129 related articles for article (PubMed ID: 25675259)
1. Investigation of the stereochemical course of ene reductase-catalysed reactions by deuterium labelling.
Brenna E; Fronza G; Fuganti C; Parmeggiani F
Isotopes Environ Health Stud; 2015; 51(1):24-32. PubMed ID: 25675259
[TBL] [Abstract][Full Text] [Related]
2. "A Study in Yellow": Investigations in the Stereoselectivity of Ene-Reductases.
Parmeggiani F; Brenna E; Colombo D; Gatti FG; Tentori F; Tessaro D
Chembiochem; 2022 Jan; 23(1):e202100445. PubMed ID: 34586700
[TBL] [Abstract][Full Text] [Related]
3. Asymmetric Ene-Reduction by F
Kang SW; Antoney J; Lupton DW; Speight R; Scott C; Jackson CJ
Chembiochem; 2023 Apr; 24(8):e202200797. PubMed ID: 36716144
[TBL] [Abstract][Full Text] [Related]
4. Site-saturation mutagenesis of tryptophan 116 of Saccharomyces pastorianus old yellow enzyme uncovers stereocomplementary variants.
Padhi SK; Bougioukou DJ; Stewart JD
J Am Chem Soc; 2009 Mar; 131(9):3271-80. PubMed ID: 19226127
[TBL] [Abstract][Full Text] [Related]
5. Ene-Reductase: A Multifaceted Biocatalyst in Organic Synthesis.
Kumar Roy T; Sreedharan R; Ghosh P; Gandhi T; Maiti D
Chemistry; 2022 Apr; 28(21):e202103949. PubMed ID: 35133702
[TBL] [Abstract][Full Text] [Related]
6. Asymmetric Ene-Reduction of α,β-Unsaturated Compounds by F
Kang SW; Antoney J; Frkic RL; Lupton DW; Speight R; Scott C; Jackson CJ
Biochemistry; 2023 Feb; 62(3):873-891. PubMed ID: 36637210
[TBL] [Abstract][Full Text] [Related]
7. A Rapid and High-Throughput Assay for the Estimation of Conversions of Ene-Reductase-Catalysed Reactions.
Forchin MC; Crotti M; Gatti FG; Parmeggiani F; Brenna E; Monti D
Chembiochem; 2015 Jul; 16(11):1571-3. PubMed ID: 26033160
[TBL] [Abstract][Full Text] [Related]
8. Comparative characterization of novel ene-reductases from cyanobacteria.
Fu Y; Castiglione K; Weuster-Botz D
Biotechnol Bioeng; 2013 May; 110(5):1293-301. PubMed ID: 23280373
[TBL] [Abstract][Full Text] [Related]
9. Bioreduction of alpha-methylcinnamaldehyde derivatives: chemo-enzymatic asymmetric synthesis of Lilial and Helional.
Stueckler C; Mueller NJ; Winkler CK; Glueck SM; Gruber K; Steinkellner G; Faber K
Dalton Trans; 2010 Sep; 39(36):8472-6. PubMed ID: 20461254
[TBL] [Abstract][Full Text] [Related]
10. Two new ene-reductases from photosynthetic extremophiles enlarge the panel of old yellow enzymes: CtOYE and GsOYE.
Robescu MS; Niero M; Hall M; Cendron L; Bergantino E
Appl Microbiol Biotechnol; 2020 Mar; 104(5):2051-2066. PubMed ID: 31930452
[TBL] [Abstract][Full Text] [Related]
11. Characterization of an ene-reductase from Meyerozyma guilliermondii for asymmetric bioreduction of α,β-unsaturated compounds.
Zhang B; Zheng L; Lin J; Wei D
Biotechnol Lett; 2016 Sep; 38(9):1527-34. PubMed ID: 27193896
[TBL] [Abstract][Full Text] [Related]
12. Loop-Grafted Old Yellow Enzymes in the Bienzymatic Cascade Reduction of Allylic Alcohols.
Reich S; Nestl BM; Hauer B
Chembiochem; 2016 Apr; 17(7):561-5. PubMed ID: 27037735
[TBL] [Abstract][Full Text] [Related]
13. Novel Old Yellow Enzyme Subclasses.
Peters C; Frasson D; Sievers M; Buller R
Chembiochem; 2019 Jun; 20(12):1569-1577. PubMed ID: 30758121
[TBL] [Abstract][Full Text] [Related]
14. Asymmetric bioreduction of alkenes using ene-reductases YersER and KYE1 and effects of organic solvents.
Yanto Y; Winkler CK; Lohr S; Hall M; Faber K; Bommarius AS
Org Lett; 2011 May; 13(10):2540-3. PubMed ID: 21510626
[TBL] [Abstract][Full Text] [Related]
15. Biocatalytic reduction of activated CC-bonds and beyond: emerging trends.
Winkler CK; Faber K; Hall M
Curr Opin Chem Biol; 2018 Apr; 43():97-105. PubMed ID: 29275291
[TBL] [Abstract][Full Text] [Related]
16. Biocatalysis with thermostable enzymes: structure and properties of a thermophilic 'ene'-reductase related to old yellow enzyme.
Adalbjörnsson BV; Toogood HS; Fryszkowska A; Pudney CR; Jowitt TA; Leys D; Scrutton NS
Chembiochem; 2010 Jan; 11(2):197-207. PubMed ID: 19943268
[TBL] [Abstract][Full Text] [Related]
17. Asymmetric Reductive Carbocyclization Using Engineered Ene Reductases.
Heckenbichler K; Schweiger A; Brandner LA; Binter A; Toplak M; Macheroux P; Gruber K; Breinbauer R
Angew Chem Int Ed Engl; 2018 Jun; 57(24):7240-7244. PubMed ID: 29689601
[TBL] [Abstract][Full Text] [Related]
18. New developments in 'ene'-reductase catalysed biological hydrogenations.
Toogood HS; Scrutton NS
Curr Opin Chem Biol; 2014 Apr; 19():107-15. PubMed ID: 24608082
[TBL] [Abstract][Full Text] [Related]
19. Asymmetric bioreduction of activated C=C bonds using enoate reductases from the old yellow enzyme family.
Stuermer R; Hauer B; Hall M; Faber K
Curr Opin Chem Biol; 2007 Apr; 11(2):203-13. PubMed ID: 17353140
[TBL] [Abstract][Full Text] [Related]
20. Biocatalytic Asymmetric Alkene Reduction: Crystal Structure and Characterization of a Double Bond Reductase from
Mansell DJ; Toogood HS; Waller J; Hughes JM; Levy CW; Gardiner JM; Scrutton NS
ACS Catal; 2013 Mar; 3(3):370-379. PubMed ID: 27547488
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
