Department of Bioengineering, Institute of Biotechnology and Antibiotics, Staroscinska 5, Warsaw, 02-516, Poland.
Microb Cell Fact. 2012 Aug 16;11:109. doi: 10.1186/1475-2859-11-109.
The most widespread, efficient prokaryotic protein-producing system is one where the T7 phage polymerase recognizes the T7 phage promoter (T7 p/p system). Unfortunately, in this system, target protein expression gradually declines and is often undetectable following 3 to 5 subcultures. Although a number of studies have attempted to stabilize the expression levels of the T7 p/p system, none has resolved the problem adequately and thus precludes the use of this system for the production of recombinant proteins on a large scale.
We created an expression cassette enabling stable, high-level expression in the T7p/p system. The cassette was tested with two different vector backbones and two target proteins. In all experiments, the expression system using the new cassette exhibited high and stable protein expression levels when compared to the traditional system.
Herein, we describe a universal expression cassette that enables high-level, stable target protein expression in T7 RNA polymerase-based expression systems. We also present the successful use of this cassette as a novel expression platform and demonstrate its ability to overcome the main deficiency of the T7 p/p system. Thus, we provide a method for using the T7 p/p system on an industrial scale.
最广泛、高效的原核蛋白产生系统是一种能够被 T7 噬菌体聚合酶识别的 T7 噬菌体启动子(T7 p/p 系统)。不幸的是,在这个系统中,目标蛋白的表达水平逐渐下降,在 3 到 5 次传代后通常无法检测到。尽管有许多研究试图稳定 T7 p/p 系统的表达水平,但没有一种方法能够充分解决这个问题,因此限制了该系统在大规模生产重组蛋白方面的应用。
我们创建了一个表达盒,能够在 T7p/p 系统中稳定、高水平地表达。该盒在两个不同的载体骨架和两种靶蛋白上进行了测试。在所有实验中,与传统系统相比,使用新盒的表达系统表现出高且稳定的蛋白表达水平。
本文描述了一种通用的表达盒,能够在 T7 RNA 聚合酶为基础的表达系统中实现高水平、稳定的靶蛋白表达。我们还成功地将该盒用作一种新型表达平台,并证明了它克服 T7 p/p 系统主要缺陷的能力。因此,我们提供了一种在工业规模上使用 T7 p/p 系统的方法。