Process for the heterotrophic production of microbial products with high concentrations of omega-3 highly unsaturated fatty acids

a technology of highly unsaturated fatty acids and heterotrophic organisms, which is applied in the field of heterotrophic organisms, can solve problems such as health effects that cannot be eliminated, and achieve the effects of extending shelf life, increasing the ph of fermentation medium, and increasing the lipid content of strains

Inactive Publication Date: 2006-07-20
DSM IP ASSETS BV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0021] Non-chloride containing sodium salts can include soda ash (a mixture of sodium carbonate and sodium oxide), sodium carbonate, sodium bicarbonate, sodium sulfate and mixtures thereof, and preferably include sodium sulfate. Soda ash, sodium carbonate and sodium bicarbonate tend to increase the pH of the fermentation medium, thus requiring control steps to maintain the proper pH of the medium. The concentration of sodium sulfate is effective to meet the salinity requirements of the microflora, preferably the sodium concentration is (expressed as g / l of Na) is greater than about 1.0 g / l, more preferably between about 1.0 g / l and about 50.0 g / l and more preferably between about 2.0 g / l and about 25 g / l.
[0022] It has been surprisingly found that fermentation of the strains in the presence of a non-chloride containing sodium salt and particularly, sodium sulfate limits the cell aggregate size of the strains to less than about 150 microns, preferably less than about 100 microns, and more preferably less than about 50 microns. As used herein, the term cell aggregate size refers to the approximate average diameter of clumps or aggregates of cells in a fermentation medium of a microfloral culture. Typically, greater than about 25 percent of the cell aggregates in a microfloral culture have cell aggregate size below the average size, more preferably greater than about 50 percent and more preferably greater than about 75 percent. Microfloral cells produced in accordance with the present invention meet cell aggregate size parameters described above while in fermentation medium as well as after freezing and / or drying of the biomass if resuspended in liquid or physically agitated, such as by a blender or vortexer. The present process is particularly important for microflora which replicate by successive bipartition (wherein a single cell replicates by dividing into two cells which each divide into two more, etc.) because as cells repeatedly and rapidly undergo this process, the cells tend to clump forming multi-cell aggregates which are often outside the cell aggregate size parameters identified above. Schizochytrium replicate by successive bipartition and by forming sporangia which release zoospores. Thraustochytrium, however, replicate only by forming sporangia and releasing zoospores. For Thraustochytrium which replicate by sporangia / zoospore formation, clumping can be a problem as well, particularly because even though the number of cells in an aggregate may not be as great as aggregates formed by successive bipartition, the individual cell sizes of Thraustochytrium tend to be larger, and thus, clumps of a small number of cells are larger. However, one deposited strain of Thraustochytrium, ATCC 26185, has been identified which does not exhibit significant aggregation.
[0023] In another aspect of the present invention, it has been found that by restricting the oxygen content of the fermentation medium during the growth of Thraustochytrium, Schizochytrium, and mixtures thereof, the lipid content of the strains can be increased. The optimum oxygen concentration for lipid production can be determined for any particular microflora by variation of the oxygen content of the medium. In particular, the oxygen content of the fermentation medium is maintained at an oxygen content of less than about 40% of saturation and preferably between about 5% of saturation and about 40% of saturation.
[0024] Growth of the strains by the invention process can be effected at any temperature conducive to satisfactory growth of the strains; for example, between about 5° C. and about 48° C., preferably between about 15° C. and about 40° C., and more preferably between about 25° C. and about 35° C. The culture medium typically becomes more alkaline during the fermentation if pH is not controlled by acid addition or buffers. The strains will grow over a pH range from 5.0-11.0 with a preferable range of about 6.0-8.5.
[0025] Various fermentation parameters for inoculating, growing and recovering microflora are discussed in detail in U.S. Pat. No. 5,130,242. The biomass harvested from a fermentation run can be dried (e.g., spray drying, tunnel drying, vacuum drying, or a similar-process) and used as a feed or food supplement for any animal whose meat or products are consumed by humans. Similarly, extracted omega-3 HUFAs can be used as a feed or food supplement. Alternatively, the harvested and washed biomass can be used directly (without drying) as a feed supplement. To extend its shelf life, the wet biomass can be acidified (approximate pH=3.5-4.5) and / or pasteurized or flash heated to inactivate enzymes and then canned, bottled or packaged under a vacuum or non-oxidizing atmosphere (e.g., N2 or CO2). The term “animal means any organism belonging to the kingdom Animalia and includes, without limitation, any animal from which poultry meat, seafood, beef, pork or lamb is derived. Seafood is derived from, without limitation, fish, shrimp and shellfish. The term “products” includes any product other than meat derived from such animals, including, without limitation, eggs or other products. When fed to such animals, omega-3 HUFAs in the harvested biomass or extracted omega-3 HUFAs are incorporated into the flesh, eggs or other products of such animals to increase the omega-3 HUFA content thereof.
[0026] A further embodiment of the present invention is the use of the harvested biomass as a food product for larval shrimp, brine shrimp, rotifers and mollusks and in particular, larval shrimp. During the larval stage of development, shrimp larvae are unable to use some food sources because the food source is too large. In particular, at certain stages of development, shrimp larvae are unable to use a food source having a diameter greater than about 150 microns. Thus, microflora grown in fermentation medium containing a non-chloride sodium salt, and particularly sodium sulfate, as broadly discussed above, are suitable for use as a shrimp food product. As discussed above, microflora grown under such conditions typically have a cell aggregate size less than about 150 microns, preferably less than about 100 microns, and more preferably less than about 50 microns.

