Mining yeast diversity unveils novel targets for improved heterologous laccase production in Saccharomyces cerevisiae.

IF 4.9 2区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Microbial Cell Factories Pub Date : 2025-03-10 DOI:10.1186/s12934-025-02677-1
Ryan Wei Kwan Wong, Marissa Foo, Jasmine R S Lay, Tiffany L T Wai, Jackson Moore, Fabien Dutreux, Cristen Molzahn, Corey Nislow, Vivien Measday, Joseph Schacherer, Thibault Mayor
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Abstract

The budding yeast Saccharomyces cerevisiae is a widely utilized host cell for recombinant protein production due to its well studied and annotated genome, its ability to secrete large and post-translationally modified proteins, fast growth and cost-effective culturing. However, recombinant protein yields from S. cerevisiae often fall behind that of other host systems. To address this, we developed a high-throughput screen of wild, industrial and laboratory S. cerevisiae isolates to identify strains with a natural propensity for greater recombinant protein production, specifically focussing on laccase multicopper oxidases from the fungi Trametes trogii and Myceliophthora thermophila. Using this method, we identified 20 non-laboratory strains with higher capacity to produce active laccase. Interestingly, lower levels of laccase mRNA were measured in most cases, indicating that the drivers of elevated protein production capacity lie beyond the regulation of recombinant gene expression. We characterized the identified strains using complementary genomic and proteomic approaches to reveal several potential pathways driving the improved expression phenotype. Gene ontology analysis suggests broad changes in cellular metabolism, specifically in genes/proteins involved in carbohydrate catabolism, thiamine biosynthesis, transmembrane transport and vacuolar degradation. Targeted deletions of the hexose transporter HXT11 and the Coat protein complex II interacting paralogs PRM8 and 9, involved in ER to Golgi transport, resulted in significantly improved laccase production from the S288C laboratory strain. Whereas the deletion of the Hsp110 SSE1 gene, guided by our proteomic analysis, also led to higher laccase activity, we did not observe major changes of the protein homeostasis network within the strains with higher laccase activity. This study opens new avenues to leverage the vast diversity of Saccharomyces cerevisiae for recombinant protein production, as well as offers new strategies and insights to enhance recombinant protein yields of current strains.

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挖掘酵母多样性揭示了改进酿酒酵母异源漆酶生产的新靶点。
出芽酵母是一种被广泛应用于重组蛋白生产的宿主细胞,因为它的基因组被充分研究和注释,能够分泌大的和翻译后修饰的蛋白质,生长速度快,培养成本低。然而,酿酒酵母的重组蛋白产量往往落后于其他宿主系统。为了解决这个问题,我们对野生、工业和实验室的酿酒葡萄球菌分离株进行了高通量筛选,以确定具有更大重组蛋白生产天然倾向的菌株,特别关注真菌Trametes trogii和嗜热丝霉菌(Myceliophthora thermoophilila)中的漆酶多铜氧化酶。利用这种方法,我们鉴定了20株具有较高生产活性漆酶能力的非实验室菌株。有趣的是,在大多数情况下检测到较低水平的漆酶mRNA,这表明提高蛋白质生产能力的驱动因素超出了重组基因表达的调节。我们使用互补的基因组学和蛋白质组学方法对鉴定的菌株进行了表征,以揭示驱动改善表达表型的几种潜在途径。基因本体论分析表明,细胞代谢发生了广泛的变化,特别是参与碳水化合物分解代谢、硫胺素生物合成、跨膜运输和液泡降解的基因/蛋白质。在实验室菌株S288C中,已糖转运蛋白HXT11和参与内质网到高尔基转运的Coat蛋白复合物II相互作用的类似物PRM8和9的靶向缺失导致漆酶产量显著提高。然而,根据我们的蛋白质组学分析,Hsp110 SSE1基因的缺失也导致了更高的漆酶活性,我们没有观察到在具有更高漆酶活性的菌株中蛋白质稳态网络的重大变化。本研究为利用酿酒酵母的巨大多样性生产重组蛋白开辟了新的途径,并为提高现有菌株的重组蛋白产量提供了新的策略和见解。
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来源期刊
Microbial Cell Factories
Microbial Cell Factories 工程技术-生物工程与应用微生物
CiteScore
9.30
自引率
4.70%
发文量
235
审稿时长
2.3 months
期刊介绍: Microbial Cell Factories is an open access peer-reviewed journal that covers any topic related to the development, use and investigation of microbial cells as producers of recombinant proteins and natural products, or as catalyzers of biological transformations of industrial interest. Microbial Cell Factories is the world leading, primary research journal fully focusing on Applied Microbiology. The journal is divided into the following editorial sections: -Metabolic engineering -Synthetic biology -Whole-cell biocatalysis -Microbial regulations -Recombinant protein production/bioprocessing -Production of natural compounds -Systems biology of cell factories -Microbial production processes -Cell-free systems
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