WO2019221981A1 - Seaweed meal and method of making the same - Google Patents
Seaweed meal and method of making the same Download PDFInfo
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- WO2019221981A1 WO2019221981A1 PCT/US2019/031218 US2019031218W WO2019221981A1 WO 2019221981 A1 WO2019221981 A1 WO 2019221981A1 US 2019031218 W US2019031218 W US 2019031218W WO 2019221981 A1 WO2019221981 A1 WO 2019221981A1
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- WIPO (PCT)
- Prior art keywords
- seaweed
- hours
- meal
- hour
- minutes
- Prior art date
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- 241001474374 Blennius Species 0.000 title claims abstract description 272
- 235000012054 meals Nutrition 0.000 title claims abstract description 90
- 238000004519 manufacturing process Methods 0.000 title description 5
- 238000000034 method Methods 0.000 claims abstract description 55
- 108010059892 Cellulase Proteins 0.000 claims abstract description 35
- 229940106157 cellulase Drugs 0.000 claims abstract description 35
- 150000003839 salts Chemical class 0.000 claims abstract description 35
- 235000013305 food Nutrition 0.000 claims abstract description 29
- 238000004061 bleaching Methods 0.000 claims abstract description 14
- 238000004140 cleaning Methods 0.000 claims abstract description 10
- 238000000227 grinding Methods 0.000 claims abstract description 8
- 238000001035 drying Methods 0.000 claims abstract description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 75
- 235000002639 sodium chloride Nutrition 0.000 claims description 40
- 239000000243 solution Substances 0.000 claims description 40
- 108090000790 Enzymes Proteins 0.000 claims description 23
- 102000004190 Enzymes Human genes 0.000 claims description 23
- 229940088598 enzyme Drugs 0.000 claims description 23
- 239000007844 bleaching agent Substances 0.000 claims description 18
- 239000000463 material Substances 0.000 claims description 15
- 239000002253 acid Substances 0.000 claims description 14
- 241001519517 Kappaphycus Species 0.000 claims description 12
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 12
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 10
- OSVXSBDYLRYLIG-UHFFFAOYSA-N dioxidochlorine(.) Chemical compound O=Cl=O OSVXSBDYLRYLIG-UHFFFAOYSA-N 0.000 claims description 10
- 239000012535 impurity Substances 0.000 claims description 10
- 238000002203 pretreatment Methods 0.000 claims description 10
- 241001428166 Eucheuma Species 0.000 claims description 9
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 8
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 claims description 8
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 6
- 230000007935 neutral effect Effects 0.000 claims description 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 6
- 239000011780 sodium chloride Substances 0.000 claims description 6
- 239000004155 Chlorine dioxide Substances 0.000 claims description 5
- 239000003513 alkali Substances 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- 239000000460 chlorine Substances 0.000 claims description 5
- 235000019398 chlorine dioxide Nutrition 0.000 claims description 5
- 239000001103 potassium chloride Substances 0.000 claims description 5
- 235000011164 potassium chloride Nutrition 0.000 claims description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
- 241000206576 Chondrus Species 0.000 claims description 4
- 241001467355 Gigartina Species 0.000 claims description 4
- 239000011736 potassium bicarbonate Substances 0.000 claims description 4
- 235000015497 potassium bicarbonate Nutrition 0.000 claims description 4
- 229910000028 potassium bicarbonate Inorganic materials 0.000 claims description 4
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 claims description 4
- 239000012266 salt solution Substances 0.000 claims description 4
- 239000011734 sodium Substances 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 4
- 235000017550 sodium carbonate Nutrition 0.000 claims description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 3
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 claims description 3
- 229910000027 potassium carbonate Inorganic materials 0.000 claims description 3
- 235000011181 potassium carbonates Nutrition 0.000 claims description 3
- GHQFLMULNSGOAR-UHFFFAOYSA-N 2,3-dihydroxybutanedioic acid;sodium Chemical compound [Na].OC(=O)C(O)C(O)C(O)=O GHQFLMULNSGOAR-UHFFFAOYSA-N 0.000 claims description 2
- 239000001509 sodium citrate Substances 0.000 claims description 2
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 claims description 2
- 235000011083 sodium citrates Nutrition 0.000 claims description 2
- 241000206572 Rhodophyta Species 0.000 claims 1
- 238000005516 engineering process Methods 0.000 abstract description 5
- 239000000796 flavoring agent Substances 0.000 abstract description 5
- 235000019634 flavors Nutrition 0.000 abstract description 5
- 230000003301 hydrolyzing effect Effects 0.000 abstract 1
- 235000010418 carrageenan Nutrition 0.000 description 25
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- 239000000679 carrageenan Substances 0.000 description 23
- 229940113118 carrageenan Drugs 0.000 description 23
- 239000000523 sample Substances 0.000 description 23
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 23
- 238000003756 stirring Methods 0.000 description 20
- 238000012360 testing method Methods 0.000 description 15
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- 210000004080 milk Anatomy 0.000 description 7
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- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 4
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- 229910019142 PO4 Inorganic materials 0.000 description 3
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- 238000004458 analytical method Methods 0.000 description 3
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- 150000002739 metals Chemical class 0.000 description 3
- 229910017604 nitric acid Inorganic materials 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- WZYRMLAWNVOIEX-BGPJRJDNSA-N 3,6-anhydro-D-galactose Chemical compound O=C[C@H](O)[C@H]1OC[C@@H](O)[C@@H]1O WZYRMLAWNVOIEX-BGPJRJDNSA-N 0.000 description 2
- 241000195493 Cryptophyta Species 0.000 description 2
- 229920001503 Glucan Polymers 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000012267 brine Substances 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- WZYRMLAWNVOIEX-UHFFFAOYSA-N cinnamtannin B-2 Natural products O=CC(O)C1OCC(O)C1O WZYRMLAWNVOIEX-UHFFFAOYSA-N 0.000 description 2
- 239000012065 filter cake Substances 0.000 description 2
- 238000001879 gelation Methods 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 238000010979 pH adjustment Methods 0.000 description 2
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- 239000005017 polysaccharide Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 235000019624 protein content Nutrition 0.000 description 2
- 235000011962 puddings Nutrition 0.000 description 2
- 235000020122 reconstituted milk Nutrition 0.000 description 2
- 235000013580 sausages Nutrition 0.000 description 2
- 230000001953 sensory effect Effects 0.000 description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000012085 test solution Substances 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- KIAPWMKFHIKQOZ-UHFFFAOYSA-N 2-[[(4-fluorophenyl)-oxomethyl]amino]benzoic acid methyl ester Chemical compound COC(=O)C1=CC=CC=C1NC(=O)C1=CC=C(F)C=C1 KIAPWMKFHIKQOZ-UHFFFAOYSA-N 0.000 description 1
- QCVGEOXPDFCNHA-UHFFFAOYSA-N 5,5-dimethyl-2,4-dioxo-1,3-oxazolidine-3-carboxamide Chemical compound CC1(C)OC(=O)N(C(N)=O)C1=O QCVGEOXPDFCNHA-UHFFFAOYSA-N 0.000 description 1
- 239000004382 Amylase Substances 0.000 description 1
- 108010065511 Amylases Proteins 0.000 description 1
- 102000013142 Amylases Human genes 0.000 description 1
- 241000228212 Aspergillus Species 0.000 description 1
- 108010084185 Cellulases Proteins 0.000 description 1
- 102000005575 Cellulases Human genes 0.000 description 1
- 102000002322 Egg Proteins Human genes 0.000 description 1
- 108010000912 Egg Proteins Proteins 0.000 description 1
- 101710121765 Endo-1,4-beta-xylanase Proteins 0.000 description 1
- 101710166469 Endoglucanase Proteins 0.000 description 1
- 108090000371 Esterases Proteins 0.000 description 1
- LLQPHQFNMLZJMP-UHFFFAOYSA-N Fentrazamide Chemical compound N1=NN(C=2C(=CC=CC=2)Cl)C(=O)N1C(=O)N(CC)C1CCCCC1 LLQPHQFNMLZJMP-UHFFFAOYSA-N 0.000 description 1
- 238000001157 Fourier transform infrared spectrum Methods 0.000 description 1
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- WDIHJSXYQDMJHN-UHFFFAOYSA-L barium chloride Chemical compound [Cl-].[Cl-].[Ba+2] WDIHJSXYQDMJHN-UHFFFAOYSA-L 0.000 description 1
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- 229910052794 bromium Inorganic materials 0.000 description 1
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- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
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- 238000004090 dissolution Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 235000014103 egg white Nutrition 0.000 description 1
- 210000000969 egg white Anatomy 0.000 description 1
