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镉胁迫下培养的红色大型植物的精细结构及X射线微分析

Fine structure and X-ray microanalysis of a red macrophyte cultured under cadmium stress.

作者信息

Talarico Laura

机构信息

Department of Biology, University of Trieste, Italy.

出版信息

Environ Pollut. 2002;120(3):813-21. doi: 10.1016/s0269-7491(02)00156-2.

Abstract

Thalli of the red alga Audouinella saviana were exposed to 600 microM Cd2+ (LC50), 1000 microM Cd2+ and 1500 microM Cd2+ (final concentrations) for 5, 10 and 15 days (each dose) by adding cadmium nitrate to the culture medium. Untreated thalli were set in triplicate as controls for each experiment. Ultrastructural modifications due to cadmium ad/absorption were observed by TEM/SEM electron microscopy. SEM-EDS X-ray microanalysis, definining the accumulation sites, was performed on cryoprepared samples. TEM studies showed striking changes in the plasmalemma of treated algae, which became irregular and convoluted. Electron-transparent exocytic vesicles, possibly related to cell wall polysaccharide synthesis, were observed. The appearance of ribosomes and Golgi bodies, not significantly present in the cytoplasms of untreated cells, suggested enhanced protein and carbohydrate biosynthesis. The cell walls lost their initial grooves and became smooth and thick. More or less electron-dense vesicular systems were formed. Electron-dense sphaeroids occurred in the plasmalemma-cell wall interface, in the cell wall itself and in nearby vesicular membrane systems. Many small vacuoles containing large metal complexes were formed. Complexes were then sequestered into a large vacuole. SEM observations demonstrated that the cell wall and the membrane systems were the most involved in the defense responses. EDS-X-ray microanalysis confirmed the presence of cadmium in these compartments. Chloroplasts, where no Cd2+ signal was detected, were the least affected organelles, showing only a partial disorganization after lengthy exposure to high Cd2+ concentrations.

摘要

通过向培养基中添加硝酸镉,将红藻萨维亚奥杜因藻的叶状体暴露于600微摩尔/升的镉离子(半数致死浓度)、1000微摩尔/升和1500微摩尔/升的镉离子(终浓度)中5天、10天和15天(每种剂量)。未处理的叶状体每组设置三个重复作为每个实验的对照。通过透射电子显微镜/扫描电子显微镜观察由于镉吸附导致的超微结构变化。对冷冻制备的样品进行扫描电子显微镜-能谱X射线微分析,以确定积累部位。透射电子显微镜研究显示,处理过的藻类的质膜发生了显著变化,变得不规则且卷曲。观察到可能与细胞壁多糖合成有关的电子透明胞吐小泡。核糖体和高尔基体的出现,在未处理细胞的细胞质中并不明显,表明蛋白质和碳水化合物生物合成增强。细胞壁失去了最初的沟槽,变得光滑且增厚。形成了或多或少电子致密的囊泡系统。电子致密的球体出现在质膜-细胞壁界面、细胞壁本身以及附近的囊泡膜系统中。形成了许多含有大量金属复合物的小液泡。然后复合物被隔离到一个大液泡中。扫描电子显微镜观察表明,细胞壁和膜系统最参与防御反应。能谱X射线微分析证实了这些区室中存在镉。未检测到镉离子信号的叶绿体是受影响最小的细胞器,在长时间暴露于高浓度镉离子后仅表现出部分解体。

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