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Isolation, identification and characterization of dehalogenase producing bacteria isolated from Labeo Rohita and its environment

机译:分离自Labeo Rohita及其环境的产脱卤素酶的细菌的鉴定,表征

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摘要

Microbial dehalogenases are involved in the biodegradation of many types of halogenated compounds. The presence of halogenated compounds in water does not only suppress the immune system of fish but adversely induces serious morbidity and mortality among cultured stocks. In this study, we attempted to screen the gut of pond-reared rohu (Labeo rohita) for isolating dehalogenase gene bacteria using molecular technique and tested the degradation ability in vitro. The present study shows eight bacterial strains studied were identified as Enterobacter mori (MK121001), Enterobacter cloacae (MK121003), Enterobacter cloacae (MK121004), Enterobacter cloacae (MK121010), Ralstonia solanacearum (121002), Acinetobacter baumannii (MK121007), Chromobacterium violaceum (MK121009) and Pantoea vagans (121011). Further analysis found three bacterial strains (MK121002, MK121007 and MK121009) were capable of degrading 2,2- dichloropropionic acid (2,2-DCP) as the sole carbon source up to a final substrate concentration of 20 mM. Their mean growth doubling time ranging from 6-23 h with the maximum of chloride ion released of 85%. Another bacterium was isolated from soil samples collected from lake water at Universiti Teknologi Malaysia, Skudai also capable of degrading 2,2-DCP. Phylogenetic analysis indicated that Serratia marcescens SE1 strain clearly shared 97% homology to the genus of Serratia marcescens according to bioinformatics analysis. Serratia marcescens has the ability to degrade 2,2-DCP with cells doubling time of 5 h and maximum chloride ion released of 38 µmolCl-/mL in the liquid growth medium.
机译:微生物脱卤酶参与许多类型卤代化合物的生物降解。水中卤代化合物的存在不仅会抑制鱼类的免疫系统,还会不利地引起养殖种群的严重发病和死亡。在这项研究中,我们尝试使用分子技术筛选池塘养殖的芜湖(Labeo rohita)的肠道以分离脱卤酶基因细菌,并测试其体外降解能力。本研究表明,已研究的八种细菌菌株分别为桑蚕肠杆菌(MK121001),阴沟肠杆菌(MK121003),阴沟肠杆菌(MK121004),阴沟肠杆菌(MK121010),青枯雷尔氏菌(121002),鲍曼不动杆菌(MK121007),绿杆菌MK121009)和Pantoea vagans(121011)。进一步分析发现,三种细菌菌株(MK121002,MK121007和MK121009)能够降解2,2-二氯丙酸(2,2-DCP)作为唯一的碳源,最终底物浓度达到20 mM。它们的平均生长倍增时间为6-23小时,最大释放的氯离子为85%。从马来西亚Skudai Teknologi大学的湖水中收集的土壤样品中分离出另一种细菌,该细菌也能够降解2,2-DCP。系统进化分析表明,根据生物信息学分析,粘质沙雷氏菌SE1菌株与粘质沙雷氏菌属具有97%的同源性。粘质沙雷氏菌具有降解2,2-DCP的能力,细胞在液体生长培养基中的倍增时间为5小时,释放的最大氯离子为38 µmolCl- / mL。

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