珊瑚礁外代谢组的微生物群落代谢扩大了不稳定溶解有机质的化学多样性

IF 4 2区 生物学 Q2 MICROBIOLOGY Environmental microbiology Pub Date : 2025-03-19 DOI:10.1111/1462-2920.70064
Zachary A. Quinlan, Craig E. Nelson, Irina Koester, Daniel Petras, Louis-Felix Nothias, Jacqueline Comstock, Brandie M. White, Lihini I. Aluwihare, Barbara A. Bailey, Craig A. Carlson, Pieter C. Dorrestein, Andreas F. Haas, Linda Wegley Kelly
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摘要

溶解有机物(DOM)由多种化合物组成,在水生生态系统中具有不同的生物利用度。DOM的来源和数量会影响微生物的生长和群落结构,从而影响生物地球化学过程。为了研究热带珊瑚礁水域中不稳定DOM的化学多样性,我们追踪了微生物对两种珊瑚和三种藻类中3000多种非靶向质谱离子特征的利用情况。这些特征中大约有一半聚集在500多个生物不稳定的光谱子网络中,这些子网络注释了不同的结构超类,包括苯类、脂类、有机酸、杂环和苯丙类,平均占每个化学类中离子丰富度和丰度的三分之一。这些不稳定化合物的不同亚群在白天和晚上由藻类和珊瑚渗出,驱动不同的微生物生长和基质利用。本研究扩展了不稳定的海洋DOM的化学多样性,并对沿海环境中的碳循环产生了影响。
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Microbial Community Metabolism of Coral Reef Exometabolomes Broadens the Chemodiversity of Labile Dissolved Organic Matter

Dissolved organic matter (DOM) comprises diverse compounds with variable bioavailability across aquatic ecosystems. The sources and quantities of DOM can influence microbial growth and community structure with effects on biogeochemical processes. To investigate the chemodiversity of labile DOM in tropical reef waters, we tracked microbial utilisation of over 3000 untargeted mass spectrometry ion features exuded from two coral and three algal species. Roughly half of these features clustered into over 500 biologically labile spectral subnetworks annotated to diverse structural superclasses, including benzenoids, lipids, organic acids, heterocyclics and phenylpropanoids, comprising on average one-third of the ion richness and abundance within each chemical class. Distinct subsets of these labile compounds were exuded by algae and corals during the day and night, driving differential microbial growth and substrate utilisation. This study expands the chemical diversity of labile marine DOM with implications for carbon cycling in coastal environments.

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来源期刊
Environmental microbiology
Environmental microbiology 环境科学-微生物学
CiteScore
9.90
自引率
3.90%
发文量
427
审稿时长
2.3 months
期刊介绍: Environmental Microbiology provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens
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