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首页> 外文期刊>Journal of Applied Phycology >Callus ontogeny of the Kappaphycus alvarezii (Rhodophyta, Gigartinales) brown tetrasporophyte strain
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Callus ontogeny of the Kappaphycus alvarezii (Rhodophyta, Gigartinales) brown tetrasporophyte strain

机译:Kappaphycus alvarezii(Rhodophyta,Gigartinales)棕色四孢子体菌株的愈伤组织个体

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This study analyzes the callus ontogeny of the Kappaphycus alvarezii brown strain tetrasporophyte using micropropagation and tissue culture. Calli were induced from axenic explants and grown for 2 months. Ontogenic analysis was made in explants collected from days 7 to 60 of culture and observed under light and transmission electron microscopy (TEM). At the end of the experimental period, 60-day samples were also analyzed by confocal microscopy. Formation of calli was initiated in the first week from medullary and cortical cells of the explant region in air contact. Alterations in the apical region of the cells were observed in TEM as cell wall thickening, proliferation of convoluted membranes, increased number of mitochondria and chloroplast alterations, indicating the dedifferentiation of these cells. Throughout the experiment, the thick cell wall of the cells which compose callus filaments showed the presence of acidic polysaccharides, suggesting a large amount of carrageenan and neutral polysaccharides. The cytoplasm showed the following main characteristics: large amount of starch grains, presence of chloroplasts with altered plastoglobules, as well as disorganized thylakoids, presence of several convoluted membranes, and vacuoles. These filaments maintained their uniseriate organization and irregular branching with many intercellular connections between them. Despite the initial stress caused by explant isolation and the beginning of callus formation, results showed that filaments were capable of reorganization and development, retaining their dedifferentiated cells, which, in turn, strongly suggested the potential of callus-based micropropagation.
机译:本研究利用微繁殖和组织培养技术分析了阿尔伯卡氏菌棕色菌株四孢子体的愈伤组织发生。从树莓外植体中诱导出愈伤组织,并使其生长2个月。在从培养的第7至60天收集的外植体中进行本体分析,并在光学和透射电子显微镜(TEM)下观察。在实验期结束时,还通过共聚焦显微镜分析了60天的样品。愈伤组织的形成在第一周从与空气接触的外植体区域的髓样和皮质细胞开始。在TEM中观察到细胞顶部区域的改变,如细胞壁增厚,回旋膜的增殖,线粒体数目增加和叶绿体改变,表明这些细胞的去分化。在整个实验过程中,组成愈伤组织细丝的细胞的厚细胞壁显示出酸性多糖的存在,表明存在大量的角叉菜胶和中性多糖。细胞质显示以下主要特征:大量淀粉粒,叶绿体的质体球发生改变,类囊体紊乱,存在数个回旋的膜和液泡。这些细丝保持其单一的组织和不规则的分支,并在它们之间具有许多胞间连接。尽管外植体分离和愈伤组织形成开始引起了最初的压力,但结果表明,细丝能够重组和发育,并保留其去分化细胞,这反过来又暗示了基于愈伤组织的微繁殖的潜力。

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