PMID:8399141
| Citation |
Loewen, PC, Switala, J, von Ossowski, I, Hillar, A, Christie, A, Tattrie, B and Nicholls, P (1993) Catalase HPII of Escherichia coli catalyzes the conversion of protoheme to cis-heme d. Biochemistry 32:10159-64 |
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| Abstract |
Catalase HPII from aerobically grown Escherichia coli normally contains heme d but cultures grown with poor or no aeration produce HPII containing a mixture of heme d and protoheme IX. The protoheme component of HPII from anaerobically grown cells is converted into heme d during treatment of the purified enzyme with hydrogen peroxide. It is concluded that heme d found in catalase HPII is formed by the cis-hydroxylation of protoheme in a reaction catalyzed by catalase HPII using hydrogen peroxide as a substrate. The distal His128 residue of HPII is absolutely required for the protoheme to heme d conversion. Two mutant enzymes, Ala128 and Asn128, are catalytically inactive and contain only protoheme, which is unaffected by hydrogen peroxide treatment. The Asn201 residue is not an absolute requirement for heme conversion. The mutant enzyme Ala201 contains predominantly heme d and is partially active. However, insertion of a histidyl residue to give the His201 enzyme interferes with the heme conversion reaction. This mutant form is isolated as a protoheme enzyme with limited activity, and a reversible conversion to a heme d-like species occurs in vitro in the presence of continuously generated hydrogen peroxide. |
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| Keywords |
Amino Acid Sequence; Ascorbic Acid/pharmacology; Azides/pharmacology; Base Sequence; Catalase/biosynthesis; Catalase/chemistry; Catalase/metabolism; Escherichia coli/enzymology; Heme/analogs & derivatives; Heme/metabolism; Hydrogen Peroxide/pharmacology; Isomerism; Kinetics; Mercaptoethanol/pharmacology; Molecular Sequence Data; Mutagenesis, Site-Directed; Oligodeoxyribonucleotides; Plasmids; Polymerase Chain Reaction; Recombinant Proteins/biosynthesis; Recombinant Proteins/chemistry; Recombinant Proteins/metabolism |
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