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Automated structure prediction of trans-acyltransferase polyketide synthase products

Nat Chem Biol. 2019-07-01; 
Eric J N Helfrich, Reiko Ueoka, Alon Dolev, Michael Rust, Roy A Meoded, Agneya Bhushan, Gianmaria Califano, Rodrigo Costa, Muriel Gugger, Christoph Steinbeck, Pablo Moreno, J?rn Piel
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Codon Optimization … The β-aminopeptidase genes from Y. lipolytica, M. smegmatis MC2 155, 169 P. horikoshii OT3, S. xenopeptidilytica 3-2W4 and S. microcystinivorans Y2 were codon 170 optimised for E. coli, synthesised and cloned into pUC57-Kan by Genscript (Piscataway, NJ). 171 … Get A Quote

摘要

Bacterial trans-acyltransferase polyketide synthases (trans-AT PKSs) are among the most complex known enzymes from secondary metabolism and are responsible for the biosynthesis of highly diverse bioactive polyketides. However, most of these metabolites remain uncharacterized, since trans-AT PKSs frequently occur in poorly studied microbes and feature a remarkable array of non-canonical biosynthetic components with poorly understood functions. As a consequence, genome-guided natural product identification has been challenging. To enable de novo structural predictions for trans-AT PKS-derived polyketides, we developed the trans-AT PKS polyketide predictor (TransATor). TransATor is a versatile bio- and chemoinform... More

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