Enzymatic hydrolysis of penicillin for 6-APA production in three-liquid-phase system.

Appl Biochem Biotechnol

Laboratory of Separation Science and Engineering, Institute of Process Engineering, Chinese Academy of Science, Beijing 100080, China.

Published: February 2008

A dodecane/thermosensitive polymer/water three-liquid-phase system was introduced for enzymatic hydrolysis of penicillin G (Pen G) for 6-aminopenicillanic acid (6-APA). The enzyme was covalently attached to the terminal of PEO-PPO-PEO polymer (L63), which would be transferred into a polymer coacervate phase at high temperature above its "cloud point". 6-APA was primarily resided in the aqueous phase due to its zwitterionic nature. More than 70% phenylacetic acid (PAA) was transferred into the organic phase using trioctylmethylammonium hydroxide and trihexyl-(tetradecyl)phosphonium bis 2,4,4-trimethylpentylphosphinate ionic liquids (Cyphos IL-104) mixture at pH 5.5, while most of Pen G resided in water. As a result, high operational pH was permitted in three-liquid-phase system, which leads to higher enzymatic activity (120 IU at 40 degrees C) and stability (enzymatic half-time up to 55 h at 60 degrees C) in comparison with the value in butyl acetate/water two-phase system. On the other hand, two products in three-liquid-phase system might be automatically separated from the enzyme sphere into different phases at the same time, which facilitated the reaction equilibrium towards the product's side with 6-APA productivity of 80% at 42 degrees C, pH 5.5.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s12010-007-8018-xDOI Listing

Publication Analysis

Top Keywords

three-liquid-phase system
16
enzymatic hydrolysis
8
hydrolysis penicillin
8
system
5
enzymatic
4
6-apa
4
penicillin 6-apa
4
6-apa production
4
three-liquid-phase
4
production three-liquid-phase
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!