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首页> 外文期刊>Biocontrol Science and Technology >Fate and behaviour of a seed-applied Pseudomonas brassicacearum strain in a winter wheat field trial, as determined by analysis with SCAR markers.
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Fate and behaviour of a seed-applied Pseudomonas brassicacearum strain in a winter wheat field trial, as determined by analysis with SCAR markers.

机译:通过使用SCAR标记进行分析,确定了在冬小麦田间试验中,种子施药的黄铜假单胞菌菌株的命运和行为。

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摘要

The fate and behaviour of the seed-applied biocontrol strain Pseudomonas brassicacearum MA250 in a field trial with winter wheat was determined using sequence-characterised amplified region (SCAR) markers. Samples of belowground plant parts from healthy and withered (due to snow mould infection) seedlings were collected approximately one and seven months after sowing, which was performed in early autumn. DNA was extracted from roots and remaining parts of seeds with adhering soil, and the abundance of the strain was determined in quantitative real-time PCR (qPCR) assays. The results show that the introduced strain persisted over the whole trial-period of seven months. On termination of the trial (after seven months) the belowground plant parts of each plant housed 106-107 cells, substantially less than the original approximately 109 cells inoculated onto the seed. In healthy seedlings, there was a shift in cell numbers from seeds to roots between the samplings, suggesting colonisation of the roots during this time. The results show that with sufficient attention given to analytical control measures and the possibility of resident background populations, SCAR markers in combination with qPCR provide valuable information regarding the fate and behaviour of biocontrol micro-organisms under field conditions.
机译:使用序列特征扩增区(SCAR)标记确定了在冬小麦田间试验中,种子施用的生防控菌株黄铜假单胞菌MA250的命运和行为。播种后大约一个月和七个月,从健康和枯萎(由于雪霉菌感染)的幼苗中收集地下植物部分的样品,该过程在初秋进行。从附着土壤的种子的根部和剩余部分中提取DNA,并通过定量实时PCR(qPCR)分析确定菌株的丰度。结果表明,引入的菌株在七个月的整个试验期内均持续存在。试验结束后(七个月后),每棵植物的地下植物部分容纳106-107个细胞,大大少于接种到种子上的原始大约109个细胞。在健康的幼苗中,两次采样之间的细胞数量从种子转移到了根,这表明在此期间根的定殖。结果表明,在充分关注分析控制措施和居民背景种群的可能性的情况下,SCAR标记与qPCR结合可提供有关田间条件下生物防治微生物的命运和行为的有价值的信息。

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