- YERABYSOHUZTPQ-UHFFFAOYSA-P endo-1,4-beta-Xylanase Chemical compound C=1C=CC=CC=1C[N+](CC)(CC)CCCNC(C(C=1)=O)=CC(=O)C=1NCCC[N+](CC)(CC)CC1=CC=CC=C1 YERABYSOHUZTPQ-UHFFFAOYSA-P 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
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- 108010093305 exopolygalacturonase Proteins 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- -1 glucanase Proteins 0.000 description 1
- 239000003324 growth hormone secretagogue Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 229940059442 hemicellulase Drugs 0.000 description 1
- 108010002430 hemicellulase Proteins 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- LPUQAYUQRXPFSQ-DFWYDOINSA-M monosodium L-glutamate Chemical compound [Na+].[O-]C(=O)[C@@H](N)CCC(O)=O LPUQAYUQRXPFSQ-DFWYDOINSA-M 0.000 description 1
- 235000013923 monosodium glutamate Nutrition 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
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- 239000013049 sediment Substances 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
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- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
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- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L17/00—Food-from-the-sea products; Fish products; Fish meal; Fish-egg substitutes; Preparation or treatment thereof
- A23L17/60—Edible seaweed
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L13/00—Meat products; Meat meal; Preparation or treatment thereof
- A23L13/50—Poultry products, e.g. poultry sausages
- A23L13/52—Comminuted, emulsified or processed products; Pastes; Reformed or compressed products from poultry meat
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L5/00—Preparation or treatment of foods or foodstuffs, in general; Food or foodstuffs obtained thereby; Materials therefor
- A23L5/20—Removal of unwanted matter, e.g. deodorisation or detoxification
- A23L5/25—Removal of unwanted matter, e.g. deodorisation or detoxification using enzymes
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y302/00—Hydrolases acting on glycosyl compounds, i.e. glycosylases (3.2)
- C12Y302/01—Glycosidases, i.e. enzymes hydrolysing O- and S-glycosyl compounds (3.2.1)
- C12Y302/01004—Cellulase (3.2.1.4), i.e. endo-1,4-beta-glucanase
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
- A23L29/20—Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents
- A23L29/206—Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents of vegetable origin
- A23L29/256—Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents of vegetable origin from seaweeds, e.g. alginates, agar or carrageenan
Definitions
- This disclosure relates to seaweed meal and a method of making the same.
- the seaweed meal disclosed herein can replace the use of carrageenan.
- the method and the seaweed meal production can be used in the field of food industry.
- Carrageenans are linear sulfated polysaccharides extracted from edible red seaweeds. They are used in food industry, particularly in dairy and meat products, to bind to food proteins and help stabilize and texturize the food products. Therefore, carrageenans have wide applications in food industry as gelling agents, thickening agents, and stabilizing agents. Carrageenan is an animal-product-free ingredient replacing gelatin in vegetarian food products.
- US Patent Application Publication No. 2015/0164125 describes a method for making seaweed meal, including the steps of harvesting the seaweed from a sea floor; chopping the seaweed; cleaning the seaweed; desiccating the seaweed; grinding the seaweed to a meal; drying the seaweed between the cleaning step and the desiccating step, the drying step is accomplished by a seaweed agitator.
- US Patent No. 4,125,392 describes a seaweed filter cake product produced by conditioning raw seaweed by mixing it with water and other substances, and then digesting the conditioned seaweed by cooking it with steam to form a steam-digested mixture. The filter cake is skimmed off the top of the resulting steam-digested mixture and used by itself, or as a starting product for producing fertilizers or plant growth stimulators in liquid or pelletized form.
- the prior-art references merely produced a simple seaweed meal or cake products, with poor gelling capability, brown or green color, and strong fishery flavor. These prior-art seaweed products are not suitable for use as gelling agent or stabilizer in food applications to replace carrageenan extracted from red seaweed. Thus, there is a need in the field to produce better quality seaweed meal suitable for food applications.
- a method of making a seaweed meal to replace carrageenan in the food industry comprises the steps of cleaning the fresh or dried red seaweed, pretreating the red seaweed with a salt under heat, and drying and grinding the treated red seaweed to obtain the seaweed meal.
- the method comprises a step of bleaching the red seaweed with a bleaching agent before the drying and grinding step.
- the method comprises a step of treating the red seaweed with an enzyme such as a cellulase before the drying and grinding step.
- the bleaching step is carried out before the enzyme treatment step.
- the bleaching step is carried out after the enzyme treatment step.
- seaweed meal produced by the method described above.
- the seaweed meal produced by the disclosed method can be used in food industry to replace carrageenan as a gelling ingredient in, for example, dairy, jelly, pudding or meat products.
- Figures 1A-1 C show the FTIR results of seaweed meal Sample 2 (top curve in each panel) in comparison to commercially available seaweed powder (Sample 9) (middle curve in each panel), and carrageenan (Sample 10) (bottom curve in each panel).
- Figure 1A shows the entire range while Figures 1 B and 1 C show the selective ranges (enlarged).
- Figures 2A-2B show the texture of the meat products obtained by the seaweed meal samples.
- Figure 2A shows the hardness and
- Figure 2B shows the chewiness of the meat produts prepared by seaweed meal samples S4, S5, and S11 in comparison to those prepared by commercially available seaweed powder (Sample 9) and carrageenan (Sample 10).
- the method is a simple process to produce a seaweed meal with desired features such as light color, good flavor and taste, good mouthfeel, high gelling capability, great stability, and ideal smoothness and slipperiness suitable for food applications.
- the seaweed meal produced by the disclosed method can be used in food industry to replace carrageenan as a gelling agent in, for example, producing dairy, jelly, pudding, or meat products.
- the method disclosed herein comprises the steps of cleaning seaweed material with water, pre-treating the clean seaweed material with a salt under heat, bleaching the pre-treated seaweed material with a bleaching agent, and treating the bleached seaweed material with an enzyme to obtain a seaweed meal suitable for food applications.
- the bleaching step is optional and can be included if a light color seaweed meal is desired.
- the enzyme treatment step is also optional and can be carried out before or after the bleaching step if both of these optional steps are included.
- Seaweed is also called macroalgae, marine algae, or seagrass.
- the seaweed material used for the disclosed method includes red seaweed, for example, Chondrus, Gigartina, Kappaphycus, and Eucheuma. In some embodiments, a combination of at least two, at least three, or at least four of the disclosed red seaweed can be used.
- the seaweed material is cleaned by water prior to any treatment. Seaweed materials in any form such as dry seaweed, or fresh seaweed, or rehydrated seaweed, material can be used. It is known in the art that fresh seaweed can be dehydrated to obtain dry seaweed. The dry seaweed can be rehydrated by soaking the dry seaweed in water. In some embodiments, the dry seaweed is rehydrated during the cleaning step.
- the dry seaweed:water ratio in the cleaning step can be between 1 :1 and 1 :40, between 1 :3 and 1 :30, between 1 :5 and 1 :25, between 1 :5 and 1 :20, between 1 :10 and 1 :20, or between 1 :5 and 1 :10; when fresh seaweed or rehydrated seaweed is used, the fresh seaweed:water ratio in the cleaning step can be between 1 :1 and 1 :3, between 1 :1 and 1 :5, between 1 :2 and 1 :5, between 1 :1 and 1 : 10, or between 1 :1 and 1 :15.
- Salt pre-treatment process is an environment-friendly process to produce a seaweed meal with good gel capability and/or stability, while retaining more natural health promoting ingredients. This simplified process generates less waste water and is more environmental friendly, compared to the traditional alkali and/or acid pre-treatment process. Therefore, the disclosed technology can produce high quality seaweed meal in a time-efficient and cost-effective manner.
- the salts that can be used for the disclosed method include one or more salts of one or more metals and one or more acids.
- the one or more metals for the one or more salts include, without limitation, alkaline metals (e.g., Li, Na, K, Rb) and alkaline-earth metals (e.g., Be, Mg, Ca, Sr), and examples of the one or more acids for the one or more salts include, without limitation, HX (e.g., X is halogen such as F, Cl, Br, I), sulfuric acid, and carbonic acid.
- suitable salt include, without limitation, sodium chloride, potassium chloride, sodium carbonate, sodium bicarbonate, potassium carbonate, potassium bicarbonate, sodium citrate, and sodium tartaric acid.
- a combination of at least two, at least three, at least four, at least five, or at least six salts can be used in the pre-treatment.
- the seaweed:salt ratio can be between 1 :1 and 1 :3, between 1 :1 and 1 :5, between 1 :2 and 1 :5, or between 1 :1 and 1 :10.
- the salt solution can be at a concentration of between 1 % and 10%, between 5% and 15%, between 3% and 20%, between 5% and 25%, between 10% and 30%, or between 5% and 30% (wt%).
- the salt pre-treatment step is performed at a temperature between 40°C and 80°C, between 50°C and 100°C, between 60°C and 90°C, or between 70°C and 120°C.
- the salt pre-treatment can be performed for a period of between 0.5 hour and 24 hours, between 0.5 hour and 20 hours, between 0.5 hour and 15 hours, between 0.5 hour and 12 hours, between 0.5 hour and 8 hours, between 0.5 hour and 6 hours, between 1 hour and 4 hours, between 1.5 hours and 3 hours, or between 0.5 hour and 4 hours.
- the seaweed is treated with a bleaching agent to obtain a light color seaweed meal.
- the bleaching agent that can be used for the disclosed method includes hypochlorous acid, sodium hypochlorous, and chlorine dioxide.
- a combination of the disclosed bleaching agents such as a combination of at least two bleaching agents, or at least three bleaching agents, can be used.
- the seaweed: bleaching agent ratio can be between 1 :1 and 1 :3, between 1 :1 and 1 :5, between 1 :2 and 1 :5, or between 1 :1 and 1 :10.
- the bleaching agent can be at a concentration of available chlorine content of between 0.01 % and 5%, between 0.02% and 3%, between 0.05% and 2%, between 0.05% and 1 %, between 0.05% and 0.5%, or between 0.01 % and 0.1 % (wt%).
- the bleaching step can be performed for a period of between 5 minutes and 240 minutes, between 10 minutes and 180 minutes, between 10 minutes and 120 minutes, between 10 minutes and 60 minutes, or between 20 minutes and 60 minutes.
- the pre-treated or bleached seaweed has an impurity of the red seaweed of less than 5%, less than 4%, less than 3%, less than 2%, or less than 1 %, and a color of light brown to light yellow.
- the enzyme treatment catalyzes the hydrolysis of the cellulose and/or related polysaccharides or the like in the pre-treated and/or bleached seaweed such that the obtained seaweed meal has an improved mouthfeel.
- Various enzymes may be used to achieve this goal, for example, cellulase, hemicellulase, pectinase, amylase, xylanase, pentosanase, glucanase, esterase.
- one or more enzymes can be used to treat the seaweed.
- cellulase including acid cellulase, neutral cellulase, and alkali cellulose, including but not limited to 1 ,4-p-D-glucan glucanohydrolase, endo-1 ,4-p-D-glucanase, 1 ,4-p-D- glucan cellobilhydrolase, exo-1 ,4-p-D-glucannase, b-1 ,4-glucosidase, from Trichoderma, Aspergillus or Penicillium. In some embodiments, a combination of at least two, at least three, or more of these cellulases can be used.
- the seaweed:enzyme ratio can be between 1 : 1 and 1 :3, between 1 :2 and 1 :5, between 1 : 1 and 1 :5, between 1 : 1 and 1 :6 or between 1 : 1 and 1 : 10.
- the enzyme can be at a concentration of between 10 U/g and 500 U/g, between 20 U/g and 400 U/g, between 30 U/g and 300U/g, between 50 U/g and 200 U/g, or between 75 U/g and 150 U/g.
- the enzyme treatment step can be performed for a period of between 0.5 hour and 12 hours, between 0.5 hour and 8 hours, between 0.5 hour and 6 hours, between 1 hour and 3 hours, or between 1 hour and 4 hours, at a pH range of between 2.0 and 10.0, between 3.0 and 9.0, between 3.0 and 8.0, between 4.0 and 7.0, or between 5.0 and 6.0, or at a temperature between 15°C and 100°C, between 20°C and 90°C, between 30°C and 80°C, between 20°C and 70°C, between 30°C and 60°C, or between 40°C and 50°C.
- a variety of acids or alkalis can be used to adjust pH.
- the alkali for pH adjustment is selected from the group consisting of sodium hydroxide, potassium hydroxide, and a combination thereof.
- the acid for pH adjustment is selected from the group consisting of hydrochloric acid, nitric acid, phosphate acid, and a combination of at least two, or at least three of these acids.
- the clean seaweed is pre-treated with between 5% and 30% (wt%) of a salt solution at a ratio of between 1 :2 and 1 :5 and at a temperature of between 50°C and 90°C, and then treated with a cellulase having a concentration of between 30 U/g and 200 U/g at a ratio of between 1 :2 and 1 :5 and at a temperature of between 40°C and 60°C.
- the treated seaweed can be dried and grinded to obtain the seaweed meal.
- the dried seaweed meal has a sulfate content of between 1 % and 50%, between 10% and 45%, between 5% to 40% or between 15% and 30%.
- the viscosity of the dried seaweed meal is at least 0.005 Pa-S.
- the dried seaweed meal has a color of light brown to light yellow.
- the seaweed meal obtained by the disclosed technology contains the following ingredients: > 50% soluble dietary fiber, about 5%- 10% insoluble dietary fiber, > 60% total dietary fiber, about 8%-40% sulfate content, and ⁇ 2% protein.
- the seaweed meal obtained by the disclosed technology has the following properties: gel strength at 0.5% >100 g/cm 2
- the seaweed meal obtained from Kappaphycus has a gel strength of about 200 g/cm 2 at 1 .5% seaweed meal in water with 0.2% KCI added.
- the seaweed meal obtained from Kappaphycus is particularly useful as a gelling agent in meat products.
- Other reagents include: hypochlorous acid, sodium hypochlorous, available chlorine contents 10%, food grade; chlorine dioxide, available chlorine contents 50%, food grade; hydrochloric acid, 36%, food grade; and sulfuric acid, nitric acid, phosphate acid, 99%, food grade; sodium hydroxide, potassium hydroxide, 99% food grade; acid cellulase, neutral cellulase, alkaline cellulase, 50,000 U/g, food grade; sodium chloride, potassium chloride, sodium carbonate, sodium bicarbonate, potassium carbonate, potassium bicarbonate, 99%, food grade.
- the clean seaweed was mixed with 50 kg 5% sodium chloride solution in the reaction tank, the mixture was heated and the temperature was kept at 50°C, with stirring at 60 RPM for 30 minutes, followed by washing the seaweed with 500 kg water. Once the water was removed, 49 kg of salt pre-treated seaweed was obtained.
- the salt pre-treated seaweed was mixed with 49 kg of 0.01 % bleaching agent, hydrochloric acid (HCIO) solution in the tank, stirred at 60 RPM for 10 minutes, then the hypochlorous acid solution was removed, and the seaweed was washed with 100 kg water. Once the water was removed 47 kg pre-treated seaweed was obtained.
- the specification of the pre-treated seaweed was: impurity of the red seaweed ⁇ 0.5%, and the color was yellow.
- the pre-treated seaweed was mixed with 47 kg of 30 U/g acid cellulase solution, pH was adjusted to 3.0 using hydrochloric acid, and the temperature was kept at 20°C, with stirring at 60 RPM for 30 minutes. Then the cellulase solution was removed and the seaweed was washed with 100 kg water. 45 kg cellulase treated seaweed was obtained. And then the seaweed was dried and grinded to obtain 4.1 kg seaweed meal.
- the pre-treated seaweed was mixed with 120 kg of 100 U/g cellulase solution, pH was adjusted to 5.0 with sulfuric acid, heated and the temperature was kept at 50°C, with stirring at 60 RPM for 120 minutes.
- the cellulase solution was removed and the seaweed was washed with 100 kg water. 44 kg of cellulase treated seaweed was obtained. And then the seaweed was dried and grinded to obtain 3.9 kg seaweed meal.
- Example 4 Preparation of Seaweed Meal from Dried Eucheuma
- the pre-treated seaweed was mixed with 210 kg of 300 U/g neutral cellulase solution, pH was adjusted to 8.0 with sodium hydroxide solution, heated and the temperature was kept at 70°C, with stirring at 60 RPM for 6 hours.
