In vitro rescue of interspecific embryos from Elaeis guineensis x E. oleifera (Arecaceae).
However, interspecific hybrid seeds induced to germinate by heat and imbibition (Nunes et al. 1998) only gave rise to approximately 30% plantlets on average (R.N.V. Cunha & R. Lopes 2008, pers. comm.), far below the 80% obtained for African oil palm seeds (Nunes et al. 1998), and slightly below the 50% observed for seeds of American oil palm.
In vitro cultivation can be useful in determining which would be the appropriate conditions to facilitate the development of somatic embryos in the future and in other applications too. This technology was used to optimize germination of avocado genotypes inflicted by precocious fruit abscission (Sanchez-Romero et al. 2007). Besides, immature embryos from Hybiscus interspecific crosses that did not produce normal fruits were recently rescued in vitro (van Laere et al. 2007).
Specifically concerning species that have oil as the principal reserve present in the seeds, plantlets of Arabidopsis thaliana were established in vitro independently of the glyoxalate cycle as long as exogenous sugars were provided (Eastmond et al. 2000). Sugar concentrations from 30 up to 90mM were sufficient to promote the germination of A. thaliana seeds in the presence of exogenous ABA, but root elongation occurred only under higher sugar concentrations (Finkelstein & Lynch 2000, Finkelstein & Gibson 2001). In vitro culture of zygotic embryos was used to rescue hybrids from Brassica napus x B. juncea and to improve the efficacy of interspecific breeding, thus overcoming the abortion of hybrid embryos caused by the differences in the number of chromosomes between the two species (Zhang et al. 2003). In vitro, B. napus isolated embryos absorbed hexoses faster than sucrose. The activities of hexokinases and sucrose synthase increased in vitro during embryo development and sucrose synthase was four fold more active than invertase (Hill et al. 2003). In vitro cultivation of tenera immature embryos produced by crossing E. guineensis types dura and pisifera was reported by Aberlenc-Bertossi et al. (2003), although the rescue of interspecific hybrids from intercrosses of E. guineensis and E. oleifera has not been evaluated.
The objectives of the present work were to evaluate sucrose and glucose as carbon sources to rescue mature hybrid embryos produced by controlled pollination of E. guineensis x E. oleifera and compost mixtures for acclimatization of the hybrid plantlets obtained in vitro.
MATERIAL AND METHODS
Plant material: Fruits were produced by controlled pollinations of selected Elaeis guineensis plants with pollen from selected plants of E. oleifera, in the Rio Urubu Experimental Station, Rio Preto da Eva, Amazonas, Brazil, 2[degrees]35' S - 59[degrees]28' W, at 200m in elevation. Fruits from progenies labeled as CI1488 and CI1603 were collect 150 days after pollination and stored at 20[degrees]C for 156 and 143 days, respectively. After removal of fruit tissues, seeds were washed with detergent, treated for 10min in 50% (v/v) commercial bleach (2 - 2.5% active chlorine) and washed in distilled autoclaved water. Embryos were immediately extracted by carefully sectioning the endosperm, taken to an aseptic environment, immersed in 5% commercial bleach (2 - 2.5% active chlorine) for 5min, washed three times in distilled autoclaved water and inoculated in culture media.
In vitro cultivation: Embryos from progenies CI1603 and CI1488 were cultivated over cellulose acetate membranes on liquid MS basal salts and vitamins (Murashige & Skoog 1962) supplemented with 10, 20 or 30g/L sucrose or 10, 20 or 30g/L glucose, under 26[+ or -]2[degrees]C and irradiated with 24[micro]mol/[m.sup.2]s of photosynthetically active photons for 16h photoperiods. The emergence of shoots and radicles with at least 2mm in length was scored up to 50 days. Experiments were conducted in a completely randomized design, with each experimental unit defined as a flask with five embryos and 15 repetitions per treatment, what made 450 mature embryos inoculated in vitro. Raw data-consisting of the average number of embryos exhibiting emerged shoots and radicles per experimental unit-were transformed to [(x + 0.5).sup.1/2] for ANOVA analyzes and the subsequent Tukey tests. These procedures comprised phase one of in vitro cultivation (P1VC). Following P1VC, plantlets that exhibited shoots and radicles were transferred to half strength MS salts, supplemented with agar (8g/L), sucrose (30g/L) and active charcoal (2.5g/L). Plantlets were maintained in this medium for 60 days, under the conditions of temperature and irradiation described previously, until acclimatization. These procedures constituted phase two of in vitro cultivation (P2VC).
