The Effect of Temperature and Growth Regulators on Callus Induction in Watermelon Anthers

HIGHLIGHTS Callogenesis was induced from watermelon anthers The auxin 2,4-D at 2.0 and 5.0 μM concentrations induced callus formation. Anthers' responses to the pre-treatment at 4 °C varied according to the watermelon genotype.

Abstract Callus induction is one of the pathways required for haploid plant regeneration through anther culture. Pollen viability, as well as the effect of growth regulators and cold pretreatment on anthers of two watermelon lines (Smile and Sugar Baby) to induce callus formation were herein evaluated. Pollen viability was estimated through the staining technique using 2% acetic carmine. Male flower buds were collected and disinfested to allow removal anthers. These anthers were placed on Murashige and Skoog medium, which was supplemented with 2,4-dichlorophenoxyacetic (2,4-D) at 0.0, 0.5, 1.0, 2.0 or 5.0 μM or with 6-benzylaminopurine at 0.0, 0.5, 1.0, 1.5, or 2.0 μM, in combination with 2.0 μM of 2,4-dichlorophenoxyacetic. Anthers were pretreated at 4 °C, for two days and then placed in vitro. Both watermelon lines provided high pollen viability rates (from 93 to 98%). The 2.0 and 5.0 μM concentrations of 2,4-D stimulated higher friable callus formation. The optimal concentration of 2,4-D was estimated at 3.78 μM and 4.17 μM, which had callus induction rates of 64% and 52%, respectively. The combination of 2.0 μM of 2,4-D and 6-benzylaminopurine did not lead to increased anther response to callus induction. The pre-treatment applied to flower buds at 4 °C enabled callus induction and the anther response to callus induction was genotype-dependent.

Selection of somaclonal variants of maracuyá (passiflora Edulis var Flavicarpa. Deneger) tolerants to water deficit / Selección de variantes somaclonales de maracuyá (Passiflora edulis var flavicarpa. Deneger) tolerantes a déficit hídrico

ABSTRACT Climate change will have an impact on the Colombian agricultural sector, by 2050 increases in temperature and distribution of erratic rainfall are expected. Passion fruit cultivation does not tolerate water deficit, it reduces flower induction, generates fruit drop and defoliation. To tackle this problem, somaclonal variants (VS) of passion fruit were selected in-vitro, seeking tolerance to water deficit. Four phases were developed: I) callogenesis, II) direct and indirect organogenesis, II) Induction and evaluation of the water deficit with Polyethylene glycol 6000 (PEG 6000) and IV) in vitro selection of VS by morphometric measurements, chlorophyll and total sugars contents. Differences in callogenesis were found with different concentrations of 2,4-D, the concentration of 2 mg L-1 presented better results producing calluses in less time and in greater quantity (8 days, 90% of the leaf area). In indirect and direct organogenesis the medium MS + ANA + BAP (0.3: 0.6), showed significant statistical differences with respect to other means, for the variables root length (15.14 cm), stem (16.72 cm) and leaves ( 14.51 cm) and root thickness (0.76 cm) stem (1.25) and leaf width (6.75). The influence of PEG 6000 showed significant differences, the treatment with 30 g L-1 showed the smallest leaf width, the greatest width was found in 25 g L1. Statistical differences were found in chlorophyll levels and total sugar contents, the highest contents were recorded in the VS 25VS1, showing the possibility of obtaining seedlings tolerant to the water deficit of passion fruit by inducing somaclonal variation.

