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Journal of Microbiological Methods

Publication date: 2016-09-01
Volume: 128 Pages: 74 - 79
Publisher: Elsevier Biomedical

Author:

Alemán-Nava, Gibran S
Cuellar-Bermudez, Sara P ; Cuaresma, Maria ; Bosma, Rouke ; Muylaert, Koenraad ; Ritmann, Bruce E ; Parra, Roberto

Keywords:

Science & Technology, Life Sciences & Biomedicine, Biochemical Research Methods, Microbiology, Biochemistry & Molecular Biology, Nile Red, Microalgae, Neutral lipids, Protocol, Biodiesel, RAPID SCREENING METHOD, BIODIESEL, QUANTIFICATION, GROWTH, BLUE, Calibration, Cell Wall, Dimethyl Sulfoxide, Edetic Acid, Fluorescent Dyes, Glycerol, Lipids, Oxazines, Temperature, 0605 Microbiology, 1108 Medical Microbiology, 3107 Microbiology

Abstract:

The use of Nile Red for rapid monitoring of the neutral lipid content in microalgae has gained interest over the last decade, since neutral lipids are feedstock for renewable transportation fuel. In this review, we discuss the main considerations needed to make an NR protocol reliable for staining neutral lipids in microalgae. Cell wall permeability must be enhanced by using stain carriers: DMSO (5% v/v to 25% v/v), glycerol (0.1 to 0.125 mg/mL), or EDTA (3.0 to 3.8 mg/mL). Temperatures between 30 and 40 °C facilitate the diffusion of NR through the cell wall without incurring excess quenching. Good NR-lipid interaction requires using a low NR/cell ratio; the NR concentration must be between 0.25 μg/ml and 2.0 μg/ml, and the cell concentration > 5x104 cells/ml. In order to have the maximum and stable NR fluorescence, it is necessary to scan the excitation/emission wavelengths for up to a 40-min of incubation time. We outline a five-step method to customize the Nile Red protocol to a specific strain: 1) Evaluate the strain's suitability by checking for the presence of neutral lipid, 2) Select of the best excitation/emission wavelength, 3) Optimization of incubation time, stain carrier, dye concentration, and temperature, 4) Prepare single-strain algal cultures with different lipid contents to calibrate NR fluorescence with neutral-lipid content, and 5) Correlate NR fluorescence intensity to neutral lipid content for the same strain. Once the protocol is customized, the NR method allows for rapid and reliable monitoring of neutral lipid content of a microalgae strain.