Nicotinamide-independent asymmetric bioreduction of CC-bonds via disproportionation of enones catalyzed by enoate reductases. - Wikidata - awgldk - TriplyDB

Nicotinamide-independent asymmetric bioreduction of CC-bonds via disproportionation of enones catalyzed by enoate reductases.

Nicotinamide-independent asymmetric bioreduction of CC-bonds via disproportionation of enones catalyzed by enoate reductases.

http://www.wikidata.org/entity/Q41378442

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The Structure of Glycerol Trinitrate Reductase NerA fromAgrobacterium radiobacterReveals the Molecular Reason for Nitro- and Ene-Reductase Activity in OYE Homologues Asymmetric bioreduction of activated alkenes to industrially relevant optically active compounds.Overcoming co-product inhibition in the nicotinamide independent asymmetric bioreduction of activated C=C-bonds using flavin-dependent ene-reductases NAD(P)H-independent asymmetric C=C bond reduction catalyzed by ene reductases by using artificial co-substrates as the hydrogen donor.Sequential Enzymatic Conversion of α-Angelica Lactone to γ-Valerolactone through Hydride-Independent C=C Bond Isomerization.Old Yellow Enzyme homologues in Mucor circinelloides: expression profile and biotransformation.Recent trends and novel concepts in cofactor-dependent biotransformations.Artificial Photosynthesis: Hybrid Systems.Nicotinamide-Dependent Ene Reductases as Alternative Biocatalysts for the Reduction of Activated Alkenes Old Yellow Enzyme-Catalyzed Dehydrogenation of Saturated Ketones

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P2860

Nicotinamide-independent asymmetric bioreduction of CC-bonds via disproportionation of enones catalyzed by enoate reductases.

http://www.wikidata.org/entity/Q41378442

description

2010 nî lūn-bûn

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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2010年论文

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name

Nicotinamide-independent asymm ...... atalyzed by enoate reductases.

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Nicotinamide-independent asymm ...... atalyzed by enoate reductases.

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Nicotinamide-independent asymm ...... atalyzed by enoate reductases.

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J.TET.2009.11.065

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Nicotinamide-independent asymm ...... atalyzed by enoate reductases.

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Clemens Stueckler

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Kurt Faber

http://www.w3.org/2001/XMLSchema#string

Nina Baudendistel

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Tamara C Reiter

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P2860

Crystal structure of 12-oxophytodienoate reductase 3 from tomato: self-inhibition by dimerization

X-ray structure of 12-oxophytodienoate reductase 1 provides structural insight into substrate binding and specificity within the family of OYE

Kinetic and structural basis of reactivity of pentaerythritol tetranitrate reductase with NADPH, 2-cyclohexenone, nitroesters, and nitroaromatic explosives

Crystal structure of bacterial morphinone reductase and properties of the C191A mutant enzyme

Catalytic promiscuity and the evolution of new enzymatic activities

Sequence and properties of pentaerythritol tetranitrate reductase from Enterobacter cloacae PB2

A homolog of old yellow enzyme in tomato. Spectral properties and substrate specificity of the recombinant protein.

Application of in situ product-removal techniques to biocatalytic processes.

Light-mediated reduction of flavoproteins with flavins as catalysts.

'New uses for an Old Enzyme'--the Old Yellow Enzyme family of flavoenzymes.

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10.1016/J.TET.2009.11.065

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3-2

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