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Biochemical Characterization of the Rice Cinnamyl Alcohol Dehydrogenase Gene Family

Cinnamyl alcohol dehydrogenase (CAD) is involved in the final step of the phenylpropanod pathway, catalyzing the NADPH-dependent reduction of hydroxy-cinnamaldehydes into the corresponding alcohols. The rice genome contains twelve CAD and CAD-like genes, collectively called OsCADs. To elucidate the...

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Autores principales: Park, Hye Lin, Kim, Tae Lim, Bhoo, Seong Hee, Lee, Tae Hoon, Lee, Sang-Won, Cho, Man-Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222663/
https://www.ncbi.nlm.nih.gov/pubmed/30332817
http://dx.doi.org/10.3390/molecules23102659
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author Park, Hye Lin
Kim, Tae Lim
Bhoo, Seong Hee
Lee, Tae Hoon
Lee, Sang-Won
Cho, Man-Ho
author_facet Park, Hye Lin
Kim, Tae Lim
Bhoo, Seong Hee
Lee, Tae Hoon
Lee, Sang-Won
Cho, Man-Ho
author_sort Park, Hye Lin
collection PubMed
description Cinnamyl alcohol dehydrogenase (CAD) is involved in the final step of the phenylpropanod pathway, catalyzing the NADPH-dependent reduction of hydroxy-cinnamaldehydes into the corresponding alcohols. The rice genome contains twelve CAD and CAD-like genes, collectively called OsCADs. To elucidate the biochemical function of the OsCADs, OsCAD1, 2, 6, and 7, which are highly expressed in rice, were cloned from rice tissues. The cloned OsCADs were heterologously expressed in Escherichia coli as His-tag fusion proteins. The activity assay of the recombinant OsCADs showed that OsCAD2, 6, and 7 have CAD activity toward hydroxycinnamaldehydes, but OsCAD1 has no detectable catalytic activity. The kinetic parameters of the enzyme reactions demonstrated that OsCAD2 has the highest catalytic activity among the examined enzymes. This result agrees well with the finding that the Zn binding and NADPH binding motifs and the residues constituting the substrate binding pocket in bona fide plant CADs were fully conserved in OsCAD2. Although they have large variations in the residue for the substrate binding pocket, OsCAD6 and 7 catalyzed the reduction of hydroxycinnamaldehydes with a similar efficiency. Alignment of amino acid sequences showed that OsCAD1 lacks the GxxxxP motif for NADPH binding and has mismatches in residues important in the reduction process, which could be responsible for the loss of catalytic activity. OsCAD2 belongs to CAD Class I with bona fide CADs from other plant species and is constitutively expressed throughout the developmental stages of rice, with preferential expression in actively lignifying tissues such as the root, stem, and panicle, suggesting that it is mainly involved in developmental lignification in rice. The expression of OsCAD2 was also induced by biotic and abiotic stresses such as Xanthomonas oryzae pv. oryzae (Xoo) infection and UV-irradiation, suggesting that it plays a role in the defense response of rice, in addition to a bona fide role in developmental lignification. OsCAD6 and 7 belong in CAD Class II. Their expression is relatively lower than that of OsCAD2 and is confined to certain tissues, such as the leaf sheath, stem, and panicle. The expression of OsCAD6 was stimulated by Xoo infection and UV-irradiation. Thus OsCAD6 appears to be an inducible OsCAD that is likely involved in the defense response of rice against biotic and abiotic stresses.
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spelling pubmed-62226632018-11-13 Biochemical Characterization of the Rice Cinnamyl Alcohol Dehydrogenase Gene Family Park, Hye Lin Kim, Tae Lim Bhoo, Seong Hee Lee, Tae Hoon Lee, Sang-Won Cho, Man-Ho Molecules Article Cinnamyl alcohol dehydrogenase (CAD) is involved in the final step of the phenylpropanod pathway, catalyzing the NADPH-dependent reduction of hydroxy-cinnamaldehydes into the corresponding alcohols. The rice genome contains twelve CAD and CAD-like genes, collectively called OsCADs. To elucidate the biochemical function of the OsCADs, OsCAD1, 2, 6, and 7, which are highly expressed in rice, were cloned from rice tissues. The cloned OsCADs were heterologously expressed in Escherichia coli as His-tag fusion proteins. The activity assay of the recombinant OsCADs showed that OsCAD2, 6, and 7 have CAD activity toward hydroxycinnamaldehydes, but OsCAD1 has no detectable catalytic activity. The kinetic parameters of the enzyme reactions demonstrated that OsCAD2 has the highest catalytic activity among the examined enzymes. This result agrees well with the finding that the Zn binding and NADPH binding motifs and the residues constituting the substrate binding pocket in bona fide plant CADs were fully conserved in OsCAD2. Although they have large variations in the residue for the substrate binding pocket, OsCAD6 and 7 catalyzed the reduction of hydroxycinnamaldehydes with a similar efficiency. Alignment of amino acid sequences showed that OsCAD1 lacks the GxxxxP motif for NADPH binding and has mismatches in residues important in the reduction process, which could be responsible for the loss of catalytic activity. OsCAD2 belongs to CAD Class I with bona fide CADs from other plant species and is constitutively expressed throughout the developmental stages of rice, with preferential expression in actively lignifying tissues such as the root, stem, and panicle, suggesting that it is mainly involved in developmental lignification in rice. The expression of OsCAD2 was also induced by biotic and abiotic stresses such as Xanthomonas oryzae pv. oryzae (Xoo) infection and UV-irradiation, suggesting that it plays a role in the defense response of rice, in addition to a bona fide role in developmental lignification. OsCAD6 and 7 belong in CAD Class II. Their expression is relatively lower than that of OsCAD2 and is confined to certain tissues, such as the leaf sheath, stem, and panicle. The expression of OsCAD6 was stimulated by Xoo infection and UV-irradiation. Thus OsCAD6 appears to be an inducible OsCAD that is likely involved in the defense response of rice against biotic and abiotic stresses. MDPI 2018-10-16 /pmc/articles/PMC6222663/ /pubmed/30332817 http://dx.doi.org/10.3390/molecules23102659 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Park, Hye Lin
Kim, Tae Lim
Bhoo, Seong Hee
Lee, Tae Hoon
Lee, Sang-Won
Cho, Man-Ho
Biochemical Characterization of the Rice Cinnamyl Alcohol Dehydrogenase Gene Family
title Biochemical Characterization of the Rice Cinnamyl Alcohol Dehydrogenase Gene Family
title_full Biochemical Characterization of the Rice Cinnamyl Alcohol Dehydrogenase Gene Family
title_fullStr Biochemical Characterization of the Rice Cinnamyl Alcohol Dehydrogenase Gene Family
title_full_unstemmed Biochemical Characterization of the Rice Cinnamyl Alcohol Dehydrogenase Gene Family
title_short Biochemical Characterization of the Rice Cinnamyl Alcohol Dehydrogenase Gene Family
title_sort biochemical characterization of the rice cinnamyl alcohol dehydrogenase gene family
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222663/
https://www.ncbi.nlm.nih.gov/pubmed/30332817
http://dx.doi.org/10.3390/molecules23102659
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