| Literature DB >> 22362652 |
Junying Ma1, Dianguang Zuo, Yongxiang Song, Bo Wang, Hongbo Huang, Yueliang Yao, Wenjun Li, Si Zhang, Changsheng Zhang, Jianhua Ju.
Abstract
The nine-membered indolactam antibiotics belong to a small group of antibiotics showing broad biological activities. However, the in vivo genetic engineering of compounds of this type has not been performed. Here we report the identification of a single gene cluster responsible for the biosynthesis of methylpendolmycin and pendolmycin, two members of this family of antibiotics, from the deep sea bacterium Marinactinospora thermotolerans SCSIO 00652. Bioinformatics analysis and gene inactivation, coupled with metabolite characterization, reveal that MpnB, a nonribosomal peptide synthetase, MpnC, a cytochrome P450, and MpnD, a prenyltransferase, are sufficient to catalyze the biosynthesis of the two antibiotics from L-Ile (or L-Val), L-Trp, and methionine. MpnD is the first identified enzyme that transfers a C5 prenyl unit in a reverse manner to the C-7 position of a Trp-derived natural product.Entities:
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Year: 2012 PMID: 22362652 DOI: 10.1002/cbic.201100700
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164