Chem. J. Chinese Universities ›› 2010, Vol. 31 ›› Issue (8): 1560.

• Articles • Previous Articles     Next Articles

Resolution of N-Acetyl-D,L-3-methoxy-alanine by Immobilized Cells with Aminoacylase

XIONG Ji-Bin, LIU Jun-Zhong, LIU Qian, JIAO Qing-Cai*   

  1. State Key Laboratory of Pharmaceutical Biotechnology, Nanjing Univeristy, Nanjing 210093, China
  • Received:2009-11-19 Online:2010-08-10 Published:2010-08-10
  • Contact: JIAO Qing-Cai. E-mail: jiaoqc@yahoo.com.cn
  • Supported by:

    国家技术创新基金(批准号: 02CJ-13-01-16)资助.

Abstract: As a pharmaceutical intermediate, L-serine plays an important role in organic synthesis and peptide synthesis. Also N-acetyl-D,L-3-methoxy-alanine is an intermediate in synthesis of L-serine from methyl α-bromo-β-methoxypropionate. In this thesis, a new method of resolution of N-acetyl-D,L-3-methoxy-alanine by immobilized cells with aminoacylase was studied. Several factors of this enzymatic reaction were investigated. The optimal temperature and pH are 50 ℃ and 7.0. In 10 mL reaction solution, the optimal concentration of N-acetyl-D,L-3-methoxy-alanine is 500 mmol/L and the amount of immobilized cells is 1 g. 10-4 mol/L of Co2+ and Mg2+ are benefit to aminoacylase, while Cu2+ and Zn2+ show clearly inhibitory effect. Under the optimal conditions, molar conversion rate of N-acetyl-L-3-methoxy-alanine is 96%.

Key words: Aminoacylase, D,L-3-Methoxy-alanine, Immobilized cell, Chiral resolution

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