Department of Life Sciences, Imperial College London, London SW7 2AZ, UK.
Microb Cell Fact. 2013 Dec 20;12:128. doi: 10.1186/1475-2859-12-128.
The success of Pichia pastoris as a heterologous expression system lies predominantly in the impressive yields that can be achieved due to high volumetric productivity. However, low specific productivity still inhibits the potential success of this platform. Multi-(gene) copy clones are potentially a quick and convenient method to increase recombinant protein titer, yet they are not without their pitfalls. It has been more than twenty years since the first reported use of multi-copy clones and it is still an active area of research to find the fastest and most efficient method for generating these strains. It has also become apparent that there is not always a linear correlation between copy number and protein titer, leading to in-depth investigations into how to minimize the negative impact of secretory stress and achieve clonal stability.
毕赤酵母作为一种异源表达系统的成功主要在于其可以通过高体积产率获得令人印象深刻的产量。然而,低比生产率仍然抑制了该平台的潜在成功。多(基因)拷贝克隆是一种提高重组蛋白滴度的快速而方便的方法,但它们并非没有缺陷。自首次报道使用多拷贝克隆以来已经超过二十年了,寻找生成这些菌株的最快和最有效的方法仍然是一个活跃的研究领域。人们也已经意识到,拷贝数与蛋白滴度之间并不总是存在线性关系,这导致人们深入研究如何最小化分泌应激的负面影响并实现克隆稳定性。