首页> 美国卫生研究院文献>Journal of Bacteriology >Identification of a membrane protein involved in activation of the KinB pathway to sporulation in Bacillus subtilis.
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Identification of a membrane protein involved in activation of the KinB pathway to sporulation in Bacillus subtilis.

机译:鉴定参与枯草芽孢杆菌中KinB途径形成孢子的膜蛋白。

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摘要

The initiation of sporulation in Bacillus subtilis is dependent on the phosphorylation of the Spo0A transcription factor mediated by the phosphorelay and by two major kinases, KinA and KinB. Temporal expression of these kinases was analyzed, and an assessment of their respective contributions to the production of Spo0A-P was undertaken. The results show that KinB is expressed and activated prior to KinA; i.e., the two kinases are solicited sequentially in the sporulation process and are thought to be activated by different signaling pathways. A strategy was developed to isolate mutations specifically affecting the KinB pathway, using the newly improved mini-Tn10 delivery vector pIC333. Several mutants were obtained, one of which carried a transposon in a gene coding for a small integral membrane protein, named KbaA. Inactivation of the kbaA gene appeared to affect KinB activity but not transcription of kinB. A Spo+ suppressor (kinB45) of the kbaA null mutation was isolated in the promoter region of kinB. An eightfold increase of kinB expression levels over wild-type levels was observed in the kinB45 mutant. Thus, overexpression of the kinB-kapB operon was sufficient to overcome the sporulation defect caused by inactivation of kbaA in a KinA- strain. Transcription of kinB was found to be repressed by SinR, while the kinB45 mutant was no longer sensitive to SinR regulation. Implications of these observations on the transcriptional regulation of kinB and the role of KbaA in KinB activation are discussed.
机译:枯草芽孢杆菌中孢子形成的起始取决于磷酸二酯和两种主要激酶KinA和KinB介导的Spo0A转录因子的磷酸化。分析了这些激酶的时间表达,并评估了它们对Spo0A-P产生的贡献。结果表明,KinB在KinA之前被表达和激活。即,这两种激酶在孢子形成过程中依次被征集,并被认为是由不同的信号传导途径激活的。使用新改良的mini-Tn10递送载体pIC333,开发了一种策略来分离特异性影响KinB途径的突变。获得了几个突变体,其中一个突变体在一个编码小的整体膜蛋白的基因(称为KbaA)的基因中带有转座子。 kbaA基因的失活似乎影响KinB活性,但不影响kinB的转录。在kinB的启动子区域中分离出了kbaA空突变的Spo +抑制子(kinB45)。在kinB45突变体中,kinB表达水平比野生型水平增加了八倍。因此,kinB-kapB操纵子的过表达足以克服KinA菌株中kbaA失活引起的孢子形成缺陷。发现kinB的转录被SinR抑制,而kinB45突变体不再对SinR调控敏感。讨论了这些观察结果对kinB的转录调控以及KbaA在KinB激活中的作用。

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