Cargando…

Asymmetric Reduction of (R)‐Carvone through a Thermostable and Organic‐Solvent‐Tolerant Ene‐Reductase

Ene‐reductases allow regio‐ and stereoselective reduction of activated C=C double bonds at the expense of nicotinamide adenine dinucleotide cofactors [NAD(P)H]. Biological NAD(P)H can be replaced by synthetic mimics to facilitate enzyme screening and process optimization. The ene‐reductase FOYE‐1, o...

Descripción completa

Detalles Bibliográficos
Autores principales:	Tischler, Dirk, Gädke, Eric, Eggerichs, Daniel, Gomez Baraibar, Alvaro, Mügge, Carolin, Scholtissek, Anika, Paul, Caroline E.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2020
Materias:	Full Papers
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216909/ https://www.ncbi.nlm.nih.gov/pubmed/31692216 http://dx.doi.org/10.1002/cbic.201900599

Ejemplares similares

Asymmetric Whole-Cell Bio-Reductions of (R)-Carvone Using Optimized Ene Reductases
por: Mähler, Christoph, et al.
Publicado: (2019)

Catalytic Performance of a Class III Old Yellow Enzyme and Its Cysteine Variants
por: Scholtissek, Anika, et al.
Publicado: (2018)

Chemoenzymatic Cascade Synthesis of Optically Pure Alkanoic Acids by Using Engineered Arylmalonate Decarboxylase Variants
por: Enoki, Junichi, et al.
Publicado: (2019)

Asymmetric Reductive Carbocyclization Using Engineered Ene Reductases
por: Heckenbichler, Kathrin, et al.
Publicado: (2018)

Flavin-dependent N-hydroxylating enzymes: distribution and application
por: Mügge, Carolin, et al.
Publicado: (2020)

Functional characterization and stability improvement of a ‘thermophilic-like’ ene-reductase from Rhodococcus opacus 1CP
por: Riedel, Anika, et al.
Publicado: (2015)

NAD(P)H-Independent Asymmetric C=C Bond Reduction Catalyzed by Ene Reductases by Using Artificial Co-substrates as the Hydrogen Donor
por: Winkler, Christoph K, et al.
Publicado: (2014)

New Carvone-Based Deep Eutectic Solvents for Siloxanes Capture from Biogas
por: Makoś-Chełstowska, Patrycja, et al.
Publicado: (2021)

Asymmetric Redox-Neutral Radical Cyclization Catalyzed by Flavin-Dependent ‘Ene’-Reductases
por: Black, Michael J., et al.
Publicado: (2019)

Influence of Organic Solvents on Enzymatic Asymmetric Carboligations
por: Gerhards, Tina, et al.
Publicado: (2012)

The Structure of Glycerol Trinitrate Reductase NerA from Agrobacterium radiobacter Reveals the Molecular Reason for Nitro- and Ene-Reductase Activity in OYE Homologues
por: Oberdorfer, Gustav, et al.
Publicado: (2013)

Chemoenzymatic Asymmetric Synthesis of Pregabalin Precursors via Asymmetric Bioreduction of β-Cyanoacrylate Esters Using Ene-Reductases
por: Winkler, Christoph K., et al.
Publicado: (2013)

Biocatalytic reduction of alkenes in micro-aqueous organic solvent catalysed by an immobilised ene reductase
por: Villa, Rocio, et al.
Publicado: (2023)

Nitrile as Activating Group in the Asymmetric Bioreduction of β-Cyanoacrylic Acids Catalyzed by Ene-Reductases
por: Winkler, Christoph K, et al.
Publicado: (2014)

Peer review of the pesticide risk assessment of the active substance carvone (substance evaluated d‐carvone)
por: Arena, Maria, et al.
Publicado: (2018)

VpStyA1/VpStyA2B of Variovorax paradoxus EPS: An Aryl Alkyl Sulfoxidase Rather than a Styrene Epoxidizing Monooxygenase
por: Tischler, Dirk, et al.
Publicado: (2018)

