Etude de la voie de biosynthèse des phlorotannins chez les algues brunes, de la caractérisation biochimique d'enzymes recombinantes à l'étude des réponses écophysiologiques

Phlorotannins are polymers of phloroglucinol that are specific phenolic compounds of brown algae (Phaeophyceae). These metabolites present antioxidant activities and are potentially involved in the formation of cell-walls but their biosynthetic pathway is currently uncharacterized. The genome annotation of the brown algae Ectocarpus provided some information about conserved genes which are implicated in the synthesis of phenolics in terrestrial plants. One polyketide synthase of type III (PKSIII) has been successfully characterized: it produces phloroglucinol. The search for other targets has been pursued in brown algae focusing mainly on chalcone isomerase-like (CHI-like) genes, as well as on phenol-sulfotransferases, which are implicated in the sulfation of flavonoids. The characterization of CHIL has revealed their implication in fatty acid binding (FAP). However, the level of interest for this new family has led to their biochemical characterization and to functional studies by complementation of gene in the Arabidopsis thaliana FAP mutant. The progressive elucidation of the phlorotannin biosynthesis pathway has been used in order to discover mechanisms which regulate this metabolism in brown algae. By combining integrated approaches of gene expression profiling with the quantification and profiling of soluble phlorotannins, we have shown that these metabolites ensure the constitutive protection in Fucus vesiculosus against UV-B radiation and could also be induced as a very early response to grazing. The development of specific molecular tools for this metabolic pathway opens some news perspectives in ecophysiological and ecological studies.Les phlorotannins, polymères du phloroglucinol, sont des composés phénoliques (CP) uniquement retrouvés chez les algues brunes (Phéophycées). Ces métabolites présentant des activités anti-oxydantes, interviendraient dans la formation de la paroi, mais à ce jour leur voie de biosynthèse reste non élucidée. L'annotation du génome de l'algue brune Ectocarpus, a permis d'identifier des gènes homologues codant pour des enzymes de la biosynthèse des CP chez les plantes terrestres. Une polyketide synthase de type III (PKSIII), a été caractérisée: elle synthétise le phloroglucinol. La recherche d'autres cibles a été poursuivie sur des gènes codant pour des chalcone-isomérases-like (CHIL), ainsi que pour des phénol-sulfotransférases homologues d'enzymes de sulfatation des flavonoïdes. Les CHIL se sont révélées être des fatty acid binding protein (FAP) impliquées dans le métabolisme des acides gras. L'intérêt pour cette nouvelle famille a justifié leur caractérisation biochimique puis fonctionnelle par complémentation de mutants FAP d'Arabidopsis thaliana. L'élucidation progressive des voies de biosynthèse des phlorotannins a servi de base pour étudier les mécanismes de régulation de ce métabolisme chez les Phaeophycées. En combinant des approches intégrées d'expression de gènes cibles, de dosages et de profilages de phlorotannins solubles, nous avons pu montrer que ces composés assurent une protection constitutive chez Fucus vesiculosus en réponse aux UV-B, et que leur métabolisme serait induit très précocement au cours de l'herbivorie. Le développement d'outils moléculaires spécifiques de ces voies métaboliques, ouvre de nouvelles perspectives en écophysiologie et en écologie

Induction of Phlorotannins and Gene Expression in the Brown Macroalga Fucus vesiculosus in Response to the Herbivore Littorina littorea

Mechanisms related to the induction of phlorotannin biosynthesis in marine brown algae remain poorly known. Several studies undertaken on fucoid species have shown that phlorotannins accumulate in the algae for several days or weeks after being exposed to grazing, and this is measured by direct quantification of soluble phenolic compounds. In order to investigate earlier inducible responses involved in phlorotannin metabolism, Fucus vesiculosus was studied between 6 and 72 h of grazing by the sea snail Littorina littorea. In this study, the quantification of soluble phenolic compounds was complemented by a Quantitative real-time PCR (qRT-PCR) approach applied on genes that are potentially involved in either the phlorotannin metabolism or stress responses. Soluble phlorotannin levels remained stable during the kinetics and increased significantly only after 12 h in the presence of grazers, compared to the control, before decreasing to the initial steady state for the rest of the kinetics. Under grazing conditions, the expression of vbpo, cyp450 and ast6 genes was upregulated, respectively, at 6 h, 12 h and 24 h, and cyp450 gene was downregulated after 72 h. Interestingly, the pksIII gene involved in the synthesis of phloroglucinol was overexpressed under grazing conditions after 24 h and 72 h. This study supports the hypothesis that phlorotannins are able to provide an inducible chemical defense under grazing activity, which is regulated at different stages of the stress response