- the cellulase solution was removed and the seaweed was washed with 200 kg water. 36 kg cellulase treated seaweed was obtained. And then the seaweed was dried and grinded to obtain 3.1 kg seaweed meal.
- the pre-treated seaweed was mixed with 41 kg of 30 U/g alkali cellulase solution, pH was adjusted to 8.0 using sodium hydroxide, and the temperature was kept at 20°C, with stirring at 60 RPM for 30 minutes.
- the cellulase solution was removed and the seaweed was washed with 100 kg water. 38 kg cellulase treated seaweed was obtained. And then the seaweed was dried and grinded to obtain 3.3 kg seaweed meal.
- the pre-treated seaweed was mixed with 120 kg of 100 U/g cellulase solution, pH was adjusted to 4.8 with phosphate acid, heated and the temperature was kept at 45°C, with stirring at 60 RPM for 120 minutes.
- the cellulase solution was removed and the seaweed was washed with 100 kg water. 43 kg of cellulase treated seaweed was obtained. And then the seaweed was dried and grinded to obtain 3.8 kg seaweed meal.
- the pre-treated seaweed was mixed with 90 kg of 60 U/g acid cellulase solution, pH was adjusted to 4.0 with nitric acid, heated and the temperature was kept at 40°C, with stirring at 60 RPM for 1 hour.
- the cellulase solution was removed and the seaweed was washed with 100 kg water. 40 kg cellulase treated seaweed was obtained. And then the seaweed was dried and grinded to obtain 3.2 kg seaweed meal.
- the pre-treated seaweed was mixed with 200 kg of 200 U/g neutral cellulase solution, pH was adjusted to 7.5 with potassium hydroxide, heated and the temperature was kept at 60°C, with stirring at 60 RPM for 240 minutes.
- the cellulase solution was removed and the seaweed was washed with 100 kg water. 41 kg cellulase treated seaweed was obtained. And then the seaweed was dried and grinded to obtain 3.6 kg seaweed meal.
- Table 2 summarizes the treatment of Examples 2-10 to obtain various seaweed meal preparations. Additionally, commercially available dried eucheuma cottonii powder from RICH MOON CO., LTD (Sample 9) and carrageenan from the Green Fresh Group (Sample 10) were used as controls.
- the sulfate test was performed as follows: 100 mg sample was dissolved in 20 ml of water (with heating if necessary), and 3 ml of barium chloride test solution and 5 ml of hydrochloric acid were added. The test solution was diluted and filtered if a precipitate formed. The solution or the filtrate was boiled for 5 minutes. A white, crystalline precipitate appeared.
- Viscosity test was performed as follows: 1.5 grams of seaweed meal was weighed and dispersed into 98.5 grams deionized water under stirring with IKA (500- 600 rpm) for 10 min, heated to 80 ° C , and the solution was kept in a water bath at 75 ° C . The viscosity was tested with Brookfield LVT, Spindle # 2, at 60 rpm. [0047] The soluble dietary fiber contents of the samples were determined by the AOAC official methods, see for example, AOAC 985.29 and AOAC 991.43. The protein contents of the samples were determined by the established kjeldahl method, published as ISO 20483:2006.
- Table 4 illustrates the process of preparing dairy products with seaweed meal.
- Table 5 summarizes the results of the basic analysis of the seaweed meal preparation samples 1-8 and 11 , obtained from Examples 2-10 in comparison with commercially available seaweed meal powder (Sample 9) and carrageenan (Sample 10).
- Samples 2 and 5 produced the best results in various tests.
- Samples 7 and 8 also produced acceptable results in various tests.
- Figure 1 shows the results of a typical Fourier Transform Infrared Spectrometer (FTIR) of Sample 2 in comparison with Sample 9, commercially obtained seaweed powder, and Sample 10, commercially obtained carrageenan.
- the spectral feature at approximately 845 cm 1 is mainly associated with D-galactose-4-sulfphate ( Figure 1 C).
- the presence of a strong band in the FTIR spectra at 930 cm 1 is indicative of the occurrence of 3,6-anhydro-D-galactose ( Figure 1 C).
- 1550-1510 cm -1 is protein N-H bending (amide bands II) ( Figure 1 B).
- FTIR demonstrates that the process disclosed herein produced a seaweed meal having a lower protein content compared to the commercially available seaweed powder and similar to carrageenan, while the content of 3,6-anhydro-D-galactose of the seaweed meal obtained by the disclosed technology is higher than that of the commercially available seaweed powder but lower than that of carrageenan.
- the gel strength test without KCI was performed as follows: 900 grams of reconstituted milk was weighed and added to a stainless-steel container having a diameter of 12 cm. The container is placed on the induction stove and under the agitator IKA. An adequate amount of the sample powder, e.g., 4.5 grams, was weighed and dispersed in the container under agitation at 1100 rpm. The induction stove (Philips HD4925) was turned on and set at the thermostat 5 (pre-heating time was between 9-12 minutes). While the temperature was on the rise, 2 drops of defoamer was added to the bottom of the container to be used for shearing. The mixture was boiled to 90°C and then the heating and stirring were stopped.
- the mixture was poured into 2 jelly cups and the testing samples were kept in an incubator at 20°C for at least 16 hours.
- the cover was gently removed by slipping on the sides of the jelly cup without damaging the gel.
- the cup was placed in the center of TXAT2i Texture Analyzer and the probe was placed above the center of the gel.
- 0.5 wt% of carrageenan was mixed with 900 grams of reconstituted milk.
- the gel strength test with KCI was performed as follows: 1.5 g of seaweed meal sample and 0.2 g of KCI were placed in a 200 ml beaker and then 100 ml distilled water was added to the beaker while stirring such that the seaweed meal sample was fully suspended in water. The mixture was heated to 90°C with slow stirring. More water was added to make up the volume to 100 ml after heating. The sample was stirred and divided into 3 intensity measurement cups, and stored at room temperature for 16 hours with a film sealing. Subsequently the samples were removed from the cups and analyzed on a TXAT2i Texture Analyzer.
- the carrageenan or seaweed meal samples were mixed with sugar.
- the mixtures were dispersed into milk at 75°C while stirring for 10 minutes and homogenized at 65-70°C, 200 bar, package filled, sterilized at 121°C for 7 minutes, and then cooled down to room temperature.
- the ingredients for the test include 80 wt% of fresh milk, 5 wt% of sugar, and 0.03 wt% of carrageenan.
- the viscosity test, sensory test, and stability test with LUMifuge were performed on the sweet milk products 1 -11 (P1 -P11 ) obtained with seaweed meal samples 1 -11 (S1 -S11 ).
- the viscosity test demonstrates that the final sweet milk products P1-P5, P7, P8 and P11 made with seaweed meal S1 -5, S7, S8 and S11 had no significant difference with sweet milk product P10 made with seaweed meal S10. But the viscosity of P6 and P9 were significantly lower than the other sweet milk products. Also, P6 and P9 were worse on water holding ability than the other by LUMi test, where higher instability index indicates lower stability. Furthermore, in the sensory test, P6 and P9 easily distinguished themselves from other products. Both P6 and P9 had an astringent and rough mouthfeel, significantly worse than P1-P5, P7, P8, P10 and P11.
- the carrageenan or seaweed meal samples were used in preparing meat products such as chicken sausages in this example.
- the ingredients are listed in Table 8 below.
- a brine was prepared by dispersing salt and sugar in cold water at 4-5°C to allow complete dissolution.
- the cured chicken breast was prepared by grinding the chicken breast with a No. 6 plate and then tumbled in brine for 8 hours by a vacuum tumbling process. One hour before the end of the tumbling process, the remaining ingredients including soy flour, flavors, seaweed meal or carrageenan, egg white, MSG, starch, and water were added.
- the chicken skin emulsion was prepared by dispersing glycerin monostearate in water and slowly adding the chicken skin to emulsify until an emulsion was obtained.
- the emulsion was kept overnight at 3-6°C to allow complete gelation, and then the chicken skin gelation was subjected to grinding with a No. 3 plate. 300 grams of the ground chicken breast and chicken skin were used to stuff 60 mm casing. The sausage was cooked to an internal temperature of 90°C for 1 hour and cooled down to room temperature.
- the texture analysis (using a TXA T2i texture analyzer) and taste evaluation were performed on the meat products obtained.
- the meat products were labeled P4, P5, P9, P10 and P11 , which were produced using seaweed meal samples S4, S5, S9, S10 and S11 , respectively.
