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Why Did Nature Choose Manganese over Cobalt to Make Oxygen Photosynthetically on the Earth? | LitMetric

All contemporary oxygenic phototrophs─from primitive cyanobacteria to complex multicellular plants─split water using a single invariant cluster comprising MnCaO (the ) as the catalyst within photosystem II, the universal oxygenic reaction center of natural photosynthesis. This cluster is unstable outside of PSII and can be reconstituted, both in vivo and in vitro, using elemental aqueous ions and light, via photoassembly. Here, we demonstrate the first functional substitution of manganese in any oxygenic reaction center by in vitro photoassembly. Following complete removal of inorganic cofactors from cyanobacterial photosystem II microcrystal (PSIIX), photoassembly with free cobalt (Co), calcium (Ca), and water (OH) restores O evolution activity. Photoassembly occurs at least threefold faster using Co versus Mn due to a higher quantum yield for PSIIX-mediated charge separation (P*): Co → P* → CoQ. However, this kinetic preference for Co over native Mn during photoassembly is offset by significantly poorer catalytic activity (∼25% of the activity with Mn) and ∼3- to 30-fold faster photoinactivation rate. The resulting reconstituted Co-PSIIX oxidizes water by the standard four-flash photocycle, although they produce 4-fold less O per PSII, suggested to arise from faster charge recombination (CoQ ← CoQ) in the catalytic cycle. The faster photoinactivation of reconstituted Co-PSIIX occurs under anaerobic conditions during the catalytic cycle, suggesting direct photodamage without the involvement of O. Manganese offers two advantages for oxygenic phototrophs, which may explain its exclusive retention throughout Darwinian evolution: significantly slower charge recombination (MnQ ← MnQ) permits more water oxidation at low and fluctuating solar irradiation (greater net energy conversion) and much greater tolerance to photodamage at high light intensities (Mn is less oxidizing than Co). Future work to identify the chemical nature of the intermediates will be needed for further interpretation.

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http://dx.doi.org/10.1021/acs.jpcb.2c00749DOI Listing

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