Metabólitos secundários são produzidos por alguns grupos vegetais e são essenciais nas diferentes estratégias de adaptação às adversidades ambientais, atuando na proteção e comunicação das plantas, sendo responsivos a diversos fatores bióticos e abióticos. Entre as diversas categorias de metabólitos secundários, os alcalóides apresentam principal função relacionada à defesa contra herbívoros; atuam também na proteção contra patógenos e na interação química com outras plantas (alelopatia). Alcalóides monoterpenos indólicos (MIAs) são uma classe de alcalóides de origem biossintética mista, e apresentam propriedades farmacológicas conhecidas (e.g. MIAs de Catharanthus roseus e Rauwolfia serpentina). MIAs provenientes de algumas espécies de Psychotria do Sul do Brasil são descritos como agentes antioxidantes, antimutagênicos, ansiolíticos, antidepressivos, antipsicóticos e analgésicos, apresentando grande potencial farmacológico. N,β-D-glicopiranosil vincosamida (GPV) é o alcalóide majoritário de Psychotria leiocarpa (Rubiaceae – APG III), apresentando estrutura semelhante a alguns alcalóides bioativos de Psychotria da região, com a peculiaridade de ser N-glicosilado. No presente trabalho, foi avaliado o efeito de dano mecânico e aplicação de jasmonato sobre o acúmulo de GPV no contexto de um possível papel do alcalóide em respostas à herbivoria, além de propriedades antioxidantes do composto. O teor de GPV se manteve constante após a aplicação dos tratamentos, ao longo de todo o experimento. Portanto, a estratégia de acúmulo deste alcalóide segue o padrão de fitoanticipina. No ensaio de dano mecânico os teores de compostos fenólicos também foram monitorados e se mantiveram constantes. Ensaios de herbivoria utilizando dois modelos generalistas e um especialista, não constataram eficácia do GPV na proteção contra estes predadores. Ensaios de atividade contra oxigênio singleto, ânions superóxido, radicais hidroxil e peróxido de hidrogênio revelaram ampla atividade antioxidante, com alguns resultados similares ao controle positivo (Trolox, um análogo da vitamina E). Os resultados obtidos neste trabalho, juntamente com dados existentes da literatura para metabólitos correlatos, sugerem uma função fundamentalmente antioxidante de MIAs de Psychotria, atuando como um modulador de estresse oxidativo. / Some plants groups accumulate secondary metabolites, which may play a major role in different strategies to deal with environmental challenges, being responsive to several biotic and abiotic factors and functioning as protection and communication agents. Among secondary metabolites, alkaloids play a major role as anti-feedant agents and are also involved in pathogen protection and chemical interaction (allelopathy). Monoterpene indole alkaloids (MIAs) are derived from two distinct biosynthetic pathways and possess well known pharmacological properties (e.g. MIAs from Catharanthus roseus and Rauwolfia serpentina). MIAs from Southern Brazilian Psychotria have been characterized as antioxidant, antimutagenic, ansyolitic, antidepressive, antipsychotic and analgesic agents, therefore bearing relevant pharmacological potential. N,β-D-glucopyranosil vincosamide (GPV) is the major alkaloid from Psychotria leiocarpa (Rubiaceae - APG III) and its structure, besides being additionally glycosylated in the N indol ring, is similar to a few bioactive alkaloids from native Psychotria species. In the present work, the effects of wounding and jasmonate application on GPV accumulation, and also antioxidant properties, were evaluated in the context of a potential role of the alkaloid in herbivory responses. GPV content remained constant after treatments, at all times of exposure. Therefore, GPV seems to present a phytoanticipin-like accumulation pattern. In the mechanical wounding assay, phenolic compounds content was also monitored and remained constant. In two herbivory assay models, a generalist and a specialist, GPV was not efficient to prevent herbivore feeding. Singlet oxygen, superoxide anions, hydroxyl radicals and hydrogen peroxide assays showed GPV has broad antioxidant activity, in some cases with activity equivalent to the positive control (Trolox, a vitamin E analog). The results obtained in this work, together with published results from our research group, strongly suggest an antioxidant role for Psychotria MIA alkaloids, which may act as oxidative stress modulators.

Metabólitos secundários são produzidos por alguns grupos vegetais e são essenciais nas diferentes estratégias de adaptação às adversidades ambientais, atuando na proteção e comunicação das plantas, sendo responsivos a diversos fatores bióticos e abióticos. Entre as diversas categorias de metabólitos secundários, os alcalóides apresentam principal função relacionada à defesa contra herbívoros; atuam também na proteção contra patógenos e na interação química com outras plantas (alelopatia). Alcalóides monoterpenos indólicos (MIAs) são uma classe de alcalóides de origem biossintética mista, e apresentam propriedades farmacológicas conhecidas (e.g. MIAs de Catharanthus roseus e Rauwolfia serpentina). MIAs provenientes de algumas espécies de Psychotria do Sul do Brasil são descritos como agentes antioxidantes, antimutagênicos, ansiolíticos, antidepressivos, antipsicóticos e analgésicos, apresentando grande potencial farmacológico. N,β-D-glicopiranosil vincosamida (GPV) é o alcalóide majoritário de Psychotria leiocarpa (Rubiaceae – APG III), apresentando estrutura semelhante a alguns alcalóides bioativos de Psychotria da região, com a peculiaridade de ser N-glicosilado. No presente trabalho, foi avaliado o efeito de dano mecânico e aplicação de jasmonato sobre o acúmulo de GPV no contexto de um possível papel do alcalóide em respostas à herbivoria, além de propriedades antioxidantes do composto. O teor de GPV se manteve constante após a aplicação dos tratamentos, ao longo de todo o experimento. Portanto, a estratégia de acúmulo deste alcalóide segue o padrão de fitoanticipina. No ensaio de dano mecânico os teores de compostos fenólicos também foram monitorados e se mantiveram constantes. Ensaios de herbivoria utilizando dois modelos generalistas e um especialista, não constataram eficácia do GPV na proteção contra estes predadores. Ensaios de atividade contra oxigênio singleto, ânions superóxido, radicais hidroxil e peróxido de hidrogênio revelaram ampla atividade antioxidante, com alguns resultados similares ao controle positivo (Trolox, um análogo da vitamina E). Os resultados obtidos neste trabalho, juntamente com dados existentes da literatura para metabólitos correlatos, sugerem uma função fundamentalmente antioxidante de MIAs de Psychotria, atuando como um modulador de estresse oxidativo. / Some plants groups accumulate secondary metabolites, which may play a major role in different strategies to deal with environmental challenges, being responsive to several biotic and abiotic factors and functioning as protection and communication agents. Among secondary metabolites, alkaloids play a major role as anti-feedant agents and are also involved in pathogen protection and chemical interaction (allelopathy). Monoterpene indole alkaloids (MIAs) are derived from two distinct biosynthetic pathways and possess well known pharmacological properties (e.g. MIAs from Catharanthus roseus and Rauwolfia serpentina). MIAs from Southern Brazilian Psychotria have been characterized as antioxidant, antimutagenic, ansyolitic, antidepressive, antipsychotic and analgesic agents, therefore bearing relevant pharmacological potential. N,β-D-glucopyranosil vincosamide (GPV) is the major alkaloid from Psychotria leiocarpa (Rubiaceae - APG III) and its structure, besides being additionally glycosylated in the N indol ring, is similar to a few bioactive alkaloids from native Psychotria species. In the present work, the effects of wounding and jasmonate application on GPV accumulation, and also antioxidant properties, were evaluated in the context of a potential role of the alkaloid in herbivory responses. GPV content remained constant after treatments, at all times of exposure. Therefore, GPV seems to present a phytoanticipin-like accumulation pattern. In the mechanical wounding assay, phenolic compounds content was also monitored and remained constant. In two herbivory assay models, a generalist and a specialist, GPV was not efficient to prevent herbivore feeding. Singlet oxygen, superoxide anions, hydroxyl radicals and hydrogen peroxide assays showed GPV has broad antioxidant activity, in some cases with activity equivalent to the positive control (Trolox, a vitamin E analog). The results obtained in this work, together with published results from our research group, strongly suggest an antioxidant role for Psychotria MIA alkaloids, which may act as oxidative stress modulators.

Metabólitos secundários são produzidos por alguns grupos vegetais e são essenciais nas diferentes estratégias de adaptação às adversidades ambientais, atuando na proteção e comunicação das plantas, sendo responsivos a diversos fatores bióticos e abióticos. Entre as diversas categorias de metabólitos secundários, os alcalóides apresentam principal função relacionada à defesa contra herbívoros; atuam também na proteção contra patógenos e na interação química com outras plantas (alelopatia). Alcalóides monoterpenos indólicos (MIAs) são uma classe de alcalóides de origem biossintética mista, e apresentam propriedades farmacológicas conhecidas (e.g. MIAs de Catharanthus roseus e Rauwolfia serpentina). MIAs provenientes de algumas espécies de Psychotria do Sul do Brasil são descritos como agentes antioxidantes, antimutagênicos, ansiolíticos, antidepressivos, antipsicóticos e analgésicos, apresentando grande potencial farmacológico. N,β-D-glicopiranosil vincosamida (GPV) é o alcalóide majoritário de Psychotria leiocarpa (Rubiaceae – APG III), apresentando estrutura semelhante a alguns alcalóides bioativos de Psychotria da região, com a peculiaridade de ser N-glicosilado. No presente trabalho, foi avaliado o efeito de dano mecânico e aplicação de jasmonato sobre o acúmulo de GPV no contexto de um possível papel do alcalóide em respostas à herbivoria, além de propriedades antioxidantes do composto. O teor de GPV se manteve constante após a aplicação dos tratamentos, ao longo de todo o experimento. Portanto, a estratégia de acúmulo deste alcalóide segue o padrão de fitoanticipina. No ensaio de dano mecânico os teores de compostos fenólicos também foram monitorados e se mantiveram constantes. Ensaios de herbivoria utilizando dois modelos generalistas e um especialista, não constataram eficácia do GPV na proteção contra estes predadores. Ensaios de atividade contra oxigênio singleto, ânions superóxido, radicais hidroxil e peróxido de hidrogênio revelaram ampla atividade antioxidante, com alguns resultados similares ao controle positivo (Trolox, um análogo da vitamina E). Os resultados obtidos neste trabalho, juntamente com dados existentes da literatura para metabólitos correlatos, sugerem uma função fundamentalmente antioxidante de MIAs de Psychotria, atuando como um modulador de estresse oxidativo. / Some plants groups accumulate secondary metabolites, which may play a major role in different strategies to deal with environmental challenges, being responsive to several biotic and abiotic factors and functioning as protection and communication agents. Among secondary metabolites, alkaloids play a major role as anti-feedant agents and are also involved in pathogen protection and chemical interaction (allelopathy). Monoterpene indole alkaloids (MIAs) are derived from two distinct biosynthetic pathways and possess well known pharmacological properties (e.g. MIAs from Catharanthus roseus and Rauwolfia serpentina). MIAs from Southern Brazilian Psychotria have been characterized as antioxidant, antimutagenic, ansyolitic, antidepressive, antipsychotic and analgesic agents, therefore bearing relevant pharmacological potential. N,β-D-glucopyranosil vincosamide (GPV) is the major alkaloid from Psychotria leiocarpa (Rubiaceae - APG III) and its structure, besides being additionally glycosylated in the N indol ring, is similar to a few bioactive alkaloids from native Psychotria species. In the present work, the effects of wounding and jasmonate application on GPV accumulation, and also antioxidant properties, were evaluated in the context of a potential role of the alkaloid in herbivory responses. GPV content remained constant after treatments, at all times of exposure. Therefore, GPV seems to present a phytoanticipin-like accumulation pattern. In the mechanical wounding assay, phenolic compounds content was also monitored and remained constant. In two herbivory assay models, a generalist and a specialist, GPV was not efficient to prevent herbivore feeding. Singlet oxygen, superoxide anions, hydroxyl radicals and hydrogen peroxide assays showed GPV has broad antioxidant activity, in some cases with activity equivalent to the positive control (Trolox, a vitamin E analog). The results obtained in this work, together with published results from our research group, strongly suggest an antioxidant role for Psychotria MIA alkaloids, which may act as oxidative stress modulators.

La pléiocarpamine est un alcaloïde indolo-monoterpénique de la famille des mavacurans. L’intérêt de cette substance naturelle réside dans sa capacité d’assemblage avec divers alcaloïdes indoliques donnant lieu à des bisindoles de structures complexes possédant des activités biologiques significatives. Plusieurs stratégies ont été étudiées pour la synthèse totale de ce composé pentacyclique. Notamment, la contraction d’un cétolactame a été envisagée pour la formation du cycle E. De manière inattendue, cette stratégie a conduit à la première synthèse totale de la (–)-17-nor-excelsinisine, un alcaloïde zwitterionique avec des activités antivirales. En parallèle, cette substance naturelle a été obtenue par cyclisation oxydante bioinspirée entre le formylester et l’atome d’azote aliphatique de la geissoschizine. La quaternarisation de ce dernier a ensuite permis de guider la chimiosélectivité de cette réaction vers le noyau indolique. Ainsi le couplage oxydant avec l’atome d’azote indolique a généré la liaison signature des mavacurans. Grâce à cette stratégie, plusieurs alcaloïdes de cette famille : (+)-taberdivarine H, (+)-16-hydroxyméthyl-pléiocarpamine et (+)-16-épi-pléiocarpamine, ont été synthétisés. Par la suite, une synthèse totale racémique de cette dernière a également été réalisée en seulement neuf étapes grâce à l’addition 1,4 intermoléculaire diastéréosélective d’un iodure de vinyle sur un indolylacrylate tétracyclique et à la fermeture finale du cycle D par substitution nucléophile. Le développement d’une version énantiosélective a été initié. Finalement, une étude a été réalisée pour la synthèse de la pycnanthinine, un bisindole dérivé de la pléiocarpamine. / Pleiocarpamine is a monoterpene indole alkaloid of the mavacuran family. The main interest of this natural product is its ability to assemble with various indole alkaloids to give structurally complex bisindoles with significant biological activities. Several strategies have been studied for the total synthesis of this pentacyclic compound. Especially, the ring contraction of a ketolactam was contemplated for E-ring formation. Unexpectedly, this strategy led to the first total synthesis of (–)-17-nor-excelsinisine, a zwitterionic alkaloid with antiviral activities. Simultaneously, this natural product was obtained via a bioinspired oxidative cyclization between the formylester and the aliphatic nitrogen atom of geissoschizine. Quaternarization of the latter allowed to guide the reaction chemoselectivity towards the indole nucleus. Therefore the oxidative coupling with the indolic nitrogen atom etablished the signature bond of the mavacurans. Thanks to this strategy, several alkaloids of this family: (+)-taberdivarine H, (+)-16-hydroxymethyl-pleiocarpamine and (+)-16-epi-pleiocarpamine, were synthetized. Subsequently, a racemic total synthesis of the latter was completed in only nine steps via a diastereoselective intermolecular 1,4 addition of a vinyl iodide into a tetracyclic indolylacrylate and a final D-ring closure by nucleophilic substitution. The development of an enantioselective version has been initiated. Finally, a study was performed for the assembly of pycnanthinine, a pleiocarpamine-derived bisindole.

Les alcaloïdes indolo-monoterpéniques (AIMs) constituent une classe de molécules naturelles très étudiée en raison d’un fort potentiel pharmacologique et thérapeutique et d’une grande diversité structurale. D’autre part, les techniques de déréplication par chromatographie liquide couplée à la spectrométrie de masse tandem ont évolué récemment, avec l’émergence de l’approche par réseaux moléculaires (molecular networking). Dans ce contexte, nous avons créé une base de données de spectres de masse tandem moyennés de 172 AIMs témoins, en collaboration avec plusieurs équipes de pharmacognosie dans le monde. Cette base de données, nommée MIADB (Monoterpene Indole Alkaloids DataBase), rendue publique, peut être utilisée comme référence dans des stratégies de déréplication fondées sur l’utilisation des réseaux moléculaires. Nous avons ensuite exploité la MIADB pour l’étude phytochimique de deux Apocynaceae : Geissospermum laeve (Vell.) Miers et Alstonia balansae Guillaumin. Dans un premier temps, l’annotation par la MIADB d’un extrait alcaloïdique des écorces de G. laeve a permis l’isolement et l’élucidation structurale de 3 nouveaux AIMs, dont deux à motif butyrolactone. Par la suite, notre approche a été améliorée par l’emploi du nouvel outil d’annotation in silico MetWork, fondé sur une prédiction métabolique et la modélisation de spectres de masse tandem. C’est ainsi que l’exploration de l’espace chimique d’un extrait alcaloïdique des feuilles d’A. balansae a permis l’identification, puis l’isolement, de 5 nouveaux AIMs du type N-oxyde-sarpagane. La stéréochimie des nouveaux composés a pu être déterminée par l’exploitation de spectres prédits et expérimentaux de dichroïsme circulaire éléctronique.Ce manuscrit décrit, après une introduction consacrée notamment aux emplois du molecular networking pour le ciblage et la découverte de petites molécules naturelles puis aux interconnections biosynthétiques en série AIM, la création puis l’évolution de la MIADB, puis son utilisation dans un workflow de déréplication efficace et de ciblage de nouveaux composés dans des mélanges complexes issus d’Apocynaceae. / Monoterpene indole alkaloids (MIAs) constitute a class of natural products that has been extensively studied due to its important pharmacological and therapeutic potentials, and to its large structural diversity. Dereplication techniques based on liquid chromatography coupled to tandem mass spectrometry have recently evolved, with the implementation of molecular networking-based approaches.In this context, we have created a spectral database that encompasses the averaged tandem mass spectra of 172 reference MIAs, in collaboration with several pharmacognosy research teams around the world. This database, named MIADB (standing for Monoterpene Indole Alkaloids DataBase), was made publicly available and can be used as a reference in the application of molecular networking as a dereplication strategy. Thereafter, we used the MIADB to carry out the phytochemical investigation of two Apocynaceae species: Geissospermum laeve (Vell.) Miers and Alstonia balansae Guillaumin. As a first application, the MIADB-based annotation of an alkaloid extract of the barks of G. laeve led to the isolation and the structural elucidation of three new MIAs, two having a butyrolactone moiety. Afterwards, this approach was improved by the application of a new tool for in silico annotation called MetWork, which is based on metabolic prediction and on the generation of predicted tandem mass spectra. Following this approach, the exploration of the chemical space of an alkaloid extract of the leaves of A. balansae allowed the anticipation and further isolation of five novel MIAs of the N-oxide-sarpagine type. The stereochemistry of all the new molecules could be determined on the basis of experimental and predicted electronic circular dichroism spectra.In the introduction of this manuscript the multiple uses of molecular networking for the identification of small natural molecules are described, as well as the biosynthetic interconnections in the MIAs group. The creation and evolution of the MIADB are then presented, followed by its utilization in efficient dereplication workflows for the targeting of new natural products within complex mixtures from Apocynaceae species.

Espécies de Psychotria encontradas no sul do Brasil produzem alcalóides do tipo monoterpeno indólicos, alguns deles com interessantes atividades biológicas e oriundos de novas rotas biossintéticas. P. leiocarpa Cham. & Schlecht. acumula N, b-D-glicopiranosilvincosamida (GPV), o primeiro alcalóide N-glicosilado desta classe a ser descrito. O extrato contendo GPV apresenta atividade analgésica inespecífica e, na planta, sua biossíntese é regulada pelo desenvolvimento e por luz. P. umbellata Vell., por sua vez, produz psicolatina, que apresenta alto potencial farmacológico, pois apresenta atividade analgésica do tipo opióide, ansiolítica e antipsicótica, interagindo com receptores de diversos sistemas de neurotransmissores no sistema nervoso central. Além disso, psicolatina é um eficiente agente redutor de peróxidos e quencher de oxigênio singlet in vitro. Os objetivos do presente trabalho foram estudar a fotorregulação de GPV em plântulas de P. leiocarpa, assim como avaliar os efeitos antioxidantes e antimutagênicos in vivo do extrato foliar bruto de P. umbellata e de psicolatina purificada, utilizando a levedura Saccharomyces cerevisiae. Essas duas últimas substâncias também foram avaliadas quanto à capacidade antioxidante contra o radical hidroxila in vitro. Em ensaios de transição luz-escuro realizados com plântulas assépticas de P. leiocarpa, o acúmulo de GPV mostrou ser responsivo a alterações na condição luminosa de cultivo. O papel negativo do escuro contínuo na biossíntese de GPV foi comprovado pela redução dos níveis deste alcalóide em plântulas cultivadas na luz e transferidas para o escuro. Por outro lado, quando plântulas cultivadas no escuro foram expostas à luz, os níveis de GPVaumentaram, indicando o caráter promotor da luz na produção de GPV. Os efeitos das transições foram mais evidentes em plântulas cultivadas em meio sem sacarose do que em plântulas cultivadas com suprimento exógeno de carboidratos. A biossíntese de GPV é regulada por diferentes faixas de luz. As regiões do azul e do vermelho-extremo aumentaram os teores de GPV. A luz vermelha não afetou de forma significativa o teor de GPV. Os resultados revelam um padrão típico de VLFRs (Very Low Fluence Responses), possivelmente envolvendo ação de PhyA em conjunto com criptocromo.Tanto o extrato bruto foliar de P. umbellata quanto psicolatina apresentaram efeito antioxidante in vivo, reduzindo a inibição do crescimento de Saccharomyces cerevisiae sob estresse oxidativo induzido por peróxido de hidrogênio e paraquat. O extrato e o alcalóide purificado também apresentaram ótima atividade antioxidante in vitro, protegendo contra o ataque do radical hidroxila. Os índices de mutagênese induzida por peróxido de hidrogêncio foram significativamente reduzidos quando as células de S. cerevisiae foram co-cultivadas na presença tanto do extrato quanto de psicolatina. / Species of Psychotria founded in southern Brazil produce a set of novel monoterpene indole alkaloids (MIAs), several of which have interesting biological activities and originate from new metabolic pathways. P. leiocarpa Cham. & Schlecht. accumulates N, b-D-glucopyranosylvincosamide (GPV), the first N-glycosylated MIA described. Leaf extracts containing GPV display nonspecific analgesic activity and, in planta, its biosynthesis is regulated by development and light. P. umbellata Vell., in turn, produces psychollatine which has significant pharmacological potential, since it yields opioid-like analgesic, anxiolytic and antipsychotic activities, interacting with receptors of different neurotransmitter systems in the central nervous system. In addition, psychollatine is an efficient peroxide reducing agent and a singlet oxygen chemical quencher in vitro. This work aimed at studying the photoregulation of GPV in P. leiocarpa seedlings, as well as at investigating the antimutagenic and antioxidant in vivo effects of the crude foliar extract of P. umbellata and purified psychollatine using the yeast Saccharomyces cerevisiae. These last substances were also evaluated for their in vitro antioxidant properties against hydroxyl radicals.In light-dark transition assays with aseptic P. leiocarpa seedlings, GPV accumulation showed to be responsive to changes in light condition. The negative role of continuous dark on GPV biosynthesis was shown by reduction of the alkaloid contents when light growing seedlings were transferred to dark. On the other hand, dark growing seedlings increased GPV contents after light exposure, suggesting a positive light regulation of GPV production. Theseresults were more evident in seedlings cultivated in media without sucrose than in seedlings cultivated with carbohydrate supplementation. GPV biosynthesys is also regulated by different light qualities. Light in the blue and far-red regions increased GPV accumulation, whereas red ligh had no significant influence on GPV yield. These results are in agreement with the profile of VLFRs (Very Low Fluence Responses), mediated by PhyA with coaction of cryptochrome. Both the crude foliar extract of P. umbellata and psychollatine showed in vivo antioxidant effects by reducing the growth inhibition of Saccharomyces cerevisiae under hydrogen peroxide- and paraquat-induced oxidative stress. The extract and the purified alkaloid also showed strong in vitro antioxidant activity against hydroxyl radicals. The levels of hydrogen peroxide-induced mutagenicity were significantly reduced when S. cerevisiae cells were cocultivated with leaf crude extract or psychollatine.

Espécies de Psychotria encontradas no sul do Brasil produzem alcalóides do tipo monoterpeno indólicos, alguns deles com interessantes atividades biológicas e oriundos de novas rotas biossintéticas. P. leiocarpa Cham. & Schlecht. acumula N, b-D-glicopiranosilvincosamida (GPV), o primeiro alcalóide N-glicosilado desta classe a ser descrito. O extrato contendo GPV apresenta atividade analgésica inespecífica e, na planta, sua biossíntese é regulada pelo desenvolvimento e por luz. P. umbellata Vell., por sua vez, produz psicolatina, que apresenta alto potencial farmacológico, pois apresenta atividade analgésica do tipo opióide, ansiolítica e antipsicótica, interagindo com receptores de diversos sistemas de neurotransmissores no sistema nervoso central. Além disso, psicolatina é um eficiente agente redutor de peróxidos e quencher de oxigênio singlet in vitro. Os objetivos do presente trabalho foram estudar a fotorregulação de GPV em plântulas de P. leiocarpa, assim como avaliar os efeitos antioxidantes e antimutagênicos in vivo do extrato foliar bruto de P. umbellata e de psicolatina purificada, utilizando a levedura Saccharomyces cerevisiae. Essas duas últimas substâncias também foram avaliadas quanto à capacidade antioxidante contra o radical hidroxila in vitro. Em ensaios de transição luz-escuro realizados com plântulas assépticas de P. leiocarpa, o acúmulo de GPV mostrou ser responsivo a alterações na condição luminosa de cultivo. O papel negativo do escuro contínuo na biossíntese de GPV foi comprovado pela redução dos níveis deste alcalóide em plântulas cultivadas na luz e transferidas para o escuro. Por outro lado, quando plântulas cultivadas no escuro foram expostas à luz, os níveis de GPVaumentaram, indicando o caráter promotor da luz na produção de GPV. Os efeitos das transições foram mais evidentes em plântulas cultivadas em meio sem sacarose do que em plântulas cultivadas com suprimento exógeno de carboidratos. A biossíntese de GPV é regulada por diferentes faixas de luz. As regiões do azul e do vermelho-extremo aumentaram os teores de GPV. A luz vermelha não afetou de forma significativa o teor de GPV. Os resultados revelam um padrão típico de VLFRs (Very Low Fluence Responses), possivelmente envolvendo ação de PhyA em conjunto com criptocromo.Tanto o extrato bruto foliar de P. umbellata quanto psicolatina apresentaram efeito antioxidante in vivo, reduzindo a inibição do crescimento de Saccharomyces cerevisiae sob estresse oxidativo induzido por peróxido de hidrogênio e paraquat. O extrato e o alcalóide purificado também apresentaram ótima atividade antioxidante in vitro, protegendo contra o ataque do radical hidroxila. Os índices de mutagênese induzida por peróxido de hidrogêncio foram significativamente reduzidos quando as células de S. cerevisiae foram co-cultivadas na presença tanto do extrato quanto de psicolatina. / Species of Psychotria founded in southern Brazil produce a set of novel monoterpene indole alkaloids (MIAs), several of which have interesting biological activities and originate from new metabolic pathways. P. leiocarpa Cham. & Schlecht. accumulates N, b-D-glucopyranosylvincosamide (GPV), the first N-glycosylated MIA described. Leaf extracts containing GPV display nonspecific analgesic activity and, in planta, its biosynthesis is regulated by development and light. P. umbellata Vell., in turn, produces psychollatine which has significant pharmacological potential, since it yields opioid-like analgesic, anxiolytic and antipsychotic activities, interacting with receptors of different neurotransmitter systems in the central nervous system. In addition, psychollatine is an efficient peroxide reducing agent and a singlet oxygen chemical quencher in vitro. This work aimed at studying the photoregulation of GPV in P. leiocarpa seedlings, as well as at investigating the antimutagenic and antioxidant in vivo effects of the crude foliar extract of P. umbellata and purified psychollatine using the yeast Saccharomyces cerevisiae. These last substances were also evaluated for their in vitro antioxidant properties against hydroxyl radicals.In light-dark transition assays with aseptic P. leiocarpa seedlings, GPV accumulation showed to be responsive to changes in light condition. The negative role of continuous dark on GPV biosynthesis was shown by reduction of the alkaloid contents when light growing seedlings were transferred to dark. On the other hand, dark growing seedlings increased GPV contents after light exposure, suggesting a positive light regulation of GPV production. Theseresults were more evident in seedlings cultivated in media without sucrose than in seedlings cultivated with carbohydrate supplementation. GPV biosynthesys is also regulated by different light qualities. Light in the blue and far-red regions increased GPV accumulation, whereas red ligh had no significant influence on GPV yield. These results are in agreement with the profile of VLFRs (Very Low Fluence Responses), mediated by PhyA with coaction of cryptochrome. Both the crude foliar extract of P. umbellata and psychollatine showed in vivo antioxidant effects by reducing the growth inhibition of Saccharomyces cerevisiae under hydrogen peroxide- and paraquat-induced oxidative stress. The extract and the purified alkaloid also showed strong in vitro antioxidant activity against hydroxyl radicals. The levels of hydrogen peroxide-induced mutagenicity were significantly reduced when S. cerevisiae cells were cocultivated with leaf crude extract or psychollatine.

Espécies de Psychotria encontradas no sul do Brasil produzem alcalóides do tipo monoterpeno indólicos, alguns deles com interessantes atividades biológicas e oriundos de novas rotas biossintéticas. P. leiocarpa Cham. & Schlecht. acumula N, b-D-glicopiranosilvincosamida (GPV), o primeiro alcalóide N-glicosilado desta classe a ser descrito. O extrato contendo GPV apresenta atividade analgésica inespecífica e, na planta, sua biossíntese é regulada pelo desenvolvimento e por luz. P. umbellata Vell., por sua vez, produz psicolatina, que apresenta alto potencial farmacológico, pois apresenta atividade analgésica do tipo opióide, ansiolítica e antipsicótica, interagindo com receptores de diversos sistemas de neurotransmissores no sistema nervoso central. Além disso, psicolatina é um eficiente agente redutor de peróxidos e quencher de oxigênio singlet in vitro. Os objetivos do presente trabalho foram estudar a fotorregulação de GPV em plântulas de P. leiocarpa, assim como avaliar os efeitos antioxidantes e antimutagênicos in vivo do extrato foliar bruto de P. umbellata e de psicolatina purificada, utilizando a levedura Saccharomyces cerevisiae. Essas duas últimas substâncias também foram avaliadas quanto à capacidade antioxidante contra o radical hidroxila in vitro. Em ensaios de transição luz-escuro realizados com plântulas assépticas de P. leiocarpa, o acúmulo de GPV mostrou ser responsivo a alterações na condição luminosa de cultivo. O papel negativo do escuro contínuo na biossíntese de GPV foi comprovado pela redução dos níveis deste alcalóide em plântulas cultivadas na luz e transferidas para o escuro. Por outro lado, quando plântulas cultivadas no escuro foram expostas à luz, os níveis de GPVaumentaram, indicando o caráter promotor da luz na produção de GPV. Os efeitos das transições foram mais evidentes em plântulas cultivadas em meio sem sacarose do que em plântulas cultivadas com suprimento exógeno de carboidratos. A biossíntese de GPV é regulada por diferentes faixas de luz. As regiões do azul e do vermelho-extremo aumentaram os teores de GPV. A luz vermelha não afetou de forma significativa o teor de GPV. Os resultados revelam um padrão típico de VLFRs (Very Low Fluence Responses), possivelmente envolvendo ação de PhyA em conjunto com criptocromo.Tanto o extrato bruto foliar de P. umbellata quanto psicolatina apresentaram efeito antioxidante in vivo, reduzindo a inibição do crescimento de Saccharomyces cerevisiae sob estresse oxidativo induzido por peróxido de hidrogênio e paraquat. O extrato e o alcalóide purificado também apresentaram ótima atividade antioxidante in vitro, protegendo contra o ataque do radical hidroxila. Os índices de mutagênese induzida por peróxido de hidrogêncio foram significativamente reduzidos quando as células de S. cerevisiae foram co-cultivadas na presença tanto do extrato quanto de psicolatina. / Species of Psychotria founded in southern Brazil produce a set of novel monoterpene indole alkaloids (MIAs), several of which have interesting biological activities and originate from new metabolic pathways. P. leiocarpa Cham. & Schlecht. accumulates N, b-D-glucopyranosylvincosamide (GPV), the first N-glycosylated MIA described. Leaf extracts containing GPV display nonspecific analgesic activity and, in planta, its biosynthesis is regulated by development and light. P. umbellata Vell., in turn, produces psychollatine which has significant pharmacological potential, since it yields opioid-like analgesic, anxiolytic and antipsychotic activities, interacting with receptors of different neurotransmitter systems in the central nervous system. In addition, psychollatine is an efficient peroxide reducing agent and a singlet oxygen chemical quencher in vitro. This work aimed at studying the photoregulation of GPV in P. leiocarpa seedlings, as well as at investigating the antimutagenic and antioxidant in vivo effects of the crude foliar extract of P. umbellata and purified psychollatine using the yeast Saccharomyces cerevisiae. These last substances were also evaluated for their in vitro antioxidant properties against hydroxyl radicals.In light-dark transition assays with aseptic P. leiocarpa seedlings, GPV accumulation showed to be responsive to changes in light condition. The negative role of continuous dark on GPV biosynthesis was shown by reduction of the alkaloid contents when light growing seedlings were transferred to dark. On the other hand, dark growing seedlings increased GPV contents after light exposure, suggesting a positive light regulation of GPV production. Theseresults were more evident in seedlings cultivated in media without sucrose than in seedlings cultivated with carbohydrate supplementation. GPV biosynthesys is also regulated by different light qualities. Light in the blue and far-red regions increased GPV accumulation, whereas red ligh had no significant influence on GPV yield. These results are in agreement with the profile of VLFRs (Very Low Fluence Responses), mediated by PhyA with coaction of cryptochrome. Both the crude foliar extract of P. umbellata and psychollatine showed in vivo antioxidant effects by reducing the growth inhibition of Saccharomyces cerevisiae under hydrogen peroxide- and paraquat-induced oxidative stress. The extract and the purified alkaloid also showed strong in vitro antioxidant activity against hydroxyl radicals. The levels of hydrogen peroxide-induced mutagenicity were significantly reduced when S. cerevisiae cells were cocultivated with leaf crude extract or psychollatine.

Catharanthus roseus est une plante tropicale qui produit spécifiquement des alcaloïdes indoliques monoterpéniques (AIM) d’intérêt thérapeutique. Chez C. roseus, la branche terpénique incluant la voie du méthylérythritol phosphate (MEP) est considérée comme limitante et présente une régulation transcriptionnelle coordonnée en réponse aux hormones inductrices de l’accumulation alcaloïdique. Lors de ce travail, suite à des analyses bioinformatiques et à la caractérisation de promoteurs de gènes de la voie MEP, nous avons identifié de nouvelles familles de facteurs de transcription impliquées dans la régulation de la biosynthèse des AIM. Des membres de la famille des ZCT, des WRKY et des RR type B interagissent avec le promoteur du gène hds de la voie MEP et régulent son activité. Ces travaux ont permis d’approfondir les connaissances sur les réseaux transcriptionnels régulateurs de la biosynthèse des AIM. L’utilisation de ces nouveaux facteurs de transcription activateurs peut désormais être envisagée dans le cadre d’expériences d’ingénierie métabolique afin d’augmenter l’accumulation d’alcaloïdes d’intérêt pharmaceutique chez C. roseus. / Catharanthus roseus is a tropical plant producing specifically monoterpene indole alkaloids (MIA) of high interest due to their therapeutical values. In C. roseus cells, the terpenoid branch including the methyl erythritol phosphate pathway (MEP) provides the MIA terpenoid moiety and is regarded as limited for MIA biosynthesis. This branch presents a coordinated transcriptional regulation in response to hormonal signals leading to MIA production. In this context, bioinformatic analysises and functional characterization of MEP pathway gene promoters allowed the identification of new transcription factor families involved in the MIA pathway regulation. Members of ZCT proteins, WRKY and type B RR families specifically interact with the hds promoter from the MEP pathway and regulate its activity. This work permits to gain into insight the transcriptional network controlling the MIA biosynthesis. It is possible now to consider using transcription factor that act as activators and target genes from the terpenoid branch to increase the accumulation of alkaloids of pharmaceutical interest in C. roseus by metabolic engineering approaches.

Les alcaloïdes indoliques monoterpéniques (AIM) sont des molécules à propriétés anti-tumorales extraites de Catharanthus roseus. Leur coût de production et les besoins encore importants de ces médicaments en chimiothérapie, en font des cibles majeures pour la recherche de stratégies de production plus efficaces. L’objectif de ce travail vise à identifier de nouveaux facteurs de transcription (FT) régulateurs de la production des AIM. Cette étude porte plus particulièrement sur la caractérisation fonctionnelle et l’implication dans la régulation de la biosynthèse des AIM, de protéines de la famille des WRKY (CrWRKYs) et des protéines de type doigt de zinc (ZCTs) précédemment isolées au sein de l’EA2106 « Biomolécules et Biotechnologies Végétales ». Nos expériences ont révélé que, parmi ces protéines, CrWRKY22, CrWRKY32, ZCT1 et ZCT2 agissent en tant que facteurs de transcription et plus spécifiquement interagissent avec le promoteur du gène Crhds. Ce dernier code une enzyme de la voie du méthyl érythritol phosphate (MEP) considérée limitante pour la production des AIM. Ces travaux ont permis d’identifier de nouveaux FT ciblant la voie du MEP dont la régulation via les FT est encore peu élucidée à ce jour et d’envisager leur utilisation en ingénierie métabolique pour augmenter la production d’AIM par la modulation du flux terpénique chez C. roseus. / Monoterpene indole alkaloids (MIA) are molecules with anti-cancer properties from Catharanthus roseus. Their production cost and the important need in chemiotherapy make them major targets for the research of more efficient production strategies. The aim of this work is to identify new transcription factors (TF) that regulate MIA production. This study focuses especially on the functional characterization and the involvement in the MIA biosynthesis regulation, of proteins previously isolated in the EA2106 “Plant Biocompounds and Biotechnology” laboratory: 3 proteins that belong to the WRKY family (CrWRKYs) and 3 zinc finger proteins named ZCTs. Our experiments revealed that among them, CrWRKY22, CrWRKY32, ZCT1 and ZCT2 act as transcription factors and more specifically interact with the promoter of Crhds gene. Crhds encodes an enzyme of the methyl erythritol phosphate (MEP) pathway that is considered as limiting for MIA production. Our work allowed identifying new TFs targeting the MEP pathway those regulation through TFs is mostly unknown. Using such transcription factors in metabolic engineering could be now considered increasing MIA production by the modulation of terpenoid flux in C. roseus.