Works about MONOOXYGENASES
Results: 1452
Generalization of Classification of AlkB Family Alkane Monooxygenases from Rhodococcus (sensu lato) Group Based on Phylogenetic Analysis and Genomic Context Comparison.
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- International Journal of Molecular Sciences, 2025, v. 26, n. 4, p. 1713, doi. 10.3390/ijms26041713
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Characterization of an Isoeugenol Monooxygenase (Iem) from Pseudomonas nitroreducens Jinl That Transforms Isoeugenol to Vanillin.
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- Bioscience, Biotechnology & Biochemistry, 2013, v. 77, n. 2, p. 289, doi. 10.1271/bbb.120715
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Transcriptional Control of the Isoeugenol Monooxygenase of Pseudomonas nitroreducens Jinl in Escherichia coli.
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- Bioscience, Biotechnology & Biochemistry, 2012, v. 76, n. 10, p. 1891, doi. 10.1271/bbb.120375
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Involvement of the CYP78A Subfamily of Cytochrome P450 Monooxygenases in Protonema Growth and Gametophore Formation in the Moss Physcomitrella patens.
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- Bioscience, Biotechnology & Biochemistry, 2011, v. 75, n. 2, p. 331, doi. 10.1271/bbb.100759
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Novel Reactivity of Dibenzothiophene Monooxygenase from Bacillus subtilis WU-S2B.
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- Bioscience, Biotechnology & Biochemistry, 2009, v. 73, n. 9, p. 2128, doi. 10.1271/bbb.90284
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Brz220 Interacts with DWF4, a Cytochrome P450 Monooxygenase in Brassinosteroid Biosynthesis, and Exerts Biological Activity.
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- Bioscience, Biotechnology & Biochemistry, 2008, v. 72, n. 1, p. 7, doi. 10.1271/bbb.70141
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Purification and Biochemical Characterization of Soluble Methane Monooxygenase Hydroxylase from Methylosinus trichosporium IMV 3011.
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- Bioscience, Biotechnology & Biochemistry, 2007, v. 71, n. 1, p. 122, doi. 10.1271/bbb.60402
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Molecular Cloning of Streptomyces Genes Encoding Vanillate Demethylase.
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- Bioscience, Biotechnology & Biochemistry, 2006, v. 70, n. 9, p. 2316, doi. 10.1271/bbb.60180
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Indole Hydroxylation by Bacterial Cytochrome P450 BM-3 and Modulation of Activity by Cumene Hydroperoxide.
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- Bioscience, Biotechnology & Biochemistry, 2005, v. 69, n. 2, p. 293, doi. 10.1271/bbb.69.293
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Thermostable Flavin Reductase That Couples with Dibenzothiophene Monooxygenase from Thermophilic Bacillus sp. DSM411: Purification, Characterization, and Gene Cloning.
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- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 8, p. 1712, doi. 10.1271/bbb.68.1712
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Total Degradation of Pentachloroethane by an Engineered Alcaligenes Strain Expressing a Modified Camphor Monooxygenase and a Hybrid Dioxygenase.
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- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 6, p. 1353, doi. 10.1271/bbb.68.1353
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Lack of an Inducible Effect of Dietary Soy Isoflavones on the mRNA Abundance of Hepatic Cytochrome P-450 Isozymes in Rats.
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- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 3, p. 508, doi. 10.1271/bbb.68.508
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Synthesis of Chiral Sulfoxides by A Cyclic Oxidation‐Reduction Multi‐Enzymatic Cascade Biocatalysis.
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- Chemistry - A European Journal, 2024, v. 30, n. 19, p. 1, doi. 10.1002/chem.202304081
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An Improved Spectrophotometric Method for Toluene‐4‐Monooxygenase Activity.
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- Chemistry - A European Journal, 2023, v. 29, n. 19, p. 1, doi. 10.1002/chem.202203322
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Frontispiece: Molecular Mechanism of Substrate Oxidation in Lytic Polysaccharide Monooxygenases: Insight from Theoretical Investigations.
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- Chemistry - A European Journal, 2023, v. 29, n. 7, p. 1, doi. 10.1002/chem.202380761
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Molecular Mechanism of Substrate Oxidation in Lytic Polysaccharide Monooxygenases: Insight from Theoretical Investigations.
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- Chemistry - A European Journal, 2023, v. 29, n. 7, p. 1, doi. 10.1002/chem.202202379
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Investigating the Active Oxidants Involved in Cytochrome P450 Catalyzed Sulfoxidation Reactions.
