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Impact of the maize rhizosphere on the genetic structure, the diversity and the atrazine-degrading gene composition of cultivable atrazine-degrading communities.

机译:玉米根际对可培养阿特拉津降解菌群的遗传结构,多样性和阿特拉津降解基因组成的影响。

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Sixty-six atrazine-degrading bacterial communities utilizing atrazine as sole N source and citrate as principal C source were isolated from unplanted and maize planted soils treated with atrazine. Ribosomal intergenic spacer analysis (RISA) fingerprints revealed that the genetic structure of atrazine-degrading bacterial communities was modified in the maize rhizosphere. To assess the underlying microbial diversity, 16S rDNA sequences amplified from each bacterial community were cloned. Libraries containing 660 16S rDNA clones were screened by restriction fragment length polymorphism (RFLP) analysis. In all, 63 clone families were identified. Rarefaction curves did not reach a clear saturation, indicating that the analysis of a greater number of clones would have revealed further diversity. Recovered 16S rDNA sequences were related to Actinobacteria, Bacteroidetes and Proteobacteria. The four dominant RFLP families were highly similar to Variovorax paradoxus, Burkholderia cepacia, Arthrobacter sp. and Bosea sp. The composition of most of the atrazine-degrading bacterial communities consisted of 2-7 different bacterial species. Various atrazine-degrading gene compositions were observed, two of these atzABCDEF, trzND and atzBCDEF, trzN being largely dominant. The first was more frequently detected in bacterial communities isolated from the maize rhizosphere whereas the second was more frequently detected in communities isolated from bulk soil. Monitoring of atrazine-degrading activity showed that 76% of the bacterial communities degraded up to 80% of the initially added atrazine within 15 days of culture. Altogether our results indicate that the maize rhizosphere has an impact on the genetic structure, the diversity and atrazine-degrading gene composition of the atrazine-degrading communities..
机译:从以阿特拉津处理的未种植和玉米种植的土壤中分离出了以阿特拉津为唯一氮源和柠檬酸为主要C源的66个降解阿特拉津的细菌群落。核糖体间基因间隔分析(RISA)指纹显示,玉米根际中阿特拉津降解细菌群落的遗传结构已被修饰。为了评估潜在的微生物多样性,克隆了从每个细菌群落扩增的16S rDNA序列。通过限制性片段长度多态性(RFLP)分析筛选了包含660个16S rDNA克隆的文库。总共鉴定出63个克隆家族。反射曲线没有达到明显的饱和度,表明对大量克隆的分析将揭示出进一步的多样性。恢复的16S rDNA序列与放线菌,拟杆菌和变形杆菌有关。四个主要的RFLP家族与Variovorax paradoxus,洋葱伯克霍尔德菌,节杆菌属高度相似。和Bosea sp。大多数降解阿特拉津的细菌群落的组成由2-7种不同的细菌组成。观察到各种降解阿特拉津的基因组成,其中两个atzABCDEF,trzND和atzBCDEF,trzN在很大程度上占优势。第一个在从玉米根际分离的细菌群落中被更频繁地检测到,而第二个在从散装土壤分离的群落中被更频繁地检测到。对of去津降解活性的监测表明,在培养的15天之内,有76%的细菌群落降解了最初添加的at去津中的80%。总之,我们的结果表明玉米根际对阿特拉津降解菌群的遗传结构,多样性和阿特拉津降解基因的组成有影响。

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