Institute of Bioengineering, Zhejiang University of Technology, 18 Chaowang Road, Hangzhou, People's Republic of China.
J Ind Microbiol Biotechnol. 2010 May;37(5):503-10. doi: 10.1007/s10295-010-0696-7. Epub 2010 Feb 23.
Immobilized cells of Delftia tsuruhatensis CCTCC M 205114 harboring R-amidase were applied in asymmetric hydrolysis of (R)-2, 2-dimethylcyclopropane carboxamide (R - 1) from racemic (R, S)-2, 2-dimethylcyclopropane carboxamide to accumulate (S)-2, 2-dimethylcyclopropane carboxamide (S - 1). Maximum R-amidase activity of 13.1 U/g wet cells (0.982 U/g beads) was obtained under conditions of 3% sodium alginate, 2.5% CaCl(2), 15 h crosslinking and 2 mm bead size, which was 53.9% of that of free cells (24.3 U/g wet cells). In addition, characterization of the immobilized cells was examined. The optimum R - 1 hydrolysis conditions were identified as follows: substrate concentration 10 mM, pH 8.5, temperature 35 degrees C and time course 40 min. Under optimum conditions, the maximum yield and enantiomeric excess of (R)-2, 2-dimethylcyclopropanecarboxylic acid were 49.5% and >99%, respectively. This afforded S - 1 with a yield >49% and an e.e. of 97.7%. With good operational stability and excellent enanotioselectivity, the immobilized cells could be potentially utilized in industrial production of S - 1.
固定化 Delftia tsuruhatensis CCTCC M 205114 细胞用于手性拆分(R)-2,2-二甲基环丙甲酰胺
(R)-2,2-二甲基环丙甲酰胺(R-1)是一种重要的手性胺,广泛应用于药物、农药和精细化学品的合成。从(R,S)-2,2-二甲基环丙甲酰胺(rac-1)制备(S)-2,2-二甲基环丙甲酰胺(S-1)的方法主要有化学拆分法、酶法拆分法和微生物发酵法。其中,酶法拆分法因其高效、高选择性和环境友好等优点,受到了广泛的关注。
本研究采用 Delftia tsuruhatensis CCTCC M 205114 细胞固定化酶,在手性拆分(R)-2,2-二甲基环丙甲酰胺(R-1)的过程中,考察了固定化细胞的酶学性质和手性拆分条件。结果表明,固定化细胞的最适酶反应条件为:海藻酸钠浓度 3%、氯化钙浓度 2.5%、交联时间 15 h、载体粒径 2 mm;最适反应条件下,(R)-2,2-二甲基环丙甲酰胺的水解转化率为 49.5%,对映体过量值(ee)大于 99%。该方法操作简便、稳定性好、对映选择性高,可用于(S)-2,2-二甲基环丙甲酰胺的工业化生产。