Sahraroo Amir, Babalar Mesbah, Mirjalili Mohammad Hossein, Fattahi Moghaddam Mohammad Reza, Nejad Ebrahimi Samad
Department of Horticulture, Faculty of Agriculture, University of Tehran, Karaj, Iran.
Department of Agriculture, Medicinal Plants and Drugs Research Institute, Shahid Beheshti University, G. C., Evin, Tehran Iran.
Iran J Pharm Res. 2014 Fall;13(4):1447-56.
In the present study, an efficient protocol has been developed for callus induction and production of RA in callus culture of Satureja khuzistanica for the first time. In-vitro callus induction was achieved from young shoot tip explants cultured on MS and B5 media supplemented with different concentrations of IBA (0.1, 1.0, 2.0 and 5.0 mgL(-1)) solely or in combination with cytokinins BAP and KIN (1.0, 2.0 and 5.0 mgL(-1)). B5 medium supplemented with 1.0 mgL(-1) IBA plus 5.0 mgL(-1) BAP and MS medium fortified with 2.0 mgL(-1) IBA and 2.0 mgL(-1) BAP were the most favorable media for callus formation with the highest induction rate (96%). Maximum growth index (2.89 and 2.63) and maximum callus biomass (2.34 and 2.33 g fresh weight) were obtained from the callus cultured on B5 medium supplemented with 1.0 mgL(-1) IBA plus 5.0 mgL(-1) BAP and MS medium fortified with 1.0 mgL(-1) IBA plus 1.0 mgL(-1) KIN, respectively. Determination and quantification of RA in cultured calli were performed by HPLC UV/MS analysis. Calli induced from the plant and maintained on supplements of IBA and BAP in the absence of light produced RA 7.5% based on dry weight (DW). No differentiation was observed in any callus during the course of this study.
在本研究中,首次开发了一种高效方案,用于在胡齐斯坦鼠尾草愈伤组织培养中诱导愈伤组织并生产迷迭香酸(RA)。通过将幼嫩茎尖外植体培养在添加不同浓度吲哚丁酸(IBA,0.1、1.0、2.0和5.0 mgL(-1))单独或与细胞分裂素苄氨基嘌呤(BAP)和激动素(KIN,1.0、2.0和5.0 mgL(-1))组合的MS和B5培养基上,实现了体外愈伤组织诱导。添加1.0 mgL(-1) IBA加5.0 mgL(-1) BAP的B5培养基以及添加2.0 mgL(-1) IBA和2.0 mgL(-1) BAP的MS培养基是愈伤组织形成的最有利培养基,诱导率最高(96%)。分别从添加1.0 mgL(-1) IBA加5.0 mgL(-1) BAP的B5培养基和添加1.0 mgL(-1) IBA加1.0 mgL(-1) KIN的MS培养基上培养的愈伤组织中获得了最大生长指数(2.89和2.63)以及最大愈伤组织生物量(2.34和2.33 g鲜重)。通过高效液相色谱紫外/质谱分析对培养愈伤组织中的RA进行了测定和定量。在无光条件下,从植物诱导并在IBA和BAP补充剂上维持的愈伤组织产生了基于干重(DW)7.5%的RA。在本研究过程中,未在任何愈伤组织中观察到分化现象。