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Combinatorial optimization of pathway, process and media for the production of p-coumaric acid by Saccharomyces cerevisiae.
Moreno-Paz, Sara; van der Hoek, Rianne; Eliana, Elif; Martins Dos Santos, Vitor A P; Schmitz, Joep; Suarez-Diez, Maria.
Afiliação
  • Moreno-Paz S; Laboratory of Systems and Synthetic Biology, Wageningen University & Research, Wageningen, The Netherlands.
  • van der Hoek R; Department of Science and Research-dsm-firmenich, Science & Research, Delft, The Netherlands.
  • Eliana E; Laboratory of Systems and Synthetic Biology, Wageningen University & Research, Wageningen, The Netherlands.
  • Martins Dos Santos VAP; Bioprocess Engineering Group, Wageningen University & Research, Wageningen, The Netherlands.
  • Schmitz J; Department of Science and Research-dsm-firmenich, Science & Research, Delft, The Netherlands.
  • Suarez-Diez M; Laboratory of Systems and Synthetic Biology, Wageningen University & Research, Wageningen, The Netherlands.
Microb Biotechnol ; 17(3): e14424, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38528768
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Proteínas de Saccharomyces cerevisiae Idioma: En Revista: Microb Biotechnol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Proteínas de Saccharomyces cerevisiae Idioma: En Revista: Microb Biotechnol Ano de publicação: 2024 Tipo de documento: Article