| Literature DB >> 29533658 |
Kenneth D Clevenger1, Rosa Ye2, Jin Woo Bok3, Paul M Thomas1,4, Md Nurul Islam2, Galen P Miley5, Matthew T Robey4, Cynthia Chen2, KaHoua Yang3, Michael Swyers2, Edward Wu2, Peng Gao1, Chengcang C Wu2, Nancy P Keller3, Neil L Kelleher1,4,5.
Abstract
The benzodiazepine benzomalvin A/D is a fungally derived specialized metabolite and inhibitor of the substance P receptor NK1, biosynthesized by a three-gene nonribosomal peptide synthetase cluster. Here, we utilize fungal artificial chromosomes with metabolomic scoring (FAC-MS) to perform molecular genetic pathway dissection and targeted metabolomics analysis to assign the in vivo role of each domain in the benzomalvin biosynthetic pathway. The use of FAC-MS identified the terminal cyclizing condensation domain as BenY-CT and the internal C-domains as BenZ-C1 and BenZ-C2. Unexpectedly, we also uncovered evidence suggesting BenY-CT or a yet to be identified protein mediates benzodiazepine formation, representing the first reported benzodiazepine synthase enzymatic activity. This work informs understanding of what defines a fungal CT domain and shows how the FAC-MS platform can be used as a tool for in vivo analyses of specialized metabolite biosynthesis and for the discovery and dissection of new enzyme activities.Entities:
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Year: 2018 PMID: 29533658 PMCID: PMC5997561 DOI: 10.1021/acs.biochem.8b00076
Source DB: PubMed Journal: Biochemistry ISSN: 0006-2960 Impact factor: 3.162