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百脉根有效结瘤所需的一种百脉根根瘤菌基因的分离与鉴定。

Isolation and characterization of a Rhizobium loti gene required for effective nodulation of Lotus pedunculatus.

作者信息

Ward L J, Rockman E S, Ball P, Jarvis B D, Scott D B

机构信息

Department of Microbiology and Genetics, Massey University, Palmerston North, New Zealand.

出版信息

Mol Plant Microbe Interact. 1989 Sep-Oct;2(5):224-32. doi: 10.1094/mpmi-2-224.

Abstract

A Rhizobium loti gene required for effective invasion of the host Lotus pedunculatus has been identified by transposon Tn5 mutagenesis. Cosmids that complemented a previously isolated mutation (239) at this invasion (inv) locus were identified by in planta complementation and used to construct a physical map of the gene region. The insertion site of Tn5 in PN239 was mapped to a 7.5-kb EcoRI fragment, which complemented the mutation when subcloned into pLAFR1. Further Tn5 mutagenesis of the 7.5-kb fragment was carried out in Escherichia coli using bacteriophage lambda 467, and the mutations homogenotized into R. loti NZP2037. Three additional Fix- mutations were isolated, and these were found to map adjacent to the position of the original mutation in strain PN239. All the other Tn5 insertions isolated in the 7.5-kb fragment gave a Fix+ phenotype on L. pedunculatus. Electron microscopic examination of the L. pedunculatus nodules induced by the isolated Fix- mutants showed that bacteria were either blocked in release from the infection threads or were unable to undergo normal bacteroid development. The inv locus as defined by the Tn5 insertions was sequenced, and a single open-reading frame (ORF) of 576 bp, corresponding to a polypeptide of 21.3 kDa, was identified. The position and orientation of this ORF were consistent with those of the isolated Tn5 Fix- insertions.

摘要

通过转座子Tn5诱变,已鉴定出根瘤菌(Rhizobium loti)有效侵染宿主百脉根(Lotus pedunculatus)所需的一个基因。通过植物体内互补鉴定出能够互补此前在该侵染(inv)位点分离得到的突变(239)的黏粒,并用于构建该基因区域的物理图谱。将PN239中Tn5的插入位点定位到一个7.5 kb的EcoRI片段上,该片段亚克隆到pLAFR1中时能够互补该突变。使用噬菌体λ467在大肠杆菌中对7.5 kb片段进行进一步的Tn5诱变,并将突变同型整合到根瘤菌NZP2037中。分离到另外三个固氮缺陷(Fix-)突变体,发现它们定位在菌株PN239中原始突变位置的相邻处。在7.5 kb片段中分离到的所有其他Tn5插入在百脉根上均表现出固氮正常(Fix+)的表型。对由分离到的Fix-突变体诱导形成的百脉根根瘤进行电子显微镜检查表明,细菌要么在从侵染线中释放时受阻,要么无法进行正常的类菌体发育。对由Tn5插入所定义的inv位点进行测序,鉴定出一个576 bp的单一开放阅读框(ORF),对应于一个21.3 kDa的多肽。该ORF的位置和方向与分离到的Tn5 Fix-插入的位置和方向一致。

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