dissected fungal polyketide
synthase and nonribosomal peptide synthetase (PKS-NRPS) hybrid enzymes
involved in biosynthesis of pseurotin and aspyridone indicate that
one α-methylation step during polyketide synthesis is a prerequisite
and a key checkpoint for chain transfer between PKS and NRPS modules.
In the absence of the resulting γ-methyl feature, the completed
polyketide intermediate is offloaded as an α-pyrone instead
of being aminoacylated by the NRPS domain. These examples illustrate
that precisely timed tailoring domain activities play critical roles
in the overall programming of the iterative PKS (and NRPS) functions.