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Quantification of total fatty acids in microalgae: comparison of extraction and transesterification methods

Determination of microalgaes’ fatty acid content is often done with chloroform and methanol according to the Bligh and Dyer extraction, though faster methods exist. A number of comparisons between the Bligh and Dyer and faster methods have resulted in contradicting data, possibly due to differences...

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Autores principales: Cavonius, Lillie R., Carlsson, Nils-Gunnar, Undeland, Ingrid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206773/
https://www.ncbi.nlm.nih.gov/pubmed/25224639
http://dx.doi.org/10.1007/s00216-014-8155-3
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author Cavonius, Lillie R.
Carlsson, Nils-Gunnar
Undeland, Ingrid
author_facet Cavonius, Lillie R.
Carlsson, Nils-Gunnar
Undeland, Ingrid
author_sort Cavonius, Lillie R.
collection PubMed
description Determination of microalgaes’ fatty acid content is often done with chloroform and methanol according to the Bligh and Dyer extraction, though faster methods exist. A number of comparisons between the Bligh and Dyer and faster methods have resulted in contradicting data, possibly due to differences in algae used and the different versions of the Bligh and Dyer method applied. Here, various forms of direct-transesterification (D-TE) and two-step transesterification (2-TE), including three versions developed in our lab, are compared with the original Bligh and Dyer (Can J Biochem Physiol 37: 911–917, 1959) extraction and two modifications thereof (Lee et al. J AOAC Int 79:487–492, 1996, and our own acidified version) on microalgae with different cell walls: Isochrysis galbana, Nannochloropsis oculata, and Phaeodactylum tricornutum. In total, fatty acid extracts from 11 methods were separated and quantified by gas chromatography with mass spectrometry. Results show that, for N. oculata and P. tricornutum, methods based on chloroform–methanol underestimated the fatty acid content compared with the 2-TE and D-TE methods, which gave similar results. Moreover, D-TE methods are faster than chloroform–methanol methods and use chemicals that are less toxic. Of the D-TE methods, the ones using hydrochloric acid and sulfuric acid recovered the most fatty acids, while boron trifluoride recovered slightly less. The main qualitative difference between the fatty acids recovered was that the chloroform–methanol methods recovered less saturated fatty acids in P. tricornutum. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00216-014-8155-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-42067732014-10-28 Quantification of total fatty acids in microalgae: comparison of extraction and transesterification methods Cavonius, Lillie R. Carlsson, Nils-Gunnar Undeland, Ingrid Anal Bioanal Chem Research Paper Determination of microalgaes’ fatty acid content is often done with chloroform and methanol according to the Bligh and Dyer extraction, though faster methods exist. A number of comparisons between the Bligh and Dyer and faster methods have resulted in contradicting data, possibly due to differences in algae used and the different versions of the Bligh and Dyer method applied. Here, various forms of direct-transesterification (D-TE) and two-step transesterification (2-TE), including three versions developed in our lab, are compared with the original Bligh and Dyer (Can J Biochem Physiol 37: 911–917, 1959) extraction and two modifications thereof (Lee et al. J AOAC Int 79:487–492, 1996, and our own acidified version) on microalgae with different cell walls: Isochrysis galbana, Nannochloropsis oculata, and Phaeodactylum tricornutum. In total, fatty acid extracts from 11 methods were separated and quantified by gas chromatography with mass spectrometry. Results show that, for N. oculata and P. tricornutum, methods based on chloroform–methanol underestimated the fatty acid content compared with the 2-TE and D-TE methods, which gave similar results. Moreover, D-TE methods are faster than chloroform–methanol methods and use chemicals that are less toxic. Of the D-TE methods, the ones using hydrochloric acid and sulfuric acid recovered the most fatty acids, while boron trifluoride recovered slightly less. The main qualitative difference between the fatty acids recovered was that the chloroform–methanol methods recovered less saturated fatty acids in P. tricornutum. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00216-014-8155-3) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2014-09-16 2014 /pmc/articles/PMC4206773/ /pubmed/25224639 http://dx.doi.org/10.1007/s00216-014-8155-3 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Research Paper
Cavonius, Lillie R.
Carlsson, Nils-Gunnar
Undeland, Ingrid
Quantification of total fatty acids in microalgae: comparison of extraction and transesterification methods
title Quantification of total fatty acids in microalgae: comparison of extraction and transesterification methods
title_full Quantification of total fatty acids in microalgae: comparison of extraction and transesterification methods
title_fullStr Quantification of total fatty acids in microalgae: comparison of extraction and transesterification methods
title_full_unstemmed Quantification of total fatty acids in microalgae: comparison of extraction and transesterification methods
title_short Quantification of total fatty acids in microalgae: comparison of extraction and transesterification methods
title_sort quantification of total fatty acids in microalgae: comparison of extraction and transesterification methods
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206773/
https://www.ncbi.nlm.nih.gov/pubmed/25224639
http://dx.doi.org/10.1007/s00216-014-8155-3
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