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Literature summary extracted from

  • Sun, H.; Gao, W.; Fan, H.; Wang, H.; Wei, D.
    Cloning, purification and evaluation of the enzymatic properties of a novel arylacetonitrilase from Luminiphilus syltensis NOR5-1B: a potential biocatalyst for the synthesis of mandelic acid and its derivatives (2015), Biotechnol. Lett., 37, 1655-1661.
    View publication on PubMed

Cloned(Commentary)

EC Number Cloned (Comment) Organism
3.5.5.5 expressed in Escherichia coli BL21(DE3) cells Luminiphilus syltensis

KM Value [mM]

EC Number KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
3.5.5.5 0.38
-
2-chloromandelonitrile at pH 7.0 and 30°C Luminiphilus syltensis

Molecular Weight [Da]

EC Number Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
3.5.5.5 43000
-
x * 43000, SDS-PAGE Luminiphilus syltensis

Organism

EC Number Organism UniProt Comment Textmining
3.5.5.5 Luminiphilus syltensis
-
-
-
3.5.5.5 Luminiphilus syltensis NOR5-1B
-
-
-

Purification (Commentary)

EC Number Purification (Comment) Organism
3.5.5.5 Ni-NTA column chromatography Luminiphilus syltensis

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3.5.5.5 (2-bromophenyl)(hydroxy)acetonitrile + H2O 74% activity compared to phenylacetonitrile Luminiphilus syltensis (2R)-(2-bromophenyl)(hydroxy)acetic acid + NH3
-
?
3.5.5.5 (2-fluorophenyl)(hydroxy)acetonitrile + H2O 439% activity compared to phenylacetonitrile Luminiphilus syltensis (2R)-(2-fluorophenyl)(hydroxy)acetic acid + NH3
-
?
3.5.5.5 (3-bromophenyl)(hydroxy)acetonitrile + H2O 706% activity compared to phenylacetonitrile Luminiphilus syltensis (2R)-(3-bromophenyl)(hydroxy)acetic acid + NH3
-
?
3.5.5.5 (3-chlorophenyl)(hydroxy)acetonitrile + H2O 810% activity compared to phenylacetonitrile Luminiphilus syltensis (2R)-(3-chlorophenyl)(hydroxy)acetic acid + NH3
-
?
3.5.5.5 (3-fluorophenyl)(hydroxy)acetonitrile + H2O 454% activity compared to phenylacetonitrile Luminiphilus syltensis (2R)-(3-fluorophenyl)(hydroxy)acetic acid + NH3
-
?
3.5.5.5 (4-bromophenyl)(hydroxy)acetonitrile + H2O 680% activity compared to phenylacetonitrile Luminiphilus syltensis (2R)-(4-bromophenyl)(hydroxy)acetic acid + NH3
-
?
3.5.5.5 (4-chlorophenyl)(hydroxy)acetonitrile + H2O 1083% activity compared to phenylacetonitrile Luminiphilus syltensis (2R)-(4-chlorophenyl)(hydroxy)acetic acid + NH3
-
?
3.5.5.5 (4-fluorophenyl)(hydroxy)acetonitrile + H2O 891% activity compared to phenylacetonitrile Luminiphilus syltensis (2R)-(4-fluorophenyl)(hydroxy)acetic acid + NH3
-
?
3.5.5.5 1,2-phenylenediacetonitrile + H2O 1.87% activity compared to phenylacetonitrile Luminiphilus syltensis 1,2-phenylenediacetic acid + NH3
-
?
3.5.5.5 2-chloromandelonitrile + H2O 33.75% activity compared to phenylacetonitrile Luminiphilus syltensis (R)-2-chloromandelic acid + NH3 enantioselectivity ee 98.2% ?
3.5.5.5 2-cyanopyridine + 2 H2O 101% activity compared to phenylacetonitrile Luminiphilus syltensis pyridine 2-carboxylic acid + NH3
-
?
3.5.5.5 2-methylglutaronitrile + 4 H2O 0.12% activity compared to phenylacetonitrile Luminiphilus syltensis 2-methylglutaric acid + 2 NH3
-
?
3.5.5.5 2-phenylbutyronitrile + H2O 0.2% activity compared to phenylacetonitrile Luminiphilus syltensis 2-phenylbutyric acid + NH3
-
?
3.5.5.5 3-cyanopyridine + 2 H2O 43.2% activity compared to phenylacetonitrile Luminiphilus syltensis pyridine 3-carboxylic acid + NH3
-
?
3.5.5.5 3-hydroxyglutaronitrile + 4 H2O 0.12% activity compared to phenylacetonitrile Luminiphilus syltensis 3-hydroxyglutaric acid + 2 NH3
-
?
3.5.5.5 3-hydroxyphenylpropionitrile + H2O 0.12% activity compared to phenylacetonitrile Luminiphilus syltensis 3-hydroxyphenylpropionic acid + NH3
-
?
3.5.5.5 3-hydroxypropionitrile + H2O 0.07% activity compared to phenylacetonitrile Luminiphilus syltensis 3-hydroxypropionic acid + NH3
-
?
3.5.5.5 4-chlorobutyronitrile + H2O 0.06% activity compared to phenylacetonitrile Luminiphilus syltensis 4-chlorobutyric acid + NH3
