52419
Ene-Reductase
recombinant, expressed in E. coli, ≥1 U/mg
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About This Item
Enzyme Commission number:
1.3.-.-
UNSPSC Code:
12352204
To inquire about this product 52419, please contact your local Merck office or dealer. Contact Technical Service
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Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Unit Definition
1 U of enzyme activity is defined as the amount of the enzyme as lyophilized powder that converts 1 μmol 2-cyclohexen-1one per hour
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Resp. Sens. 1 - Skin Sens. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Dong Chen et al.
BMC biotechnology, 12, 89-89 (2012-11-28)
Biliverdin IXα is produced when heme undergoes reductive ring cleavage at the α-methene bridge catalyzed by heme oxygenase. It is subsequently reduced by biliverdin reductase to bilirubin IXα which is a potent endogenous antioxidant. Biliverdin IXα, through interaction with biliverdin
Maciej Szaleniec
Pharmacological reports : PR, 64(4), 761-781 (2012-10-23)
Artificial Neural Networks (ANNs) are introduced as robust and versatile tools in quantitative structure-activity relationship (QSAR) modeling. Their application to the modeling of enzyme reactivity is discussed, along with methodological issues. Methods of input variable selection, optimization of network internal
Kuan Hu et al.
The Biochemical journal, 449(1), 79-89 (2012-10-12)
TERs (trans-2-enoyl-CoA reductases; EC 1.3.1.44), which specifically catalyse the reduction of crotonyl-CoA to butyryl-CoA using NADH as cofactor, have recently been applied in the design of robust synthetic pathways to produce butan-1-ol as a biofuel. We report in the present
Ayushi Kamthan et al.
Scientific reports, 2, 951-951 (2012-12-12)
Crop genetic engineering mostly aims at improving environmental stress (biotic and abiotic) tolerance as well as nutritional quality. Empowering a single crop with multiple traits is highly demanding and requires manipulation of more than one gene. However, we report improved
Caroline E Paul et al.
Organic letters, 15(1), 180-183 (2012-12-22)
A series of synthetic nicotinamide cofactors were synthesized to replace natural nicotinamide cofactors and promote enoate reductase (ER) catalyzed reactions without compromising the activity or stereoselectivity of the bioreduction process. Conversions and enantioselectivities of >99% were obtained for C═C bioreductions
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