Abstract
BackgroundEnantiomerically pure alcohols are important building blocks for production of chiral pharmaceuticals, flavors, agrochemicals and functional materials and appropriate whole-cell biocatalysts offer a highly enantioselective, minimally polluting route to these valuable compounds. At present, most of these biocatalysts follow Prelog’s rule, and thus the (S)-alcohols are usually obtained when the smaller substituent of the ketone has the lower CIP priority. Only a few anti-Prelog (R)-specific whole cell biocatalysts have been reported. In this paper, the biocatalytic anti-Prelog reduction of 2-octanone to (R)-2-octanol was successfully conducted with high enantioselectivity using whole cells of Acetobacter pasteurianus GIM1.158.ResultsCompared with other microorganisms investigated, Acetobacter pasteurianus GIM1.158 was shown to be more effective for the reduction reaction, affording much higher yield, product enantiomeric excess (e.e.) and initial reaction rate. The optimal temperature, buffer pH, co-substrate and its concentration, substrate concentration, cell concentration and shaking rate were 35°C, 5.0, 500 mmol/L isopropanol, 40 mmol/L, 25 mg/mL and 120 r/min, respectively. Under the optimized conditions, the maximum yield and the product e.e. were 89.5% and >99.9%, respectively, in 70 minutes. Compared with the best available data in aqueous system (yield of 55%), the yield of (R)-2-octanol was greatly increased. Additionally, the efficient whole-cell biocatalytic process was feasible on a 200-mL preparative scale and the chemical yield increased to 95.0% with the product e.e. being >99.9%. Moreover, Acetobacter pasteurianus GIM1.158 cells were proved to be capable of catalyzing the anti-Prelog bioreduction of other prochiral carbonyl compounds with high efficiency.ConclusionsVia an effective increase in the maximum yield and the product e.e. with Acetobacter pasteurianus GIM1.158 cells, these results open the way to use of whole cells of this microorganism for challenging enantioselective reduction reactions on laboratory and commercial scales.
Highlights
Pure alcohols are important building blocks for production of chiral pharmaceuticals, flavors, agrochemicals and functional materials and appropriate whole-cell biocatalysts offer a highly enantioselective, minimally polluting route to these valuable compounds
Comparison of the biocatalytic enantioselective reduction of 2-octanone with Acetobacter pasteurianus GIM1.158 and other potential microorganisms A variety of microorganisms have been reported to be efficient in catalyzing prochrial ketones to enantiomerically pure chrial alcohols [16,25,26,27,28,29]
AS2.2241, Pseudomonas oleovorans GIM1.304)were comparatively tested for their potential for the preparation of (R)-2-octanol via asymmetric reduction of 2-octanone in TEA-HCl buffer (50 mmol/L, pH 5.0)
Summary
Pure alcohols are important building blocks for production of chiral pharmaceuticals, flavors, agrochemicals and functional materials and appropriate whole-cell biocatalysts offer a highly enantioselective, minimally polluting route to these valuable compounds. Most of these biocatalysts follow Prelog’s rule, and the (S)-alcohols are usually obtained when the smaller substituent of the ketone has the lower CIP priority. (R)-2-octanol is a versatile intermediate for the synthesis of FLCD (ferroelectric liquid crystals FLCs) and several optically active pharmaceuticals such as steroid and follow Prelog’s rule [11], and the (S)-alcohols are usually obtained when the smaller substituent of the ketone has the lower CIP priority. As far as we know, most of the previously reported anti-Prelog microorganisms have not been used for industrial preparation of chiral alcohols for their relatively low catalytic activity and stereoselectivity. The discovery of more efficient microorganisms would be of great significance
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