Silva Rafael de C, Camillo Julcéia, Scherwinski-Pereira Jonny E
Post-Graduate Program in Biotechnology, Federal University of Amazonas, 69077-000 Manaus, AM, Brazil.
Rev Biol Trop. 2012 Mar;60(1):473-82. doi: 10.15517/rbt.v60i1.2782.
Actually, the germplasm of Jatropha spp. is conserved as whole plants in field collections. Under this storage method, the genetic resources are exposed to disease, pest and natural hazards such as human error, drought and weather damage. Besides, field genebanks are costly to maintain and with important requirements of trained personnel. Thus, the development of efficient techniques to ensure its safe conservation and regeneration is therefore of paramount importance. In this work we describe a method for Jatropha curcas seeds cryoexposure and seedling recovery after thawed. In a first experiment, an efficient protocol for in vitro plant recovery was carried out using zygotic embryo or seeds with or without coat. In a second experiment, desiccated seeds with or without coat were exposed to liquid nitrogen and evaluated after cryoexposure. Germination percentages were variable among treatments, and seeds demonstrated tolerance to liquid nitrogen exposure under certain conditions. Seeds of J. curcas presented up to 99.6% germination after seed coat removal. Seeds with coat cultured in vitro did not germinate, and were 60% contaminated. The germination of the zygotic embryos was significantly higher in the 1/2 MS medium (93.1%) than in WPM medium (76.2%), but from zygotic embryo, abnormal seedlings reached up to 99%. Seeds with coat exposed to liquid nitrogen showed 60% germination in culture after coat removal with good plant growth, and seeds cryopreserved without coat presented 82% germination, but seedlings showed a reduced vigor and a significant increase in abnormal plants. Seeds cultured in vitro with coat did not germinate, independently of cryoexposure or not. This study reports the first successful in vitro seedling recovery methodology for Jatropha curcas seeds, after a cryopreservation treatment, and is recommended as an efficient procedure for in vitro plant recovery, when seeds are conserved in germplasm banks by low or cryotemperatures.
实际上,麻风树属植物的种质是以整株植物的形式保存在田间收集库中。在这种保存方法下,遗传资源会受到病虫害以及诸如人为失误、干旱和天气损害等自然灾害的影响。此外,田间基因库维护成本高昂,且对专业技术人员有重要要求。因此,开发高效技术以确保其安全保存和再生至关重要。在这项工作中,我们描述了一种麻疯树种子冷冻处理及解冻后幼苗恢复的方法。在第一个实验中,使用有胚乳或无胚乳的合子胚或种子进行了体外植株恢复的有效方案。在第二个实验中,将有或无种皮的干燥种子暴露于液氮中,并在冷冻处理后进行评估。不同处理间的发芽率各不相同,种子在某些条件下表现出对液氮暴露的耐受性。去除种皮后的麻疯树种子发芽率高达99.6%。带种皮在体外培养的种子未发芽,且污染率为60%。合子胚在1/2 MS培养基中的发芽率(93.1%)显著高于在WPM培养基中的发芽率(76.2%),但由合子胚发育而来的异常幼苗高达99%。带种皮暴露于液氮中的种子,去除种皮后在培养中的发芽率为60%,植株生长良好;无种皮冷冻保存的种子发芽率为82%,但幼苗活力降低,异常植株显著增加。带种皮在体外培养的种子,无论是否经过冷冻处理均未发芽。本研究报道了麻疯树种子冷冻保存处理后首次成功的体外幼苗恢复方法,当种子在种质库中通过低温或冷冻保存时,该方法被推荐为体外植株恢复的有效程序。