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Literature summary for 1.5.1.20 extracted from

  • Clark, J.E.; Ljungdahl, L.G.
    Purification and properties of 5,10-methylenetetrahydrofolate reductase from Clostridium formicoaceticum (1986), Methods Enzymol., 122, 392-399.
    View publication on PubMed

General Stability

General Stability Organism
0.005 mM FAD stabilizes enzyme during purification procedure Clostridium formicaceticum

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
0.12
-
5-methyltetrahydrofolate
-
Clostridium formicaceticum
11.1
-
benzyl viologen
-
Clostridium formicaceticum

Metals/Ions

Metals/Ions Comment Organism Structure
Iron 15.2 molecules iron per enzyme molecule, enzyme contains iron-sulfur clusters Clostridium formicaceticum
iron-sulfur centre enzyme contains 15.2 molecules iron and 19.5 molecules acid-labile sulfur as iron-sulfur clusters Clostridium formicaceticum
Zinc 2.3 molecules zinc per enzyme molecule Clostridium formicaceticum

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
26000
-
alpha4,beta4, 4 * 26000 + 4 * 35000, SDS-PAGE Clostridium formicaceticum
35000
-
alpha4,beta4, 4 * 26000 + 4 * 35000, SDS-PAGE Clostridium formicaceticum
237000
-
gel filtration Clostridium formicaceticum

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
5,10-methylenetetrahydrofolate + reduced ferredoxin Clostridium formicaceticum physiological important reaction: enzyme catalyzes reduction of 5,10-methylenetetrahydrofolate with reduced ferredoxin 5-methyltetrahydrofolate + oxidized ferredoxin
-
?
5,10-methylenetetrahydrofolate + reduced ferredoxin Clostridium formicaceticum enzyme is part of synthesis pathway of acetate from CO2 via a unique tetrahydrofolate-corrinoid pathway 5-methyltetrahydrofolate + oxidized ferredoxin
-
?

Organism

Organism UniProt Comment Textmining
Clostridium formicaceticum
-
strain ATCC 23439
-

Oxidation Stability

Oxidation Stability Organism
oxygen labile, half-life: less than 1 h in aerobic buffer, sodium dithionite prevents inactivation by oxygen Clostridium formicaceticum

Purification (Commentary)

Purification (Comment) Organism
-
Clostridium formicaceticum

Specific Activity [micromol/min/mg]

Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
139
-
-
Clostridium formicaceticum

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
5,10-methylenetetrahydrofolate + reduced acceptor forward reaction: reduced acceptor is FADH2 Clostridium formicaceticum 5-methyltetrahydrofolate + oxidized acceptor
-
r
5,10-methylenetetrahydrofolate + reduced acceptor reverse reaction: menadione as electron acceptor Clostridium formicaceticum 5-methyltetrahydrofolate + oxidized acceptor
-
r
5,10-methylenetetrahydrofolate + reduced acceptor reverse reaction: FAD, rubredoxin, benzyl viologen and methylene blue as electron acceptor Clostridium formicaceticum 5-methyltetrahydrofolate + oxidized acceptor
-
r
5,10-methylenetetrahydrofolate + reduced acceptor forward reaction: reduced ferredoxin as reduced acceptor Clostridium formicaceticum 5-methyltetrahydrofolate + oxidized acceptor
-
r
5,10-methylenetetrahydrofolate + reduced ferredoxin physiological important reaction: enzyme catalyzes reduction of 5,10-methylenetetrahydrofolate with reduced ferredoxin Clostridium formicaceticum 5-methyltetrahydrofolate + oxidized ferredoxin
-
?
5,10-methylenetetrahydrofolate + reduced ferredoxin enzyme is part of synthesis pathway of acetate from CO2 via a unique tetrahydrofolate-corrinoid pathway Clostridium formicaceticum 5-methyltetrahydrofolate + oxidized ferredoxin
-
?
5-methyltetrahydrofolate + NAD+
-
Clostridium formicaceticum 5,10-methylenetetrahydrofolate + NADH + H+
-
r
additional information no direct activity with pyridine nucleotides Clostridium formicaceticum ?
-
?
additional information not as electron donor: reduced rubredoxin Clostridium formicaceticum ?
-
?
nitrate + reduced benzyl viologen
-
Clostridium formicaceticum nitrite + benzyl viologen
-
?

Subunits

Subunits Comment Organism
octamer alpha4,beta4, 4 * 26000 + 4 * 35000, SDS-PAGE Clostridium formicaceticum

Cofactor

Cofactor Comment Organism Structure
FAD 1.7 molecules enzyme-bound FAD per enzyme molecule Clostridium formicaceticum
FAD flavoprotein, oxidized acceptor in reverse reaction Clostridium formicaceticum
FADH2 flavoprotein, reduced acceptor in forward reaction Clostridium formicaceticum
additional information no direct activity with pyridine nucleotides: NADH, NADPH Clostridium formicaceticum