- Seaweed meals S4, S5, and S11 all improved the hardness and chewiness of the meat products such that P4, P5, and P11 demonstrated a comparable texture to P10, which was obtained using commercially available carrageenan S10. All of these meat products had a better texture than P9, which was obtained using a commercially available seaweed meal S9.
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Abstract
Provided are methods of making high quality seaweed meal suitable for food applications. The method comprises the steps of cleaning the fresh, dried, or rehydrated red seaweed, pretreating the red seaweed with a salt under heat, and drying and grinding the treated red seaweed to obtain the seaweed meal. Optionally, the method comprises bleaching the red seaweed, and/or hydrolyzing the red seaweed with cellulase. The seaweed meal produced by the disclosed technology has a light color, good flavor and taste, good mouthfeel, high gelling capability, great stability, and ideal smoothness and slipperiness suitable for food applications.
Description
SEAWEED MEAL AND METHOD OF MAKING THE SAME
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation-in-part of U.S. Patent Application No. 16/010,343, filed June 15, 2018, which claims the benefit of U.S. Provisional Patent Application No. 62/671 ,302, filed May 14, 2018. This application also claims the benefit of U.S. Provisional Patent Application No. 62/781 ,529, filed December 18, 2018. All of these applications are incorporated herein by reference in their entireties.
TECHNICAL FIELD
[0002] This disclosure relates to seaweed meal and a method of making the same. The seaweed meal disclosed herein can replace the use of carrageenan. The method and the seaweed meal production can be used in the field of food industry.
BACKGROUND
[0003] Carrageenans are linear sulfated polysaccharides extracted from edible red seaweeds. They are used in food industry, particularly in dairy and meat products, to bind to food proteins and help stabilize and texturize the food products. Therefore, carrageenans have wide applications in food industry as gelling agents, thickening agents, and stabilizing agents. Carrageenan is an animal-product-free ingredient replacing gelatin in vegetarian food products.
[0004] Clean Label and disruptive Green have become more and more popular in food industrials, and have been listed in the“Top 10 Innova’s 2017 Trends,” resulting in strong interests in naturalness and clean label. This trend has been growing globally for the past couple of years and is the new standard in the industry. It provides vast market space development potential for seaweed meal to replace carrageenan in food application.
[0005] US Patent Application Publication No. 2015/0164125 describes a method for making seaweed meal, including the steps of harvesting the seaweed from a sea floor; chopping the seaweed; cleaning the seaweed; desiccating the seaweed; grinding the seaweed to a meal; drying the seaweed between the cleaning step and the
desiccating step, the drying step is accomplished by a seaweed agitator. US Patent No. 4,125,392 describes a seaweed filter cake product produced by conditioning raw seaweed by mixing it with water and other substances, and then digesting the conditioned seaweed by cooking it with steam to form a steam-digested mixture. The filter cake is skimmed off the top of the resulting steam-digested mixture and used by itself, or as a starting product for producing fertilizers or plant growth stimulators in liquid or pelletized form.
[0006] The prior-art references merely produced a simple seaweed meal or cake products, with poor gelling capability, brown or green color, and strong fishery flavor. These prior-art seaweed products are not suitable for use as gelling agent or stabilizer in food applications to replace carrageenan extracted from red seaweed. Thus, there is a need in the field to produce better quality seaweed meal suitable for food applications.
SUMMARY
[0007] In one aspect, provided herein is a method of making a seaweed meal to replace carrageenan in the food industry. The method comprises the steps of cleaning the fresh or dried red seaweed, pretreating the red seaweed with a salt under heat, and drying and grinding the treated red seaweed to obtain the seaweed meal. Optionally, the method comprises a step of bleaching the red seaweed with a bleaching agent before the drying and grinding step. Optionally, the method comprises a step of treating the red seaweed with an enzyme such as a cellulase before the drying and grinding step. In some embodiments, the bleaching step is carried out before the enzyme treatment step. In some embodiments, the bleaching step is carried out after the enzyme treatment step. The disclosure provides a simple process to produce a seaweed meal with light color, good flavor and taste, good mouthfeel, high gelling capability, great stability, and ideal smoothness and slipperiness suitable for“clean label” food applications.
[0008] In a related aspect, provided herein is a seaweed meal produced by the method described above. The seaweed meal produced by the disclosed method can be used in food industry to replace carrageenan as a gelling ingredient in, for example, dairy, jelly, pudding or meat products.
BRIEF DESCRIPTION OF THE DRAWINGS
[0009] This application contains at least one drawing executed in color. Copies of this application with color drawing(s) will be provided by the Office upon request and payment of the necessary fees.
[0010] Figures 1A-1 C show the FTIR results of seaweed meal Sample 2 (top curve in each panel) in comparison to commercially available seaweed powder (Sample 9) (middle curve in each panel), and carrageenan (Sample 10) (bottom curve in each panel). Figure 1A shows the entire range while Figures 1 B and 1 C show the selective ranges (enlarged).
[0011] Figures 2A-2B show the texture of the meat products obtained by the seaweed meal samples. Figure 2A shows the hardness and Figure 2B shows the chewiness of the meat produts prepared by seaweed meal samples S4, S5, and S11 in comparison to those prepared by commercially available seaweed powder (Sample 9) and carrageenan (Sample 10).
DETAILED DESCRIPTION
[0012] Methods for making high quality seaweed meal suitable for food applications are provided herein. The method is a simple process to produce a seaweed meal with desired features such as light color, good flavor and taste, good mouthfeel, high gelling capability, great stability, and ideal smoothness and slipperiness suitable for food applications. The seaweed meal produced by the disclosed method can be used in food industry to replace carrageenan as a gelling agent in, for example, producing dairy, jelly, pudding, or meat products.
[0013] In some embodiments, the method disclosed herein comprises the steps of cleaning seaweed material with water, pre-treating the clean seaweed material with a salt under heat, bleaching the pre-treated seaweed material with a bleaching agent, and treating the bleached seaweed material with an enzyme to obtain a seaweed meal suitable for food applications. The bleaching step is optional and can be included if a light color seaweed meal is desired. The enzyme treatment step is also optional and can be carried out before or after the bleaching step if both of these optional steps are included.
[0014] Seaweed is also called macroalgae, marine algae, or seagrass. The seaweed material used for the disclosed method includes red seaweed, for example, Chondrus, Gigartina, Kappaphycus, and Eucheuma. In some embodiments, a combination of at least two, at least three, or at least four of the disclosed red seaweed can be used. The seaweed material is cleaned by water prior to any treatment. Seaweed materials in any form such as dry seaweed, or fresh seaweed, or rehydrated seaweed, material can be used. It is known in the art that fresh seaweed can be dehydrated to obtain dry seaweed. The dry seaweed can be rehydrated by soaking the dry seaweed in water. In some embodiments, the dry seaweed is rehydrated during the cleaning step. When dry seaweed is used, the dry seaweed:water ratio in the cleaning step can be between 1 :1 and 1 :40, between 1 :3 and 1 :30, between 1 :5 and 1 :25, between 1 :5 and 1 :20, between 1 :10 and 1 :20, or between 1 :5 and 1 :10; when fresh seaweed or rehydrated seaweed is used, the fresh seaweed:water ratio in the cleaning step can be between 1 :1 and 1 :3, between 1 :1 and 1 :5, between 1 :2 and 1 :5, between 1 :1 and 1 : 10, or between 1 :1 and 1 :15.
[0015] Salt pre-treatment process is an environment-friendly process to produce a seaweed meal with good gel capability and/or stability, while retaining more natural health promoting ingredients. This simplified process generates less waste water and is more environmental friendly, compared to the traditional alkali and/or acid pre-treatment process. Therefore, the disclosed technology can produce high quality seaweed meal in a time-efficient and cost-effective manner.
