Dufault-Thompson K, Levy S, Hall B, Jiang X
ISME J. 2024; 18(1).
PMID: 39658189
PMC: 11669818.
DOI: 10.1093/ismejo/wrae242.
Zahn L, Gannon P, Rajakovich L
Metallomics. 2024; 16(11).
PMID: 39504489
PMC: 11574389.
DOI: 10.1093/mtomcs/mfae049.
Sahrawat A, Polidori N, Kroutil W, Gruber K
ACS Catal. 2024; 14(3):1257-1266.
PMID: 38327643
PMC: 10845114.
DOI: 10.1021/acscatal.3c04362.
Knaus T, Corrado M, Mutti F
ACS Catal. 2022; 12(23):14459-14475.
PMID: 36504913
PMC: 9724091.
DOI: 10.1021/acscatal.2c03052.
Luzny M, Krzywda M, Kozlowska E, Kostrzewa-Suslow E, Janeczko T
Molecules. 2019; 24(17).
PMID: 31480751
PMC: 6749209.
DOI: 10.3390/molecules24173185.
Stereoselectivity Switch in the Reduction of α-Alkyl-β-Arylenones by Structure-Guided Designed Variants of the Ene Reductase OYE1.
Crotti M, Parmeggiani F, Ferrandi E, Gatti F, Sacchetti A, Riva S
Front Bioeng Biotechnol. 2019; 7:89.
PMID: 31080798
PMC: 6497740.
DOI: 10.3389/fbioe.2019.00089.
C3 and C6 Modification-Specific OYE Biotransformations of Synthetic Carvones and Sequential BVMO Chemoenzymatic Synthesis of Chiral Caprolactones.
Issa I, Toogood H, Johannissen L, Raftery J, Scrutton N, Gardiner J
Chemistry. 2018; 25(12):2983-2988.
PMID: 30468546
PMC: 6468273.
DOI: 10.1002/chem.201805219.
Asymmetric Reductive Carbocyclization Using Engineered Ene Reductases.
Heckenbichler K, Schweiger A, Brandner L, Binter A, Toplak M, Macheroux P
Angew Chem Int Ed Engl. 2018; 57(24):7240-7244.
PMID: 29689601
PMC: 6033016.
DOI: 10.1002/anie.201802962.
Sequential Enzymatic Conversion of α-Angelica Lactone to γ-Valerolactone through Hydride-Independent C=C Bond Isomerization.
Turrini N, Eger E, Reiter T, Faber K, Hall M
ChemSusChem. 2016; 9(24):3393-3396.
PMID: 27885835
PMC: 5574032.
DOI: 10.1002/cssc.201601363.
Functional Annotation of a Presumed Nitronate Monoxygenase Reveals a New Class of NADH:Quinone Reductases.
Ball J, Salvi F, Gadda G
J Biol Chem. 2016; 291(40):21160-21170.
PMID: 27502282
PMC: 5076524.
DOI: 10.1074/jbc.M116.739151.
The Chemistry of Gut Microbial Metabolism of Polyphenols.
Stevens J, Maier C
Phytochem Rev. 2016; 15(3):425-444.
PMID: 27274718
PMC: 4888912.
DOI: 10.1007/s11101-016-9459-z.
Better than Nature: Nicotinamide Biomimetics That Outperform Natural Coenzymes.
Knaus T, Paul C, Levy C, de Vries S, Mutti F, Hollmann F
J Am Chem Soc. 2016; 138(3):1033-9.
PMID: 26727612
PMC: 4731831.
DOI: 10.1021/jacs.5b12252.
STRUCTURAL AND FUNCTIONAL CONSEQUENCES OF CIRCULAR PERMUTATION ON THE ACTIVE SITE OF OLD YELLOW ENZYME.
Daugherty A, Horton J, Cheng X, Lutz S
ACS Catal. 2015; 5(2):892-899.
PMID: 25692074
PMC: 4327928.
DOI: 10.1021/cs501702k.
Structure of an Aspergillus fumigatus old yellow enzyme (EasA) involved in ergot alkaloid biosynthesis.
Chilton A, Ellis A, Lamb A
Acta Crystallogr F Struct Biol Commun. 2014; 70(Pt 10):1328-32.
PMID: 25286934
PMC: 4188074.
DOI: 10.1107/S2053230X14018962.
Comparative structural modeling of six old yellow enzymes (OYEs) from the necrotrophic fungus Ascochyta rabiei: insight into novel OYE classes with differences in cofactor binding, organization of active site residues and stereopreferences.
Nizam S, Gazara R, Verma S, Singh K, Verma P
PLoS One. 2014; 9(4):e95989.
PMID: 24776850
PMC: 4002455.
DOI: 10.1371/journal.pone.0095989.
NAD(P)H-independent asymmetric C=C bond reduction catalyzed by ene reductases by using artificial co-substrates as the hydrogen donor.
Winkler C, Clay D, Entner M, Plank M, Faber K
Chemistry. 2014; 20(5):1403-9.
PMID: 24382795
PMC: 4413776.
DOI: 10.1002/chem.201303897.
Overcoming co-product inhibition in the nicotinamide independent asymmetric bioreduction of activated C=C-bonds using flavin-dependent ene-reductases.
Winkler C, Clay D, van Heerden E, Faber K
Biotechnol Bioeng. 2013; 110(12):3085-92.
PMID: 23794404
PMC: 4034509.
DOI: 10.1002/bit.24981.
Asymmetric bioreduction of activated carbon-carbon double bonds using Shewanella yellow enzyme (SYE-4) as novel enoate reductase.
Iqbal N, Rudroff F, Brige A, Van Beeumen J, Mihovilovic M
Tetrahedron. 2012; 68(37):7619-7623.
PMID: 22991485
PMC: 3415682.
DOI: 10.1016/j.tet.2012.05.092.
Asymmetric bioreduction of activated alkenes to industrially relevant optically active compounds.
Winkler C, Tasnadi G, Clay D, Hall M, Faber K
J Biotechnol. 2012; 162(4):381-9.
PMID: 22498437
PMC: 3521962.
DOI: 10.1016/j.jbiotec.2012.03.023.
Nicotinamide-independent asymmetric bioreduction of C=C-bonds via disproportionation of enones catalyzed by enoate reductases.
Stueckler C, Reiter T, Baudendistel N, Faber K
Tetrahedron. 2011; 66(3-2):663-667.
PMID: 21270958
PMC: 3007678.
DOI: 10.1016/j.tet.2009.11.065.