Molecular Biology and Functional Genomics, TH Wildau, Bahnhofstr, 1, 15745 Wildau, Germany.
BMC Biotechnol. 2011 Nov 30;11:118. doi: 10.1186/1472-6750-11-118.
Currently established methods to identify viable and non-viable cells of cyanobacteria are either time-consuming (eg. plating) or preparation-intensive (eg. fluorescent staining). In this paper we present a new and fast viability assay for unicellular cyanobacteria, which uses red chlorophyll fluorescence and an unspecific green autofluorescence for the differentiation of viable and non-viable cells without the need of sample preparation.
The viability assay for unicellular cyanobacteria using red and green autofluorescence was established and validated for the model organism Synechocystis sp. PCC 6803. Both autofluorescence signals could be observed simultaneously allowing a direct classification of viable and non-viable cells. The results were confirmed by plating/colony count, absorption spectra and chlorophyll measurements. The use of an automated fluorescence microscope and a novel ImageJ based image analysis plugin allow a semi-automated analysis.
The new method simplifies the process of viability analysis and allows a quick and accurate analysis. Furthermore results indicate that a combination of the new assay with absorption spectra or chlorophyll concentration measurements allows the estimation of the vitality of cells.
目前用于鉴定蓝藻活细胞和死细胞的方法要么耗时(例如平板培养法),要么准备工作繁琐(例如荧光染色法)。本文提出了一种新的快速单细胞蓝藻活力检测方法,该方法利用红色叶绿素荧光和非特异性绿色自发荧光来区分死活细胞,无需进行样品制备。
建立并验证了使用红色和绿色自发荧光的单细胞蓝藻活力检测方法,该方法适用于模式生物集胞藻 6803。两种自发荧光信号可以同时观察,从而可以直接对活细胞和死细胞进行分类。结果通过平板计数/菌落计数、吸收光谱和叶绿素测量得到了证实。使用自动化荧光显微镜和新的基于 ImageJ 的图像分析插件可以实现半自动分析。
该新方法简化了活力分析过程,实现了快速准确的分析。此外,结果表明,将新检测方法与吸收光谱或叶绿素浓度测量相结合,可用于评估细胞活力。