Identification of a novel growth-associated promoter for biphasic expression of heterogenous proteins in Pichia pastoris

Author:

Shen Qi123ORCID,Cui Jie123,Wang Yang123,Hu Zhong-Ce123,Xue Ya-Ping123ORCID,Zheng Yu-Guo123

Affiliation:

1. Key Laboratory of Bioorganic Synthesis of Zhejiang Province, College of Biotechnology and Bioengineering, Zhejiang University of Technology, Hangzhou, China

2. Engineering Research Center of Bioconversion and Biopurification of Ministry of Education, Zhejiang University of Technology, Hangzhou, China

3. National and Local Joint Engineering Research Center for Biomanufacturing of Chiral Chemicals, Zhejiang University of Technology, Hangzhou, China

Abstract

ABSTRACT Pichia pastoris ( P. pastoris ) is one of the most popular cell factories for expressing exogenous proteins and producing useful chemicals. The alcohol oxidase 1 promoter (P AOX1 ) is the most commonly used strong promoter in P. pastoris and has the characteristic of biphasic expression. However, the inducer for P AOX1 , methanol, has toxicity and poses risks in industrial settings. In the present study, analyzing transcriptomic data of cells collected at different stages of growth found that the formate dehydrogenase (FDH) gene ranked 4960th in relative expression among 5032 genes during the early logarithmic growth phase but rose to the 10th and 1st during the middle and late logarithmic growth phases, respectively, displaying a strict biphasic expression characteristic. The unique transcriptional regulatory profile of the FDH gene prompted us to investigate the properties of its promoter (P FDH800 ). Under single-copy conditions, when a green fluorescent protein variant was used as the expression target, the P FDH800 achieved 119% and 69% of the activity of the glyceraldehyde-3-phosphate dehydrogenase promoter and P AOX1 , respectively. After increasing the copy number of the expression cassette in the strain to approximately four copies, the expression level of GFPuv driven by P FDH800 increased to approximately 2.5 times that of the strain containing GFPuv driven by a single copy of P AOX1 . Our P FDH800 -based expression system exhibited precise biphasic expression, ease of construction, minimal impact on normal cellular metabolism, and high strength. Therefore, it has the potential to serve as a new expression system to replace the P AOX1 promoter. IMPORTANCE The alcohol oxidase 1 promoter (PAOX1) expression system has the characteristics of biphasic expression and high expression levels, making it the most widely used promoter in the yeast Pichia pastoris . However, PAOX1 requires methanol induction, which can be toxic and poses a fire hazard in large quantities. Our research has found that the activity of PFDH800 is closely related to the growth state of cells and can achieve biphasic expression without the need for an inducer. Compared to other reported non-methanol-induced biphasic expression systems, the system based on the PFDH800 offers several advantages, including high expression levels, simple construction, minimal impact on cellular metabolism, no need for an inducer, and the ability to fine-tune expression.

Funder

MOST | National Key Research and Development Program of China

MOST | NSFC | NSFC-Zhejiang Joint Fund | Basic Public Welfare Research Program of Zhejiang Province

Major Research Program of Zhejiang Provincial National Natural Science Foundation of China

Publisher

American Society for Microbiology

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