-
?
3.5.5.5 4-cyanopyridine + 2 H2O 142% activity compared to phenylacetonitrile Luminiphilus syltensis pyridine 4-carboxylic acid + NH3
-
?
3.5.5.5 acrylonitrile + H2O 0.05% activity compared to phenylacetonitrile Luminiphilus syltensis acrylic acid + NH3
-
?
3.5.5.5 acrylonitrile + H2O 0.05% activity compared to phenylacetonitrile Luminiphilus syltensis NOR5-1B acrylic acid + NH3
-
?
3.5.5.5 alpha-methylphenylacetonitrile + H2O 0.14% activity compared to phenylacetonitrile Luminiphilus syltensis alpha-methylphenylacetic acid + NH3
-
?
3.5.5.5 benzonitrile + 2 H2O 21% activity compared to phenylacetonitrile Luminiphilus syltensis benzoic acid + NH3
-
?
3.5.5.5 cinnamonitrile + H2O 0.07% activity compared to phenylacetonitrile Luminiphilus syltensis cinnamic acid + NH3
-
?
3.5.5.5 dodecanenitrile + H2O 0.04% activity compared to phenylacetonitrile Luminiphilus syltensis dodecanoic acid + NH3
-
?
3.5.5.5 fumaronitrile + H2O 0.72% activity compared to phenylacetonitrile Luminiphilus syltensis fumaric acid + NH3
-
?
3.5.5.5 fumaronitrile + H2O 0.72% activity compared to phenylacetonitrile Luminiphilus syltensis NOR5-1B fumaric acid + NH3
-
?
3.5.5.5 glycolonitrile + H2O 0.08% activity compared to phenylacetonitrile Luminiphilus syltensis glycolic acid + NH3
-
?
3.5.5.5 hydroxy(2-methoxyphenyl)acetonitrile + H2O 178% activity compared to phenylacetonitrile Luminiphilus syltensis (2R)-hydroxy(2-methoxyphenyl)acetic acid + NH3
-
?
3.5.5.5 hydroxy(2-methylphenyl)acetonitrile + H2O 194% activity compared to phenylacetonitrile Luminiphilus syltensis (2R)-hydroxy(2-methylphenyl)acetic acid + NH3
-
?
3.5.5.5 hydroxy(phenyl)acetonitrile + H2O 404% activity compared to phenylacetonitrile Luminiphilus syltensis (2R)-hydroxy(phenyl)acetic acid + NH3
-
?
3.5.5.5 iminodiacetonitrile + 2 H2O 0.05% activity compared to phenylacetonitrile Luminiphilus syltensis iminodiacetic acid + 2 NH3
-
?
3.5.5.5 iminodiacetonitrile + 2 H2O 0.05% activity compared to phenylacetonitrile Luminiphilus syltensis NOR5-1B iminodiacetic acid + 2 NH3
-
?
3.5.5.5 indole-3-acetonitrile + H2O 35% activity compared to phenylacetonitrile Luminiphilus syltensis indole-3-acetic acid + NH3
-
?
3.5.5.5 malononitrile + H2O 3.7% activity compared to phenylacetonitrile Luminiphilus syltensis malonic acid + NH3
-
?
3.5.5.5 malononitrile + H2O 3.7% activity compared to phenylacetonitrile Luminiphilus syltensis NOR5-1B malonic acid + NH3
-
?
3.5.5.5 mandelonitrile + 2 H2O best substrate, 164% activity compared to phenylacetonitrile Luminiphilus syltensis mandelic acid + NH3
-
?
3.5.5.5 mandelonitrile + 2 H2O best substrate, 164% activity compared to phenylacetonitrile Luminiphilus syltensis NOR5-1B mandelic acid + NH3
-
?
3.5.5.5 octanedinitrile + H2O 0.14% activity compared to phenylacetonitrile Luminiphilus syltensis ? + NH3
-
?
3.5.5.5 succinonitrile + H2O 0.12% activity compared to phenylacetonitrile Luminiphilus syltensis succinic acid + NH3
-
?
3.5.5.5 valeronitrile + H2O 0.08% activity compared to phenylacetonitrile Luminiphilus syltensis valeric acid + NH3
-
?

Subunits

EC Number Subunits Comment Organism
3.5.5.5 ? x * 43000, SDS-PAGE Luminiphilus syltensis

Synonyms

EC Number Synonyms Comment Organism
3.5.5.5 arylacetonitrile-specific nitrilase
-
Luminiphilus syltensis
3.5.5.5 GPnor51
-
Luminiphilus syltensis

Temperature Optimum [°C]

EC Number Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
3.5.5.5 40
-
-
Luminiphilus syltensis

Temperature Range [°C]

EC Number Temperature Minimum [°C] Temperature Maximum [°C] Comment Organism
3.5.5.5 30 45 more than half maximal activity at 30 and 45°C Luminiphilus syltensis

Temperature Stability [°C]

EC Number Temperature Stability Minimum [°C] Temperature Stability Maximum [°C] Comment Organism
3.5.5.5 50
-
the enzyme retains 50% of its initial activity after incubation at 50°C for 30 min Luminiphilus syltensis

pH Optimum

EC Number pH Optimum Minimum pH Optimum Maximum Comment Organism
3.5.5.5 7
-
-
Luminiphilus syltensis