RESUMEN El cambio climático tendrá impactos en el sector agropecuario colombiano, para el 2050 se prevén aumentos de temperatura y distribución de lluvias erráticas. El cultivo de maracuyá no tolera el déficit hídrico, este disminuye la inducción floral, genera caída de frutos y defoliación. Para abordar esta problemática se seleccionaron in-vitro variantes somaclonales (VS) de maracuyá, buscando tolerancia al déficit hídrico. Se desarrollaron cuatro fases: I) callogénesis, II) organogénesis directa e indirecta, III) Inducción y evaluación del déficit hídrico con Polientilenglicol 6000 (PEG 6000) y IV) selección in vitro de VS por mediciones morfométricas, contenidos de clorofila y azúcares totales. Se hallaron diferencias en callogénesis con diferentes concentraciones de 2,4-D, la concentración de 2 mg-L-1 presentó mejores resultados produciendo callos en menor tiempo y en mayor cantidad (8 días, 90% del área foliar); en organogénesis indirecta y directa el medio MS + ANA + BAP (0.3:0.6), mostró diferencias estadísticas significativas respecto a otros medios, para las variables longitud de raíz (15.14 cm), tallo (16.72 cm) y hojas (14.51 cm) y grosor de raíz (0.76 cm) tallo (1.25) y ancho de hojas (6.75). La influencia de PEG 6000 mostró diferencias significativas, el tratamiento con 30 g-L-1 mostró menor ancho de hojas, el mayor ancho se encontró en 25 g-L-1. Se hallaron diferencias estadísticas en niveles de clorofila y contenidos de azúcares totales, los mayores contenidos se registraron en el VS 25VS1, mostrando la posibilidad de obtener plántulas tolerantes al déficit hídrico de maracuyá mediante la inducción de variación somaclonal.

Induction, biochemical trait and phytochemical screening of calluses of Amburana cearensis (Allemão) A. C. Smith

Amburana cearensisis an arboreal legume of the Fabaceaefamily,with high phytotherapic and medicinal potential due the presence of secondary metabolites. The objective of this study was to evaluate the effect of 2,4-dichlorophenoxyacetic acid (2,4-D) and 4-amino-2,5,6-trichloro-2-pyridinecarboxylic acid (picloram) on the in vitroinduction of callogenesis of A. cearensisand analyze the biochemical and phytochemical potential of these calluses. For callus induction, leaf and cotyledon segments were used as explants, which were inoculated in woody plant medium (WPM) supplemented with different concentrations of 2,4-D (0, 5, 10, 20, 40 μM) or picloram (0, 5, 10, 20, 40, 80 μM). The callus growth curve was estimated based on fresh weight, measured at 7-day intervals until 28 days after inoculation. The calluses were analyzed by biochemical tests to quantify the reducing sugars and total proteins. Phytochemical screening and high-performance liquid chromatography were performed to establish the phytochemical profile of extracts from calluses. The concentrations of 21.94 μMand 26.46 μMof 2,4-Dinduced the greatest formation of compact and friable calluses from the leaf and cotyledon segments, respectively. The growth curve had two distinct phases(lag and exponential) for both types of calluses evaluated. The maximum levels of reducing sugars and total proteins in the calluses from leaf and cotyledon segments were obtained on the day of inoculation and after 28 days of cultivation, respectively. The results of the phytochemical analysis identified the presence of coumarin in all the extracts evaluated, this secondary metabolite has high pharmacological potential.

Micropropagacion in vitro de Rosa rosa sp. a partir de yemas axilares y respuesta callogénica / Rose rosa sp. in vitro micropropagation from axillary buds and callogenic response

El objetivo de este trabajo fue obtener plántulas de Rosa sp y respuesta callogénica a partir de yemas axilares y hojas. Se utilizó Murashige y Skoog (MS) al 100%, como medio de cultivo para la fase de establecimiento, adicionado con myo-inositol 0,1 mg/L, ácido ascórbico 0,1 mg/L, tiamina 0,2 mg/L, sacarosa 30 g, benzylaminopurina (BAP) 0,4 mg/L, kinetina 0,3 mg/L, ácido naftaleno-acético (ANA) 0,3 mg/L, y Agar sigma 6 g; ajustando el pH a 5,8; esterilizados en autoclave a 120°C bajo 15 lb de presión. El análisis de varianza para la fase de multiplicación y enraizamiento determinó que existen diferencias altamente significativas para la variable altura ( p=0,000), para determinar en cuáles medias son significativamente diferentes se realizó la prueba de Kruskal ­ Wallis. Para las variables presencia de raíz (p = 0,3398), número de hojas (p = 0,4775) y formación de callos (p = 0,1964), sin diferencias estadísticamente significativas.

