Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 4.2.1.103 extracted from

  • Sato, H.; Hashimoto, Y.; Fukatsu, H.; Kobayashi, M.
    Novel isonitrile hydratase involved in isonitrile metabolism (2010), J. Biol. Chem., 285, 34793-34802.
    View publication on PubMedView publication on EuropePMC

Cloned(Commentary)

Cloned (Comment) Organism
InhB, DNA and amino acid sequence determination and analysis, cloning and expression in Escherichia coli strain DH10B Arthrobacter pascens

Inhibitors

Inhibitors Comment Organism Structure
4-chloromercuribenzoate 99.8% inhibition at 1 mM Arthrobacter pascens
5,5'-dithiobis-(2-nitrobenzoate) 34.9% inhibition at 1 mM Arthrobacter pascens
8-hydroxyquinoline 26.1% inhibition at 1 mM Arthrobacter pascens
Ag+ complete inhibition at 1 mM Arthrobacter pascens
Al3+ 21.4% inhibition at 1 mM Arthrobacter pascens
Cd2+ 71.6% inhibition at 1 mM Arthrobacter pascens
Co2+ 89.5% inhibition at 1 mM Arthrobacter pascens
Cu2+ complete inhibition at 1 mM Arthrobacter pascens
Fe2+ 7.6% inhibition at 1 mM Arthrobacter pascens
Fe3+ 19.7% inhibition at 1 mM Arthrobacter pascens
H2O2 45.0% inhibition at 1 mM Arthrobacter pascens
Hg2+ complete inhibition at 1 mM Arthrobacter pascens
additional information the hydrophilic thiol reagent iodoacetate does not influence the enzyme activity. No inhibition by LiCl, NaCl, MgCl, CaCl2, MnCl2, RbCl, CsCl, SrCl2, hydroxylamine, phenylhydrazine, semicarbazide, aminoguanidine, 2,2'-dipyridyl, o-phenanthroline, EDTA, diethyldithiocarbamate, KCN, dithiothreitol, 2-mercaptoethanol, Na2S2O4, and diisopropyl fluorophosphate, poor inhibition by Na2MoO4, ammonium persulfate, and NaN3 Arthrobacter pascens
N-ethylmaleimide 48.1% inhibition at 1 mM Arthrobacter pascens
Ni2+ 95.0% inhibition at 1 mM Arthrobacter pascens
Pb2+ 11.9% inhibition at 1 mM Arthrobacter pascens
PMSF 49.4% inhibition at 1 mM Arthrobacter pascens
Sn2+ 41.7% inhibition at 1 mM Arthrobacter pascens
Zn2+ 51.9% inhibition at 1 mM Arthrobacter pascens

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
additional information
-
additional information Michaelis-Menten-type kinetics Arthrobacter pascens
0.95
-
cyclohexyl isocyanide pH 7.5, 25°C Arthrobacter pascens

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
43000
-
12 * 43000, SDS-PAGE Arthrobacter pascens
530000
-
gel filtration Arthrobacter pascens

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
cyclohexyl isocyanide + H2O Arthrobacter pascens
-
N-cyclohexyl formamide
-
?
cyclohexyl isocyanide + H2O Arthrobacter pascens F164
-
N-cyclohexyl formamide
-
?

Organism

Organism UniProt Comment Textmining
Arthrobacter pascens E1CJF8
-
-
Arthrobacter pascens F164 E1CJF8
-
-

Purification (Commentary)

Purification (Comment) Organism
native enzyme 14.6fold by ammonium sulfate fractionation followed by two steps of hydrophobic interaction chromatography Arthrobacter pascens

Source Tissue

Source Tissue Comment Organism Textmining
cell culture the enzyme is expressed in cells growing on isonitrile as the sole carbon and nitrogen sources, highest enzyme activity is strain F164 in a nutrient medium containing N-benzylformamide. No induction by growth on glycerol and (NH4)2SO4 as the sole carbon and nitrogen sources, respectively Arthrobacter pascens
-

Specific Activity [micromol/min/mg]

Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
0.935
-
purified enzyme, substrate is cyclohexyl isocyanide, pH 7.5, 25°C Arthrobacter pascens

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1-pentyl isocyanide + H2O
-
Arthrobacter pascens N-1-pentylformamide
-
?
1-pentyl isocyanide + H2O
-
Arthrobacter pascens F164 N-1-pentylformamide
-
?
benzyl isocyanide + H2O
-
Arthrobacter pascens N-benzylformamide
-
?
benzyl isocyanide + H2O
-
Arthrobacter pascens F164 N-benzylformamide
-
?
cyclohexyl isocyanide + H2O
-
Arthrobacter pascens N-cyclohexyl formamide
-
?
cyclohexyl isocyanide + H2O the substrate is partly decomposed into N-cyclohexylformamide on spontaneous and chemical, nonenzymatic reaction under acidic conditions under pH 6.0, but is over pH 6.5 Arthrobacter pascens N-cyclohexyl formamide
-
?
cyclohexyl isocyanide + H2O
-
Arthrobacter pascens F164 N-cyclohexyl formamide
-
?
cyclohexyl isocyanide + H2O the substrate is partly decomposed into N-cyclohexylformamide on spontaneous and chemical, nonenzymatic reaction under acidic conditions under pH 6.0, but is over pH 6.5 Arthrobacter pascens F164 N-cyclohexyl formamide
-
?
ethyl isocyanoacetate + H2O
-
Arthrobacter pascens N-formylglycine ethyl ester
-
?
methyl isocyanoacetate + H2O
-
Arthrobacter pascens N-formylglycine methyl ester
-
?
additional information substrate specificity, isocyanomethyl phosphonic acid diethyl ether is a poor substrate giving isocyanomethyl phosphonic acid diethyl ether, overview Arthrobacter pascens ?
-
?
additional information substrate specificity, isocyanomethyl phosphonic acid diethyl ether is a poor substrate giving isocyanomethyl phosphonic acid diethyl ether, overview Arthrobacter pascens F164 ?
-
?
tert-butyl isocyanide + H2O
-
Arthrobacter pascens N-tert-butylformamide
-
?

Subunits

Subunits Comment Organism
dodecamer 12 * 43000, SDS-PAGE Arthrobacter pascens

Synonyms

Synonyms Comment Organism
InhB
-
Arthrobacter pascens
isonitrile hydratase
-
Arthrobacter pascens

Temperature Optimum [°C]

Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
25
-
assay at Arthrobacter pascens

Temperature Stability [°C]

Temperature Stability Minimum [°C] Temperature Stability Maximum [°C] Comment Organism
35 40 most stable at 35°C, enzyme activity is rapidly lost above 40°C Arthrobacter pascens

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
7.5
-
assay at Arthrobacter pascens

pH Stability

pH Stability pH Stability Maximum Comment Organism
5.5 9.7 most stable in the range of pH 5.5-9.7 Arthrobacter pascens

Expression

Organism Comment Expression
Arthrobacter pascens the enzyme is induced by N-benzylformamide and isonitriles benzyl isocyanide and cyclohexyl isocyanide, while benzylamine and N-benzylacetamide do not induce isonitrile hydratase activity up

General Information

General Information Comment Organism
metabolism isonitrile hydratase is involved in the first step of isonitrile metabolism hydrating isonitrile to the corresponding N-substituted formamide Arthrobacter pascens