Chai Yunrong, Chu Frances, Kolter Roberto, Losick Richard
Department of Molecular and Cellular Biology, The Biological Laboratories, Harvard University, Cambridge, MA 02138, USA.
Mol Microbiol. 2008 Jan;67(2):254-63. doi: 10.1111/j.1365-2958.2007.06040.x. Epub 2007 Nov 28.
Biofilms of Bacillus subtilis consist of long chains of cells that are held together in bundles by an extracellular matrix of exopolysaccharide and the protein TasA. The exopolysaccharide is produced by enzymes encoded by the epsA-O operon and the gene encoding TasA is located in the yqxM-sipW-tasA operon. Both operons are under the control of the repressor SinR. Derepression is mediated by the antirepressor SinI, which binds to SinR with a 1:1 stoichiometry. Paradoxically, in medium promoting derepression of the matrix operons, the overall concentration of SinR in the culture greatly exceeded that of SinI. We show that under biofilm-promoting conditions sinI, which is under the control of the response regulator Spo0A, was expressed only in a small subpopulation of cells, whereas sinR was expressed in almost all cells. Activation of Spo0A is known to be subject to a bistable switch, and we infer that SinI reaches levels sufficient to trigger matrix production only in the subpopulation of cells in which Spo0A is active. Additionally, evidence suggests that sinI is expressed at intermediate, but not low or high, levels of Spo0A activity, which may explain why certain nutritional conditions are more effective in promoting biofilm formation than others.
枯草芽孢杆菌的生物膜由细胞长链组成,这些细胞通过胞外多糖和蛋白质TasA的细胞外基质捆绑在一起。胞外多糖由epsA - O操纵子编码的酶产生,编码TasA的基因位于yqxM - sipW - tasA操纵子中。这两个操纵子都受阻遏物SinR的控制。去阻遏由抗阻遏物SinI介导,SinI与SinR以1:1的化学计量比结合。矛盾的是,在促进基质操纵子去阻遏的培养基中,培养物中SinR的总浓度大大超过SinI。我们发现,在促进生物膜形成的条件下,受应答调节因子Spo0A控制的sinI仅在一小部分细胞中表达,而sinR几乎在所有细胞中都表达。已知Spo0A的激活存在双稳态开关,我们推断只有在Spo0A活跃的细胞亚群中,SinI才能达到足以触发基质产生的水平。此外,有证据表明,sinI在Spo0A活性处于中等水平而非低水平或高水平时表达,这可能解释了为什么某些营养条件比其他条件更有效地促进生物膜形成。