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Improved production of epi-cedrol and santalene by fusion protein expression: Stability study and cyclization mechanism of epi-cedrol biosynthesis

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dc.contributor.advisor Dharne, M. S. en
dc.contributor.author Navale, G. R. en
dc.date.accessioned 2021-01-05T04:14:19Z en
dc.date.available 2021-01-05T04:14:19Z en
dc.date.issued 2021-01-01 en
dc.identifier TH2451
dc.identifier.citation Navale G.R. (Thesis) Improved production of epi-cedrol and santalene by fusion protein expression: Stability study and cyclization mechanism of epi-cedrol biosynthesis, 2020. en
dc.identifier.uri http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/5904 en
dc.description.abstract A wide range of secondary metabolites are produced by living organisms such as plants, bacteria and fungi as a part of their defense system against herbivores, pests and pathogens etc. Isoprenoids often called as terpenoids, are the most abundant and highly diverse family of natural organic compounds. In Plants, they plays a diverse part in photosynthetic pigments, hormones, electron carrier, structural components of membrane, as well as an important role in communication and defense. Many isoprenoids have useful applications in the pharmaceutical, nutraceutical, and chemical industries. Isoprenoids synthesized in living organisms by Methyl D-Erythritol 4- Phosphate (MEP) pathway and Mevalonate (MVA) pathway. The recent advancement in metabolic engineering and synthetic biology techniques have enabled the engineering of these important isoprenoid biosynthetic pathways in the heterologous host systems like Escherichia coli and Saccharomyces cerevisiae. Both engineered systems are induced for large scale production of value added isoprenoids. In this chapter, the engineering in MEP pathway and MVA pathway for synthesizing isoprene units (C5) and its poly-isoprene chains for terpenoid productions have been summarized. This introduction chapter particularly highlighted the efforts taken for the production of hemiterpenoids (C5), monoterpenoids (C10), and sesquiterpenoids (C15) by various metabolic engineering techniques in host E. coli and S. cerevisiae over a decade. en
dc.description.sponsorship CSIR‐Senior Research Fellowship (31/11(1026)/2018 EME I) en
dc.format.extent 222 p. en
dc.language.iso en_US en
dc.publisher CSIR-National Chemical Laboratory, Pune en
dc.subject Biotechnology en
dc.subject Biochemistry en
dc.title Improved production of epi-cedrol and santalene by fusion protein expression: Stability study and cyclization mechanism of epi-cedrol biosynthesis en
dc.type Thesis(Ph.D.) en
local.division.division Biochemical Sciences Division en
dc.description.university AcSIR en
dc.identifier.accno 11911 en


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