Acclimatization: During ex vitro transfer, plantlets were evaluated and randomly distributed in 200[cm.sup.3] plastic tubes with drainage holes fitted in square cages and filled with commercial horticultural compost (constituted principally of milled wood) pure or mixed 3:1 or 1:1 with sand. Plantlets in tubes were maintained under greenhouse conditions with approximately 70% shading and manual water supplying and evaluated 43, 100 and 125 days after transfer. At transfer and in the final evaluation, roots and leaves were counted along with the measurement of the longest root and the longest leaf per plant. For intermediary evaluations only the number of leaves and the length of the longest leaf were recorded. Data from plantlets damaged during transfer were excluded from further analyzes. Each plantlet constituted an experimental unit and the experiments were conducted with 43/44 repetitions per treatment. ANOVA analysis for acclimatization was performed from raw data (Kruskal-Wallis one way analysis of variance on ranks) and the medians were compared by Dunn test. The Mann-Whitney ranks sum test was applied to compare the medians of groups of data recorded for different evaluation days. Spearman's ranks order correlation was used to test the correlation among groups of data. Data from different evaluations were compared by the t-test. All the statistical analyzes were performed with SigmaStat v. 2.0 (Fox et al. 1995).
Elaeis guineensis x E. oleifera hybrid embryos displayed no significant differences in average values observed for shoot emergence per experimental unit under distinct glucose treatments (n = 45, F = 2.337, p = 0.115) but significantly higher averages (n = 45, F = 13.742, p < 0.001 and Tukey, p < 0.05) were observed for radicle emergence under glucose 20 (110mM) and 30g/L (165mM) (Table 1).
For cultivation in sucrose-containing media the average values observed for radicle (n = 45, F = 5.441, p = 0.010) and shoot (n = 45, F = 21.899, p < 0.001) emergence were highest for the highest concentration tested. There was no significant difference between 30g/L (87mM) and 10g/L (29mM) for shoot emergence (Tukey, p [greater than or equal to] 0.05), but radicle emergence was significantly higher in 30g/L sucrose (Table 1).
It became evident that germinating oil palm interspecific embryos exhibited higher shoot emergence frequencies in comparison to radicle emergence, independently of the sugar source in the cultivation media (Table 1). Although radicle development had not been evaluated quantitatively until the end of P2VC and transference to acclimatization, it could be observed that it was the principal barrier to plantlet establishment in P1VC. Indeed from the results obtained under glucose-containing media, it was noticed that alleviation of the impairment in root elongation was achieved in 20g/L (110mM) or highest concentration of this sugar. Shoot emergence was similarly frequent for plantlets maintained in medium containing 10 (55mM), 20 (110mM) or 30g/L (165mM) glucose, however during the 50 days of P1VC, the percentage of plantlets displaying developed shoots and radicles simultaneously was only significantly increased in media containing 20g/L (110mM) glucose or higher (Table 1). Accordingly, among sucrose treatments, increase in the emergence of radicles with subsequent development was observed almost exclusively for the highest concentration (30g/L or 89mM, Fig. 1), despite it has not been as high as in glucose 20 and 30g/L (t-test, p < 0.05).
Most plantlets germinating under 10 and 20g/L sucrose and 10g/L glucose could not be forwarded to P2VC due to the observed staggered root development. Consequently these three treatments were eliminated from acclimatization experiments.
From P1VC, 130 plantlets were transferred to the greenhouse. Data collect during ex vitro transfer revealed the absence of significant influence of culture media used during P1VC (20 or 30g/L glucose or 30g/L sucrose) on the number of leaves per plant (n = 130, H = 0.0361, p = 0.982), on the lengths of the longest roots (n = 118, H = 0.719, p = 0.698) or on the longest leaves (n = 130, H = 1.171, p = 0.425).
