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通过选择性释放、双水相分配和超滤分离大肠杆菌青霉素酰化酶。

E. coli penicillin acylase isolation by selective release, aqueous two-phase partitioning and ultrafiltration.

作者信息

Guan Y, Treffry T E, Lilley T H

机构信息

Department of Molecular Biology and Biotechnology, The University, Sheffield, UK.

出版信息

Bioseparation. 1994 Apr;4(2):89-99.

PMID:7765042
Abstract

A procedure has been developed for the purification of penicillin acylase from E. coli fermentation broths. The method described is based primarily on selective release from biomass, charge-directed partitioning in an aqueous two-phase system, and the use of ultrafiltration membranes to recycle the modified polyethylene glycol required and to further purify the enzyme. Each step has been discussed and comparisons have been made with other approaches, where possible. Suggestions have been made for optimisation in process engineering. The approach developed may be applicable to other beta-lactam antibiotic acylases or more generally to some of the other E. coli periplasmic proteins.

摘要

已开发出一种从大肠杆菌发酵液中纯化青霉素酰化酶的方法。所述方法主要基于从生物质中选择性释放、在双水相系统中进行电荷导向分配,以及使用超滤膜来循环所需的改性聚乙二醇并进一步纯化酶。已对每个步骤进行了讨论,并在可能的情况下与其他方法进行了比较。还对过程工程中的优化提出了建议。所开发的方法可能适用于其他β-内酰胺抗生素酰化酶,或更广泛地适用于一些其他大肠杆菌周质蛋白。

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