Engineering Biology Research Center, Kobe University, Kobe, Japan.
Graduate School of Science, Technology and Innovation, Kobe University, Kobe, Japan.
Commun Biol. 2022 Jun 8;5(1):561. doi: 10.1038/s42003-022-03475-w.
Expression of secreted recombinant proteins burdens the protein secretion machinery, limiting production. Here, we describe an approach to improving protein production by the non-conventional yeast Komagataella phaffii comprised of genome-wide screening for effective gene disruptions, combining them in a single strain, and recovering growth reduction by adaptive evolution. For the screen, we designed a multiwell-formatted, streamlined workflow to high-throughput assay of secretion of a single-chain small antibody, which is cumbersome to detect but serves as a good model of proteins that are difficult to secrete. Using the consolidated screening system, we evaluated >19,000 mutant strains from a mutant library prepared by a modified random gene-disruption method, and identified six factors for which disruption led to increased antibody production. We then combined the disruptions, up to quadruple gene knockouts, which appeared to contribute independently, in a single strain and observed an additive effect. Target protein and promoter were basically interchangeable for the effects of knockout genes screened. We finally used adaptive evolution to recover reduced cell growth by multiple gene knockouts and examine the possibility for further enhancing protein secretion. Our successful, three-part approach holds promise as a method for improving protein production by non-conventional microorganisms.
分泌重组蛋白会给蛋白分泌机制带来负担,从而限制产量。在这里,我们描述了一种通过全基因组筛选有效的基因缺失,将它们组合在一个单一的菌株中,并通过适应性进化来恢复生长减少,从而提高非常规酵母毕赤酵母生产蛋白的方法。在筛选过程中,我们设计了一种多孔格式的简化工作流程,用于高通量检测单链小分子抗体的分泌,这种方法虽然繁琐,但可以作为很难分泌的蛋白的良好模型。利用整合的筛选系统,我们评估了超过 19000 株来自改良随机基因敲除方法制备的突变文库中的突变株,发现 6 个因素的敲除会导致抗体产量增加。然后,我们在单个菌株中组合了这些敲除,最多可达四倍基因敲除,这些敲除似乎是独立贡献的,并且具有累加效应。靶蛋白和启动子对于筛选的敲除基因的作用基本上是可互换的。最后,我们利用适应性进化来恢复因多个基因敲除而导致的细胞生长减少,并研究进一步提高蛋白分泌的可能性。我们成功的三部分方法有望成为提高非常规微生物蛋白生产的一种方法。