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首页> 外文期刊>MBio >Novel Mechanism for Scavenging of Hypochlorite Involving a Periplasmic Methionine-Rich Peptide and Methionine Sulfoxide Reductase
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Novel Mechanism for Scavenging of Hypochlorite Involving a Periplasmic Methionine-Rich Peptide and Methionine Sulfoxide Reductase

机译:清除次氯酸盐涉及周质富含蛋氨酸和蛋氨酸亚砜还原酶的新机制。

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ABSTRACT Reactive chlorine species (RCS) defense mechanisms are important for bacterial fitness in diverse environments. In addition to the anthropogenic use of RCS in the form of bleach, these compounds are also produced naturally through photochemical reactions of natural organic matter and in vivo by the mammalian immune system in response to invading microorganisms. To gain insight into bacterial RCS defense mechanisms, we investigated Azospira suillum strain PS, which produces periplasmic RCS as an intermediate of perchlorate respiration. Our studies identified an RCS response involving an RCS stress-sensing sigma/anti-sigma factor system (SigF/NrsF), a soluble hypochlorite-scavenging methionine-rich periplasmic protein (MrpX), and a putative periplasmic methionine sulfoxide reductase (YedY1). We investigated the underlying mechanism by phenotypic characterization of appropriate gene deletions, chemogenomic profiling of barcoded transposon pools, transcriptome sequencing, and biochemical assessment of methionine oxidation. Our results demonstrated that SigF was specifically activated by RCS and initiated the transcription of a small regulon centering around yedY1 and mrpX . A yedY1 paralog ( yedY2 ) was found to have a similar fitness to yedY1 despite not being regulated by SigF. Markerless deletions of yedY2 confirmed its synergy with the SigF regulon. MrpX was strongly induced and rapidly oxidized by RCS, especially hypochlorite. Our results suggest a mechanism involving hypochlorite scavenging by sacrificial oxidation of the MrpX in the periplasm. Reduced MrpX is regenerated by the YedY methionine sulfoxide reductase activity. The phylogenomic distribution of this system revealed conservation in several Proteobacteria of clinical importance, including uropathogenic Escherichia?coli and Brucella spp., implying a putative role in immune response evasion in vivo . IMPORTANCE Bacteria are often stressed in the environment by reactive chlorine species (RCS) of either anthropogenic or natural origin, but little is known of the defense mechanisms they have evolved. Using a microorganism that generates RCS internally as part of its respiratory process allowed us to uncover a novel defense mechanism based on RCS scavenging by reductive reaction with a sacrificial methionine-rich peptide and redox recycling through a methionine sulfoxide reductase. This system is conserved in a broad diversity of organisms, including some of clinical importance, invoking a possible important role in innate immune system evasion.
机译:摘要活​​性氯物种(RCS)防御机制对于多种环境中的细菌适应性很重要。除了人为使用的RCS漂白剂外,这些化合物还可以通过天然有机物的光化学反应自然产生,并通过哺乳动物免疫系统响应入侵微生物在体内产生。为了深入了解细菌的RCS防御机制,我们研究了Azospira suillum菌株PS,该菌株产生周质RCS作为高氯酸盐呼吸的中间产物。我们的研究确定了涉及RCS应力感应sigma / anti-sigma因子系统(SigF / NrsF),可溶性次氯酸盐清除蛋氨酸富集的周质蛋白(MrpX)和推定的周质蛋氨酸亚砜还原酶(YedY1)的RCS响应。我们通过表型表征适当的基因缺失,条形码转座子池的化学基因组分析,转录组测序以及蛋氨酸氧化的生化评估,研究了潜在的机制。我们的结果表明,SigF被RCS特异性激活并启动了以yedY1和mrpX为中心的小调控子的转录。发现yedY1旁系同源物(yedY2)与yedY1具有相似的适用性,尽管不受SigF的调节。 yedY2的无标记缺失证实了它与SigF regulon的协同作用。 MrpX被RCS特别是次氯酸盐强烈诱导并迅速被氧化。我们的结果提出了一种机制,该机制涉及通过在质膜中牺牲性氧化MrpX清除次氯酸盐。还原的MrpX由YedY蛋氨酸亚砜还原酶活性再生。该系统的系统生物学分布揭示了在几种具有重要临床意义的变形杆菌中的保守性,包括尿路致病性大肠杆菌和布鲁氏菌属,这暗示了体内逃避免疫应答的假定作用。重要信息细菌通常在环境中受到人为或自然来源的反应性氯物种(RCS)的压力,但人​​们对其形成的防御机制知之甚少。使用在呼吸过程中内部产生RCS的微生物,使我们能够发现新的防御机制,该机制是通过与牺牲性蛋氨酸富集的肽进行还原反应并通过蛋氨酸亚砜还原酶进行氧化还原循环来清除RCS的。该系统在各种各样的生物体中都得到了保护,包括某些具有临床重要性的生物体,从而在逃避先天免疫系统中发挥了重要作用。

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