Study of the biosynthesis pathway of phlorotannins in brown algae, toward biochemical characterization of recombinant enzymes and study of ecophysiological responses

Les phlorotannins, polymères du phloroglucinol, sont des composés phénoliques (CP) uniquement retrouvés chez les algues brunes (Phéophycées). Ces métabolites présentant des activités anti-oxydantes, interviendraient dans la formation de la paroi, mais à ce jour leur voie de biosynthèse reste non élucidée. L'annotation du génome de l'algue brune Ectocarpus, a permis d'identifier des gènes homologues codant pour des enzymes de la biosynthèse des CP chez les plantes terrestres. Une polyketide synthase de type III (PKSIII), a été caractérisée: elle synthétise le phloroglucinol. La recherche d'autres cibles a été poursuivie sur des gènes codant pour des chalcone-isomérases-like (CHIL), ainsi que pour des phénol-sulfotransférases homologues d'enzymes de sulfatation des flavonoïdes. Les CHIL se sont révélées être des fatty acid binding protein (FAP) impliquées dans le métabolisme des acides gras. L'intérêt pour cette nouvelle famille a justifié leur caractérisation biochimique puis fonctionnelle par complémentation de mutants FAP d'Arabidopsis thaliana. L'élucidation progressive des voies de biosynthèse des phlorotannins a servi de base pour étudier les mécanismes de régulation de ce métabolisme chez les Phaeophycées. En combinant des approches intégrées d'expression de gènes cibles, de dosages et de profilages de phlorotannins solubles, nous avons pu montrer que ces composés assurent une protection constitutive chez Fucus vesiculosus en réponse aux UV-B, et que leur métabolisme serait induit très précocement au cours de l'herbivorie. Le développement d'outils moléculaires spécifiques de ces voies métaboliques, ouvre de nouvelles perspectives en écophysiologie et en écologie.Phlorotannins are polymers of phloroglucinol that are specific phenolic compounds of brown algae (Phaeophyceae). These metabolites present antioxidant activities and are potentially involved in the formation of cell-walls but their biosynthetic pathway is currently uncharacterized. The genome annotation of the brown algae Ectocarpus provided some information about conserved genes which are implicated in the synthesis of phenolics in terrestrial plants. One polyketide synthase of type III (PKSIII) has been successfully characterized: it produces phloroglucinol. The search for other targets has been pursued in brown algae focusing mainly on chalcone isomerase-like (CHI-like) genes, as well as on phenol-sulfotransferases, which are implicated in the sulfation of flavonoids. The characterization of CHIL has revealed their implication in fatty acid binding (FAP). However, the level of interest for this new family has led to their biochemical characterization and to functional studies by complementation of gene in the Arabidopsis thaliana FAP mutant. The progressive elucidation of the phlorotannin biosynthesis pathway has been used in order to discover mechanisms which regulate this metabolism in brown algae. By combining integrated approaches of gene expression profiling with the quantification and profiling of soluble phlorotannins, we have shown that these metabolites ensure the constitutive protection in Fucus vesiculosus against UV-B radiation and could also be induced as a very early response to grazing. The development of specific molecular tools for this metabolic pathway opens some news perspectives in ecophysiological and ecological studies

Constitutive or Inducible Protective Mechanisms against UV-B Radiation in the Brown Alga Fucus vesiculosus? A Study of Gene Expression and Phlorotannin Content Responses.

A role as UV sunscreens has been suggested for phlorotannins, the phenolic compounds that accumulate in brown algae in response to a number of external stimuli and take part in cell wall structure. After exposure of the intertidal brown alga Fucus vesiculosus to artificial UV-B radiation, we examined its physiological responses by following the transcript level of the pksIII gene encoding a phloroglucinol synthase, likely to be involved in the first step of phlorotannins biosynthesis. We also monitored the expression of three targeted genes, encoding a heat shock protein (hsp70), which is involved in global stress responses, an aryl sulfotransferase (ast), which could be involved in the sulfation of phlorotannins, and a vanadium bromoperoxidase (vbpo), which can potentially participate in the scavenging of Reactive Oxygen Species (ROS) and in the cross-linking and condensation of phlorotannins. We investigated whether transcriptional regulation of these genes is correlated with an induction of phlorotannin accumulation by establishing metabolite profiling of purified fractions of low molecular weight phlorotannins. Our findings demonstrated that a high dose of UV-B radiation induced a significant overexpression of hsp70 after 12 and 24 hours following the exposure to the UV-B treatment, compared to control treatment. The physiological performance of algae quantified by the photosynthetic efficiency (Fv/Fm) was slightly reduced. However UV-B treatment did not induce the accumulation of soluble phlorotannins in F. vesiculosus during the kinetics of four weeks, a result that may be related to the lack of induction of the pksIII gene expression. Taken together these results suggest a constitutive accumulation of phlorotannins occurring during the development of F.vesiculosus, rather than inducible processes. Gene expression studies and phlorotannin profiling provide here complementary approaches to global quantifications currently used in studies of phenolic compounds in brown algae

