High-Yield Lasso Peptide Production in a Burkholderia Bacterial Host by Plasmid Copy Number Engineering

被引:7
|
作者
Fernandez, Hannah N. [1 ,2 ]
Kretsch, Ashley M. [3 ,4 ]
Kunakom, Sylvia [1 ,2 ]
Kadjo, Adjo E. [1 ,2 ]
Mitchell, Douglas A. [3 ,4 ]
Eustaquio, Alessandra S. [1 ,2 ]
机构
[1] Univ Illinois, Dept Pharmaceut Sci, Coll Pharm, Chicago, IL 60607 USA
[2] Univ Illinois, Coll Pharm, Ctr Biomol Sci, Chicago, IL 60607 USA
[3] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[4] Univ Illinois, Carl R Woese Inst Genom Biol, Urbana, IL 61801 USA
来源
ACS SYNTHETIC BIOLOGY | 2024年 / 13卷 / 01期
基金
美国国家卫生研究院;
关键词
lasso peptide; RiPP; natural product; secondary metabolite; bacteria; heterologousexpression; Burkholderiaceae; BIOSYNTHESIS; EXPRESSION; TRANSCRIPTION; REPLICATION; CAPISTRUIN;
D O I
10.1021/acssynbio.3c00597
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The knotted configuration of lasso peptides confers thermal stability and proteolytic resistance, addressing two shortcomings of peptide-based drugs. However, low isolation yields hinder the discovery and development of lasso peptides. While testing Burkholderia sp. FERM BP-3421 as a bacterial host to produce the lasso peptide capistruin, an overproducer clone was previously identified. In this study, we show that an increase in the plasmid copy number partially contributed to the overproducer phenotype. Further, we modulated the plasmid copy number to recapitulate titers to an average of 160% relative to the overproducer, which is 1000-fold higher than previously reported with E. coli, reaching up to 240 mg/L. To probe the applicability of the developed tools for lasso peptide discovery, we targeted a new lasso peptide biosynthetic gene cluster from endosymbiont Mycetohabitans sp. B13, leading to the isolation of mycetolassin-15 and mycetolassin-18 in combined titers of 11 mg/L. These results validate Burkholderia sp. FERM BP-3421 as a production platform for lasso peptide discovery.
引用
收藏
页码:337 / 350
页数:14
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