At transfer, a correlation between the lengths of the longest leaf and the longest root was significant (Spearman, n = 118, r = 0.330, p < 0.001). Nevertheless, this inclusive result was highly influenced by the values observed for plantlets cultivated in 20 or 30g/L glucose during P1VC (Spearman, n = 75, r = 0.405, p < 0.001), since the correlation between shoot and root lengths was not significant under cultivation on 30g/L sucrose (Spearman, n = 43 r = 0.203, p = 0.191). This result is in agreement with the higher frequency of plantlets showing radicle development in 20 or 30g/L glucose than in 30g/L sucrose along P1VC (and Table 1).
Plants surviving up to the second evaluation under greenhouse conditions 43 days after transfer corresponded to 55% (71 plants). This result was similar to the 58.33% survival observed for coconut plantlets (Ledo et al. 2007). From the total, 24 plants were transferred to pure horticultural compost, 24 to 3:1 compost:sand and 23 to 1:1 compost: sand mixtures. Only five plants died after the second evaluation.
[FIGURE 1 OMITTED]
Plantlets gained on average 0.04cm/day in length of the longest leaf during the first 43 days in the greenhouse. Subsequent progress was significantly better (t-tests, p < 0.05) comparing data registered upon ex vitro transfer versus subsequent evaluations. It was observed the increase in the number of leaves and the lengthening of the longest leaf (Table 2), with gains of 0.123cm/day between the second and third evaluations and 0.110cm/day from the third to the final evaluations were observed. A correlation between the length of the longest leaf and the number of leaves not observed at transfer was established by the second evaluation (Spearman, n = 71, r = 0.778, p < 0.001) and persisted through the experiment.
Distinct compost mixtures had no influence on shoot development until the final evaluation, when the number of leaves was higher for pure commercial compost (n = 66, H = 11.23, p = 0.004). Root length followed a similar pattern and was equally high in pure compost or 3:1 compost: sand mixture (n = 66, H = 7.66, p = 0.022).
The phase of reserve (including sucrose and proteins) accumulation ends approximately 110 days after pollination, when the acquisition of tolerance to desiccation is initiated, for seeds of Elaeis guineensis type tenera. About 120 days after pollination, water loss stops, embryos preserve a water content slightly higher than the values commonly observed for orthodox species and the seed remains dormant until fruit abscission, which can last 60 additional days or for longer periods (Aberlenc-Bertossi et al. 2003). Besides sucrose accumulation, abscisic acid (ABA) and late embryogenesis abundant (LEA) proteins are possibly involved in this process and the acquired desiccation tolerance is likely to be lost after germination (Aberlenc-Bertossi et al. 2003). This process could be somewhat different for interspecific hybrids, since E. oleifera seeds have relatively lower viability and the combination of genomes from two species can produce novel phenotypes for a massive number of traits. For instance, different Arabidopsis landraces or ecotypes vary in their degree of seed dormancy (Bentsink et al. 2006). Nevertheless, E. guineensis remains the most suitable reference for the study of interspecific hybrids, and since fruits were collect 150 days after pollination and stored, they were considered to be dormant.
The hormone ABA can accumulate in roots of dormant species just after emergence (Kende & Zeevaart 1997), is involved in embryo dormancy (Koornneef et al. 2002) and in the inhibition of invertase activity and root elongation, which are complex signal transduction processes orchestrated by sugars, water and light (Bewley 1997, Finkelstein & Gibson 2001). The impairment in root elongation is gradually supplanted while the radicle becomes a photosynthate sink (Finkelstein & Gibson 2001), and this physiological mechanism is possibly coordinated with the accumulation of sufficient sucrose in shoots. Embryos of E. guineensis type tenera exposed to light display chlorophyll accumulation in the haustorium due to chloroplast development, and subsequent starch accumulation (Rabechault & Cas 1974). In plants, haustorium functions to transfer reserves from the endosperm to the germinating embryo (Carvalho 2000) and is not exposed to light. In the present study, greening of haustoria was observed. Accumulation of starch would also agree with the availability of hexoses in the shoots while root invertases are inhibited by ABA. Efficient reserve accumulation in the shoots and transfer to the radicles, among other factors (as the presence of light during germination), would account for the observation of highest frequencies of plantlets showing normal root development in glucose 20 and 30g/L media, when compared to 10g/L of the same sugar, and in the highest concentration of sucrose compared to the lower concentrations tested (Table 1). The optimum absorption and metabolism of glucose in the shoots (Hill et al. 2003) would compensate for a possible inhibition of root invertases following emergence (Finkelstein & Lynch 2000).
