کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
69514 | 48777 | 2015 | 7 صفحه PDF | دانلود رایگان |
• GoCR from G. oxydans could catalyze the reduction of halogenated acetophenones.
• Only S-configuration alcohols (>99% ee) were produced.
• 500 mM o-chloroacetophenone was reduced at 96% conversion.
• For o-chloroacetophenone reduction, 2.0 eq. of isopropanol served as co-substrate.
• Molecular docking explained the mechanism of the high enantioselectivity of GoCR.
A carbonyl reductase from Gluconobacter oxydans (GoCR) exhibited good activity and strict enantioselectivity for the asymmetric reduction of a series of halogenated acetophenones, resulting in the corresponding S-alcohols. For efficient synthesis of alcohol products, an economical and satisfactory substrate-coupled cofactor regeneration system was constructed employing isopropanol as the co-substrate to regenerate NADH in situ. In the presence of 2.0 molar eq. of isopropanol, 500 mM o-chloroacetophenone was reduced to (S)-1-(2-chlorophenyl)-ethanol with >99% ee and a high conversion rate of 96% by recombinant Escherichia coli BL21 cells overexpressing GoCR. In this reaction system, a slight excess of isopropanol as hydride source could drive the reduction reaction to near completion due to the speculated forming of an intramolecular hydrogen bond between the Cl group and the new obtained alcohol moiety of (S)-1-(2-chlorophenyl)-ethanol. Furthermore, other tested halogenated acetophenones at 100 or 200 mM substrate load were also reduced at 71–96% conversion, affording S-configuration alcohols with >99% ee. Homology modeling and molecular dynamics simulation were performed to uncover the structural basis for the excellent enantioselectivity of GoCR toward halogenated acetophenones. These results imply the high potential of GoCR in the production of halogenated 1-phenylethanols, such as (S)-1-(2-chlorophenyl)-ethanol, an important chiral building block with wide application in pharmaceutical chemistry and fine chemicals.
Figure optionsDownload as PowerPoint slide
Journal: Journal of Molecular Catalysis B: Enzymatic - Volume 118, August 2015, Pages 1–7