Identification and functional analysis of the fusaricidin biosynthetic gene of Paenibacillus polymyxa E681

被引:91
作者
Choi, Soo-Keun
Park, Soo-Young
Kim, Rumi
Lee, Choong-Hwan
Kim, Jihyun F.
Park, Seung-Hwan
机构
[1] Syst Microbiol Res Ctr, KRIBB, Taejon 305806, South Korea
[2] Nat Med Res Ctr, KRIBB, Taejon 305806, South Korea
关键词
Paenibacillus polymyxa; fusaricidin; fusaricidin synthetase gene; NRPS;
D O I
10.1016/j.bbrc.2007.10.147
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fusaricidin, a peptide antibiotic consisting of six amino acids, has been identified as a potential antifungal agent from Paellibacillus polymyxa. Here, we report the complete sequence of the fusaricidin synthetase gene (fusA) identified from the genome sequence of a rhizobacterium, P. polymyxa E681. The gene encodes a polypeptide consisting of six modules in a single open-reading frame. Interestingly, module six of FusA does not contain an epimerization domain, which suggests that the sixth amino acids of the fusaricidin analogs produced by P. polymyxa E681 may exist as an L-form, although all reported fusaricidins contain D-form alanines in their sixth amino acid residues. Alternatively, the sixth adenylation domain of the FusA may directly recognize the D-form alanine. The inactivation of fusA led to the complete loss of antifungal activity against Fusarium oxysporum. LC/MS analysis confirmed the incapability of fusaricidin production in the fusA mutant strain, thus demonstrating that fusA is involved in fusaricidin biosynthesis. Our findings suggested that FusA can produce more than one kind of fusaricidin, as various forms of fusaricidins were identified from P. polymyxa E681. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:89 / 95
页数:7
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