Issue 4, 1977

Biosynthesis of the natural (type-III) porphyrins: proof that rearrangement occurs after head-to-tail bilane formation

Abstract

The aminomethylbilane corresponding to head-to-tail combination of four porphobilinogen units is unambiguously synthesised and it is converted (rearranged) by the deaminase–cosynthetase enzyme system into uro'gen-III, the precursor of the natural porphyrins, chlorins, and corrins; 13C-labelling establishes the specificity of the conversion.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1977, 113-115

Biosynthesis of the natural (type-III) porphyrins: proof that rearrangement occurs after head-to-tail bilane formation

A. R. Battersby, E. McDonald, D. C. Williams and H. K. W. Wurziger, J. Chem. Soc., Chem. Commun., 1977, 113 DOI: 10.1039/C39770000113

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