组合碱响应型杂交启动子作为酿酒酵母异源蛋白表达的工具。

IF 5.2 2区 生物学
Abdelghani Zekhnini, Antonio Casamayor, Joaquín Ariño
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引用次数: 0

摘要

近年来,对强而易诱导的启动子在酿酒酵母中产生异源蛋白的需求引起了人们的广泛关注。在这种生物体中,碱化引发广泛且特征明确的转录反应,包括钙依赖性钙调磷酸酶- crz1和磷酸盐反应性PHO途径的激活。在这里,我们构建了包含Crz1-和pho4结合序列的多种组合的随机文库,并表明这些元件能够通过简单地向培养基中添加KOH来促进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素对GFP产生的相对贡献。我们还发现,添加含有Stp1/2位点的ENA1启动子60 bp片段的单个拷贝进一步增强了表达。最后,我们证明了这些结构驱动分泌漆酶的强烈表达,这是一种加工木质素生物聚合物的工业酶,并且表达水平可以通过改变培养基的pH值来调节。总之,我们的工作提出了一种新的表达系统,其诱导简单,便宜,易于监测,并且可能成为当前研究和工业蛋白质生产目的的表达平台的有吸引力的替代方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Combinatorial Alkali-Responsive Hybrid Promoters as Tools for Heterologous Protein Expression in Saccharomyces cerevisiae

Combinatorial Alkali-Responsive Hybrid Promoters as Tools for Heterologous Protein Expression in Saccharomyces cerevisiae

Combinatorial Alkali-Responsive Hybrid Promoters as Tools for Heterologous Protein Expression in Saccharomyces cerevisiae

Combinatorial Alkali-Responsive Hybrid Promoters as Tools for Heterologous Protein Expression in Saccharomyces cerevisiae

Combinatorial Alkali-Responsive Hybrid Promoters as Tools for Heterologous Protein Expression in Saccharomyces cerevisiae

Combinatorial Alkali-Responsive Hybrid Promoters as Tools for Heterologous Protein Expression in Saccharomyces cerevisiae

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.

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来源期刊
Microbial Biotechnology
Microbial Biotechnology Immunology and Microbiology-Applied Microbiology and Biotechnology
CiteScore
11.20
自引率
3.50%
发文量
162
审稿时长
1 months
期刊介绍: Microbial Biotechnology publishes papers of original research reporting significant advances in any aspect of microbial applications, including, but not limited to biotechnologies related to: Green chemistry; Primary metabolites; Food, beverages and supplements; Secondary metabolites and natural products; Pharmaceuticals; Diagnostics; Agriculture; Bioenergy; Biomining, including oil recovery and processing; Bioremediation; Biopolymers, biomaterials; Bionanotechnology; Biosurfactants and bioemulsifiers; Compatible solutes and bioprotectants; Biosensors, monitoring systems, quantitative microbial risk assessment; Technology development; Protein engineering; Functional genomics; Metabolic engineering; Metabolic design; Systems analysis, modelling; Process engineering; Biologically-based analytical methods; Microbially-based strategies in public health; Microbially-based strategies to influence global processes
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