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Literature summary for 3.5.1.137 extracted from

  • Chaudhry, G.R.; Mateen, A.; Kaskar, B.; Bloda, M.; Riazuddin, S.
    Purification and biochemical characterization of the carbamate hydrolase from Pseudomonas sp. 50432 (2002), Biotechnol. Appl. Biochem., 36, 63-70 .
    View publication on PubMed

General Stability

General Stability Organism
the enzyme is stable in Triton X-100 and other detergents such as CHAPS Pseudomonas sp. 50432

Inhibitors

Inhibitors Comment Organism Structure
2-mercaptoethanol the enzyme shows 10% activity in the presence of 0.1% (v/v) 2-mercaptoethanol. Higher concentrations completely inactivate the enzyme. However, the activity of the enzyme is recovered when 2-mercaptoethanol was removed by dialysis Pseudomonas sp. 50432
dithiothreitol the enzyme shows 10% activity in the presence of 0.1% (v/v) dithiothreitol. Higher concentrations completely inactivate the enzyme Pseudomonas sp. 50432
additional information EDTA does not affect the enzyme activity Pseudomonas sp. 50432

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
0.012
-
Carbaryl at pH 7.0 and 25°C Pseudomonas sp. 50432
0.016
-
carbofuran at pH 7.0 and 25°C Pseudomonas sp. 50432

Localization

Localization Comment Organism GeneOntology No. Textmining
cytosol
-
Pseudomonas sp. 50432 5829
-

Metals/Ions

Metals/Ions Comment Organism Structure
additional information cations do not affect the enzyme activity Pseudomonas sp. 50432

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
88000
-
gel filtration Pseudomonas sp. 50432

Organism

Organism UniProt Comment Textmining
Pseudomonas sp. 50432
-
-
-

Purification (Commentary)

Purification (Comment) Organism
DEAE-cellulose column chromatography, Sephadex G-200 gel filtration, and Macro-prep tert-butyl column chromatography Pseudomonas sp. 50432

Specific Activity [micromol/min/mg]

Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
0.5
-
crude cell extract, at pH 7.0 and 25°C Pseudomonas sp. 50432
1016
-
after 2032fold purification, at pH 7.0 and 25°C Pseudomonas sp. 50432

Storage Stability

Storage Stability Organism
-20 or -70°C, purified enzyme in 10 mM K2HPO4 (pH 7.5) in the presence of 20% (v/v) glycerol, 1 month, no loss of activity Pseudomonas sp. 50432
4°C, purified enzyme in 10 mM K2HPO4 (pH 7.5), 1 month, 25% loss of activity Pseudomonas sp. 50432
4°C, purified enzyme in 10 mM K2HPO4 (pH 7.5), 1 week, no loss of activity Pseudomonas sp. 50432

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1-naphthyl acetate + H2O
-
Pseudomonas sp. 50432 1-naphthol + acetate
-
?
carbaryl + H2O
-
Pseudomonas sp. 50432 1-naphthol + methylamine + CO2
-
?
carbofuran + H2O
-
Pseudomonas sp. 50432 7-phenol + methylamine + CO2
-
?
additional information the purified enzyme does not hydrolyze 2-nitrophenyl dimethylcarbamate Pseudomonas sp. 50432 ?
-
-

Subunits

Subunits Comment Organism
monomer 1 * 88000, SDS-PAGE Pseudomonas sp. 50432

Synonyms

Synonyms Comment Organism
carbamate hydrolase
-
Pseudomonas sp. 50432
carbofuran hydrolase
-
Pseudomonas sp. 50432

Temperature Optimum [°C]

Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
37
-
-
Pseudomonas sp. 50432

Temperature Stability [°C]

Temperature Stability Minimum [°C] Temperature Stability Maximum [°C] Comment Organism
60
-
when heated at 60°C for 5 min, the catalytic activity of the enzyme is completely lost Pseudomonas sp. 50432

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
8.5
-
-
Pseudomonas sp. 50432

pI Value

Organism Comment pI Value Maximum pI Value
Pseudomonas sp. 50432 isoelectric focusing
-
6.9