首页> 外文期刊>Antonie van Leeuwenhoek: Journal of Microbiology and serology >Rapid detection and identification of the free-living nitrogen fixing genus Azospirillum by 16S rRNA-gene-targeted genus-specific primers.
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Rapid detection and identification of the free-living nitrogen fixing genus Azospirillum by 16S rRNA-gene-targeted genus-specific primers.

机译:通过16S rRNA基因靶向的属特异性引物快速检测和鉴定自生固氮菌属螺旋藻属。

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摘要

The modern agricultural practice utilizing plant growth promoting rhizobacteria (PGPR) has brought great benefits in the promotion of crop growth. Among PGPR, Azospirillum is considered as an important genus which is not only closely-associated with plants but also shows potential in the degradation of organic contaminants. However, lack of media for selective isolation or techniques for specific detection or identification limit the exploration of these rhizobacteria. This motivated us to design a genus-specific oligonucleotide primer pair which could assist in rapid detection of species of the genus Azospirillum by means of PCR-specific amplification. The sensitivity and specificity of the newly designed primer pair Azo494-F/Azo756-R were tested against 12 Azospirillum type strains and other closely-related genera. The Azospirillum-specific 16S rRNA gene fragment (263 bp) was successfully amplified for all the reference Azospirillum species with the designed primer pair. No amplification was noted for closely-related species from other genera. The genus specificity was validated with 18 strains including environmental isolates. Interestingly, two strains assigned earlier as Azospirillum amazonense (DSM 2787(T)) and Azospirillum irakense (DSM 11586(T)) failed to produce an Azospirillum-specific fragment with this primer pair. Further phylogenetic analysis of these two isolates based on 16S rRNA gene sequences shows that these two strains might belong to other genera rather than Azospirillum. Preliminary screening of isolates and soil samples with the Azospirillum-specific primers was successful in terms of the rapid detection of Azospirillum isolates. By using real-time PCR analysis the minimum limit of Azospirillum detection was 10(2) CFU g(-1) in the seeded soil sample. The newly designed primers can be used to study the diversity of Azospirillum in ecosystems and aid in the exploration of novel species.
机译:利用促进植物生长的根际细菌(PGPR)的现代农业实践在促进作物生长方面带来了巨大的好处。在PGPR中,固氮螺菌被认为是重要的属,不仅与植物紧密相关,而且在降解有机污染物方面显示出潜力。然而,缺乏用于选择性分离的培养基或用于特异性检测或鉴定的技术限制了对这些根瘤菌的探索。这促使我们设计属特异的寡核苷酸引物对,该引物对可通过PCR特异性扩增来帮助快速检测偶氮螺旋菌属的物种。测试了新设计的引物对Azo494-F / Azo756-R对12种偶氮螺旋菌菌株和其他密切相关属的敏感性和特异性。使用设计的引物对,成功扩增了所有参照拟螺菌属物种的拟螺菌特异性16S rRNA基因片段(263 bp)。没有发现来自其他属的密切相关物种的扩增。用包括环境分离物的18个菌株验证了属特异性。有趣的是,先前被指定为亚马逊细螺旋体(DSM 2787(T))和伊拉克奇细螺旋体(DSM 11586(T))的两个菌株均无法通过该引物对产生细螺旋体特异性片段。基于16S rRNA基因序列对这两个分离株的进一步系统进化分析表明,这两个菌株可能属于其他属而不是固氮螺菌属。就Azospirillum分离物的快速检测而言,使用Azospirillum特异性引物进行的分离物和土壤样品的初步筛选是成功的。通过使用实时PCR分析,播种土壤样品中偶氮螺旋菌的最低检测限为10(2)CFU g(-1)。新设计的引物可用于研究生态系统中固氮螺菌的多样性,并有助于探索新物种。

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