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Profiling of heavy metal(loid)-resistant bacterial community structure by metagenomic-DNA fingerprinting using PCR–DGGE for monitoring and bioremediation of contaminated environment

机译:分析重金属(根)防细菌社区结构metagenomic-DNA使用PCR-DGGE监测和指纹污染环境的生物修复

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Abstract Frequent exposure of microbes to hazardous metalloids/heavy metals in contaminated environment results in the development of heavy metal(loid)-resistance properties. The study attempted to assess the profile of elevated arsenic (As), cadmium (Cd) and mercury (Hg)—resistant bacterial community structures of sludge (S1, India), sludge and sediment (S2 and S3, Japan) and sediment (S4, Vietnam) samples by metagenomic-DNA fingerprinting using polymerase chain reaction-denaturing gradient gel electrophoresis ( PCR–DGGE) for monitoring and bioremediation of hazardous metal(loid) contamination in environment. The results revealed that As-resistant bacteria were dominant compared to Cd- and Hg-resistant bacteria with higher species diversity ( Lysinibacillus sp., Uncultured soil bacterium clone, Staphylococcus sciuri , Bacillus fastidiosus , Bacillus niacini , Clostridium sp. and Bacillus sp.) in S1 and S4 than that of S2 and S3 samples. The occurrence of dominant As-resistant bacteria may indicate arsenic contamination in the investigated coastal habitats of India, Japan and Vietnam. The As-, Cd- and Hg-resistant bacteria/bacterial consortiums showed appreciable uptake ability of respective metal(loid) (0.042–0.125 mg As/l, 0.696–0.726 mg Cd/l and 0.34–0.412 mg Hg/l). Therefore, it might be concluded that the profiling of metalloids/heavy metal-resistant bacterial community structure by metagenomic-DNA fingerprinting using PCR–DGGE could be used to explore high metal(loid)-resistant bacteria for applying in metal(loid) bioremediation and as an indicator for monitoring hazardous metal(loid) contamination in environment.
机译:抽象的频繁接触的微生物危险的准金属/重金属污染环境发展的结果重金属(根)为属性。试图评估高架的概要文件砷(As)、镉(Cd)和水星(Hg)防细菌社区结构污泥(S1、印度),污泥和沉积物(S2和S3、日本)和沉积物(S4、越南)样品metagenomic-DNA指纹使用聚合酶链reaction-denaturing梯度凝胶为监控和电泳(PCR-DGGE)生物修复的有害金属(根)污染环境。显示与顽固性细菌占主导地位Cd相比,Hg-resistant细菌更高的物种多样性(Lysinibacillus sp。未耕作的土壤细菌克隆,葡萄球菌sciuri, fastidiosus, niacini杆菌芽孢杆菌、sp.梭状芽胞杆菌和芽孢杆菌sp)在S1和S4比S2和S3样本。主导与顽固性细菌可能表明砷污染的调查沿海栖息地的印度、日本和越南。Cd -和Hg-resistant细菌/细菌财团显示明显的吸收能力各自的金属(根)(0.042 - -0.125 mg / l,0.696 - -0.726毫克Cd / l和0.34 - -0.412毫克Hg / l)。因此,它可能会得出结论,分析准金属/重型耐金属由metagenomic-DNA细菌群落结构使用PCR-DGGE可以用于指纹探索高防金属(根)细菌应用在金属(根)生物修复和作为指标监测有害金属(根)污染环境。

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