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Anaerobic degradation of hexadecane and phenanthrene coupled to sulfate reduction by enriched consortia from northern Gulf of Mexico seafloor sediment

机译:墨西哥湾北部海底沉积物的富集财团对十六烷和菲的厌氧降解与硫酸盐的还原相结合

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摘要

To advance understanding of the fate of hydrocarbons released from the Deepwater Horizon oil spill and deposited in marine sediments, this study characterized the microbial populations capable of anaerobic hydrocarbon degradation coupled with sulfate reduction in non-seep sediments of the northern Gulf of Mexico. Anaerobic, sediment-free enrichment cultures were obtained with either hexadecane or phenanthrene as sole carbon source and sulfate as a terminal electron acceptor. Phylogenetic analysis revealed that enriched microbial populations differed by hydrocarbon substrate, with abundant SSU rRNA gene amplicon sequences from hexadecane cultures showing high sequence identity (up to 98%) to Desulfatibacillum alkenivorans (family Desulfobacteraceae), while phenanthrene-enriched populations were most closely related to Desulfatiglans spp. (up to 95% sequence identity; family Desulfarculaceae). Assuming complete oxidation to CO2, observed stoichiometric ratios closely resembled the theoretical ratios of 12.25:1 for hexadecane and 8.25:1 for phenanthrene degradation coupled to sulfate reduction. Phenanthrene carboxylic acid was detected in the phenanthrene-degrading enrichment cultures, providing evidence to indicate carboxylation as an activation mechanism for phenanthrene degradation. Metagenome-assembled genomes (MAGs) revealed that phenanthrene degradation is likely mediated by novel genera or families of sulfate-reducing bacteria along with their fermentative syntrophic partners, and candidate genes linked to the degradation of aromatic hydrocarbons were detected for future study.
机译:为了进一步了解从“深水地平线”溢油中释放出来并沉积在海洋沉积物中的碳氢化合物的命运,这项研究对能够在墨西哥湾北部非深度沉积物中进行厌氧性碳氢化合物降解和硫酸盐还原的微生物种群进行了表征。以十六烷或菲为唯一碳源,硫酸盐为末端电子受体,得到无氧,无沉淀的富集培养物。系统发育分析表明,富集的微生物种群因烃底物而异,十六烷培养物中丰富的SSU rRNA基因扩增子序列与脱硫枯草杆菌(家族脱硫杆菌科)显示出很高的序列同一性(高达98%),而富菲的种群与脱硫葡萄球菌(高达95%的序列同一性;脱硫菊科)。假设完全氧化成CO2,所观察到的化学计量比与十六烷的理论比为12.25:1,对于菲降解与硫酸盐还原反应的理论比为8.25:1。在菲降解富集培养物中检测到菲羧酸,提供了证据表明羧化是菲降解的激活机制。元基因组组装的基因组(MAGs)表明,菲的降解很可能是由新的硫酸盐还原菌属或家族及其发酵同养伴侣介导的,并且检测了与芳香烃降解相关的候选基因,以备将来研究。

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