Initiation of coconut cell suspension culture from shoot meristem derived embryogenic calli: A preliminary study

U. Bhavyashree, K. Jayaraj, K. S. Muralikrishna, K. K. Sajini, M. K. Rajesh, A. Karun
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引用次数: 3

Abstract

An attempt was made to establish highly competent embryogenic cell suspension culture in coconut, a species recalcitrant to in vitro culture. Embryogenic calli were initiated from shoot meristem explants of coconut. Y3 medium supplemented with 2.4-D (4.5 μM) and glutamine (34.2 μM) was found to be the best medium to initiate cell suspension. Growth evaluation was done by packed cell volume (PCV) and it was found that maximum growth volume of 9.9% was reached at 200 days of culture initiation. About 52% of viable cells were detected through fluorescent microscopy. Cell aggregation was noticed in Y3 medium supplemented with glutamine (34.2 μM), malt extract (100mg/l), biotin (40.9 μM) and kinetin (9.3 μM), but further progress could not be achieved. It was also observed that embryogenic calli were not of a friable type, but were associated with densely aggregated cells. Because of its hard nature, we were unsuccessful to obtain high quality cell suspension.
椰芽分生组织胚性愈伤组织悬浮培养的初步研究
在对离体培养有抗性的椰子中,建立了高能力的胚性细胞悬浮培养。以椰子茎部分生组织为外植体,培养出胚性愈伤组织。发现添加2.4-D (4.5 μM)和谷氨酰胺(34.2 μM)的Y3培养基是引发细胞悬浮的最佳培养基。用填充细胞体积法(PCV)对其生长进行评价,发现在培养开始200 d时,其最大生长量达到9.9%。荧光显微镜检测到约52%的活细胞。在添加谷氨酰胺(34.2 μM)、麦芽提取物(100mg/l)、生物素(40.9 μM)和动素(9.3 μM)的Y3培养基中发现细胞聚集,但未见进一步进展。胚性愈伤组织不是易碎型,而是由密集聚集的细胞组成。由于其坚硬的性质,我们未能获得高质量的细胞悬液。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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