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Literature summary for 3.4.24.37 extracted from

  • Bolumar, T.; Sanz, Y.; Aristoy, M.C.; Toldra, F.
    Purification and characterisation of proteases A and D from Debaryomyces hansenii (2008), Int. J. Food Microbiol., 124, 135-141.
    View publication on PubMed

Activating Compound

Activating Compound Comment Organism Structure
iodoacetate 11% activation at 1 mM Debaryomyces hansenii

Inhibitors

Inhibitors Comment Organism Structure
1,10-phenanthroline complete inhibition at 0.1 mM Debaryomyces hansenii
2-mercaptoethanol 19% inhibition at 5 mM Debaryomyces hansenii
3,4-dichloroisocoumarin 71% inhibition at 1 mM Debaryomyces hansenii
4-chloromercuribenzoate complete inhibition at 0.1 mM Debaryomyces hansenii
Cd2+ 33% inhibition at 0.5 mM Debaryomyces hansenii
DTT 19% inhibition at 1 mM Debaryomyces hansenii
EGTA 35% inhibition at 5 mM Debaryomyces hansenii
Hg2+ complete inhibition at 0.05 mM Debaryomyces hansenii
Mg2+ 21% inhibition at 0.5 mM Debaryomyces hansenii
additional information no inhibition by EDTA at 5 mM Debaryomyces hansenii
pepstatin A 15% inhibition at 1 mM Debaryomyces hansenii
PMSF 50% inhibition at 1 mM Debaryomyces hansenii
Zn2+ 73% inhibition at 0.5 mM Debaryomyces hansenii

Metals/Ions

Metals/Ions Comment Organism Structure
additional information metalloprotease, not affeted by Cu2+, Co2+, Mn2+, and Ca2+ Debaryomyces hansenii

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
65000
-
1 * 65000, SDS-PAGE Debaryomyces hansenii
68000
-
gel filtration Debaryomyces hansenii

Organism

Organism UniProt Comment Textmining
Debaryomyces hansenii
-
isolated from the natural microflora of fermented sausages and selected as possible starter culture on the basis of its physiological and biochemical properties and its ability to compete during sausage manufacturing processes
-
Debaryomyces hansenii CECT 12487
-
isolated from the natural microflora of fermented sausages and selected as possible starter culture on the basis of its physiological and biochemical properties and its ability to compete during sausage manufacturing processes
-

Purification (Commentary)

Purification (Comment) Organism
native enzyme 2560fold by fractionation with protamine sulfate, anion exchange chromatography on a weak followed by a strong anion exchange resin, and gel filtration Debaryomyces hansenii

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
N-succinyl-Leu-Tyr-7-amido-4-methylcoumarin + H2O
-
Debaryomyces hansenii N-succinyl-Leu-Tyr + 7-amino-4-methylcoumarin
-
?
N-succinyl-Leu-Tyr-7-amido-4-methylcoumarin + H2O
-
Debaryomyces hansenii CECT 12487 N-succinyl-Leu-Tyr + 7-amino-4-methylcoumarin
-
?
N-succinyl-Leu-Tyr-7-amido-4-methylcoumarin + H2O
-
Debaryomyces hansenii CECT12487 N-succinyl-Leu-Tyr + 7-amino-4-methylcoumarin
-
?

Subunits

Subunits Comment Organism
monomer 1 * 65000, SDS-PAGE Debaryomyces hansenii

Synonyms

Synonyms Comment Organism
PrD
-
Debaryomyces hansenii
protease D
-
Debaryomyces hansenii

Temperature Optimum [°C]

Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
37
-
assay at Debaryomyces hansenii

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
7 8
-
Debaryomyces hansenii