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茎瘤固氮根瘤菌ORS571中一个功能性nodD基因的鉴定与表征

Identification and characterization of a functional nodD gene in Azorhizobium caulinodans ORS571.

作者信息

Goethals K, Van den Eeede G, Van Montagu M, Holsters M

机构信息

Laboratorium yoor Genetica, Rijksuniversiteit Gent, Belgium.

出版信息

J Bacteriol. 1990 May;172(5):2658-66. doi: 10.1128/jb.172.5.2658-2666.1990.

Abstract

Azorhizobium caulinodans ORS571, a bacterium capable of nodulating roots and stems of the tropical legume Sesbania rostrata, has been shown to have no nodD-like gene located immediately upstream from its common nodABC locus. A clone carrying a functional nodD gene of strain ORS571 has now been isolated from a pLAFR1 gene library by screening for naringenin-induced expression of the common nod genes in an Agrobacterium background. Tn5 mutagenesis of the cloned insert DNA delimited the inducing activity to a +/- 0.8-kilobase-pair fragment. One of the Tn5 insertions in the activator locus was homogenotized in the ORS571 genome. This resulted in a mutant strain (ORS571-3) that was unable to induce common nod gene expression in the presence of host plant exudate or the flavanone naringenin and that had lost the capacity to nodulate the roots and stems of S. rostrata. Complementation of both mutant phenotypes was achieved upon introduction of the cloned nodD gene. Sequencing of the nodD locus indicated the presence of a single, 942-base-pair-long open reading frame (ORFD) with significant homology to the nodD gene of (brady)rhizobia. The level of homology, however, is the lowest thus far reported for this kind of gene. ORFD most likely initiates translation with a TTG start codon. Upstream from ORFD, a divergently oriented nod box-like sequence is present, the function of which remains to be determined.

摘要

茎瘤固氮根瘤菌ORS571能够使热带豆科植物喙荚田菁的根和茎结瘤,已证明在其普通的nodABC基因座上游紧邻处没有类nodD基因。现在,通过在农杆菌背景中筛选柚皮素诱导的普通结瘤基因表达,从pLAFR1基因文库中分离出了一个携带茎瘤固氮根瘤菌ORS571功能型nodD基因的克隆。对克隆的插入DNA进行Tn5诱变,将诱导活性限定在一个±0.8千碱基对的片段上。激活基因座中的一个Tn5插入在ORS571基因组中实现了同源整合。这产生了一个突变菌株(ORS571-3),该菌株在宿主植物分泌物或黄烷酮柚皮素存在的情况下无法诱导普通结瘤基因表达,并且失去了使喙荚田菁的根和茎结瘤的能力。导入克隆的nodD基因后,两种突变表型都得到了互补。nodD基因座的测序表明存在一个单一的、942个碱基对长的开放阅读框(ORFD),与(慢生)根瘤菌的nodD基因具有显著同源性。然而,同源性水平是迄今为止这类基因报道中最低的。ORFD很可能以TTG起始密码子开始翻译。在ORFD上游,存在一个反向排列的类nod盒序列,其功能尚待确定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dad4/208910/83ac810f04c5/jbacter00119-0476-a.jpg

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