首页> 中文期刊> 《催化学报》 >酵母静息细胞催化丙酮酸乙酯不对称还原制(S)-乳酸乙酯

酵母静息细胞催化丙酮酸乙酯不对称还原制(S)-乳酸乙酯

         

摘要

Thirty six strains that exhibited the catalytic activity for asymmetric reduction of ethyl pyruvate to (S)-ethyl lactate were isolated from sewage of a chemical factory in Chengdu, China and the neighboring soil. Among them, yeast strain BTY 18-6 has high catalytic activity. The asymmetric reduction of ethyl pyruvate to (S)-ethyl lactate catalyzed by BTY18-6 resting cells in an aqueous phase was examined,and the parameters influencing the bio-reduction were optimized. The results showed that, under the optimized conditions of 2.5% glucose as co-substrate, the initial reaction pH = 6.8, the initial cell concentration at 0.175 g/ml (wet mass) cultured for 48 h, the initial ethyl pyruvate concentration at 65 mmol/L, temperature 32 ℃, and reaction time 48 h, the ethyl pyruvate conversion reached 95.5% with enantiomeric excess of 92.1%.%从污水处理池及其附近土壤中分离到36株可将丙酮酸乙酯不对称还原成(S-乳酸乙酯的菌株,经多次复筛,最终得到一株具有较高催化活性的酵母菌BTY18-6.以BTY18-6的静息细胞为催化剂,在水相中进行丙酮酸乙酯不对称还原成(S)-乳酸乙酯的反应,并对反应条件进行了优化.结果表明,以2.5%葡萄糖为辅助底物,反应体系初始pH=6.8,发酵培养48 h的菌体湿度0.175 g/ml,丙酮酸乙酯初始浓度65 mmol/L,于32℃反应48 h的条件下,丙酮酸乙酯转化率达95.5%,产物对映体过量值(ee值)为92.1%.

著录项

相似文献

  • 中文文献
  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号