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首页> 外文期刊>Physiology and Molecular Biology of Plants >Evaluation of in vitro shoot multiplication and ISSR marker based assessment of somaclonal variants at different subcultures of vanilla (Vanilla planifolia Jacks)
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Evaluation of in vitro shoot multiplication and ISSR marker based assessment of somaclonal variants at different subcultures of vanilla (Vanilla planifolia Jacks)

机译:基于体外拍摄倍增和基于ISSR标记的Somaclonal变体评估(Vanilla Planifolia Jacks)

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摘要

The effect of subculture cycles on somaclonal variation of V. planifolia using intersimple sequence repeat (ISSR) markers was analyzed. Nodal segments of 2 cm in length were established in vitro and multiplied by 10 subculture cycles in Murashige andSkoog (MS) medium supplemented with 8.86 uM BAP (benzylaminopurine). After 45 days in each culture, the length and number of shoots per explant were evaluated. For ISSR markers, ten shoots per each subculture and the mother plant were used. Ten ISSR primers were used and a total of 118 bands were obtained. The polymorphism (%) was calculated and a dendrogram based on Jaccard's genetic distance between the subcultures and the donor plant was obtained. These results show that the multiplication rate tendsto increase until subculture five, whereas shoot length decreases as the number of subcultures increases. The ISSR markers revealed an increase in the polymorphism percentage after the fifth culture cycle. The dendrogram showed the formation of two groups. The first group, with less genetic variability, is the donor plant andsubcultures 1-5; the second group has greater genetic distance and is formed by subcultures 6-10. The results revealed that the number of subcultures with 8.86 uM BAP is a factor that affects the somaclonal variation during in vitro regeneration of V. planifolia. In conclusion, the subculture number affects somaclonal variation and in vitro development of V. planifolia.
机译:分析了亚栽培循环对使用晶序列重复(ISSR)标记的Plaifolia糖髓变化的影响。在体外建立2厘米的节点段,并在Murashige和Skoog(MS)培养基中乘以10.86μmBap(苄氨基嘌呤)的10个脱殖民科循环。每种培养45天后,评估每种外植体的芽的长度和数量。对于ISSR标记,使用每种亚栽培的10个芽和母植物。使用十个ISSR引物,并获得118个带。计算多态性(%),得到基于jaccard之间的jaccard与供体植物之间的遗传距离的树枝图。这些结果表明,随着延长次数的增加,繁殖率倾向于增加,而射击长度降低。 ISSR标记显示第五培养循环后多态性百分比的增加。树枝图显示两组的形成。遗传变异性较少的第一组是施主植物和大草1-5;第二组具有更大的遗传距离,并通过推子6-10形成。结果表明,具有8.86μmBap的传代培养物的数量是影响V.Plinifolia体外再生过程中的糖髓变化的因素。总之,亚栽培号影响V.Plinifolia的糖髓变异和体外发育。

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