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- Chemistry - A European Journal, 2022, v. 28, n. 72, p. 1, doi. 10.1002/chem.202202428
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Enabling Aromatic Hydroxylation in a Cytochrome P450 Monooxygenase Enzyme through Protein Engineering.
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- Chemistry - A European Journal, 2022, v. 28, n. 67, p. 1, doi. 10.1002/chem.202201895
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Discovery of (±)‐Penindolenes Reveals an Unusual Indole Ring Cleavage Pathway Catalyzed by P450 Monooxygenase.
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- Angewandte Chemie, 2024, v. 136, n. 26, p. 1, doi. 10.1002/ange.202403963
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Engineering Biocatalysts for the C−H Activation of Fatty Acids by Ancestral Sequence Reconstruction.
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- Angewandte Chemie, 2024, v. 136, n. 18, p. 1, doi. 10.1002/ange.202314869
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Flavin‐N5OOH Functions as both a Powerful Nucleophile and a Base in the Superfamily of Flavoenzymes.
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- Angewandte Chemie, 2024, v. 136, n. 14, p. 1, doi. 10.1002/ange.202318629
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Novel Biocatalysts from Specialized Metabolism.
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- Angewandte Chemie, 2024, v. 136, n. 4, p. 1, doi. 10.1002/ange.202309284
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Anchoring a Structurally Editable Proximal Cofactor‐like Module to Construct an Artificial Dual‐center Peroxygenase.
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- Angewandte Chemie, 2023, v. 135, n. 51, p. 1, doi. 10.1002/ange.202311259
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Somalactams A–D: Anti‐inflammatory Macrolide Lactams with Unique Ring Systems from an Arctic Actinomycete Strain.
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- Angewandte Chemie, 2023, v. 135, n. 18, p. 1, doi. 10.1002/ange.202218085
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Innentitelbild: Strukturelle und mechanistische Studien zur Substrat‐ und Stereoselektivität der Indol‐Monooxygenase VpIndA1: Neue Wege für biokatalytische Epoxidationen und Sulfoxidationen (Angew. Chem. 17/2023).
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- Angewandte Chemie, 2023, v. 135, n. 17, p. 1, doi. 10.1002/ange.202300657
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Total Biosynthesis of Mutaxanthene Unveils a Flavoprotein Monooxygenase Catalyzing Xanthene Ring Formation.
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- Angewandte Chemie, 2023, v. 135, n. 13, p. 1, doi. 10.1002/ange.202218660
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Photoinduced Promiscuity of Cyclohexanone Monooxygenase for the Enantioselective Synthesis of α‐Fluoroketones.
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- Angewandte Chemie, 2022, v. 134, n. 50, p. 1, doi. 10.1002/ange.202211199
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Biosynthesis of Nodulisporic Acids: A Multifunctional Monooxygenase Delivers a Complex and Highly Branched Array.
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- Angewandte Chemie, 2022, v. 134, n. 49, p. 1, doi. 10.1002/ange.202213364
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Atropopeptides are a Novel Family of Ribosomally Synthesized and Posttranslationally Modified Peptides with a Complex Molecular Shape.
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- Angewandte Chemie, 2022, v. 134, n. 41, p. 1, doi. 10.1002/ange.202208361
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Multienzyme Redox System with Cofactor Regeneration for Cyclic Deracemization of Sulfoxides.
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- Angewandte Chemie, 2022, v. 134, n. 37, p. 1, doi. 10.1002/ange.202209272
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Sequential Allylic Alcohol Formation by a Multifunctional Cytochrome P450 Monooxygenase with Rare Redox Partners.
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- Angewandte Chemie, 2022, v. 134, n. 26, p. 1, doi. 10.1002/ange.202203264
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Catalytic Control of Spiroketal Formation in Rubromycin Polyketide Biosynthesis.
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- Angewandte Chemie, 2021, v. 133, n. 52, p. 27166, doi. 10.1002/ange.202109384
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An NADPH‐Dependent Ketoreductase Catalyses the Tetracyclic to Pentacyclic Skeletal Rearrangement in Chartreusin Biosynthesis.
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- Angewandte Chemie, 2021, v. 133, n. 50, p. 26582, doi. 10.1002/ange.202112047
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The Cytochrome P450 Catalyzing C−S Bond Formation in S‐Heterocyclization of Chuangxinmycin Biosynthesis.
