Isolation and purification of penicillin G acylase obtained from Escherichia coli (NCIM-2400) and immobilisation on Eupergit C for the production of 6 amino penicillanic acid.

Hindustan antibiotics bulletin Pub Date : 1997-02-01
M M Hegde, S B Thadani, U Singh, S R Naik
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Abstract

Penicillin G-Acylase is produced by submerged cultivation of E. Coli (NCIM-2400) and extracted from the harvested fermented broth, purified (affinity chromatography) and immobilised on Eupergit C (Synthetic polymer in bead form). The immobilised penicillin G acylase properties are studied and compared with soluble penicillin G-acylase. The control parameters for conversion of penicillin G-K to 6 APA are optimised [e.g. substrate (Pen G-K) concentration ratio to immobilised penicillin G-acylase, temperature, pH etc.] in a stirred tank reactor. Our findings suggest that immobilised penicillin G-acylase can be used commercially and the productivity of 1 kg. of immobilised enzyme is around 400 kg of 6 APA under given desired stipulated conditions.

从大肠杆菌中分离纯化青霉素G酰化酶(NCIM-2400)并固定化Eupergit C生产6氨基青霉酸。
青霉素g -酰化酶是通过大肠杆菌(NCIM-2400)的深层培养产生的,从收获的发酵肉液中提取,纯化(亲和层析)并固定在Eupergit C(珠状合成聚合物)上。研究了固定化青霉素G酰化酶的性质,并与可溶性青霉素G酰化酶进行了比较。在搅拌槽反应器中优化了青霉素G-K转化为6apa的控制参数[例如底物(Pen G-K)与固定化青霉素g -酰化酶的浓度比、温度、pH等]。我们的研究结果表明,固定化青霉素g -酰化酶可以商业化使用,产量为1公斤。在给定所需的规定条件下,固定酶约为400公斤的6apa。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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