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Literature summary for 4.2.1.53 extracted from

  • Hiseni, A.; Arends, I.; Otten, L.
    New cofactor-independent hydration biocatalysts Structural, biochemical, and biocatalytic characteristics of carotenoid and oleate hydratases (2015), ChemCatChem, 7, 29-37 .
No PubMed abstract available

Application

Application Comment Organism
synthesis (R)-10-hydroxyoctadecanoic acid, produced by the oleate hydratase is a precursor for gamma-dodecalactone which is an important fragrance and flavour compound Lactobacillus acidophilus
synthesis (R)-10-hydroxyoctadecanoic acid, produced by the oleate hydratase is a precursor for gamma-dodecalactone which is an important fragrance and flavour compound Stenotrophomonas maltophilia
synthesis (R)-10-hydroxyoctadecanoic acid, produced by the oleate hydratase is a precursor for gamma-dodecalactone which is an important fragrance and flavour compound Elizabethkingia meningoseptica
synthesis (R)-10-hydroxyoctadecanoic acid, produced by the oleate hydratase is a precursor for gamma-dodecalactone which is an important fragrance and flavour compound Macrococcus caseolyticus
synthesis (R)-10-hydroxyoctadecanoic acid, produced by the oleate hydratase is a precursor for gamma-dodecalactone which is an important fragrance and flavour compound Streptococcus pyogenes
synthesis (R)-10-hydroxyoctadecanoic acid, produced by the oleate hydratase is a precursor for gamma-dodecalactone which is an important fragrance and flavour compound Lysinibacillus fusiformis
synthesis (R)-10-hydroxyoctadecanoic acid, produced by the oleate hydratase is a precursor for gamma-dodecalactone which is an important fragrance and flavour compound Lacticaseibacillus rhamnosus
synthesis (R)-10-hydroxyoctadecanoic acid, produced by the oleate hydratase is a precursor for gamma-dodecalactone which is an important fragrance and flavour compound Lactiplantibacillus plantarum
synthesis (R)-10-hydroxyoctadecanoic acid, produced by the oleate hydratase is a precursor for gamma-dodecalactone which is an important fragrance and flavour compound Bifidobacterium breve
synthesis (R)-10-hydroxyoctadecanoic acid, produced by the oleate hydratase is a precursor for gamma-dodecalactone which is an important fragrance and flavour compound Bifidobacterium animalis subsp. lactis
synthesis one of the largest bottlenecks in producing lactones is the hydroxylation of the fatty acids. The exploitation of oleate hydratase to hydrate oleic acid, which can easily be turned into gamma-dodecalactone after beta-elimination, is therefore the perfect solution to produce this valuable compound from cheap renewable materials (e.g. vegetable oil). The specificity and enantioselectivity of the enzyme will provide the correct lactone Lactobacillus acidophilus
synthesis one of the largest bottlenecks in producing lactones is the hydroxylation of the fatty acids. The exploitation of oleate hydratase to hydrate oleic acid, which can easily be turned into gamma-dodecalactone after beta-elimination, is therefore the perfect solution to produce this valuable compound from cheap renewable materials (e.g. vegetable oil). The specificity and enantioselectivity of the enzyme will provide the correct lactone Stenotrophomonas maltophilia
synthesis one of the largest bottlenecks in producing lactones is the hydroxylation of the fatty acids. The exploitation of oleate hydratase to hydrate oleic acid, which can easily be turned into gamma-dodecalactone after beta-elimination, is therefore the perfect solution to produce this valuable compound from cheap renewable materials (e.g. vegetable oil). The specificity and enantioselectivity of the enzyme will provide the correct lactone Elizabethkingia meningoseptica
synthesis one of the largest bottlenecks in producing lactones is the hydroxylation of the fatty acids. The exploitation of oleate hydratase to hydrate oleic acid, which can easily be turned into gamma-dodecalactone after beta-elimination, is therefore the perfect solution to produce this valuable compound from cheap renewable materials (e.g. vegetable oil). The specificity and enantioselectivity of the enzyme will provide the correct lactone Macrococcus caseolyticus
synthesis one of the largest bottlenecks in producing lactones is the hydroxylation of the fatty acids. The exploitation of oleate hydratase to hydrate oleic acid, which can easily be turned into gamma-dodecalactone after beta-elimination, is therefore the perfect solution to produce this valuable compound from cheap renewable materials (e.g. vegetable oil). The specificity and enantioselectivity of the enzyme will provide the correct lactone Streptococcus pyogenes
synthesis one of the largest bottlenecks in producing lactones is the hydroxylation of the fatty acids. The exploitation of oleate hydratase to hydrate oleic acid, which can easily be turned into gamma-dodecalactone after beta-elimination, is therefore the perfect solution to produce this valuable compound from cheap renewable materials (e.g. vegetable oil). The specificity and enantioselectivity of the enzyme will provide the correct lactone Lysinibacillus fusiformis
synthesis one of the largest bottlenecks in producing lactones is the hydroxylation of the fatty acids. The exploitation of oleate hydratase to hydrate oleic acid, which can easily be turned into gamma-dodecalactone after beta-elimination, is therefore the perfect solution to produce this valuable compound from cheap renewable materials (e.g. vegetable oil). The specificity and enantioselectivity of the enzyme will provide the correct lactone Lacticaseibacillus rhamnosus
synthesis one of the largest bottlenecks in producing lactones is the hydroxylation of the fatty acids. The exploitation of oleate hydratase to hydrate oleic acid, which can easily be turned into gamma-dodecalactone after beta-elimination, is therefore the perfect solution to produce this valuable compound from cheap renewable materials (e.g. vegetable oil). The specificity and enantioselectivity of the enzyme will provide the correct lactone Lactiplantibacillus plantarum
synthesis one of the largest bottlenecks in producing lactones is the hydroxylation of the fatty acids. The exploitation of oleate hydratase to hydrate oleic acid, which can easily be turned into gamma-dodecalactone after beta-elimination, is therefore the perfect solution to produce this valuable compound from cheap renewable materials (e.g. vegetable oil). The specificity and enantioselectivity of the enzyme will provide the correct lactone Bifidobacterium breve
synthesis one of the largest bottlenecks in producing lactones is the hydroxylation of the fatty acids. The exploitation of oleate hydratase to hydrate oleic acid, which can easily be turned into gamma-dodecalactone after beta-elimination, is therefore the perfect solution to produce this valuable compound from cheap renewable materials (e.g. vegetable oil). The specificity and enantioselectivity of the enzyme will provide the correct lactone Bifidobacterium animalis subsp. lactis

