首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Assessment of competitiveness of rhizobia infecting Galega orientalis on the basis of plant yield nodulation and strain identification by antibiotic resistance and PCR.
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Assessment of competitiveness of rhizobia infecting Galega orientalis on the basis of plant yield nodulation and strain identification by antibiotic resistance and PCR.

机译:根据植物产量结瘤和通过抗生素抗性和PCR鉴定菌株评估根瘤菌感染侧柏的竞争力。

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摘要

Competition between effective and ineffective Rhizobium galegae strains nodulating Galega orientalis was examined on the basis of plant growth, nodulation, antibiotic resistance, and PCR results. In a preliminary experiment in Leonard's jars, ineffective R. galegae strains HAMBI 1207 and HAMBI 1209 competed in similar manners with the effective strain R. galegae HAMBI 1174. In a pot experiment, soil was inoculated with 0 to 10(5) HAMBI 1207 cells per g before G. orientalis was sown. Seeds of G. orientalis were surface inoculated with 2 x 10(4) and 2 x 10(5) cells of HAMBI 1174 per seed (which represent half and fivefold the commercially recommended amount of inoculant, respectively). Plant yield and nodulation by the effective strain were significantly reduced, with as few as 10(2) ineffective rhizobia per g of soil, and the inoculation response was not improved by the 10-fold greater dose of the inoculant. Bacteria occupying the nodules were identified by antibiotic resistance and PCR with primers specific for R. galegae HAMBI 1174, R. galegae, and genes coding for bacterial 16S rRNA (bacterial 16S rDNA). Sixty-two large nodules examined were occupied by the effective strain HAMBI 1174, as proven by antibiotic resistance and amplification of the strain-specific fragment. From 20 small nodules, only the species-specific fragment could be amplified, and isolated bacteria had the same antibiotic resistance and 16S PCR restriction pattern as strain HAMBI 1207. PCR with our strain-specific and species-specific primers provides a powerful tool for strain identification of R. galegae directly from nodules without genetic modification of the bacteria.
机译:根据植物生长,结瘤,抗生素抗性和PCR结果,研究了根瘤菌侧根瘤有效和无效的根瘤菌菌株之间的竞争。在伦纳德的广口瓶中进行的初步实验中,无效的R. galegae菌株HAMBI 1207和HAMBI 1209与有效的R. galegae HAMBI 1174菌株竞争。在盆栽实验中,土壤中接种了0至10(5)HAMBI 1207细胞每克播种前每克。每只种子表面接种2 x 10(4)和2 x 10(5)HAMBI 1174细胞(分别代表商业推荐量的接种量的一半和五倍),以接种G.orientis种子。有效菌株的植物产量和根瘤形成显着降低,每克土壤少有10(2)根瘤菌无效菌,接种量增加10倍后接种反应不会得到改善。通过抗生素抗性和PCR鉴定占据细菌结节的细菌,该引物对R.galegae HAMBI 1174,R.galegae和编码细菌16S rRNA(细菌16S rDNA)的基因具有特异性。抗菌素耐药性和菌株特异性片段的扩增证明,有效菌株HAMBI 1174占据了检查的六十二个大结节。从20个小结节中,只能扩增出物种特异性片段,并且分离出的细菌具有与HAMBI 1207菌株相同的抗生素抗性和16S PCR限制模式。使用我们的菌株特异性和物种特异性引物进行PCR可为菌株提供强大的工具无需对细菌进行基因修饰即可直接从结核中鉴定出半乳糖丙型杆菌。

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