| Year |
Citation |
Score |
| 2021 |
Yi X, Khey J, Kazlauskas RJ, Travisano M. Plasmid hypermutation using a targeted artificial DNA replisome. Science Advances. 7. PMID 34272238 DOI: 10.1126/sciadv.abg8712 |
0.545 |
|
| 2020 |
Jones BJ, Evans RL, Mylrea NJ, Chaudhury D, Luo C, Guan B, Pierce CT, Gordon WR, Wilmot CM, Kazlauskas RJ. Larger active site in an ancestral hydroxynitrile lyase increases catalytically promiscuous esterase activity. Plos One. 15: e0235341. PMID 32603354 DOI: 10.1371/Journal.Pone.0235341 |
0.341 |
|
| 2020 |
Yi X, Kazlauskas R, Travisano M. Evolutionary innovation using EDGE, a system for localized elevated mutagenesis. Plos One. 15: e0232330. PMID 32353078 DOI: 10.1371/Journal.Pone.0232330 |
0.579 |
|
| 2017 |
Lin H, Kazlauskas RJ, Travisano M. Developmental evolution facilitates rapid adaptation. Scientific Reports. 7: 15891. PMID 29162942 DOI: 10.1038/S41598-017-16229-0 |
0.573 |
|
| 2017 |
Jones BJ, Lim HY, Huang J, Kazlauskas RJ. Comparison of five protein engineering strategies to stabilize an α/β-hydrolase. Biochemistry. PMID 29087185 DOI: 10.1021/Acs.Biochem.7B00571 |
0.319 |
|
| 2017 |
Lee PG, Kim J, Kim EJ, Lee SH, Choi KY, Kazlauskas RJ, Kim BG. Biosynthesis of (-)-5-hydroxy-equol and 5-hydroxy-dehydroequol from soy isoflavone, genistein using microbial whole cell bioconversion. Acs Chemical Biology. PMID 28985044 DOI: 10.1021/Acschembio.7B00624 |
0.308 |
|
| 2017 |
Lee HR, Kazlauskas RJ, Park TH. One-step pretreatment of yellow poplar biomass using peracetic acid to enhance enzymatic digestibility. Scientific Reports. 7: 12216. PMID 28939889 DOI: 10.1038/S41598-017-12542-W |
0.314 |
|
| 2017 |
Jones BJ, Bata Z, Kazlauskas RJ. Identical active sites in hydroxynitrile lyases show opposite enantioselectivity and reveal possible ancestral mechanism. Acs Catalysis. 7: 4221-4229. PMID 28798888 DOI: 10.1021/Acscatal.7B01108 |
0.33 |
|
| 2017 |
Ding Q, Kazlauskas RJ. Improving Pseudomonas fluorescens esterase for hydrolysis of lactones Catalysis Science & Technology. 7: 4756-4765. DOI: 10.1039/C7Cy01770G |
0.347 |
|
| 2017 |
Lee HR, Lee HW, Lee YW, Kazlauskas RJ, Park TH. Improved pretreatment of yellow poplar biomass using hot compressed water and enzymatically-generated peracetic acid Biomass & Bioenergy. 105: 190-196. DOI: 10.1016/J.Biombioe.2017.07.004 |
0.321 |
|
| 2017 |
Lee HR, Kazlauskas RJ, Park TH. Mild pretreatment of yellow poplar biomass using sequential dilute acid and enzymatically-generated peracetic acid to enhance cellulase accessibility Biotechnology and Bioprocess Engineering. 22: 405-412. DOI: 10.1007/S12257-017-0139-7 |
0.327 |
|
| 2016 |
Lin H, Travisano M, Kazlauskas RJ. The Fungus Trichoderma Regulates Submerged Conidiation Using the Steroid Pregnenolone. Acs Chemical Biology. PMID 27413801 DOI: 10.1021/Acschembio.6B00376 |
0.568 |
|
| 2016 |
Lin H, Travisano M, Kazlauskas RJ. Experimental Evolution of Trichoderma citrinoviride for Faster Deconstruction of Cellulose. Plos One. 11: e0147024. PMID 26820897 DOI: 10.1371/Journal.Pone.0147024 |
0.593 |
|
| 2016 |
