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在无菌条件下杜氏盐藻的最佳生长以用于除草剂测定。

Optimal growth of Dunaliella primolecta in axenic conditions to assay herbicides.

作者信息

Santín-Montanyá I, Sandín-España P, García Baudín J M, Coll-Morales J

机构信息

Departamento de Protección Vegetal, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Ctra. de la Coruña Km. 7.5, 28040 Madrid, Spain.

出版信息

Chemosphere. 2007 Jan;66(7):1315-22. doi: 10.1016/j.chemosphere.2006.07.019. Epub 2006 Sep 18.

Abstract

To develop an assay for herbicides in marine environments using microalgae, we have optimized the specie, cell culture media and physical conditions to obtain maximal cellular densities in a 96 well micro format to allow mass assays. We first surveyed several species of 7 unicellular eukaryotic algae genera (Dunaliella, Tetraselmis, Chlorella, Ellipsoidon, Isochrysis, Nannochloropsis, and Phaeodactylum) for vigorous in vitro axenic growth. Once the genus Dunaliella was selected, Dunaliella primolecta was preferred among 9 species (bioculata, minuta, parva, peircei, polymorpha, primolecta, quartolecta, salina and tertiolecta) because it showed the highest growth rates. The components (oligo elements, sugars, amino acids and vitamins) and conditions (light, CO(2), temperature) of the culture media were further optimized to obtain the highest cellular densities (up to 60x10(6)cellsml(-1)) and the shortest cell cycle duration ( approximately 12h) for D. primolecta. Then the toxicity of four representative herbicides, alloxydim, and sethoxydim (inhibitors of acetyl-coA carboxilase), metamitron (inhibitor of photosynthesis) and clopyralid (inhibitor of respiration), were assayed on the optimal culture conditions for D. primolecta during 96h. The results showed that D. primolecta was susceptible to those herbicides in the following order: metamitron > sethoxydim > alloxydim. In contrast, clopyralid did not have any effects. Therefore, D. primolecta microcultures can be used to assay a large number of samples for the presence of herbicides under a saline environment.

摘要

为了开发一种利用微藻检测海洋环境中除草剂的分析方法,我们对藻种、细胞培养基和物理条件进行了优化,以在96孔微孔板中获得最大细胞密度,从而实现大规模分析。我们首先调查了7个单细胞真核藻类属(杜氏藻属、四爿藻属、小球藻属、椭圆藻属、等鞭金藻属、微拟球藻属和三角褐指藻属)的几个物种,以寻找在体外无菌培养条件下生长旺盛的藻种。一旦选定杜氏藻属,在9个物种(双凹杜氏藻、微小杜氏藻、小形杜氏藻、皮尔西杜氏藻、多形杜氏藻、原始杜氏藻、第四杜氏藻、盐生杜氏藻和第三杜氏藻)中,原始杜氏藻表现出最高的生长速率,因此被选为首选。进一步优化了培养基的成分(微量元素、糖类、氨基酸和维生素)和条件(光照、二氧化碳、温度),以获得原始杜氏藻的最高细胞密度(高达60×10⁶个细胞/毫升)和最短细胞周期时长(约12小时)。然后,在原始杜氏藻的最佳培养条件下,对四种代表性除草剂——烯禾啶、稀禾啶(乙酰辅酶A羧化酶抑制剂)、苯嗪草酮(光合作用抑制剂)和氯吡嘧磺隆(呼吸作用抑制剂)进行了96小时的毒性测定。结果表明,原始杜氏藻对这些除草剂的敏感程度依次为:苯嗪草酮>稀禾啶>烯禾啶。相比之下,氯吡嘧磺隆没有任何影响。因此,原始杜氏藻微培养可用于在盐环境下检测大量样品中除草剂的存在。

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