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Literature summary for 1.8.98.1 extracted from

  • Heiden, S.; Hedderich, R.; Setzke, E.; Thauer, R.K.
    Purification of a two-subunit cytochrome-b-containing heterodisulfide reductase from methanol-grown Methanosarcina barkeri (1994), Eur. J. Biochem., 221, 855-861.
    View publication on PubMed

General Stability

General Stability Organism
more stable in presence of CHAPS than in the presence of dodecyl beta-D-maltoside Methanosarcina barkeri

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
0.25
-
coenzyme B pH 7.0, 37°C Methanosarcina barkeri
0.4
-
N-(7-[(2-sulfoethyl)dithio]heptanoyl)-3-O-phospho-L-threonine pH 7.0, 37°C, reaction with reduced benzyl viologen Methanosarcina barkeri
0.8
-
coenzyme M pH 7.0, 37°C Methanosarcina barkeri

Localization

Localization Comment Organism GeneOntology No. Textmining
membrane
-
Methanosarcina barkeri 16020
-

Metals/Ions

Metals/Ions Comment Organism Structure
Iron the enzyme contains 280 nmol of non-heme iron per mg of protein Methanosarcina barkeri

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
23000
-
x * 46000 + x * 23000, the 23000 Da subunit is cytochrome b, SDS-PAGE Methanosarcina barkeri
46000
-
x * 46000 + x * 23000, the 23000 Da subunit is cytochrome b, SDS-PAGE Methanosarcina barkeri

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
N-(7-[(2-sulfoethyl)dithio]heptanoyl)-3-O-phospho-L-threonine + H2 Methanosarcina barkeri
-
coenzyme B + coenzyme M
-
?

Organism

Organism UniProt Comment Textmining
Methanosarcina barkeri
-
-
-

Purification (Commentary)

Purification (Comment) Organism
-
Methanosarcina barkeri

Source Tissue

Source Tissue Comment Organism Textmining
culture condition:methanol-grown cell
-
Methanosarcina barkeri
-

Specific Activity [micromol/min/mg]

Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
3 8
-
Methanosarcina barkeri

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
coenzyme B + coenzyme M + methylene blue
-
Methanosarcina barkeri N-(7-[(2-sulfoethyl)dithio]heptanoyl)-3-O-phospho-L-threonine + reduced methylene blue
-
?
N-(7-[(2-sulfoethyl)dithio]heptanoyl)-3-O-phospho-L-threonine + H2
-
Methanosarcina barkeri coenzyme B + coenzyme M
-
?
N-(7-[(2-sulfoethyl)dithio]heptanoyl)-3-O-phospho-L-threonine + reduced methylviologen
-
Methanosarcina barkeri coenzyme B + coenzyme M + methyl viologen
-
?

Subunits

Subunits Comment Organism
? x * 46000 + x * 23000, the 23000 Da subunit is cytochrome b, SDS-PAGE Methanosarcina barkeri

Temperature Optimum [°C]

Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
50
-
-
Methanosarcina barkeri

pH Range

pH Minimum pH Maximum Comment Organism
5 7.5 activity with reduced benzyl viologen and N-(7-[(2-sulfoethyl)dithio]heptanoyl)-3-O-phospho-L-threonine increases continously with decreasing pH in the range between pH 7.5 and pH 5.0 Methanosarcina barkeri

Cofactor

Cofactor Comment Organism Structure
cytochrome b the 23000 Da subunit is the cytochrome b, cytochrome b serves as electron donor for the heterodisulfide reduction Methanosarcina barkeri
FAD the enzyme contains 3 mol of FAD per mg of protein Methanosarcina barkeri