Gottig Natalia, Pedrido María Eugenia, Méndez Marcelo, Lombardía Esteban, Rovetto Adrián, Philippe Valeria, Orsaria Lelia, Grau Roberto
Departamento de Microbiología, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario and Instituto de Biología Molecular y Celular de Rosario, IBR-CONICET, Suipacha 531, Rosario (2000), Argentina.
J Bacteriol. 2005 Apr;187(8):2662-72. doi: 10.1128/JB.187.8.2662-2672.2005.
Even though there is a large body of information concerning the harmful effects of alcohol on different organisms, the mechanism(s) that affects developmental programs, at a single-cell level, has not been clearly identified. In this respect, the spore-forming bacterium Bacillus subtilis constitutes an excellent model to study universal questions of cell fate, cell differentiation, and morphogenesis. Here, we demonstrate that treatment with subinhibitory concentrations of alcohol that did not affect vegetative growth inhibited the initiation of spore development through a selective blockage of key developmental genes under the control of the master transcription factor Spo0A approximately P. Isopropyl-beta-D-thiogalactopyranoside-directed expression of a phosphorylation-independent form of Spo0A (Sad67) and the use of an in vivo mini-Tn10 insertional library permitted the identification of the developmental SinR repressor and RapA phosphatase as the effectors that mediated the inhibitory effect of alcohol on spore morphogenesis. A double rapA sinR mutant strain was completely resistant to the inhibitory effects of different-C-length alcohols on sporulation, indicating that the two cell fate determinants were the main or unique regulators responsible for the spo0 phenotype of wild-type cells in the presence of alcohol. Furthermore, treatment with alcohol produced a significant induction of rapA and sinR, while the stationary-phase induction of sinI, which codes for a SinR inhibitor, was completely turned off by alcohol. As a result, a dramatic repression of spo0A and the genes under its control occurred soon after alcohol addition, inhibiting the onset of sporulation and permitting the evaluation of alternative pathways required for cellular survival.
尽管有大量关于酒精对不同生物体有害影响的信息,但在单细胞水平上影响发育程序的机制尚未明确确定。在这方面,形成孢子的枯草芽孢杆菌是研究细胞命运、细胞分化和形态发生等普遍问题的优秀模型。在这里,我们证明,用不影响营养生长的亚抑制浓度酒精处理,通过选择性阻断主转录因子Spo0A大约P控制下的关键发育基因,抑制了孢子发育的起始。异丙基-β-D-硫代半乳糖苷定向表达磷酸化非依赖性形式的Spo0A(Sad67)以及使用体内mini-Tn10插入文库,使得能够鉴定出发育性SinR阻遏物和RapA磷酸酶是介导酒精对孢子形态发生抑制作用的效应物。双rapA sinR突变菌株对不同碳链长度酒精对孢子形成的抑制作用完全具有抗性,这表明这两个细胞命运决定因素是在有酒精存在时负责野生型细胞spo0表型的主要或唯一调节因子。此外,酒精处理导致rapA和sinR显著诱导,而编码SinR抑制剂的sinI在稳定期的诱导被酒精完全关闭。结果,在添加酒精后不久,spo0A及其控制下的基因发生了显著抑制,抑制了孢子形成的起始,并允许评估细胞存活所需的替代途径。