Acid or erythromycin stress significantly improves transformation efficiency through regulating expression of DNA binding proteins in Lactococcus lactis F44

被引:4
|
作者
Wang, Binbin [1 ,2 ,3 ]
Zhang, Huawei [1 ,2 ,3 ]
Liang, Dongmei [1 ,2 ,3 ]
Hao, Panlong [1 ,2 ,3 ]
Li, Yanni [1 ,2 ,3 ]
Qiao, Jianjun [1 ,2 ,3 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Dept Pharmaceut Engn, Tianjin 300072, Peoples R China
[2] Minist Educ Tianjin, Key Lab Syst Bioengn, Tianjin 300072, Peoples R China
[3] Collaborat Innovat Ctr Chem Sci & Engn, SynBio Res Platform, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
Lactococcus lactis; transformation efficiency; acid/erythromycin stress; DNA binding protein; BACTERIAL COMPETENCE; GENES; ELECTROPORATION; REPLICATION; MECHANISMS; SEARCH; CELLS; DPS;
D O I
10.3168/jds.2017-13101
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Lactococcus lactis is a gram-positive bacterium used extensively in the dairy industry and food fermentation, and its biological characteristics are usually improved through genetic manipulation. However, poor transformation efficiency was the main restriction factor for the construction of engineered strains. In this study, the transformation efficiency of L. lactis F44 showed a 56.1-fold increase in acid condition (pH 5.0); meanwhile, erythromycin stress (0.04 mu g/mL) promoted the transformation efficiency more significantly (76.9-fold). Notably, the transformation efficiency of F44e (L. lactis F44 harboring empty pLEB124) increased up to 149.1-fold under the synergistic stresses of acid and erythromycin. In addition, the gene expression of some DNA binding proteins (DprA, RadA, RadC, RecA, RecQ, and SsbA) changed correspondingly. Especially for radA, 25.1-fold improvement was detected when F44e was exposed to pH 5.0. Overexpression of some DNA binding proteins could improve the transformation efficiency. The results suggested that acid or erythromycin stress could improve the transformation efficiency of L. lactis through regulating gene expression of DNA binding proteins. We have proposed a simple but promising strategy for improving the transformation efficiency of L. lactis and other hard-transformed microorganisms.
引用
收藏
页码:9532 / 9538
页数:7
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