Nagórska Krzysztofa, Hinc Krzysztof, Strauch Mark A, Obuchowski Michał
Department of Medical Biotechnology, Medical University of Gdańsk, Gdańsk, Poland.
J Bacteriol. 2008 May;190(10):3546-56. doi: 10.1128/JB.01665-07. Epub 2008 Mar 7.
Bacillus subtilis forms structured communities of biofilms encased in an exopolysaccharide matrix on solid surfaces and at the air-liquid interface. It is postulated that nonoptimal growth conditions induce this multicellular behavior. We showed that under laboratory conditions a strain deleted for sigB was unable to form a floating pellicle on the surface of a liquid medium. However, overexpression of yxaB, encoding a putative exopolysaccharide synthase, from a p(Spac) promoter in a sigB-deleted strain resulted in partial recovery of the wild-type phenotype, indicating the participation of the YxaB protein in this multicellular process. We present data concerning the regulation of transcription of genes yxaB and yxaA, encoding a putative glycerate kinase. Both genes are cotranscribed as a single transcription unit from a sigma(A)-dependent promoter during vegetative growth of a liquid bacterial culture. The promoter driving transcription of the yxaAB operon is regulated by AbrB. In addition, the second gene in the operon, yxaB, possesses its own promoter, which is recognized by RNA polymerase containing the sigma(B) subunit. This transcription start site is used under general stress conditions, resulting in increased expression.
枯草芽孢杆菌在固体表面和气液界面形成由胞外多糖基质包裹的生物膜结构化群落。据推测,非最佳生长条件会诱导这种多细胞行为。我们发现,在实验室条件下,sigB基因缺失的菌株无法在液体培养基表面形成漂浮菌膜。然而,在sigB基因缺失的菌株中,从p(Spac)启动子过表达编码假定胞外多糖合酶的yxaB,导致野生型表型部分恢复,表明YxaB蛋白参与了这一多细胞过程。我们提供了关于编码假定甘油酸激酶的yxaB和yxaA基因转录调控的数据。在液体细菌培养的营养生长阶段,这两个基因作为一个单一转录单元从依赖sigma(A)的启动子共转录。驱动yxaAB操纵子转录的启动子受AbrB调控。此外,操纵子中的第二个基因yxaB拥有自己的启动子,该启动子可被含有sigma(B)亚基的RNA聚合酶识别。这个转录起始位点在一般应激条件下被使用,导致表达增加。