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Literature summary for 3.5.5.1 extracted from

  • Singh, R.; Sharma, R.; Tewari, N.; Tewari, N.; Rawat, D.S.
    Nitrilase and its application as a green catalyst (2006), Chem. Biodivers., 3, 1279-1287.
    View publication on PubMed
Search for more literature for 3.5.5.1

Application

Application Comment Organism
synthesis attractive as green, mild, and selective catalysts for setting stereogenic centers in fine-chemical synthesis and enantiospecific synthesis of a variety of carboxylic acid derivatives Alcaligenes faecalis
synthesis attractive as green, mild, and selective catalysts for setting stereogenic centers in fine-chemical synthesis and enantiospecific synthesis of a variety of carboxylic acid derivatives Hordeum vulgare
synthesis attractive as green, mild, and selective catalysts for setting stereogenic centers in fine-chemical synthesis and enantiospecific synthesis of a variety of carboxylic acid derivatives Arabidopsis thaliana
synthesis attractive as green, mild, and selective catalysts for setting stereogenic centers in fine-chemical synthesis and enantiospecific synthesis of a variety of carboxylic acid derivatives Rhodococcus rhodochrous
synthesis attractive as green, mild, and selective catalysts for setting stereogenic centers in fine-chemical synthesis and enantiospecific synthesis of a variety of carboxylic acid derivatives Pseudomonas sp.
synthesis attractive as green, mild, and selective catalysts for setting stereogenic centers in fine-chemical synthesis and enantiospecific synthesis of a variety of carboxylic acid derivatives Klebsiella pneumoniae
synthesis attractive as green, mild, and selective catalysts for setting stereogenic centers in fine-chemical synthesis and enantiospecific synthesis of a variety of carboxylic acid derivatives Bacillus sp. (in: Bacteria)
synthesis attractive as green, mild, and selective catalysts for setting stereogenic centers in fine-chemical synthesis and enantiospecific synthesis of a variety of carboxylic acid derivatives Comamonas testosteroni
synthesis attractive as green, mild, and selective catalysts for setting stereogenic centers in fine-chemical synthesis and enantiospecific synthesis of a variety of carboxylic acid derivatives Rhodococcus sp.
synthesis attractive as green, mild, and selective catalysts for setting stereogenic centers in fine-chemical synthesis and enantiospecific synthesis of a variety of carboxylic acid derivatives Acinetobacter sp.
synthesis attractive as green, mild, and selective catalysts for setting stereogenic centers in fine-chemical synthesis and enantiospecific synthesis of a variety of carboxylic acid derivatives Acidovorax facilis
synthesis attractive as green, mild, and selective catalysts for setting stereogenic centers in fine-chemical synthesis and enantiospecific synthesis of a variety of carboxylic acid derivatives Fusarium solani
synthesis attractive as green, mild, and selective catalysts for setting stereogenic centers in fine-chemical synthesis and enantiospecific synthesis of a variety of carboxylic acid derivatives Fusarium oxysporum
synthesis attractive as green, mild, and selective catalysts for setting stereogenic centers in fine-chemical synthesis and enantiospecific synthesis of a variety of carboxylic acid derivatives Penicillium multicolor
synthesis attractive as green, mild, and selective catalysts for setting stereogenic centers in fine-chemical synthesis and enantiospecific synthesis of a variety of carboxylic acid derivatives Aeribacillus pallidus

