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Ultrastructural calli analysis of Inga vera Willd. subsp. Affinis (DC.) T.D. Penn

机译:Inga Vera Willd的超微结构Calli分析。亚普。 Affinis(DC。)T.D.Penn

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Subcellular changes are relevant to understand plant organogenesis and embryogenesis in the early stages of cell development. The cytology during cell development in tissue culture is however still poorly characterized. This study aimed to characterize the ultrastructural differences related to callogenesis of anthers, ovaries, leaf and nodal segments of Inga vera Willd. subsp. Affinis (DC.) T.D. Penn. Flower buds, nodal segments and leaves were disinfected and inoculated in test tubes containing MS medium with 3% sucrose and 4.5μM 2.4-D, except for leaf callogenesis, where 9μM of this auxin was used, and for the callogenesis of anthers and ovaries, where the culture medium was enriched with 0.25% activated charcoal and 90μM PVP. After 45 days in culture medium, the anther, ovary, leaf and nodal segment calli were fixed in Karnovisky and prepared for visualization by scanning and transmission electron microscopy. Ultrastructural differences were observed among the callus cells of anthers, ovaries, segments and leaves. There was no evidence of somatic embryo formation in the anther, leaf and nodal segment calli, in spite of some embryogenic characteristics in the cells. The ovary calli, with indications of embryo formation, seem to be the most responsive explant source for embryogenesis.
机译:亚细胞变化与植物有机组织和胚胎发生在细胞发育的早期阶段相关。然而,组织培养中细胞发育过程中的细胞学表征仍然很差。本研究旨在表征与Inga Vera Willd的花药,卵巢,叶片和节点段相关的超微结构差异。亚普。 Affinis(DC)T.D.Penn。在含有3%蔗糖的含有3%蔗糖和4.5μm2.4-d的试管中消毒并接种在含有3%蔗糖的试管中,除了叶胼un,其中使用了9μm,卵巢,富含0.25%活化的炭和90μmPVP的培养基。在培养基中45天后,在Karnovisky中固定花药,卵巢,叶子和节点愈伤组织,并准备通过扫描和透射电子显微镜进行可视化。在花药,卵巢,段和叶子的愈伤组织细胞中观察到超微结构差异。尽管细胞中有一些胚性特性,但在花药,叶和节点段愈伤组织中没有表现出细胞胚胎形成。卵巢Calli,胚胎形成的迹象,似乎是胚胎发生的最敏感的外植体源。

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