New generation of biocatalysts for organic synthesis BM Nestl, SC Hammer, BA Nebel, B Hauer Angewandte Chemie International Edition 53 (12), 3070-3095, 2014 | 395 | 2014 |
Recent progress in industrial biocatalysis BM Nestl, BA Nebel, B Hauer Current opinion in chemical biology 15 (2), 187-193, 2011 | 303 | 2011 |
Engineering of flexible loops in enzymes BM Nestl, B Hauer Acs Catalysis 4 (9), 3201-3211, 2014 | 173 | 2014 |
Enzyme toolbox: novel enantiocomplementary imine reductases PN Scheller, S Fademrecht, S Hofelzer, J Pleiss, F Leipold, NJ Turner, ... ChemBioChem 15 (15), 2201-2204, 2014 | 140 | 2014 |
Bacterial CYP153A monooxygenases for the synthesis of omega-hydroxylated fatty acids SH Malca, D Scheps, L Kühnel, E Venegas-Venegas, A Seifert, BM Nestl, ... Chemical communications 48 (42), 5115-5117, 2012 | 125 | 2012 |
Imine reductase‐catalyzed intermolecular reductive amination of aldehydes and ketones PN Scheller, M Lenz, SC Hammer, B Hauer, BM Nestl ChemCatChem 7 (20), 3239-3242, 2015 | 120 | 2015 |
Regioselective ω-hydroxylation of medium-chain n-alkanes and primary alcohols by CYP153 enzymes from Mycobacterium marinum and Polaromonas sp. strain JS666 D Scheps, SH Malca, H Hoffmann, BM Nestl, B Hauer Organic & biomolecular chemistry 9 (19), 6727-6733, 2011 | 112 | 2011 |
Synthesis of ω‐hydroxy dodecanoic acid based on an engineered CYP153A fusion construct D Scheps, S Honda Malca, SM Richter, K Marisch, BM Nestl, B Hauer Microbial biotechnology 6 (6), 694-707, 2013 | 109 | 2013 |
Squalene hopene cyclases are protonases for stereoselective Brønsted acid catalysis SC Hammer, A Marjanovic, JM Dominicus, BM Nestl, B Hauer Nature chemical biology 11 (2), 121-126, 2015 | 105 | 2015 |
Recent advances in imine reductase-catalyzed reactions M Lenz, N Borlinghaus, L Weinmann, BM Nestl World Journal of Microbiology and Biotechnology 33, 1-10, 2017 | 77 | 2017 |
Squalene hopene cyclases: highly promiscuous and evolvable catalysts for stereoselective CC and CX bond formation SC Hammer, PO Syrén, M Seitz, BM Nestl, B Hauer Current opinion in chemical biology 17 (2), 293-300, 2013 | 74 | 2013 |
Engineering Rieske Non‐Heme Iron Oxygenases for the Asymmetric Dihydroxylation of Alkenes C Gally, BM Nestl, B Hauer Angewandte Chemie International Edition 54 (44), 12952-12956, 2015 | 65 | 2015 |
Biokatalysatoren für die organische Synthese–die neue Generation BM Nestl, SC Hammer, BA Nebel, B Hauer Angewandte Chemie 126 (12), 3132-3158, 2014 | 63 | 2014 |
Synthesis of heterocyclic terpenoids by promiscuous squalene-hopene cyclases. M Seitz, PO Syrén, L Steiner, J Klebensberger, BM Nestl, B Hauer Chembiochem: a European Journal of Chemical Biology 14 (4), 436-439, 2013 | 63 | 2013 |
Asymmetric ketone reduction by imine reductases M Lenz, J Meisner, L Quertinmont, S Lutz, J Kästner, BM Nestl ChemBioChem 18 (3), 253-256, 2017 | 60 | 2017 |
Asymmetric enzymatic hydration of unactivated, aliphatic alkenes RM Demming, SC Hammer, BM Nestl, S Gergel, S Fademrecht, J Pleiss, ... Angewandte Chemie 131 (1), 179-183, 2019 | 59 | 2019 |
Identification of imine reductase‐specific sequence motifs S Fademrecht, PN Scheller, BM Nestl, B Hauer, J Pleiss Proteins: Structure, Function, and Bioinformatics 84 (5), 600-610, 2016 | 59 | 2016 |
Variations in the stability of NCR ene reductase by rational enzyme loop modulation S Reich, N Kress, BM Nestl, B Hauer Journal of structural biology 185 (2), 228-233, 2014 | 58 | 2014 |
Squalene-hopene cyclases—evolution, dynamics and catalytic scope PO Syren, S Henche, A Eichler, BM Nestl, B Hauer Current opinion in structural biology 41, 73-82, 2016 | 53 | 2016 |
Biocatalytic approaches for the quantitative production of single stereoisomers from racemates P Gadler, SM Glueck, W Kroutil, BM Nestl, B Larissegger-Schnell, ... Biochemical Society Transactions 34 (2), 296-300, 2006 | 49 | 2006 |