Abstract
Fast and accurate determination of lipid content in microalgal cultures is a required step for algal bioprocess development and optimization. An improved high-throughput Nile Red staining protocol using a microplate fluorescence reader is proposed, resulting in an increased correlation coefficient and a reduction in the relative standard deviation of 84% when compared to previously reported staining protocols. Differences in the staining efficacy of Nile Red among different algal strains were observed, even though the performance of the proposed method was found to be satisfactory for the different Trebouxiophyceae and Chlorophyceae microalgal cultures evaluated. Therefore, the proposed Nile Red method should only be used for evaluating lipid content variations in previously standardized strains. BODIPY 505/515 was evaluated as a potential substitute for Nile Red, but was found to be unsuitable as a quantitative stain for algal lipids in the microplate-based staining technique.
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