The objective of this work was to obtain Rosa sp seedlings and callogenic response from axillary buds and leaves. Murashige and Skoog (MS) 100%, was used as culture medium for the establishment phase, added with myo-inositol 0.1 mg / L, ascorbic acid 0.1 mg / L, thiamin 0.2 mg / L, sucrose 30 g, benzylaminopurine (BAP) 0.4 mg / L, kinetin 0.3 mg / L, indole-acetic acid (IAA) 0.3 mg / L, and Sigma agar 6 g; adjusting the pH to 5.8; sterilized in an autoclave at 120 °C under 15 lb of pressure. The analysis of variance for the phase of multiplication and rooting determined that there are highly significant differences for the variable height (p = 0.000), in order to determine which means are significantly different, the Kruskal - Wallis test was performed. For the variables presence of root (p = 0. 3398), number of leaves (p = 0.4775) and callus formation (p = 0.1964), without statistically significant differences.

Induction and growth curve of calli from leaf and nodal explants of genipap / Indução e curva de crescimento de calos obtidos de explantes foliares e nodais de jenipapeiro

The aim of this study was to determine the effect of the auxin 2,4-D (2,4-dichlorophenoxyacetic) in calli formation from leaf and nodal segments of genipap and to characterize its growth curve. Explants obtained from shoots previously established from in vitro seedlings were used for calli induction. The experimental design was completely randomized in a 3x5x2 factorial with three accessions (NB, SA, SAL), five concentrations of 2,4-D (0.0; 2.0; 4.0, 6.0 or 8.0 mg L-1) and two times of measurement for calli fresh weight (30 and 60 days). There was callus formation in all treatments tested. It was observed that the best response for callus induction from leaf segments was with 2.0 mg L-1 of 2,4-D. For the nodal segment, the response among the accessions was different due to 2,4-D concentrations. The growth curve was plotted according to the fresh weight of callus obtained at intervals of 10 days up to 60 days. Through the established growth curve, the nodal-derived calli from accession SA should be transferred to a new medium, after 40 days of culture.

O objetivo desse trabalho foi determinar o efeito da auxina 2,4-D (ácido diclorofenoxiacético) na calogênese de segmentos foliar e nodal de jenipapeiro e caracterizar sua curva de crescimento. Explantes obtidos de brotações pré-estabelecidas a partir de plântulas in vitro foram utilizados na indução de calos. O delineamento experimental utilizado foi o inteiramente casualizado em esquema fatorial 3x5x2, com três acessos (NB, SA e SAL), cinco concentrações de 2,4-D (0,0; 2,0; 4,0; 6,0 ou 8,0 mg L-1) e dois tempos de avaliação (30 e 60 dias) da massa fresca de calos. Houve formação de calos em todos os tratamentos testados. Observou-se que a melhor resposta de indução ocorreu na concentração de 2,0 mg L-1 para calos oriundos de segmentos foliares. Para o segmento nodal a resposta entre os acessos foi diferenciada em função das concentrações de 2,4-D. A curva de crescimento foi plotada a partir da massa fresca dos calos obtida em intervalos de 10 dias até os 60 dias. Através da curva de crescimento estabelecida, os calos derivados de segmentos nodais do acesso SA devem ser transferidos para um novo meio de cultura, 40 dias após à inoculação.

