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Phosphate removal and recovery using immobilized phosphate binding proteins.

ABSTRACT: Progress towards a more circular phosphorus economy necessitates development of innovative water treatment systems which can reversibly remove inorganic phosphate (Pi) to ultra-low levels (<100??g?L-1), and subsequently recover the Pi for reuse. In this study, a novel approach using the high-affinity E. coli phosphate binding protein (PBP) as a reusable Pi bio-adsorbent was investigated. PBP was expressed, extracted, purified and immobilized on NHS-activated Sepharose beads. The resultant PBP beads were saturated with Pi and exposed to varying pH (pH 4.7 to 12.5) and temperatures (25-45?°C) to induce Pi release. Increase in temperature from 25 to 45?°C and pH conditions between 4.7 and 8.5 released less than 20% of adsorbed Pi. However, 62% and 86% of the adsorbed Pi was released at pH 11.4 and 12.5, respectively. Kinetic experiments showed that Pi desorption occurred nearly instantaneously (<5?min), regardless of pH conditions, which is advantageous for Pi recovery. Additionally, no loss in Pi adsorption or desorption capacity was observed when the PBP beads were exposed to 10 repeated cycles of adsorption/desorption using neutral and high pH (?12.5) washes, respectively. The highest average Pi adsorption using the PBP beads was 83?±?5%, with 89?±?4.1% average desorption using pH 12.5 washes over 10 wash cycles at room temperature. Thermal shift assay of the PBP showed that the protein was structurally stable after 10 cycles, with statistically similar melting temperatures between pH 4 and 12.5. These results indicate that immobilized high-affinity PBP has the potential to be an effective and reversible bio-adsorbent suitable for Pi recovery from water/wastewater.

SUBMITTER: Venkiteshwaran K

PROVIDER: S-EPMC6549937 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature

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Phosphate removal and recovery using immobilized phosphate binding proteins.

Venkiteshwaran Kaushik K Pokhrel Nilisha N Hussein Faten F Antony Edwin E Mayer Brooke K BK

Water research X 20181005

Progress towards a more circular phosphorus economy necessitates development of innovative water treatment systems which can reversibly remove inorganic phosphate (Pi) to ultra-low levels (<100 μg L-1), and subsequently recover the Pi for reuse. In this study, a novel approach using the high-affinity E. coli phosphate binding protein (PBP) as a reusable Pi bio-adsorbent was investigated. PBP was expressed, extracted, purified and immobilized on ...[more]

PMID: 31194063

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Project description:The capacities of immature and mature rat brain myelin, bovine myelin and human myelin to be agglutinated by soya-bean agglutinin, Ricinus communis agglutinin, wheatgerm agglutinin, and Lotus tetragonolobus agglutinin were examined. The first two lectins, which are specific for galactose and N-acetylgalactosamine, strongly agglutinated immature and mature rat myelin, weakly agglutinated bovine myelin, but did not affect human myelin. The other myelin and lectin combinations resulted in very weak or no agglutination. [(3)H]Fucose-labelled glycoproteins of purified adult rat brain myelin were solubilized with sodium dodecyl sulphate and allowed to bind to concanavalin A-Sepharose and each of the other lectins mentioned above, which had been immobilized on agarose. About 60% of the radioactive fucose was in glycoproteins that bound to concanavalin A-Sepharose and these glycoproteins could be eluted with solutions containing methyl alpha-d-mannoside and sodium dodecyl sulphate. Periodate/Schiff staining or radioactive counting of analytical gels showed that most of the major myelin-associated glycoprotein (apparent mol.wt. approx. 100000) bound to the concanavalin A, whereas the glycoproteins that did not bind were mostly of lower molecular weight. Preparative polyacrylamide-gel electrophoresis of the glycoprotein fraction that was eluted with methyl alpha-d-mannoside yielded a relatively pure preparation of the myelin-associated glycoprotein. Similar results were obtained with each of the other lectins, i.e. the myelin-associated glycoprotein was in the fraction that bound to the immobilized lectin. Double-labelling experiments utilizing [(3)H]fucose-labelled glycoproteins from adult myelin and [(14)C]fucose-labelled glycoproteins from 14-day-old rat brain myelin did not reveal any difference in the binding of the mature and immature glycoproteins to any of the immobilized lectins. The results in this and the preceding paper [McIntyre, Quarles & Brady (1979) Biochem. J.183, 205-212] suggest that the myelin-associated glycoprotein is one of the principal receptors for concanavalin A and other lectins in myelin, and that this property can be utilized for the purification of this glycoprotein.

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Phosphate removal and recovery using immobilized phosphate binding proteins.

Publications

Phosphate removal and recovery using immobilized phosphate binding proteins.

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