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Types and concentrations of cytokinins in the micropropagation of Anthurium maricense

机译:桃红掌微繁殖中细胞分裂素的类型和浓度

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Faced with the demand for plants potted for their foliage, Anthurium maricense is seen as a viable option. However, most of the studies on obtaining micropropagated plantlets are for A. andraeanum, with nothing yet reported for A. maricense. The aim of this study therefore, was to evaluate the effect of four cytokinins in different concentrations, on the in vitro induction of shoots from nodal segments of A. maricense. The experimental design was completely randomised in a 4 x 4 factorial scheme, with four cytokinins (BAP, ZEA, CIN and 2iP) and 4 concentrations (0, 2.22, 4.44 and 6.66 μM), for a total of 16 treatments, with 6 replications of five test tubes, and using one nodal segment. Cultures were kept in a growth room at 25 ± 2°C, a photoperiod of 16 h and a light intensity of 30 μmolm-2 s-1 for 60 days. After this period, the number of shoots formed per node was evaluated. The addition of a cytokinin to the culture medium was determinant for the in vitro regeneration of shoots in A. maricense. The greatest estimated number of shoot formations in A. maricense were obtained in the culture media containing ZEA (3.87) and BAP (3.30), both at concentration of 6.66 μM.
机译:面对盆栽植物的需求,红掌被认为是可行的选择。但是,大多数获得微繁苗的研究都是针对红曲霉的,尚未报道过有关地中海蓟的报道。因此,本研究的目的是评估四种浓度不同的细胞分裂素对离体从A. maricense的芽诱导的体外作用。实验设计以4 x 4因子分解方案完全随机化,使用四种细胞分裂素(BAP,ZEA,CIN和2iP)和4种浓度(0、2.22、4.44和6.66μM)进行总共16种治疗,重复6次五支试管,并使用一个节段。将培养物在25±2°C,光周期为16 h,光强度为30μmolm-2s-1的生长室中放置60天。在这段时间之后,评估每个结点形成的芽数。向培养基中添加细胞分裂素是决定拟南芥中芽的体外再生的决定因素。在含有ZEA(3.87)和BAP(3.30)的培养基中,均以6.66μM的浓度获得了估计的褐飞曲霉芽形成的最大数量。

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