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首页> 外文期刊>Journal of Basic Microbiology: An International Journal on Morphology, Physiology, Genetics, and Ecology of Microorganisms >Bacterial community analysis of cypermethrin enrichment cultures and bioremediation of cypermethrin contaminated soils
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Bacterial community analysis of cypermethrin enrichment cultures and bioremediation of cypermethrin contaminated soils

机译:氯氰菊酯富集培养和氯氰菊酯污染土壤的生物修复的细菌群落分析。

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摘要

Cypermethrin is widely used for insect control; however, its toxicity toward aquatic life requires its complete removal from contaminated areas where the natural degradation ability of microbes can be utilized. Agricultural soil with extensive history of CM application was used to prepare enrichment cultures using cypermethrin as sole carbon source for isolation of cypermethrin degrading bacteria and bacterial community analysis using PCR-DGGE of 16S rRNA gene. DGGE analysis revealed that dominant members of CM enrichment culture were associated with -proteobacteria followed by -proteobacteria, Firmicutes, and Actinobacteria. Three potential CM-degrading isolates identified as Ochrobactrum anthropi JCm1, Bacillus megaterium JCm2, and Rhodococcus sp. JCm5 degraded 86-100% of CM (100mgL(-1)) within 10 days. These isolates were also able to degrade other pyrethroids, carbofuran, and cypermethrin degradation products. Enzyme activity assays revealed that enzymes involved in CM-degradation were inducible and showed activity when strains were grown on cypermethrin. Degradation kinetics of cypermethrin (200mgkg(-1)) in soils inoculated with isolates JCm1, JCm2, and JCm5 suggested time-dependent disappearance of cypermethrin with rate constants of 0.0516, 0.0425, and 0.0807d(-1), respectively, following first order rate kinetics. The isolated bacterial strains were among dominant genera selected under CM enriched conditions and represent valuable candidates for in situ bioremediation of contaminated soils and waters.
机译:氯氰菊酯被广泛用于昆虫防治。然而,其对水生生物的毒性要求将其从可利用微生物自然降解能力的受污染地区彻底清除。使用具有广泛CM应用历史的农业土壤,以氯氰菊酯为唯一碳源,制备富集培养物,以分离氯氰菊酯降解细菌,并使用16S rRNA基因PCR-DGGE进行细菌群落分析。 DGGE分析表明,CM富集培养的主要成员与-proteobacteria,-proteobacteria,Firmicutes和Actinobacteria相关。三个潜在的CM降解分离株被鉴定为人牙O JCm1,巨大芽孢杆菌JCm2和红球菌sp.。 JCm5在10天内降解了86-100%的CM(100mgL(-1))。这些分离物还能够降解其他拟除虫菊酯,呋喃丹和氯氰菊酯的降解产物。酶活性测定表明,与CM降解有关的酶是可诱导的,并且当菌株在氯氰菊酯上生长时显示出活性。氯氰菊酯(200mgkg(-1))在分离株JCm1,JCm2和JCm5接种的土壤中的降解动力学表明,氯氰菊酯的时间依赖性消失,速率常数分别为0.0516、0.0425和0.0807d(-1)。速率动力学。分离出的细菌菌株是在富含CM的条件下选择的优势菌种,它们代表着对污染土壤和水体进行原位生物修复的有价值的候选物。

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