Asymmetric reduction of 3,5-bistrifluoromethyl acetophenone to produce(S)-3,5-bistrifluoromethylphenyl ethanol was successfully carried out with sodium alginate immobilized Saccharomyces rhodotorula cells in an aqueou...Asymmetric reduction of 3,5-bistrifluoromethyl acetophenone to produce(S)-3,5-bistrifluoromethylphenyl ethanol was successfully carried out with sodium alginate immobilized Saccharomyces rhodotorula cells in an aqueous-organic solvent biphasic system.The possible influential factors were examined thoroughly according to their effects on conversion rate and e.e of the product.Organic solvents were rated by their biocompatibility and conversion potential.The immobilized cells [125 mg/mL in 20 mmol/L Tris-HCl buffer and 5%(j) octane at pH 8] showed the best conversion with a substrate concentration of 1.42 g/L at 30℃ with glucose as co-substrate for cofactor regeneration.Sequential 8-batch process was carried out with immobilized cells with a slow decrease in conversion and e.e.The immobilized cells showed stable catalytic activity with 50% reserved activity and are superior especially in reusability in comparison with resting cells.展开更多
THE oxidative dehydrogenation of propane （ODP） to propene is one of the potentially important catalytic processes for the effective utilization of light alkanes. The VMgO catalysts which have better catalytic perfor...THE oxidative dehydrogenation of propane （ODP） to propene is one of the potentially important catalytic processes for the effective utilization of light alkanes. The VMgO catalysts which have better catalytic performances for the reaction have aroused much interest and argument.Kung et al. proposed that the active phase was magnesium orthovanadate （Mg<sub>3</sub>V<sub>2</sub>O<sub>8</sub>）, but Volta et al. suggested that magnesium pyrovanadate （α-Mg<sub>2</sub>V<sub>2</sub>O<sub>7</sub>） was the active phase; in this phase, V<sup>4+</sup> ions which are associated to the formation of oxygen vacancies could stably exist, and Mg<sub>3</sub>V<sub>2</sub>O<sub>8</sub> is responsible for the total oxidation due to nonexistence of V<sup>4+</sup> ions.展开更多
基金support from the National Natural Science Foundation of China(No.20573015)the Program for New Century Excellent Talents in University(No.NCET-07-0138)the Science and Technology Project in Universities from the Education Department of Liaoning Province(No.2008T233)
文摘Asymmetric reduction of 3,5-bistrifluoromethyl acetophenone to produce(S)-3,5-bistrifluoromethylphenyl ethanol was successfully carried out with sodium alginate immobilized Saccharomyces rhodotorula cells in an aqueous-organic solvent biphasic system.The possible influential factors were examined thoroughly according to their effects on conversion rate and e.e of the product.Organic solvents were rated by their biocompatibility and conversion potential.The immobilized cells [125 mg/mL in 20 mmol/L Tris-HCl buffer and 5%(j) octane at pH 8] showed the best conversion with a substrate concentration of 1.42 g/L at 30℃ with glucose as co-substrate for cofactor regeneration.Sequential 8-batch process was carried out with immobilized cells with a slow decrease in conversion and e.e.The immobilized cells showed stable catalytic activity with 50% reserved activity and are superior especially in reusability in comparison with resting cells.
文摘THE oxidative dehydrogenation of propane （ODP） to propene is one of the potentially important catalytic processes for the effective utilization of light alkanes. The VMgO catalysts which have better catalytic performances for the reaction have aroused much interest and argument.Kung et al. proposed that the active phase was magnesium orthovanadate （Mg<sub>3</sub>V<sub>2</sub>O<sub>8</sub>）, but Volta et al. suggested that magnesium pyrovanadate （α-Mg<sub>2</sub>V<sub>2</sub>O<sub>7</sub>） was the active phase; in this phase, V<sup>4+</sup> ions which are associated to the formation of oxygen vacancies could stably exist, and Mg<sub>3</sub>V<sub>2</sub>O<sub>8</sub> is responsible for the total oxidation due to nonexistence of V<sup>4+</sup> ions.
