首页> 外文期刊>Genes and Development: a Journal Devoted to the Molecular Analysis of Gene Expression in Eukaryotes, Prokaryotes, and Viruses >Respiration control of multicellularity in Bacillus subtilis by a complex of the cytochrome chain with a membrane-embedded histidine kinase
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Respiration control of multicellularity in Bacillus subtilis by a complex of the cytochrome chain with a membrane-embedded histidine kinase

机译:通过细胞色素链与膜包埋的组氨酸激酶的复合物控制枯草芽孢杆菌的多细胞呼吸作用

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摘要

Bacillus subtilis forms organized multicellular communities known as biofilms wherein the individual cells are held together by a self-produced extracellular matrix. The environmental signals that promote matrix synthesis remain largely unknown. We discovered that one such signal is impaired respiration. Specifically, high oxygen levels suppressed synthesis of the extracellular matrix. In contrast, low oxygen levels, in the absence of an alternative electron acceptor, led to increased matrix production. The response to impaired respiration was blocked in a mutant lacking cytochromes caa3 and bc and markedly reduced in a mutant lacking kinase KinB. Mass spectrometry of proteins associated with KinB showed that the kinase was in a complex with multiple components of the aerobic respiratory chain. We propose that KinB is activated via a redox switch involving interaction of its second transmembrane segment with one or more cytochromes under conditions of reduced electron transport. In addition, a second kinase (KinA) contributes to the response to impaired respiration. Evidence suggests that KinA is activated by a decrease in the nicotinamide adenine dinucleotide (NAD+)/NADH ratio via binding of NAD+ to the kinase in a PAS domain A-dependent manner. Thus, B. subtilis switches from a unicellular to a multicellular state by two pathways that independently respond to conditions of impaired respiration.
机译:枯草芽孢杆菌形成有组织的多细胞群落,称为生物膜,其中各个细胞通过自身产生的细胞外基质保持在一起。促进基质合成的环境信号在很大程度上仍然未知。我们发现一种这样的信号是呼吸受损。具体而言,高氧水平抑制了细胞外基质的合成。相反,在没有替代电子受体的情况下,低氧含量导致基质产量增加。在缺乏细胞色素caa3和bc的突变体中,对呼吸受损的反应被阻断,而在缺乏激酶KinB的突变体中,其反应显着降低。与KinB相关的蛋白质的质谱分析表明,该激酶与需氧呼吸链的多个组成部分复合。我们建议KinB是通过氧化还原开关激活的,该开关涉及其第二跨膜片段与一种或多种细胞色素在减少的电子传输条件下的相互作用。此外,第二种激酶(KinA)有助于对呼吸受损的反应。有证据表明,通过以PAS域A依赖性方式将NAD +与激酶结合,烟酰胺腺嘌呤二核苷酸(NAD +)/ NADH比值降低可激活KinA。因此,枯草芽孢杆菌通过两条途径独立地响应呼吸困难的条件从单细胞状态切换到多细胞状态。

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