Organism

Organism UniProt Comment Textmining
Acidovorax facilis
-
-
-
Acidovorax facilis 72W
-
-
-
Acinetobacter sp.
-
-
-
Acinetobacter sp. AK226
-
-
-
Aeribacillus pallidus
-
-
-
Aeribacillus pallidus Dac521
-
-
-
Alcaligenes faecalis
-
 strain ATCC 8750
-
Arabidopsis thaliana
-
-
-
Bacillus sp. (in: Bacteria)
-
-
-
Bacillus sp. (in: Bacteria) OxB-1
-
-
-
Comamonas testosteroni
-
-
-
Fusarium oxysporum
-
-
-
Fusarium solani
-
-
-
Fusarium solani IMI196840
-
-
-
Hordeum vulgare
-
-
-
Klebsiella pneumoniae
-
-
-
Penicillium multicolor
-
-
-
Pseudomonas sp.
-
 strain DSM 7155
-
Rhodococcus rhodochrous
-
-
-
Rhodococcus rhodochrous
-
 strains PA-34 and JI
-
Rhodococcus rhodochrous K22
-
-
-
Rhodococcus sp.
-
 strains NCIB11215, ATCC39484, and NCIB11216
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
(E/Z)-2-methylbut-2-enenitrile + H2O
-
 Rhodococcus rhodochrous (E)-2-methylbut-2-enoic acid + NH3
-
 ?
(E/Z)-2-methylbut-2-enenitrile + H2O
-
 Comamonas testosteroni (E)-2-methylbut-2-enoic acid + NH3
-
 ?
(E/Z)-2-methylbut-2-enenitrile + H2O
-
 Acidovorax facilis (E)-2-methylbut-2-enoic acid + NH3
-
 ?
(E/Z)-2-methylbut-2-enenitrile + H2O
-
 Rhodococcus rhodochrous K22 (E)-2-methylbut-2-enoic acid + NH3
-
 ?
(E/Z)-2-methylbut-2-enenitrile + H2O
-
 Acidovorax facilis 72W (E)-2-methylbut-2-enoic acid + NH3
-
 ?
2-methylglutaronitrile + 2 H2O
-
 Rhodococcus rhodochrous 4-cyanopentanoic acid + NH3
-
 ?
2-methylglutaronitrile + 2 H2O
-
 Rhodococcus rhodochrous K22 4-cyanopentanoic acid + NH3
-
 ?
3-hydroxyglutaronitrile + 2 H2O
-
 Rhodococcus rhodochrous (R)-3-hydroxy-4-cyanobutanoic acid + NH3
-
 ?
3-phenylpropanenitrile + H2O
-
 Arabidopsis thaliana phenylacetic acid + NH3
-
 ?
3-phenylpropanenitrile + H2O
-
 Rhodococcus rhodochrous phenylacetic acid + NH3
-
 ?
3-trans-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dienyl]prop-2-enenitrile + H2O
-
 Arabidopsis thaliana (2E)-3-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dien-1-yl]prop-2-enoic acid + NH3
-
 ?
3-trans-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dienyl]prop-2-enenitrile + H2O
-
 Rhodococcus rhodochrous (2E)-3-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dien-1-yl]prop-2-enoic acid + NH3
-
 ?
3-trans-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dienyl]prop-2-enenitrile + H2O
-
 Rhodococcus sp. (2E)-3-[(5S,6R)-5,6-dihydroxycyclohexa-1,3-dien-1-yl]prop-2-enoic acid + NH3
-
 ?
benzonitrile + 2 H2O
-
 Hordeum vulgare benzoic acid + NH3
-
 ?
benzonitrile + 2 H2O
-
 Rhodococcus rhodochrous benzoic acid + NH3
-
 ?
benzonitrile + 2 H2O
-
 Pseudomonas sp. benzoic acid + NH3
-
 ?
benzonitrile + 2 H2O
-
 Klebsiella pneumoniae benzoic acid + NH3
-
 ?
benzonitrile + 2 H2O
-
 Bacillus sp. (in: Bacteria) benzoic acid + NH3
-
 ?
benzonitrile + 2 H2O
-
 Rhodococcus sp. benzoic acid + NH3
-
 ?
benzonitrile + 2 H2O
-
 Acinetobacter sp. benzoic acid + NH3
-
 ?
benzonitrile + 2 H2O
-
 Fusarium solani benzoic acid + NH3
-
 ?
benzonitrile + 2 H2O
-
 Fusarium oxysporum benzoic acid + NH3
-
 ?
benzonitrile + 2 H2O
-
 Penicillium multicolor benzoic acid + NH3
-
 ?
benzonitrile + 2 H2O
-
 Aeribacillus pallidus benzoic acid + NH3
-
 ?
benzonitrile + 2 H2O
-
 Fusarium solani IMI196840 benzoic acid + NH3
-
 ?
benzonitrile + 2 H2O
-
 Acinetobacter sp. AK226 benzoic acid + NH3
-
 ?
benzonitrile + 2 H2O
-
 Bacillus sp. (in: Bacteria) OxB-1 benzoic acid + NH3
-
 ?
benzonitrile + 2 H2O
-
 Rhodococcus rhodochrous K22 benzoic acid + NH3
-
 ?
benzonitrile + 2 H2O
-
 Aeribacillus pallidus Dac521 benzoic acid + NH3
-
 ?
cis-5,6-dihydroxy-cyclohexa-1,3-diene-1-carbonitrile + H2O
-
 Rhodococcus rhodochrous (5R,6S)-5,6-dihydroxycyclohexa-1,3-diene-1-carboxylic acid + NH3
-
 ?
cis-5,6-dihydroxy-cyclohexa-1,3-diene-1-carbonitrile + H2O
-
 Rhodococcus sp. (5R,6S)-5,6-dihydroxycyclohexa-1,3-diene-1-carboxylic acid + NH3
-
 ?
indole-3-acetonitrile + H2O the reaction is catalyzed by the branch 1 of the nitrilase superfamily Rhodococcus rhodochrous indole-3-acetic acid + NH3
-
 ?
indole-3-acetonitrile + H2O the reaction is catalyzed by the branch 1 of the nitrilase superfamily Rhodococcus rhodochrous K22 indole-3-acetic acid + NH3
-
 ?
mandelonitrile + 2 H2O
-
 Alcaligenes faecalis (R)-mandelic acid + NH3
-
 ?
mandelonitrile + 2 H2O
-
 Rhodococcus rhodochrous (R)-mandelic acid + NH3
-
 ?
mandelonitrile + 2 H2O
-
 Rhodococcus rhodochrous K22 (R)-mandelic acid + NH3
-
 ?
additional information does not convert cis-5,6-dihydroxy-cyclohexa-1,3-diene-1-carbonitrile Arabidopsis thaliana ?
-
 ?

Synonyms

Synonyms Comment Organism
NIT1
-
 Arabidopsis thaliana
NIT2
-
 Arabidopsis thaliana
NIT3
-
 Arabidopsis thaliana