Combinatorial optimization of pathway, process and media for the production of p-coumaric acid by Saccharomyces cerevisiae

IF 5.7 2区 生物学 Microbial Biotechnology Pub Date : 2024-03-25 DOI:10.1111/1751-7915.14424
Sara Moreno-Paz, Rianne van der Hoek, Elif Eliana, Vitor A. P. Martins dos Santos, Joep Schmitz, Maria Suarez-Diez
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Abstract

Microbial cell factories are instrumental in transitioning towards a sustainable bio-based economy, offering alternatives to conventional chemical processes. However, fulfilling their potential requires simultaneous screening for optimal media composition, process and genetic factors, acknowledging the complex interplay between the organism's genotype and its environment. This study employs statistical design of experiments to systematically explore these relationships and optimize the production of p-coumaric acid (pCA) in Saccharomyces cerevisiae. Two rounds of fractional factorial designs were used to identify factors with a significant effect on pCA production, which resulted in a 168-fold variation in pCA titre. Moreover, a significant interaction between the culture temperature and expression of ARO4 highlighted the importance of simultaneous process and strain optimization. The presented approach leverages the strengths of experimental design and statistical analysis and could be systematically applied during strain and bioprocess design efforts to unlock the full potential of microbial cell factories.

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组合优化酿酒酵母生产对香豆酸的途径、工艺和培养基。
微生物细胞工厂有助于向可持续生物经济过渡,为传统化学工艺提供了替代品。然而,要发挥其潜力,需要同时筛选最佳的培养基成分、工艺和遗传因素,并认识到生物基因型与其环境之间复杂的相互作用。本研究采用统计实验设计来系统地探索这些关系,并优化酿酒酵母中对香豆酸(pCA)的生产。研究采用了两轮分数因子设计来确定对 pCA 产量有显著影响的因素,结果发现 pCA 滴度的变化为 168 倍。此外,培养温度与 ARO4 表达之间存在明显的交互作用,这凸显了同时优化工艺和菌株的重要性。所介绍的方法充分利用了实验设计和统计分析的优势,可在菌株和生物工艺设计过程中系统应用,以充分挖掘微生物细胞工厂的潜力。
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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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