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A Genomewide Evolution-Based CRISPR/Cas9 with Donor-Free (GEbCD) for Developing Robust and Productive Industrial Yeast.
Zhang, Jinwei; Zhao, Guomiao; Bai, Wenxin; Chen, Ying; Zhang, Yuan; Li, Fan; Wang, Manyi; Shen, Yue; Wang, Yun; Wang, Xiaoyan; Li, Chun.
Afiliación
  • Zhang J; Nutrition & Health Research Institute, COFCO Corporation, Beijing 102209, China.
  • Zhao G; Key Laboratory of Medical Molecule Science and Pharmaceutics Engineering, Ministry of Industry and Information Technology, Institute of Biochemical Engineering, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 100081, China.
  • Bai W; School of Life Science, Yan'an University, Yan'an, Shaanxi 716000, China.
  • Chen Y; Nutrition & Health Research Institute, COFCO Corporation, Beijing 102209, China.
  • Zhang Y; Nutrition & Health Research Institute, COFCO Corporation, Beijing 102209, China.
  • Li F; Key Laboratory of Medical Molecule Science and Pharmaceutics Engineering, Ministry of Industry and Information Technology, Institute of Biochemical Engineering, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 100081, China.
  • Wang M; Guangdong Provincial Key Laboratory of Genome Read and Write, BGI Research, Shenzhen 518083, China.
  • Shen Y; College of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
  • Wang Y; Nutrition & Health Research Institute, COFCO Corporation, Beijing 102209, China.
  • Wang X; Nutrition & Health Research Institute, COFCO Corporation, Beijing 102209, China.
  • Li C; Nutrition & Health Research Institute, COFCO Corporation, Beijing 102209, China.
ACS Synth Biol ; 13(8): 2335-2346, 2024 Aug 16.
Article en En | MEDLINE | ID: mdl-39012160
ABSTRACT
Developing more robust and productive industrial yeast is crucial for high-efficiency biomanufacturing. However, the challenges posed by the long time required and the low abundance of mutations generated through genomewide evolutionary engineering hinder the development and optimization of desired hosts for industrial applications. To address these issues, we present a novel solution called the Genomewide Evolution-based CRISPR/Cas with Donor-free (GEbCD) system, in which nonhomologous-end-joining (NHEJ) repair can accelerate the acquisition of highly abundant yeast mutants. Together with modified rad52 of the DNA double-strand break repair in Saccharomyces cerevisiae, a hypermutation host was obtained with a 400-fold enhanced mutation ability. Under multiple environmental stresses the system could rapidly generate millions of mutants in a few rounds of iterative evolution. Using high-throughput screening, an industrial S. cerevisiae SISc-Δrad52-G4-72 (G4-72) was obtained that is strongly robust and has higher productivity. G4-72 grew stably and produced ethanol efficiently in multiple-stress environments, e.g. high temperature and high osmosis. In a pilot-scale fermentation with G4-72, the fermentation temperature was elevated by 8 °C and ethanol production was increased by 6.9% under the multiple stresses posed by the industrial fermentation substrate. Overall, the GEbCD system presents a powerful tool to rapidly generate abundant mutants and desired hosts, and offers a novel strategy for optimizing microbial chassis with regard to demands posed in industrial applications.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Saccharomyces cerevisiae / Sistemas CRISPR-Cas Idioma: En Revista: ACS Synth Biol Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Saccharomyces cerevisiae / Sistemas CRISPR-Cas Idioma: En Revista: ACS Synth Biol Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos