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The major facilitator superfamily-type protein LbtC promotes the utilization of the legiobactin siderophore by Legionella pneumophila

机译:主要的促进剂超小心型蛋白质LBTC促进了军团菌肺炎的乳糜蛋白纵横物细胞的利用

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The Gram-negative bacterium Legionella pneumophila elaborates the siderophore legiobactin. We previously showed that cytoplasmic LbtA helps mediate legiobactin synthesis, inner-membrane LbtB promotes export of legiobactin, and outer-membrane LbtU acts as the ferrisiderophore receptor. RT-PCR analyses now identified lbtC as an iron-repressed gene that is the final gene in an operon containing lbtA and lbtB. In silico analysis predicted that LbtC is an inner-membrane protein that belongs to the major facilitator superfamily (MFS). Although capable of normal growth in standard media, lbtC mutants were defective for growth on iron-depleted agar media. While producing normal levels of legiobactin, lbtC mutants were unable to utilize supplied legiobactin to stimulate growth on iron-depleted media and displayed an impaired ability to take up radiolabelled iron. All lbtC mutant phenotypes were complemented by reintroduction of an intact copy of lbtC. When a cloned copy of both lbtC and lbtU was introduced into a heterologous bacterium (Legionella longbeachae), the organism acquired the ability to utilize legiobactin to grow better on low-iron media. Together, these data indicate that LbtC is involved in the uptake of legiobactin, and based upon its predicted location is most likely the mediator of ferrilegiobactin transport across the inner membrane. The data are also a unique documentation of how an MFS protein can promote bacterial iron-siderophore import, standing in contrast to the vast majority of studies which have defined ABC-type permeases as the mediators of siderophore import across the Gram-negative inner membrane or the Gram-positive cytoplasmic membrane.
机译:革兰阴性细菌军团菌肺炎群岛阐述了剑道的legiobactin。我们以前表明,细胞质LBTA有助于介导的乳糖酰胺蛋白合成,内膜LBTB促进乳杆菌蛋白的出口,外膜LBTU作为铁霉菌受体。 RT-PCR分析现在将LBTC作为铁抑制基因鉴定为含有LBTA和LBTB的操纵子中的最终基因。在硅分析中,LBTC是一种属于主要促进剂超家族(MFS)的内膜蛋白。虽然能够正常在标准培养基中生长,但LBTC突变体对铁耗尽琼脂培养基的生长有缺陷。在产生正常水平的乳糖酰胺时,LBTC突变体无法利用供应的乳酰粘蛋白来刺激铁耗尽介质上的生长,并显示出占用放射性标记铁的损害能力。所有LBTC突变表型都是通过重新引入LBTC的完整拷贝的所有LBTC突变表型。当将LBTC和LBTU的克隆副本引入异源细菌(Legionella longbeace)中,生物体获得了利用乳糖酰胺在低铁介质上生长的能力。这些数据在一起表明,LBTC参与了乳糖酰胺的摄取,并且基于其预测位置最有可能在内膜穿过内膜的铁牛肉蛋白输送的介体。该数据也是MFS蛋白质如何促进细菌铁 - 铁道进口的独特文献,与绝大多数研究相反,这些研究具有定义了ABC型易易透过革兰氏阴性内膜的介质或革兰氏阳性细胞质膜。

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