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一个参与茎瘤固氮根瘤菌ORS571脂多糖产生以及在喙荚田菁茎和根上形成根瘤的基因座。

An Azorhizobium caulinodans ORS571 locus involved in lipopolysaccharide production and nodule formation on Sesbania rostrata stems and roots.

作者信息

Goethals K, Leyman B, Van Den Eede G, Van Montagu M, Holsters M

机构信息

Laboratorium voor Genetica, Universiteit Gent, Belgium.

出版信息

J Bacteriol. 1994 Jan;176(1):92-9. doi: 10.1128/jb.176.1.92-99.1994.

Abstract

Azorhizobium caulinodans ORS571 is able to nodulate roots and stems of the tropical legume Sesbania rostrata. An ORS571 Tn5 insertion mutant, strain ORS571-X15, had a rough colony morphology, was nonmotile, and showed clumping behavior on various media. When this pleiotropic mutant was inoculated on roots or stems of the host, no nodules developed (Nod-). Compared with the wild type, strain ORS571-X15 produced lipopolysaccharides (LPS) with an altered ladder pattern on sodium dodecyl sulfate-polyacrylamide gel electrophoresis gels, suggestive of a different O-antigen structure with a lower degree of polymerization. A cosmid clone, pRG20, that fully complemented all phenotypes of ORS571-X15 was isolated. With a 6-kb EcoRI subfragment of pRG20, clumping was relieved and nodulation was almost completely restored, but the strain was still nonmotile. LPS preparations from these complemented strains resembled the wild-type LPS, although minor quantitative and qualitative differences were evident. The sequence of the locus hit by the Tn5 in ORS571-X15 (the oac locus) revealed a striking homology with the rfb locus of Salmonella typhimurium, which is involved in O-antigen biosynthesis. The Tn5 insertion position was mapped to the oac3 gene, homologous to rfbA, encoding dTDP-D-glucose synthase. Biochemical assaying showed that ORS571-X15 is indeed defective in dTDP-D-glucose synthase activity, essential for the production of particular deoxyhexoses. Therefore, it was proposed that the O antigen of the mutant strain is devoid of such sugars.

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形成根瘤。一株ORS571的Tn5插入突变体,即菌株ORS571-X15,具有粗糙的菌落形态,无运动性,并且在各种培养基上表现出聚集行为。当将这个多效性突变体接种到宿主的根或茎上时,没有形成根瘤(结瘤阴性)。与野生型相比,菌株ORS571-X15在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳凝胶上产生的脂多糖(LPS)具有改变的梯状模式,这表明其O抗原结构不同,聚合度较低。分离出了一个完全互补ORS571-X15所有表型的黏粒克隆pRG20。用pRG20的一个6 kb EcoRI亚片段,聚集现象得到缓解,结瘤几乎完全恢复,但该菌株仍然无运动性。这些互补菌株的LPS制剂类似于野生型LPS,尽管存在明显的微小定量和定性差异。ORS571-X15中被Tn5插入的位点(oac位点)的序列显示与鼠伤寒沙门氏菌的rfb位点有显著同源性,rfb位点参与O抗原的生物合成。Tn5插入位置被定位到与rfbA同源的oac3基因,rfbA编码dTDP-D-葡萄糖合酶。生化分析表明,ORS571-X15在dTDP-D-葡萄糖合酶活性方面确实存在缺陷,而dTDP-D-葡萄糖合酶活性是产生特定脱氧己糖所必需的。因此,有人提出突变菌株的O抗原缺乏这类糖类。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce74/205018/c522a098c7e3/jbacter00019-0118-a.jpg

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