期刊文献+

Asymmetric Reduction of 3,5-Bistrifluoromethyl Acetophenone with NADH Regeneration by Immobilized Cells of Saccharomyces rhodotorula in Aqueous-Organic Solvent Biphasic System 被引量:1

Asymmetric Reduction of 3,5-Bistrifluoromethyl Acetophenone with NADH Regeneration by Immobilized Cells of Saccharomyces rhodotorula in Aqueous-Organic Solvent Biphasic System
原文传递
导出
摘要 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. 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.
出处 《过程工程学报》 CAS CSCD 北大核心 2011年第5期840-845,共6页 The Chinese Journal of Process Engineering
关键词 asymmetric reduction 3 5-bistrifluoromethyl acetophenone 3 5-bistrifluoromethylphenyl ethanol immobilized cell aqueous-organic solvent biphasic system asymmetric reduction 3 5-bistrifluoromethyl acetophenone 3 5-bistrifluoromethylphenyl ethanol immobilized cell aqueous-organic solvent biphasic system
  • 相关文献

参考文献27

  • 1Gonzalo G, Lavandem I, Durchschein K, et al. Asymmetric Biocatalytic Reduction of Ketones Using Hydroxy-functionalised Water-miscible Ionic Liquids as Solvent [J]. Tetrahedron: Asymmetry, 2007, 18(21): 2541-2546.
  • 2Panke S, Wubbolts M. Advances in Biocatalytic Synthesis of Pharmaceutical Intermediates [J]. Curr. Opin. Chem. Biol., 2005, 9(2): 188-194.
  • 3Tufvesson P, Fu W, Jensen J S, et al. Process Considerations for the Scale-up and Implementation of Biocatalysis [J]. Food and Bioproducts Processing, 2010, 88(1): 3-11.
  • 4Pinedo-Rivilla, Cafeu M C, Casatejada J A, et al. Asymmetric Microbial Reduction of Ketones: Absolute Configuration of Trans-4-ethyl-1-(1S-hydroxyethyl) Tyclohexanol [J]. Tetrahedron: Asymmetry, 2009, 20(23): 2666-2672.
  • 5Rekuc A, Jastrzembska B, Liesiene J, et al. Comparative Studies on Immobilized Laccase Behaviour in Packed-bed and Batch Reactors [J]. J. Mol. Catal. B: Enzym., 2009, 57(1/4): 216-222.
  • 6Kurbanoglu E B, Zilbeyaz K, Ozdal M, et al. Asymmetric Reduction of Substituted Acetophenones Using Once Immobilized Rhodotorulaglutinis Cells [J]. Bioresour. Technol., 2010, 101(11): 3825-3829.
  • 7Zhu D, Malik H T, Hua L. Asymmetric Ketone Reduction by a Hyperthermophilic Alcohol Dehydrogenase: The Substrate Specificity, Enantioselectivity and Tolerance of Organic Solvents [J]. Tetrahedron Asymmetry, 2006, 17(21): 3010-3014.
  • 8Yang W, Xu J H, Pan J, et al. Efficient Reduction of Aromatic Ketones with NADPH Regeneration by Using Crude Enzyme from Rhodotorula Cells and Mannitol as Cosubstrate [J]. Biochem. Ical. Eng. J., 2008, 42(1): 1-5.
  • 9Qiu H, Li Y, Ji G L, et al. Immobilization of Lignin Peroxidase on Nanoporous Gold: Enzymatic Properties and in situ Release of H2O2 by Co-immobilized Glucose Oxidase [J]. Bioresour. Technol., 2009, 100(17): 3837-3841.
  • 10Huisman G W, Liang J, Krebber A. Practical Chiral Alcohol Manufacture Using Ketoreductases [J]. Curr. Opin. Chem. Biol., 2010,14(2): 122-129.

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部