Srimathi M, Suganthi M, Sugitha S, Ashok Kumar K, Ramprasath C, Abirami G
Department of Biotechnology, School of Life Sciences, Vels Institute of Science Technology and Advanced Studies, Pallavaram, Chennai, Tamil Nadu India.
Eukpro Biotech Private Limited, Chrompet, Chennai, Tamil Nadu India.
Indian J Microbiol. 2024 Dec;64(4):1697-1709. doi: 10.1007/s12088-024-01222-9. Epub 2024 Mar 7.
The spillage of petroleum hydrocarbons, one of the most versatile energy resources, leads to disastrous environmental pollution. The present study aims to degrade oil using enzymes from bacterial strains. A total of 39 bacteria were isolated from six different soil samples collected from Ullal Beach, Mangalore, Karnataka, located at 12°52'N latitude and 74°49'E longitude, India. All 39 bacterial isolates were screened for the production of four industrially important extracellular enzymes. Among these isolates, ten showed the highest lipase production. These cultures were further screened for bio-surfactant assays, including oil displacement and drop collapse assay and Emulsification Index. EBPL0613-F2 exhibited the best reaction in crude oil degradation. A polyphasic taxonomical approach identified the crude oil-degrading bacterium EBPL0613-F2 as and submitted in NCBI and the Accession Number is PP059616. It was then cultivated in ocean water media with tween 20 and 1% crude oil as the sole carbon and energy source. The strain was screened for lipase quantitative and qualitative assay and the protein content was also estimated. The identified bacterial strain EBPL0613-F2 demonstrated moderate lipase activity, with 76 U/ml and 24 U/ml, respectively, after 48-72 h of incubation in the crude oil substrate. For Tween 20 substrates, it exhibited 36 U/ml and 34 U/ml, respectively. FTIR analysis was used to examine the properties of crude oil following the biodegradation. The results suggest that, EBPL0613-F2 recorded the highest degradation rate so this culture has the potential for use in the degradation of crude oil in a greener manner.
石油碳氢化合物作为用途最为广泛的能源资源之一,其泄漏会导致灾难性的环境污染。本研究旨在利用细菌菌株中的酶来降解石油。从印度卡纳塔克邦芒格洛尔的乌拉尔海滩采集了六个不同的土壤样本,共分离出39株细菌,该海滩位于北纬12°52′、东经74°49′。对所有39株细菌分离物进行了四种工业上重要的胞外酶产生情况的筛选。在这些分离物中,有十株显示出最高的脂肪酶产量。对这些培养物进一步进行生物表面活性剂测定筛选,包括油置换和液滴塌陷测定以及乳化指数测定。EBPL0613 - F2在原油降解方面表现出最佳反应。采用多相分类方法将原油降解细菌EBPL0613 - F2鉴定为[具体菌种名称未给出],并提交至NCBI,登录号为PP059616。然后将其在含有吐温20和1%原油作为唯一碳源和能源的海水培养基中培养。对该菌株进行脂肪酶定量和定性测定筛选,并对蛋白质含量进行了估算。经鉴定的细菌菌株EBPL0613 - F2在原油底物中培养48 - 72小时后,分别表现出中等的脂肪酶活性,为76 U/ml和24 U/ml。对于吐温20底物,其分别表现出36 U/ml和34 U/ml。采用傅里叶变换红外光谱(FTIR)分析来检测生物降解后原油的性质。结果表明,EBPL0613 - F2的降解率最高,因此该培养物具有以更环保方式用于降解原油的潜力。