[0016] The salts that can be used for the disclosed method include one or more salts of one or more metals and one or more acids. Examples of the one or more metals for the one or more salts include, without limitation, alkaline metals (e.g., Li, Na, K, Rb) and alkaline-earth metals (e.g., Be, Mg, Ca, Sr), and examples of the one or more acids for the one or more salts include, without limitation, HX (e.g., X is halogen such as F, Cl, Br, I), sulfuric acid, and carbonic acid. Examples of suitable salt include, without limitation, sodium chloride, potassium chloride, sodium carbonate, sodium bicarbonate, potassium carbonate, potassium bicarbonate, sodium citrate, and sodium tartaric acid. In some embodiments, a combination of at least two, at least three, at
least four, at least five, or at least six salts can be used in the pre-treatment. In the pre- treatment step, the seaweed:salt ratio can be between 1 :1 and 1 :3, between 1 :1 and 1 :5, between 1 :2 and 1 :5, or between 1 :1 and 1 :10. The salt solution can be at a concentration of between 1 % and 10%, between 5% and 15%, between 3% and 20%, between 5% and 25%, between 10% and 30%, or between 5% and 30% (wt%). In some embodiments, the salt pre-treatment step is performed at a temperature between 40°C and 80°C, between 50°C and 100°C, between 60°C and 90°C, or between 70°C and 120°C. In some embodiments, the salt pre-treatment can be performed for a period of between 0.5 hour and 24 hours, between 0.5 hour and 20 hours, between 0.5 hour and 15 hours, between 0.5 hour and 12 hours, between 0.5 hour and 8 hours, between 0.5 hour and 6 hours, between 1 hour and 4 hours, between 1.5 hours and 3 hours, or between 0.5 hour and 4 hours.
[0017] Optionally, the seaweed is treated with a bleaching agent to obtain a light color seaweed meal. The bleaching agent that can be used for the disclosed method includes hypochlorous acid, sodium hypochlorous, and chlorine dioxide. Alternatively, a combination of the disclosed bleaching agents, such as a combination of at least two bleaching agents, or at least three bleaching agents, can be used. In the bleaching step, the seaweed: bleaching agent ratio can be between 1 :1 and 1 :3, between 1 :1 and 1 :5, between 1 :2 and 1 :5, or between 1 :1 and 1 :10. The bleaching agent can be at a concentration of available chlorine content of between 0.01 % and 5%, between 0.02% and 3%, between 0.05% and 2%, between 0.05% and 1 %, between 0.05% and 0.5%, or between 0.01 % and 0.1 % (wt%). In some embodiments, the bleaching step can be performed for a period of between 5 minutes and 240 minutes, between 10 minutes and 180 minutes, between 10 minutes and 120 minutes, between 10 minutes and 60 minutes, or between 20 minutes and 60 minutes.
[0018] In some embodiments, the pre-treated or bleached seaweed has an impurity of the red seaweed of less than 5%, less than 4%, less than 3%, less than 2%, or less than 1 %, and a color of light brown to light yellow.
[0019] The enzyme treatment catalyzes the hydrolysis of the cellulose and/or
related polysaccharides or the like in the pre-treated and/or bleached seaweed such that the obtained seaweed meal has an improved mouthfeel. Various enzymes may be used to achieve this goal, for example, cellulase, hemicellulase, pectinase, amylase, xylanase, pentosanase, glucanase, esterase. In some embodiments, one or more enzymes can be used to treat the seaweed. An example of the suitable enzyme is cellulase, including acid cellulase, neutral cellulase, and alkali cellulose, including but not limited to 1 ,4-p-D-glucan glucanohydrolase, endo-1 ,4-p-D-glucanase, 1 ,4-p-D- glucan cellobilhydrolase, exo-1 ,4-p-D-glucannase, b-1 ,4-glucosidase, from Trichoderma, Aspergillus or Penicillium. In some embodiments, a combination of at least two, at least three, or more of these cellulases can be used. In the enzyme treatment step, the seaweed:enzyme ratio can be between 1 : 1 and 1 :3, between 1 :2 and 1 :5, between 1 : 1 and 1 :5, between 1 : 1 and 1 :6 or between 1 : 1 and 1 : 10. The enzyme can be at a concentration of between 10 U/g and 500 U/g, between 20 U/g and 400 U/g, between 30 U/g and 300U/g, between 50 U/g and 200 U/g, or between 75 U/g and 150 U/g. In some embodiments, the enzyme treatment step can be performed for a period of between 0.5 hour and 12 hours, between 0.5 hour and 8 hours, between 0.5 hour and 6 hours, between 1 hour and 3 hours, or between 1 hour and 4 hours, at a pH range of between 2.0 and 10.0, between 3.0 and 9.0, between 3.0 and 8.0, between 4.0 and 7.0, or between 5.0 and 6.0, or at a temperature between 15°C and 100°C, between 20°C and 90°C, between 30°C and 80°C, between 20°C and 70°C, between 30°C and 60°C, or between 40°C and 50°C.
[0020] A variety of acids or alkalis can be used to adjust pH. For example, the alkali for pH adjustment is selected from the group consisting of sodium hydroxide, potassium hydroxide, and a combination thereof. The acid for pH adjustment is selected from the group consisting of hydrochloric acid, nitric acid, phosphate acid, and a combination of at least two, or at least three of these acids.
[0021] In some embodiments, the clean seaweed is pre-treated with between 5% and 30% (wt%) of a salt solution at a ratio of between 1 :2 and 1 :5 and at a temperature of between 50°C and 90°C, and then treated with a cellulase having a concentration of between 30 U/g and 200 U/g at a ratio of between 1 :2 and 1 :5 and at a temperature of
between 40°C and 60°C.
[0022] The treated seaweed can be dried and grinded to obtain the seaweed meal. In some embodiments, the dried seaweed meal has a sulfate content of between 1 % and 50%, between 10% and 45%, between 5% to 40% or between 15% and 30%. In some embodiments, the viscosity of the dried seaweed meal is at least 0.005 Pa-S. In some embodiments, the dried seaweed meal has a color of light brown to light yellow.
[0023] In some embodiments, the seaweed meal obtained by the disclosed technology contains the following ingredients: > 50% soluble dietary fiber, about 5%- 10% insoluble dietary fiber, > 60% total dietary fiber, about 8%-40% sulfate content, and < 2% protein. In some embodiments, the seaweed meal obtained by the disclosed technology has the following properties: gel strength at 0.5% >100 g/cm2
[0024] In some embodiments, the seaweed meal obtained from Kappaphycus has a gel strength of about 200 g/cm2 at 1 .5% seaweed meal in water with 0.2% KCI added. The seaweed meal obtained from Kappaphycus is particularly useful as a gelling agent in meat products.
[0025] The following examples are intended to illustrate various embodiments of the invention. As such, the specific embodiments discussed are not to be construed as limitations on the scope of the invention. It will be apparent to one skilled in the art that various equivalents, changes, and modifications may be made without departing from the scope of invention, and it is understood that such equivalent embodiments are to be included herein. Further, all references cited in the disclosure are hereby incorporated by reference in their entirety, as if fully set forth herein.
EXAMPLES
Example 1 : Materials and Methods
[0027] Other reagents include: hypochlorous acid, sodium hypochlorous, available chlorine contents 10%, food grade; chlorine dioxide, available chlorine contents 50%, food grade; hydrochloric acid, 36%, food grade; and sulfuric acid, nitric acid, phosphate acid, 99%, food grade; sodium hydroxide, potassium hydroxide, 99% food grade; acid cellulase, neutral cellulase, alkaline cellulase, 50,000 U/g, food grade; sodium chloride, potassium chloride, sodium carbonate, sodium bicarbonate, potassium carbonate, potassium bicarbonate, 99%, food grade.
Example 2: Preparation of Seaweed Meal from Dried Eucheuma
[0028] 10 kg dried Eucheuma was mixed with 50 kg water in the tank, stirred at
60 RPM for 30 minutes to clean the seaweed, and then the water was removed to obtain 50 kg clean seaweed. The clean seaweed was mixed with 50 kg 5% sodium chloride solution in the reaction tank, the mixture was heated and the temperature was kept at 50°C, with stirring at 60 RPM for 30 minutes, followed by washing the seaweed with 500 kg water. Once the water was removed, 49 kg of salt pre-treated seaweed was obtained. The salt pre-treated seaweed was mixed with 49 kg of 0.01 % bleaching agent, hydrochloric acid (HCIO) solution in the tank, stirred at 60 RPM for 10 minutes, then the hypochlorous acid solution was removed, and the seaweed was washed with 100 kg water. Once the water was removed 47 kg pre-treated seaweed was obtained.
The specification of the pre-treated seaweed was: impurity of the red seaweed < 0.5%, and the color was yellow.
[0029] Subsequently, the pre-treated seaweed was mixed with 47 kg of 30 U/g acid cellulase solution, pH was adjusted to 3.0 using hydrochloric acid, and the temperature was kept at 20°C, with stirring at 60 RPM for 30 minutes. Then the cellulase solution was removed and the seaweed was washed with 100 kg water. 45 kg cellulase treated seaweed was obtained. And then the seaweed was dried and grinded to obtain 4.1 kg seaweed meal.
