首页> 外文期刊>International Journal of Microbiology and Biotechnology >Phenotypic and Molecular Screening of Laccase-producing Bacteria Isolated from Automobile Workshop Soil Samples in Ado-Ekiti
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Phenotypic and Molecular Screening of Laccase-producing Bacteria Isolated from Automobile Workshop Soil Samples in Ado-Ekiti

机译:从Ado-Ekiti汽车车间土壤样品中分离的漆酶生产细菌的表型和分子筛选

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This work was carried out to isolate hydrocarbon-degrading bacteria from oil contaminated soil sample in Ado-Ekiti and screen them for laccase production. Soil samples were collected and analyzed using standard microbiological techniques. The isolates were initially screened for hydrocarbon degrading ability on minimal salt medium supplemented with 1% crude oil and incubated for 14days. The isolates were further screened for their ability to produce laccase enzyme using plate screening and molecular techniques. Four of the isolates that gave the best results on tannic-agar plates were selected for PCR amplification of laccase gene using specific primers. The isolates were identified as Lactobacillus sakei, Pseudomonas aeruginosa, Bacillus cereus and Gracilibacter thermotolerans based on 16SrRNA sequencing. The DNA of these bacteria amplified the primer specific for laccase gene with 1300bp, 1400bp, 1600bp and 350bp respectively. For bioremediation to be effective, microorganisms must enzymatically attack the pollutants and convert them to harmless products. Therefore, laccase production potentials in these bacteria make them useful in bioremediation as laccase is known to break heavy phenol containing hydrocarbons. Further work can be done to determine the activity of this enzyme during the degradation of crude oil.
机译:进行该工作以将碳氢化合物降解的细菌分离在Ado-Ekiti中的油污污染的土壤样品,并筛选它们进行漆酶生产。收集土壤样品并使用标准微生物技术进行分析。最初筛选分离物,用于烃基降解能力的最小盐培养基,其补充有1%原油并孵育14天。进一步筛选分离株,用于使用平板筛选和分子技术产生漆酶酶的能力。使用特异性引物选择给予鞣酸琼脂平板上最佳结果的4个分离物用于PCRAse基因的PCR扩增。将分离物鉴定为基于16SRNA测序的杆菌,芽孢杆菌,芽孢杆菌,芽孢杆菌和Gracilibacter Hotoroterans。这些细菌的DNA分别扩增了具有1300bp,1400bp,1600bp和350bp的漆酶基因的引物。对于生物修复有效,微生物必须酶促攻击污染物并将其转换为无害的产品。因此,这些细菌中的漆酶生产电位使它们在生物修复中有用,因为已知漆酶破坏含重对含烃的烃。可以进行进一步的工作以在原油降解过程中确定该酶的活性。

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