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- Angewandte Chemie, 2021, v. 133, n. 28, p. 15527, doi. 10.1002/ange.202015814
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How Oxygen Binding Enhances Long‐Range Electron Transfer: Lessons From Reduction of Lytic Polysaccharide Monooxygenases by Cellobiose Dehydrogenase.
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- Angewandte Chemie, 2021, v. 133, n. 5, p. 2415, doi. 10.1002/ange.202011408
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Activation of a Non‐Heme Fe<sup>III</sup>‐OOH by a Second Fe<sup>III</sup> to Hydroxylate Strong C−H Bonds: Possible Implications for Soluble Methane Monooxygenase.
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- Angewandte Chemie, 2019, v. 131, n. 25, p. 8572, doi. 10.1002/ange.201903465
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Unprecedented [5.5.5.6]Dioxafenestrane Ring Construction in Fungal Insecticidal Sesquiterpene Biosynthesis.
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- Angewandte Chemie, 2019, v. 131, n. 20, p. 6641, doi. 10.1002/ange.201813722
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Regio‐ and Enantio‐selective Chemo‐enzymatic C−H‐Lactonization of Decanoic Acid to (S)‐δ‐Decalactone.
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- Angewandte Chemie, 2019, v. 131, n. 17, p. 5724, doi. 10.1002/ange.201901242
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Biomimetic and Biocatalytic Synthesis of Bruceol.
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- Angewandte Chemie, 2019, v. 131, n. 5, p. 1441, doi. 10.1002/ange.201812432
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Chemo‐ and Regioselective Dihydroxylation of Benzene to Hydroquinone Enabled by Engineered Cytochrome P450 Monooxygenase.
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- Angewandte Chemie, 2019, v. 131, n. 3, p. 774, doi. 10.1002/ange.201812093
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Individual differences in in vitro and in vivo metabolic clearances of the antipsychotic drug olanzapine from non-smoking and smoking Japanese subjects genotyped for cytochrome P4502D6 and flavincontaining monooxygenase 3.
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- Human Psychopharmacology: Clinical & Experimental, 2016, v. 31, n. 2, p. 83, doi. 10.1002/hup.2515
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Diversity and distribution of CYP gene family in Bactrian camel.
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- Functional & Integrative Genomics, 2018, v. 18, n. 1, p. 23, doi. 10.1007/s10142-017-0571-y
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Chemical composition and pharmacological activity of the leaves of Pueraria hirsuta L. grown in Georgia.
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- Pharmaceutical Chemistry Journal, 2008, v. 42, n. 6, p. 340, doi. 10.1007/s11094-008-0131-9
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Rapid evaluation of the functional activity of the hepatic monooxygenase system.
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- Pharmaceutical Chemistry Journal, 2007, v. 41, n. 12, p. 631, doi. 10.1007/s11094-008-0033-x
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Effect of birch bark dry extract on the key biotransformation enzymes (cytochrome P-450) and microsomal membranes in rat liver.
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- Pharmaceutical Chemistry Journal, 2007, v. 41, n. 5, p. 264, doi. 10.1007/s11094-007-0058-6
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The Effects of Benzonal, Halonal, and Halodif on the Development of Postischemic Liver Disorders in Rats.
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- Pharmaceutical Chemistry Journal, 2003, v. 37, n. 12, p. 623, doi. 10.1023/B:PHAC.0000022078.14847.77
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- Article
Hepatoprotector Properties of Eryxin in Animals with Acute Drug-Induced Hepatitis Model.
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- Pharmaceutical Chemistry Journal, 2003, v. 37, n. 2, p. 63, doi. 10.1023/A:1024025424825
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The cytochrome P450 complement ( CYPome) of Mycosphaerella graminicola.
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- Biotechnology & Applied Biochemistry, 2013, v. 60, n. 1, p. 52, doi. 10.1002/bab.1062
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Novel family members of CYP109 from Sorangium cellulosum So ce56 exhibit characteristic biochemical and biophysical properties.
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- Biotechnology & Applied Biochemistry, 2013, v. 60, n. 1, p. 18, doi. 10.1002/bab.1087
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Cytochrome P450 of wood-rotting basidiomycetes and biotechnological applications.
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- Biotechnology & Applied Biochemistry, 2013, v. 60, n. 1, p. 71, doi. 10.1002/bab.1061
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