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苜蓿中华根瘤菌高分子量质粒上结瘤和固氮基因的定位

Location of nodulation and nitrogen fixation genes on a high molecular weight plasmid of R. meliloti.

作者信息

Bánfalvi Z, Sakanyan V, Koncz C, Kiss A, Dusha I, Kondorosi A

出版信息

Mol Gen Genet. 1981;184(2):318-25. doi: 10.1007/BF00272925.

Abstract

R. meliloti strain 41 (Rm41) was shown to harbour two indigenous plasmids with molecular weights of 140 Mdal (pRme41a) and more than 300 Mdal (pRme41b), respectively. Using a heat-treatment procedure, derivatives of Rm41 defective in nodulation (Nod-) or nitrogen fixation (Fix-) have been readily obtained. In some Nod- mutants the deletion of a segment of plasmid pRme41b was found. Based on the demonstrated homology between the nitrogen fixation (nif) genes of Klebsiella pneumoniae and of R. meliloti the Rhizobium nif region has been cloned into the cosmid vector pHC79, then recloned into pBR322 and the restriction map of the nif region has been determined. 32P-labelled nick-translated probe prepared from the cloned nif DNA fragment hybridized to pRme41b of Rm41 but for most Nod- mutants this hybridization was not detected. Hybridization of a cosmid containing Rm41 DNA to total DNA digest from the wild-type bacterium and from a series of Nod- mutants revealed that at least a 2 kb DNA fragment including the nif structural genes was missing from most of the Nod- mutants. These results, together with the genetic analyses of these symbiotic mutations suggest that some nod and fix genes are located on pRme41b.

摘要

苜蓿中华根瘤菌菌株41(Rm41)被证明分别携带两个内源质粒,分子量分别为140Mdal(pRme41a)和超过300Mdal(pRme41b)。使用热处理程序,很容易获得在结瘤(Nod-)或固氮(Fix-)方面有缺陷的Rm41衍生物。在一些Nod-突变体中,发现质粒pRme41b的一段片段缺失。基于肺炎克雷伯菌和苜蓿中华根瘤菌固氮(nif)基因之间已证明的同源性,根瘤菌nif区域已被克隆到黏粒载体pHC79中,然后再克隆到pBR322中,并确定了nif区域的限制性图谱。从克隆的nif DNA片段制备的32P标记的缺口平移探针与Rm41的pRme41b杂交,但对于大多数Nod-突变体,未检测到这种杂交。含有Rm41 DNA的黏粒与野生型细菌和一系列Nod-突变体的总DNA消化产物杂交表明,大多数Nod-突变体至少缺失了一个包括nif结构基因的2kb DNA片段。这些结果,连同对这些共生突变的遗传分析表明,一些nod和fix基因位于pRme41b上。

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