Method for extracting soluble proteins from microalgal biomass
AssigneeCorbion Biotech, Inc.
InventorSamuel Patinier
Life of this patent
Estimating the term…
Abstract
A method for preparing a protein isolate of the biomass of microalgae of the genus Chlorella, includes the following steps: supplying a microalgal biomass produced by fermentation, washing the biomass so as to eliminate the soluble interstitial compounds and concentrating the biomass, mechanically grinding the washed and concentrated biomass in a horizontal ball grinder-type system in order to produce an emulsion, destructuring the emulsion thus produced, triple-phase separation so as to separate the soluble fraction from the fractions containing the lipids and the cell debris, recovery of the soluble fraction thus produced in order to produce the soluble protein isolate, then evaporation, pasteurization and atomization of the protein isolate.
Claims10
A method for preparing a protein isolate from the biomass of microalgae of the Chlorella genus, comprising:
- providing a microalgal biomass produced by fermentation of microalgae of the Chlorella genus, wherein the fermentation is carried out for more than 36 hours at 28° C. with agitation and at a pH of 6.5,
- washing the microalgal biomass so as to eliminate interstitial soluble compounds and concentrate the microalgal biomass,
- mechanical milling of the washed and concentrated microalgal biomass, carried out in a horizontal bead mill type system, to obtain an emulsion,
- destructuring the obtained emulsion by (i) or (ii), thus resulting in a destructured emulsion:
- (i) by enzymatic predigestion, by treatment with polar solvent, and/or by controlled alkaline treatment targeting the protein fraction of the emulsion for a duration of 2-8 hours at a temperature of more than 30° C. and a pH of greater than 7;
- or
- (ii) by treatment with a polar solvent, and/or by enzymatic digestion targeting the interface with the lipid fraction of the emulsion for a duration of 6 hours at a temperature of 50° C. and a pH of 5-6;
- triphase separation so as to separate the soluble fraction from the fractions containing lipids and cell debris,
- recovering the soluble fraction obtained in this way in order to obtain the soluble protein isolate, then
- evaporation, pasteurization and atomization of the protein isolate.
Dependencies are inferred from the claim text.