RESUMO
Paracoccus pantotrophus cytochrome cd(1) is a physiological nitrite reductase and an in vitro hydroxylamine reductase. The oxidised "as isolated" form of the enzyme has bis-histidinyl coordinated c-heme and upon reduction its coordination changes to histidine/methionine. Following treatment of reduced enzyme with hydroxylamine, a novel, oxidised, conformer of the enzyme is obtained. We have devised protocols for freeze-quench near-ir-MCD spectroscopy that have allowed us to establish unequivocally the c-heme coordination of this species as His/Met. Thus it is shown that the catalytically competent, hydroxylamine reoxidised, form of P. pantotrophus cytochrome cd(1) has different axial ligands to the c-heme than "as isolated" enzyme.
Assuntos
Citocromos/química , Citocromos/metabolismo , Nitrito Redutases/química , Nitrito Redutases/metabolismo , Paracoccus/enzimologia , Grupo dos Citocromos c , Espectroscopia de Ressonância de Spin Eletrônica/métodos , Congelamento , Oxirredução , Conformação Proteica , Espectrofotometria Infravermelho/métodosAssuntos
L-Lactato Desidrogenase/química , NAD/química , Plasmodium falciparum/enzimologia , Conformação Proteica , Animais , Antimaláricos , Desenho de Fármacos , Inibidores Enzimáticos , L-Lactato Desidrogenase/antagonistas & inibidores , Modelos Moleculares , NAD/metabolismo , Ácido Oxâmico/químicaRESUMO
The alpha- and beta-anomers of D-cellobiose were resolved by 1H NMR spectroscopy. Addition of cellobiose dehydrogenase purified from the white-rot P. chrysosporium led to selective conversion of beta-D-cellobiose. The product was identical to cellobionolactone as synthesized from Ca-cellobionate. Overnight incubation of the product led to an altered NMR spectrum, which was also obtained by incubation of cellobionolactone. The new spectrum matched that for Ca-cellobionate. The instability of cellobionolactone explains the detection of cellobionic acid as product in earlier studies.