Induction of Phlorotannins and Gene Expression in the Brown Macroalga Fucus vesiculosus in Response to the Herbivore Littorina littorea

Mechanisms related to the induction of phlorotannin biosynthesis in marine brown algae remain poorly known. Several studies undertaken on fucoid species have shown that phlorotannins accumulate in the algae for several days or weeks after being exposed to grazing, and this is measured by direct quantification of soluble phenolic compounds. In order to investigate earlier inducible responses involved in phlorotannin metabolism, Fucus vesiculosus was studied between 6 and 72 h of grazing by the sea snail Littorina littorea. In this study, the quantification of soluble phenolic compounds was complemented by a Quantitative real-time PCR (qRT-PCR) approach applied on genes that are potentially involved in either the phlorotannin metabolism or stress responses. Soluble phlorotannin levels remained stable during the kinetics and increased significantly only after 12 h in the presence of grazers, compared to the control, before decreasing to the initial steady state for the rest of the kinetics. Under grazing conditions, the expression of vbpo, cyp450 and ast6 genes was upregulated, respectively, at 6 h, 12 h and 24 h, and cyp450 gene was downregulated after 72 h. Interestingly, the pksIII gene involved in the synthesis of phloroglucinol was overexpressed under grazing conditions after 24 h and 72 h. This study supports the hypothesis that phlorotannins are able to provide an inducible chemical defense under grazing activity, which is regulated at different stages of the stress response

Quantification of total soluble phenol contents (mg equivalent phloroglucinol.g^-1 DW) before purification in controlled condition (white square) and exposed to UV-B (black square).

<p>Values represent means of three independent replicates and bars represent the SD.</p

Primers used for the qRT-PCR analysis on control and UV-B conditions.

<p>Primers used for the qRT-PCR analysis on control and UV-B conditions.</p

Structure/Function analysis of a type iii polyketide synthase in the brown alga Ectocarpus siliculosus reveals a biochemical pathway in phlorotannin monomer biosynthesis.

International audienceBrown algal phlorotannins are structural analogs of condensed tannins in terrestrial plants and, like plant phenols, they have numerous biological functions. Despite their importance in brown algae, phlorotannin biosynthetic pathways have been poorly characterized at the molecular level. We found that a predicted type III polyketide synthase in the genome of the brown alga Ectocarpus siliculosus, PKS1, catalyzes a major step in the biosynthetic pathway of phlorotannins (i.e., the synthesis of phloroglucinol monomers from malonyl-CoA). The crystal structure of PKS1 at 2.85-Å resolution provided a good quality electron density map showing a modified Cys residue, likely connected to a long chain acyl group. An additional pocket not found in other known type III PKSs contains a reaction product that might correspond to a phloroglucinol precursor. In vivo, we also found a positive correlation between the phloroglucinol content and the PKS III gene expression level in cells of a strain of Ectocarpus adapted to freshwater during its reacclimation to seawater. The evolution of the type III PKS gene family in Stramenopiles suggests a lateral gene transfer event from an actinobacterium

Relative gene expression in <i>Fucus vesiculosus</i> in controlled condition (white square) and exposed to UV-B (black square) during 72 hours are presented for <i>pksIII</i> (a), <i>ast6</i> (b), <i>hsp70</i> (c), and <i>vbpo</i> (d).

<p>The expression of a gene is normalized to the geometric mean of the expression of 2 reference genes (<i>ef1α</i>, <i>tua</i>) in the same algal sample and to the mean of its expression in the three control algae at each time point. Values represent means of three independent replicates and bars represent the SE. Letters indicate significant difference (LSMEANS 0.05).</p