[1] XU G C,YU H L,SHANG Y P,et al. Enantioselective bioreductive preparation of chiral halohydrins employing two newly identified stereocmpleentary reductase[J]. RSC Advances,2015,5(29):22703-22711. [2] NI Y,XU J H. Asymmetric reduction of aryl ketones with a new isolate Rhodotorula sp. AS2.2241[J]. Journal of Molecular Catalysis B:Enzymatic,2002,18(4):233-241. [3] GOLDBERG K,SEHROER K,LUTZ S,et al. Biocatalytic ketone reduction-a powerful tool for the production of chiral alcohols—Part I:processes with isolated enzymes[J]. Applied Microbiology and Biotechnology,2007,76(2):237-248. [4] ISHIGE T,HONDA K,SHIMIZU S. Whole organism biocatalysis[J]. Current Opinion in Chemical Biology,2005,9(2):174-180. [5] PAPANIKOLAOU S,AGGELIS G. Yarrowia lipolytica:a model microorganism used for the production of tailor-made lipids[J]. European Journal of Lipid Science and Technology,2010,112(6):639-654. [6] LAGOS F M,CARBALLEIRA J D,BERMUDEZ J L,et al. Highly stereoselective reduction of haloketones using three new yeasts:Application to the synthesis of (S)-adrenergic β-blockers related to propranolol[J]. Tetrahedron:Asymmetry,2004,15(5):763-770. [7] FANTIN G,FOGANGNOLO,GIOVANNINI P P,et al. Anti-Prelog microbial reduction of prochiral carbonyl compounds[J]. Tetrahedrom,1996,52(10):3547-3552. [8] KURBANOGLU E B,ZILBEYAZ K,KURBANOGLUC N I,et al. Highly enantioselective reduction of acetophenone by locally isolated Alternaria alternata using ram horn peptone[J]. Tetrahedron:Asymmetry,2007,18(13):1529-1532. [9] SONI P,BANERJEE U C. Enantioselective reduction of acetophenone and its derivatives with a new yeast isolate Candida tropicalis PBR-2 MTCC 5158[J]. Journal of Biotechnology,2006,1(1):80-85. [10] 杨忠华,曾嵘,吴高明,等. 水-有机溶剂两相体系中面包酵母不对称还原苯乙酮合成手性苯乙醇的研究[J]. 高校化学工程学报,2009,23(3):450-454. [11] XIAO M T,YE J,ZHANG Y W,et al. Reaction characteristics of asymmetric synthesis of (2S,5S)-2,5-hexanediol catalyzed with baker's yeast number 6[J]. Chinese Journal of Chemical Engineering,2009,17(3):493-499. [12] XIAO M T,HUANG Y Y,SHI X A,et al. Bioreduction of phenylglyoxylic acid to R-(-)-mandelic acid by Saccharomyces cerevisiae FD11b[J]. Enzyme and Microbial Technology,2005,37(6):589-596. [13] POLIZZI K M,BOMMARIUS A S,BROERING J M,et al. Stability of biocatalysts[J]. Current Opinion in Chemical Biology,2007,11(2):220-225. [14] PHILLIPS R S. Temperature modulation of the stereochemistry of enzymatic catalysis:prospects for exploitation[J]. Trends in Biotechnology,1996,14(1):13-16. [15] 刘湘,孙培冬,李明,等. 面包酵母用于苯乙酮的不对称还原研究[J]. 分子催化,2002,16(2):107-110. [16] CHIN-JOEI,STRAATHOF A J J,PRONK J T,et al. Influence of the ethanol and glucose supply rate on the rate and enantioselectivity of 3-oxo ester reduction by baker's yeast[J]. Biotechnology and Bioengineering,2001,75(1):29-38. [17] HILKER I,GUTIERREZ M C,FURSTOSS R,et al. Preparative scale Baeyer-Villiger biooxidation at high conversion using recombinant Escherichia coli and in situ substrate feeding and product removal process[J]. Nature Protocols,2008,3(3):546-554. [18] MATSUDA T,YAMANAKA R,NAKAMURA K. Recent progress in biocatalysis for asymmetric oxidation and reduction[J]. Tetrahedron:Asymmetry,2009,20(5):513-557. [19] 刘湘,方志杰,许建和,等. 酵母细胞催化芳香酮的不对称还原反应[J]. 催化学报,2006,27(1):20-24. [20] LOU W Y,ZONG M H,SMITH T J. Use of ionic liquids to improve whole-cell biocatalytic asymmetric reduction of acetyltrimethylsilane for efficient synthesis of enantiopure (S)-1-trimethylsilylethanol[J]. Green Chemistry,2006,8(2):147-155. [21] KURBANOGLU E B,ZILBEYAZ K,OZDAL M,et al. Asymmetric reduction of substituted acetophenones using once immobilized Rhodotorula glutinis cells[J]. Bioresource Technology,2010,101(11):3825-3829 |