AI Article Synopsis

  • Enzymes containing nickel, iron, and sulfur are crucial for prokaryotes to facilitate reactions that impact global carbon and hydrogen cycles.
  • The enzymes discussed—[NiFe] hydrogenases, Ni,Fe carbon monoxide dehydrogenases, and acetyl-CoA synthases—likely originated from ancient abiotic processes, despite having different active site compositions.
  • All three enzymes rely on nickel for substrate binding and activation, with sulfur connecting nickel to iron, contributing to the process in complex and not yet fully understood ways.

Article Abstract

Enzymes relying on the interplay of nickel, iron, and sulfur in their active sites are used by prokaryotes to catalyze reactions driving the global carbon and hydrogen cycles. The three enzymes, [NiFe] hydrogenases, Ni,Fe-containing carbon monoxide dehydrogenases and acetyl-CoA synthases share an ancient origin possibly derived from abiotic processes. Although their active sites have different compositions and assemble Ni, Fe, and S in different ways and for different purposes, they share a central role of Ni in substrate binding and activation, with sulfur linking the Ni ion to one or more Fe ions, which, although indispensable for function, supports the catalytic process in less understood ways. The review gives a short overview on the properties of the three individual enzymes highlighting their parallels and differences.

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Source
http://dx.doi.org/10.1515/9783110589757-017DOI Listing

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