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中国农学通报 ›› 2011, Vol. 27 ›› Issue (13): 121-125.

所属专题: 生物技术

• 林学 园艺 园林 • 上一篇    下一篇

甘草不同时期愈伤组织细胞形态与线粒体变化的研究

曹君迈 张欣 刘建利 郑素娇   

  • 收稿日期:2010-09-15 修回日期:2010-10-13 出版日期:2011-06-05 发布日期:2011-06-05
  • 基金资助:

    宁夏自然科学基金甘草脱分化过程中细胞结构变化的研究

Study on Change Cell Morphology and Mitochondria from Different Callus Licorice in Different Culture Stage

  • Received:2010-09-15 Revised:2010-10-13 Online:2011-06-05 Published:2011-06-05

摘要:

此实验为甘草愈伤组织继代培养和进一步研究提供方法依据。以乌拉尔甘草不同来源愈伤组织为材料,采用石蜡切片法观察了不同时期甘草愈伤组织细胞大小变化;采用悬滴法观察了不同时期甘草愈伤组织线粒体形态、大小变化。试验结果表明:愈伤组织细胞大小受外植体来源影响显著(P<0.05),芽来源愈伤组织细胞大小(均值31.40 μm)大于叶来源愈伤组织细胞大小(均值29.41 μm)且大于根来源愈伤组织细胞大小(均值25.67 μm);愈伤组织细胞大小受培养时期影响极显著(P<0.01),培养到30天时细胞达最大,均值为37.45 μm,之后到40天时,细胞平均减小到29.55 μm。芽和叶来源愈伤组织细胞内的哑铃状线粒体数目高于根来源愈伤组织细胞内的哑铃状线粒体数目。愈伤组织细胞线粒体大小与外植体来源及培养时期有显著交互作用(P<0.05),根来源愈伤组织在培养30天时线粒体长度均值最大,达2.60 μm。芽来源愈伤组织在培养40天时线粒体长度均值最大,达2.07 μm。叶来源愈伤组织在细胞培养40天时线粒体长度均值最大,达2.01 μm;培养时期对愈伤组织细胞线粒体大小影响极显著(P<0.01),培养到30天时细胞最大,均值为2.06 μm。此研究结果,为甘草愈伤组织继代培养奠定了基础,同时为甘草脱分化及再分化调控提供细胞学方面的依据。

关键词: 有机肥 钾肥 水稻 土壤供钾能力, 有机肥 钾肥 水稻 土壤供钾能力

Abstract:

The experiment provided the method basis for the Glycyrrhiza uralensis callus’ subculture and further studies. Taking callus from different sources of Glycyrrhiza uralensis as trial material, the cell size of callus in different culture stages were observed with paraffin section, and the changes of mitochondria shape and the size from Glycyrrhiza uralensis callus in the different culture stages, was observed with pendent drop. The results showed that the length of cell from callus had a significant effect on source of explant (P<0.5), the length of cell from leaf callus (average 29.41 μm) was greater than from rhizome’s (average 25.67 μm), but was smaller than from bud’s (average 31.40 μm). The length of cell from callus had a very significant effect on their development stages(P<0.01), the largest cell (average 37.45 μm) appeared after 30 days’ culture, and then reduce ,when cultured 40 days, the average length was reduced to 29.55μm.The number of dumbbelllike mitochondria in the cell from bud and leaf callus was more than rhizome’s. It had a notable interaction in size of mitochondria, the source of explant and the period of culture (P<0.05). The length of mitochondria from rhizome callus was 2.60 μm (maximum) after 30 days’ culturing, while bud’ 2.07 μm and leaf’ 2.01 μm after 40 days’ culturing. The culture stage had a very significant effect on the size of mitochondria (P<0.01), when 30 days’ cultivation, the average length of cell can reach to 2.06 μm (maximum). This finding laid the foundation for Glycyrrhiza uralensis callus successive subculture, simultaneously to provide the cytology aspect basis for differentiation and the redifferentiation for the Glycyrrhiza uralensis.

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