Search bioRxiv⌕ Search

Biology subjects

Sobol, M.

Publications and source records attributed to Sobol, M..

3 recordsLinked to original sources

Ecological constraints and evolutionary trade-offs shape nitrogen fixation across habitats

From its earliest beginnings, lifes expansion into new habitats has been profoundly shaped by its reciprocal interactions with Earths changing environments. Understanding how ancient metabolisms co-evolved with their environments requires uncovering the ecological and evolutionary processes that structured the functionally linked genes and networks underlying these metabolisms. Here, we focus on nitrogen (N2) fixation, one of lifes most critical metabolisms, and investigate the drivers of complexity in its associated gene machinery today. We used a large-scale comparative genomics framework to construct a comprehensive catalog of extant N2 fixation-associated genes and assessed their distribution across diverse microbial genomes and environmental backgrounds. Genomes enriched in N2 fixation genes generally have larger genome sizes, broader metabolic capabilities, wider habitat ranges, and are predominantly associated with mesophilic and aerobic lifestyles. Evolutionary reconstructions reveal a pattern of early gene gains in ancestral diazotrophs followed by lineage-specific gene losses in later diverging taxa, suggesting evolutionary trade-offs shaped by changing environments. These findings demonstrate that the evolution of N2 fixation has been intertwined with the composition and organization of the genes supporting the overarching N2 metabolism, driven by feedback between genome evolution and shifting environmental and ecological conditions.

microbiology↗

Biological molybdenum usage stems back to 3.4 billion years ago

Molybdenum (Mo) is an essential nutrient for most living organisms, serving as a cofactor in a diverse array of molybdoenzymes that catalyze key reactions in several elemental cycles. However, geochemical data suggest that dissolved Mo concentrations in the Archean ocean (before 2.5 billion years ago) were 1-2 orders of magnitude lower than today, raising questions about its bioavailability to early life. Here, we apply a phylogenomic approach to chart the modern biological and environmental distribution of Mo-related enzymes and use phylogenetic reconciliations to reconstruct the evolutionary history of biological Mo usage. Our results reveal the ubiquity of molybdoenzymes across contemporary organisms inhabiting diverse environments. Furthermore, phylogenetic evidence indicates that the earliest molybdoenzymes stem back to the Paleo/Mesoarchean (~3.5-3.0 Gya), facilitating critical energy-harnessing reactions in some of Earths most ancient life forms. Taken together, our findings challenge the prevailing view of limited Mo bioavailability on the anoxic early Earth.

evolutionary biology↗

Ecological resource competition as a driver of metallome evolution

The oldest nitrogenase isozyme, emerging a billion years or more before the Great Oxidation Event (GOE), required a molybdenum (Mo)-based cofactor. "Alternative" nitrogenases using iron (Fe) or vanadium (V) cofactors evolved only after the GOE. This history is puzzling because environmental Fe availability decreased after the GOE, while Mo availability increased, due to the contrasting environmental redox behaviors of these elements. Why, then, did the alternatives emerge only after the GOE? Using a model constrained by known microbial Mo quotas, we demonstrate that a strong selection pressure for the use of metals in nitrogenase other than Mo is a plausible consequence of competition between nitrogen-fixing prokaryotes and nitrate-reducing microbes, which require Mo for nitrate reduction and assimilation. This competition would have intensified after the GOE due to increasing availability of nitrate, explaining the evolutionary timing of nitrogenases isozymes. Ecological resource competition therefore emerges as a third driver of metallome evolution in deep-time, alongside the relative environmental availabilities and adaptive advantages of particular metals.

evolutionary biology↗