Example 3: Preparation of Seaweed Meal from Fresh Eucheuma
[0030] 50 kg fresh Eucheuma was mixed with 120 kg water in the tank, and stirred at 60 RPM for 30 minutes to clean the seaweed. The water was removed to obtain 48 kg clean seaweed. The clean seaweed was mixed with 120 kg of 20% potassium chloride solution in the reaction tank. The mixture was heated and the temperature was kept at 80°C, with stirring at 60 RPM for 120 minutes. The seaweed was washed with 600 kg water, and the water was removed to obtain 47 kg salt pre- treated seaweed. The salt pre-treated seaweed was mixed with 120 kg of 0.05% bleaching agent, sodium hypochlorous acid solution, stirred at 60 RPM for 30 minutes, the sodium hypochlorous acid solution was removed, and followed by washing with 100 kg water. The water was removed to obtain 46 kg pre-treated seaweed. The specification of the pre-treated seaweed was: impurity of the red seaweed < 0.3%, and the color was light yellow.
[0031] The pre-treated seaweed was mixed with 120 kg of 100 U/g cellulase solution, pH was adjusted to 5.0 with sulfuric acid, heated and the temperature was kept at 50°C, with stirring at 60 RPM for 120 minutes. The cellulase solution was removed and the seaweed was washed with 100 kg water. 44 kg of cellulase treated seaweed was obtained. And then the seaweed was dried and grinded to obtain 3.9 kg seaweed meal.
Example 4: Preparation of Seaweed Meal from Dried Eucheuma
[0032] 10 kg dried Eucheuma was mixed with 250 kg water in the tank, and stirred at 60 RPM for 30 minutes to clean the seaweed. The water was removed to obtain 50 kg clean seaweed. The clean seaweed was mixed with 250 kg 30% sodium carbonate solution in the reaction tank. The mixture was heated and kept at a temperature of 100°C, with stirring at 60 RPM for 12 hours. Then the seaweed was washed with 600 kg water. The water was removed to obtain 45 kg salt pre-treated seaweed. The salt pre-treated seaweed was mixed with 225 kg 0.5% bleaching agent, chlorine dioxide solution, stirred at 60 RPM for 120 minutes, and then the chlorine dioxide solution was removed, followed by washing with 200 kg water. The water was removed to obtain 42 kg pre-treated seaweed. The specification of the pre-treated seaweed was: impurity of the red seaweed < 0.6%, and the color was yellow.
[0033] The pre-treated seaweed was mixed with 210 kg of 300 U/g neutral cellulase solution, pH was adjusted to 8.0 with sodium hydroxide solution, heated and the temperature was kept at 70°C, with stirring at 60 RPM for 6 hours. The cellulase solution was removed and the seaweed was washed with 200 kg water. 36 kg cellulase treated seaweed was obtained. And then the seaweed was dried and grinded to obtain 3.1 kg seaweed meal.
Example 5: Preparation of Seaweed Meal from Fresh Kappaphycus
[0034] 50 kg fresh Kappaphycus was mixed with 50 kg water in the tank, and stirred at 60 RPM for 30 minutes to clean the seaweed. The water was removed to obtain 49 kg clean seaweed. The clean seaweed was mixed with 49 kg 5% sodium bicarbonate solution in the reaction tank. The mixture was heated and kept at a temperature of 50°C, with stirring at 60 RPM for 30 minutes, then the seaweed was washed with 500 kg water. The water was removed to obtain 42 kg salt pre-treated seaweed. The salt pre-treated seaweed was mixed with 42 kg of 0.01 % bleaching agent, hypochlorous acid (HCIO) solution, stirred at 60 RPM for 10 minutes. And then the hypochlorous acid solution was removed, and the seaweed was washed with 100 kg water. The water was removed to obtain 41 kg pre-treated seaweed. The specification
of the pre-treated seaweed was: impurity of the red seaweed < 0.4%, and the color was yellow.
[0035] The pre-treated seaweed was mixed with 41 kg of 30 U/g alkali cellulase solution, pH was adjusted to 8.0 using sodium hydroxide, and the temperature was kept at 20°C, with stirring at 60 RPM for 30 minutes. The cellulase solution was removed and the seaweed was washed with 100 kg water. 38 kg cellulase treated seaweed was obtained. And then the seaweed was dried and grinded to obtain 3.3 kg seaweed meal.
Example 6: Preparation of Seaweed Meal from Dried Kappaphycus
[0036] 10 kg dried Kappaphycus was mixed with 120 kg water in the tank, and stirred at 60 RPM for 30 minutes to clean the seaweed. The water was removed to obtain 49 kg clean seaweed. The clean seaweed was mixed with 120 kg of 20% sodium chloride solution in the reaction tank. The mixture was heated and kept at a temperature of 80°C, with stirring at 60 RPM for 120 minutes, and then washed with 600 kg water. The water was removed to obtain 48 kg salt pre-treated seaweed. The salt pre-treated seaweed was mixed with 120 kg of 0.05% bleaching agent, hypochlorous acid solution, stirred at 60 RPM for 30 minutes. The hypochlorous acid solution was removed, and the seaweed was washed with 100 kg water. The water was removed to obtain 46 kg pre-treated seaweed. The specification of the pre-treated seaweed was: impurity of the red seaweed < 0.2%, and the color was light yellow.
[0037] The pre-treated seaweed was mixed with 120 kg of 100 U/g cellulase solution, pH was adjusted to 4.8 with phosphate acid, heated and the temperature was kept at 45°C, with stirring at 60 RPM for 120 minutes. The cellulase solution was removed and the seaweed was washed with 100 kg water. 43 kg of cellulase treated seaweed was obtained. And then the seaweed was dried and grinded to obtain 3.8 kg seaweed meal.
Example 7: Preparation of Seaweed Meal from Dried Kappaphycus
[0038] 10 kg Kappaphycus was mixed with 150 kg water in the tank, and stirred at 60 RPM for 30 minutes to clean the seaweed. The water was removed to obtain 49
kg clean seaweed. The clean seaweed was dried and grinded to obtain 4.8 kg seaweed meal.
Example 8: Preparation of Seaweed Meal from Dried Gigartina
[0039] 10 kg dried Gigartina was mixed with 80 kg water in the tank, and stirred at 60 RPM for 2 hours to clean the seaweed. The water was removed to obtain 49 kg clean seaweed. The clean seaweed was mixed with 80 kg of 8% potassium bicarbonate solution in the reaction tank. The mixture was heated and kept at a temperature of 60°C, with stirring at 60 RPM for 1 hour, and then washed with 600 kg water. The water was removed to obtain 45 kg salt pre-treated seaweed. The salt pre- treated seaweed was mixed with 80 kg of 0.03% bleaching agent, sodium hypochlorous acid solution, and stirred at 60 RPM for 20 minutes. The sodium hypochlorous acid solution was removed, and the seaweed was washed with 100 kg water. The water was removed to obtain 45 kg pre-treated seaweed. The specification of the pre-treated seaweed was: impurity of the red seaweed < 0.6%, and the color was light brown.
[0040] The pre-treated seaweed was mixed with 90 kg of 60 U/g acid cellulase solution, pH was adjusted to 4.0 with nitric acid, heated and the temperature was kept at 40°C, with stirring at 60 RPM for 1 hour. The cellulase solution was removed and the seaweed was washed with 100 kg water. 40 kg cellulase treated seaweed was obtained. And then the seaweed was dried and grinded to obtain 3.2 kg seaweed meal.
Example 9: Preparation of Seaweed Meal from Dried Chondrus
[0041] 10 kg dried Chondrus was mixed with 200 kg water in the tank, and stirred at 60 RPM for 30 minutes to clean the seaweed. The water was removed to obtain 49 kg clean seaweed. The clean seaweed was mixed with 200 kg of 25% potassium chloride solution in the reaction tank, heated and kept at a temperature of 90°C, with stirring at 60 RPM for 8 hours, and then washed with 600 kg water. The water was removed to obtain 45 kg salt pre-treated seaweed. The salt pre-treated seaweed was mixed with 200 kg of 0.08% bleaching agent, sodium hypochlorous acid solution, stirred at 60 RPM for 90 minutes, and then the sodium hypochlorous acid solution was
removed, and the seaweed was washed with 100 kg water. The water was removed to obtain 44 kg pre-treated seaweed. The specification of the pre-treated seaweed was: impurity of the red seaweed < 0.5%, and the color was light brown.
