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双荧光法检测越冬蓝藻活力的效果。

Efficacy of a dual fluorescence method in detecting the viability of overwintering cyanobacteria.

机构信息

CAS Key Laboratory of Algal Biology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, Hubei, China.

出版信息

Lett Appl Microbiol. 2013 Sep;57(3):174-80. doi: 10.1111/lam.12095. Epub 2013 May 20.

Abstract

Chill in the light is the major environmental stress that cyanobacteria encounter in winter. Cyanobacterial cells may acquire chill-light tolerance upon exposure to low temperature in autumn and early winter. We sought to establish the efficacy of the dual fluorescence method in detecting the viability of overwintering cyanobacteria and to provide further evidence for the chill-light tolerance of preconditioned cyanobacteria. Synechocystis sp. PCC 6803 and Microcystis aeruginosa PCC 7806 were exposed to chill (5°C)-light stress with or without pretreatment at 15°C and stained with SYTO 9 and propidium iodide. Live and dead cells were observed under a fluorescence microscope, and the percentage of viable cells was quantified on a microplate reader. The dual fluorescence method showed consistent results with tests of the ability to reinitiate growth. Cell viability was quantitatively correlated with ratio of SYTO 9/propidium iodide fluorescence. Previously, Microcystis colonies in Lake Taihu had been found to accumulate RNA-binding protein 1 in autumn and winter. Use of this method directly showed the viability of such Microcystis colonies throughout the winter.

摘要

光照低温是蓝藻在冬季遇到的主要环境胁迫。蓝藻细胞在秋季和初冬低温暴露下可能会获得耐光照低温能力。我们试图通过建立双重荧光法来检测越冬蓝藻的活力,并为预先处理的蓝藻的耐光照低温能力提供进一步的证据。我们将集胞藻 PCC 6803 和铜绿微囊藻 PCC 7806 暴露于有或没有 15°C 预处理的光照低温(5°C)胁迫下,并用 SYTO 9 和碘化丙啶染色。在荧光显微镜下观察活细胞和死细胞,并在微孔板读数器上定量计算活细胞的百分比。双重荧光法与重新起始生长能力的测试结果一致。细胞活力与 SYTO 9/碘化丙啶荧光的比值定量相关。此前,已发现太湖中的微囊藻在秋季和冬季积累 RNA 结合蛋白 1。使用该方法直接显示了整个冬季这些微囊藻群体的活力。

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