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Detection of polychlorinated biphenyl-degrading bacteria in soil

机译:土壤中多氯联苯降解菌的检测

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This work is based on research which focuses on the study of the possible mutual relationship of microorganisms and plants in PCB metabolism. Three different plant species - Nicotiana tabacum (tobacco), Solanum nigrum (black nightshade) and Medicago sativa (alfalfa) - were cultivated in real soil from an industrial site. After six months the decrease of PCB content in soil and the PCB accumulation in plant tissue was analysed. The highest decrease of PCB concentration was measured from the soil vegetated with tobacco. From this polluted soil, bacteria which potentially participate in the biodegradation of PCBs were isolated and were screened for the presence of bphA1 and bphC genes. These genes are a part of the bph operon, which is very important for PCB degradation. The PCR primers were designed for conserved regions of bphA1 and bphC genes from an alignment of previously published sequences. The degradative capabilities of the isolates were confirmed by growing in the presence of biphenyl as a cosubstrate. For the extraction of DNA directly from soil a commercial DNA purification kit and a laboratory-devised method based on mechanical lysis were used.
机译:这项工作是基于研究的,该研究的重点是研究PCB代谢中微生物与植物之间可能的相互关系。在工业区的真实土壤中种植了三种不同的植物品种:烟草(烟草),茄子(黑色茄子)和紫花苜蓿(苜蓿)。六个月后,分析土壤中PCB含量的减少和植物组织中PCB的积累。从烟草种植的土壤中测出的PCB浓度下降幅度最大。从这种污染的土壤中,分离出可能参与多氯联苯生物降解的细菌,并筛选是否存在bphA1和bphC基因。这些基因是bph操纵子的一部分,对PCB降解非常重要。从先前公布的序列的比对,设计PCR引物用于bphA1和bphC基因的保守区。分离物的降解能力通过在联苯作为共底物的存在下生长得到证实。为了直接从土壤中提取DNA,使用了商业DNA纯化套件和基于机械裂解的实验室设计方法。

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