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一种新的小分子调控蛋白 HmuP 调节苜蓿中华根瘤菌血红素的获取。

A new small regulatory protein, HmuP, modulates haemin acquisition in Sinorhizobium meliloti.

机构信息

Laboratorio de Bioquímica y Genómica Microbianas, Instituto de Investigaciones Biológicas Clemente Estable, MEC, Unidad Asociada a la Facultad de Ciencias, Av. Italia 3318, Montevideo 11600, Uruguay.

Sección Bioquímica, Facultad de Ciencias, Iguá 4225, Montevideo 11400, Uruguay.

出版信息

Microbiology (Reading). 2010 Jun;156(Pt 6):1873-1882. doi: 10.1099/mic.0.037713-0. Epub 2010 Feb 18.

Abstract

Sinorhizobium meliloti has multiple systems for iron acquisition, including the use of haem as an iron source. Haem internalization involves the ShmR haem outer membrane receptor and the hmuTUV locus, which participates in haem transport across the cytoplasmic membrane. Previous studies have demonstrated that expression of the shmR gene is negatively regulated by iron through RirA. Here, we identify hmuP in a genetic screen for mutants that displayed aberrant control of shmR. The normal induction of shmR in response to iron limitation was lost in the hmuP mutant, showing that this gene positively affects shmR expression. Moreover, the HmuP protein is not part of the haemin transporter system. Analysis of gene expression and siderophore production indicates that disruption of hmuP does not affect other genes related to the iron-restriction response. Our results strongly indicate that the main function of HmuP is the transcriptional regulation of shmR. Sequence alignment of HmuP homologues and comparison with the NMR structure of Rhodopseudomonas palustris CGA009 HmuP protein revealed that certain amino acids localized within predicted beta-sheets are well conserved. Our data indicate that at least one of the beta-sheets is important for HmuP activity.

摘要

苜蓿中华根瘤菌有多种获取铁的系统,包括利用血红素作为铁源。血红素内化涉及 ShmR 血红素外膜受体和 hmuTUV 基因座,该基因座参与血红素穿过细胞质膜的运输。先前的研究表明,shmR 基因的表达受到 RirA 通过铁的负调控。在这里,我们在突变体的遗传筛选中鉴定出 hmuP,这些突变体表现出 shmR 异常控制。hmuP 突变体中失去了对铁限制的正常 shmR 诱导,表明该基因对 shmR 表达有积极影响。此外,HmuP 蛋白不是血红素转运系统的一部分。基因表达和铁载体生产分析表明,hmuP 的破坏不影响其他与铁限制反应相关的基因。我们的结果强烈表明,HmuP 的主要功能是 shmR 的转录调节。HmuP 同源物的序列比对和与 Rhodopseudomonas palustris CGA009 HmuP 蛋白的 NMR 结构比较表明,某些位于预测β-折叠内的氨基酸高度保守。我们的数据表明,至少一个β-折叠对于 HmuP 的活性很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f545/3068671/6f178e7c7c30/1873fig1.jpg

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