Devamani T, Rauwerdink AM, Lunzer M, Jones BJ, Mooney JL, Tan MA, Zhang ZJ, Xu JH, Dean AM, Kazlauskas RJ. Catalytic promiscuity of ancestral esterases and hydroxynitrile lyases. Journal of the American Chemical Society. PMID 26736133 DOI: 10.1021/Jacs.5B12209 |
0.373 |
|
| 2015 |
Rauwerdink A, Kazlauskas RJ. How the Same Core Catalytic Machinery Catalyzes 17 Different Reactions: the Serine-Histidine-Aspartate Catalytic Triad of α/β-Hydrolase Fold Enzymes. Acs Catalysis. 5: 6153-6176. PMID 28580193 DOI: 10.1021/Acscatal.5B01539 |
0.389 |
|
| 2015 |
Jung DH, Kim EJ, Jung E, Kazlauskas RJ, Choi KY, Kim BG. Production of p-hydroxybenzoic acid from p-coumaric acid by Burkholderia glumae BGR1. Biotechnology and Bioengineering. PMID 26693833 DOI: 10.1002/Bit.25908 |
0.335 |
|
| 2015 |
Rauwerdink A, Lunzer M, Devamani T, Jones B, Mooney J, Zhang ZJ, Xu JH, Kazlauskas RJ, Dean AM. Evolution of a Catalytic Mechanism. Molecular Biology and Evolution. PMID 26681154 DOI: 10.1093/Molbev/Msv338 |
0.356 |
|
| 2015 |
Huang J, Jones BJ, Kazlauskas RJ. Stabilization of an α/β-Hydrolase by Introducing Proline Residues: Salicylic Acid Binding Protein 2 from Tobacco. Biochemistry. 54: 4330-41. PMID 26110207 DOI: 10.1021/Acs.Biochem.5B00333 |
0.326 |
|
| 2014 |
von Langermann J, Nedrud DM, Kazlauskas RJ. Increasing the reaction rate of hydroxynitrile lyase from Hevea brasiliensis toward mandelonitrile by copying active site residues from an esterase that accepts aromatic esters. Chembiochem : a European Journal of Chemical Biology. 15: 1931-8. PMID 25044660 DOI: 10.1002/Cbic.201402081 |
0.401 |
|
| 2014 |
Eum H, Kazlauskas RJ, Ha HJ. Molecular basis for the enantio- and diastereoselectivity of burkholderia cepacia lipase toward γ-Butyrolactone primary alcohols Iubmb Life. 356: 3585-3599. DOI: 10.1002/Adsc.201400510 |
0.353 |
|
| 2013 |
Choi KY, Jung EO, Yun H, Yang YH, Kazlauskas RJ, Kim BG. Development of colorimetric HTS assay of cytochrome p450 for ortho-specific hydroxylation, and engineering of CYP102D1 with enhanced catalytic activity and regioselectivity. Chembiochem : a European Journal of Chemical Biology. 14: 1231-8. PMID 23780920 DOI: 10.1002/Cbic.201300212 |
0.304 |
|
| 2013 |
Yin DT, Purpero VM, Fujii R, Jing Q, Kazlauskas RJ. New structural motif for carboxylic acid perhydrolases. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 3037-46. PMID 23325572 DOI: 10.1002/Chem.201202027 |
0.681 |
|
| 2013 |
Jung DH, Choi W, Choi KY, Jung E, Yun H, Kazlauskas RJ, Kim BG. Bioconversion of p-coumaric acid to p-hydroxystyrene using phenolic acid decarboxylase from B. amyloliquefaciens in biphasic reaction system. Applied Microbiology and Biotechnology. 97: 1501-11. PMID 23081771 DOI: 10.1007/S00253-012-4358-8 |
0.309 |
|
| 2012 |
Yin DT, Kazlauskas RJ. Revised molecular basis of the promiscuous carboxylic acid perhydrolase activity in serine hydrolases. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 8130-9. PMID 22618813 DOI: 10.1002/Chem.201200052 |
0.677 |
|
| 2012 |
Malla S, Koffas MA, Kazlauskas RJ, Kim BG. Production of 7-O-methyl aromadendrin, a medicinally valuable flavonoid, in Escherichia coli. Applied and Environmental Microbiology. 78: 684-94. PMID 22101053 DOI: 10.1128/Aem.06274-11 |
0.327 |
|
| 2012 |
