沙巴蛇草(Clinacanthus nutans)流式细胞仪优化方案和基因组大小估计

Kandaiah Vidhyaini, Singaram Nallammai, Isparan Kandasamy Kodi
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引用次数: 1

摘要

胡桃木是一种经济上重要的药用植物,在亚洲地区的许多国家都有种植。抗癌、抗菌和抗病毒等有用的药物特性,加上其高含量的植物化学化合物,如卵黄蛋白、异卵黄蛋白、豆甾醇和羽扇豆醇,增加了市场对坚果的需求。使用新鲜样品对其含量和药理活性进行了广泛的研究,但对坚果梭菌体外培养的研究有限。目前尚未对坚果C.nutans进行基因组大小估计。本研究的目的是用流式细胞术分析坚果核DNA的含量。制备不同的细胞核分离缓冲液,并用碘化丙啶进行化学计量DNA染色。以Glycine max cv.Polanka为内标,对坚果C.nutans的基因组大小进行了估算,并将其与离体植株进行了比较。流式细胞仪分析表明,坚果细胞核2C DNA含量估计为1.75±0.006pg。流式细胞术分析的变异系数在5%以内,表明结果是可靠的,Tris.MgCl2是最佳的细胞核分离缓冲液。在野外生长和体外培养的坚果中没有观察到显著差异。这一发现将有助于进一步进行Clinacanthus spp.的基因组大小进化分析,并确定活性化合物和生物量增加的多倍体。在不同的日子进行复制。在所有实验中,测量了至少5000个核至10000个核的荧光。从皮克(pg)到碱基对数的转换如下:1 pg DNA相当于0.978×109bp(Dolezel等人,2007)。结果采用SPSS 25版单因素方差分析(ANOVA)进行分析。为了获得显著效果,进行了Tukey的成对比较,p值≤0.05。。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Optimized flow cytometric protocol and genome size estimation of Sabah snake grass (Clinacanthus nutans)
Clinacanthus nutans is an economically important medicinal plant that can be found grown in many countries in the Asian region. Useful medicine properties such as anti-cancer, anti-bacteria, and anti-viral, backed by its high content of phytochemical compounds such vitexin, isovitexin, stigmasterol and lupeol has increased the demand for C. nutans in the market. Extensive work had been carried out on its content and pharmacological activity using fresh samples but limited studies for in vitro cultures of C. nutans . No genome size estimation has been done for C. nutans . Objective of this study was to analyse nuclear DNA content of C. nutans using flow cytometry. Preparation of different nuclei isolation buffer and stoichiometric DNA staining using propidium iodide was carried out. The genome size of C. nutans was estimated using Glycine max cv. Polanka as internal standard and its genome size was compared with in vitro plantlets of C. nutans. Flow cytometry analysis revealed that nuclear 2C DNA of C. nutans content is estimated at 1.75 ± 0.006 pg. Coefficient of variation in flow cytometric analysis was within the limit of 5% implying that the results were reliable with the Tris.MgCl 2 being the best nuclei isolation buffer. No significant difference was observed from field grown and in vitro C. nutans . This finding will assist further in genome size evolution analysis of Clinacanthus spp. and to determine polyploids for increased active compounds and biomass. replicate being performed on different days. In all the experiments, the fluorescence of at least 5000 nuclei to 10000 nuclei was measured. Conversion from picograms (pg) to base pair numbers was done as follows: 1 pg DNA is equivalent to 0.978 × 10 9 bp (Dolezel et al., 2007). The results were analysed using one way analysis of variance (ANOVA) using SPSS version 25. For significant effect, Tukey’s pairwise comparison was carried out with p value ≤ 0.05..
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