During the first 43 days under acclimatization process, hybrid plantlets dying were presumably those with a higher number of leaves or younger leaves, since no records of plants bearing four leaves at the second evaluation were observed, despite plants at that stage were observed at transfer. In the same period, a reduction in the average length of the longest leaf was not observed (Table 2). Plantlets bearing more leaves would lose higher contents of water due to the higher number of stomata and thinner superficial wax layer (Abdelouahhab & Hughes 1995), thus demanding more absorption from an insufficiently developed root system.
To attain better results in future studies, embryos at different maturation stages will be evaluated as reported for avocado (Sanchez-Romero et al. 2007) and the effects of growth regulators on germination will be tested (Aberlenc-Bertossi et al. 2003, Ledo et al. 2007). Despite the higher percentage of plantlets obtained in vitro in comparison to the average number of interspecific hybrid seeds germinating from progeny pools, the loss of plantlets during acclimatization was of concern. This losses could be reduced by a longer P2VC, by pruning of the roots and by the use of an automated system to control the moisture in the greenhouse. Germination rates and subsequent plantlet development may, in addition, be influenced by embryo genotype, and therefore, different results may be found in future experiments.
In conclusion, interspecific zygotic embryos of E. guineensis x E. oleifera succeeded in metabolize the glucose provided in the media for in vitro culture, and displayed the highest frequencies of emerged and developed roots when this sugar concentration reached 110mM or more (20 or 30g/L glucose). A balanced shoot/root development was observed only for plantets rescued from these two treatments, by the end of P2VC and transfer to acclimatization took place. From embryos cultivated in 20g/L glucose, 76% developed normal shoots and roots simultaneously at the end of P1VC. The highest tested concentration of sucrose produced the highest frequency of plantlets bearing developed shoots and radicles. After four months in the greenhouse, plants grown solely in horticulture compost displayed simultaneously higher number of leaves and longer roots.
To CNPq for financial support, as grant number 401078/04-3. To Rosimar F. de Souza, Jeferson C. da Cruz and Hilma A. R. do Couto at Embrapa Western Amazon Plant Biotechnology Laboratory for technical support. To Nelson L. de Paula, Raimundo O. do Nascimento and Raimundo C. P. de Moraes for carefully handling the embryos.
Abdelouahhab, Z. & H. Hughes. 1995. In vitro acclimatization of date palm (Phoenix dactylifera L.) plantlets: a quantitative comparison of epicuticular leaf wax as a function of polyethylene glycol treatment. Plant Cell Rep. 15: 111-114.
Aberlenc-Bertossi, F., N. Chabrillange, F. Corbineau & Y. Duval. 2003. Acquisition of desiccation tolerance in developing oil palm (Elaeis guineensis Jacq.) embryos in planta and in vitro in relation to sugar content. Seed Sci. Res. 13: 179-186.
Barcelos, E., C.D.M. Nunes & R.N.V. Cunha. 2000. Melhoramento genetico e producao de sementes comerciais de dendezeiro, p. 145-174. In I.J.M. Viegas & A.A. Muller (eds.). A cultura do dendezeiro na Amazonia brasileira. Embrapa Amazonia Oriental/ Embrapa Amazonia Ocidental, Belem, Para, Brasil.
Bentsink, L., J. Jowett, C.J. Hanhart & M. Koornneef. 2006. Cloning of DOG1, a quantitative trait locus controlling seed dormancy in Arabidopsis. PNAS 103: 17042-17047.
