García-Calvo Laura, Kummen Charlotte, Rustad Solvor, Rønning Sissel Beate, Fagerlund Annette
Nofima - Norwegian Institute of Food, Fisheries and Aquaculture Research, Ås, Norway.
Microb Cell Fact. 2025 May 3;24(1):97. doi: 10.1186/s12934-025-02716-x.
The yeast Komagataella phaffii (formerly known as Pichia pastoris) has been widely used for functional expression of recombinant proteins, including plant and animal food proteins. CRISPR/Cas9 genome editing systems can be used for insertion of heterologous genes without the use of selection markers. The study aimed to create a convenient markerless knock-in method for integrating expression cassettes into the chromosome of K. phaffii using CRISPR/Cas9 technology. The approach was based on the hierarchical, modular, Golden Gate assembly employing the GoldenPiCS toolkit. Furthermore, the aim was to evaluate the system's efficiency and suitability for producing secreted recombinant food proteins.
Three Cas9/sgRNA plasmids were constructed, along with corresponding donor helper plasmids containing homology regions for chromosomal integration via homology-directed repair. The integration efficiency of an enhanced green fluorescent protein (eGFP) expression cassette was assessed at three genomic loci (04576, PFK1, and ROX1). The 04576 locus showed the highest integration efficiency, while ROX1 had the highest transformation efficiency. Whole genome sequencing revealed variable copy numbers of eGFP expression cassettes among clones, corresponding with increasing levels of fluorescence. Furthermore, the system's applicability for producing recombinant food proteins was validated by successfully expressing and secreting chicken ovalbumin. This constitutes the first report of CRISPR/Cas9 applied to produce recombinant chicken ovalbumin.
The adapted GoldenPiCS toolkit combined with CRISPR/Cas9 technology enabled efficient and precise genome integration in K. phaffii. This approach holds promise for expanding the production of high-value recombinant proteins. Future research should focus on optimizing integration sites and improving cloning procedures to enhance the system's efficiency and versatility.
巴斯德毕赤酵母(以前称为毕赤酵母)已被广泛用于重组蛋白的功能表达,包括植物和动物食品蛋白。CRISPR/Cas9基因组编辑系统可用于在不使用选择标记的情况下插入异源基因。本研究旨在创建一种便捷的无标记敲入方法,利用CRISPR/Cas9技术将表达盒整合到巴斯德毕赤酵母的染色体中。该方法基于采用GoldenPiCS工具包的分层、模块化金门组装。此外,目的是评估该系统生产分泌型重组食品蛋白的效率和适用性。
构建了三种Cas9/sgRNA质粒,以及相应的供体辅助质粒,这些质粒包含通过同源定向修复进行染色体整合的同源区域。在三个基因组位点(04576、PFK1和ROX1)评估了增强型绿色荧光蛋白(eGFP)表达盒的整合效率。04576位点显示出最高的整合效率,而ROX1具有最高的转化效率。全基因组测序揭示了克隆中eGFP表达盒的可变拷贝数,这与荧光水平的增加相对应。此外,通过成功表达和分泌鸡卵清蛋白验证了该系统生产重组食品蛋白的适用性。这是CRISPR/Cas9应用于生产重组鸡卵清蛋白的首次报道。
改进后的GoldenPiCS工具包与CRISPR/Cas9技术相结合,能够在巴斯德毕赤酵母中实现高效、精确的基因组整合。这种方法有望扩大高价值重组蛋白的生产。未来的研究应集中在优化整合位点和改进克隆程序,以提高该系统的效率和通用性。