Literature DB >> 18291318

Elucidation of the Streptomyces coelicolor pathway to 2-undecylpyrrole, a key intermediate in undecylprodiginine and streptorubin B biosynthesis.

SangJoon Mo1, Paulina K Sydor, Christophe Corre, Mamoun M Alhamadsheh, Anna E Stanley, Stuart W Haynes, Lijiang Song, Kevin A Reynolds, Gregory L Challis.   

Abstract

The red gene cluster of Streptomyces coelicolor directs production of undecylprodiginine. Here we report that this gene cluster also directs production of streptorubin B and show that 2-undecylpyrrole (UP) is an intermediate in the biosynthesis of undecylprodiginine and streptorubin B. The redPQRKL genes are involved in UP biosynthesis. RedL and RedK are proposed to generate UP from dodecanoic acid or a derivative. A redK(-) mutant produces a hydroxylated undecylprodiginine derivative, whereas redL(-) and redK(-) mutants require addition of chemically synthesized UP for production of undecylprodiginine and streptorubin B. Fatty acid biosynthetic enzymes can provide dodecanoic acid, but efficient and selective prodiginine biosynthesis requires RedPQR. Deletion of redP, redQ, or redR leads to an 80%-95% decrease in production of undecylprodiginine and an array of prodiginine analogs with varying alkyl chains. In a redR(-) mutant, the ratio of these can be altered in a logical manner by feeding various fatty acids.

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Year:  2008        PMID: 18291318     DOI: 10.1016/j.chembiol.2007.11.015

Source DB:  PubMed          Journal:  Chem Biol        ISSN: 1074-5521


  28 in total

1.  Dual positive feedback regulation of protein degradation of an extra-cytoplasmic function σ factor for cell differentiation in Streptomyces coelicolor.

Authors:  Xu-Ming Mao; Ning Sun; Feng Wang; Shuai Luo; Zhan Zhou; Wei-Hong Feng; Fang-Liang Huang; Yong-Quan Li
Journal:  J Biol Chem       Date:  2013-09-06       Impact factor: 5.157

2.  Large-Scale Transposition Mutagenesis of Streptomyces coelicolor Identifies Hundreds of Genes Influencing Antibiotic Biosynthesis.

Authors:  Zhong Xu; Yemin Wang; Keith F Chater; Hong-Yu Ou; H Howard Xu; Zixin Deng; Meifeng Tao
Journal:  Appl Environ Microbiol       Date:  2017-03-02       Impact factor: 4.792

3.  Identification of a prodigiosin cyclization gene in the roseophilin producer and production of a new cyclized prodigiosin in a heterologous host.

Authors:  Shoko Kimata; Masumi Izawa; Takashi Kawasaki; Yoichi Hayakawa
Journal:  J Antibiot (Tokyo)       Date:  2016-07-27       Impact factor: 2.649

4.  MarH, a Bifunctional Enzyme Involved in the Condensation and Hydroxylation Steps of the Marineosin Biosynthetic Pathway.

Authors:  Wanli Lu; Papireddy Kancharla; Kevin A Reynolds
Journal:  Org Lett       Date:  2017-03-08       Impact factor: 6.005

5.  Elimination of butylcycloheptylprodigiosin as a known natural product inspired by an evolutionary hypothesis for cyclic prodigiosin biosynthesis.

Authors:  Brian T Jones; Dennis X Hu; Brett M Savoie; Regan J Thomson
Journal:  J Nat Prod       Date:  2013-09-20       Impact factor: 4.050

6.  Synthesis of the spiroiminal moiety of marineosins A and B.

Authors:  Xiao-Chuan Cai; Xiaoxing Wu; Barry B Snider
Journal:  Org Lett       Date:  2010-04-02       Impact factor: 6.005

Review 7.  Exploitation of the Streptomyces coelicolor A3(2) genome sequence for discovery of new natural products and biosynthetic pathways.

Authors:  Gregory L Challis
Journal:  J Ind Microbiol Biotechnol       Date:  2013-12-10       Impact factor: 3.346

8.  Modular access to complex prodiginines: total synthesis of (+)-roseophilin via its 2-azafulvene prototropisomer.

Authors:  James H Frederich; Patrick G Harran
Journal:  J Am Chem Soc       Date:  2013-03-01       Impact factor: 15.419

Review 9.  Molecular regulation of antibiotic biosynthesis in streptomyces.

Authors:  Gang Liu; Keith F Chater; Govind Chandra; Guoqing Niu; Huarong Tan
Journal:  Microbiol Mol Biol Rev       Date:  2013-03       Impact factor: 11.056

10.  Synthesis of the spiroiminal moiety and approaches to the synthesis of marineosins A and B.

Authors:  Xiao-Chuan Cai; Barry B Snider
Journal:  J Org Chem       Date:  2013-11-21       Impact factor: 4.354

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