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Literature summary for 1.14.14.155 extracted from

  • Beecher, J.; Willetts, A.
    Biotransformation of organic sulfides. Predictive active site models for sulfoxidation catalyzed by 2,5-diketocamphane 1,2-monooxygenase and 3,6-diketocamphane 1,6-monooxygenase, enantiocomplementary enzymes from Pseudomonas putida NCIMB 10007 (1998), Tetrahedron, 9, 1899-1916.
No PubMed abstract available

Application

Application Comment Organism
synthesis production of useful chiral synthons for chemoenzymatic synthesis Pseudomonas putida

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
(-)-bornane-2,5-dione + FMNH2 + O2 Pseudomonas putida inducible by growth on racemic camphor ?
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additional information Pseudomonas putida catalyzes stereoselective electrophilic biooxidation of a wide range of prochiral organic sulfoxides to the corresponding chiral sulfoxides as well as the nucleophilic biooxidation of ketones to lactones with different enantio- and stereoselectivity, overview ?
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?

Organism

Organism UniProt Comment Textmining
Pseudomonas putida
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Pseudomonas putida
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2 isozymes termed 2,5-diketocamphane-1,2-monooxygenase and 3,6-diketocamphane-1,6-monooxygenase
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Pseudomonas putida NCIMB 10007
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Purification (Commentary)

Purification (Comment) Organism
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Pseudomonas putida

Reaction

Reaction Comment Organism Reaction ID
(-)-bornane-2,5-dione + reduced rubredoxin + O2 + FMNH2 = (-)-5-oxo-1,2-campholide + FMN + H2O mechanism Pseudomonas putida
(-)-bornane-2,5-dione + reduced rubredoxin + O2 + FMNH2 = (-)-5-oxo-1,2-campholide + FMN + H2O catalysis of 2 mechanistically different types of biochemical reactions within the confines of the same active site Pseudomonas putida
(-)-bornane-2,5-dione + reduced rubredoxin + O2 + FMNH2 = (-)-5-oxo-1,2-campholide + FMN + H2O belongs to group of Bayer-Villiger monooxygenases of the NADH plus FMN-dependent type 2 enzymes Pseudomonas putida
(-)-bornane-2,5-dione + reduced rubredoxin + O2 + FMNH2 = (-)-5-oxo-1,2-campholide + FMN + H2O cubic space active site model, topography Pseudomonas putida
(-)-bornane-2,5-dione + reduced rubredoxin + O2 + FMNH2 = (-)-5-oxo-1,2-campholide + FMN + H2O isozyme, enantiocomplementary and isofunctional isozymes 2,5-DKCMO EC 1.14.15.2 and 3,6-DKCMO EC 1.14.15.x Pseudomonas putida
(-)-bornane-2,5-dione + reduced rubredoxin + O2 + FMNH2 = (-)-5-oxo-1,2-campholide + FMN + H2O higher activity in oxidation of sulfides to the corresponding sulfoxides than in lactonization of ketones Pseudomonas putida

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
(-)-bornane-2,5-dione + FMNH2 + O2 6-dione i.e. 3,6-diketocamphane Pseudomonas putida 1,8,8-trimethyl-2-oxabicyclo[3.2.1]octane-3,6-dione + FMN + H2O
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(-)-bornane-2,5-dione + FMNH2 + O2 inducible by growth on racemic camphor Pseudomonas putida ?
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?
(-)-bornanone + FMNH2 + O2 i.e. (-)-camphor Pseudomonas putida ?
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additional information enzyme is associated with a NADH oxidase Pseudomonas putida ?
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additional information rubredoxin not mentioned Pseudomonas putida ?
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additional information catalyzes stereoselective electrophilic biooxidation of a wide range of prochiral organic sulfoxides to the corresponding chiral sulfoxides as well as the nucleophilic biooxidation of ketones to lactones with different enantio- and stereoselectivity, overview Pseudomonas putida ?
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?

Synonyms

Synonyms Comment Organism
3,6-diketocamphane 1,6-monooxygenase isozyme, enantiocomplementary and isofunctional isozymes 2,5-DKCMO EC 1.14.15.2 and 3,6-DKCMO EC 1.14.15.x Pseudomonas putida
3,6-diketocamphane 1,6-monooxygenase i.e. 3,6-DKCMO Pseudomonas putida
3,6-diketocamphane 1,6-monooxygenase isoform, which is probably a different enzyme Pseudomonas putida
3,6-diketocamphane-monooxygenase
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Pseudomonas putida