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Enhanced Biosynthesis of d-Allulose from a d-Xylose-Methanol Mixture and Its Self-Inductive Detoxification by Using Antisense RNAs in Escherichia coli.
Guo, Qiang; Zheng, Ling-Jie; Zheng, Shang-He; Zheng, Hui-Dong; Lin, Xiao-Cheng; Fan, Li-Hai.
Affiliation
  • Guo Q; College of Chemical Engineering, Fujian Engineering Research Center of Advanced Manufacturing Technology for Fine Chemicals, Fuzhou University, Fuzhou 350108, People's Republic of China.
  • Zheng LJ; College of Chemical Engineering, Fujian Engineering Research Center of Advanced Manufacturing Technology for Fine Chemicals, Fuzhou University, Fuzhou 350108, People's Republic of China.
  • Zheng SH; Qingyuan Innovation Laboratory, Quanzhou 362801, People's Republic of China.
  • Zheng HD; College of Chemical Engineering, Fujian Engineering Research Center of Advanced Manufacturing Technology for Fine Chemicals, Fuzhou University, Fuzhou 350108, People's Republic of China.
  • Lin XC; College of Chemical Engineering, Fujian Engineering Research Center of Advanced Manufacturing Technology for Fine Chemicals, Fuzhou University, Fuzhou 350108, People's Republic of China.
  • Fan LH; Qingyuan Innovation Laboratory, Quanzhou 362801, People's Republic of China.
J Agric Food Chem ; 72(26): 14821-14829, 2024 Jul 03.
Article in En | MEDLINE | ID: mdl-38897918
ABSTRACT
d-Allulose, a C-3 epimer of d-fructose, has great market potential in food, healthcare, and medicine due to its excellent biochemical and physiological properties. Microbial fermentation for d-allulose production is being developed, which contributes to cost savings and environmental protection. A novel metabolic pathway for the biosynthesis of d-allulose from a d-xylose-methanol mixture has shown potential for industrial application. In this study, an artificial antisense RNA (asRNA) was introduced into engineered Escherichia coli to diminish the flow of pentose phosphate (PP) pathway, while the UDP-glucose-4-epimerase (GalE) was knocked out to prevent the synthesis of byproducts. As a result, the d-allulose yield on d-xylose was increased by 35.1%. Then, we designed a d-xylose-sensitive translation control system to regulate the expression of the formaldehyde detoxification operon (FrmRAB), achieving self-inductive detoxification by cells. Finally, fed-batch fermentation was carried out to improve the productivity of the cell factory. The d-allulose titer reached 98.6 mM, with a yield of 0.615 mM/mM on d-xylose and a productivity of 0.969 mM/h.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Xylose / RNA, Antisense / Methanol / Escherichia coli / Fermentation Language: En Journal: J Agric Food Chem Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Xylose / RNA, Antisense / Methanol / Escherichia coli / Fermentation Language: En Journal: J Agric Food Chem Year: 2024 Document type: Article
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