How the O₂-dependent Mg-protoporphyrin monomethyl ester cyclase forms the fifth ring of chlorophylls.

ABSTRACT: Mg-protoporphyrin IX monomethyl ester (MgPME) cyclase catalyses the formation of the isocyclic ring, producing protochlorophyllide a and contributing substantially to the absorption properties of chlorophylls and bacteriochlorophylls. The O₂-dependent cyclase is found in both oxygenic phototrophs and some purple bacteria. We overproduced the simplest form of the cyclase, AcsF, from Rubrivivax gelatinosus, in Escherichia coli. In biochemical assays the di-iron cluster within AcsF is reduced by ferredoxin furnished by NADPH and ferredoxin:NADP⁺ reductase, or by direct coupling to Photosystem I photochemistry, linking cyclase to the photosynthetic electron transport chain. Kinetic analyses yielded a turnover number of 0.9 min^-1, a Michaelis-Menten constant of

SUBMITTER: Chen GE 

PROVIDER: S-EPMC7610348 | biostudies-literature | 2021 Mar

REPOSITORIES: biostudies-literature