冷冻观察青木木瓜的体外受精芽与Pvs2的水合物、装货和脱水处理及其修改

Fitriyana Wardani, J. Witono, Darda Efendi, D. Dinarti
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摘要

木瓜是一种开放授粉的植物,其基因型和表型很容易因环境变化而改变,因此具有很高的遗传变异性。低温保存是一种在液氮(-196℃)中保存种质资源的方法,可以保持种质资源的基因型和表型。本实验旨在获得番木瓜‘Sukma’离体苗的最佳预培养、装载和脱水条件。在预培养中,我们将幼芽种植在含有0.3 M和0.4 M蔗糖的MS培养基上,分别种植1、2和3天。在加载处理中,我们将嫩枝浸泡在加载液(液体MS+1.2M甘油+0.4M蔗糖)中,分别浸泡0、10、20、30分钟。为了脱水,我们将嫩枝浸泡在冷冻保护剂(PVS2及其改性剂)中5分钟、10分钟和15分钟。然后,将芽浸泡在液氮中。结果表明,芽在添加0.3 M蔗糖的MS培养基上预培养3 d,成活率最高。最佳加载处理时间为20 ~ 30分钟。PVS2改性10 min为最佳脱水处理。冷冻保存后的嫩枝无法恢复,因此可以得出结论,体外木瓜Sukma嫩枝的冷冻保存尚未成功。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kriopreservasi Tunas in Vitro Pepaya ‘Sukma’ Dengan Perlakuan Prakultur, Loading, Dan Dehidrasi Dengan Pvs2 Dan Modifikasinya
Papaya has high genetic variability because it is an open-pollinated plant and has genotype and phenotypeare that are easily changed due to environment changes. Cryopreservation is a storing method of germplasm in liquid nitrogen (-196 oC) which can maintain the genotype and phenotype of germplasm. The experiment aimed to obtain the best preculture, loading, and dehydration for cryopreservation of papaya ‘Sukma’ in vitro shoots. For preculture, we planted shoots on MS media with 0.3 M and 0.4 M sucrose for 1, 2, and 3 days. In the loading treatment, we immersed shoots in loading solution (liquid MS+1.2M glycerol+0.4M sucrose) for 0, 10, 20, and 30 minutes. For dehydration, we immersed shoots in cryoprotectant (PVS2 and its modification) for 5, 10, and 15 minutes. Then, shoots were immersed in liquid nitrogen. The results showed thatshoots had the best survival rate while they had been precultured on MS medium with 0.3 M sucrose for 3 days. The best loading treatment time was 20–30 minutes. The best dehydration treatment was obtained by modification of PVS2 for 10 minutes. The shoots have not been able to recovery after cryopreservation, so it can be concluded that cryopreservation of in vitro papaya ‘Sukma’ shoots has not been successful.
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