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如何触发重组体中的周质释放:一项比较分析。

How to trigger periplasmic release in recombinant : A comparative analysis.

作者信息

Wurm David J, Slouka Christoph, Bosilj Tadej, Herwig Christoph, Spadiut Oliver

机构信息

Research Division Biochemical Engineering Institute of Chemical Engineering Vienna University of Technology Vienna Austria.

Christian Doppler Laboratory for Mechanistic and Physiological Methods for Improved Bioprocesses Institute of Chemical Engineering Vienna University of Technology Vienna Austria.

出版信息

Eng Life Sci. 2016 Oct 5;17(2):215-222. doi: 10.1002/elsc.201600168. eCollection 2017 Feb.

Abstract

Recombinant protein production in usually leads to accumulation of the product inside the cells. To capture the product, cells are harvested, resuspended, and lysed. However, in cases where the product is transported to the periplasm, selective disruption of the outer membrane leads to much purer crude extracts compared to complete cell lysis, as only 4-8% of the native host cell proteins are located in the periplasmic space. A variety of different strategies to enable selective release of the product from the periplasm is available. However, in most of these studies cells are harvested before they are resuspended in permeabilization agent and no differentiation between leakiness and lysis is made. Here, we tested and compared different strategies to trigger leakiness. In contrast to other studies, we performed these experiments during cultivation and quantified both leakiness and lysis. In summary, we recommend incubation with 350 mM TRIS at constant pH for several hours followed by a mild heat treatment up to 38°C to trigger leakiness with only minimal lysis. This study represents a comparative summary of different strategies to trigger leakiness and describes a solid basis for further experiments in this field.

摘要

通常情况下,重组蛋白在细胞内产生并积累。为了获取产物,需要收获细胞、重悬并裂解细胞。然而,当产物被转运到周质空间时,与完全裂解细胞相比,选择性破坏外膜可得到纯度更高的粗提物,因为只有4 - 8%的天然宿主细胞蛋白位于周质空间。目前有多种不同策略可实现从周质中选择性释放产物。然而,在大多数此类研究中,细胞在重悬于透化剂之前就被收获了,并且没有区分渗漏和裂解。在此,我们测试并比较了不同的引发渗漏的策略。与其他研究不同的是,我们在培养过程中进行这些实验,并对渗漏和裂解进行了定量。总之,我们建议在恒定pH值下用350 mM三羟甲基氨基甲烷(TRIS)孵育数小时,然后进行温和的热处理至38°C,以引发渗漏且仅产生最小程度的裂解。本研究对引发渗漏的不同策略进行了比较总结,并为该领域的进一步实验奠定了坚实基础。

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