Cloned(Commentary)

Cloned (Comment) Organism
expression in Escherichia coli Lactobacillus acidophilus
expression in Escherichia coli Stenotrophomonas maltophilia
expression in Escherichia coli Elizabethkingia meningoseptica
expression in Escherichia coli Macrococcus caseolyticus
expression in Escherichia coli Streptococcus pyogenes
expression in Escherichia coli Lysinibacillus fusiformis
expression in Escherichia coli Lacticaseibacillus rhamnosus
expression in Escherichia coli Lactiplantibacillus plantarum
expression in Escherichia coli Bifidobacterium breve
expression in Escherichia coli Bifidobacterium animalis subsp. lactis

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
67000
-
-
Lactobacillus acidophilus
67000
-
-
Stenotrophomonas maltophilia
67000
-
-
Elizabethkingia meningoseptica
67000
-
-
Macrococcus caseolyticus
67000
-
-
Streptococcus pyogenes
67000
-
-
Lysinibacillus fusiformis
67000
-
-
Lacticaseibacillus rhamnosus
67000
-
-
Lactiplantibacillus plantarum
67000
-
-
Bifidobacterium breve
82000
-
-
Bifidobacterium animalis subsp. lactis

Organism

Organism UniProt Comment Textmining
Bifidobacterium animalis subsp. lactis A0A1C7FUY1
-
-
Bifidobacterium breve A0A2N6TXX1
-
-
Elizabethkingia meningoseptica C7DLJ6
-
-
Lacticaseibacillus rhamnosus A0A249DBU8
-
-
Lactiplantibacillus plantarum A0A0G9FDC3
-
-
Lactobacillus acidophilus
-
-
-
Lysinibacillus fusiformis A0A1E4R6K3
-
-
Macrococcus caseolyticus B9E972
-
-
Stenotrophomonas maltophilia
-
-
-
Streptococcus pyogenes B5XK69
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
(6Z,9Z,12Z)-octadec-6,9,12-trienoic acid + H2O
-
Stenotrophomonas maltophilia (6Z,12Z)-10-hydroxyoctadec-6,12-dienoic acid
-
?
(6Z,9Z,12Z)-octadec-6,9,12-trienoic acid + H2O
-
Macrococcus caseolyticus (6Z,12Z)-10-hydroxyoctadec-6,12-dienoic acid
-
?
(6Z,9Z,12Z)-octadec-6,9,12-trienoic acid + H2O
-
Streptococcus pyogenes (6Z,12Z)-10-hydroxyoctadec-6,12-dienoic acid
-
?
(6Z,9Z,12Z)-octadec-6,9,12-trienoic acid + H2O
-
Lysinibacillus fusiformis (6Z,12Z)-10-hydroxyoctadec-6,12-dienoic acid
-
?
(9Z)-hexadec-9-enoic acid + H2O
-
Lactobacillus acidophilus 10-hydroxyhexadecanoic acid
-
?
(9Z)-hexadec-9-enoic acid + H2O
-
Stenotrophomonas maltophilia 10-hydroxyhexadecanoic acid
-
?
(9Z)-hexadec-9-enoic acid + H2O
-
Elizabethkingia meningoseptica 10-hydroxyhexadecanoic acid
-
?
(9Z)-hexadec-9-enoic acid + H2O
-
Macrococcus caseolyticus 10-hydroxyhexadecanoic acid
-
?
(9Z)-hexadec-9-enoic acid + H2O
-
Streptococcus pyogenes 10-hydroxyhexadecanoic acid
-
?
(9Z)-hexadec-9-enoic acid + H2O
-