Problems solved by technology

However, there are several significant problems with these fish oil supplements, including bioaccumulation of fat-soluble vitamins and high levels of saturated and omega-6 fatty acids, both of which can have deleterious health effects.

Method used

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  • Process for the heterotrophic production of microbial products with high concentrations of omega-3 highly unsaturated fatty acids
  • Process for the heterotrophic production of microbial products with high concentrations of omega-3 highly unsaturated fatty acids
  • Process for the heterotrophic production of microbial products with high concentrations of omega-3 highly unsaturated fatty acids

Examples

Experimental program
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Effect test

example 1

Collection and Screening

[0038] A 150 ml water sample was collected from a shallow, inland saline pond and stored in a sterile polyethylene bottle. Special effort was made to include-some of the living plant material and naturally occurring detritus (decaying plant and animal matter) along with the water sample. The sample was placed on ice until return to the laboratory. In the lab, the water sample was shaken for 15-30 seconds, and 1-10 ml of the sample was pipetted or poured into a filter unit containing 2 types of filters: 1) on top, a sterile 47 mm diameter Whatman #4 filter having a pore size about 25 μm; and 2) underneath the Whatman filter, a 47 mm diameter polycarbonate filter with about 1.0 μm pore size. Given slight variations of nominal pore sizes for the filters, the cells collected on the polycarbonate filter range in size from about 1.0 μm to about 25 μm.

[0039] The Whatman filter was removed and discarded. The polycarbonate filter was placed on solid F-1 media in a p...

example 2

Maintaining Unrestricted Growth: PO4 and Yeast Extract

[0041] Cells of Schizochytrium aggregatum (ATCC 28209) were picked from solid F-1 medium and inoculated into 50 ml of FFM medium. (Fuller et al., 1964). This medium contains: seawater, 1000 ml; glucose, 1.0 g; gelatin hydrolysate, 1.0 g; liver extract, 0.01 g; yeast extract, 0.1 g; PII metals, 5 ml; 1 ml B-vitamins solution (Goldstein et al., 1969); and 1 ml of an antibiotic solution (25 g / l streptomycin sulfate and penicillin-G). 11.0 ml of the vitamin mix (pH 7.2) contains: thiamine HCl, 200 μg; biotin, 0.5 μg; cyanocobalamin, 0.05 μg; nicotinic acid, 100 μg; calcium pantothenate, 100 μg; riboflavin, 5.0 μg; pyridoxine HCl, 40.0 μg; pyridoxamine 2HCl, 20.0 μg; p-aminobenzoic acid, 10 μg; chlorine HCl, 500 kg; inositol, 1.0 mg; thymine, 0.8 mg; orotic acid, 0.26 mg; folinic acid, 0.2 μg; and folic acid, 2.5 μg. The culture was placed on a rotary shaker (200 rpm) at 27° C. After 3-4 days, 1 ml of this culture was transferred to ...

