3.9 Article

Diversion of metabolic flux towards 5-deoxy(iso)flavonoid production via enzyme self-assembly in Escherichia coli

期刊

出版社

ELSEVIER
DOI: 10.1016/j.mec.2021.e00185

关键词

Self-assembled enzymes; Protein-protein interaction; Enzyme scaffolds; 5-Deoxyflavonoid; Chalcone reductase

资金

  1. National Key R&D Program of China [2018YFA0900600]
  2. National Natural Science Foundation of China [22077129, 32070328, 41876084]
  3. Research Program of State Key Laboratory of Bioreactor Engineering
  4. Tianjin Synthetic Biotechnology Innovation Capacity Improvement Project [TSBICIP-KJGG-002-15]
  5. Program of Shanghai Academic Research Leader [20XD1404400]
  6. Strategic Priority Research Program 'Molecular mechanism of Plant Growth and Development' of CAS [XDB27020202]
  7. Construction of the Registry and Database of Bioparts for Synthetic Biology of the Chinese Academy of Science [ZSYS-016]
  8. International Partnership Program of Chinese Academy of Science [153D31KYSB20170121]
  9. National Key Laboratory of Plant Molecular Genetics, SIPPE, CAS
  10. Fundation of Youth Innovation Promotion Association of the Chinese Academy of Sciences

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5-deoxy(iso)flavonoids are important compounds in plants with potential applications in pharmaceuticals, nutraceuticals, and food additives. By utilizing specific enzymes and protein-protein interaction strategies, production of 5-deoxy(iso)flavonoids can be improved and product quality can be optimized.
5-Deoxy(iso)flavonoids are structural representatives of phenylpropanoid-derived compounds and play critical roles in plant ecophysiology. Recently, 5-deoxy(iso)flavonoids gained significant interest due to their potential applications as pharmaceuticals, nutraceuticals, and food additives. Given the difficulties in their isolation from native plant sources, engineered biosynthesis of 5-deoxy(iso)flavonoids in a microbial host is a highly promising alternative approach. However, the production of 5-deoxy(iso)flavonoids is hindered by metabolic flux imbalances that result in a product profile predominated by non-reduced analogues. In this study, GmCHS7 (chalcone synthase from Glycine max) and GuCHR (chalcone reductase from Glycyrrhizza uralensis) were preliminarily utilized to improve the CHR ratio (CHR product to total CHS product). The use of this enzyme combination improved the final CHR ratio from 39.7% to 50.3%. For further optimization, a protein-protein interaction strategy was employed, basing on the spatial adhesion of GmCHS7:PDZ and GuCHR:PDZlig. This strategy further increased the ratio towards the CHR-derived product (54.7%), suggesting partial success of redirecting metabolic flux towards the reduced branch. To further increase the total carbon metabolic flux, 15 protein scaffolds were programmed with stoichiometric arrangement of the three sequential catalysts GmCHS7, GuCHR and MsCHI (chalcone isomerase from Medicago sativa), resulting in a 1.4-fold increase in total flavanone production, from 69.4 mg/L to 97.0 mg/L in shake flasks. The protein self-assembly strategy also improved the production and direction of the lineage-specific compounds 7,4'-dihydroxyflavone and daidzein in Escherichia coli. This study presents a significant advancement of 5-deoxy(iso)flavonoid production and provides the foundation for production of value-added 5-deoxy(iso)flavonoids in microbial hosts.

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