ABSTRACT
The coordination between phytohormones regulation, stomatal behaviour (stomatal index and opening/closing) and gas exchange are potent determinants of plant survival under drought stress. However, we found a knowledge gap in the mechanism regulating the fine-tuning of these features during drought. In order to address this we evaluated gas exchange, stomatal behaviour and endogenous phytohormones content in two cotton varieties (LRA-5166 and NBRI-67) differing in drought sensitivity during water deficit conditions. Variety specific differences were recorded in net photosynthesis rate (A), transpiration rate (E) and stomatal conductance (gs) with significantly less decrease in drought tolerant LRA-5166 than drought sensitive NBRI-67. The abscisic acid (ABA) accumulation was significantly increased in LRA-5166 while reduced in NBRI-67 under water deficit, which was accompanied by relatively less reduced 6-benzylaminopurine (6-BAP) level in LRA-5166 than NBRI-67.Thus, improved ABA/6-BAP ratio was observed in both the varieties of cotton. Critically, LRA- 5166 has reduced stomatal index, aperture size and significantly higher A and intrinsic water use efficiency (WUEi), thus higher drought tolerance than NBRI-67. Furthermore, we found that endogenous ABA predominantly maintains the stomatal behaviour and regulates its physiology either by antagonizing 6-BAP or alone to coordinate with water deficit signals. Overall, our findings describe a new insight as to how drought modulates endogenous ABA and 6-BAP homeostasis in cotton leaf and the mechanism of stomatal regulation by ABA and 6-BAP in cotton.
ABSTRACT
The objective of this study was to promote the establishment of an in vitro culture of Brassavola tuberculata, testing different concentrations of naphthalene acetic acid (NAA) and 6-benzylaminopurine (BAP) on multiplication and rooting, evaluating different substrates during acclimatization, as well as the effect of in vitro treatments. After germination, the seedlings of B. tuberculata were subjected to culture on MS medium supplemented with different concentrations of NAA and BAP, and multiplication and rooting were assessed. During acclimatization, different substrates were tested: S1, Plantmax® and vermiculite (1: 1); S2, Plantmax® and grit (1: 1); and S3, dust fern. Also the effect of the in vitro culture treatments was evaluated: T1, control; T5, (2.5 µM NAA +5 µM BAP); and T7, (5 µM NAA + 0 µM BAP). The favorable balance of cytokinins promoted by treatment T5 yielded the largest number of shoots and leaves in B. tuberculata. The greatest length of leaves and roots, and highest root number were observed in the treatment T7, favored by the presence of auxin. This treatment had a positive effect with respect to plant acclimatization: T7 associated with substrate S1 provided the most suitable conditions for acclimatization of seedlings of B. tuberculata, providing greater number and length of leaves, and high survival rate.
Objetivou-se, com este trabalho, promover o estabelecimento do cultivo in vitro de Brassavola tuberculata, testando diferentes concentrações de ANA e BAP na multiplicação e no enraizamento, e avaliar diferentes substratos e o efeito dos tratamentos de cultivo in vitro na aclimatização. Após a germinação das sementes, as plântulas de B. tuberculata foram submetidas ao cultivo em meio MS suplementado com diferentes concentrações de ácido naftaleno acético (ANA) e 6-benzilaminopurina (BAP), sendo avaliados a multiplicação e o enraizamento. Foram testados diferentes substratos: S1 (Plantmax e vermiculita (1:1)); S2 (Plantmax e areia (1:1)) e S3 (pó de xaxim) na aclimatização e, posteriormente, o efeito dos tratamentos do cultivo in vitro: T1 (controle), T5 (2,5 ANA + 5 BAP) e T7 (5 ANA + 0 BAP), na aclimatização. O balanço favorável às citocininas promovido pelo tratamento T5 (2,5 µM ANA + 5 µM BAP) promoveu maior número de brotos e de folhas em B. tuberculata. O maior comprimento das folhas, das raízes e maior número de raízes foi observado no tratamento T7 (5 µM ANA e 0 µM BAP), favorável a auxina. Este tratamento apresentou efeito positivo com relação a aclimatização das plantas: T7 associado ao substrato S1, Plantmax e vermiculita (1:1) proporcionou melhores condições para a aclimatização das plântulas de B. tuberculata, propiciando maior número e comprimento das folhas, e elevada taxa de sobrevivência.
Subject(s)
In Vitro Techniques , Substrates for Biological Treatment , Germination , OrchidaceaeABSTRACT
Azadirachta indica, es una planta con múltiples aplicaciones tanto forestal como farmacológica. Por ende, el establecimiento del sistema de cultivo in vitro por embriogénesis somática ofrece diversas y variadas ventajas, tales como obtener plantas altamente productivas en metabolitos. En este estudio, se utilizaron secciones foliares y cotiledonares, inducidas en medios MS (1962) suplementados con: BAP sólo y combinado con ANA / 2,4-D, TDZ sólo y con ABA. La regeneración fue con MS sólo o con K + AIA y BAP + AIA. Como resultado se estableció un sistema eficiente con secciones de cotiledones, observándose organogénesis a bajas concentraciones de BAP, mientras a altos niveles de BAP (2,5 mg.L-1), así como con TDZ + ABA (0,02 + 1 mg.L-1) respectivamente favorecieron la embriogénesis somática primaria y secundaria en un 96 % y 71 % respectivamente. La regeneración fue 71 % con MS, mientras que el enraizamiento fue de 86,67 % con MS½, obteniéndose plantas completas a corto plazo.
