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Viscosity effects on eukaryotic nitrate reductase activity.
- Source :
-
The Journal of biological chemistry [J Biol Chem] 2005 Jul 15; Vol. 280 (28), pp. 26049-54. Date of Electronic Publication: 2005 May 16. - Publication Year :
- 2005
-
Abstract
- Rate-limiting processes of catalysis by eukaryotic molybdenum-containing nitrate reductase (NaR, EC 1.7.1.1-3) were investigated using two viscosogens (glycerol and sucrose) and observing their impact on NAD(P)H:NaR activity of corn leaf NaR and recombinant Arabidopsis and yeast NaR. Holo-NaR has two "hinge" sequences between stably folded regions housing its internal electron carriers: 1) Hinge 1 between the molybdenum-containing nitrate reducing module and cytochrome b domain containing heme and 2) Hinge 2 between cytochrome b and cytochrome b reductase (CbR) module containing FAD. Solution viscosity negatively impacted the activity of these holo-NaR forms, which suggests that the rate-limiting events in catalysis were likely to involve large conformational changes that restrict or "gate" internal electron-proton transfers (IET). Little effect of viscosity was observed on recombinant CbR module and methyl viologen nitrate reduction by holo-NaR, suggesting that these activities involved no large conformational changes. To determine whether Hinge 2 is involved in gating the first step in IET, the effects of viscosogen on cytochrome c and ferricyanide reductase activities of holo-NaR and ferricyanide reductase activity of the recombinant molybdenum reductase module (CbR, Hinge 2, and cytochrome b) were analyzed. Solution viscosity negatively impacted these partial activities, as if Hinge 2 were involved in gating IET in both enzyme forms. We concluded that both Hinges 1 and 2 appear to be involved in gating IET steps by restricting the movement of the cytochrome b domain relative to the larger nitrate-reducing and electron-donating modules of NaR.
- Subjects :
- Amino Acid Sequence
Arabidopsis metabolism
Binding Sites
Buffers
Catalysis
Cytochrome Reductases chemistry
Cytochromes b chemistry
Dose-Response Relationship, Drug
Electrons
Ferricyanides chemistry
Fungal Proteins metabolism
Glycerol pharmacology
Kinetics
Models, Biological
Models, Chemical
Molecular Sequence Data
Nitrate Reductase
Nitrate Reductases metabolism
Oxidation-Reduction
Paraquat chemistry
Protein Conformation
Protein Folding
Protein Structure, Tertiary
Protons
Recombinant Proteins chemistry
Sequence Homology, Amino Acid
Sucrose pharmacology
Viscosity
Zea mays metabolism
Nitrate Reductases chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 0021-9258
- Volume :
- 280
- Issue :
- 28
- Database :
- MEDLINE
- Journal :
- The Journal of biological chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 15897195
- Full Text :
- https://doi.org/10.1074/jbc.M409694200