九重葛悬浮液栽培的细胞形态

Christian Marely Rodriguez-Salazar, José Roman-Reynosa, S. V. Ávila-Reyes, Franklin Loring-Younce, A. Jiménez–Aparicio, S. Evangelista-Lozano
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摘要

这项工作的目的是描述的主要细胞形式的生长动力学阶段在九重葛品种的惊喜悬浮培养。在Murashige和Skoog (MS)基础培养基中添加6种不同浓度和组合的植物生长调节剂(VGR)型生长素(2,4- d和NAA)和细胞分裂素(BAP) (0.2 ~ 5.3 mg/L)和对照。在MS固体培养基中,以植酸酯为胶凝剂,以2.2 g/L的胶凝量培养叶片外植体,获得脆性愈伤组织。取部分愈伤组织(1.0 g)作为细胞接种物,在控制条件(50 mL, 120 rpm, 25℃,48 μmol m/s发光强度)下培养。BAP与NAA的激素关系为2:1,鲜重产量在1.7905 ~ 5.8340 g之间,占70%左右,差异显著(p≤0.05)。鲜重曲线0 ~ 14 d为适应期;第14天到第19天是指数阶段,第21天是递减阶段。适应期细胞形态以细长细胞为主,少数呈球状,少数呈肾状。在指数期,这些细胞形成球状细胞的小聚集体。死亡期细胞呈褐色、伸长、破损、碎裂。利用这些数据,可以确定在新鲜培养基中的继代时间。
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Cellular Forms in Cultivation in Suspension of Bougainvillea glabra Choisy Variety Surprise
The objective of this work was to describe the predominant cell forms in the phases of growth kinetics in a suspension culture of the Bougainvillea glabra Choisy variety Surprise. Treatments in suspension with Murashige and Skoog (MS) basal culture medium were supplemented with six different concentrations and combinations of vegetable growth regulator (VGR) of type auxin (2,4-D and NAA) and cytokinin (BAP) (0.2-5.3 mg/L) and a control. Friable callus was obtained from leaf explants ex vitro to in vitro culture in solid MS medium using Phytagel as gelling agent to 2.2 g/L. A portion of callus (1.0 g) was used as cellular inoculum and grown under controlled conditions (50 mL, 120 rpm, 25 °C and luminous intensity of 48 μmol m/s). The best treatment with significant differences (p ≤ 0.05) were with a hormonal relation of 2:1 of BAP and NAA, respectively, with a fresh weight yield ranging from 1.7905 g to 5.8340 g, which represents around 70%. An adaptation phase was observed from day 0 to day 14 on the curve of fresh weight; an exponential phase at day 14 to day 19 and a declination phase at day 21. Cellular forms in the adaptation phase were elongated cells, a few globular and a few with kidney shape. In the exponential phase, these cells formed small aggregates of globular cells. In the death phase, brown, elongated, damaged and fragmented cells were found. Whit this data obtained it is possible to establish the subculture time in fresh medium.
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