Abstract

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.

Highlights

  • IntroductionHydroxycinnamyl alcohols are the final metabolites in the phenylpropanoid pathway and serve as precursors for lignin polymers and diverse phenolic compounds, such as lignans and phenylpropenes.Lignin is a complex phenolic polymer mainly derived from p-coumaryl alcohol, coniferyl alcohol, and sinapyl alcohol (called monolignols) [1,2]

  • Hydroxycinnamyl alcohols are the final metabolites in the phenylpropanoid pathway and serve as precursors for lignin polymers and diverse phenolic compounds, such as lignans and phenylpropenes.Lignin is a complex phenolic polymer mainly derived from p-coumaryl alcohol, coniferyl alcohol, and sinapyl alcohol [1,2]

  • OsCAD5 and OsCAD8B and C) are 1032–1140 nucleotides, encoding polypeptides 343–379 amino acids long (Table 1), which is similar to the bona fide Cinnamyl alcohol dehydrogenase (CAD) from Arabidopsis, maize, wheat, sorghum, and Populus, which range from 1068 to 1131 nucleotides [25,26,27,28,30,31]

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Summary

Introduction

Hydroxycinnamyl alcohols are the final metabolites in the phenylpropanoid pathway and serve as precursors for lignin polymers and diverse phenolic compounds, such as lignans and phenylpropenes.Lignin is a complex phenolic polymer mainly derived from p-coumaryl alcohol, coniferyl alcohol, and sinapyl alcohol (called monolignols) [1,2]. Hydroxycinnamyl alcohols are the final metabolites in the phenylpropanoid pathway and serve as precursors for lignin polymers and diverse phenolic compounds, such as lignans and phenylpropenes. Because of its complexity and physical toughness, lignin plays an important role in plant defense, and its synthesis and deposition can be induced by biotic and abiotic stresses [3,6,7,8]. Coniferyl alcohol and its glycosylated derivatives have been found to accumulate and be involved in the defense against fungal pathogens [9]. Lignans are defense-related phenolic compounds, typically dimers of hydroxycinnamyl alcohols formed by the oxidative coupling of the monomers [1,10,11,12]. In Arabidopsis, the lignans lariciresinol and pinoresinol were found to be accumulated in response to an infection of the fungal pathogen

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