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1.
Biosci. j. (Online) ; 32(3): 619-626, may/june 2016. tab, graf
Artigo em Inglês | LILACS | ID: biblio-965500

RESUMO

Micropropagation is an alternative to produce orchid plants in large scale. However, this process presents losses during acclimatization. Exogenous proline use in vitro plant tissue culture can reduce the stress of the plant acclimatization phase. We aimed to verify the growth of orchids in different micropropagation systems with the addition of proline in the culture medium. Cattleya walkeriana plants were obtained from the germination of seeds in culture medium. Seeds were germinated in MS medium, added 20 g. L-1 of sucrose, solidified with 6 g. L-1 of agar and pH adjusted for 5,8. The cultures were incubated in a growth room with temperature of 24 ± 2 0C, under photoperiod of 16 h. After 5 months, 1-cm long seedlings were placed in a culture vessel according to the treatments, which were composed of two micropropagation systems (conventional and natural ventilation) and three proline concentrations (0, 1, and 2 g·L-1). The experiment was carried out in an entirely randomized design consisting of a 2 × 3 factorial, for a total of 6 treatments, each with 5 replicates. The natural ventilation system with the use of proline (1 g·L-1) promoted higher dry mass accumulation and better control of water loss by plants.


A micropropagação é uma alternativa para a produção de plantas de orquídeas em larga escala. Entretanto, este processo apresenta perdas durante a fase de aclimatização. O emprego de prolina exógena na cultura de tecidos vegetais é uma alternativa para reduzir o estresse das plantas na fase de aclimatização. O objetivo da presente pesquisa foi verificar o crescimento de orquídeas em diferentes sistemas de micropropagação com prolina adicionada no meio de cultura. Plantas de Cattleya walkeriana foram obtidas a partir da germinação de sementes em meio de cultura. Sementes foram germinadas em meio MS, adicionado de 20 g. L-1 de sacarose, solidificado com 6 g. L-1 de ágar e pH ajustado para 5,8. Após 5 meses, plântulas com 1 cm de comprimento foram inoculadas nos frascos de cultivo de acordo com os tratamentos, os quais foram compostos por dois sistemas de micropropagação (convencional e ventilação natural) em combinação com prolina (0, 1 e 2 g L-1). O experimento foi conduzido em esquema inteiramente casualizado, constando de um fatorial 2x3, totalizando 6 tratamentos com 5 repetições. O sistema de ventilação natural com o uso de prolina (1 g L-1) promoveu o maior acúmulo de massa seca e melhor controle da perda de água das plantas.


Assuntos
Técnicas In Vitro , Germinação , Orchidaceae/crescimento & desenvolvimento
2.
Ann Bot ; 112(1): 17-29, 2013 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-23618898

RESUMO

BACKGROUND AND AIMS: A positive correlation between tissue thickness and crassulacean acid metabolism (CAM) expression has been frequently suggested. Therefore, this study addressed the question of whether water availability modulates photosynthetic plasticity in different organs of two epiphytic orchids with distinct leaf thickness. METHODS: Tissue morphology and photosynthetic mode (C3 and/or CAM) were examined in leaves, pseudobulbs and roots of a thick-leaved (Cattleya walkeriana) and a thin-leaved (Oncidium 'Aloha') epiphytic orchid. Morphological features were studied comparing the drought-induced physiological responses observed in each organ after 30 d of either drought or well-watered treatments. KEY RESULTS: Cattleya walkeriana, which is considered a constitutive CAM orchid, displayed a clear drought-induced up-regulation of CAM in its thick leaves but not in its non-leaf organs (pseudobulbs and roots). The set of morphological traits of Cattleya leaves suggested the drought-inducible CAM up-regulation as a possible mechanism of increasing water-use efficiency and carbon economy. Conversely, although belonging to an orchid genus classically considered as performing C3 photosynthesis, Oncidium 'Aloha' under drought seemed to express facultative CAM in its roots and pseudobulbs but not in its leaves, indicating that such photosynthetic responses might compensate for the lack of capacity to perform CAM in its thin leaves. Morphological features of Oncidium leaves also indicated lower efficiency in preventing water and CO2 losses, while aerenchyma ducts connecting pseudobulbs and leaves suggested a compartmentalized mechanism of nighttime carboxylation via phosphoenolpyruvate carboxylase (PEPC) (pseudobulbs) and daytime carboxylation via Rubisco (leaves) in drought-exposed Oncidium plants. CONCLUSIONS: Water availability modulated CAM expression in an organ-compartmented manner in both orchids studied. As distinct regions of the same orchid could perform different photosynthetic pathways and variable degrees of CAM expression depending on the water availability, more attention should be addressed to this in future studies concerning the abundance of CAM plants.


Assuntos
Orchidaceae/anatomia & histologia , Orchidaceae/metabolismo , Fotossíntese/fisiologia , Folhas de Planta/anatomia & histologia , Carbono/metabolismo , Secas , Malato Desidrogenase/metabolismo , Orchidaceae/fisiologia , Fosfoenolpiruvato Carboxilase/metabolismo , Folhas de Planta/metabolismo , Raízes de Plantas/anatomia & histologia , Raízes de Plantas/metabolismo , Raízes de Plantas/fisiologia , Água/metabolismo
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