scholarly journals Nile Red Staining for Oil Determination in Microalgal Cells: A New Insight through Statistical Modelling

2015 ◽  
Vol 2015 ◽  
pp. 1-14 ◽  
Author(s):  
Ronald Halim ◽  
Paul A. Webley

In the wake of global warming and rapid fossil fuel depletion, microalgae emerge as promising feedstocks for sustainable biofuel production. Nile red staining acts as a rapid diagnostic tool to measure the amount of biodiesel-convertible lipid that the cells accumulate. There is a need for the development of a more uniform staining procedure. In its first phase, this study examined the dependence of microalgal Nile red fluorescence (Tetraselmis suecica) in terms of its most pertinent staining variables. A quadratic surface model that successfully described the Nile red fluorescence intensity as a composite function of its variables was generated (r2=0.86). Cell concentration was shown to have a significant effect on the fluorescence intensity. Up to a certain threshold, fluorescence intensity was shown to increase with Nile red dye concentration. In its second phase, the study reviewed findings from previous Nile red studies to elucidate some of the fundamental mechanism underlying the diffusion of Nile red dye molecules into the microalgal cells and their subsequent interaction with intracellular lipids. Through the review process, we were able to develop a simple framework that provided a set of guidelines for the standardization of the Nile red staining procedure across different microalgal species.

2015 ◽  
Vol 49 (4) ◽  
pp. 249-254 ◽  
Author(s):  
M. S. Pilipenko ◽  
A. V. Koshkin ◽  
V. A. Sazhnikov ◽  
M. V. Alfimov

2015 ◽  
Vol 290 ◽  
pp. 115-120
Author(s):  
Ewa Rogoża ◽  
◽  
Katarzyna Drzewiecka ◽  

Fingerprints disclosed by cyanoacrylate on non-absorbent substrates, in order to improve readabiIity, require additional contrasting fluorescent dyes. Nile Red is one of them. Its effectiveness was tested under conditions similar to those of daily laboratory practice. The highest Nile Red fluorescence occurred in an excitation light of blue-green and a wavelength of 505nm. Spectral analysis showed that the emission of light oscillates in the wavelength of about 630nm. In order to cut off the light, longpass edge filters of the colours yellow, orange or red can be used. Filter selection depends on the characteristics of the substrate and can be chosen empirically. Nile Red fluorescence does not change over a longer period of time, which allows for the registration of fingerprints to be performed within a time convenient for the testing, without fear of losing their quality. Nile Red may be an alternative to other fluorescent dyes used for visualization in fingerprint testing.


Data ◽  
2020 ◽  
Vol 5 (3) ◽  
pp. 77
Author(s):  
Mauricio Ramirez-Castrillon ◽  
Victoria Jaramillo-Garcia ◽  
Helio Barros ◽  
João Henriques ◽  
Valter Stefani ◽  
...  

We used Nile red to estimate lipid content in oleaginous yeasts using a high-throughput approach. We measured the fluorescence intensity of Nile red using different solvents, yeast strains, and incubation times in optimized excitation/emission wavelengths. The data show the relative fluorescence units (RFU) for Nile red excitation, using 1× PBS, 1× PBS and 5% v/v isopropyl alcohol, 50% v/v glycerol, culture medium A-gly broth, and A-gly broth supplemented with 5% v/v DMSO. In addition, we showed the RFU for the Nile red dye for different oleaginous and non-oleaginous yeast strains, such as Meyerozyma guilliermondii BI281A, Yarrowia lipolytica QU21 and Saccharomyces cerevisiae MRC164. Other measurements of lipid accumulation kinetics were shown for the above and additional yeast strains. These datasets provide the guidelines to obtain the optimal solvent system and the minimal interaction time for the Nile red dye to enter in the cells and obtain a stable readout.


Sign in / Sign up

Export Citation Format

Share Document