Department of Plant Biology, Faculty of Sciences, University of Damascus, Damascus, Syria.
Department of Biotechnology, Faculty of Applied Sciences, University of Kalamoon, Damascus Countryside, Deirattiah, Syria.
Saudi J Biol Sci. 2014 Sep;21(4):317-23. doi: 10.1016/j.sjbs.2013.12.002. Epub 2014 Jan 3.
Ziziphora tenuior L. (Lamiaceae) is an aromatic herb used for its medicinal values against fungi, bacteria. Micropropagation can be used for large-scale multiplication of essential oil producing plants thus avoiding an overexploitation of natural resources. This work aims to develop a reliable protocol for the in vitro propagation of Z. tenuior, and to compare the antioxidant activity between in vitro propagated and wild plants. The explants were sterilized and cultured on MS medium containing different concentrations of growth regulators naphthalene acetic acid (NAA) or indole-3-butyric acid (IBA) with 0.5 mg/L of kinetin (Kin) callus formation was 70.2% after 45 days of incubation in dark on medium supplemented with 1.5 mg/L of NAA. After one month of callus culture on medium supplemented with 2 mg/L BA the shoot number was 5.12 and for the multiplication stage. The shoot number was 4.21 and length was 6.17 cm on medium supplemented with 1 mg/L Kin + 0.1 mg/L NAA. DPPH• reagent was used to test the antioxidant activity. The aqueous and methanol extracts of in vitro plants which were treated with 1.5 and 1 mg/L of kin plus 0.1 mg/L of NAA showed a strong DPPH• scavenging activity where IC50 was 0.307 and 0.369 mg/ml, respectively, while the IC50 of aqueous and methanol extracts of wild plants was 0.516 and 9.229 mg/ml, respectively. Our results suggested that plant growth regulators and in vitro culture conditions increased the antioxidant activity.
荆芥(唇形科)是一种芳香草本植物,具有抗真菌、细菌的药用价值。微繁殖可用于大规模繁殖产生精油的植物,从而避免对自然资源的过度开发。本工作旨在建立荆芥离体繁殖的可靠方案,并比较体外繁殖和野生植物的抗氧化活性。外植体经消毒后在含有不同浓度萘乙酸(NAA)或吲哚丁酸(IBA)的 MS 培养基上培养,加入 0.5 mg/L 的激动素(Kin),在黑暗中培养 45 天后,愈伤组织形成率为 70.2%。在添加 1.5 mg/L NAA 的培养基上培养一个月的愈伤组织后,每个培养物的芽数为 5.12 个,用于增殖阶段。在添加 1 mg/L Kin + 0.1 mg/L NAA 的培养基上,芽数为 4.21 个,长度为 6.17 cm。DPPH•试剂用于测试抗氧化活性。用 1.5 和 1 mg/L Kin + 0.1 mg/L NAA 处理的体外植物的水提物和甲醇提取物表现出很强的 DPPH•清除活性,IC50 分别为 0.307 和 0.369 mg/ml,而野生植物的水提物和甲醇提取物的 IC50 分别为 0.516 和 9.229 mg/ml。我们的结果表明,植物生长调节剂和体外培养条件增加了抗氧化活性。