Lysinibacillus fusiformis 10-hydroxyhexadecanoic acid
-
?
(9Z)-hexadec-9-enoic acid + H2O
-
Lacticaseibacillus rhamnosus 10-hydroxyhexadecanoic acid
-
?
(9Z)-hexadec-9-enoic acid + H2O
-
Lactiplantibacillus plantarum 10-hydroxyhexadecanoic acid
-
?
(9Z)-hexadec-9-enoic acid + H2O
-
Bifidobacterium breve 10-hydroxyhexadecanoic acid
-
?
(9Z)-hexadec-9-enoic acid + H2O
-
Bifidobacterium animalis subsp. lactis 10-hydroxyhexadecanoic acid
-
?
(9Z)-octadec-9-enoic acid + H2O
-
Stenotrophomonas maltophilia (R)-10-hydroxyoctadecanoic acid
-
?
(9Z)-octadec-9-enoic acid + H2O
-
Macrococcus caseolyticus (R)-10-hydroxyoctadecanoic acid
-
?
(9Z)-octadec-9-enoic acid + H2O
-
Streptococcus pyogenes (R)-10-hydroxyoctadecanoic acid
-
?
(9Z)-octadec-9-enoic acid + H2O
-
Lysinibacillus fusiformis (R)-10-hydroxyoctadecanoic acid
-
?
(9Z,12Z)-octadec-9,12-dienoic acid + H2O
-
Lactobacillus acidophilus (12Z)-10-hydroxyoctadec-12-enoic acid
-
?
(9Z,12Z)-octadec-9,12-dienoic acid + H2O
-
Stenotrophomonas maltophilia (12Z)-10-hydroxyoctadec-12-enoic acid
-
?
(9Z,12Z)-octadec-9,12-dienoic acid + H2O
-
Elizabethkingia meningoseptica (12Z)-10-hydroxyoctadec-12-enoic acid
-
?
(9Z,12Z)-octadec-9,12-dienoic acid + H2O
-
Macrococcus caseolyticus (12Z)-10-hydroxyoctadec-12-enoic acid
-
?
(9Z,12Z)-octadec-9,12-dienoic acid + H2O
-
Streptococcus pyogenes (12Z)-10-hydroxyoctadec-12-enoic acid
-
?
(9Z,12Z)-octadec-9,12-dienoic acid + H2O
-
Lysinibacillus fusiformis (12Z)-10-hydroxyoctadec-12-enoic acid
-
?
(9Z,12Z)-octadec-9,12-dienoic acid + H2O
-
Lacticaseibacillus rhamnosus (12Z)-10-hydroxyoctadec-12-enoic acid
-
?
(9Z,12Z)-octadec-9,12-dienoic acid + H2O
-
Lactiplantibacillus plantarum (12Z)-10-hydroxyoctadec-12-enoic acid
-
?
(9Z,12Z)-octadec-9,12-dienoic acid + H2O
-
Bifidobacterium breve (12Z)-10-hydroxyoctadec-12-enoic acid
-
?
(9Z,12Z)-octadec-9,12-dienoic acid + H2O
-
Bifidobacterium animalis subsp. lactis (12Z)-10-hydroxyoctadec-12-enoic acid
-
?
(9Z,12Z,15Z)-octadec-9,12,15-trienoic acid + H2O
-
Stenotrophomonas maltophilia (12Z,15Z)-10-hydroxyoctadec-12,15-dienoic acid
-
?
(9Z,12Z,15Z)-octadec-9,12,15-trienoic acid + H2O
-
Elizabethkingia meningoseptica (12Z,15Z)-10-hydroxyoctadec-12,15-dienoic acid
-
?
(9Z,12Z,15Z)-octadec-9,12,15-trienoic acid + H2O
-
Macrococcus caseolyticus (12Z,15Z)-10-hydroxyoctadec-12,15-dienoic acid
-
?
(9Z,12Z,15Z)-octadec-9,12,15-trienoic acid + H2O
-
Streptococcus pyogenes (12Z,15Z)-10-hydroxyoctadec-12,15-dienoic acid
-
?
(9Z,12Z,15Z)-octadec-9,12,15-trienoic acid + H2O
-
Lysinibacillus fusiformis (12Z,15Z)-10-hydroxyoctadec-12,15-dienoic acid
-
?

