{"title":"Utilisation of 2,2DCP by Staphyloccocus aureus ZT and In Silico Analysis of Putative Dehalogenase","authors":"Zatty Zawani Zaidi, F. Huyop","doi":"10.15294/BIOSAINTIFIKA.V13I1.26322","DOIUrl":null,"url":null,"abstract":"Halogenated compound such as 2,2-dichloropropionic acid is known for its toxicity and polluted many areas especially with agricultural activities. This study focused on the isolation and characterization of the bacterium that can utilise 2,2-dichloropropionic acid from palm oil plantation in Lenga, Johor and in silico analysis of putative dehalogenase obtained from NCBI database of the same genus and species. The bacterium was isolated using an enrichment culture media supplemented with 20 mM 2,2-dicholoropropionic acid as a carbon source. The cells were grown at 30˚C with cells doubling time of 2.00±0.005 hours with the maximum growth at A680nm of 1.047 overnight. The partial biochemical tests and morphological examination concluded that the bacterium belongs to the genus Staphylococcus sp.. This is the first reported studies of  Staphylococcus sp. with the ability to grow on 2,2-dichloropropionic acid. The genomic DNA from NCBI database of the same species was analysed assuming the same genus and has identical genomic sequence. The full genome of Staphylococcus sp. was screened for dehalogenase gene and  haloacid dehalogenase gene was detected in the mobile genetic element of the species revealed that the dehalogenase sequence has little identities to the previously reported dehalogenases.The main outcome of the studies suggesting an in situ bioremediation can be regarded as a natural process to detoxify the contaminated sites provided that the microorganisms contained a specialised gene sequence within its genome that served the nature for many long years. Whether microorganisms will be successful in destroying man-made contaminants entirely rely on what types of organisms play a role in in situ bioremediation and which contaminants are most susceptible to bioremediation. ","PeriodicalId":30622,"journal":{"name":"Biosaintifika Journal of Biology Biology Education","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biosaintifika Journal of Biology Biology Education","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15294/BIOSAINTIFIKA.V13I1.26322","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Halogenated compound such as 2,2-dichloropropionic acid is known for its toxicity and polluted many areas especially with agricultural activities. This study focused on the isolation and characterization of the bacterium that can utilise 2,2-dichloropropionic acid from palm oil plantation in Lenga, Johor and in silico analysis of putative dehalogenase obtained from NCBI database of the same genus and species. The bacterium was isolated using an enrichment culture media supplemented with 20 mM 2,2-dicholoropropionic acid as a carbon source. The cells were grown at 30ËšC with cells doubling time of 2.00±0.005 hours with the maximum growth at A680nm of 1.047 overnight. The partial biochemical tests and morphological examination concluded that the bacterium belongs to the genus Staphylococcus sp.. This is the first reported studies of  Staphylococcus sp. with the ability to grow on 2,2-dichloropropionic acid. The genomic DNA from NCBI database of the same species was analysed assuming the same genus and has identical genomic sequence. The full genome of Staphylococcus sp. was screened for dehalogenase gene and  haloacid dehalogenase gene was detected in the mobile genetic element of the species revealed that the dehalogenase sequence has little identities to the previously reported dehalogenases.The main outcome of the studies suggesting an in situ bioremediation can be regarded as a natural process to detoxify the contaminated sites provided that the microorganisms contained a specialised gene sequence within its genome that served the nature for many long years. Whether microorganisms will be successful in destroying man-made contaminants entirely rely on what types of organisms play a role in in situ bioremediation and which contaminants are most susceptible to bioremediation.Â
卤代化合物如2,2-二氯丙酸因其毒性而闻名,并污染了许多地区,特别是农业活动。本研究的重点是分离和鉴定可以利用柔佛州Lenga棕榈油种植园中的2,2-二氯丙酸的细菌,并对从NCBI数据库中获得的同一属和物种的推定脱卤酶进行了硅分析。采用添加20 mM 2,2-二氯丙酸作为碳源的富集培养基分离细菌。Â细胞在30ËšC处生长,细胞倍增时间为2.00±0.005 h,在A680nm处的最大生长时间为1.047过夜。经部分生化试验和形态学检查,该细菌属于葡萄球菌属。这是首次报道研究Â葡萄球菌具有在2,2-二氯丙酸上生长的能力。对NCBI数据库中同一物种的基因组DNA进行分析,假设其属相同且基因组序列相同。Â对葡萄球菌进行全基因组脱卤酶基因筛选,Â在该物种的移动遗传元件中检测到卤酸脱卤酶基因,结果表明该脱卤酶序列与之前报道的脱卤酶几乎没有同源性。这些研究的主要结果表明,就地生物修复可以被视为一种自然过程,以解毒受污染的地点,前提是微生物在其基因组中包含一个专门的基因序列,该序列可以为自然服务多年。微生物是否能够成功地完全摧毁人造污染物取决于在原位生物修复中发挥作用的生物类型以及哪些污染物最容易受到bioremediation.Â的影响