Artificial Transcription Factors for Tuneable Gene Expression in Pichia pastoris

毕赤酵母 拟南芥 生物 转录因子 拟南芥 酿酒酵母 基因 毕赤酵母 发起人 酵母 转录调控 遗传学 计算生物学 基因表达 突变体 重组DNA
作者
Gita Naseri,Kevin Prause,Housam Haj Hamdo,Christoph Arenz
出处
期刊:Frontiers in Bioengineering and Biotechnology [Frontiers Media SA]
卷期号:9 被引量:7
标识
DOI:10.3389/fbioe.2021.676900
摘要

The non-conventional yeast Pichia pastoris (syn. Komagataella phaffii ) has become a powerful eukaryotic expression platform for biopharmaceutical and biotechnological applications on both laboratory and industrial scales. Despite the fundamental role that artificial transcription factors (ATFs) play in the orthogonal control of gene expression in synthetic biology, a limited number of ATFs are available for P. pastoris . To establish orthogonal regulators for use in P. pastoris , we characterized ATFs derived from Arabidopsis TFs. The plant-derived ATFs contain the binding domain of TFs from the plant Arabidopsis thaliana , in combination with the activation domains of yeast GAL4 and plant EDLL and a synthetic promoter harboring the cognate cis -regulatory motifs. Chromosomally integrated ATFs and their binding sites (ATF/BSs) resulted in a wide spectrum of inducible transcriptional outputs in P. pastoris , ranging from as low as 1- to as high as ∼63-fold induction with only small growth defects. We demonstrated the application of ATF/BSs by generating P. pastoris cells that produce β-carotene. Notably, the productivity of β-carotene in P. pastoris was ∼4.8-fold higher than that in S. cerevisiae , reaching ∼59% of the β-carotene productivity obtained in a S. cerevisiae strain optimized for the production of the β–carotene precursor, farnesyl diphosphate, by rewiring the endogenous metabolic pathways using plant-derived ATF/BSs. Our data suggest that plant-derived regulators have a high degree of transferability from S. cerevisiae to P. pastoris . The plant-derived ATFs, together with their cognate binding sites, powerfully increase the repertoire of transcriptional regulatory modules for the tuning of protein expression levels required in metabolic engineering or synthetic biology in P. pastoris .
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