120 related articles for article (PubMed ID: 38428763)
1. Identification and characterization of an ene-reductase from Corynebacterium casei.
Wu S; Ma X; Yan H
Int J Biol Macromol; 2024 Apr; 264(Pt 1):130427. PubMed ID: 38428763
[TBL] [Abstract][Full Text] [Related]
2. Identification of a novel ene reductase from
Zhang B; Sun J; Zheng Y; Mao X; Lin J; Wei D
RSC Adv; 2022 May; 12(22):13924-13931. PubMed ID: 35558851
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Asymmetric Reduction of (R)-Carvone through a Thermostable and Organic-Solvent-Tolerant Ene-Reductase.
Tischler D; Gädke E; Eggerichs D; Gomez Baraibar A; Mügge C; Scholtissek A; Paul CE
Chembiochem; 2020 Apr; 21(8):1217-1225. PubMed ID: 31692216
[TBL] [Abstract][Full Text] [Related]
5. 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]
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. 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]
8. 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]
9. 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]
10. Rhodococcus strains as source for ene-reductase activity.
Chen BS; Médici R; van der Helm MP; van Zwet Y; Gjonaj L; van der Geest R; Otten LG; Hanefeld U
Appl Microbiol Biotechnol; 2018 Jul; 102(13):5545-5556. PubMed ID: 29705954
[TBL] [Abstract][Full Text] [Related]
11. Loop 6 and the β-hairpin flap are structural hotspots that determine cofactor specificity in the FMN-dependent family of ene-reductases.
Kerschbaumer B; Totaro MG; Friess M; Breinbauer R; Bijelic A; Macheroux P
FEBS J; 2024 Apr; 291(7):1560-1574. PubMed ID: 38263933
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Stereoselective synthesis of (R)-phenylephrine using recombinant Escherichia coli cells expressing a novel short-chain dehydrogenase/reductase gene from Serratia marcescens BCRC 10948.
Peng GJ; Kuan YC; Chou HY; Fu TK; Lin JS; Hsu WH; Yang MT
J Biotechnol; 2014 Jan; 170():6-9. PubMed ID: 24291189
[TBL] [Abstract][Full Text] [Related]
14. Enantioselective synthesis of enantiopure chiral alcohols using carbonyl reductases screened from Yarrowia lipolytica.
Zhang HL; Zhang C; Pei CH; Han MN; Li W
J Appl Microbiol; 2019 Jan; 126(1):127-137. PubMed ID: 30291666
[TBL] [Abstract][Full Text] [Related]
15. Identification of four ene reductases and their preliminary exploration in the asymmetric synthesis of (R)-dihydrocarvone and (R)-profen derivatives.
Shi Q; Jia Y; Wang H; Li S; Li H; Guo J; Dou T; Qin B; You S
Enzyme Microb Technol; 2021 Oct; 150():109880. PubMed ID: 34489033
[TBL] [Abstract][Full Text] [Related]
16. A novel NADPH-dependent reductase of Sulfobacillus acidophilus TPY phenol hydroxylase: expression, characterization, and functional analysis.
Li M; Guo W; Chen X
Appl Microbiol Biotechnol; 2016 Dec; 100(24):10417-10428. PubMed ID: 27376793
[TBL] [Abstract][Full Text] [Related]
17. Biocatalytic properties of a recombinant aldo-keto reductase with broad substrate spectrum and excellent stereoselectivity.
Ni Y; Li CX; Ma HM; Zhang J; Xu JH
Appl Microbiol Biotechnol; 2011 Feb; 89(4):1111-8. PubMed ID: 20981419
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. A thermophilic-like ene-reductase originating from an acidophilic iron oxidizer.
Scholtissek A; Ullrich SR; Mühling M; Schlömann M; Paul CE; Tischler D
Appl Microbiol Biotechnol; 2017 Jan; 101(2):609-619. PubMed ID: 27542380
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]