11:00 AM - 11:22 AM
[BCG03-07] Mineral-catalyzed hydrothermal CO2 reduction that generated primordial autotrophic metabolisms
★Invited Papers
Keywords:Origin of life, Chemical evolution, Hydrothermal vent, CO2 reduction, Autotrophs
Minerals are thought to play a crucial role in chemical evolution by driving the production of biomolecules via their catalytic activity. Especially in autotrophic theories for the origin of life, mineral catalysts are believed to enhance the continuous generation of organic molecules from inorganics such as CO2 under the relatively moderate geochemical settings in the Hadean Earth; such as hydrothermal vents. Biochemistry suggests that such primordial CO2 fixation reactions are preserved as “metabolic fossils” within the extant reductive acetyl-CoA pathway, the most primitive CO2 fixation pathway, of organisms utilizing CO2 and H2, because of the similarity of the key components and reaction flows. In these theories, the most fundamental step that provides the necessary building blocks for autotrophic chemical evolution is reduction of CO2. Hydrogen is thought to be the primary electron donor for the reaction on the Hadean Earth. Generation of H2 occurs by water-rock interaction, namely serpentinization, in the Earth’s crust, providing H2-rich water to hydrothermal vents fueling the catalytic reduction of CO2 by minerals. Over the past decades, many studies have attempted to find possible chemical routes analogous to the acetyl-CoA pathway assaying CO2 reduction by H2 using commonly observed metal sulfides in hydrothermal vents, such as FeS and NiS. However, no efficient reactions have been reported until recently. Recently, a series of new trials have been conducted using minerals formed by serpentinization and/or originated from meteorites rather than conventionally used metal sulfides. The presenter has reconsidered the geochemical settings of the serpentinization reaction and its relevant by-product minerals to assay their potential for CO2 reduction by H2 in hydrothermal systems. Greigite (Fe3S4), a mixed-valence iron sulfide, was found to catalyze CO2 reduction by H2, generating formate, acetate, and CH4 as products under versatile hydrothermal conditions (pH~10, ~100 °C, and ~100 bar). Similar reaction route catalyzed by other minerals synthesized as serpentinization product, namely magnetite (Fe3O4) and awaruite (Ni3Fe), has also been discovered independently in the different laboratories. Magnetite and awaruite have been shown to catalyze the synthesis of pyruvate and ethanol, in addition to formate and acetate, from CO2. The product profile of these minerals was similar to those of the intermediates and the end products of the extant reductive acetyl-CoA pathway. These facts suggest the significant involvement of these minerals in the abiotic synthesis of organics from CO2 with H2, providing building blocks required for the ancient reductive acetyl-CoA pathway in the chemical evolution. These findings support the theory that the first life could have formed from the primordial catalytic network based on CO2 fixation catalyzed by geochemical reactions, preceding the enzyme-catalyzed biochemistry. In this presentation, a series of notable progress in mineral-catalyzed CO2 reduction studies, including the recently discovered reaction route described above, will be introduced. Afterwards, research for ancient metalloenzymes which the presenter is conducting now will also be introduced in the context of the mineral-catalyzed chemical evolution process. Finally, the limitations and future perspectives on the autotrophic origin of life research will be discussed.