Bewley, J.D. 1997. Seed germination and dormancy. Plant Cell 9: 1055-1066.
Carvalho, C.J.R. 2000. Ecofisiologia do dendezeiro Elaeis guineensis JACQ), p. 89-124. In I.J.M. Viegas & A.A. Muller (eds). A cultura do dendezeiro na Amazonia brasileira. Embrapa Amazonia Oriental/ Embrapa Amazonia Ocidental, Belem, Para, Brasil.
Eastmond, P.J., V. Germain, P.R. Lange, J.H. Bryce, S.M. Smith & I.A. Graham. 2000. Postgerminative growth and lipid catabolism in oilseeds lacking the glyoxalate cycle. PNAS 97: 5669-5674.
Finkelstein, R.R. & T.J. Lynch. 2000. Abscisic acid inhibition of radicle emergence but not seedling growth is suppressed by sugars. Plant Physiol. 122: 1179-1186.
Finkelstein, R.R. & S.I. Gibson. 2001. ABA and sugar interactions regulating development: cross-talk or voices in a crowd? Curr. Opin. Plant Biol. 5: 26-32.
Fiorese, C. 2008. Noticias da Amazonia. (Downloaded: March 1, 2010, www.noticiasdaamazonia.com. br/2521-com-fabrica-no-para-natura-aposta-naindustria-sustentavel/).
Fox, E., K. Shotton & C. Ulrich. 1995. SigmaStat Users Manual. Jandel Corporation, USA.
Hill, L.M., E.R. Morley-Smith & S. Rawsthorne. 2003. Metabolism of sugars in the endosperm of developing seeds of oilseed rape. Plant Physiol. 131: 228-236.
Homma, O., J. Furlan Junior, R.A. Carvalho & C.A.P. Ferreira. 2000. Bases para uma politica de desenvolvimento da cultura do dendezeiro na Amazonia, p.11-30. In I.J.M. Viegas & A.A. Muller (eds.). A cultura do dendezeiro na Amazonia brasileira. Embrapa Amazonia Oriental/Embrapa Amazonia Ocidental, Belem, Para, Brasil.
Kende, H. & J.A.D. Zeevart. 1997. The five classical plant hormones. Plant Cell 9: 1197-1210.
Koornneef, M., L. Bentsink & H. Hilhorst. 2002. Seed dormancy and germination. Curr. Opin. Plant Biol. 5: 33-36.
Ledo, A.S., K.K.P. Gomes, S.B.S.C. Barboza, G.S.S. Vieira, E.A. Tupinamba & W.M. Aragao. 2007. Cultivo in vitro de embrioes zigoticos e aclimatacao de plantulas de coqueiro-anao. PAB 42: 147-154.
Lopes, R., R.N.V. Cunha, M.R.L. Rodrigues, P.C. Teixeira, R.N.C. Rocha & W.A.A. Lima. 2008. Palmaceas, p. 767-786. In A.C.S. Albuquerque, A.G. Silva (eds.). Agricultura tropical: quatro decadas de inovacoes tecnologicas, institucionais e politicas. v. 1. Embrapa Informacao Tecnologica, Brasilia, DF, Brasil.
Murashige, T. & F. Skoog. 1962. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol. Plant 15: 473-497.
Natura. 2010. NaturaEkos. (Downloaded: March 1, 2010, www. naturaekos.com.br/pt/naturaekos/ cadeia-sustentavel/).
Nunes, C.D.M., D. Lima & R.N.V. Cunha. 1998. Germinacao de sementes de dende (Elaeis guineensis Jacq.), utilizando o metodo de calor seco. Instrucoes Tecnicas, 12. Embrapa Amazonia Ocidental, Manaus, Amazonas, Brasil.
Rabechault, H. & S. Cas. 1974. Recherches sur la culture in vitro des embryons de palmier a huile (Elaeis guineensis Jacq. var. dura Becc.). Oleagineux 29: 73-78.