In vitro callogenesis of Poincianella pyramidalis (catingueira)

ABSTRACT This work describes the establishment of procedures to induce in vitro callogenesis from Poincianella pyramidalis (Tul.) L. P. Queiroz, Fabaceae, explants. Nodal, internodal and leaf segments were isolated from in vitro germinated seedlings and cultured in MS medium with 0, 2.5, 5 and 10 mg l-1 of 2,4-dichlorophenoxyacetic acid. After 30 days, the explants with induced callus showed a quadratic response for the segments nodal, internodal and leaf, with increasing the callus formation in 2,4-dichlorophenoxyacetic acid concentrations of 6.28, 6.49 and 4.91 mg l-1, respectively. In 30 days there was a linear oxidation rise with the increase to the 2,4-dichlorophenoxyacetic acid. After 60 days, oxidation values were minimum, at 2,4-dichlorophenoxyacetic acid concentrations of 5.13 mg l-1 (internodal) and 3.98 mg l-1 (leaf). The highest callus production was observed after 30 days in the presence of 6.09 mg l-1, 5.82 mg l-1 and 4.91 mg l-1 of 2,4-dichlorophenoxyacetic acid in nodal, internodal and leaf segments, respectively. After 60 days these segments showed peaks of production at 7.0 mg l-1 (nodal), 6.15 mg l-1 (internodal) and 5.08 mg l-1 (leaf) of 2,4-dichlorophenoxyacetic acid. For callus induction the intake of 2,4-dichlorophenoxyacetic acid was essential. The greater intensity in callus formation was observed in 4.91 mg l-1 in leaf segments after 30 days.

Induction and growth pattern of callus from Piper permucronatum leaves / Indução e padrão de crescimento de calos de folhas de Piper permucronatum

ABSTRACT Piper permucronatum is a perennial shrub, a medicinal plant native to the Amazon Rainforest. Traditionally, the tea of its leaves is used to combat menstrual and intestinal cramps, stomach pain, digestive problems, diarrhea, hemorrhage, and nausea. Its leaf’s essential oil is effective against Aedes aegypti larvae; its flavones and flavanones have a fungicidal effect against Clamidosporium cladosporioides and C. sphaerospermum; its hexanic extract is effective against Leishmania amazonensis. The objective of this study was to provide a protocol for callus induction from P. permucronatum leaves and an identification of the callus growth pattern, focusing on the deceleration phase, when the callus cells must be subcultured into liquid medium in order to produce a cell suspension cultures. Leaf explants were inoculated in a solid MS medium supplemented with factorial combinations of 2,4-D, BA, NAA and GA3. Callus formation was evaluated weekly until the 49th day. Subsequently, new explants were inoculated at the hormonal combination that resulted in the highest callus cell proliferation and, every seven days during a period of 70 days, samples were dried and weighed to determine the callus growth pattern. NAA and GA3 were not effective for callus induction. Combinations of 2,4-D and BA resulted in callus induction and proliferation. The highest percentage of callus induction was observed with the combination of 4.52 µM 2,4-D and 4.44 µM BA. The calluses thereby produced were friable and whitish. The callus growth pattern followed a sigmoid shape. The deceleration phase started on the 56th day of culture.

RESUMO Indução e padrão de crescimento de calos de folhas de Piper permucronatum. Piper permucronatum é um arbusto perene, uma planta medicinal native da Floresta Amazônica. Tradicionalmente, o chá de suas folhas é usado em casos de cólicas menstruais e intestinais, dores de estômago, problemas digestivos, diarreia, hemorragia e náusea. O óleo essencial das folhas é efetivo contra a larva de Aedes aegypti; suas flavonas e flavanonas têm efeito fungicida contra Clamidosporium cladosporioides e C. sphaerospermum; seu extrato hexânico é efetivo contra Leishmania amazonensis. O objetivo deste trabalho foi determinar um protocolo para indução de calos em folhas de P. permucronatum e identificar o padrão de crescimento dos calos, com foco na fase de desaceleração, quando as células de calo devem ser subcultivadas em meio líquido para produzir culturas de células em suspensão. Explantes foliares foram inoculados em meio MS sólido suplementado com combinações fatoriais de 2,4-D, BAP, ANA e GA3. A formação de calos foi avaliada semanalmente até o 49º dia. Posteriormente, novos explantes foram inoculados na combinação hormonal que resultou na maior proliferação de células de calo e, a cada sete dias durante 70 dias, amostras foram secas e pesadas para determinar o padrão de crescimento dos calos. ANA e GA3 não foram efetivas para a indução de calos. Combinações de 2,4-D e BAP resultaram em indução e proliferação de calos. A maior porcentagem de indução de calos foi observada com a combinação de 4,52 µM de 2,4-D e 4,44 µM de BAP. Os calos produzidos eram friáveis e esbranquiçados. O crescimento dos calos seguiu um padrão sigmoide. A fase de desaceleração iniciou no 56º dia de cultivo.

