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Quantification of Azospirillum brasilense FP2 Bacteria in Wheat Roots by Strain-Specific Quantitative PCR

机译:通过菌株特异性定量PCR定量测定小麦根中的巴西固氮螺旋菌FP2细菌

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摘要

Azospirillum is a rhizobacterial genus containing plant growth-promoting species associated with different crops worldwide. Azospirillum brasilense strains exhibit a growth-promoting effect by means of phytohormone production and possibly by N2 fixation. However, one of the most important factors for achieving an increase in crop yield by plant growth-promoting rhizobacteria is the survival of the inoculant in the rhizosphere, which is not always achieved. The objective of this study was to develop quantitative PCR protocols for the strain-specific quantification of A. brasilense FP2. A novel approach was applied to identify strain-specific DNA sequences based on a comparison of the genomic sequences within the same species. The draft genome sequences of A. brasilense FP2 and Sp245 were aligned, and FP2-specific regions were filtered and checked for other possible matches in public databases. Strain-specific regions were then selected to design and evaluate strain-specific primer pairs. The primer pairs AzoR2.1, AzoR2.2, AzoR5.1, AzoR5.2, and AzoR5.3 were specific for the A. brasilense FP2 strain. These primer pairs were used to monitor quantitatively the population of A. brasilense in wheat roots under sterile and nonsterile growth conditions. In addition, coinoculations with other plant growth-promoting bacteria in wheat were performed under nonsterile conditions. The results showed that A. brasilense FP2 inoculated into wheat roots is highly competitive and achieves high cell numbers (∼107 CFU/g [fresh weight] of root) in the rhizosphere even under nonsterile conditions and when coinoculated with other rhizobacteria, maintaining the population at rather stable levels for at least up to 13 days after inoculation. The strategy used here can be applied to other organisms whose genome sequences are available.
机译:固氮螺菌属(Azospirillum)是根瘤菌属,其包含与全世界不同作物相关的促进植物生长的物种。巴西固氮螺菌菌株通过植物激素的产生并可能通过N 2固定表现出促进生长的作用。但是,通过促进植物生长的根际细菌实现作物增产的最重要因素之一是接种剂在根际中的存活,但并非总是如此。这项研究的目的是开发定量PCR方案,用于巴西乳杆菌FP2的菌株特异性定量。基于对同一物种内基因组序列的比较,一种新颖的方法被用于鉴定菌株特异性DNA序列。将巴西拟南芥FP2和Sp245的基因组草图序列进行比对,并过滤FP2特定区域,并在公共数据库中检查其他可能的匹配。然后选择菌株特异性区域来设计和评估菌株特异性引物对。引物对AzoR2.1,AzoR2.2,AzoR5.1,AzoR5.2和AzoR5.3对巴西拟南芥FP2菌株具有特异性。这些引物对用于在无菌和非无菌生长条件下定量监测小麦根中巴西农杆菌的种群。此外,在非无菌条件下与小麦中其他促进植物生长的细菌共接种。结果表明,即使在非无菌条件下和在不育时,接种到小麦根中的巴西根茎FP2竞争性很高,在根际中获得高细胞数(约10 7 CFU / g [鲜重]根)。与其他根瘤菌同时接种,在接种后至少13天之内将种群维持在相当稳定的水平。此处使用的策略可以应用于其基因组序列可用的其他生物。

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