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Literature summary for 1.7.7.2 extracted from

  • Seki-Chiba, S.; Ishimoto, M.
    Studies on nitrate reductase of Clostridium perfringens. Purification, some properties, and effect of tungstate on its formation (1977), J. Biochem., 82, 1663-1671.
    View publication on PubMed

Activating Compound

Activating Compound Comment Organism Structure
additional information enzyme synthesis is induced by nitrate Clostridium perfringens

Inhibitors

Inhibitors Comment Organism Structure
azide 74% inhibition Clostridium perfringens
cyanide 10 mM, 87% inhibition Clostridium perfringens
additional information not inhibited by 0.1 mM p-chloromercuribenzoate, enzyme formation is induced by nitrate and inhibited by 0.5 mM tungstate, but recovered by 0.1 mM molybdate Clostridium perfringens

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
0.1
-
nitrate
-
Clostridium perfringens

Localization

Localization Comment Organism GeneOntology No. Textmining
cytoplasm enzyme functions in the soluble state in the cytoplasm Clostridium perfringens 5737
-

Metals/Ions

Metals/Ions Comment Organism Structure
Ca2+ stimulates activity about 30% Clostridium perfringens
Fe2+ stimulates activity about 50% Clostridium perfringens
Iron molybdenum iron-sulfur protein Clostridium perfringens
iron-sulfur centre molybdo-iron-sulfur protein Clostridium perfringens
Mg2+ stimulates activity about 30% Clostridium perfringens
Mn2+ stimulates activity about 50%, stimulates reaction rate and level of nitrite formation Clostridium perfringens
Molybdenum molybdenum iron-sulfur protein Clostridium perfringens

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
80000
-
gel filtration Clostridium perfringens
90000
-
ultracentrifugation Clostridium perfringens

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
nitrate + reduced ferredoxin Clostridium perfringens nitrate fermentation, ferredoxin is utilized as direct electron donor in nitrate reduction nitrite + oxidized ferredoxin
-
?

Organism

Organism UniProt Comment Textmining
Clostridium perfringens
-
-
-

Purification (Commentary)

Purification (Comment) Organism
-
Clostridium perfringens

Specific Activity [micromol/min/mg]

Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
52
-
-
Clostridium perfringens

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information not as electron donors: NADH, NADPH, FADH2, FMNH2, rubredoxin Clostridium perfringens ?
-
?
nitrate + reduced ferredoxin ferredoxin as electron donor at neutral pH and pH 8, but not at pH 9 Clostridium perfringens nitrite + H2O + oxidized ferredoxin
-
?
nitrate + reduced ferredoxin nitrate fermentation, ferredoxin is utilized as direct electron donor in nitrate reduction Clostridium perfringens nitrite + oxidized ferredoxin
-
?
nitrate + reduced methyl viologen nitrite formation 10times higher at pH 9 than at pH 8 Clostridium perfringens nitrite + oxidized methyl viologen
-
?
nitrate + reduced methyl viologen enzyme uses also reduced methyl viologen as reductant Clostridium perfringens nitrite + oxidized methyl viologen
-
?
nitrate + reduced methyl viologen enzyme also has methyl viologen-linked activity Clostridium perfringens nitrite + oxidized methyl viologen
-
?

Subunits

Subunits Comment Organism
monomer 1 * 90000, SDS-PAGE Clostridium perfringens

Temperature Optimum [°C]

Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
37
-
assay at Clostridium perfringens

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
9
-
reduced methyl viologen as electron donor Clostridium perfringens

pH Range

pH Minimum pH Maximum Comment Organism
8.3 9.8 at pH 8.3 and 9.8: about 50% of activity maximum Clostridium perfringens