Kazlauskas R. Biology evolves to fight chemistry Chemistry and Biology. 19: 435-437. DOI: 10.1016/J.Chembiol.2012.04.004 |
0.307 |
|
| 2011 |
Jochens H, Hesseler M, Stiba K, Padhi SK, Kazlauskas RJ, Bornscheuer UT. Protein engineering of α/β-hydrolase fold enzymes. Chembiochem : a European Journal of Chemical Biology. 12: 1508-17. PMID 21506229 DOI: 10.1002/Cbic.201000771 |
0.336 |
|
| 2011 |
Jiang Y, Morley KL, Schrag JD, Kazlauskas RJ. Different active-site loop orientation in serine hydrolases versus acyltransferases. Chembiochem : a European Journal of Chemical Biology. 12: 768-76. PMID 21351219 DOI: 10.1002/Cbic.201000693 |
0.332 |
|
| 2011 |
Yin DT, Jing Q, AlDajani WW, Duncan S, Tschirner U, Schilling J, Kazlauskas RJ. Improved pretreatment of lignocellulosic biomass using enzymatically-generated peracetic acid. Bioresource Technology. 102: 5183-92. PMID 21345668 DOI: 10.1016/J.Biortech.2011.01.079 |
0.668 |
|
| 2011 |
Colton IJ, Yin DT, Grochulski P, Kazlauskas RJ. Insights into the molecular basis of chiral acid recognition by Candida rugosa lipase from an X-ray crystal structure of a bound phosphonate transition state analog Advanced Synthesis & Catalysis. 353: 2529-2544. DOI: 10.2210/Pdb3Rar/Pdb |
0.641 |
|
| 2011 |
Colton IJ, Yin D, Grochulski P, Kazlauskas RJ. Molecular basis of chiral acid recognition by Candida rugosa lipase: X-ray structure of transition state analog and modeling of the hydrolysis of methyl 2-methoxy-2-phenylacetate Advanced Synthesis and Catalysis. 353: 2529-2544. DOI: 10.1002/Adsc.201100459 |
0.681 |
|
| 2010 |
Padhi SK, Fujii R, Legatt GA, Fossum SL, Berchtold R, Kazlauskas RJ. Switching from an esterase to a hydroxynitrile lyase mechanism requires only two amino acid substitutions. Chemistry & Biology. 17: 863-71. PMID 20797615 DOI: 10.1016/J.Chembiol.2010.06.013 |
0.326 |
|
| 2010 |
Yin de LT, Bernhardt P, Morley KL, Jiang Y, Cheeseman JD, Purpero V, Schrag JD, Kazlauskas RJ. Switching catalysis from hydrolysis to perhydrolysis in Pseudomonas fluorescens esterase. Biochemistry. 49: 1931-42. PMID 20112920 DOI: 10.1021/Bi9021268 |
0.405 |
|
| 2010 |
Duncan S, Jing Q, Katona A, Kazlauskas RJ, Schilling J, Tschirner U, Aldajani WW. Increased saccharification yields from aspen biomass upon treatment with enzymatically generated peracetic acid. Applied Biochemistry and Biotechnology. 160: 1637-52. PMID 19484411 DOI: 10.1007/S12010-009-8639-3 |
0.35 |
|
| 2009 |
Park JH, Ha HJ, Lee WK, Généreux-Vincent T, Kazlauskas RJ. Molecular basis for the stereoselective ammoniolysis of N-alkyl aziridine-2-carboxylates catalyzed by Candida antarctica lipase B. Chembiochem : a European Journal of Chemical Biology. 10: 2213-22. PMID 19672908 DOI: 10.1002/Cbic.200900343 |
0.364 |
|
| 2009 |
Jochens H, Stiba K, Savile C, Fujii R, Yu JG, Gerassenkov T, Kazlauskas RJ, Bornscheuer UT. Converting an esterase into an epoxide hydrolase. Angewandte Chemie (International Ed. in English). 48: 3532-5. PMID 19350592 DOI: 10.1002/Anie.200806276 |
0.348 |
|
| 2009 |
Kazlauskas R, Lutz S. Engineering enzymes by 'intelligent' design. Current Opinion in Chemical Biology. 13: 1-2. PMID 19272831 DOI: 10.1016/J.Cbpa.2009.02.022 |
0.334 |
|
| 2009 |
