scholarly journals Biochemical and Structural Characterization of Bisubstrate Inhibitors of BasE, the Self-Standing Nonribosomal Peptide Synthetase Adenylate-Forming Enzyme of Acinetobactin Synthesis,

Biochemistry ◽  
2010 ◽  
Vol 49 (43) ◽  
pp. 9292-9305 ◽  
Author(s):  
Eric J. Drake ◽  
Benjamin P. Duckworth ◽  
João Neres ◽  
Courtney C. Aldrich ◽  
Andrew M. Gulick
Keyword(s):  
Structural Characterization ◽  
Nonribosomal Peptide Synthetase ◽  
The Self ◽  
Nonribosomal Peptide ◽  
Peptide Synthetase ◽  
Bisubstrate Inhibitors

scholarly journals Characterization of the Saframycin A Gene Cluster from Streptomyces lavendulae NRRL 11002 Revealing a Nonribosomal Peptide Synthetase System for Assembling the Unusual Tetrapeptidyl Skeleton in an Iterative Manner

2007 ◽  
Vol 190 (1) ◽  
pp. 251-263 ◽  
Author(s):  
Lei Li ◽  
Wei Deng ◽  
Jie Song ◽  
Wei Ding ◽  
Qun-Fei Zhao ◽  
...  
Keyword(s):  
Gene Cluster ◽  
Biosynthetic Gene Cluster ◽  
Nonribosomal Peptide Synthetase ◽  
Combinatorial Biosynthesis ◽  
Common Mechanism ◽  
Nonribosomal Peptide ◽  
Streptomyces Lavendulae ◽  
Peptide Synthetase

ABSTRACT Saframycin A (SFM-A), produced by Streptomyces lavendulae NRRL 11002, belongs to the tetrahydroisoquinoline family of antibiotics, and its core is structurally similar to the core of ecteinascidin 743, which is a highly potent antitumor drug isolated from a marine tunicate. In this study, the biosynthetic gene cluster for SFM-A was cloned and localized to a 62-kb contiguous DNA region. Sequence analysis revealed 30 genes that constitute the SFM-A gene cluster, encoding an unusual nonribosomal peptide synthetase (NRPS) system and tailoring enzymes and regulatory and resistance proteins. The results of substrate prediction and in vitro characterization of the adenylation specificities of this NRPS system support the hypothesis that the last module acts in an iterative manner to form a tetrapeptidyl intermediate and that the colinearity rule does not apply. Although this mechanism is different from those proposed for the SFM-A analogs SFM-Mx1 and safracin B (SAC-B), based on the high similarity of these systems, it is likely they share a common mechanism of biosynthesis as we describe here. Construction of the biosynthetic pathway of SFM-Y3, an aminated SFM-A, was achieved in the SAC-B producer (Pseudomonas fluorescens). These findings not only shed new insight on tetrahydroisoquinoline biosynthesis but also demonstrate the feasibility of engineering microorganisms to generate structurally more complex and biologically more active analogs by combinatorial biosynthesis.

scholarly journals Characterization of AusA: A Dimodular Nonribosomal Peptide Synthetase Responsible for the Production of Aureusimine Pyrazinones

Biochemistry ◽  
2013 ◽  
Vol 52 (5) ◽  
pp. 926-937 ◽  
Author(s):  
Daniel J. Wilson ◽  
Ce Shi ◽  
Aaron M. Teitelbaum ◽  
Andrew M. Gulick ◽  
Courtney C. Aldrich
Keyword(s):  
Nonribosomal Peptide Synthetase ◽  
Nonribosomal Peptide ◽  
Peptide Synthetase

scholarly journals In Vitro Characterization of a Heterologously Expressed Nonribosomal Peptide Synthetase Involved in Phosphinothricin Tripeptide Biosynthesis

Biochemistry ◽  
2009 ◽  
Vol 48 (23) ◽  
pp. 5054-5056 ◽  
Author(s):  
Jin-Hee Lee ◽  
Bradley S. Evans ◽  
Gongyong Li ◽  
Neil L. Kelleher ◽  
Wilfred A. van der Donk
Keyword(s):  
Nonribosomal Peptide Synthetase ◽  
Nonribosomal Peptide ◽  
In Vitro Characterization ◽  
Peptide Synthetase
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