Physical mechanism for inactivation of metallo-enzymes by characteristic X-rays. 1986

H H Jawad, and D E Watt

Measurements have been made of the inactivation of the metallo-enzyme dihydro-oratic dehydrogenase in solution by characteristic X-rays at energies above and below the K absorption edge of the constituent iron atom. From the dose-survival curves and knowledge of the equilibrium electron spectrum generated by the X-ray 'field', inactivation cross-sections are deduced and expressed in terms of intrinsic efficiencies for the various proposed direct and indirect mechanisms of inactivation. It is concluded that the inactivation is caused by direct X-ray interaction in an area equivalent to about 30 per cent of the mean geometrical cross-section of the molecule, and is independent of whether the target is wet or dry. The contribution from Auger electron cascades, Coulomb charges etc. initiated by the inner-shell vacancy in the metal atom is negligible--possibly due to saturation effects. It seems that the presence of the metal atom simply serves to enhance the overall interaction probability with the molecule in a manner consistent with expectations from the photon absorption coefficients. No anomalously large damage is detected. These conclusions are supported by comparison with published results for other metallo-enzymes and bromine-loaded bacteria.

UI MeSH Term Description Entries
D008667 Metalloproteins Proteins that have one or more tightly bound metal ions forming part of their structure. (Dorland, 28th ed) Metalloprotein
D010088 Oxidoreductases The class of all enzymes catalyzing oxidoreduction reactions. The substrate that is oxidized is regarded as a hydrogen donor. The systematic name is based on donor:acceptor oxidoreductase. The recommended name will be dehydrogenase, wherever this is possible; as an alternative, reductase can be used. Oxidase is only used in cases where O2 is the acceptor. (Enzyme Nomenclature, 1992, p9) Dehydrogenases,Oxidases,Oxidoreductase,Reductases,Dehydrogenase,Oxidase,Reductase
D004081 Dihydroorotate Oxidase An enzyme that in the course of pyrimidine biosynthesis, catalyzes the oxidation of dihydro-orotic acid to orotic acid utilizing oxygen as the electron acceptor. This enzyme is a flavoprotein which contains both FLAVIN-ADENINE DINUCLEOTIDE and FLAVIN MONONUCLEOTIDE as well as iron-sulfur centers. EC 1.3.3.1. Dihydro-Orotate Oxidase,Dihydro Orotate Oxidase,Oxidase, Dihydro-Orotate,Oxidase, Dihydroorotate

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