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首页> 外文期刊>Phycological Research >Applicability of the fluorescein diacetate assay for metabolic activity measurement of Microcystis aeruginosa (Chroococcales, Cyanobacteria)
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Applicability of the fluorescein diacetate assay for metabolic activity measurement of Microcystis aeruginosa (Chroococcales, Cyanobacteria)

机译:荧光素双乙酸盐测定法在铜绿微囊藻(色球菌,蓝细菌)的代谢活性测定中的适用性

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摘要

The fluorescein diacetate (FDA) assay has been widely used to measure metabolic activity in phytoplankton. It was found that FDA fluorescence values did not decrease in some stressed cells, demonstrating that the applicability of the method needs to be assessed further in the context of growth-influencing conditions. In the present study, changes of FDA fluorescence values were studied in bloom-forming cyanobacterial Microcystis aeruginosa Kutz cells under stress conditions such as nitrogen (N) or phosphorus (P) deficiency, or darkness and low temperature (10 degrees C), respectively. The results demonstrated that esterase activity decreased immediately in dark-stressed cells, which correlated with the decline of biomass and photosynthetic activity. Under the other three stress conditions, however, especially at low temperature, the cells lost photosynthetic activity but had the highest esterase activity, which was five times higher than the control group. These findings contrast with the assay criteria that the expression of a stain should reflect the change of photosynthetic activity and that stressed cells should have a lower staining intensity than the control cells. According to these results, the esterase activity response was dependent on environmental factors. Furthermore, higher fluorescence intensity did not mean higher metabolic activity, but a discrepant value indicated a severe stress.
机译:荧光素二乙酸酯(FDA)分析已被广泛用于测量浮游植物的代谢活性。发现在某些应激细胞中,FDA荧光值并未降低,这表明该方法的适用性需要在影响生长的条件下进行进一步评估。在本研究中,分别在氮(N)或磷(P)缺乏,黑暗和低温(10摄氏度)等胁迫条件下,对形成水华的蓝藻铜绿微囊藻库兹氏细胞中FDA荧光值的变化进行了研究。结果表明,在黑暗胁迫的细胞中,酯酶活性立即下降,这与生物量和光合活性的下降有关。然而,在其他三种胁迫条件下,特别是在低温下,细胞丧失了光合作用活性,但具有最高的酯酶活性,是对照组的五倍。这些发现与测定标准相反,测定标准是染色剂的表达应反映光合作用的变化,应激细胞的染色强度应低于对照细胞。根据这些结果,酯酶活性反应取决于环境因素。此外,较高的荧光强度并不意味着较高的代谢活性,但是相差的值表示严重的压力。

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