Jing Q, Okrasa K, Kazlauskas RJ. Stereoselective hydrogenation of olefins using rhodium-substituted carbonic anhydrase--a new reductase. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 1370-6. PMID 19115310 DOI: 10.1002/Chem.200801673 |
0.348 |
|
| 2008 |
Mugford PF, Wagner UG, Jiang Y, Faber K, Kazlauskas RJ. Enantiocomplementary enzymes: classification, molecular basis for their enantiopreference, and prospects for mirror-image biotransformations. Angewandte Chemie (International Ed. in English). 47: 8782-93. PMID 18850616 DOI: 10.1002/Anie.200705159 |
0.329 |
|
| 2008 |
Gorke JT, Srienc F, Kazlauskas RJ. Hydrolase-catalyzed biotransformations in deep eutectic solvents. Chemical Communications (Cambridge, England). 1235-7. PMID 18309428 DOI: 10.1039/B716317G |
0.36 |
|
| 2008 |
Mugford PF, Wagner UG, Jiang Y, Faber K, Kazlauskas RJ. Enantiokomplementäre Enzyme: Klassifizierung, molekulare Grundlage der Enantiopräferenz und Prognosen für spiegelbildliche Biotransformationen Angewandte Chemie. 120: 8912-8923. DOI: 10.1002/Ange.200705159 |
0.306 |
|
| 2006 |
Kazlauskas RJ. Engineering a multipurpose catalyst. Nature Chemical Biology. 2: 514-5. PMID 16983384 DOI: 10.1038/Nchembio1006-514 |
0.304 |
|
| 2006 |
Lavandera I, Fernández S, Magdalena J, Ferrero M, Grewal H, Savile CK, Kazlauskas RJ, Gotor V. Remote interactions explain the unusual regioselectivity of lipase from Pseudomonas cepacia toward the secondary hydroxyl of 2'-deoxynucleosides. Chembiochem : a European Journal of Chemical Biology. 7: 693-8. PMID 16491501 DOI: 10.1002/Cbic.200500451 |
0.353 |
|
| 2006 |
Okrasa K, Kazlauskas RJ. Manganese-substituted carbonic anhydrase as a new peroxidase. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 1587-96. PMID 16416502 DOI: 10.1002/Chem.200501413 |
0.313 |
|
| 2006 |
Morley KL, Chauve G, Kazlauskas R, Dupont C, Shareck F, Marchessault RH. Acetyl xylan esterase-catalyzed deacetylation of chitin and chitosan Carbohydrate Polymers. 63: 310-315. DOI: 10.1016/J.Carbpol.2005.07.034 |
0.35 |
|
| 2006 |
Savile CK, Kazlauskas RJ. The 3-(3-pyridine)propionyl anchor group for protease-catalyzed resolutions: p-toluenesulfinamide and sterically hindered secondary alcohols Advanced Synthesis and Catalysis. 348: 1183-1192. DOI: 10.1002/Adsc.200606040 |
0.339 |
|
| 2005 |
Kazlauskas R. Biological chemistry: Enzymes in focus Nature. 436: 1096-1097. PMID 16121163 DOI: 10.1038/4361096A |
0.345 |
|
| 2005 |
Lavandera I, Fernández S, Magdalena J, Ferrero M, Kazlauskas RJ, Gotor V. An inverse substrate orientation for the regioselective acylation of 3',5'-diaminonucleosides catalyzed by Candida antarctica lipase B? Chembiochem : a European Journal of Chemical Biology. 6: 1381-90. PMID 15977272 DOI: 10.1002/Cbic.200400422 |
0.353 |
|
| 2005 |
Mugford PF, Magloire VP, Kazlauskas RJ. Unexpected subtilisin-catalyzed hydrolysis of a sulfinamide bond in preference to a carboxamide bond in N-acyl sulfinamides. Journal of the American Chemical Society. 127: 6536-7. PMID 15869266 DOI: 10.1021/Ja0506105 |
0.302 |
|
| 2005 |
Morley KL, Kazlauskas RJ. Improving enzyme properties: when are closer mutations better? Trends in Biotechnology. 23: 231-7. PMID 15866000 DOI: 10.1016/J.Tibtech.2005.03.005 |
