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
Recommended Products
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
signalword
Danger
hcodes
Hazard Classifications
Resp. Sens. 1 - Skin Sens. 1
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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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
Linda T Hiraki et al.
Genetic epidemiology, 37(1), 92-98 (2012-11-09)
The primary circulating form of vitamin D is 25-hydroxy vitamin D (25(OH)D), a modifiable trait linked with a growing number of chronic diseases. In addition to environmental determinants of 25(OH)D, including dietary sources and skin ultraviolet B (UVB) exposure, twin-
Olivia Trummer et al.
Clinical chemistry, 59(5), 793-797 (2013-01-16)
Decreased circulating 25-hydroxy-vitamin D (25-OH-vitamin D) concentrations have been associated with mortality rates, but it is unclear whether this association is causal. We performed a Mendelian randomization study and analyzed whether 3 common single-nucleotide polymorphisms (SNPs) associated with 25-OH-vitamin D
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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