Durán Roberto E, Méndez Valentina, Rodríguez-Castro Laura, Barra-Sanhueza Bárbara, Salvà-Serra Francisco, Moore Edward R B, Castro-Nallar Eduardo, Seeger Michael
Laboratorio de Microbiología Molecular y Biotecnología Ambiental, Departamento de Química - Centro de Biotecnología, Universidad Técnica Federico Santa María, Valparaíso, Chile.
Department of Infectious Diseases, Institute for Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Front Microbiol. 2019 Apr 5;10:528. doi: 10.3389/fmicb.2019.00528. eCollection 2019.
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 spp. and to characterize the genetic determinants and the physiological response of QD168 to model environmental stressors (benzene, oxidizing agents, and salt). Phylogenomic analyses, using 35 housekeeping genes, clustered QD168 with four other strains of spp. ( BU33N, JQ135, UBA3227, and UBA7629). Genomic sequence analyses of QD168 with 25 spp., using ANIb, indicated that 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. 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 () and catechol 1,2-dioxygenase (). 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 QD168 is notably more resistant to paraquat than to HO. Genetic determinants (47 genes) for osmoprotective responses were identified, correlating with observed high halotolerance by strain QD168. The physiological adaptation of QD168 to environmental stressors such as pollutants, oxidative stress and salinity may be exploited for bioremediation of oil-polluted saline sites.
QD168是一种海洋芳烃降解细菌,从金特罗湾的油污沉积物中分离得到,金特罗湾是一个长期受到多种污染物影响的工业沿海区域。本研究的目的是确定QD168菌株的系统发育位置,并表征其对模拟环境应激源(苯、氧化剂和盐)的遗传决定因素和生理反应。利用35个管家基因进行的系统发育分析将QD168与其他四株菌属菌株(BU33N、JQ135、UBA3227和UBA7629)聚类在一起。使用ANIb对QD168与25株菌属菌株进行基因组序列分析表明,BU33N是最密切相关的菌株,ANIb相似度为96.8%。菌株QD168含有95个编码七种中心分解代谢途径蛋白质的基因,以及16种芳香化合物的外周分解代谢途径/反应。QD168能够以3-羟基苯甲酸、4-羟基苯甲酸、苯甲酸、苯、3-羟基肉桂酸、肉桂酸、邻氨基苯甲酸、苯甲酰胺、4-氨基苯甲酸、烟酸、甲苯、联苯和色氨酸作为唯一碳源或氮源生长。通过生长、代谢物鉴定和基因表达分析进一步分析了苯的降解情况。苯强烈诱导编码苯酚羟化酶和儿茶酚1,2-双加氧酶的基因表达。此外,还鉴定了30个编码转录调节因子、清除酶、氧化损伤修复系统和参与氧化应激反应的同工酶的基因。表征了菌株QD168对过氧化氢和百草枯的氧化应激反应,表明QD168对百草枯的耐受性明显高于对过氧化氢的耐受性。确定了渗透保护反应的遗传决定因素(47个基因),这与观察到的菌株QD168的高耐盐性相关。QD168对污染物、氧化应激和盐度等环境应激源的生理适应性可用于油污盐渍地的生物修复。