Research Division Biochemical Engineering, Institute of Chemical, Environmental and Biological Engineering, TU Wien, Gumpendorfer Strasse 1a, 1060, Vienna, Austria.
Christian Doppler Laboratory for Mechanistic and Physiological Methods for Improved Bioprocesses, Institute of Chemical, Environmental and Biological Engineering, TU Wien, Vienna, Austria.
Microb Cell Fact. 2017 Sep 13;16(1):152. doi: 10.1186/s12934-017-0768-8.
The methylotrophic yeast Pichia pastoris is a well-studied host organism for recombinant protein production, which is usually regulated either by a constitutive promoter (e.g. promoter of glyceraldehyde-3-phosphate dehydrogenase; P) or an inducible promoter (e.g. promoter of alcohol oxidase 1; P). Both promoter systems have several advantages and disadvantages; with one of the main disadvantages being their lack of tunability. Various novel promoter systems, which are either inducible or de-repressed, allowing higher degrees of freedom, have been reported. Recently, bi-directional promoter systems in P. pastoris with two promoter systems regulating recombinant expression of one or more genes were developed. In this study, we introduce a novel bi-directional promoter system combining a modified catalase promoter system (P; derepressible and inducible) and the traditional P, allowing tunable recombinant protein production.
We characterized a recombinant P. pastoris strain, carrying the novel bi-directional promoter system, during growth and production in three dynamic bioreactor cultivations. We cloned the model enzyme cellobiohydralase downstream of either promoter and applied different feeding strategies to determine the physiological boundaries of the strain. We succeeded in demonstrating tunability of recombinant protein production solely in response to the different feeding strategies and identified a mixed feed regime allowing highest productivity.
In this feasibility study, we present the first controlled bioreactor experiments with a recombinant P. pastoris strain carrying a novel bi-directional promotor combination of a catalase promoter variant (P) and the traditional P. We demonstrated that this bi-directional promoter system allows tunable recombinant protein expression only in response to the available C-sources. This bi-directional promoter system offers a high degree of freedom for bioprocess design and development, making bi-directional promoters in P. pastoris highly attractive for recombinant protein production.
甲醇营养型酵母毕赤酵母是一种研究较为深入的重组蛋白生产宿主,其表达通常受组成型启动子(如甘油醛-3-磷酸脱氢酶启动子;P)或诱导型启动子(如醇氧化酶 1 启动子;P)调控。这两种启动子系统各有优缺点;其中一个主要缺点是缺乏可调性。已报道了各种新型启动子系统,这些启动子系统可以是诱导型或去阻遏型的,从而具有更高的自由度。最近,毕赤酵母中开发了具有两个启动子系统的双向启动子系统,这两个启动子系统可以调控一个或多个基因的重组表达。在本研究中,我们引入了一种新型的双向启动子系统,该系统结合了改良的过氧化氢酶启动子系统(P;可诱导和去阻遏)和传统的 P,从而允许对重组蛋白生产进行可调控制。
我们在三次动态生物反应器培养中对携带新型双向启动子系统的重组毕赤酵母菌株进行了生长和生产特性的表征。我们将模型酶纤维二糖水解酶克隆到任一个启动子的下游,并应用不同的补料策略来确定该菌株的生理极限。我们成功地证明了仅通过不同的补料策略即可实现重组蛋白生产的可调性,并确定了一种混合补料策略可以实现最高的生产率。
在这项可行性研究中,我们首次进行了携带新型双向启动子组合(一种过氧化氢酶启动子变体(P)和传统的 P)的重组毕赤酵母菌株的受控生物反应器实验。我们证明,这种双向启动子系统仅在响应可用 C 源的情况下允许可调的重组蛋白表达。这种双向启动子系统为生物过程设计和开发提供了高度的自由度,使得毕赤酵母中的双向启动子非常适合用于重组蛋白生产。