2014
DOI: 10.12691/jfnr-3-1-3
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Extraction and Separation of Phycocyanin from <i>Spirulina</i> using Aqueous Two-Phase Systems of Ionic Liquid and Salt

Abstract: To explore a new and simple rapid extraction and purification technique for phycocyanin, an ionic liquids(ILs)-based aqueous two-phase system(ATPS) was developed for the purification of phycocyanin from Spirulina extracts. Effects of various process parameters such as the concentrations of [Bmim]Cl, the concentrations of KH 2 PO 4 , the concentrations of crude phycocyanin, the system pH and the temperature on partitioning of phycocyanin were evaluated. The obtained data indicated that phycocyanin was preferent… Show more

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Cited by 23 publications
(17 citation statements)
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“…Under this condition, the high temperature led to the destruction in hydrogen bonding interaction between the surface water of protein and amino acid residue and thus reduced the purity ratio (Zhang et al . ).…”
Section: Resultsmentioning
confidence: 97%
“…Under this condition, the high temperature led to the destruction in hydrogen bonding interaction between the surface water of protein and amino acid residue and thus reduced the purity ratio (Zhang et al . ).…”
Section: Resultsmentioning
confidence: 97%
“…They found that 82.7–100% of the protein, bovine serum albumin (BSA), migrated to the top phase, while the carbohydrates were preferentially concentrated in the bottom phase. These results demonstrated that IL-ABS were effective in the selective separation of proteins and carbohydrates, and in this sense, further studies were carried out. Nonetheless, to the best of our knowledge, the fractionation of polysaccharides and proteins and the isolation of specific polysaccharide structures have never been reported in a single step and using IL-based ABS.…”
Section: Introductionmentioning
confidence: 86%
“…The ATPS system, formed by [Emim]­[EtSO 4 ] (IL), K 2 HPO 4 (salt), and water, was prepared in 25 mL centrifuge glass tubes that contained the appropriate amounts of all the three components above. Before adding the crude extract into the ATPS system, the pH was adjusted to 6.5 using HCl (ACS reagent, 37%, Sigma-Aldrich) because PC is stable within the pH range 6.0–7.0 and starts degradation at pH values above 7. , Then, the ATPS system and the crude extract were mixed in a vortex for 1 min. The blend was centrifuged at 4000 rpm for 5 min to complete the separation of both phases.…”
Section: Methodsmentioning
confidence: 99%