Induction and Morpho-Ultrastructural Analysis of Organogenic Calli of a Wild Passionfruit

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.

Indução e análise histológica de calos em explantes foliares de Jatropha curcas L. (Euphorbiaceae) / Induction and histological analysis of callus leaf explants of Jatropha curcas L. (Euphorbiaceae)

O objetivo deste trabalho foi avaliar o efeito de BAP e AIB sobre a formação de calos a partir de explantes foliares de Jatropha curcas L. (acesso JCUFS-012), descrever a curva de crescimento e realizar análise histológica dos calos. O delineamento experimental foi o inteiramente casualizado, em esquema fatorial 5x4, com cinco concentrações de BAP (0,0; 0,5; 1,0; 2,0 e 3,0 mg.L-1) e quatro de AIB (0,0; 0,5; 0,75 e 1,0 mg.L-1). Durante o experimento, a curva de crescimento dos calos foi acompanhada e mensurada aos 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60 dias de cultivo. A análise histológica foi realizada a partir de calos crescidos em meio MS acrescido de 1,0 mg.L-1 de BAP e 0,5 mg.L-1 de AIB, após 60 dias de cultivo. A interação dos reguladores de crescimento BAP e AIB proporcionou a formação de calos compactos e posterior regeneração de brotações. Um maior número médio (6,2) de brotos por calo foi observado quando se adicionou ao meio de cultivo 1,65 mg.L-1 de BAP. A curva de crescimento de calos apresentou cinco fases distintas: lag, exponencial, linear, estacionária e desaceleração. Na análise histológica dos calos de J. curcas fica evidenciado a organogênese indireta pela formação de brotos adventícios, que apresentam conexão cambial com os tecidos dos calos.

The aim of this study was to evaluate the effect of IBA and BAP on callus formation from leaf explants of Jatropha curcas L. (accession JCUFS-012), describing the growth curve and histological analysis of the callus. The experimental design was completely randomized in a 5x4 factorial design with five concentrations of BAP (0.0, 0.5, 1.0, 2.0 and 3.0 mg. L-1) and four of IBA (0.0, 0.5, 0.75 and 1.0 mg.L-1). During the experiment, the growth curve of the calli was monitored and measured at 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60 days of cultivation. Histological analysis was performed from calli grown on MS medium supplemented with 1.0 mg.L-1 of BAP and 0.5 mg.L-1 of IBA after 60 days of cultivation. The interaction of the growth regulators BAP and IBA provided the formation of compact calli and subsequent regeneration of shoots. A higher number (6.2) of shoots per callus was observed when 1.65 mg.L-1 of BAP was added to the culture medium. The growth curve of calli showed five distinct phases: lag, exponential, linear, stationary and deceleration. On histological analysis of callus J. curcas, indirect organogenesis was evidenced by the formation of adventitious shoots, that presented cambial connection with the callus tissue.

