Literature DB >> 1330552

X-ray crystallographic characterisation of type-2-depleted ascorbate oxidase from zucchini.

A Messerschmidt1, W Steigemann, R Huber, G Lang, P M Kroneck.   

Abstract

The type-2 depleted form of ascorbate oxidase from zucchini has been prepared in crystals and characterised by X-ray crystallography and EPR spectroscopy. The X-ray structure analysis by difference-Fourier techniques and refinement shows that, on average, about 1.3 Cu atoms/ascorbate oxidase monomer are removed. The copper is lost from the trinuclear site whereby the EPR-active type-2 copper is depleted most; type-1 copper is not affected. This observation indicates preferential formation of a 1 Cu-depleted form with the hole equally distributed over all three copper sites. Each of these 1 Cu-depleted species may represent an anti-ferromagnetically coupled copper pair which is EPR-silent and could explain the disappearance of the type-2 EPR signal.

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Year:  1992        PMID: 1330552     DOI: 10.1111/j.1432-1033.1992.tb17325.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  5 in total

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3.  Reduction thermodynamics of the T1 Cu site in plant and fungal laccases.

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4.  The glutathione redox couple modulates zinc transfer from metallothionein to zinc-depleted sorbitol dehydrogenase.

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5.  Stability of Japanese-lacquer-tree (Rhus vernicifera) laccase to thermal and chemical denaturation: comparison with ascorbate oxidase.

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  5 in total

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