Lin Nai-Xin, He Rui-Zhen, Xu Yan, Yu Xiao-Wei
Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi, 214122, People's Republic of China.
Biotechnol Biofuels. 2021 Jul 20;14(1):160. doi: 10.1186/s13068-021-02013-w.
Pichia pastoris (syn. Komagataella phaffii) is an important yeast system for heterologous protein expression. A robust P. pastoris mutant with oxidative and thermal stress cross-tolerance was acquired in our previous study. The robust mutant can express a 2.5-fold higher level of lipase than its wild type (WT) under methanol induction conditions.
In this study, we found that the robust mutant not only can express a high level of lipase, but also can express a high level of other heterogeneous proteins (e.g., green fluorescence protein) under methanol induction conditions. Additionally, the intracellular reactive oxygen species (ROS) levels in the robust mutant were lower than that in the WT under methanol induction conditions. To figure out the difference of cellular response to methanol between the WT and the robust mutant, RNA-seq was detected and compared. The results of RNA-seq showed that the expression levels of genes related to antioxidant, MAPK pathway, ergosterol synthesis pathway, transcription factors, and the peroxisome pathway were upregulated in the robust mutant compared to the WT. The upregulation of these key pathways can improve the oxidative stress tolerance of strains and efficiently eliminate cellular ROS. Hence, we inferred that the high heterologous protein expression efficiency in the robust mutant may be due to its enhanced oxidative stress tolerance. Promisingly, we have indeed increased the expression level of lipase up to 1.6-fold by overexpressing antioxidant genes in P. pastoris.
This study demonstrated the impact of methanol on the expression levels of genes in P. pastoris and emphasized the contribution of oxidative stress tolerance on heterologous protein expression in P. pastoris. Our results shed light on the understanding of protein expression mechanism in P. pastoris and provided an idea for the rational construction of robust yeast with high expression ability.
巴斯德毕赤酵母(同义词:法夫酵母)是用于异源蛋白表达的重要酵母系统。在我们之前的研究中获得了一种具有氧化和热应激交叉耐受性的健壮巴斯德毕赤酵母突变体。在甲醇诱导条件下,该健壮突变体表达脂肪酶的水平比其野生型高2.5倍。
在本研究中,我们发现该健壮突变体不仅在甲醇诱导条件下能高水平表达脂肪酶,还能高水平表达其他异源蛋白(如绿色荧光蛋白)。此外,在甲醇诱导条件下,健壮突变体的细胞内活性氧(ROS)水平低于野生型。为了弄清楚野生型和健壮突变体对甲醇的细胞反应差异,对RNA测序进行了检测和比较。RNA测序结果表明,与野生型相比,健壮突变体中与抗氧化、丝裂原活化蛋白激酶(MAPK)途径、麦角固醇合成途径、转录因子和过氧化物酶体途径相关的基因表达水平上调。这些关键途径的上调可以提高菌株的氧化应激耐受性并有效消除细胞内的ROS。因此,我们推断健壮突变体中异源蛋白表达效率高可能是由于其氧化应激耐受性增强。有希望的是,我们通过在巴斯德毕赤酵母中过表达抗氧化基因,确实将脂肪酶的表达水平提高到了1.6倍。
本研究证明了甲醇对巴斯德毕赤酵母基因表达水平的影响,并强调了氧化应激耐受性对巴斯德毕赤酵母异源蛋白表达的贡献。我们的结果有助于理解巴斯德毕赤酵母中的蛋白质表达机制,并为合理构建具有高表达能力的健壮酵母提供了思路。