Health Benefits and Pharmacological Properties of Carvone
por: Bouyahya, Abdelhakim, et al.
Publicado: (2021)

Degradation and Pathways of Carvone in Soil and Water
por: Huang, Chenyu, et al.
Publicado: (2022)

The use of carvone in consecutive patch testing
por: Enberg, Johanna, et al.
Publicado: (2022)

Asymmetric Glyoxylate-Ene Reactions Catalyzed by Chiral Pd(II) Complexes in the Ionic Liquid [bmim][PF(6)]
por: He, Xi Jun, et al.
Publicado: (2007)

In vitro anti-MRSA activity of carvone with gentamicin
por: MUN, SU-HYUN, et al.
Publicado: (2014)

Hypolipidaemic and Insulin Secretagogue Activities of (R)-(−)-Carvone
por: Abbas, Manal Ahmad, et al.
Publicado: (2020)

Rhodococcus strains as source for ene-reductase activity
por: Chen, Bi-Shuang, et al.
Publicado: (2018)

Vanillyl alcohol oxidase from Diplodia corticola: Residues Ala420 and Glu466 allow for efficient catalysis of syringyl derivatives
por: Eggerichs, Daniel, et al.
Publicado: (2023)

Sustainable Asymmetric Organolithium Chemistry: Enantio‐ and Chemoselective Acylations through Recycling of Solvent, Sparteine, and Weinreb “Amine”
por: Monticelli, Serena, et al.
Publicado: (2019)

Enhanced Production and Characterization of a Solvent Stable Amylase from Solvent Tolerant Bacillus tequilensis RG-01: Thermostable and Surfactant Resistant
por: Tiwari, Soni, et al.
Publicado: (2014)

Metagenomic ene-reductases for the bioreduction of sterically challenging enones
por: Dobrijevic, Dragana, et al.
Publicado: (2019)

“A Study in Yellow”: Investigations in the Stereoselectivity of Ene‐Reductases
por: Parmeggiani, Fabio, et al.
Publicado: (2021)

Overcoming co-product inhibition in the nicotinamide independent asymmetric bioreduction of activated C=C-bonds using flavin-dependent ene-reductases
por: Winkler, Christoph K, et al.
Publicado: (2013)

The plant terpenoid carvone is a chemotaxis repellent for C. elegans
por: Ellington, Clayton T., et al.
Publicado: (2020)

Highly thermostable carboxylic acid reductases generated by ancestral sequence reconstruction
por: Thomas, Adam, et al.
Publicado: (2019)

Engineering of a Thermostable Biocatalyst for the Synthesis of 2‐O‐Glucosylglycerol
por: Franceus, Jorick, et al.
Publicado: (2021)

Engineering of Thermostable β‐Hydroxyacid Dehydrogenase for the Asymmetric Reduction of Imines
por: Stockinger, Peter, et al.
Publicado: (2020)

Production of thermostable phycocyanin in a mesophilic cyanobacterium
por: Puzorjov, Anton, et al.
Publicado: (2021)

Process optimization for production and purification of a thermostable, organic solvent tolerant lipase from Acinetobacter sp. AU07
por: Gururaj, P., et al.
Publicado: (2016)

An Improved Three Step Synthesis of (-)-3β-Hydroxycarvone from (-)-Carvone
por: dos Santos, Reginaldo B., et al.
Publicado: (2002)

Comparison by Life-Cycle Assessment of Alternative Processes for Carvone and Verbenone Production
por: Becerra, Jaime-Andrés, et al.
Publicado: (2022)

C=C-Ene-Reductases Reduce the C=N Bond of Oximes
por: Velikogne, Stefan, et al.
Publicado: (2020)

Discovery of an ene-reductase for initiating flavone and flavonol catabolism in gut bacteria
por: Yang, Gaohua, et al.
Publicado: (2021)

Mechanistic Insights into the Ene-Reductase-Catalyzed Promiscuous Reduction of Oximes to Amines
por: Breukelaar, Willem B., et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_9r39q8s6j155740q2tjralk0qp