Solventless extraction process
View Patent ↗The present invention provides a method for extracting lipids from microorganisms without using organic solvent as an extraction solvent. In particular, the present invention provides a method for extracting lipids from microorganisms by lysing cells and removing water soluble compound and/or materials by washing the lysed cell mixtures with aqueous washing solutions until a substantially non-emulsified lipid is obtained.
1. A process for recovering lipids from microorganisms comprising:
(a) growing said microorganisms in a culture medium;
(b) treating microorganism cells from said culture medium without drying said cells to release intercellular lipids;
(c) subjecting the culture medium containing the released intercellular lipids to gravity separation to form a light lipid-containing phase and a heavy phase;
(d) separating said heavy phase from said light phase;
(e) treating said light phase to break an emulsion formed between said lipid and water; and
(f) recovering a crude lipid,
wherein the process comprises extracting lipids from a microbial biomass containing at least about 10% by weight entrained water and wherein a solventless extraction process is used.
2. The process of claim 1 , wherein said light phase comprises an emulsified lipid.
3. The process of claim 2 , wherein said emulsified lipid comprises a suspension of said lipid in an aqueous solution.
4. The process of claim 3 , wherein said aqueous solution comprises solid cell materials.
5. The process of claim 1 , wherein said microorganisms are obtained from a fermentation process.
6. The process of claim 1 , wherein said microorganism is selected from the group consisting of algae, fungi, bacteria and protists.
7. The process of claim 6 , wherein said microorganisms comprise microorganisms of the order Thraustochytriales.
8. The process of claim 7 , wherein said microorganisms are selected from the genus Thraustochytrium, Schizochytrium and mixtures thereof.
9. The process of claim 1 , wherein said microorganisms are capable of producing at least about 0.1 grams per liter per hour of lipids, wherein said lipids are omega 3 and highly unsaturated fatty acids comprising eicosapentaenoic acid, docosapentaenoic acid, and docosahexaenoic acid, or mixtures thereof.
10. The process of claim 1 , wherein at least about 20% of said lipid is omega 3 highly unsaturated fatty acids comprising eicosapentaenoic acid, docosapentaenoic acid, and docosahexaenoic acid, or mixtures thereof.
11. The process of claim 1 , wherein said treatment of the cells includes a treatment selected from the group consisting of heating said cells, exposing said cells to basic conditions, exposing said cells to a chelating compound or combinations thereof.
12. The process of claim 1 , wherein said treatment of the cells comprises heating the cells to at least 50° C. before, during or after exposing the cells to a basic condition, a chelating compound or mixtures thereof.
13. The process of claim 1 , wherein said gravity separation of step (c) comprises passing the culture medium containing the released intracellular lipids through a stacked-disc, separator or decanter centrifuge.
14. The process of claim 1 , wherein the treatment to break the emulsion comprises mixing the emulsion with water, alcohol and/or acetone and subjecting the mixture to gravity separation.
15. The process of claim 14 , wherein said gravity separation comprises centrifugation.
16. The process of claim 15 , wherein said centrifugation includes treatment in a stacked-disc-, separator- or decanter-type centrifuge.
17. The process of claim 14 , wherein said treatment is repeated at least 3 times to obtain said crude lipid.
18. The process of claim 1 , wherein said crude lipid is subjected to further refining or purification to obtain a refined lipid.
19. The process of claim 18 , wherein said crude lipid is bleached and deodorized.