In vitro conservation of mangaba (Hancornia speciosa Gomes): An important fruit tree of Brazilian Cerrado

D. C. M. Pires, S. A. Asmar, J. M. Luz, M. Pasqual, R. A. L. S. Rezende, J. Dória
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Abstract

This study aimed at evaluating the effect of osmotic agents, sucrose, and abscisic acid on the in vitro conservation of mangaba trees by slow growth. Two experiments were carried out. Nodal segments were inoculated in the MS medium with the addition of 1) osmotic agents (15, 20, and 25 g L-1 of mannitol and 10, 20, and 40 g L-1 of sorbitol) + control; 2) sucrose (0, 10, 20 and 30 g L-1) and abscisic acid – ABA (0 and 0.5 mg L-1). After carrying out the experiments, both were performed again, this time with the addition of 2 g L-1 activated charcoal to the medium for comparison. The survival rate and number of green leaves were evaluated after 45 and 90 days. For growth recovery, the explants were transferred to a specific growth medium, consisting of MS medium supplemented with 7 g L-1 agar, 1 mg L-1 6-benzylaminopurine (BAP), 1 mg L-1 1-naphthaleneacetic acid (NAA), 2 g L-1 activated charcoal. At 60 days, survival rate, number of green leaves, number of nodes, shoot length and fresh weight of the explants were assessed. The results showed that the use of 2 g L-1 of activated charcoal improves the growth and development of the explants. The tested doses of osmotic agents also did not influence the evaluated characteristics. However, there was significant effect of osmotic agent and time on survival rate and treatment x time interaction for the number of green leaves, having been influenced also by the use of osmotic agent at 45 days, in addition to significant differences between the control and the other treatments for this characteristic. The osmotic agents were not effective in plant conservation as well as the use of ABA. According to the conditions of this study, it is recommended the use of 30 g L-1 sucrose to the culture medium for up to 90 days in a row of in vitro conservation of mangaba plants.
巴西塞拉多一种重要果树芒果树的离体保护
本研究旨在探讨渗透剂、蔗糖和脱落酸对孟加板树体外缓生长保护的影响。进行了两个实验。在MS培养基中接种节段,加入1)渗透剂(15、20、25 g L-1甘露醇和10、20、40 g L-1山梨醇)+对照;2)蔗糖(0、10、20和30 g L-1)和脱落酸- ABA(0和0.5 mg L-1)。实验完成后,再次进行实验,这次在培养基中加入2g L-1活性炭进行比较。45 d和90 d后分别测定植株成活率和绿叶数。为了恢复生长,将外植体转移到特定的生长培养基中,该培养基由MS培养基添加7 g L-1琼脂,1 mg L-1 6-氨基嘌呤(BAP), 1 mg L-1 1-萘乙酸(NAA), 2 g L-1活性炭组成。60 d时,测定外植体的成活率、绿叶数、节数、茎长和鲜重。结果表明,使用2 g L-1的活性炭可促进外植体的生长发育。渗透剂的测试剂量也不影响所评估的特性。然而,渗透剂和时间对存活率和处理x时间互作对绿叶数有显著影响,在45天渗透剂的使用也有影响,除了对照和其他处理在这一特性上有显著差异外。渗透剂对植物保护和ABA的利用效果不佳。根据本研究条件,推荐在培养基中添加30 g L-1蔗糖,连续培养达90天。
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