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Biochemical and Molecular Characterization of the Rice Chalcone Isomerase Family
Chalcone isomerase (CHI) is a key enzyme in flavonoid biosynthesis. In plants, CHIs occur in multigene families, and they are divided into four types, types I–IV. Type I and II CHIs are bona fide CHIs with CHI activity, and type III and IV CHIs are non-catalytic members with different functions. Ric...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8540780/ https://www.ncbi.nlm.nih.gov/pubmed/34685873 http://dx.doi.org/10.3390/plants10102064 |
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author | Park, Sang-Il Park, Hye-Lin Bhoo, Seong-Hee Lee, Sang-Won Cho, Man-Ho |
author_facet | Park, Sang-Il Park, Hye-Lin Bhoo, Seong-Hee Lee, Sang-Won Cho, Man-Ho |
author_sort | Park, Sang-Il |
collection | PubMed |
description | Chalcone isomerase (CHI) is a key enzyme in flavonoid biosynthesis. In plants, CHIs occur in multigene families, and they are divided into four types, types I–IV. Type I and II CHIs are bona fide CHIs with CHI activity, and type III and IV CHIs are non-catalytic members with different functions. Rice contains seven CHI family genes (OsCHIs). Molecular analysis suggested that OsCHI3 is a type I CHI, and the other OsCHIs were classified into types III and IV. To elucidate their biochemical functions, OsCHI1, OsCHI3, OsCHI6, and OsCHI7 were expressed in Escherichia coli, and the recombinant OsCHI proteins were purified. An activity assay of recombinant OsCHIs showed that OsCHI3 catalyzed the isomerization of naringenin chalcone and isoliquiritigenin, whereas the other recombinant OsCHIs had no CHI activity. OsCHI3 also exhibited a strong preference to naringenin chalcone compared to isoliquiritigenin, which agrees well with the catalytic properties of type I CHIs. These results ascertain OsCHI3 to be a bona fide CHI in rice. OsCHI3 and the other OsCHIs were expressed constitutively throughout the rice growth period and different tissues. OsCHI3 expression was induced immediately in response to ultra-violet (UV) stress, suggesting its involvement in the biosynthesis of sakuranetin, a flavonoid phytoalexin in rice. |
format | Online Article Text |
id | pubmed-8540780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85407802021-10-24 Biochemical and Molecular Characterization of the Rice Chalcone Isomerase Family Park, Sang-Il Park, Hye-Lin Bhoo, Seong-Hee Lee, Sang-Won Cho, Man-Ho Plants (Basel) Article Chalcone isomerase (CHI) is a key enzyme in flavonoid biosynthesis. In plants, CHIs occur in multigene families, and they are divided into four types, types I–IV. Type I and II CHIs are bona fide CHIs with CHI activity, and type III and IV CHIs are non-catalytic members with different functions. Rice contains seven CHI family genes (OsCHIs). Molecular analysis suggested that OsCHI3 is a type I CHI, and the other OsCHIs were classified into types III and IV. To elucidate their biochemical functions, OsCHI1, OsCHI3, OsCHI6, and OsCHI7 were expressed in Escherichia coli, and the recombinant OsCHI proteins were purified. An activity assay of recombinant OsCHIs showed that OsCHI3 catalyzed the isomerization of naringenin chalcone and isoliquiritigenin, whereas the other recombinant OsCHIs had no CHI activity. OsCHI3 also exhibited a strong preference to naringenin chalcone compared to isoliquiritigenin, which agrees well with the catalytic properties of type I CHIs. These results ascertain OsCHI3 to be a bona fide CHI in rice. OsCHI3 and the other OsCHIs were expressed constitutively throughout the rice growth period and different tissues. OsCHI3 expression was induced immediately in response to ultra-violet (UV) stress, suggesting its involvement in the biosynthesis of sakuranetin, a flavonoid phytoalexin in rice. MDPI 2021-09-30 /pmc/articles/PMC8540780/ /pubmed/34685873 http://dx.doi.org/10.3390/plants10102064 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Park, Sang-Il Park, Hye-Lin Bhoo, Seong-Hee Lee, Sang-Won Cho, Man-Ho Biochemical and Molecular Characterization of the Rice Chalcone Isomerase Family |
title | Biochemical and Molecular Characterization of the Rice Chalcone Isomerase Family |
title_full | Biochemical and Molecular Characterization of the Rice Chalcone Isomerase Family |
title_fullStr | Biochemical and Molecular Characterization of the Rice Chalcone Isomerase Family |
title_full_unstemmed | Biochemical and Molecular Characterization of the Rice Chalcone Isomerase Family |
title_short | Biochemical and Molecular Characterization of the Rice Chalcone Isomerase Family |
title_sort | biochemical and molecular characterization of the rice chalcone isomerase family |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8540780/ https://www.ncbi.nlm.nih.gov/pubmed/34685873 http://dx.doi.org/10.3390/plants10102064 |
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