Subunits

Subunits Comment Organism
dimer
-
Stenotrophomonas maltophilia
dimer
-
Macrococcus caseolyticus
dimer
-
Streptococcus pyogenes
dimer
-
Lysinibacillus fusiformis

Synonyms

Synonyms Comment Organism
OHase
-
Lactobacillus acidophilus
OHase
-
Stenotrophomonas maltophilia
OHase
-
Elizabethkingia meningoseptica
OHase
-
Macrococcus caseolyticus
OHase
-
Streptococcus pyogenes
OHase
-
Lysinibacillus fusiformis
OHase
-
Lacticaseibacillus rhamnosus
OHase
-
Lactiplantibacillus plantarum
OHase
-
Bifidobacterium breve
OHase
-
Bifidobacterium animalis subsp. lactis

Cofactor

Cofactor Comment Organism Structure
FAD with the multiple sequence alignment a motif indicative of FAD binding is identified Lactobacillus acidophilus
FAD with the multiple sequence alignment a motif indicative of FAD binding is identified Stenotrophomonas maltophilia
FAD with the multiple sequence alignment a motif indicative of FAD binding is identified Elizabethkingia meningoseptica
FAD with the multiple sequence alignment a motif indicative of FAD binding is identified Macrococcus caseolyticus
FAD with the multiple sequence alignment a motif indicative of FAD binding is identified Streptococcus pyogenes
FAD with the multiple sequence alignment a motif indicative of FAD binding is identified Lysinibacillus fusiformis
FAD with the multiple sequence alignment a motif indicative of FAD binding is identified Lacticaseibacillus rhamnosus
FAD with the multiple sequence alignment a motif indicative of FAD binding is identified Lactiplantibacillus plantarum
FAD with the multiple sequence alignment a motif indicative of FAD binding is identified Bifidobacterium breve
FAD with the multiple sequence alignment a motif indicative of FAD binding is identified Bifidobacterium animalis subsp. lactis