Zekhnini Abdelghani, Casamayor Antonio, Ariño Joaquín
Institut de Biotecnologia i Biomedicina & Departament de Bioquímica i Biologia Molecular, Universitat Autònoma de Barcelona, Cerdanyola del Vallès, Spain.
Microb Biotechnol. 2025 Sep;18(9):e70213. doi: 10.1111/1751-7915.70213.
The demand for strong and easily inducible promoters to produce heterologous proteins in Saccharomyces cerevisiae has attracted considerable attention in the last years. In this organism, alkalinisation triggers a wide and well-characterised transcriptional response that includes activation of the calcium-dependent calcineurin-Crz1 and the phosphate-responsive PHO pathways. Here, we present the construction of random libraries containing multiple combinations of Crz1- and Pho4-binding sequences, and we show that these elements are able to promote efficient expression of GFP by simple addition of KOH to the medium. The expression in Crz1 or Pho4-deficient cells allowed us to define the relative contribution of these elements to GFP production. We also show that the addition of a single copy of a 60-bp fragment of the ENA1 promoter containing an Stp1/2 site further enhances expression. Finally, we demonstrate that these constructs drive strong expression of secretable laccase, an enzyme of industrial interest in processing lignin biopolymers, and that the level of expression can be adjusted by modifying the pH of the medium. In conclusion, our work presents a novel expression system whose induction is simple, cheap, and easy to monitor, and that could be an attractive alternative to current expression platforms for both research and industrial protein production purposes.
近年来,在酿酒酵母中生产异源蛋白时,对强大且易于诱导的启动子的需求引起了广泛关注。在这种生物体中,碱化会引发广泛且特征明确的转录反应,其中包括钙依赖性钙调神经磷酸酶 - Crz1和磷酸盐反应性PHO途径的激活。在此,我们展示了包含Crz1和Pho4结合序列多种组合的随机文库的构建,并且我们表明通过向培养基中简单添加KOH,这些元件能够促进GFP的高效表达。在Crz1或Pho4缺陷细胞中的表达使我们能够确定这些元件对GFP产生的相对贡献。我们还表明,添加含有Stp1/2位点的ENA1启动子的60bp片段的单拷贝可进一步增强表达。最后,我们证明这些构建体可驱动可分泌漆酶的强表达,漆酶是一种在木质素生物聚合物加工中具有工业价值的酶,并且表达水平可通过调节培养基的pH来调整。总之,我们的工作提出了一种新型表达系统,其诱导简单、廉价且易于监测,并且对于研究和工业蛋白质生产目的而言,可能是当前表达平台的有吸引力的替代方案。