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Directed evolution of the 3-hydroxypropionic acid production pathway by engineering aldehyde dehydrogenase using a synthetic selection device
  • Seok, Joo Yeon ;
  • Yang, Jina ;
  • Choi, Sang Jin ;
  • Lim, Hyun Gyu ;
  • Choi, Un Jong ;
  • Kim, Kyung Jin ;
  • Park, Sunghoon ;
  • Yoo, Tae Hyeon ;
  • Jung, Gyoo Yeol
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Publication Year
2018-05-01
Publisher
Academic Press Inc.
Citation
Metabolic Engineering, Vol.47, pp.113-120
Keyword
3-hydroxypropionic acidDirected evolutionMetabolic engineeringScreeningSynthetic biologyTranscription factor
Mesh Keyword
3-Hydroxypropionic acidAldehyde dehydrogenaseBiological productionCatalytic efficienciesDirected evolutionEvolutionary approachSemialdehyde dehydrogenaseSynthetic biologyAldehyde DehydrogenaseDirected Molecular EvolutionEscherichia coliEscherichia coli ProteinsLactic Acid
All Science Classification Codes (ASJC)
BiotechnologyBioengineeringApplied Microbiology and Biotechnology
Abstract
3-Hydroxypropionic acid (3-HP) is an important platform chemical, and biological production of 3-HP from glycerol as a carbon source using glycerol dehydratase (GDHt) and aldehyde dehydrogenase (ALDH) has been revealed to be effective because it involves a relatively simple metabolic pathway and exhibits higher yield and productivity than other biosynthetic pathways. Despite the successful attempts of 3-HP production from glycerol, the biological process suffers from problems arising from low activity and inactivation of the two enzymes. To apply the directed evolutionary approach to engineer the 3-HP production system, we constructed a synthetic selection device using a 3-HP-responsive transcription factor and developed a selection approach for screening 3-HP-producing microorganisms. The method was applied to an ALDH library, specifically aldehyde-binding site library of alpha-ketoglutaric semialdehyde dehydrogenase (KGSADH). Only two serial cultures resulted in enrichment of strains showing increased 3-HP production, and an isolated KGSADH variant enzyme exhibited a 2.79-fold higher catalytic efficiency toward its aldehyde substrate than the wild-type one. This approach will provide the simple and efficient tool to engineer the pathway enzymes in metabolic engineering.
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/30143
DOI
https://doi.org/10.1016/j.ymben.2018.03.009
Fulltext

Type
Article
Funding
This research was supported by the Advanced Biomass R&D Center (ABC) of Global Frontier Project (grant number ABC-2015M3A6A2066119 ) and the National Research Foundation of Korea (NRF) (grant number NRF-2015R1A2A1A10056126 ), funded by the Ministry of Science and ICT, Korea . This research was also supported by the Korea Institute of Energy Technology Evaluation and Planning (KETEP) and the Ministry of Trade, Industry & Energy (MOTIE) of the Republic of Korea (grant number 20174030201600 ).
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Yoo, Tae Hyeon유태현
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