Microbial Systems and Computational Biology Research Team, Thailand Bioresource Research Center, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Pathum Thani, Thailand.
Microbial Cell Factory Research Team, Biorefinery and Bioproduct Technology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Pathum Thani, Thailand.
Yeast. 2021 May;38(5):316-325. doi: 10.1002/yea.3548. Epub 2021 Jan 14.
The thermotolerant methylotrophic yeast Ogataea thermomethanolica TBRC656 is a potential host for heterologous protein production. However, overproduction of heterologous protein can induce cellular stress and limit the level of its secretion. To improve the secretion of heterologous protein, we identified the candidate proteins with altered production during production of heterologous protein in O. thermomethanolica by using a label-free comparative proteomic approach. Four hundred sixty-four proteins with various biological functions showed differential abundance between O. thermomethanolica expressing fungal xylanase (OT + Xyl) and a control strain. The induction of proteins in transport and proteasomal proteolysis was prominently observed. Eight candidate proteins involved in cell wall biosynthesis (Chs3, Gas4), chaperone (Sgt2, Pex19), glycan metabolism (Csf1), protein transport (Ypt35), and vacuole and protein sorting (Cof1, Npr2) were mutated by a CRISPR/Cas9 approach. An Sgt2 mutant showed higher phytase and xylanase activity compared with the control strain (13%-20%), whereas mutants of other genes including Cof1, Pex19, Gas4, and Ypt35 showed lower xylanase activity compared with the control strain (15%-25%). In addition, an Npr2 mutant showed defective growth, while overproduction of Npr2 enhanced xylanase activity. These results reveal genes that can be mutated to modulate heterologous protein production and growth of O. thermomethanolica TBRC656.
嗜热甲醇营养酵母 Ogataea thermomethanolica TBRC656 是一种潜在的异源蛋白生产宿主。然而,过量生产异源蛋白会诱导细胞应激,限制其分泌水平。为了提高异源蛋白的分泌量,我们采用无标记比较蛋白质组学方法,鉴定了在 O. thermomethanolica 生产异源蛋白过程中产量发生变化的候选蛋白。在表达真菌木聚糖酶(OT+Xyl)的 O. thermomethanolica 和对照菌株之间,有 464 种具有各种生物学功能的蛋白质显示出不同的丰度。观察到蛋白质在运输和蛋白酶体蛋白水解中的诱导作用明显。涉及细胞壁生物合成(Chs3、Gas4)、伴侣蛋白(Sgt2、Pex19)、聚糖代谢(Csf1)、蛋白质转运(Ypt35)和液泡及蛋白质分拣(Cof1、Npr2)的 8 个候选蛋白通过 CRISPR/Cas9 方法发生突变。与对照菌株相比,Sgt2 突变体的植酸酶和木聚糖酶活性更高(13%-20%),而包括 Cof1、Pex19、Gas4 和 Ypt35 在内的其他基因的突变体的木聚糖酶活性则低于对照菌株(15%-25%)。此外,Npr2 突变体的生长受到影响,而 Npr2 的过表达则增强了木聚糖酶的活性。这些结果揭示了可以突变的基因,以调节 O. thermomethanolica TBRC656 中异源蛋白的生产和生长。