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利用TnphoA融合技术检测苜蓿根瘤菌外生基因在自由生活细胞和植物体内的调控。

Regulation of Rhizobium meliloti exo genes in free-living cells and in planta examined by using TnphoA fusions.

作者信息

Reuber T L, Long S, Walker G C

机构信息

Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.

出版信息

J Bacteriol. 1991 Jan;173(2):426-34. doi: 10.1128/jb.173.2.426-434.1991.

Abstract

The exo loci of Rhizobium meliloti are necessary for the production of an acidic exopolysaccharide, EPS I, that is needed for alfalfa nodule invasion by strain Rm1021. We have isolated and characterized alkaline phosphatase fusions made with TnphoA in several exo loci of R. meliloti and used these fusions to examine the subcellular localization of exo gene products and the regulation of exo genes in free-living cells and in planta. In the course of this work, we isolated a new exo locus, exoT. We have obtained evidence that several of the exo loci may encode membrane proteins. The activity of TnphoA fusions in several exo loci is increased two- to fivefold in the presence of the regulatory mutations exoR95 and exoS96. While examining the regulation of the exo gens by exoR95 and exoS96, we found that certain classes of exo mutations are lethal in an exoR95 or exoS96 background unless a plasmid complementing the exo mutation is present. This result has possible implications for the role of these exo loci in EPS I biosynthesis. We have developed a method for staining nodules specifically for the alkaline phosphatase activity present in the inducing bacteria and used this method to show that an exoF::TnphoA fusion is expressed mainly in the invasion zone of the nodule.

摘要

苜蓿中华根瘤菌的exo基因座对于酸性胞外多糖EPS I的产生是必需的,而EPS I是Rm1021菌株侵染苜蓿根瘤所必需的。我们已分离并鉴定了用TnphoA在苜蓿中华根瘤菌的几个exo基因座构建的碱性磷酸酶融合体,并利用这些融合体来检测exo基因产物的亚细胞定位以及在自由生活细胞和植物体内exo基因的调控。在这项工作过程中,我们分离出一个新的exo基因座exoT。我们已获得证据表明几个exo基因座可能编码膜蛋白。在存在调控突变exoR95和exoS96的情况下,几个exo基因座中TnphoA融合体的活性提高了2至5倍。在检测exoR95和exoS96对exo基因的调控时,我们发现某些类型的exo突变在exoR95或exoS96背景下是致死的,除非存在互补该exo突变的质粒。这一结果可能对这些exo基因座在EPS I生物合成中的作用具有启示意义。我们已开发出一种方法,可特异性地对根瘤中诱导细菌中存在的碱性磷酸酶活性进行染色,并利用该方法表明exoF::TnphoA融合体主要在根瘤的侵染区表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0fd/207029/c11b0c8b841f/jbacter00092-0026-a.jpg

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