Son Yeon Jeong, Ryu Ae Jin, Li Ling, Han Nam Soo, Jeong Ki Jun
Department of Chemical and Biomolecular Engineering, BK21 Plus PROGRAM, KAIST, 291 Daehak-ro, Yuseong-gu, Daejeon, 34141, Republic of Korea.
Division of Animal, Horticultural and Food Sciences, Brain Korea 21 Center for Bio-Resource Development, Chungbuk National University, Cheongju, 28644, Republic of Korea.
Microb Cell Fact. 2016 Jan 15;15:12. doi: 10.1186/s12934-015-0400-8.
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.
明串珠菌是一种异型发酵乳酸菌,其在乳制品行业的重要性已得到广泛认可。然而,由于包括用于明串珠菌的质粒在内的遗传工具有限,目前对明串珠菌的遗传学和基因工程研究还不太广泛。因此,迫切需要高拷贝数质粒用于明串珠菌中有用基因的操作和重组蛋白的过量表达。
利用现有的低拷贝质粒,通过随机诱变,随后基于荧光激活细胞分选(FACS)的高通量筛选来增加质粒的拷贝数。首先,通过随机化柠檬明串珠菌中负责复制的区域构建了一个随机质粒文库;此外,使用超折叠绿色荧光蛋白(sfGFP)作为报告蛋白。通过高速FACS分选仪富集高荧光细胞,经过两轮分选后,分离出表现出最高水平sfGFP的单克隆。通过定量PCR(qPCR)测定分离出的质粒(pCB4270)的拷贝数。发现分离出的质粒的拷贝数比原始质粒高约30倍(约每细胞70个拷贝)。通过序列分析,在第4690位发现了一个单突变(C→T),并且我们证实这个单突变导致了质粒拷贝数的增加。利用两种蛋白模型谷胱甘肽 - S - 转移酶(GST)和α - 淀粉酶成功证明了分离出的高拷贝数质粒用于重组蛋白过量表达的有效性。
通过基于FACS的高通量筛选柠檬明串珠菌中的质粒文库,成功分离出了高拷贝数质粒。分离出的质粒可能是用于明串珠菌中高水平基因表达的有用遗传工具,并且可用于将这种有用细菌的应用扩展到乳制品和制药行业的各个领域。