example 3

Maintaining Unrestricted Growth: Substitution of Corn Steep Liquor for Yeast Extract

[0042] Cells of Schizochytrium sp. S31 (ATCC No. 20888) were picked from solid F-1 medium and placed into 50 ml of M-5 medium. This medium consists of (on a per liter basis): yeast extract, 1 g; NaCl, 25 g; MgSO40.7H2O, 5 g; KCl, 1 g; CaCl., 200 mg; glucose, 5 g; glutamate, 5 g; KHZPO4, 1 g; PII metals, 5 ml; A-vitamins solution, 1 ml; and antibiotic solution, 1 ml. The pH of the solution was adjusted to 7.0 and the solution was filter sterilized. Sterile solutions of corn steep liquor (4 g / 40 ml; pH 7.0) and yeast extract (1 g / 40 ml; pH 7.0) were prepared. To one set of M-5 medium flasks, the following amount of yeast extract solution was added: 1) 2 ml; 2) 1.5 ml; 3) 1 ml; 4) 0.5 ml; and 5) 0.25 ml. To another set of M-5 medium flasks the yeast extract and corn steep liquor solutions were added at the following levels: 1) 2 ml yeast extract; 2) 1.5 ml yeast extract and 0.5 ml corn steep liquor; 3)...

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Abstract

Disclosed is a process for growing the microflora Thraustochytrium, Schizochytrium, and mixtures thereof, which includes the growing of the microflora in fermentation medium containing non-chloride containing sodium salts, in particular sodium sulfate. In a preferred embodiment of the present invention, the process produces microflora having a cell aggregate size useful for the production of food products for use in aquaculture. Further disclosed is a food product which includes Thraustochytrium, Schizochytrium, and mixtures thereof, and a component selected from flaxseed, rapeseed, soybean and avocado meal. Such a food product includes a balance of long chain and short chain omega-3 highly unsaturated fatty acids.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS [0001] This application is a continuation-in-part of copending and commonly assigned U.S. patent application Ser. No. 07 / 911,760, filed Jul. 10, 1992 which is incorporated herein in its entirety by reference which is a divisional of U.S. patent application Ser. No. 07 / 580,778, filed Sep. 11, 1990 which is incorporated herein in its entirety which issued as U.S. Pat. No. 5,130,242 which is a continuation-in-part of copending and commonly assigned U.S. patent application Ser. No. 07 / 439,093, filed Nov. 17, 1989 which is incorporated herein in its entirety by reference which is a continuation-in-part of U.S. patent application Ser. No. 07 / 241,410, filed Sep. 7, 1988 which was previously expressly abandoned.FIELD OF THE INVENTION [0002] The field of this invention relates to heterotrophic organisms and a process for culturing them for the production of lipids with high concentrations of omega-3 highly unsaturated fatty acids (HUFA) suitable for hu...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C12N1/20A01K61/00A23K1/00A23K1/16A23K1/18A23L1/30A23L11/00A23L13/00A23L13/40A23L13/50A23L15/00A23L17/00A23L17/40A23L19/00A23L25/00A23L29/00A61K31/20A61K31/202C11B1/10C12N1/12C12N1/14C12N1/38C12P7/64C12R1/645
CPCA23K1/003A23K1/008A23K1/164A23K1/18A23K1/1813A23K1/1826A23K1/188A23L1/0345A23L1/2006A23L1/2128A23L1/3008A23L1/31A23L1/31454A23L1/315A23L1/3204A23L1/325A23L1/3252A23L1/33A23L1/366A61K31/20A61K31/202C11B1/10C12N1/10C12N1/14C12P7/6409C12P7/6427C12P7/6463C12P7/6472C12P7/649Y10S435/911Y10S426/805Y10S435/946Y10S426/807Y02E50/13A23K10/16A23K20/158A23K50/00A23K50/10A23K50/75A23K50/80A23L29/065A23L11/07A23L19/09A23L33/12A23L13/00A23L13/43A23L13/50A23L15/20A23L17/00A23L17/65A23L17/40A23L25/30Y02A40/818Y02E50/10A23K40/25A23K40/20C12N1/12C12P7/6432
Inventor BARCLAY, WILLIAM R.
Owner DSM IP ASSETS BV
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