Sustainable valorization of meat processing wastewater with synergetic eutectic mixture based purification of R-Phycoerythrin from porphyrium cruentium
[Display omitted] •Six protic deep eutectic solvents synthesised and thermophysical assessment done.•Meat processing wastewater valorised as potential nutrient source for algal culture.•Microwave-cavitation assisted disruptive microextraction of R-PE was employed.•Kinetics of disruptive purification...
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Veröffentlicht in: | Bioresource technology 2021-09, Vol.336, p.125357-125357, Article 125357 |
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Format: | Artikel |
Sprache: | eng |
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•Six protic deep eutectic solvents synthesised and thermophysical assessment done.•Meat processing wastewater valorised as potential nutrient source for algal culture.•Microwave-cavitation assisted disruptive microextraction of R-PE was employed.•Kinetics of disruptive purification for microwave cavitation extraction determined.•Selective purification of R-PE by size exclusion and anion exchange chromatography.
Wastewater effluent from meat processing industries are enriched with nutrients but remain underutilized. Therefore, an efficient method was administered by employing this resource for the cultivation of Porphyreum cruentium. The cultured biomass was exposed to a one-step disruption and selective purification method using a protic deep eutectic solvent to obtain a commercially significant pigment, R-Phycoerythrin (R-PE). Six protic deep eutectic solvents (pDES) were synthesized and their thermophysical activity determined. A synergy between microwave and cavitation (MACE-DLPME) has been achieved for the effective recovery of these membrane proteins. The addition of pDES provides the selective medium for the concentration of R-PE. Optimization of the MACE-DLPME method yields 95.9% (w/w) of R-PE. Preparative size exclusion chromatography resulted in (28 µg/g) of R-PE. Further ultra-purification by anion exchange chromatography enhances the purity fold of R-PE to 125. The resulting ultrapure fraction exhibits enhanced anti-platelet activity (1.56 mg/g ascorbic acid equivalent). |
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ISSN: | 0960-8524 1873-2976 |
DOI: | 10.1016/j.biortech.2021.125357 |