2022
DOI: 10.1016/j.jbiotec.2021.11.004
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Foam fractionation of a recombinant biosurfactant apolipoprotein

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Cited by 10 publications
(3 citation statements)
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“…Its widespread offline utilization is due to the purification capacity of intact proteins with mild chromatographic conditions to permit further additional sample preparation steps with minimal impact on the conformational structure. The type of analytes and samples investigated by SEC in recent studies included exosomal proteins in human plasma [30], plasma exosomal proteins of corneal epithelial injury [31], extracellular vesicles in cancer cells [32,33], foam of recombinant biosurfactant apolipoprotein [34], peptides in alcalase hydrolisated pollen [35], circulating microparticles proteins to identify preterm babies before the end of 35 weeks of gestation [36], extracellular vesicle in cord blood of preterm and term births [37], α-Glucosidase-inhibitory peptides in dry-cured ham [38], extracellular vesicle in blood plasma [39], proteins in endogenous membrane proteins [40], N-Glycoproteins and phosphoproteins in human urine [41], high-density lipoproteins from plasma [42], proteins in antivenoms [43] and venoms of snakes [44], artificially created immune complexes on human serum [45], labelled proteins of E. coli lysate [46], extracellular vesicles in serum [47], β-Type Hemocyanin in shrimps [48], and extracellular vesicles in PLB-985 neutrophil-like cells [49].…”
Section: 1mentioning
confidence: 99%
“…Its widespread offline utilization is due to the purification capacity of intact proteins with mild chromatographic conditions to permit further additional sample preparation steps with minimal impact on the conformational structure. The type of analytes and samples investigated by SEC in recent studies included exosomal proteins in human plasma [30], plasma exosomal proteins of corneal epithelial injury [31], extracellular vesicles in cancer cells [32,33], foam of recombinant biosurfactant apolipoprotein [34], peptides in alcalase hydrolisated pollen [35], circulating microparticles proteins to identify preterm babies before the end of 35 weeks of gestation [36], extracellular vesicle in cord blood of preterm and term births [37], α-Glucosidase-inhibitory peptides in dry-cured ham [38], extracellular vesicle in blood plasma [39], proteins in endogenous membrane proteins [40], N-Glycoproteins and phosphoproteins in human urine [41], high-density lipoproteins from plasma [42], proteins in antivenoms [43] and venoms of snakes [44], artificially created immune complexes on human serum [45], labelled proteins of E. coli lysate [46], extracellular vesicles in serum [47], β-Type Hemocyanin in shrimps [48], and extracellular vesicles in PLB-985 neutrophil-like cells [49].…”
Section: 1mentioning
confidence: 99%
“…Reactors and apparatus involving a gas-liquid or gas-liquidsolid phase have been applied to various processes including foam fractionation-based bioseparation [74], enzymatic oxidation reactions [75,76], water treatments [77], and cell cultures [78]. An external loop airlift bubble column (ELBC) is one of the practical and promising apparatus for biochemical engineering processes [75] because of its well-characterized and relatively mild flow conditions and wide scalability [79].…”
Section: Gas-liquid Flow-induced Characteristics Of Liposomesmentioning
confidence: 99%
“…During the removal of surfactant micropollutants from a liquid in a bubble column, surfactant molecules are adsorbed on air bubble surfaces, and the generated foam contains a higher amount of the surfactant than the remaining liquid solution . This method is called bubble separation or foam fractionation, which is used in protein purifications, pharmaceutical and micropollutant removals, and wastewater treatments. This is very important considering that some of these chemicals are also surfactants, and foam fractionation is an effective separation method for surfactant removal from a solution containing a low surfactant concentration.…”
Section: Introductionmentioning
confidence: 99%