Expression of chalcone synthase and chalcone isomerase from Polygonum minus huds. in Escherichia coli, gene characterization, and structure elucidation of chalcone isomerase
Flavonoids are commonly found in plants and possessed vast benefits particularly towards the improvement of human health. These compounds that are attracting scientific attention, have been traditionally extracted from plant sources and synthesized chemically. Nevertheless, methods such as heat refl...
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| Format: | Thesis |
| Language: | English |
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2020
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| Online Access: | http://psasir.upm.edu.my/id/eprint/92797/ http://psasir.upm.edu.my/id/eprint/92797/1/FBSB%202021%208%20IR.pdf |
| Summary: | Flavonoids are commonly found in plants and possessed vast benefits particularly towards the improvement of human health. These compounds that are attracting scientific attention, have been traditionally extracted from plant sources and synthesized chemically. Nevertheless, methods such as heat reflux and Soxhlet extractions are commercially infeasible, laborious, waste plant sources, and are environmentally unsafe due to the use of toxic solvents. Polygonum minus Huds. is a household-plant with flavonoids as one of its major compounds, hence engineering a plant’s phenylpropanoid pathway into microbial hosts for flavonoid production is an option, where these metabolites are produced without facing the issues mentioned. This study aims to identify and isolate chalcone isomerase (CHI) from P. minus, to express chalcone synthase (CHS) and CHI in Escherichia coli, and to predict the threedimensional (3D) structure of CHI protein from P. minus. The Open Reading Frame (ORF) of CHI gene was isolated through PCR amplification from P. minus cDNA. Various bioinformatics analyses were carried out to analyze the identified PmCHI protein sequence. Then, CHS and CHI genes from P. minus were codonoptimized, synthesized, and individually cloned into an expression vector. The recombinant vectors were later transformed into E. coli BL21(DE3). Temperature differences applied during the growth of recombinant E. coli BL21(DE3) expressing these enzymes were investigated, followed by western blot analysis and partial purification of these enzymes. As the 3D structure of PmCHS was predicted previously, Yet Another Scientific Artificial Reality Application (YASARA) software was used to construct the PmCHI model by using the CHI protein model of Deschampsia antartica Desv. (PDB ID: 5YX4) as template. The predicted model was analyzed, and previously theorized active site residues were highlighted. Then, the predicted model was validated by using validation programs and servers available online. ORF of PmCHI was identified to be ~700-bp ... |
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