97 related articles for article (PubMed ID: 22526807)
1. Asymmetric bioreduction of activated alkenes by a novel isolate of Achromobacter species producing enoate reductase.
Liu YJ; Pei XQ; Lin H; Gai P; Liu YC; Wu ZL
Appl Microbiol Biotechnol; 2012 Aug; 95(3):635-45. PubMed ID: 22526807
[TBL] [Abstract][Full Text] [Related]
2. An enoate reductase Achr-OYE4 from Achromobacter sp. JA81: characterization and application in asymmetric bioreduction of C=C bonds.
Wang HB; Pei XQ; Wu ZL
Appl Microbiol Biotechnol; 2014 Jan; 98(2):705-15. PubMed ID: 23644746
[TBL] [Abstract][Full Text] [Related]
3. Asymmetric reduction of activated alkenes using an enoate reductase from Gluconobacter oxydans.
Richter N; Gröger H; Hummel W
Appl Microbiol Biotechnol; 2011 Jan; 89(1):79-89. PubMed ID: 20717668
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Recombinant expression and characterisation of the oxygen-sensitive 2-enoate reductase from Clostridium sporogenes.
Mordaka PM; Hall SJ; Minton N; Stephens G
Microbiology (Reading); 2018 Feb; 164(2):122-132. PubMed ID: 29111967
[TBL] [Abstract][Full Text] [Related]
6. An ene reductase from Clavispora lusitaniae for asymmetric reduction of activated alkenes.
Ni Y; Yu HL; Lin GQ; Xu JH
Enzyme Microb Technol; 2014 Mar; 56():40-5. PubMed ID: 24564901
[TBL] [Abstract][Full Text] [Related]
7. Novel gene clusters involved in arsenite oxidation and resistance in two arsenite oxidizers: Achromobacter sp. SY8 and Pseudomonas sp. TS44.
Cai L; Rensing C; Li X; Wang G
Appl Microbiol Biotechnol; 2009 Jun; 83(4):715-25. PubMed ID: 19283378
[TBL] [Abstract][Full Text] [Related]
8. Chemoselective biocatalytic reduction of conjugated nitroalkenes: new application for an Escherichia coli BL21(DE3) expression strain.
Jovanovic P; Jeremic S; Djokic L; Savic V; Radivojevic J; Maslak V; Ivkovic B; Vasiljevic B; Nikodinovic-Runic J
Enzyme Microb Technol; 2014 Jun; 60():16-23. PubMed ID: 24835095
[TBL] [Abstract][Full Text] [Related]
9. Cloning, expression, and directed evolution of carbonyl reductase from Leifsonia xyli HS0904 with enhanced catalytic efficiency.
Wang NQ; Sun J; Huang J; Wang P
Appl Microbiol Biotechnol; 2014 Oct; 98(20):8591-601. PubMed ID: 24788330
[TBL] [Abstract][Full Text] [Related]
10. Stereoselective synthesis of (R)-3-quinuclidinol through asymmetric reduction of 3-quinuclidinone with 3-quinuclidinone reductase of Rhodotorula rubra.
Uzura A; Nomoto F; Sakoda A; Nishimoto Y; Kataoka M; Shimizu S
Appl Microbiol Biotechnol; 2009 Jun; 83(4):617-26. PubMed ID: 19234697
[TBL] [Abstract][Full Text] [Related]
11. Oxidation of arsenite by two β-proteobacteria isolated from soil.
Bachate SP; Khapare RM; Kodam KM
Appl Microbiol Biotechnol; 2012 Mar; 93(5):2135-45. PubMed ID: 21983709
[TBL] [Abstract][Full Text] [Related]
12. Recombinant S. cerevisiae expressing Old Yellow Enzymes from non-conventional yeasts: an easy system for selective reduction of activated alkenes.
Romano D; Contente ML; Molinari F; Eberini I; Ruvutuso E; Sensi C; Amaretti A; Rossi M; Raimondi S
Microb Cell Fact; 2014 Apr; 13():60. PubMed ID: 24767246
[TBL] [Abstract][Full Text] [Related]
13. Asymmetric alkene reduction by yeast old yellow enzymes and by a novel Zymomonas mobilis reductase.
Müller A; Hauer B; Rosche B
Biotechnol Bioeng; 2007 Sep; 98(1):22-9. PubMed ID: 17657768
[TBL] [Abstract][Full Text] [Related]
14. Asymmetric bioreduction of activated alkenes to industrially relevant optically active compounds.
Winkler CK; Tasnádi G; Clay D; Hall M; Faber K
J Biotechnol; 2012 Dec; 162(4):381-9. PubMed ID: 22498437
[TBL] [Abstract][Full Text] [Related]
15. Genome sequence of the highly efficient arsenite-oxidizing bacterium Achromobacter arsenitoxydans SY8.
Li X; Hu Y; Gong J; Lin Y; Johnstone L; Rensing C; Wang G
J Bacteriol; 2012 Mar; 194(5):1243-4. PubMed ID: 22328747
[TBL] [Abstract][Full Text] [Related]
16. Asymmetric bioreduction of activated alkenes using cloned 12-oxophytodienoate reductase isoenzymes OPR-1 and OPR-3 from Lycopersicon esculentum (tomato): a striking change of stereoselectivity.
Hall M; Stueckler C; Kroutil W; Macheroux P; Faber K
Angew Chem Int Ed Engl; 2007; 46(21):3934-7. PubMed ID: 17431865
[No Abstract] [Full Text] [Related]
17. A highly efficient ADH-coupled NADH-recycling system for the asymmetric bioreduction of carbon-carbon double bonds using enoate reductases.
Tauber K; Hall M; Kroutil W; Fabian WM; Faber K; Glueck SM
Biotechnol Bioeng; 2011 Jun; 108(6):1462-7. PubMed ID: 21328323
[TBL] [Abstract][Full Text] [Related]
18. Biochemical characterization and substrate profiling of a new NADH-dependent enoate reductase from Lactobacillus casei.
Gao X; Ren J; Wu Q; Zhu D
Enzyme Microb Technol; 2012 Jun; 51(1):26-34. PubMed ID: 22579387
[TBL] [Abstract][Full Text] [Related]
19. Asymmetric biocatalytic reduction of 3,5-bis(trifluoromethyl) acetophenone to (1R)-[3,5-bis(trifluoromethyl)phenyl] ethanol using whole cells of newly isolated Leifsonia xyli HS0904.
Wang P; Cai JB; Ouyang Q; He JY; Su HZ
Appl Microbiol Biotechnol; 2011 Jun; 90(6):1897-904. PubMed ID: 21614678
[TBL] [Abstract][Full Text] [Related]
20. Isolation and characterization of novel human short-chain dehydrogenase/reductase SCDR10B which is highly expressed in the brain and acts as hydroxysteroid dehydrogenase.
Huang C; Wan B; Gao B; Hexige S; Yu L
Acta Biochim Pol; 2009; 56(2):279-89. PubMed ID: 19436836
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]