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Appl Microbiol Biotechnol. 2015 Dec;99(23):10237-47. doi: 10.1007/s00253-015-6909-2. Epub 2015 Aug 16.

Direct quantification of fatty acids in wet microalgal and yeast biomass via a rapid in situ fatty acid methyl ester derivatization approach.

Author information

1
Department of Biological Systems Engineering, Washington State University, Pullman, WA, 99164-6120, USA.
2
Department of Biological Systems Engineering, Washington State University, Pullman, WA, 99164-6120, USA. chens@wsu.edu.

Abstract

Accurate determination of fatty acid contents is routinely required in microalgal and yeast biofuel studies. A method of rapid in situ fatty acid methyl ester (FAME) derivatization directly from wet fresh microalgal and yeast biomass was developed in this study. This method does not require prior solvent extraction or dehydration. FAMEs were prepared with a sequential alkaline hydrolysis (15 min at 85 °C) and acidic esterification (15 min at 85 °C) process. The resulting FAMEs were extracted into n-hexane and analyzed using gas chromatography. The effects of each processing parameter (temperature, reaction time, and water content) upon the lipids quantification in the alkaline hydrolysis step were evaluated with a full factorial design. This method could tolerate water content up to 20% (v/v) in total reaction volume, which equaled up to 1.2 mL of water in biomass slurry (with 0.05-25 mg of fatty acid). There were no significant differences in FAME quantification (p>0.05) between the standard AOAC 991.39 method and the proposed wet in situ FAME preparation method. This fatty acid quantification method is applicable to fresh wet biomass of a wide range of microalgae and yeast species.

KEYWORDS:

Biofuel; Esterification; FAME; GC analysis; Microalgae; Yeast

PMID:
26276545
DOI:
10.1007/s00253-015-6909-2
[Indexed for MEDLINE]

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