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基于蕨类孢子线粒体活性开发自然小型化检测方法:一种新型高等植物生物测定法。

Development of a naturally miniaturised testing method based on the mitochondrial activity of fern spores: a new higher plant bioassay.

作者信息

Catala Myriam, Esteban Marta, Rodríguez-Gil José-Luis, Quintanilla Luis G

机构信息

Departamento de Geología y Biología, ESCET, Campus de Móstoles, Universidad Rey Juan Carlos, E-28933 Móstoles, Madrid, Spain.

出版信息

Chemosphere. 2009 Nov;77(7):983-8. doi: 10.1016/j.chemosphere.2009.07.080. Epub 2009 Sep 29.

Abstract

One of the main concerns of current environmental toxicology is the low number of taxa used for standard bioassays. Ferns, with more than 10,000 living species, are the second largest group of vascular plants and are important components of numerous plant communities. Fern spores and gametophytes have long been recognized as useful models for plant research since they constitute a naturally miniaturised and economic higher plant model. Mitochondria are the main energy source in eukaryotic cells and any toxic damage will affect the whole organism. The reduction of tetrazolium salts to water-insoluble coloured formazan salts by the respiratory chain has been used for more than 50 years as a measure of cell mitochondrial activity and viability in eukaryotic organisms. Here, the reduction of 2,3,5-triphenyltetrazolium chloride (TTC) by mitochondria is adapted and optimized to measure fern spore or gametophyte viability. Procedures selected as optimum in the model species Dryopteris guanchica are as follows: bleach sterilization, incubation without shaking at 20 degrees C in the dark for 1-4h with 0.05-1.5% TTC in Dyer medium supplemented with 0.001-0.005% Tween 20 at pH 8. We conclude that this method constitutes a promising low cost bioassay for higher plant toxicity during development.

摘要

当前环境毒理学的主要关注点之一是用于标准生物测定的分类单元数量较少。蕨类植物有超过10000个现存物种,是维管植物的第二大类群,也是众多植物群落的重要组成部分。蕨类植物的孢子和配子体长期以来一直被认为是植物研究的有用模型,因为它们构成了一个天然小型化且经济的高等植物模型。线粒体是真核细胞的主要能量来源,任何毒性损伤都会影响整个生物体。呼吸链将四氮唑盐还原为水不溶性有色甲臜盐,50多年来一直被用作衡量真核生物细胞线粒体活性和活力的指标。在此,对线粒体还原2,3,5-三苯基氯化四氮唑(TTC)的方法进行了调整和优化,以测定蕨类植物孢子或配子体的活力。在模式物种关氏鳞毛蕨中选择的最佳程序如下:漂白消毒,在20℃黑暗中不摇晃培养1-4小时,使用添加了0.001-0.005%吐温20、pH值为8的戴尔培养基中0.05-1.5%的TTC。我们得出结论,该方法构成了一种有前景的低成本生物测定法,用于评估高等植物发育过程中的毒性。

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