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苜蓿中华根瘤菌中磷胁迫诱导基因的表达与调控

Expression and regulation of phosphate stress inducible genes in Sinorhizobium meliloti.

作者信息

Summers M L, Elkins J G, Elliott B A, McDermott T R

机构信息

Department of Land Resources and Environmental Sciences, Montana State University, Bozeman 59717-3120, USA.

出版信息

Mol Plant Microbe Interact. 1998 Nov;11(11):1094-101. doi: 10.1094/MPMI.1998.11.11.1094.

Abstract

Sinorhizobium meliloti 104A14 was mutated with transposon Tn5B22, which creates lacZ transcriptional fusions when inserted in the correct orientation relative to the promoter. This promoter reporter allowed us to identify six phosphate stress inducible (psi) genes in S. meliloti that are up-regulated in response to inorganic phosphate (Pi) starvation. The transposon and flanking DNA were cloned from each psi::Tn5B22 reporter mutant and the junction DNA sequenced. High identity/similarity of the inferred peptides with those in major data bases allowed identification of the following genes: dnaK, expC, pssB, ackA, vipC, and prkA. The prkA homolog was also found to be up-regulated in response to carbon starvation and when nitrate replaced ammonium as the nitrogen source. Through allele replacement techniques, PhoB- mutants were generated for the expC, ackA, vipC, and pssB reporter strains. Loss of a functional PhoB resulted in the absence of Pi-sensitive induction in all four genes. These experiments suggest the Pho regulon in S. meliloti includes genes that presumably are not directly linked to Pi acquisition or assimilation. The psi strains were tested for their symbiotic properties under growth conditions that were Pi-limiting or Pi-nonlimiting for the host plant. All were Nod+ and Fix+ except the reporter strain of dnaK transcription, which was less effective than the wild-type strain under both P treatments, indicating DnaK is required for optimum symbiotic function.

摘要

苜蓿中华根瘤菌104A14用转座子Tn5B22进行诱变,当以相对于启动子的正确方向插入时,该转座子会产生lacZ转录融合体。这种启动子报告基因使我们能够在苜蓿中华根瘤菌中鉴定出六个磷酸盐胁迫诱导(psi)基因,这些基因在无机磷酸盐(Pi)饥饿时会上调。从每个psi::Tn5B22报告突变体中克隆转座子和侧翼DNA,并对连接DNA进行测序。推断的肽段与主要数据库中的肽段具有高度同一性/相似性,从而鉴定出以下基因:dnaK、expC、pssB、ackA、vipC和prkA。还发现prkA同源物在碳饥饿以及硝酸盐替代铵作为氮源时会上调。通过等位基因置换技术,为expC、ackA、vipC和pssB报告菌株构建了PhoB-突变体。功能性PhoB的缺失导致所有四个基因中都没有Pi敏感诱导。这些实验表明,苜蓿中华根瘤菌中的Pho调节子包括可能与Pi获取或同化没有直接联系的基因。在宿主植物Pi限制或非限制的生长条件下,对psi菌株的共生特性进行了测试。除了dnaK转录的报告菌株外,所有菌株都是结瘤阳性(Nod+)和固氮阳性(Fix+),在两种磷处理下,该报告菌株都比野生型菌株效果差,这表明DnaK是最佳共生功能所必需的。

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