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Monooxygenases, bacterial

Organic chemists often use enantiomencally homogeneous starting materials for the synthe SIS of complex molecules (see Chiral Drugs p 296) A novel preparation of the S enantiomer of compound B has been descnbed using a bacterial cyclohexanone monooxygenase enzyme system... [Pg.749]

Enantioselective oxidation of cyclic dithioacetals to monosulfoxides catalyzed by bacterial cyclohexanone monooxygenases 96CC2303. [Pg.208]

Wieser M, B Wagner, J Eberspacher, F Lingens (1997) Puriflcation and characterization of 2,4,6-trichloro-phenol-4-monooxygenase, a dehalogenating enzyme imm Azotobacter sp. strain GPL J Bacterial 179 202-208. [Pg.90]

Eppink MHM, SA Boeren, J Vervoort, WJH van Berkel (1997) Purification and properties of 4-hydroxybenzoate 1-hydroxylase (decarboxylating), a novel flavin adenine dinucleotide-dependent monooxygenase from Candida parapsilosis CBS604. J Bacterial 179 668-6687. [Pg.138]

Fukumori F, RP Hausinger (1993a) Alcaligenes eutrophus JMP 134 2,4-chlorophenoxyacetate monooxygenase is an a-ketoglutarate-dependent dioxygenase. J Bacterial 175 2083-2086. [Pg.138]

Xun L (1996) Purification and characterization of chlorophenol 4-monooxygenase from Burkholderia cepacia ACnOO. J Bacterial 178 2645-2649. [Pg.147]

Zahn JA, AA DiSpirito (1996) Membrane associated methane monooxygenase from Methylococcus capsula-tus (Bath). J Bacterial 178 1018-1029. [Pg.147]

Whited GM, DT Gibson (1991) Separation and partial characterization of the enzymes of the toluene-4-monooxygenase catabolic pathway in Pseudomonas mendocina KRl. J Bacterial 173 3017-3020. [Pg.240]

A number of bacterial strains with monooxygenase activity have been described, and different types of MMO have played important roles in the degradation of a range of aliphatic componnds. MMO may exist in either a soluble (sMMO) form that has been more extensively studied or in a particulate (pMMO) form. These forms display different substrate ranges and different rates of transformation rates, and most methanotrophs express only the particnlate form of the enzyme (Hanson and Hanson 1996). [Pg.297]

Payne JW, H Bolton, JA Campbell, L Xun (1998) Purification and characterization of EDTA monooxygenase from the EDTA-degrading bacterium BNCl. J Bacterial 180 3823-3827. [Pg.332]

Small FJ, SA Ensign (1997) Alkene monooxygenase from Xanthobacter strain Py2. Purification and characterization of a four-component system central to the bacterial metabolism of aliphatic alkenes. J Biol Chem 272 24913-24920. [Pg.334]

Hartmans S, MJ van der Werf, JAM de Bont (1990) Bacterial degradation of styrene involving a novel flavin adenenine dinucleotide-dependent styrene monooxygenase. Appl Environ Microbiol 41 1045-1054. [Pg.396]

Zhou N-Y, J Al-Dulayymi, MS Baird, PA Williams (2002) Salicylate 5-hydroxylase from Ralstonia sp. strain U2 a monooxygenase with close relationships to and shared electron transport proteins with naphthalene dioxygenase. J Bacterial 184 1547-1555. [Pg.424]

Martin G, S Dijols, C Capeillere-Blandin, 1 Arnaud (1999) Hydroxylation reaction catalyzed by the Burk-holderia cepacia ACllOO bacterial strain. Involvement of the chlorophenol-4-monooxygenase. Eur J Bioichem 261 533-538. [Pg.444]

Walsh and coworkers oxidized ethyl p-tolyl sulfide on an analytical scale to the S-sulfoxide of 64% enantiomeric purity using a bacterial flavoenzyme cyclohexanone monooxygenase derived from Adnetobacter . Using a flavin adenine dinucleotide containing monooxygenase purified from hog liver microsomes yielded the R-sulfoxide of 90% enantiomeric purity. HPLC on a column containing a 3,5-dinitrobenzoyl-D-phenylglycine chiral stationary phase was used to determine the optical purity of the sulfoxides. [Pg.78]

Marasco, E. and C. Schmidt-Dannert (2008). Identification of bacterial carotenoid cleavage dioxygenase homologs that cleave the interphenyl u,(J double bond of stilbene derivatives via a monooxygenase reaction. Chembiochem. 9(9) 1450-1461. [Pg.413]


See other pages where Monooxygenases, bacterial is mentioned: [Pg.256]    [Pg.256]    [Pg.350]    [Pg.368]    [Pg.371]    [Pg.374]    [Pg.78]    [Pg.254]    [Pg.1590]    [Pg.309]    [Pg.90]    [Pg.252]    [Pg.227]    [Pg.108]    [Pg.116]    [Pg.106]    [Pg.410]    [Pg.585]    [Pg.650]    [Pg.682]    [Pg.165]    [Pg.702]    [Pg.1383]    [Pg.236]   


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