Suppr超能文献

乳酸乳球菌MG1363环丙烷脂肪酸合酶基因在低pH值下的转录分析

Transcriptional analysis of the cyclopropane fatty acid synthase gene of Lactococcus lactis MG1363 at low pH.

作者信息

Budin-Verneuil Aurélie, Maguin Emmanuelle, Auffray Yanick, Ehrlich S Dusko, Pichereau Vianney

机构信息

Laboratoire de Microbiologie de l'Environnement, EA956-USC INRA 2017, IRBA, Université de Caen, 14032 Caen Cedex, France.

出版信息

FEMS Microbiol Lett. 2005 Sep 15;250(2):189-94. doi: 10.1016/j.femsle.2005.07.007.

Abstract

Cyclopropane fatty acid synthase (cfa) catalyses the transfer of a methyl group from S-adenosylmethionine (SAM) to unsaturated fatty acids. Northern blot experiments demonstrated that the Lactococcus lactis MG1363 cfa gene is mainly expressed as a bicistronic transcript together with metK, the gene encoding SAM synthetase, and is highly induced by acidity. The cfa promoter was characterized by 5'-RACE PCR, and fused to beta-galactosidase by cloning into the pAK80 plasmid. This transcriptional fusion was highly induced by acidity (23-fold at pH 5) as well as during entry into the stationary phase (8-fold) in L. lactis. Interestingly, the cfa promoter expression is repressed in a L. lactis relA* mutant which accumulates (p)ppGpp, whereas its induction by acidity appeared independent of (p)ppGpp in L. lactis and in Escherichia coli.

摘要

环丙烷脂肪酸合酶(cfa)催化将甲基从S-腺苷甲硫氨酸(SAM)转移至不饱和脂肪酸。Northern印迹实验表明,乳酸乳球菌MG1363的cfa基因主要与metK(编码SAM合成酶的基因)一起作为双顺反子转录本表达,并且受到酸度的高度诱导。通过5'-RACE PCR对cfa启动子进行了表征,并通过克隆到pAK80质粒中与β-半乳糖苷酶融合。这种转录融合在乳酸乳球菌中受到酸度(pH 5时为23倍)以及进入稳定期(8倍)的高度诱导。有趣的是,cfa启动子的表达在积累(p)ppGpp的乳酸乳球菌relA*突变体中受到抑制,而其在乳酸乳球菌和大肠杆菌中受酸度诱导似乎与(p)ppGpp无关。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验