深海冷渗漏中微生物还原脱卤的证据及其对生物地球化学循环的意义。

IF 12.7 1区 生物学 Q1 MICROBIOLOGY
Yingchun Han, Zhaochao Deng, Yongyi Peng, Jiaxue Peng, Lei Cao, Yangru Xu, Yi Yang, Hao Zhou, Chen Zhang, Dongdong Zhang, Minxiao Wang, Chunfang Zhang, Chris Greening, Xiyang Dong
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引用次数: 0

摘要

背景:还原性脱卤对卤素循环和环境修复至关重要,但其生态作用尚未完全了解,特别是在深海环境中。为了解决这一空白,我们研究了深海冷渗漏中编码还原脱卤酶催化亚基(RdhAs)的基因的多样性和表达,以及潜在的有机卤化物还原剂的生态生理。深海冷渗漏是富含卤化化合物的环境。结果:通过对165份全球冷渗沉积物样本的基因组解析宏基因组分析,根据其特征和系统发育关系鉴定出4种rdha样序列:典型呼吸、跨膜呼吸、细胞质和一种新的进化支。研究人员发现,与其他海洋沉积物相比,冷渗漏中含有更高丰度的rdha样基因,这凸显了它们作为微生物还原脱卤热点的潜力。这些rdha样基因由4个古细菌和36个细菌门的广泛微生物编码,显著扩大了已知的有机卤化物还原剂的多样性。卤素地球化学、实验室孵育、超转录组学数据和代谢组学分析证实,这些沉积物中存在浓度高达18 mg/g的有机卤化物,并表明微生物还原脱卤的可能性。我们的研究结果表明,从与碳、氢、氮、硫和微量元素循环相关的基因的存在推断,冷渗沉积物中的有机卤化物还原剂可能参与了多种生物地球化学过程。此外,来自冷渗漏的rdha样蛋白在不同的基因群中具有不同的n端结构。结论:这些发现共同表明,还原脱卤是深海环境中一个重要的过程,由多种微生物和新型酶介导。丰富多样的rdha样基因的发现,以及它们的基因组背景和潜在的代谢联系,突出了冷渗漏作为微生物多样性储藏库的作用,可能对环境修复产生影响。视频摘要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evidence of microbial reductive dehalogenation in deep-sea cold seeps and its implications for biogeochemical cycles.

Background: Reductive dehalogenation is crucial for halogen cycling and environmental remediation, yet its ecological role is not completely understood, especially in deep-sea environments. To address this gap, we investigated the diversity and expression of genes encoding reductive dehalogenase catalytic subunits (RdhAs), and ecophysiology of potential organohalide reducers in deep-sea cold seeps, which are environments rich in halogenated compounds.

Results: Through genome-resolved metagenomic analysis of 165 global cold seep sediment samples, 4 types of RdhA-like sequences were identified based on their features and phylogenetic relationships: prototypical respiratory, transmembrane respiratory, cytosolic, and a novel clade. Cold seeps were found to harbor a higher abundance of these rdhA-like genes compared to other marine sediments, highlighting their potential as microbial reductive dehalogenation hotspots. These rdhA-like genes are encoded by a wide range of microorganisms across 4 archaeal and 36 bacterial phyla, significantly expanding the known diversity of organohalide reducers. Halogen geochemistry, laboratory incubations, metatranscriptomic data, and metabolomic profiling confirmed the presence of organohalides at concentrations of up to 18 mg/g in these sediments and suggested the potential for microbial reductive dehalogenation. Our findings suggest that organohalide reducers in cold seep sediments may participate in diverse biogeochemical processes, as inferred from the presence of genes related to carbon, hydrogen, nitrogen, sulfur, and trace element cycling. Additionally, RdhA-like proteins from cold seeps have diverse N-terminal structures across different gene groups.

Conclusions: These findings collectively suggest that reductive dehalogenation is an important process in deep-sea environments, mediated by a diverse array of microbes and novel enzymes. The discovery of diverse and abundant rdhA-like genes, along with their genomic context and potential metabolic linkages, highlights the role of cold seeps as reservoirs of microbial diversity with possible implications for environmental remediation. Video Abstract.

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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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