Tissue culture of Cecropia glaziovii Sneth (urticaceae): vegetative micropropagation and plant regeneration from callus / Cultura de tecidos de Cecropia glaziovii Sneth (Urticaceae): micropropagação vegetativa e regeneração de plantas via calos

Cecropia glaziovii is a tree with used in Brazilian popular medicine. Methods allowing the clonal propagation of this species are of great interest for superior genotype multiplication and perpetuation. For this reason, we examined the effect of different culture media and different types of explants on adventitious shoot regeneration from callus and buds of C. glaziovii. Leaves, petioles and stipules obtained from aseptically grown seedlings or from pre-sterilized plants were used to initiate cultures. Adventitious shoot regeneration was achieved when apical and axillary buds were inoculated on gelled Murashige & Skoog (MS) medium supplemented with 6-benzylaminopurine alone (BAP) (1.0, 5.0 or 10.0 mg L-1) or combined with -naphthalene acetic acid (NAA) (1.0 or 2.0 mg L-1), after 40 days of culture. Best callus production was obtained after 30 days of petioles' culture on gelled MS medium with 2,4 dichlorophenoxyacetic acid (2,4-D) (5.0 mg L-1) combined with BAP (1.0 mg L-1). Successful shoot regeneration from callus was achieved when MS medium supplemented with zeatin (ZEA) (0.1 mg L-1) alone or combined with 2,4-D (1.0 or 5.0 mg L-1) was inoculated with friable callus obtained from petioles. All shoots were rooted by inoculation on MS medium supplemented with indole-3-acetic acid (IAA) (1.0 mg L-1). Rooted plants transferred to potting soil were successfully established. All in vitro regenerated plantlets showed to be normal, without morphological variations, being also identical to the source plant. Our study has shown that C. glaziovii can be propagated by tissue culture methods, allowing large scale multiplication of superior plants for pharmacological purposes.

Cecropia glaziovii é uma planta lenhosa, popularmente usada no Brasil como medicinal. Métodos que visem a sua propagação clonal podem ser de grande utilidade na preservação de seus genótipos de elite. Foram examinados efeitos de diferentes reguladores de crescimento e explantes na formação de brotações múltiplas a partir de calos e a partir de brotos apicais. Folhas, pecíolos e estípulas obtidas de plântulas assépticas e da esterilização de sementes ou através da esterilização direta dos explantes foram utilizados para iniciar os cultivos. Brotações múltiplas foram obtidas quando brotos apicais ou axilares foram inoculados em meios compostos de sais de Murashige & Skoog (MS), suplementado com apenas 6-benzilaminopurine (BAP) (1,0, 5,0 ou 10,0 mg L-1) ou combinado com ácido -naftaleno acético (ANA) (1,0 ou 2,0 mg L-1), depois de 40 dias. A produção de calos foi obtida após 30 dias, quando pecíolos foram inoculados em meio MS acrescido de acido 2,4 diclorofenoxiacético (2,4-D) (5,0 mg L-1) combinado com BAP (1,0 mg L-1). A regeneração de brotos a partir de calos foi obtida quando meio MS acrescido de apenas zeatina (ZEA) (0,1 mg L-1) ou combinado com 2,4-D (1,0 ou 5,0 mg L-1) foi inoculado com calos friáveis obtidos de pecíolos. As plântulas foram enraizadas em MS suplementado com ácido 3-indol acético (AIA) (1.0 mg L-1). A aclimatação das plântulas enraizadas foi estabelecida pela transferência para vasos contendo substrato orgânico e vermiculita sob umidade relativa 100 por cento. As plântulas regeneradas "in vitro" apresentaram aparência normal e idênticas à planta-mãe. Nosso estudo concluiu que genótipos de elite de C. glaziovii podem ser propagados em larga escala através de métodos "in vitro", proporcionando uma fonte confiável de matéria prima para estudos farmacológicos.

