Abstract

Chalcone synthase (CHS) family are plant type III polyketide synthases that participate in the flavonoid synthesis pathway to induce plant resistance to various biotic and abiotic stresses. Zostera marina, a common seagrass, migrated to terrestrial conditions and returned to the sea, achieving the most severe habitat shift of flowering plants. Given the special evolutionary process, we conducted genome-wide, expression and enzyme activity analyses of the ZosmaCHS family to understand its phylogenetic implications. Various duplication modes led to the expansion of 11 CHS homologs in Z. marina. Based on the phylogenetic relationships, ZosmaCHSs were classified into three clades. Further quantitative real time-PCR analyses of the ZosmaCHS homologs showed different light responses and tissue-specific expression, indicating functional diversification of the ZosmaCHSs. Moreover, the ZosmaCHS proteins clustering with the validated chalcone synthases were recombined into prokaryotic expression systems. All the recombinant proteins showed CHS activity to generate naringenin chalcone with varying catalytic efficiencies. ZosmaCHS07 was regarded as the dominant CHS because of its significant light response and the higher catalytic efficiency. Taken together, the disparity of the expression and enzyme activity indicated that sub-functionalization is the primary mechanism of the expansion of the ZosmaCHSs family.

Highlights

  • The chalcone synthase (CHS) superfamily mainly participates in the biosynthesis of various plant secondary metabolites

  • To identify the CHS family members in Z. marina, CHS profiles (PF00195 and PF02797) downloaded from the Pfam database1 were used as queries to perform BLASTP searches against Z. marina database (Olsen et al, 2016) on Phytozome website2

  • ZosmaCHS09 was the smallest protein with 23 kDa, while the remaining were about 43 kDa

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Summary

Introduction

The chalcone synthase (CHS) superfamily mainly participates in the biosynthesis of various plant secondary metabolites. The metabolites include chalcones, stilbenes, phloroglucinols, resorcinols, benzophenones, biphenyls, bibenzyls, chromones, acridones, pyrones, and curcuminoids (Austin and Noel, 2003; Abe and Morita, 2010). These metabolites play key roles in tissue pigmentation, auxin transport, pathogen defense, pollen fertility, and light protection (Dao et al, 2011; Pandith et al, 2016, 2019). CHS (EC 2.3.1.74), the most representative member, carries out the sequential decarboxylative condensation of p-coumaroyl-CoA with three malonyl-CoA molecules This process generates naringenin chalcone, the starting molecule in the biosynthesis of various flavonoids (Kuo et al, 2019).

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