2020
DOI: 10.3390/pr9010010
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Microalgae Biomolecules: Extraction, Separation and Purification Methods

Abstract: Several microalgae species have been exploited due to their great biotechnological potential for the production of a range of biomolecules that can be applied in a large variety of industrial sectors. However, the major challenge of biotechnological processes is to make them economically viable, through the production of commercially valuable compounds. Most of these compounds are accumulated inside the cells, requiring efficient technologies for their extraction, recovery and purification. Recent improvements… Show more

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Cited by 67 publications
(22 citation statements)
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“…Ion exchange chromatography uses the difference between the charge properties of molecules to promote separation. By manipulating the pH, it is possible to change the net surface charge of charged biomolecules to achieve higher selectivity [48]. Size exclusion chromatography can be used to separate microalgal polysaccharides with different molecular weights or molecular sizes [49].…”
Section: Extraction and Fractionation/purificationmentioning
confidence: 99%
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“…Ion exchange chromatography uses the difference between the charge properties of molecules to promote separation. By manipulating the pH, it is possible to change the net surface charge of charged biomolecules to achieve higher selectivity [48]. Size exclusion chromatography can be used to separate microalgal polysaccharides with different molecular weights or molecular sizes [49].…”
Section: Extraction and Fractionation/purificationmentioning
confidence: 99%
“…Gel permeation chromatography is a widely used size exclusion chromatography for separating macromolecules. For microalgae, this technique has been applied to characterize polysaccharides [48]. In affinity chromatography, the target molecule charged by the mobile phase binds to the immobilized ligand on the stationary phase by affinity.…”
Section: Extraction and Fractionation/purificationmentioning
confidence: 99%
“…The components of C. pyrenoidosa were analyzed to be 9.94% carbohydrate (55% glucose and 45% galactose), 0.64% fiber, 56.61% protein, 4.55% lipid, and 7.86% ash [15]. The sugar extraction process was performed with 2% hydrochloric acid and a solid-liquid ratio of 100 g/L in an Erlenmeyer flask, using an autoclave (VS-1221-100, Vision science, Daejeon, South Korea) at 121 • C for 15 min, after which the pH was regulated to 7 by using NaOH [12].…”
Section: Sugar Extraction Of Chlorella Pyrenoidosa Using Hydrochloric Acidmentioning
confidence: 99%
“…Presently, algae-sea plants-are being focused on as the next generation carbon source. Because sea algae also photosynthesize, they have all the merits of land plants [12]. Additionally, it is well known that they grow rapidly because they have higher photosynthesis efficiency than land plants, and they have a 1.5-fold to 2-fold higher carbon dioxide fixation effect [13,14].…”
Section: Introductionmentioning
confidence: 99%
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