Plant regeneration from cotyledonary explants of Eucalyptus camaldulensis dehn and histological study of organogenesis in vitro

The present work aimed at regenerating plants of Eucalyptus camaldulensis from the cotyledonary explants and describing the anatomy of the tissues during callogenesis and organogenesis processes, in order to determine the origin of the buds. The cotyledonary leaves of E. camaldulensis were cultured in Murashige and Skoog (MS), WPM and JADS media supplemented with 2.7 µM NAA and 4.44 µM BAP. The best results for bud regeneration were obtained on MS and WPM media (57.5 and 55 percent of calluses formed buds, respectively). Shoot elongation and rooting (80 percent) were obtained on MS/2 medium (with half-strength salt concentration) with 0.2 percent activated charcoal. Acclimatization was performed in the growth chamber for 48 h and then the plants were transferred to a soil:vermiculite mixture and cultured in a greenhouse. Histological studies revealed that the callogenesis initiated in palisade parenchyma cells and that the adventitious buds were formed from the calluses, indicating indirect organogenesis.

Este trabalho teve como objetivo a obtenção de plantas de Eucalyptus camaldulensis a partir de folhas cotiledonares e o estudo da anatomia dos tecidos durante a calogênese e organogênese para determinar a origem das gemas. Folhas cotiledonares foram cultivadas em meios de cultura MS, WPM e JADS suplementados com 2,7 µM de ANA e 4,44 µM de BAP. Os melhores resultados para a regeneração de gemas foram obtidos com os meios MS e WPM. Para o alongamento e enraizamento, o meio de cultura MS/2 contendo 0,2 por cento de carvão ativado apresentou-se eficiente para ambas as etapas. A aclimatização foi realizada mediante a abertura dos frascos na sala de crescimento por 48 horas, seguido da transferência para casa-de-vegetação com nebulização intermitente. Estudos histológicos foram conduzidos e revelaram que a calogênese teve início nas células do parênquima paliçádico e que as gemas adventícias formaram-se a partir dos calos, indicando a organogênese indireta.

Early somatic embryogenesis in Heliconia chartacea Lane ex Barreiros cv. Sexy Pink ovary section explants

The present work evaluated the development of embryogenic callus from transversal ovary sections. The experiments were carried out under two experimental regimes using combinations of IAA (0; 5.71; 8.56; 11.42; 14.27μM) and 2,4-D (0; 13.57; 18.10; 22.62μM) or combinations of 2,4-D with BA (0; 4.43; 6.65; 8.87; 11.09μM). Assessments were made of anatomical aspects of the callus and for the presence of embryogenic structures using cytochemical and histological analyses and stereomicroscopic and scanning electronic microscopic observations. Treatments with 2,4-D and IAA produced friable calluses demonstrating cellular acquisition of morphogenetic competence as well as the formation of pro-embryogenic sectors. The expression of embryogenic program could be observed, with proembryogenic cell clusters developing into globular embryos. These results offer the possibility of using new types of explants for culturing helicons that avoid the growth of endophytic bacteria.

Este trabalho teve como objetivo avaliar a resposta de secções transversais de ovários e o desenvolvimento de calos embriogênicos. O experimento constou de dois ensaios. No primeiro avaliou-se combinações entre AIA (0; 5.71; 8.56; 11.42; 14.27μM) e 2,4-D (0; 13.57; 18.10; 22.62μM) e no segundo avaliou-se as concentrações de 2,4-D supracitadas, combinadas com concentrações de BA (0; 4.43; 6.65; 8.87; 11.09μM). Os calos formados foram avaliados quanto à presença de estruturas embriogênicas utilizando-se estereomicroscópio, microscópio eletrônico de varredura, além de análises citoquímicas e histológicas. Combinações entre 2,4-D e AIA induziram a formação de calos friáveis com setores pró-embriogênicos, refletindo a aquisição de competência morfogenética. Posteriormente foi observada a expressão do programa embriogênico quando massas pró-embriogências desenvolveram-se formando embriões somáticos. Esses resultados apresentam uma alternativa para a utilização de um tipo de explante que possibilita o cultivo in vitro de helicônia sem o desenvolvimento de bactérias endofíticas.