0.34 |
|
| 2005 |
Mezzetti A, Schrag JD, Cheong CS, Kazlauskas RJ. Mirror-image packing in enantiomer discrimination molecular basis for the enantioselectivity of B.cepacia lipase toward 2-methyl-3-phenyl-1-propanol. Chemistry & Biology. 12: 427-37. PMID 15850979 DOI: 10.1016/J.Chembiol.2005.01.016 |
0.34 |
|
| 2005 |
Kazlauskas RJ. Enhancing catalytic promiscuity for biocatalysis. Current Opinion in Chemical Biology. 9: 195-201. PMID 15811805 DOI: 10.1016/J.Cbpa.2005.02.008 |
0.355 |
|
| 2005 |
Bernhardt P, Hult K, Kazlauskas RJ. Molecular basis of perhydrolase activity in serine hydrolases. Angewandte Chemie (International Ed. in English). 44: 2742-6. PMID 15803517 DOI: 10.1002/Anie.200463006 |
0.32 |
|
| 2005 |
Savile CK, Magloire VP, Kazlauskas RJ. Subtilisin-catalyzed resolution of N-acyl arylsulfinamides. Journal of the American Chemical Society. 127: 2104-13. PMID 15713087 DOI: 10.1021/Ja045397B |
0.303 |
|
| 2005 |
Park S, Morley KL, Horsman GP, Holmquist M, Hult K, Kazlauskas RJ. Focusing mutations into the P. fluorescens esterase binding site increases enantioselectivity more effectively than distant mutations. Chemistry & Biology. 12: 45-54. PMID 15664514 DOI: 10.1016/J.Chembiol.2004.10.012 |
0.693 |
|
| 2004 |
Bornscheuer UT, Kazlauskas RJ. Catalytic promiscuity in biocatalysis: using old enzymes to form new bonds and follow new pathways. Angewandte Chemie (International Ed. in English). 43: 6032-40. PMID 15523680 DOI: 10.1002/Anie.200460416 |
0.382 |
|
| 2004 |
Mugford PF, Lait SM, Keay BA, Kazlauskas RJ. Enantiocomplementary enzymatic resolution of the chiral auxiliary: cis,cis-6-(2,2-dimethylpropanamido)spiro[4.4]nonan-1-ol and the molecular basis for the high enantioselectivity of subtilisin Carlsberg. Chembiochem : a European Journal of Chemical Biology. 5: 980-7. PMID 15239056 DOI: 10.1002/Cbic.200300909 |
0.33 |
|
| 2004 |
Cheeseman JD, Tocilj A, Park S, Schrag JD, Kazlauskas RJ. Structure of an aryl esterase from Pseudomonas fluorescens. Acta Crystallographica. Section D, Biological Crystallography. 60: 1237-43. PMID 15213385 DOI: 10.1107/S0907444904010522 |
0.312 |
|
| 2004 |
Morley KL, Magloire VP, Guérard C, Kazlauskas RJ. Parallel synthesis of an ester library for substrate mapping of esterases and lipases Tetrahedron Asymmetry. 15: 3005-3009. DOI: 10.1016/J.Tetasy.2004.07.048 |
0.326 |
|
| 2004 |
Somers NA, Kazlauskas RJ. Mapping the substrate selectivity and enantioselectivity of esterases from thermophiles Tetrahedron Asymmetry. 15: 2991-3004. DOI: 10.1016/J.Tetasy.2004.07.044 |
0.319 |
|
| 2004 |
Bornscheuer UT, Kazlauskas RJ. Untreue Enzyme in der Biokatalyse: mit alten Enzymen zu neuen Bindungen und Synthesewegen Angewandte Chemie. 116: 6156-6165. DOI: 10.1002/Ange.200460416 |
0.305 |
|
| 2003 |
Horsman GP, Liu AM, Henke E, Bornscheuer UT, Kazlauskas RJ. Mutations in distant residues moderately increase the enantioselectivity of Pseudomonas fluorescens esterase towards methyl 3bromo-2-methylpropanoate and ethyl 3phenylbutyrate. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 1933-9. PMID 12740839 DOI: 10.1002/Chem.200204551 |
0.677 |
|
| 2003 |
