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Selection and optimisation of a method for efficient metabolites extraction from microalgae
[Display omitted] ► Nine disruption techniques were tested on two microalgae models. ► Image analysis was used to evaluate the efficiency of disruption techniques. ► The best grinding method was the mixer mill with polypropylen grinding jars. ► The disruption method was optimised in the objective of...
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Published in: | Bioresource technology 2012-11, Vol.124, p.311-320 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
► Nine disruption techniques were tested on two microalgae models. ► Image analysis was used to evaluate the efficiency of disruption techniques. ► The best grinding method was the mixer mill with polypropylen grinding jars. ► The disruption method was optimised in the objective of high throughput screening. ► Pigments were good candidates to follow extraction of fragile metabolites.
Over the last decade, the use of microalgae for biofuel production and carbon dioxide sequestration has become a challenge worldwide. Processing costs are still too high for these methods to be profitable though, leading to a need to find high value by-products to optimise the added value of this biomass. For high-throughput screening of such metabolites, it is essential to reach the inner content of the cell. This paper presents research and development of a technique enabling a high extraction yield of any metabolite, taking into account the difficulty of extracting bound and or inaccessible molecules with a wide variety of polarities. To this end, several disruption techniques were tested at laboratory scale on two biological models: Porphyridium purpureum and Phaeodactylum tricornutum. A mixer mill gave the best results, offering access to a broad diversity of metabolites from microalgae for high-throughput screening. |
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ISSN: | 0960-8524 1873-2976 |
DOI: | 10.1016/j.biortech.2012.07.105 |