Sanchez-Romero, C., R. Peran-Quesada, B. Marquez-Martin, A. Barcelo-Munoz & F. Pliego-Alfaro. 2007. In vitro rescue of immature avocado (Persea americana Mill.) embryos. Sci. Hort. 111: 365-370.
van Laere, K., J.M. van Huylenbroeck & E. van Bockstaele. 2007. Interspecific hybridization between Hibiscus syriacus, Hibiscus sinosyriacus and Hibiscus paramutabilis. Euphytica 155: 271-283.
Veiga, A.S., L. Smit & L.R.R. Furia. 2000. Avaliacao do dendezeiro como opcao para o sequestro de carbono na Amazonia, p. 125-144. In I.J.M. Viegas & A.A. Muller (eds.). A cultura do dendezeiro na Amazonia brasileira. Embrapa Amazonia Oriental/Embrapa Amazonia Ocidental, Belem, Para, Brazil.
Zhang, G.Q., W.J. Zhou, H.H. Gu, W.J. Song & E.J.J. Momoh. 2003. Plant regeneration from the hybridization of Brassica juncea and B. napus through embryo culture. J. Agron. Crop. Sci. 189: 347-350.
Paula Cristina da Silva Angelo, Larissa Alexandra Cardoso Moraes, Ricardo Lopes, Nelcimar Reis Sousa, Raimundo Nonato Vieira da Cunha & Regina Caetano Quisen
Researchers at Embrapa Western Amazon, Rodovia AM 010, km 29, CP 319, CEP 69010-970, Manaus-AM, Brazil; firstname.lastname@example.org, email@example.com, firstname.lastname@example.org, email@example.com, firstname.lastname@example.org, email@example.com
TABLE 1 Average values per experimental unit (absolute numbers) unit and the percentage of Elaeis guineensis x E. oleifera interspecific hybrid plantlets bearing shoots and radicles at least 2mm long in 50 days of in vitro cultivation (P1VC) Glucose g/l m/M Shoot Radicle Shoot + radicle (%) 30 165 4.533 a 3.333 a 66.66 20 110 4.867 a 3.367 a 73.34 10 55 4.933 a 1.467 b 29.34 Sucrose 30 87 3.533 a 1.677 a 33.54 20 58 2.400 b 0 b 0 10 29 2.800 ab 0.200 b 4.00 Values followed by the same letters in columns are statistically similar (Tukey test, p [greater than or equal to] 0.05). TABLE 2 Number of leaves (NL), length of the longest leaf (LL) and the longest root (LR) observed for Elaeis guineensis x E. oleifera interspecific hybrid plantlets during acclimatization Data At transfer NL mean [+ or -] SD 1.22 [+ or -] 0.52 min - max 1.0 - 4.0 LL mean [+ or -] SD 6.48 [+ or -] 2.28 (cm) min - max 1.5 - 13.0 LR mean [+ or -] SD 1.82 [+ or -] 1.81 (cm) min - max 0.2 - 11.3 43 DAT 100 DAT NL 1.73 [+ or -] 0.56 2.65 [+ or -] 0.68 1.0 - 3.0 1.0 - 4.0 LL 7.57 [+ or -] 3.35 13.93 [+ or -] 5.79 (cm) 1.0 - 20.0 1.0 - 23.5 LR NE NE (cm) 125 DAT NL 3.15 [+ or -] 0.81 1.0 - 4.0 LL 17.05 [+ or -] 6.03 (cm) 4.0 - 27.0 LR 11.33 [+ or -] 6.55 (cm) 1.0 - 28.0 OBS: DAT = days after transfer for acclimatization. NE = not evaluated.
|Printer friendly Cite/link Email Feedback|
|Author:||da Silva Angelo, Paula Cristina; Cardoso Moraes, Larissa Alexandra; Lopes, Ricardo; Reis Sousa, Nelc|
|Publication:||Revista de Biologia Tropical|
|Date:||Sep 1, 2011|
|Previous Article:||Soil seed bank and the effect of needle litter layer on seedling emergence in a tropical pine plantation.|
|Next Article:||Antioxidant and antitopoisomerase activities in plant extracts of some Colombian flora from La Marcada Natural Regional Park.|