Park S, Viklund F, Hult K, Kazlauskas RJ. Vacuum-driven lipase-catalysed direct condensation of L-ascorbic acid and fatty acids in ionic liquids: Synthesis of a natural surface active antioxidant Green Chemistry. 5: 715-719. DOI: 10.1039/B307715B |
0.31 |
|
| 2003 |
Mezzetti A, Keith C, Kazlauskas RJ. Highly enantioselective kinetic resolution of primary alcohols of the type Ph-X-CH(CH3)-CH2OH by Pseudomonas cepacia lipase: Effect of acyl chain length and solvent Tetrahedron Asymmetry. 14: 3917-3924. DOI: 10.1016/J.Tetasy.2003.09.049 |
0.33 |
|
| 2003 |
Park S, Forró E, Grewal H, Fülöp F, Kazlauskas RJ. Molecular Basis for the Enantioselective Ring Opening of β-Lactams Catalyzed by Candida antarctica Lipase B Advanced Synthesis and Catalysis. 345: 986-995. DOI: 10.1002/Adsc.200303069 |
0.335 |
|
| 2003 |
Kazlauskas RJ. (S)‐(−)‐ and (R)‐(+)‐1,1′‐Bi‐2‐Naphthol Organic Syntheses. 60-60. DOI: 10.1002/0471264180.Os070.08 |
0.309 |
|
| 2001 |
Gascoyne DG, Finkbeiner HL, Chan KP, Gordon JL, Stewart KR, Kazlauskas RJ. Molecular basis for enantioselectivity of lipase from Chromobacterium viscosum toward the diesters of 2,3-dihydro-3-(4'-hydroxyphenyl)-1,1,3-trimethyl-1H-inden-5-ol. The Journal of Organic Chemistry. 66: 3041-8. PMID 11325269 DOI: 10.1021/Jo005681V |
0.362 |
|
| 2001 |
Liu AMF, Somers NA, Kazlauskas RJ, Brush TS, Zocher F, Enzelberger MM, Bornscheuer UT, Horsman GP, Mezzetti A, Schmidt-Dannert C, Schmid RD. Mapping the substrate selectivity of new hydrolases using colorimetric screening: Lipases from Bacillus thermocatenulatus and Ophiostoma piliferum, esterases from Pseudomonas fluorescens and Streptomyces diastatochromogenes Tetrahedron Asymmetry. 12: 545-556. DOI: 10.1016/S0957-4166(01)00072-6 |
0.691 |
|
| 2000 |
Kazlauskas RJ. Molecular modeling and biocatalysis: explanations, predictions, limitations, and opportunities. Current Opinion in Chemical Biology. 4: 81-8. PMID 10679382 DOI: 10.1016/S1367-5931(99)00056-3 |
0.307 |
|
| 1999 |
Tuomi WV, Kazlauskas RJ. Molecular Basis for Enantioselectivity of Lipase from Pseudomonas cepacia toward Primary Alcohols. Modeling, Kinetics, and Chemical Modification of Tyr29 to Increase or Decrease Enantioselectivity. The Journal of Organic Chemistry. 64: 2638-2647. PMID 11674331 DOI: 10.1021/Jo981783Y |
0.334 |
|
| 1999 |
Zhang M, Kazlauskas R. First preparation of enantiopure indane monomer, (S)-(-)- and (R)-(+)- 2,3-dihydro-3-(4'-hydroxyphenyl)-1,1,3-trimethyl-1H-inden-5-ol, via a unique enantio- and regioselective enzymatic kinetic resolution Journal of Organic Chemistry. 64: 7498-7503. DOI: 10.1021/Jo990795W |
0.352 |
|
| 1999 |
Janes LE, Cimpoia A, Kazlauskas RJ. Protease-mediated separation of cis and trans diastereomers of 2(R,S)- benzyloxymethyl-4(S)-carboxylic acid 1,3-dioxolane methyl ester: Intermediates for the synthesis of dioxolane nucleosides Journal of Organic Chemistry. 64: 9019-9029. DOI: 10.1021/Jo990757C |
0.339 |
|
| 1999 |
Weber HK, Weber H, Kazlauskas RJ. 'Watching' lipase-catalyzed acylations using 1H NMR: Competing hydrolysis of vinyl acetate in dry organic solvents Tetrahedron Asymmetry. 10: 2635-2638. DOI: 10.1016/S0957-4166(99)00274-8 |
0.349 |
|
| 1998 |
