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Microbial enzymes for aromatic compound hydroxylation.Organization and regulation of meta cleavage pathway genes for toluene and o-xylene derivative degradation in Pseudomonas stutzeri OX1.Carcinogenicity prediction of noncongeneric chemicals by augmented top priority fragment classification.Formation of bound residues by naphthalene and cis-naphthalene-1,2-dihydrodiol.Regulated expression systems for the development of whole-cell biocatalysts expressing oxidative enzymes in a sequential manner.Novel auto-inducing expression systems for the development of whole-cell biocatalysts.Styrene lower catabolic pathway in Pseudomonas fluorescens ST: identification and characterization of genes for phenylacetic acid degradation.Predicting toxicity: a mechanism of action model of chemical mutagenicity.Aldol reactions of the trans-o-hydroxybenzylidenepyruvate hydratase-aldolase (tHBP-HA) from Pseudomonas fluorescens N3.From dioxin to dioxin congeners: understanding the differences in hydrophobic aggregation in water and absorption into lipid membranes by means of atomistic simulations.Characterization of the aldol condensation activity of the trans-o-hydroxybenzylidenepyruvate hydratase-aldolase (tHBP-HA) cloned from Pseudomonas fluorescens N3.Selective enzymatic reduction of aldehydes.Production of substituted naphthalene dihydrodiols by engineered Escherichia coli containing the cloned naphthalene 1,2-dioxygenase gene from Pseudomonas fluorescens N3.Insect pest control agents: Novel chiral butanoate esters (juvenogens)Electroreduction of volatile organic halides on activated silver cathodesSilver as a powerful electrocatalyst for organic halide reduction: the critical role of molecular structureCathode and medium effects on the electroreductive glucosidation of phenolsMultienzymatic preparation of 3-[(1R)-1-hydroxyethyl]benzoic acid and (2S)-hydroxy(phenyl)ethanoic acidMultienzymatic preparation of (−)-[3-(oxiran-2-yl)phenyl]methanol and (−)-3-(oxiran-2-yl)benzoic acidBiocatalyst expressing cis-naphthalene dihydrodiol dehydrogenase from Pseudomonas fluorescens N3 catalyzes alcohol and 1,2-diol dehydrogenase reactionsIsolation, cloning and synthetic use of the tHBP aldolase from Pseudomonas fluorescens N3One-Pot Wittig Reactions in Water and in the Presence of a SurfactantSynthesis of enantiopure 2-amino-1-phenyl and 2-amino-2-phenyl ethanols using enantioselective enzymatic epoxidation and regio- and diastereoselective chemical aminolysis(1S,2S)-1-Amino-2-hydroxy-1,2,3,4-tetrahydronaphthalene: a new chiral auxiliary for asymmetric Reformatsky reactionsBacterial monooxygenase mediated preparation of nonracemic chiral oxiranes: study of the effects of substituent nature and positionOrganic phase effect in the biphasic bioconversion of substituted naphthalenes by engineered E. coli containing P. fluorescens N3 dioxygenaseA chemoenzymatic synthesis of (2R)-8-substituted-2-aminotetralinsEnantiopure vic-amino alcohols and vic-diamines from (1R,2S)-1,2-dihydroxy-1,2-dihydronaphthaleneDevelopment of biocatalysts carrying naphthalene dioxygenase and dihydrodiol dehydrogenase genes inducible in aerobic and anaerobic conditions1,2-Dihydro-1,2-dihydroxynaphthalene dehydrogenase containing recombinant strains: Preparation, isolation and characterisation of 1,2-dihydroxynaphthalenes and 1,2-naphthoquinonesBioconversion of Substituted Naphthalenes to the Corresponding 1,2-Dihydroxy Derivatives by Escherichia coli Recombinant StrainsSynthesis and biological evaluation of new 3-amino-2-azetidinone derivatives as anti-colorectal cancer agents.Analysis of a theoretical model based on similarity for studying RNA base pairingsPrediction of organic reaction products: determining the best reaction conditionsSpecificity of substrate recognition by Pseudomonas fluorescens N3 dioxygenase. The role of the oxidation potential and molecular geometryReaction centre accessibility. I. Calculation of reaction centre congestion and influence of structure flexibilityReaction centre accessibility. II. Role of reaction centre congestion in the calculation of reaction centre accessibilityTop-priority fragment QSAR approach in predicting pesticide aquatic toxicityHydrophobic aggregation and collective absorption of dioxin into lipid membranes: insights from atomistic simulationsDetermination of toxicant mode of action by augmented top priority fragment class
P50
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P50
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wetenschapper
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հետազոտող
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Guido Sello
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Guido Sello
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Guido Sello
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Guido Sello
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Guido Sello
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Guido Sello
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Guido Sello
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Guido Sello
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Guido Sello
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Guido Sello
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Guido Sello
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Guido Sello
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P106
P1153
7003773782
P31
P496
0000-0003-2538-9107