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J Biol Chem ; 275(28): 20996-1001, 2000 Jul 14.
Artigo em Inglês | MEDLINE | ID: mdl-10801830

RESUMO

The chloroplastic NADP-malate dehydrogenase is activated by reduction of its N- and C-terminal disulfides by reduced thioredoxin. The activation is inhibited by NADP(+), the oxidized form of the cofactor. Previous studies suggested that the C-terminal disulfide was involved in this process. Recent structural data pointed toward a possible direct interaction between the C terminus of the oxidized enzyme and the cofactor. In the present study, the relationship between the cofactor specificity for catalysis and for inhibition of activation has been investigated by changing the cofactor specificity of the enzyme by substitution of selected residues of the cofactor-binding site. An NAD-specific thiol-regulated MDH was engineered. Its activation was inhibited by NAD(+) but no longer by NADP(+). These results demonstrate that the oxidized cofactor is bound at the same site as the reduced cofactor and support the idea of a direct interaction between the negatively charged C-terminal end of the enzyme and the positively charged nicotinamide ring of the cofactor, in agreement with the structural data. The structural requirements for cofactor specificity are modeled and discussed.


Assuntos
Cloroplastos/enzimologia , Malato Desidrogenase/metabolismo , NADP/metabolismo , NAD/metabolismo , Plantas/enzimologia , Tiorredoxinas/metabolismo , Sequência de Aminoácidos , Substituição de Aminoácidos , Animais , Dissulfetos , Humanos , Cinética , Malato Desidrogenase/química , Malato Desidrogenase (NADP+) , Modelos Moleculares , Dados de Sequência Molecular , Mutagênese Sítio-Dirigida , Oxirredução , Conformação Proteica , Proteínas Recombinantes/química , Proteínas Recombinantes/metabolismo , Alinhamento de Sequência , Homologia de Sequência de Aminoácidos
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