科威特石油污染土壤中多环芳烃(PAHs)降解菌伯克霍尔德氏菌P14的分子特征

Q2 Agricultural and Biological Sciences
A. Akbar, Rita Rahmeh, Mohamad Kishk, Batool Akbar, Mustafa Al-Shamali, D. Al-Baijan
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引用次数: 0

摘要

多环芳烃(PAHs)和重金属污染是影响土壤质量的主要问题。生物修复是一种净化这些污染物的有效方法,同时对环境构成的风险最低。该技术的基础是识别具有降解污染物代谢潜力的微生物。研究了科威特石油污染土壤的理化性质。土壤为碱性pH(8.36),盐度为0.08%,多环芳烃含量较高(芘1212 mg/kg)、菲710 mg/kg和芴326 mg/kg)。土壤样品中还检测到铁、铝、钠、镁、钒、铜等重金属。然后,通过菌落形成单位(colony forming units, CFU)和16S rDNA基因序列对多环芳烃降解物进行选择性筛选,确定其生长特征和分类鉴定。共筛选出21株耐多环芳烃菌株,包括假单胞菌(9株)、伯克霍尔德菌(6株)、芽孢杆菌(2株)、博德氏菌(1株)、微细菌(1株)、微球菌(1株)和科库利亚菌(1株)。其中,伯克霍尔德菌sp. P14在存在菲和芴的情况下,在第5 ~ 8天保持稳定生长,菌数为6 log CFU/ml。污染伯克霍尔德菌P14菌株的基因组草图包含68个contigs, 8,584,157bp, GC含量66%,4个rRNA和75个tRNA。共有80个基因参与了苯甲酯、萘和多环芳烃的降解。编码多环芳烃降解的基因被分成四个不同的组,包括pcaHG、pcaB、pcaIJ和pcaKFR,分别存在于污染芽孢杆菌P14的第5、11、8和13组中。KEGG分析表明P14中的多环芳烃通过β-酮己酸原儿茶酸降解途径的原儿茶酸和儿茶酚分支降解。P14的基因组岛区与参考基因组M14的基因组岛区不同,表明该菌株具有新颖性和基因组重组性。P14的基因组信息有助于阐明参与多环芳烃分解代谢的分子机制。污染伯克霍尔德菌P14菌株对油污染土壤的生物修复有促进作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular characterization of a polycyclic aromatic hydrocarbons (PAHs) degrader, Burkholderia contaminans strain P14, isolated from aged oil-contaminated soil in Kuwait
Soil contamination by polycyclic aromatic hydrocarbons (PAHs) and heavy metals is a major concern affecting soil quality. Bioremediation is an efficient approach to decontaminate these pollutants while posing the lowest risk to the environment. This technique is based on identifying microorganisms with the metabolic potential to degrade the pollutants. In this study, the physiochemical properties of oil-contaminated soils in Kuwait were investigated. The soil had alkaline pH (8.36) with a salinity of 0.08% and PAHs compounds were detected at high concentrations (pyrene, 1212 mg/kg), (phenanthrene, 710 mg/kg) and (fluorene 326 mg/kg). Heavy metals such as iron, aluminum, sodium, magnesium, vanadium, copper, etc., were also detected in the soil samples. Then, selective screening for PAH degraders was performed and assessed by colony forming units (CFU) and 16S rDNA gene sequences to determine their growth profiles and taxonomical identification. In total, 21 strains were selected for their resistance to PAHs, which include Pseudomonas (9), Burkholderia (6), Bacillus (2), Bordetella (1), Microbacterium (1), Micrococcus (1), and Kocuria (1). Among all, the growth by Burkholderia sp. P14, in the presence of phenanthrene and fluorene, has maintained a stationary phase from day 5 to 8 with a 6 log CFU/ml bacterial count. The draft genome of the Burkholderia contaminans P14 strain comprised 68 contigs with 8,584,157bp, 66% GC content, 4 rRNA and 75 tRNA. A total of 80 genes were involved in the degradation of the benzoate, naphthalene, and PAH . Genes that encode the PAH degradation were clustered into four distinct groups, including pcaHG, pcaB, pcaIJ, and pcaKFR and were found to be in contigs 5, 11, 8 and 13 of B. contaminans P14, respectively. KEGG analysis suggested that PAHs were degraded in P14 via the protocatechuate and catechol branches of the β-ketoadipate protocatechuate degradation pathway. The genomic island regions in P14 differed from those in the reference genome of B. contaminans M14, indicating the novelty and genomic recombination of the strain. Genomic information on P14 has helped clarify the molecular mechanisms involved in PAH catabolism. Burkholderia contaminans P14 strain will enhance the bioremediation of oil-contaminated soils.
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来源期刊
Applied Environmental Biotechnology
Applied Environmental Biotechnology Agricultural and Biological Sciences-Agricultural and Biological Sciences (miscellaneous)
CiteScore
3.70
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0.00%
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2
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