Azadirachta indica, is a plant with multiple forest and pharmacological application. Therefore, the establishment of in vitro culture system for somatic embryogenesis offers several distinct advantages such as obtaining highly productive plant metabolites. In this study, were used sections cotyledon and leaf, induced on MS medium (1962) supplemented with: BAP alone and combined with NAA / 2,4-D, TDZ alone and ABA. Regeneration was with MS alone or with K + BAP + IAA and IAA. As a result was established an efficient system with cotyledon sections, being observed organogenesis at low concentrations of BAP, while high levels of BAP (2.5 mg.L-1) with 96 % and TDZ + ABA (0.02 + 1 mg.L-1) with 71 %, favoring the primary and secondary somatic embryogenesis. Regeneration was 71 % with MS; rooting was 86.67 % with MS½, presenting whole plants obtained short term.
ABSTRACT
Existen varios protocolos de regeneración de plantas vía embriogénesis somática de Sorghum bicolor (L.) Moench, sin embargo los porcentajes de formación de callos con estructuras embriogénicas y regeneración de plantas son bajos. Es por ello que esta investigación tuvo como objetivo generar embriones somáticos en sorgo rojo variedad CIAP 132-R. Se ensayaron diferentes concentraciones de 2,4-D para la formación de callos, así como tres concentraciones de ácido ascórbico para eliminar la exudación de compuestos fenólicos por el explante. También para la formación de los embriones somáticos a partir de los callos se evaluaron diferentes concentraciones de 2,4-D y 6-BAP. El mayor porcentaje de formación de callos (57,5 %) se alcanzó con 18,1 µM de 2,4-D. Con la adición al medio de cultivo de 50,0 mg.l-1 de ácido ascórbico fue posible eliminar los compuestos fenólicos en el explante y en el medio de cultivo, además permitió incrementar el porcentaje de formación de callos con estructuras embriogénicas hasta un 95 %. El número mayor de embriones somáticos por callo se alcanzó en el medio de cultivo con concentraciones de 4,52 µM de 2,4- D, combinada con 2,22 µM de 6-BAP. Por primera vez, se logró la formación eficiente de embriones somáticos a partir de los callos obtenidos de semillas inmaduras germinadas como explante inicial en la variedad CIAP 132-R.
Several protocols of plant regeneration via somatic embryogenesis from Sorghum bicolor (L.) Moench have been development, however the percentage of calluses with embryogenic structures and plant regeneration are low. Therefore this study aimed to generate somatic embryos in red sorghum variety CIAP 132-R. Different concentrations of 2,4-D for callus formation, and three concentrations of ascorbic acid to remove phenolics exudation were assayed by explant. For the formation of embryos different concentrations of 2,4-D and 6-BAP were evaluated. The highest percentage of callus formation (57.5 %) was achieved with 18.1 µM 2,4-D. With the addition to the culture medium of 50.0 mg.l-1 of ascorbic acid was possible to eliminate the phenolic compounds in the explant and in the culture medium; also it allows increasing the percentage of calluses with embryogenic structures up to 95 %. The highest number of somatic embryos per callus was achieved with a reduction in the culture medium of 2,4-D to 4.52 µM in combination with 2.22 µM 6-BAP. For the first time, the efficiency of somatic embryo formation was obtained from the freshly germinated sprouts of immature seeds as initial explant CIAP 132-R.
ABSTRACT
germination of S. emarginatus in vitro cotyledon explants in BAP/Kn/TDZ (1.0-3.0 mg/L) supplemented MS medium and (2) in plant treatment with BAP/Kn/TDZ (3.0 mg/ L) in combination of 1AA (0.5 mg/L) of the cotyledon explants of plants and maintained under sterile conditions. While the former method resulted in as many as (7.5±8.6 shoot buds) from the cotyledonary explants within four weeks, the latter yielded on average approximately 8 shoot buds from each treated node in eight weeks. The cytokinin treatment in plant consisted of placing sterile filter paper moistened with sterile distilled water over the node and adding different concentrations of 6- benzylaminopurine. The best results for shoot bud regeneration were obtained with cotyledons, when cultured in the presence of (0.5 mg/L) IAA in combination with (3.0 mg/L). The shoots elongated and rooted directly in vermiculite after a pulse treatment with IBA (2.5 mg/L) for 15 min. Fungus growth, a serious problem in S. emarginatus tissue culture, was controlled using a fungicide, Bavistin, along with elimination of organic nutrients from the growth medium.
