Development of a high-copy plasmid for enhanced production of recombinant proteins in Leuconostoc citreum

被引:23
|
作者
Son, Yeon Jeong [1 ]
Ryu, Ae Jin [1 ]
Li, Ling [2 ]
Han, Nam Soo [2 ]
Jeong, Ki Jun [1 ,3 ]
机构
[1] Korea Adv Inst Sci & Technol, Plus PROGRAM BK21, Dept Chem & Biomol Engn, Daejeon 34141, South Korea
[2] Chungbuk Natl Univ, Div Anim Hort & Food Sci, Brain Korea Ctr Bioresource Dev 21, Cheongju 28644, South Korea
[3] Korea Adv Inst Sci & Technol, Inst BioCentury, Daejeon 34141, South Korea
来源
MICROBIAL CELL FACTORIES | 2016年 / 15卷
基金
新加坡国家研究基金会;
关键词
Lactic acid bacteria; Leuconostoc citreum; High copy plasmid; Plasmid engineering; FACS; SMALL CRYPTIC PLASMID; LACTIC-ACID BACTERIA; ESCHERICHIA-COLI; GENE-EXPRESSION; SHUTTLE VECTOR; NUMBER; IDENTIFICATION; FERMENTATION; DERIVATIVES; MUTATION;
D O I
10.1186/s12934-015-0400-8
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
Background: Leuconostoc is a hetero-fermentative lactic acid bacteria, and its importance is widely recognized in the dairy industry. However, due to limited genetic tools including plasmids for Leuconostoc, there has not been much extensive research on the genetics and engineering of Leuconostoc yet. Thus, there is a big demand for high-copy-number plasmids for useful gene manipulation and overproduction of recombinant proteins in Leuconostoc. Results: Using an existing low-copy plasmid, the copy number of plasmid was increased by random mutagenesis followed by FACS-based high-throughput screening. First, a random library of plasmids was constructed by randomizing the region responsible for replication in Leuconostoc citreum; additionally, a superfolder green fluorescent protein (sfGFP) was used as a reporter protein. With a high-speed FACS sorter, highly fluorescent cells were enriched, and after two rounds of sorting, single clone exhibiting the highest level of sfGFP was isolated. The copy number of the isolated plasmid (pCB4270) was determined by quantitative PCR (qPCR). It was found that the isolated plasmid has approximately a 30-fold higher copy number (approx. 70 copies per cell) than that of the original plasmid. From the sequence analysis, a single mutation (C -> T) at position 4690 was found, and we confirmed that this single mutation was responsible for the increased plasmid copy number. The effectiveness of the isolated high-copy-number plasmid for the overproduction of recombinant proteins was successfully demonstrated with two protein models Glutathione-S-transferase (GST) and alpha-amylase. Conclusions: The high-copy number plasmid was successfully isolated by FACS-based high-throughput screening of a plasmid library in L. citreum. The isolated plasmid could be a useful genetic tool for high-level gene expression in Leuconostoc, and for extending the applications of this useful bacteria to various areas in the dairy and pharmaceutical industries.
引用
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页数:11
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