Magnesium-protoporphyrin IX monomethyl ester (oxidative) cyclase (EC 1.14.13.81), is an enzyme with systematic name magnesium-protoporphyrin-IX 13-monomethyl ester, ferredoxin:oxygen oxidoreductase (hydroxylating).[1] In plants this enzyme catalyses the following overall chemical reaction
Magnesium-protoporphyrin IX monomethyl ester (oxidative) cyclase | |||||||||
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Identifiers | |||||||||
EC no. | 1.14.13.81 | ||||||||
CAS no. | 92353-62-3 | ||||||||
Databases | |||||||||
IntEnz | IntEnz view | ||||||||
BRENDA | BRENDA entry | ||||||||
ExPASy | NiceZyme view | ||||||||
KEGG | KEGG entry | ||||||||
MetaCyc | metabolic pathway | ||||||||
PRIAM | profile | ||||||||
PDB structures | RCSB PDB PDBe PDBsum | ||||||||
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Recent evidence[2] shows that the necessary electrons which cycle the enzyme from oxidised to reduced form come from ferredoxin. In green tissue, ferredoxin can receive these electrons directly from photosystem I so that NADPH need not be involved. However, in the dark, ferredoxin can also be reduced via Ferredoxin—NADP(+) reductase, allowing the reaction to proceed in that case. It is therefore more accurate to show the individual steps as follows:
This enzyme requires Fe(II) for activity. In barley the cyclase protein is named XanL and is encoded by the Xantha-l gene. An associated protein, Ycf54, seems to be required for proper maturation of the XanL enzyme,[2] which is part of the biosynthetic pathway to chlorophylls.[3][4][5] In anaerobic organisms such as Rhodobacter sphaeroides the same overall transformation occurs but the oxygen incorporated into magnesium-protoporphyrin IX 13-monomethyl ester comes from water in the reaction EC 1.21.98.3.[6]