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当前位置: 首页 > 文章 > 同源重组法构建副干酪乳杆菌组氨酸蛋白激酶基因缺失突变株 食品科学 2017 (12) 15-20
Position: Home > Articles > Construction of prcK Gene Deletion Mutant of Lactobacillus paracasei by Homologous Recombination FOOD SCIENCE 2017 (12) 15-20

同源重组法构建副干酪乳杆菌组氨酸蛋白激酶基因缺失突变株

作  者：
岳元春;王洋;由田;高冬妮;平文祥;葛菁萍
单  位：
黑龙江大学农业微生物技术教育部工程研究中心;黑龙江大学生命科学学院微生物省高校重点实验室
关键词：
副干酪乳杆菌;细菌素;组氨酸蛋白激酶基因;同源重组
摘  要：
构建副干酪乳杆菌(Lactobacillus paracasei)组氨酸蛋白激酶prcK基因缺失突变株,为prcK基因功能研究提供实验工具。采用同源重组技术构建质粒p KLKRT(含prcK::Tet~r基因),将其电转化进入L.paracaseiHD1.7中,使prcK::Tet~r基因同源重组到L.paracasei HD1.7的染色体上,通过四环素耐药、氨苄青霉素敏感等特性筛选出含有prcK::Tet~r基因的新L.paracasei HD1.7。结果表明,经聚合酶链式反应(polymerase chain reaction,PCR)验证及酶切验证后确定质粒p KLKRT构建成功,并成功转化入L.paracasei HD1.7中,经PCR确认L.paracasei HD1.7 prcK基因缺失突变株构建成功。该突变株产生的细菌素效价比出发菌株低23.61%。采用同源重组方法成功构建L.paracasei HD1.7 prcK基因缺失突变株,为研究L.paracasei HD1.7群体效应相关基因的分子机理奠定基础。
译  名：
Construction of prcK Gene Deletion Mutant of Lactobacillus paracasei by Homologous Recombination
作  者：
YUE Yuanchun;WANG Yang;YOU Tian;GAO Dongni;PING Wenxiang;GE Jingping;Key Laboratory of Microbiology,Life Science College,Heilongjiang University;Engineering Research Center of Agricultural Microbiology Technology,Ministry of Education,Heilongjiang University;
关键词：
Lactobacillus paracasei;;bacteriocin;;histidine protein kinase;;homologous recombination
摘  要：
This study aimed to construct a histidine protein kinase gene(prcK) deletion mutant of Lactobacillus paracasei HD1.7 for providing an experiment tool for research on the function of the prcK gene. In this research, homologous recombination method was used. Plasmid p KLKRT(including prcK::Tet~r) was constructed and used to transform L. paracasei HD1.7 by eletroporation. The prcK::Tet~r in place of prcK was integrated into the chromosome of L. paracasei HD1.7 by homologous recombination. One strain that grew only on plates with tetracycline but not on plates with ampicillin was selected. The PCR amplification and endonuclease digestion analysis indicated that plasmid p KLKRT was successfully constructed and introduced into L. paracasei HD1.7. The prcK gene deletion mutant was confirmed by PCR amplification. In conclusion, a prcK gene deletion mutant of L. paracasei HD1.7 has been successfully constructed by homologous recombination, which will lay the basis for understanding the molecular mechanism of the quorum sensing-related genes in L. paracasei HD1.7.

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