Kazlauskas RJ, Weber HK. Improving hydrolases for organic synthesis. Current Opinion in Chemical Biology. 2: 121-6. PMID 9667912 DOI: 10.1016/S1367-5931(98)80043-4 |
0.332 |
|
| 1998 |
Janes LE, Löwendahl AC, Kazlauskas RJ. Quantitative screening of hydrolase libraries using pH indicators: Identifying active and enantioselective hydrolases Chemistry - a European Journal. 4: 2324-2331. DOI: 10.1002/(Sici)1521-3765(19981102)4:11<2324::Aid-Chem2324>3.0.Co;2-I |
0.315 |
|
| 1997 |
Kazlauskas RJ, Weissfloch ANE. A structure-based rationalization of the enantiopreference of subtilisin toward secondary alcohols and isosteric primary amines Journal of Molecular Catalysis - B Enzymatic. 3: 65-72. DOI: 10.1016/S1381-1177(96)00040-9 |
0.352 |
|
| 1997 |
Janes LE, Kazlauskas RJ. Empirical rules for the enantiopreference of lipase from Aspergillus niger toward secondary alcohols and carboxylic acids, especially α-amino acids Tetrahedron Asymmetry. 8: 3719-3733. DOI: 10.1016/S0957-4166(97)00524-7 |
0.336 |
|
| 1996 |
Nobes GAR, Kazlauskas RJ, Marchessault RH. Lipase-catalyzed ring-opening polymerization of lactones: a novel route to poly(hydroxyalkanoate)s Macromolecules. 29: 4829-4833. DOI: 10.1021/Ma951774G |
0.3 |
|
| 1995 |
Serreqi AN, Kazlauskas RJ. Kinetic Resolution Of Sulfoxides With Pendant Acetoxy Groups Using Cholesterol Esterase : Substrate Mapping And An Empirical Rule For Chiral Phenols Canadian Journal of Chemistry. 73: 1357-1367. DOI: 10.1139/V95-167 |
0.352 |
|
| 1995 |
Colton IJ, Ahmed SN, Kazlauskas RJ. A 2-propanol treatment increases the enantioselectivity of Candida rugosa lipase toward esters of chiral carboxylic acids The Journal of Organic Chemistry. 60: 212-217. DOI: 10.1021/Jo00106A036 |
0.318 |
|
| 1994 |
Grochulski P, Bouthillier F, Kazlauskas RJ, Serreqi AN, Schrag JD, Ziomek E, Cygler M. Analogs of reaction intermediates identify a unique substrate binding site in Candida rugosa lipase. Biochemistry. 33: 3494-500. PMID 8142346 DOI: 10.1021/Bi00178A005 |
0.346 |
|
| 1994 |
Kazlauskas RJ. Elucidating structure-mechanism relationships in lipases: prospects for predicting and engineering catalytic properties. Trends in Biotechnology. 12: 464-72. PMID 7765546 DOI: 10.1016/0167-7799(94)90022-1 |
0.371 |
|
| 1994 |
Ahmed SN, Kazlauskas RJ, Morinville AH, Grochulski P, Schrag JD, Cygler M. Enantioselectivity of candida rugosa lipase toward carboxylic acids: A predictive rule from substrate mapping and x-ray crystallography Biocatalysis and Biotransformation. 9: 209-225. DOI: 10.3109/10242429408992121 |
0.352 |
|
| 1994 |
Ng-Youn-Chen MC, Serreqi AN, Huang Q, Kazlauskas RJ. Kinetic resolution of pipecolic acid using partially-purified lipase from Aspergillus niger Journal of Organic Chemistry. 59: 2075-2081. DOI: 10.1021/Jo00087A023 |
0.362 |
|
| 1994 |
Caron G, Kazlauskas RJ. Isolation of racemic 2,4-pentanediol and 2,5-hexanediol from commercial mixtures of racemic and meso isomers by way of cyclic sulfites. Tetrahedron: Asymmetry. 5: 657-664. DOI: 10.1016/0957-4166(94)80028-6 |
0.322 |
|
| 1993 |
Caron G, Kazlauskas RJ. Sequential kinetic resolution of (±)-2,3-butanediol in organic solvent using lipase from Pseudomonas cepacia. Tetrahedron: Asymmetry. 4: 1995-2000. DOI: 10.1016/S0957-4166(00)82248-X |
