Institutional Repository of Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences
Assembly of the protoplasm of Codium fragile (Bryopsidales, Chlorophyta) into new protoplasts | |
Li, Demao1,3,4; Lue, Fang1,4; Wang, Guangce1,2; Zhou, Baicheng1 | |
2008-06-01 | |
发表期刊 | JOURNAL OF INTEGRATIVE PLANT BIOLOGY |
ISSN | 1672-9072 |
卷号 | 50期号:6页码:752-760 |
文章类型 | Article |
摘要 | The cell organelles of the coenocytic alga Codium fragile (Sur.) Hariot aggregated rapidly and protoplasts were formed when its protoplasm was extruded out in seawater. Continuous observation showed that there were long and gelatinous threads connecting the cell organelles. The threads contracted, and thus the cell organelles aggregated into protoplasmic masses. The enzyme digestion experiments and Coomassie Brilliant Blue and Anthrone stainings showed that the long and gelatinous threads involved in the formation of the protoplasts might include protein and saccharides as structure components. Nile Red staining indicated that the protoplast primary envelope was non-lipid at first, and then lipid materials integrated into its surface gradually. The fluorescent brightener staining indicated that the cell wall did not regenerate in the newly formed protoplasts and they all disintegrated within 72 h after formation. Transmission electron microscopy of the cell wall of wild C. fragile showed electron-dense material embedded in the whole cell wall at regular intervals. The experiments indicated that C. fragile would be a suitable model alga for studying the formation of protoplasts.; The cell organelles of the coenocytic alga Codium fragile (Sur.) Hariot aggregated rapidly and protoplasts were formed when its protoplasm was extruded out in seawater. Continuous observation showed that there were long and gelatinous threads connecting the cell organelles. The threads contracted, and thus the cell organelles aggregated into protoplasmic masses. The enzyme digestion experiments and Coomassie Brilliant Blue and Anthrone stainings showed that the long and gelatinous threads involved in the formation of the protoplasts might include protein and saccharides as structure components. Nile Red staining indicated that the protoplast primary envelope was non-lipid at first, and then lipid materials integrated into its surface gradually. The fluorescent brightener staining indicated that the cell wall did not regenerate in the newly formed protoplasts and they all disintegrated within 72 h after formation. Transmission electron microscopy of the cell wall of wild C. fragile showed electron-dense material embedded in the whole cell wall at regular intervals. The experiments indicated that C. fragile would be a suitable model alga for studying the formation of protoplasts. |
关键词 | Codium Fragile Protoplasm Protoplast Cell Wall |
DOI | 10.1111/j.1744-7909.2008.00671.x |
URL | 查看原文 |
收录类别 | SCI |
语种 | 英语 |
WOS记录号 | WOS:000256532500014 |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | http://ir.qdio.ac.cn/handle/337002/6286 |
专题 | 实验海洋生物学重点实验室 |
作者单位 | 1.Chinese Acad Sci, Inst Oceanol, Qingdao 266071, Peoples R China 2.Tainjin Univ Sci & Technol, Coll Marine Sci & Engn, Tianjin 300457, Peoples R China 3.Liaocheng Univ, Coll Agr, Dept Food Sci, Liaocheng 252059, Peoples R China 4.Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China |
第一作者单位 | 中国科学院海洋研究所 |
推荐引用方式 GB/T 7714 | Li, Demao,Lue, Fang,Wang, Guangce,et al. Assembly of the protoplasm of Codium fragile (Bryopsidales, Chlorophyta) into new protoplasts[J]. JOURNAL OF INTEGRATIVE PLANT BIOLOGY,2008,50(6):752-760. |
APA | Li, Demao,Lue, Fang,Wang, Guangce,&Zhou, Baicheng.(2008).Assembly of the protoplasm of Codium fragile (Bryopsidales, Chlorophyta) into new protoplasts.JOURNAL OF INTEGRATIVE PLANT BIOLOGY,50(6),752-760. |
MLA | Li, Demao,et al."Assembly of the protoplasm of Codium fragile (Bryopsidales, Chlorophyta) into new protoplasts".JOURNAL OF INTEGRATIVE PLANT BIOLOGY 50.6(2008):752-760. |
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