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苜蓿根瘤菌结瘤基因区域的物理图谱和遗传图谱以及nodC的核苷酸序列

Physical and genetic map of a Rhizobium meliloti nodulation gene region and nucleotide sequence of nodC.

作者信息

Jacobs T W, Egelhoff T T, Long S R

出版信息

J Bacteriol. 1985 May;162(2):469-76. doi: 10.1128/jb.162.2.469-476.1985.

Abstract

Infection of alfalfa by the soil bacterium Rhizobium meliloti proceeds by deformation of root hairs and bacterial invasion of host tissue by way of an infection thread. We studied an 8.7-kilobase (kb) segment of the R. meliloti megaplasmid, which contains genes required for infection. Site-directed Tn5 mutagenesis was used to examine this fragment for nodulation genes. A total of 81 R. meliloti strains with mapped Tn5 insertions in the 8.7-kb fragment were evaluated for nodulation phenotype on alfalfa plants; 39 of the insertions defined a 3.5-kb segment containing nodulation functions. Of these 39 mutants, 37 were completely nodulation deficient (Nod-), and 2 at the extreme nif-distal end were leaky Nod-. Complementation analysis was performed by inoculating plants with strains carrying a genomic Tn5 at one location and a plasmid-borne Tn5 at another location in the 3.5-kb nodulation segment. Mutations near the right border of the fragment behaved as two distinct complementation groups. The segment in which these mutations are located was analyzed by DNA sequencing. Several open reading frames were found in this region, but the one most likely to function is 1,206 bases long, reading from left to right (nif distal to proximal) and spanning both mutation groups. The genetic behavior of this segment may be due either to the gene product having two functional domains or to a recombinational hot spot between the apparent complementation groups.

摘要

土壤细菌苜蓿根瘤菌对苜蓿的感染是通过根毛变形以及细菌通过感染丝侵入宿主组织来进行的。我们研究了苜蓿根瘤菌大质粒的一个8.7千碱基(kb)片段,该片段包含感染所需的基因。采用定点Tn5诱变来检测这个片段中的结瘤基因。对81株在8.7 kb片段中Tn5插入位点已定位的苜蓿根瘤菌菌株进行了苜蓿植株结瘤表型评估;其中39个插入位点确定了一个包含结瘤功能的3.5 kb片段。在这39个突变体中,37个完全缺乏结瘤能力(Nod-),在最远端固氮基因(nif)处的2个为渗漏型结瘤缺陷(Nod-)。通过用在3.5 kb结瘤片段的一个位置携带基因组Tn5且在另一个位置携带质粒携带的Tn5的菌株接种植物来进行互补分析。片段右边界附近的突变表现为两个不同的互补组。对这些突变所在的片段进行了DNA测序分析。在该区域发现了几个开放阅读框,但最有可能起作用的那个开放阅读框从左到右(从固氮基因远端到近端)长1206个碱基,跨越两个突变组。该片段的遗传行为可能是由于基因产物具有两个功能结构域,或者是由于明显互补组之间的重组热点。

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