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"Chilling a Biochemical Hot Potato: Stable Acyl-thioester Analogs to Study Fatty Acid & Polyketide Biosynthesis"

Date:
-
Location:
CP 114
Speaker(s) / Presenter(s):
Dr. Jeremy Lohman

Dr. Jeremy Lohman

Abstract: The biosynthesis of both fatty acids and polyketides involves a common reaction, the iterative carbon-carbon bond formation between acyl-thioesters and malonyl-thioesters. While fatty acids and polyketides are essential to society for a plethorea of reasons, how the underlying carbon-carbon bond forming reactions occur remains an open question. Malonyl-thioesters are akin to biochemical hot-potatoes, because they are prone to hydrolysis and decarboxylation. While these two high-energy reactions are exploited by nature for biosynthetic purpose, they plague the structural biologist. We developed molecules that look like malonyl-thioesters but are much more stable, thus we have chilled the hot-potato. These stable malonyl-thioester analogs have provided us with insight into the catalysis of three enzymes. Our preliminary studies with these malonyl-thioester analogs demonstrate that we will be able to generate insight into fatty acid and polyketide biosynthesis, paving the way for new routes to drugs, agrochemicals and biofuels.

 

Files:
Lohman_Flyer.pdf (5.25 MB)
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