Iwanicki Adam, Hinc Krzysztof, Seror Simone, Wegrzyn Grzegorz, Obuchowski Michal
Department of Medical Biotechnology, Intercollegiate Faculty of Biotechnology, Medical University of Gdańsk, Debinki st. 1, 80-211, Gdańsk, Poland.
Arch Microbiol. 2005 Sep;183(6):421-30. doi: 10.1007/s00203-005-0015-2. Epub 2005 Oct 13.
The prpC and prkC genes encode two proteins with opposing activities, eukaryotic-like protein phosphatase and protein kinase involved in the sporulation and biofilm formation processes. The prpC gene overlaps 3 bp of the prkC gene; prkC is followed by the essential gene, yloQ. The organisation of the prpC, prkC and yloQ genes is conserved among several Gram-positive bacteria. In this work, we have found two promoters which function within the region of these genes and we also described conditions in which these promoters become activated. One promoter appears to be located upstream of prpC resulting in transcription of both prpC and prkC, as well as the yloQ gene. A second promoter is located 7 bp upstream of the start codon of yloQ. The yloQ promoter was activated during ethanol stress, but was sigmaB-independent. We also showed that prpC, prkC and yloQ genes form an operon.
prpC和prkC基因编码两种具有相反活性的蛋白质,即参与芽孢形成和生物膜形成过程的类真核蛋白磷酸酶和蛋白激酶。prpC基因与prkC基因重叠3个碱基对;prkC基因后面是必需基因yloQ。prpC、prkC和yloQ基因的组织方式在几种革兰氏阳性细菌中是保守的。在这项研究中,我们发现了两个在这些基因区域内起作用的启动子,并且我们还描述了这些启动子被激活的条件。一个启动子似乎位于prpC上游,导致prpC、prkC以及yloQ基因的转录。第二个启动子位于yloQ起始密码子上游7个碱基对处。yloQ启动子在乙醇胁迫期间被激活,但不依赖于sigmaB。我们还表明prpC、prkC和yloQ基因形成一个操纵子。