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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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dc.contributor.authorSeok, Joo Yeon-
dc.contributor.authorYang, Jina-
dc.contributor.authorChoi, Sang Jin-
dc.contributor.authorLim, Hyun Gyu-
dc.contributor.authorChoi, Un Jong-
dc.contributor.authorKim, Kyung Jin-
dc.contributor.authorPark, Sunghoon-
dc.contributor.authorYoo, Tae Hyeon-
dc.contributor.authorJung, Gyoo Yeol-
dc.date.issued2018-05-01-
dc.identifier.urihttps://dspace.ajou.ac.kr/dev/handle/2018.oak/30143-
dc.description.abstract3-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.-
dc.description.sponsorshipThis 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 ).-
dc.language.isoeng-
dc.publisherAcademic Press Inc.-
dc.subject.mesh3-Hydroxypropionic acid-
dc.subject.meshAldehyde dehydrogenase-
dc.subject.meshBiological production-
dc.subject.meshCatalytic efficiencies-
dc.subject.meshDirected evolution-
dc.subject.meshEvolutionary approach-
dc.subject.meshSemialdehyde dehydrogenase-
dc.subject.meshSynthetic biology-
dc.subject.meshAldehyde Dehydrogenase-
dc.subject.meshDirected Molecular Evolution-
dc.subject.meshEscherichia coli-
dc.subject.meshEscherichia coli Proteins-
dc.subject.meshLactic Acid-
dc.titleDirected evolution of the 3-hydroxypropionic acid production pathway by engineering aldehyde dehydrogenase using a synthetic selection device-
dc.typeArticle-
dc.citation.endPage120-
dc.citation.startPage113-
dc.citation.titleMetabolic Engineering-
dc.citation.volume47-
dc.identifier.bibliographicCitationMetabolic Engineering, Vol.47, pp.113-120-
dc.identifier.doi10.1016/j.ymben.2018.03.009-
dc.identifier.pmid29545147-
dc.identifier.scopusid2-s2.0-85044109129-
dc.identifier.urlhttp://www.elsevier.com/inca/publications/store/6/2/2/9/1/3/index.htt-
dc.subject.keyword3-hydroxypropionic acid-
dc.subject.keywordDirected evolution-
dc.subject.keywordMetabolic engineering-
dc.subject.keywordScreening-
dc.subject.keywordSynthetic biology-
dc.subject.keywordTranscription factor-
dc.description.isoafalse-
dc.subject.subareaBiotechnology-
dc.subject.subareaBioengineering-
dc.subject.subareaApplied Microbiology and Biotechnology-
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