0.306 |
|
| 1987 |
Crans DC, Kazlauskas RJ, Hirschbein BL, Wong CH, Abril O, Whitesides GM. Enzymatic regeneration of adenosine 5'-triphosphate: acetyl phosphate, phosphoenolpyruvate, methoxycarbonyl phosphate, dihydroxyacetone phosphate, 5-phospho-alpha-D-ribosyl pyrophosphate, uridine-5'-diphosphoglucose. Methods in Enzymology. 136: 263-80. PMID 2446104 DOI: 10.1016/S0076-6879(87)36027-6 |
0.615 |
|
| 1985 |
Kazlauskas RJ, Whitesides GM. Synthesis of methoxycarbonyl phosphate, a new reagent having high phosphoryl donor potential for use in ATP cofactor regeneration Journal of Organic Chemistry. 50: 1069-1076. DOI: 10.1021/Jo00207A031 |
0.405 |
|
| 1983 |
Whitesides GM, Kazlauskas RJ, Josephson L. Magnetic separations in biotechnology Trends in Biotechnology. 1: 144-148. DOI: 10.1016/0167-7799(83)90005-7 |
0.339 |
|
| 1982 |
Wrighton MS, Graff JL, Kazlauskas RJ, Mitchener JC, Reichel CL. Photogeneration Of Reactive Organometallic Species Pure and Applied Chemistry. 54: 161-176. DOI: 10.1351/Pac198254010161 |
0.479 |
|
| 1982 |
Klein B, Kazlauskas RJ, Wrighton MS. Photochemistry of solution and surface-confined alkyl- and benzyltricarbonylcyclopentadienyltungsten complexes Organometallics. 1: 1338-1350. DOI: 10.1021/Om00070A016 |
0.423 |
|
| 1982 |
Kazlauskas RJ, Wrighton MS. Photochemistry of alkyldicarbonyl(.eta.5-cyclopentadienyl)iron and -ruthenium. Ligand substitution and alkene elimination via photogenerated sixteen-valence-electron intermediates Organometallics. 1: 602-611. DOI: 10.1021/Om00064A006 |
0.448 |
|
| 1982 |
Kazlauskas RJ, Wrighton MS. Photochemistry of metal carbonyl alkyls. Study of thermal β-hydrogen transfer in photogenerated, 16-valence-electron alkyldicarbonylcyclopentadienylmolybdenum and -tungsten complexes Journal of the American Chemical Society. 104: 6005-6015. DOI: 10.1021/Ja00386A029 |
0.455 |
|
| 1982 |
Kazlauskas RJ, Wrighton MS. Application of rapid-scan Fourier transform infrared spectroscopy to characterize the monodentate intermediate in the photochemical formation of tetracarbonyl(4,4′-dialkyl-2,2′-bipyridine)metal from hexacarbonylmetal Journal of the American Chemical Society. 104: 5784-5786. DOI: 10.1002/Chin.198303306 |
0.446 |
|
| 1982 |
Kazlauskas RJ, Wrighton MS. Photochemistry of alkyldicarbonyl(η5-cyclopentadienyl)iron and -ruthenium. Ligand substitution and alkene elimination via photogenerated 16-valence-electron intermediates Organometallics. 1: 602-611. |
0.379 |
|
| 1980 |
Kazlauskas RJ, Wrighton MS. Photogeneration of intermediates involved in catalytic cycles. .beta.-Hydride elimination from the 16-electron alkyl species generated by irradiation of tricarbonyl(.eta.5-cyclopentadienyl)(n-pentyl)tungsten(II) Journal of the American Chemical Society. 102: 1727-1730. DOI: 10.1021/Ja00525A048 |
0.453 |
|
| 1980 |
Kazlauskas RJ, Wrighton MS. Photogeneration of intermediates involved in catalytic cycles. β-Hydride elimination from the 16-electron alkyl species generated by irradiation of tricarbonyl(η5-cyclopentadienyl)(n-pentyl)tungsten(II) [7] Journal of the American Chemical Society. 102: 1727-1730. |
0.402 |
|
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