首页> 外文期刊>Frontiers in Microbiology >Genomic and Physiological Traits of the Marine Bacterium Alcaligenes aquatilis QD168 Isolated From Quintero Bay, Central Chile, Reveal a Robust Adaptive Response to Environmental Stressors
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Genomic and Physiological Traits of the Marine Bacterium Alcaligenes aquatilis QD168 Isolated From Quintero Bay, Central Chile, Reveal a Robust Adaptive Response to Environmental Stressors

机译:从智利中部昆特罗湾分离的海洋细菌 alcaligenes aquatilis QD168的基因组和生理性状显示出对环境胁迫的强大适应性响应

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Alcaligenes aquatilis QD168 is a marine, aromatic hydrocarbon-degrading bacterium, isolated from an oil-polluted sediment of Quintero Bay, an industrial-coastal zone that has been chronically impacted by diverse pollutants. The aims of this study were to characterize the phylogenomic positions of Alcaligenes spp. and to characterize the genetic determinants and the physiological response of A. aquatilis QD168 to model environmental stressors (benzene, oxidizing agents, and salt). Phylogenomic analyses, using 35 housekeeping genes, clustered A. aquatilis QD168 with four other strains of Alcaligenes spp. ( A. aquatilis BU33N, A. faecalis JQ135, A. faecalis UBA3227, and A. faecalis UBA7629). Genomic sequence analyses of A. aquatilis QD168 with 25 Alcaligenes spp., using ANIb, indicated that A. aquatilis BU33N is the closest related strain, with 96.8% ANIb similarity. Strain QD168 harbors 95 genes encoding proteins of seven central catabolic pathways, as well as sixteen peripheral catabolic pathways/reactions for aromatic compounds. A. aquatilis QD168 was able to grow on 3-hydroxybenzoate, 4-hydroxybenzoate, benzoate, benzene, 3-hydroxycinnamate, cinnamate, anthranilate, benzamide, 4-aminobenzoate, nicotinate, toluene, biphenyl and tryptophan, as sole carbon or nitrogen source. Benzene degradation was further analyzed by growth, metabolite identification and gene expression analyses. Benzene strongly induced the expression of the genes encoding phenol hydroxylase ( dmpP ) and catechol 1,2-dioxygenase ( catA ). Additionally, 30 genes encoding transcriptional regulators, scavenging enzymes, oxidative damage repair systems and isozymes involved in oxidative stress response were identified. Oxidative stress response of strain QD168 to hydrogen peroxide and paraquat was characterized, demonstrating that A. aquatilis QD168 is notably more resistant to paraquat than to H _(2)O _(2). Genetic determinants (47 genes) for osmoprotective responses were identified, correlating with observed high halotolerance by strain QD168. The physiological adaptation of A. aquatilis QD168 to environmental stressors such as pollutants, oxidative stress and salinity may be exploited for bioremediation of oil-polluted saline sites.
机译:水生产碱杆菌QD168是一种海洋性芳香族烃降解细菌,从受工业污染的Quintero湾的油污沉积物中分离出来,该地区一直受到各种污染物的长期影响。这项研究的目的是表征产碱菌的种系的位置。并表征A. aquatilis QD168的遗传决定因素和生理反应,以模拟环境胁迫因子(苯,氧化剂和盐)。使用35个管家基因进行系统遗传学分析,将A. aquatilis QD168与其他4种Alcaligenes spp菌株聚在一起。 (A.aquatilis BU33N,A.faecalis JQ135,A.faecalis UBA3227和A.faecalis UBA7629)。使用ANIb对具有25种产碱菌的A. aquatilis QD168进行基因组序列分析,表明A. aquatilis BU33N是最接近的相关菌株,与96.8%ANIb相似。 QD168菌株包含95个基因,这些基因编码7个中央分解代谢途径的蛋白质,以及16个对芳香族化合物的周边分解代谢途径/反应。 A. aquatilis QD168能够在3-羟基苯甲酸酯,4-羟基苯甲酸酯,苯甲酸酯,苯,3-羟基肉桂酸酯,肉桂酸酯,邻氨基苯甲酸酯,苯甲酰胺,4-氨基苯甲酸酯,烟酸酯,甲苯,联苯和色氨酸上生长,作为唯一的碳或氮源。通过生长,代谢物鉴定和基因表达分析进一步分析苯的降解。苯强烈诱导了编码酚羟化酶(dmpP)和邻苯二酚1,2-二加氧酶(catA)的基因的表达。此外,鉴定了30种编码转录调节因子,清除酶,氧化损伤修复系统和氧化应激反应涉及的同工酶的基因。表征了菌株QD168对过氧化氢和百草枯的氧化应激响应,表明水产农杆菌QD168对百草枯的抵抗力明显强于对H _(2)O _(2)的抵抗力。鉴定了用于渗透保护反应的遗传决定因素(47个基因),与菌株QD168观察到的高耐盐性相关。可以利用A. aquatilis QD168对环境应激物(例如污染物,氧化应激和盐度)的生理适应性来进行生物修复油污染的盐碱地。

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