TY  - JOUR
N1  - The copyright  of this article belongs to Elsevier 
ID  - open2999
UR  - https://www.sciencedirect.com/science/article/abs/pii/S2352554122000134
A1  - Verma, Nitish Kumar
A1  - Kumar, Sachin
A1  - Prasad, G S
A1  - Bhattacharyya, Mani Shankar
Y1  - 2022/05//
N2  - Enantiopure alcohols are key intermediates for the synthesis of a plethora of pharmaceuticals, agrochemicals and fine chemicals. Present study reports the deracemization of racemic naphthyl ethanols into their enantiopure S-forms by CHF-15P (Rhodotorula kratochvilovae, MTCC 13029) whole cells, isolated from the high altitude of the Himalayan mountain range. Initially, the biocatalyst was able to deracemize rac-1-(6-methoxy-2-naphthyl)ethanol to S-1-(6-methoxy-2-naphthyl)ethanol with 86.3% yield and 82.6% eeS. The studies on the effect of physicochemical parameters showed 92.3% yield with eeS>99% of product in a medium containing 2 mM substrate concentration and 2% glucose at 30 °C temperature, pH 7.0 (0.2 M sodium phosphate buffer), with 100 mg/mL cell concentration. In addition, the deracemization of rac-1-(6-methyl-2-naphthyl)ethanol and rac-1-(2-naphthyl)ethanol was achieved within 12 h at 30 °C with 96.4 and 98.8% of yield (98.2% and >99% eeS), respectively. The process of deracemization occurs via the formation of a ketone intermediate. The appearance of ketone has been demonstrated by high performance liquid chromatography (HPLC) and confocal laser scanning microscopy. However, rac-1-(1-naphthyl)ethanol and rac-1-(4-fluoro-1-naphthyl)ethanol were not deracemized under the same condition. In gram scale preparation, 92.8% yield with eeS>99% was obtained.
PB  - Elsevier
JF  - Sustainable Chemistry and Pharmacy
VL  - 26
KW  - Stereoinversion; Rhodotorula kratochvilovae; Deracemization; Reductase; Oxidase
TI  - Biocatalytic deracemization of racemic naphthyl alcohols by using a novel yeast isolate Rhodotorula kratochvilovae (MTCC 13029)
ER  -