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

Overview of attention for article published in Microbial Cell Factories, January 2016
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Title
Development of a high-copy plasmid for enhanced production of recombinant proteins in Leuconostoc citreum
Published in
Microbial Cell Factories, January 2016
DOI 10.1186/s12934-015-0400-8
Pubmed ID
Authors

Yeon Jeong Son, Ae Jin Ryu, Ling Li, Nam Soo Han, Ki Jun Jeong

Abstract

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. 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 α-amylase. 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.

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Mendeley readers

The data shown below were compiled from readership statistics for 39 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
India 1 3%
China 1 3%
Unknown 37 95%

Demographic breakdown

Readers by professional status Count As %
Researcher 7 18%
Student > Ph. D. Student 5 13%
Student > Master 5 13%
Student > Bachelor 4 10%
Student > Doctoral Student 2 5%
Other 5 13%
Unknown 11 28%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 12 31%
Agricultural and Biological Sciences 9 23%
Engineering 3 8%
Immunology and Microbiology 2 5%
Chemistry 1 3%
Other 1 3%
Unknown 11 28%