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Comparative transcriptome analysis reveals the redirection of metabolic flux from cell growth to astaxanthin biosynthesis in Yarrowia lipolytica.
Wang, Dan-Ni; Yu, Chen-Xi; Feng, Jie; Wei, Liu-Jing; Chen, Jun; Liu, Zhijie; Ouyang, Liming; Zhang, Lixin; Liu, Feng; Hua, Qiang.
Affiliation
  • Wang DN; State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, China.
  • Yu CX; State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, China.
  • Feng J; State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, China.
  • Wei LJ; State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, China.
  • Chen J; State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, China.
  • Liu Z; Key Laboratory of Fermentation Engineering (Ministry of Education), Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Wuhan, China.
  • Ouyang L; Hubei Key Laboratory of Industrial Microbiology, Hubei University of Technology, Wuhan, China.
  • Zhang L; State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, China.
  • Liu F; State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, China.
  • Hua Q; Shanghai Collaborative Innovation Center for Biomanufacturing Technology, Shanghai, China.
Yeast ; 41(6): 369-378, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38613186
ABSTRACT
Engineering Yarrowia lipolytica to produce astaxanthin provides a promising route. Here, Y. lipolytica M2 producing a titer of 181 mg/L astaxanthin was isolated by iterative atmospheric and room-temperature plasma mutagenesis and diphenylamine-mediated screening. Interestingly, a negative correlation was observed between cell biomass and astaxanthin production. To reveal the underlying mechanism, RNA-seq analysis of transcriptional changes was performed in high producer M2 and reference strain M1, and a total of 1379 differentially expressed genes were obtained. Data analysis revealed that carbon flux was elevated through lipid metabolism, acetyl-CoA and mevalonate supply, but restrained through central carbon metabolism in strain M2. Moreover, upregulation of other pathways such as ATP-binding cassette transporter and thiamine pyrophosphate possibly provided more cofactors for carotenoid hydroxylase and relieved cell membrane stress caused by astaxanthin insertion. These results suggest that balancing cell growth and astaxanthin production may be important to promote efficient biosynthesis of astaxanthin in Y. lipolytica.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Gene Expression Profiling / Yarrowia / Xanthophylls Language: En Journal: Yeast Journal subject: MICROBIOLOGIA Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Gene Expression Profiling / Yarrowia / Xanthophylls Language: En Journal: Yeast Journal subject: MICROBIOLOGIA Year: 2024 Document type: Article Affiliation country: Country of publication: