982 resultados para Cultura de tecidos vegetais


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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

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This work studied a new protocol for organogenic calli induction and characterization of the morphology and ultrastructure of callogenesis in leaf explants of Passiflora gibertii N. E. Brown, a native passion fruit species from Brazil. Calli induction was performed in different growth conditions (light and dark), different MS medium salt concentrations (MS and MS half strength) and the presence or absence of coconut water. The leaf explants maintained in the dark were more responsive to bud formation. In order to reduce spending on in vitro culture, the most suitable induction medium for P. gibertii organogenesis could, therefore be the MS half strength salt concentration medium maintained in the dark. The addition of coconut water to the culture medium was essential for both calli induction and bud formation. The morphological and ultrastructural features of the organogenic calli were isodiametric cells, characterized by an organized cellular system, nucleus with prominent nucleoli, presence of starch grains and dense cytoplasm rich in endoplasmic reticulum. The scanning electron microscopy demonstrated that buds were present on these calli.

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Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

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The experiment was carried out aiming to analyze the dry mass production and distribution and the content and accumulation of macronutrients in sourgrass (Digitaria insularis) plants cultivated under mineral nutrition standard conditions. Plants grew in 7-liter pots filled with sand substrate and daily irrigated with nutrient solution, being maintained under greenhouse conditions. Treatments consisted of times of evaluation (21, 35, 49, 63, 77, 91, 105, 119, and 133 days after emergence - DAE) and were arranged in a completely randomized design with four replicates. Sourgrass showed small accumulation of dry mass (0.3 g per plant) and macronutrients (3.7 mg of N per plant, 0.4 mg of P per plant, 5.6 mg of K per plant, 0.9 mg of Ca per plant, 0.7 mg of Mg per plant, and 0.3 mg of S per plant) at vegetative growth stage (< 49 DAE). Those accumulations increased mainly after 77 DAE, reaching the maximum theoretical value at 143, 135, 141, 129, 125, 120, and 128 DAE, for dry mass (12.4 g per plant), N (163.2 mg per plant), P (27.1 mg per plant), K (260.5 mg per plant), Ca (47.6 mg per plant), Mg (30.9 mg per plant), and S (13.7 mg per plant), respectively. K and N were found with higher rates and, as a consequence, they were required and accumulated in greater amounts in plant tissues of sourgrass.

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This experiment was carried out to analyze dry mass production and distribution, and the content and accumulation of macronutrients in arrowleaf sida (Sida rhombifolia) plants cultivated under mineral nutrition standard conditions. Plants grew in seven liter pots filled with sand substrate and daily irrigated with nutrient solution, under greenhouse conditions. Treatments consisted of times of evaluation (21, 35, 49, 63, 77, 91, 105, 119, and 133 days after emergence - DAE) and were arranged in a completely randomized design with four replicates. Arrowleaf sida plants showed small accumulation of dry mass (0.3 g per plant) and macronutrients (6.9 mg N per plant, 0.7 mg P per plant, 8.6 mg K per plant, 4.9 mg Ca per plant, 2,6 mg Mg per plant, and 0.3 mg S per plant) at the vegetative growth stage (< 49 DAE). Those accumulations increased, mainly after 63 DAE, and the daily accumulation rate was crescent up to 94 DAE (dry mass - DM), 89 DAE (N and P), 98 DAE (K), 95 DAE (Ca and S), and 93 DAE (Mg), when there was accumulation of 26.3 g DM per plant, 402.6 mg N per plant, 45.6 mg P per plant, 359.3 mg K per plant, 337.6 mg Ca per plant, 71.9 mg Mg per plant, and 20.9 mg S per plant. N and K had the highest rates and, consequently, were the most required and accumulated in greater amounts in plant tissues of arrowleaf sida.

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Pós-graduação em Agronomia (Energia na Agricultura) - FCA

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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

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O sucesso do desenvolvimento da dinâmica das formações vegetais depende das relações estabelecidas entre as espécies vegetais com outros organismos e com o meio físico. Tais relações estão sujeitas a situações de estresse, podendo esse ser de caráter abiótico, como condições elevadas de radiação solar e temperatura e déficit hídrico ou de caráter biótico, como a herbivoria e o ataque de patógenos. Dessa maneira, em virtude à necessidade de um sistema de defesa, as plantas utilizam compostos químicos, como compostos fenólicos e ligninas, para se desenvolverem com proteção. Os compostos fenólicos são compostos oriundos do metabolismo secundário vegetal e ocorrem na parede celular dos tecidos vegetais, constituindo assim uma rápida linha de defesa vegetal a lesões e infecções e funcionando como substrato para atuação de enzimas de defesa como peroxidases e polifenoloxidases. Junto com a atuação dos compostos fenólicos, as ligninas fornecem à planta maior resistência mecânica e impermeabilidade suficiente aos vasos condutores do xilema, proporcionando, assim, desde um fundamental auxílio aos vegetais na conquista do ambiente terrestre até o estabelecimento de uma barreira protetora eficiente contra o ataque de microorganismos. Assim, por meio da extração e análise dos teores de compostos fenólicos e de ligninas de porção de raiz, caule, ápice caulinar e folhas maduras e imaturas de indivíduos de Erythrina speciosa Andrews, Eugenia uniflora L., Hevea brasiliensis M. Arg., Hymenaea courbaril L. var. stilbocarpa (Hayne) Lee et Lang, Joannesia princeps Vell., Lecythis pisonis Cambess, Licania tomentosa (Benth.) Fritsch, Pachira aquatica Aubl. e Psidium guajava L., classificou-se como espécies pioneiras Erythrina speciosa Andrews, Hymenaea courbaril L. var. stilbocarpa (Hayne) Lee et Lang, Joannesia princeps Vell., Pachira aquatica Aubl... (Resumo completo, clicar acesso eletrônico abaixo)

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The experiment was carried out aiming to analyze dry mass production and distribution, and the content and accumulation of macronutrients in Urochloa arrecta plants cultivated under mineral nutrition standard conditions. Plants grew in seven-liter pots filled with sand substrate, were daily irrigated with nutrient solution, and maintained under greenhouse conditions. Treatments corresponded to assessment periods (21, 35, 49, 63, 77, 91, 105, 119, 133, 147, and 161 days after emergence - DAE) and were arranged in a completely randomized design with four replicates. Plants of U. arrecta showed low accumulation (less than 7% of the maximum accumulation at 161 DAE) of dry mass (5.1 g DM per planta) and of macronutrients (57.7 mg N per planta, 8.9 mg P per planta, 167.8 mg K per planta, 21.3 mg Ca per planta, 14.7 mg Mg per planta, and 9.2 mg S per planta) up to 49 DAE. Such accumulations increased mainly after 91 DAE. Daily accumulation rate was crescent up to 130 DAE (DM and S), 137 DAE (N), 125 DAE (P), 119 DAE (K), 144 DAE (Ca), and 128 DAE (Mg), when there was accumulation of 87.7 g DM per planta, 918.0 mg N per planta, 105.8 mg P per planta, 1,643.9 K per planta, 390.4 mg Ca per planta, 200.0 mg Mg per planta, and 103.5 mg S per planta. K and N were found to have the highest rates and, hence, they were the most demanded and accumulated in the greatest amounts in U. arrecta plant tissues.

