Kazlauskas, Romas, 1956-
Romas J. Kazlauskas researcher
Kazlauskas, R. J. (Romas J.), 1956-
Kazlauskas, Romas J., 1956-....
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
Kazlauskas, Romas J.
Kazlauskas, Romas
VIAF ID: 25449648 (Personal)
Permalink: http://viaf.org/viaf/25449648
Preferred Forms
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100 1 _ ‡a Kazlauskas, R. J. ‡q (Romas J.), ‡d 1956-
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100 1 _ ‡a Kazlauskas, R. J. ‡q (Romas J.), ‡d 1956-
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100 1 _ ‡a Kazlauskas, R. J. ‡q (Romas J.), ‡d 1956-
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100 1 0
‡a
Kazlauskas, R. J.
‡q
(Romas J.),
‡d
1956-
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100 1 _ ‡a Kazlauskas, Romas
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100 1 _ ‡a Kazlauskas, Romas J.
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100 1 _
‡a
Kazlauskas, Romas J.
‡d
1956-
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100 1 _
‡a
Kazlauskas, Romas J.,
‡d
1956-....
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100 1 _ ‡a Kazlauskas, Romas ‡d (1956- ).
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100 1 _
‡a
Kazlauskas, Romas
‡d
1956-
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100 1 _ ‡a Kazlauskas, Romas, ‡d 1956-
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100 0 _
‡a
Romas J. Kazlauskas
‡c
researcher
4xx's: Alternate Name Forms (9)
Works
| Title | Sources |
|---|---|
| Amplification of screening sensitivity through selective destruction: theory and screening of a library of carbonic anhydrase inhibitors. |
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| Analogs of reaction intermediates identify a unique substrate binding site in Candida rugosa lipase |
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| Biocatalysis--becoming more predictable and selective |
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| Biocatalysis for green chemistry and chemical process development |
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| Biocatalysis in ionic liquids - advantages beyond green technology |
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| Bioconversion of p-coumaric acid to p-hydroxystyrene using phenolic acid decarboxylase from B. amyloliquefaciens in biphasic reaction system. |
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| Biological chemistry: enzymes in focus |
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| Biology evolves to fight chemistry |
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| Biosynthesis of (-)-5-Hydroxy-equol and 5-Hydroxy-dehydroequol from Soy Isoflavone, Genistein Using Microbial Whole Cell Bioconversion |
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| Catalytic promiscuity in biocatalysis: using old enzymes to form new bonds and follow new pathways. |
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| Chemical biotechnology in progress |
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| Cloning, expression and characterization of CYP102D1, a self-sufficient P450 monooxygenase from Streptomyces avermitilis. |
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| Development of colorimetric HTS assay of cytochrome p450 for ortho-specific hydroxylation, and engineering of CYP102D1 with enhanced catalytic activity and regioselectivity |
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| Developmental evolution facilitates rapid adaptation |
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| Different active-site loop orientation in serine hydrolases versus acyltransferases |
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| Enantiocomplementary enzymes: classification, molecular basis for their enantiopreference, and prospects for mirror-image biotransformations. |
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| Engineering a multipurpose catalyst |
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| Engineering enzymes by 'intelligent' design. |
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| Engineering the third wave of biocatalysis |
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| Enzymatic synthesis of poly(hydroxyalkanoates) in ionic liquids |
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| Evolution of a Catalytic Mechanism. |
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| Evolutionary innovation using EDGE, a system for localized elevated mutagenesis |
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| Experimental Evolution of Trichoderma citrinoviride for Faster Deconstruction of Cellulose |
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| Extracellular production of Streptomyces lividans acetyl xylan esterase A in Escherichia coli for rapid detection of activity. |
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| From nature to industry: Harnessing enzymes for biocatalysis |
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| The Fungus Trichoderma Regulates Submerged Conidiation Using the Steroid Pregnenolone |
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| High-Level Production of Lysine in the Yeast Saccharomyces cerevisiae by Rational Design of Homocitrate Synthase |
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| How substrate solvation contributes to the enantioselectivity of subtilisin toward secondary alcohols. |
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| How the Same Core Catalytic Machinery Catalyzes 17 Different Reactions: the Serine-Histidine-Aspartate Catalytic Triad of α/β-Hydrolase Fold Enzymes. |
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| Hydrolase-catalyzed biotransformations in deep eutectic solvents |
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| Hydrolases in organic synthesis regio- and stereoselective biotransformations |
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| Improved preparation and use of room-temperature ionic liquids in lipase-catalyzed enantio- and regioselective acylations. |
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| Improving enzyme properties: when are closer mutations better? |
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| Increased saccharification yields from aspen biomass upon treatment with enzymatically generated peracetic acid. |
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| Increasing the reaction rate of hydroxynitrile lyase from Hevea brasiliensis toward mandelonitrile by copying active site residues from an esterase that accepts aromatic esters. |
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| Integrating biocatalysis into organic synthesis : special issue |
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| Larger active site in an ancestral hydroxynitrile lyase increases catalytically promiscuous esterase activity |
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| Manganese-substituted carbonic anhydrase as a new peroxidase |
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| Mapping the substrate selectivity of new hydrolases using colorimetric screening: lipases from Bacillus thermocatenulatus and Ophiostoma piliferum, esterases from Pseudomonas fluorescens and Streptomyces diastatochromogenes |
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| Mirror-image packing in enantiomer discrimination molecular basis for the enantioselectivity of B.cepacia lipase toward 2-methyl-3-phenyl-1-propanol. |
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| Molecular Basis for Enantioselectivity of Lipase from Pseudomonas cepacia toward Primary Alcohols. Modeling, Kinetics, and Chemical Modification of Tyr29 to Increase or Decrease Enantioselectivity. |
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| Molecular basis for the stereoselective ammoniolysis of N-alkyl aziridine-2-carboxylates catalyzed by Candida antarctica lipase B. |
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| Mutations in distant residues moderately increase the enantioselectivity of Pseudomonas fluorescens esterase towards methyl 3bromo-2-methylpropanoate and ethyl 3phenylbutyrate |
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| Natural product biosynthesis: the road to L |
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| New structural motif for carboxylic acid perhydrolases. |
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| One-step pretreatment of yellow poplar biomass using peracetic acid to enhance enzymatic digestibility. |
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| Production of 7-O-methyl aromadendrin, a medicinally valuable flavonoid, in Escherichia coli. |
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| Production of p-hydroxybenzoic acid from p-coumaric acid by Burkholderia glumae BGR1. |
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| Receptor-assisted combinatorial chemistry: thermodynamics and kinetics in drug discovery |
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| Remote interactions explain the unusual regioselectivity of lipase from Pseudomonas cepacia toward the secondary hydroxyl of 2'-deoxynucleosides. |
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| Revised molecular basis of the promiscuous carboxylic acid perhydrolase activity in serine hydrolases |
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| Stabilization of an α/β-Hydrolase by Introducing Proline Residues: Salicylic Acid Binding Protein 2 from Tobacco |
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| Survey of protein engineering strategies |
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| Switching Catalysis from Hydrolysis to Perhydrolysis in Pseudomonas fluorescens Esterase |
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| Switching from an esterase to a hydroxynitrile lyase mechanism requires only two amino acid substitutions |
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| Tech.Sight. Modeling--a tool for experimentalists |
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| Uncovering divergent evolution of α/β-hydrolases: a surprising residue substitution needed to convert Hevea brasiliensis hydroxynitrile lyase into an esterase |
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| Unexpected subtilisin-catalyzed hydrolysis of a sulfinamide bond in preference to a carboxamide bond in N-acyl sulfinamides. |
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