Robes Jose Miguel D, Liebergesell Tashi C E, Beals Delaney G, Yu Xinhui, Brazelton William J, Puri Aaron W
Department of Chemistry, University of Utah, Salt Lake City, UT 84112.
Henry Eyring Center for Cell and Genome Science, University of Utah, Salt Lake City, UT 84112.
Proc Natl Acad Sci U S A. 2025 Sep 9;122(36):e2507323122. doi: 10.1073/pnas.2507323122. Epub 2025 Sep 3.
Methane is a potent greenhouse gas and a target for near-term climate change mitigation. In many natural ecosystems, methane is sequestered by microbial communities, yet little is known about how constituents of methane-oxidizing communities interact with each other and their environment. This lack of mechanistic understanding is a common issue for many important microbial communities, but it is difficult to draw links between available sequencing information and the metabolites that govern community interactions. Here, we develop and apply a technique called inverse stable isotope probing-metabolomics (InverSIP) to bridge the gap between metagenomic and metabolomic information and functionally characterize interactions in a complex methane-oxidizing community. Using InverSIP, we link a highly transcribed biosynthetic gene cluster in the community with its secondary metabolite product: methylocystabactin, a triscatecholate siderophore not previously observed in nature. We find that production of methylocystabactin is widespread among methanotrophic alphaproteobacteria and that it can be used by another methanotroph in the community that does not produce this siderophore itself. Functional assays reveal that methylocystabactin supports methanotroph growth and the activity of the methane-oxidizing enzyme soluble methane monooxygenase under conditions where bioavailable iron is limited, establishing an important molecular link between methane-oxidation and the insoluble iron found in many natural environments. These findings contribute to a molecular-level understanding of these environmentally important bacterial communities and establish InverSIP as a broadly applicable genomics-guided strategy for characterizing metabolites in microbial ecosystems.
甲烷是一种强效温室气体,也是近期减缓气候变化的目标。在许多自然生态系统中,甲烷由微生物群落封存,但对于甲烷氧化群落的组成部分如何相互作用以及与环境相互作用却知之甚少。这种对机制的缺乏理解是许多重要微生物群落的常见问题,但很难将现有的测序信息与控制群落相互作用的代谢物联系起来。在这里,我们开发并应用了一种称为反向稳定同位素探测-代谢组学(InverSIP)的技术,以弥合宏基因组学和代谢组学信息之间的差距,并在复杂的甲烷氧化群落中对相互作用进行功能表征。使用InverSIP,我们将群落中一个高度转录的生物合成基因簇与其次生代谢产物联系起来:甲基囊菌素,一种自然界中以前未观察到的三儿茶酚铁载体。我们发现甲基囊菌素的产生在甲烷营养型α-变形杆菌中广泛存在,并且可以被群落中另一种自身不产生这种铁载体的甲烷营养菌利用。功能分析表明,在生物可利用铁有限的条件下,甲基囊菌素支持甲烷营养菌的生长和甲烷氧化酶可溶性甲烷单加氧酶的活性,在甲烷氧化与许多自然环境中发现的不溶性铁之间建立了重要的分子联系。这些发现有助于从分子水平理解这些对环境重要的细菌群落,并将InverSIP确立为一种广泛适用的基因组学指导策略,用于表征微生物生态系统中的代谢物。