Heterologous production of non-ribosomal peptide LLD-ACV in Saccharomyces cerevisiae

被引:37
|
作者
Siewers, Verena [1 ]
Chen, Xiao [1 ]
Huang, Le [1 ]
Zhang, Jie [1 ]
Nielsen, Jens [1 ]
机构
[1] Tech Univ Denmark, Dept Syst Biol, Ctr Microbial Biotechnol, DK-2800 Lyngby, Denmark
关键词
Secondary metabolites; Non-ribosomal peptide synthetase; Phosphopantetheinyl transferase; S; cerevisiae; LOW-TEMPERATURE INCREASES; PENICILLIN BIOSYNTHESIS; SECONDARY METABOLITES; NATURAL-PRODUCT; GENE-CLUSTER; EXPRESSION; PROTEIN; TRANSFERASE; SYNTHETASE; CHRYSOGENUM;
D O I
10.1016/j.ymben.2009.08.002
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Non-ribosomal peptides (NRPs) are a diverse family of secondary metabolites with a broad range of biological activities. We started to develop an eukaryotic microbial platform based on the yeast Saccharomyces cerevisiae for heterologous production of NRPs using delta-(L-alpha-aminoadipyl)-L-cysteinyl-D- valine (ACV) as a model NRP. The Penicillium chrysogenum gene pcbAB encoding ACV synthetase was expressed in S. cerevisiae from a high-copy plasmid together with phosphopantetheinyl transferase (PPTase) encoding genes from Aspergillus nidulans, P. chrysogenum and Bacillus subtilis, and in all the three cases production of ACV was observed. To improve ACV synthesis, several factors were investigated. Codon optimization of the 50 end of pcbAB did not significantly increase ACV production. However, a 30-fold enhancement was achieved by lowering the cultivation temperature from 30 to 20 degrees C. When ACVS and PPT a seen coding genes were integrated into the yeast genome, a 6-fold decrease in ACV production was observed indicating that gene copy number was one of the rate-limiting factors for ACV production in yeast. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:391 / 397
页数:7
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