继代培养时间对抗性黑松体胚发生的影响

Effects of Subculture Time on Somatic Embryogenesis of Nematode-resistant Pinus thunbergii

  • 摘要: 以继代培养0.5、1.5 a和3.5 a的抗性黑松37#家系胚性愈伤组织为材料,观察不同培养时间胚性细胞的形态和体胚成熟的过程,并对愈伤组织的增殖率、每克愈伤形成的体胚数量及体胚萌发率和植株成活率进行测定。结果表明:在继代培养过程中,胚性胚柄细胞团(ESM)结构逐渐疏松,胚柄细胞呈现缩短、增粗的现象;培养时间对抗性黑松愈伤组织的增殖、分化、体胚萌发及植株成活率均有显著影响。3种不同培养时间愈伤组织的增殖率分别为200.37%、182.47%和111.63%,每克胚性愈伤组织形成成熟体细胞胚分别为77、31、5个,萌发率分别为84.43%、51.10%、11.13%;植株成活率分别为73.00%、50.00%、6.70%,均呈下降趋势;3种愈伤体胚成熟的时间也存在显著差异,继代培养时间越长,体胚分化成熟过程越慢,愈伤组织形成子叶胚的时间最短为46 d,最长为74 d。因此,抗性黑松胚性愈伤组织在继代培养过程中胚性逐步降低,体胚发生和植株再生能力下降,短期培养的胚性愈伤组织(0.5 a)为抗性黑松体胚发生较为理想的初始材料,且愈伤组织继代培养时间不宜超过1.5 a。

     

    Abstract: The callus of 37#family used for the experimentwas cultured for 0.5 years,1.5 years and 3.5 years, respectively. During this period, the cell morphology and the maturation stage of somatic embryos were observed. In addition, the proliferation rate, the number of somatic embryos per gram of embryonic callus, the normal germination rate and survival rate of plants were measured. The results revealed that embryonic somatic mass (ESM) gradually became loose and cell stalk was short, thick and deformed in the long-term subculture process. The time of subculture had significant effects not only on the proliferation and differentiation of callus but also somatic embryo germination and survival rate of plants. The proliferation rate of 3 kinds callus was 200.37%, 182.47% and 111.63%, the number of somatic embryos was 77, 31 and 5, the normal germination rate was 84.43%, 51.10% and 11.13%, and the survival rate of plants was 73.00%, 50.00% and 6.70%, respectively, all showing a downward trend. Additionally, there were significant differences in the time of embryo maturation among 3 kinds callus. The callus formed the cotyledon embryo for a minimum of 46 days and a maximum of 74 days. As the subculture time increased, the process of somatic embryo differentiation became slower and slower. It can be seen that the potential of embryogenic callus of nematode-resistant Pinus thunbergii was gradually reduced and the abilities of somatic embryogenesis and plants regeneration were decreased during the subculture. And the short-term cultured embryogenic callus (0.5 years) was an ideal starting material for somatic embryogenesis of nematode-resistant P. thunbergii, and the callus culture time should be less than 1.5 years.

     

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