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研究蓝藻鱼腥藻 PCC 7120 对缺锌响应的特征。

Characterization of the response to zinc deficiency in the cyanobacterium Anabaena sp. strain PCC 7120.

机构信息

Instituto de Bioquímica Vegetal y Fotosíntesis, CSIC, Universidad de Sevilla, Seville, Spain.

出版信息

J Bacteriol. 2012 May;194(10):2426-36. doi: 10.1128/JB.00090-12. Epub 2012 Mar 2.

Abstract

Zur regulators control zinc homeostasis by repressing target genes under zinc-sufficient conditions in a wide variety of bacteria. This paper describes how part of a survey of duplicated genes led to the identification of the open reading frame all2473 as the gene encoding the Zur regulator of the cyanobacterium Anabaena sp. strain PCC 7120. All2473 binds to DNA in a zinc-dependent manner, and its DNA-binding sequence was characterized, which allowed us to determine the relative contribution of particular nucleotides to Zur binding. A zur mutant was found to be impaired in the regulation of zinc homeostasis, showing sensitivity to elevated concentrations of zinc but not other metals. In an effort to characterize the Zur regulon in Anabaena, 23 genes containing upstream putative Zur-binding sequences were identified and found to be regulated by Zur. These genes are organized in six single transcriptional units and six operons, some of them containing multiple Zur-regulated promoters. The identities of genes of the Zur regulon indicate that Anabaena adapts to conditions of zinc deficiency by replacing zinc metalloproteins with paralogues that fulfill the same function but presumably with a lower zinc demand, and with inducing putative metallochaperones and membrane transport systems likely being involved in the scavenging of extracellular zinc, including plasma membrane ABC transport systems and outer membrane TonB-dependent receptors. Among the Zur-regulated genes, the ones showing the highest induction level encode proteins of the outer membrane, suggesting a primary role for components of this cell compartment in the capture of zinc cations from the extracellular medium.

摘要

在各种细菌中,Zur 调控因子通过在锌充足的条件下抑制靶基因来控制锌稳态。本文描述了在重复基因调查的一部分中,如何确定开放阅读框 all2473 是蓝藻 Anabaena sp. PCC 7120 的 Zur 调控因子的基因。All2473 以锌依赖的方式与 DNA 结合,并且其 DNA 结合序列被表征,这使我们能够确定特定核苷酸对 Zur 结合的相对贡献。发现 Zur 突变体在锌稳态的调节中受损,对高浓度锌敏感,但对其他金属不敏感。为了在 Anabaena 中表征 Zur 调控组,鉴定了含有上游推定 Zur 结合序列的 23 个基因,并发现它们受 Zur 调控。这些基因组织在六个单一转录单位和六个操纵子中,其中一些包含多个 Zur 调节的启动子。Zur 调控组的基因身份表明,Anabaena 通过用具有相同功能但可能需要较低锌的同源物替代锌金属蛋白酶来适应锌缺乏条件,并诱导假定的金属伴侣和膜转运系统,这些系统可能参与从细胞外环境中摄取锌,包括质膜 ABC 转运系统和外膜 TonB 依赖性受体。在 Zur 调节的基因中,诱导水平最高的基因编码外膜蛋白,表明该细胞区室的成分在从细胞外介质中捕获锌阳离子方面具有主要作用。

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