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<Emphasis Type="Italic">Escherichia coli</Emphasis> modular coculture system for resveratrol glucosides production
Authors:Nguyen Huy Thuan  Nguyen Thanh Trung  Nguyen Xuan Cuong  Duong Van Cuong  Dong Van Quyen  Sailesh Malla
Institution:1.Center for Molecular Biology,Duy Tan University,Da Nang,Vietnam;2.Laboratory of Marine Medicinal Materials, Institute of Marine Biochemistry (IMBC),Vietnam Academy of Science and Technology, (VAST),Hanoi,Vietnam;3.Faculty of Biotechnology and Food Technology,Thainguyen University of Agriculture and Forestry, Thainguyen University,Thai Nguyen,Vietnam;4.Laboratory of Molecular Microbiology, Institute of Biotechnology,Vietnam Academy of Science and Technology, (VAST),Hanoi,Vietnam;5.University of Science and Technology of Hanoi,Vietnam Academy of Science and Technology,Hanoi,Vietnam;6.Novo Nordisk Foundation Center for Biosustainability,Technical University of Denmark,Kongens Lyngby,Denmark
Abstract:In bio-based fermentation, the overall bioprocess efficiency is significantly affected by the metabolic burden associated with the expression of complete biosynthetic pathway as well as precursor and cofactor generating enzymes into a single microbial cell. To attenuate such burden by compartmentalizing the enzyme expression, recently synthetic biologists have used coculture or poly-culture techniques for biomolecules synthesis. In this paper, coculture system of two metabolically engineered Escherichia coli populations were employed which comprises upstream module expressing two enzymes converting para-coumaric acid into resveratrol and the downstream module expressing glucosyltransferase to convert the resveratrol into its glucosidated forms; polydatin and resveratroloside. Upon optimization of the initial inoculum ratio of two E. coli populations, 92 mg resveratrol glucosides/L (236 µM) was produced i.e. achieving 84% bioconversion from 280 µM of p-coumaric acid in 60 h by 3 L fed batch fermentor. This is the report of applying coculture system to produce resveratrol glucosides by expressing the aglycone formation pathway and sugar dependent pathway into two different cells.
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