ABSTRACT
El objetivo de esta investigación fue lograr el establecimiento in vitro de la especie Terminalia amazonia y Vochysia allenii debido a la dificultad de propagarlas sexual y asexualmente con técnicas convencionales. Se logró establecer segmentos nodales de ambas especies en condiciones in vitro empleando el HgCl2 0,1 % con un tiempo de exposición de 5 minutos. El mejor medio de cultivo para nudos fue el WPM 100 % de sales para T.amazonia y para V. allenii fue el WPM 50 % de sales. Después de 28 días de cultivo se obtuvo un 42 % de nudos establecidos para T. amazonia y 10% para V. allenii. En ambas especies se evaluó el efecto sobre la brotación de cinco concentraciones de 6-bencilaminopurina (6-BAP) (0,0; 2.22, 4.44, 6.66, 8.88 μM L-1) y cinco de tidiazuron (TDZ) (0,0; 0.22, 0.45, 0.68, 0.90 μM L-1). Se obtuvó en promedio un brote por explante en los cinco tratamientos de BAP y TDZ utilizados.
The objective of this research was to achieve the in vitro establishment of the species Terminalia amazonia and Vochysia allenii due to the difficulty propagate sexually and asexually with conventional techniques. It was possible to establish the nodal segments of both species in in vitro conditions using 0.1 % HgCl2 with an exposure time of 5 minutes. The best nodal culture medium was 100 % WPM salts in T. amazonia and V. allenii was WPM 50% salts. After 28 days of culture 42 % of nodal segments to T. amazonia and V. allenii 10% was obtained. In both species, the effect on sprouting of five concentrations of 6-benzylaminopurine (6-BAP) (0.0, 2.22, 4.44, 6.66, 8.88 μM L-1) and five thidiazuron (TDZ) (0.0, 0.22, 0.45, 0.68, 0.90 μM L-1) was evaluated. Outbreak was scored on average per explant in the five treatments of BAP and TDZ used.
ABSTRACT
Realizou-se um estudo para avaliar o efeito de fontes de luz na micropropagação de morangueiro, com níveis crescentes de BAP no meio de cultivo. Para tanto, inocularam-se gemas de brotações da cultivar 'Sabrosa' em meio MS com 30g L-1 de sacarose, 100mg L-1 de mio-inositol, 7g L-1 de ágar e BAP (0; 0,3; 0,6; 0,9; e 1,5mg L-1), em pH 5,8. Os explantes foram cultivados a 25+2°C, com 16 horas de fotoperíodo e luminosidade de 20µmol m-2 s-1, esta última fornecida por diferentes fontes de luz (LED azul-EDEB 3LA1, LED verde-EDET 3LA1, LED vermelho-EDER 3LA3, lâmpada fluorescente Growlux e lâmpada fluorescente branca). Os tratamentos foram dispostos em delineamento inteiramente ao acaso em um fatorial 5x5 (concentrações de BAP x fontes de luz), com seis repetições. O experimento foi repetido em três subcultivos sucessivos de 35 dias cada. Nestes avaliaram-se o número de brotações por explante e a altura das brotações. Ao final do terceiro subcultivo, determinaram-se, ainda, as concentrações de carotenoides e de clorofilas a e b, independentemente do nível de BAP. Maior número de brotações por explante foi obtido sob LEDs vermelhos e verdes. Concentrações de BAP no meio de cultura entre 0,82 e 1,22mg L-1, dependendo da fonte de luz, proporcionaram maior multiplicação in vitro de brotações. Sob todas as fontes de luz foram obtidas brotações de maior comprimento em meio isento de BAP. Brotações cultivadas sob LEDs vermelhos apresentaram maior quantidade de pigmentos fotossintéticos, enquanto aquelas sob LEDs verdes e lâmpadas Growlux apresentaram a menor.
The objective of this research was to evaluate the effect of different sources of light in strawberry micropropagation, under increasing levels of BAP in culture medium. 'Sabrosa' shoots were inoculated in MS medium supplemented with 30g L-1 sucrose, 100mg L-1 myo-inositol, 7 agar g L-1 and BAP (0; 0.3; 0.6; 0.9; e 1.5mg L-1), pH 5.8. The explants were cultivated at 25+2°C, 16 hours photoperiod and 20µmol m-2 s-1. The luminosity was supplied by different sources of light (blue-EDEB 3LA1 LED, green-EDET 3LA1 LED, red-EDER 3LA3 LED, Growlux fluorescent lamp and white fluorescent lamp). The experimental design was a factorial entirely randomized (5 concentrations of BAP x 5 light sources) with six replications. The experiment was repeated in three successive subcultures of 35 days each, being evaluated the shoot number per explant and shoot height. The carotenoids and chlorophyll a and b determinations were carried out after the third subculture, independently of BAP concentration. Shoot number per explant was higher under red and green LEDs. BAP concentrations between 0.82 and 1.22mg L-1 in culture medium showed higher multiplication rate depending on the light source. Shoot length was highest in culture medium without BAP under all light sources. Shoots cultivated under red LEDs showed higher concentration of photosynthetic pigments, while those under green LEDs and Growlux light bulbs showed the lowest.