首页> 美国卫生研究院文献>Journal of Genetic Engineering Biotechnology >Colchicine effect on the DNA content and stomata size of Glycyrrhiza glabra var.glandulifera and Carthamus tinctorius L. cultured in vitro
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Colchicine effect on the DNA content and stomata size of Glycyrrhiza glabra var.glandulifera and Carthamus tinctorius L. cultured in vitro

机译:秋水仙碱对甘草和红花的DNA含量和气孔大小的影响。

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摘要

In vitro induction of polyploids using colchicine causes an increase in DNA content in plants. This is of high importance especially for plants that have medicinal and commercial values. Seeds of two medicinal plants, licorice Glycyrrhiza glabra L. var.glandulifera and safflower Carthamus tinctorius were treated with different concentrations of colchicine, 0%, 0.03%, 0.05%, 0.08%, 0.1% (W/V) in vitro for 24 and 48 h. Treated seeds then were cultured on solid Murashige and Skoog (MS) media under controlled conditions. After a month, the length of the stomata was measured to study the effect of colchicine on stomata size. Cellular DNA content of the regenerated plants was measured by spectrophotometry. Flow cytometry was used for confirming the results obtained from stomata size measurement and spectrophotometry. Results suggested that treated plants have a fair amount of larger stomata, significantly in licorice plantlets that were treated with 0.1% colchicine for 24 h and safflower plantlets that were treated with 0.03%, 0.05% and 0.1% colchicine. Safflower DNA content in all treatments enhanced significantly, but in licorice only DNA content of plantlets that were treated with 0.05% colchicine for 24 h and 0.1%, 0.03% colchicine for 48 h found to be increased significantly. The morphological features of treated plantlets such as shoot and leaf thickness were found to be increased. Flow cytometry confirmed the previously mentioned results and suggested tetraploids in all treated safflower plantlets and licorice plantlets obtained from treatment with 0.08% of colchicine and mixoploids in licorice plantlets obtained from treatment with 0.1% of colchicine.
机译:使用秋水仙碱的多倍体的体外诱导导致植物中DNA含量的增加。这对于具有药用和商业价值的植物尤其重要。分别用0%,0.03%,0.05%,0.08%,0.1%(W / V)的秋水仙碱浓度分别对甘草甘草和红花红花这两种药用植物的种子进行体外处理24和48小时然后将处理过的种子在受控条件下在固体Murashige和Skoog(MS)培养基上培养。一个月后,测量气孔的长度以研究秋水仙碱对气孔大小的影响。通过分光光度法测量再生植物的细胞DNA含量。流式细胞术用于确认从气孔大小测量和分光光度法获得的结果。结果表明,处理过的植物有相当大的气孔,在用0.1%秋水仙素处理24小时的甘草苗和用0.03%,0.05%和0.1%秋水仙素处理的红花植物中,气孔明显更大。在所有处理中,红花的DNA含量均显着增加,但是在甘草中,仅用0.05%秋水仙碱处理24小时和0.1%,0.03%秋水仙碱处理48小时的幼苗的DNA含量显着增加。发现处理过的小植株的形态特征如芽和叶的厚度增加。流式细胞术证实了前面提到的结果,并建议在所有用0.08%秋水仙素处理的红花苗和甘草苗中的四倍体和在用0.1%秋水仙素处理的甘草苗中的四倍体。

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