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O objetivo deste trabalho foi avaliar os efeitos de BAP (6-benzilaminopurina) e NAA (ácido naftaleno acético) na indução, na multiplicação in vitro de gemas, nas brotações de Ananas comosus da cultivar 'IAC Gomo-de-mel' e a correlação desses efeitos com a atividade de peroxidase e o teor de proteína solúvel total. Foram utilizadas gemas axilares retiradas da coroa de frutos sadios, inoculadas em tubo de ensaio contendo meio de cultura MS solidificado com ágar a 5%, pH ajustado para 5,7, contendo os tratamentos que incluíam diferentes concentrações e combinações de BAP (0, 0,5, 1,0 e 1,5mg L-1) e NAA (0, 0,5 e 1,0mg L-1). Nessa fase, aos 65 dias, ocorreu a formação de 2,24 brotações, utilizando-se 1mg L-1 de BAP. Após o desenvolvimento, as gemas foram inoculadas em meio MS líquido associado a dois tratamentos (1,0mg L-1 BAP + 0,5mg L-1 NAA e 1,0mg L-1 BAP + 1,0mg L-1 NAA) e, aos 95 dias, o meio de cultura mais adequado foi aquele que continha 1,0mg L-1 BAP + 0,5mg L-1 NAA, proporcionando 7,42 brotações, menor porcentagem de hiper-hidricidade, maior número de brotações e indução de gemas. As proteínas solúveis apresentaram relação negativa com hiper-hidricidade e comprimento de brotações. A atividade da peroxidase foi maior em plantas com maior número de brotos e com maior porcentagem de hiper-hidricidade.

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Este trabalho teve como objetivo estudar o efeito das poliaminas espermidina e espermina no crescimento de calos Hancornia speciosa Gomes. Calos com 0,5 cm de diâmetro foram inoculados em meio Murashige & Skoog (1962) (MS) a 50% + 100 mg L-1 de caseína hidrolisada + 200 mg L-1 de levedura de cerveja, variando os tratamentos:A: 1 mmol de espermina + 2 mg L-1 de 2,4-D (ácido 2,4 diclorofenoxiacético) + 0,5 mg L-1 de NAA (ácido naftalenoacético); B: 1 mmol de espermidina + 2 mg L-1 de 2,4-D + 0,5 mg L-1 de NAA; C: 2 mg L-1 de 2,4-D + 0,5 mg L-1 de NAA. Não houve influência das poliaminas no crescimento dos calos. observou-se, nos calos tratados com espermidina, maior concentração celular de putrescina (582,37 µg g mf-1) aos 60 dias, maior teor de espermidina (502,54 µg g mf-1) e espermina (868,53 µg g mf-1) aos 40 dias de cultivo, quando se aplicou a própria poliamina. Conclui-se que a aplicação exógena de poliaminas em Hancornia speciosa não proporciona aumento no crescimento de calos. A oxidação promovida por longos períodos de cultivo in vitro induz aumento nos níveis de putrescina.

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Pós-graduação em Agronomia (Genética e Melhoramento de Plantas) - FCAV

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Fundação de Apoio à Pesquisa do Estado de São Paulo (FAPESP)

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Rangpur lime (Citrus limonia Osbeck) in vitro organogenesis was studied based on explant type and cytokinin culture media supplementation. Four explants types collected from epicotyl or hypocotyl regions of in vitro germinated seedlings were evaluated. The epicotyl-derived explants consisted of epicotyl segments and the hypocotyl-derived explants consisted of the entire hypocotyl segment, the hypocotyl segment attached to a cotyledon fragment, and the hypocotyl segment divided longitudinally. The explants were cultured on EME culture medium supplemented with benzylaminopurine (0, 0.5, 1.0, or 1.5 mg L-1). The evaluation was performed after 6 weeks. Best results considering both the explant responsiveness and number of shoots developed per explants were obtained when epicotyl segments-derived explants were evaluated. Considering the explant responsiveness of hypocotyl segments-derived explants no difference was detected between the entire hypocotyl segment and the hypocotyl segment attached to a cotyledon fragment. Moreover, the percentage of responsive explants decreased when hypocotyl segments divided longitudinally were tested. No difference was detected for the number of shoots developed per explant considering the three types of hypocotyl-derived explants. Culture media supplementation with BAP was not essential for Rangpur lime in vitro organogenesis. However, adventitious shoot development was stimulated in concentrations between 0.5 - 1.0 mg L-1.