[0042] The pre-treated seaweed was mixed with 200 kg of 200 U/g neutral cellulase solution, pH was adjusted to 7.5 with potassium hydroxide, heated and the temperature was kept at 60°C, with stirring at 60 RPM for 240 minutes. The cellulase solution was removed and the seaweed was washed with 100 kg water. 41 kg cellulase treated seaweed was obtained. And then the seaweed was dried and grinded to obtain 3.6 kg seaweed meal.
Example 10: Preparation of Seaweed Meal from Dried Kappaphycus
[0043] 10 kg dried Kappaphycus was mixed with 120 kg water in the tank, and stirred at 60 RPM for 30 minutes to clean the seaweed. The water was removed to obtain 48 kg clean seaweed. The clean seaweed was mixed with 120 kg of 20% sodium chloride solution in the reaction tank. The mixture was heated and kept at a temperature of 85°C, with stirring at 60 RPM for 120 minutes, and then washed with 600 kg water. The water was removed to obtain 48 kg salt pre-treated seaweed. The specification of the pre-treated seaweed was: impurity of the red seaweed < 0.2%, and the color was yellow. 45 kg of cellulase treated seaweed was obtained. And then the seaweed was dried and grinded to obtain 4.0 kg seaweed meal.
Example 11 : Basic Analysis of the Seaweed Meal Preparations
[0044] Table 2 summarizes the treatment of Examples 2-10 to obtain various seaweed meal preparations. Additionally, commercially available dried eucheuma cottonii powder from RICH MOON CO., LTD (Sample 9) and carrageenan from the Green Fresh Group (Sample 10) were used as controls.
[0045] The sulfate test was performed as follows: 100 mg sample was dissolved in 20 ml of water (with heating if necessary), and 3 ml of barium chloride test solution and 5 ml of hydrochloric acid were added. The test solution was diluted and filtered if a precipitate formed. The solution or the filtrate was boiled for 5 minutes. A white, crystalline precipitate appeared.
[0046] Viscosity test was performed as follows: 1.5 grams of seaweed meal was weighed and dispersed into 98.5 grams deionized water under stirring with IKA (500- 600 rpm) for 10 min, heated to 80 °C , and the solution was kept in a water bath at 75 °C . The viscosity was tested with Brookfield LVT, Spindle # 2, at 60 rpm.
[0047] The soluble dietary fiber contents of the samples were determined by the AOAC official methods, see for example, AOAC 985.29 and AOAC 991.43. The protein contents of the samples were determined by the established kjeldahl method, published as ISO 20483:2006.
[0048] Application test was performed in neutral dairy, with a formula of the prototype in Table 3.
[0049] Table 4 illustrates the process of preparing dairy products with seaweed meal.
[0050] Table 5 summarizes the results of the basic analysis of the seaweed meal preparation samples 1-8 and 11 , obtained from Examples 2-10 in comparison with commercially available seaweed meal powder (Sample 9) and carrageenan (Sample 10).
[0051] Samples 2 and 5 produced the best results in various tests. Samples 7 and 8 also produced acceptable results in various tests.
[0052] Figure 1 shows the results of a typical Fourier Transform Infrared Spectrometer (FTIR) of Sample 2 in comparison with Sample 9, commercially obtained seaweed powder, and Sample 10, commercially obtained carrageenan. The spectral feature at approximately 845 cm 1 is mainly associated with D-galactose-4-sulfphate (Figure 1 C). The presence of a strong band in the FTIR spectra at 930 cm 1 is indicative of the occurrence of 3,6-anhydro-D-galactose (Figure 1 C). 1550-1510 cm-1 is protein N-H bending (amide bands II) (Figure 1 B). Thus, FTIR demonstrates that the process disclosed herein produced a seaweed meal having a lower protein content compared to the commercially available seaweed powder and similar to carrageenan, while the content of 3,6-anhydro-D-galactose of the seaweed meal obtained by the disclosed
technology is higher than that of the commercially available seaweed powder but lower than that of carrageenan.
Example 11 : Gel Strength Test of the Seaweed Meal Samples
[0053] The gel strength test without KCI was performed as follows: 900 grams of reconstituted milk was weighed and added to a stainless-steel container having a diameter of 12 cm. The container is placed on the induction stove and under the agitator IKA. An adequate amount of the sample powder, e.g., 4.5 grams, was weighed and dispersed in the container under agitation at 1100 rpm. The induction stove (Philips HD4925) was turned on and set at the thermostat 5 (pre-heating time was between 9-12 minutes). While the temperature was on the rise, 2 drops of defoamer was added to the bottom of the container to be used for shearing. The mixture was boiled to 90°C and then the heating and stirring were stopped. The mixture was poured into 2 jelly cups and the testing samples were kept in an incubator at 20°C for at least 16 hours. When the sample was ready to be measured, the cover was gently removed by slipping on the sides of the jelly cup without damaging the gel. The cup was placed in the center of TXAT2i Texture Analyzer and the probe was placed above the center of the gel. For the carrageenan control, 0.5 wt% of carrageenan was mixed with 900 grams of reconstituted milk.
[0054] The gel strength test with KCI was performed as follows: 1.5 g of seaweed meal sample and 0.2 g of KCI were placed in a 200 ml beaker and then 100 ml distilled water was added to the beaker while stirring such that the seaweed meal sample was fully suspended in water. The mixture was heated to 90°C with slow stirring. More water was added to make up the volume to 100 ml after heating. The sample was stirred and divided into 3 intensity measurement cups, and stored at room temperature for 16 hours with a film sealing. Subsequently the samples were removed from the cups and analyzed on a TXAT2i Texture Analyzer.
[0055] Based on the syneresis observation, products made with Sample 6 and Sample 9 were worse on protein syneresis and the protein sediment could be found in both products. Also, products made with Sample 6 and Sample 9 had weaker gel strength than other products made with Samples 1 -5, 7, 8, 10 and 11. Samples 1-5, 7, 8, 11 can replace carrageenan, demonstrating equivalent or even better properties. Samples 4, 5 and 11 demonstrated great gel strength with added KCI and can be used in meat products replacing carrageenan.
Example 12: Use of Seaweed Meal Samples in Preparing Sweet Milk
[0056] The carrageenan or seaweed meal samples were mixed with sugar. The mixtures were dispersed into milk at 75°C while stirring for 10 minutes and homogenized at 65-70°C, 200 bar, package filled, sterilized at 121°C for 7 minutes, and then cooled down to room temperature. The ingredients for the test include 80 wt% of fresh milk, 5 wt% of sugar, and 0.03 wt% of carrageenan. The viscosity test, sensory test, and stability test with LUMifuge were performed on the sweet milk products 1 -11 (P1 -P11 ) obtained with seaweed meal samples 1 -11 (S1 -S11 ).
[0057] The viscosity test demonstrates that the final sweet milk products P1-P5, P7, P8 and P11 made with seaweed meal S1 -5, S7, S8 and S11 had no significant difference with sweet milk product P10 made with seaweed meal S10. But the viscosity of P6 and P9 were significantly lower than the other sweet milk products. Also, P6 and P9 were worse on water holding ability than the other by LUMi test, where higher instability index indicates lower stability. Furthermore, in the sensory test, P6 and P9 easily distinguished themselves from other products. Both P6 and P9 had an astringent and rough mouthfeel, significantly worse than P1-P5, P7, P8, P10 and P11.
Example 13: Use of Seaweed Meal Samples in Preparing Meat Product
[0058] The carrageenan or seaweed meal samples were used in preparing meat products such as chicken sausages in this example. The ingredients are listed in Table 8 below.
[0059] A brine was prepared by dispersing salt and sugar in cold water at 4-5°C to allow complete dissolution. The cured chicken breast was prepared by grinding the chicken breast with a No. 6 plate and then tumbled in brine for 8 hours by a vacuum tumbling process. One hour before the end of the tumbling process, the remaining ingredients including soy flour, flavors, seaweed meal or carrageenan, egg white, MSG, starch, and water were added. The chicken skin emulsion was prepared by dispersing glycerin monostearate in water and slowly adding the chicken skin to emulsify until an emulsion was obtained. The emulsion was kept overnight at 3-6°C to allow complete gelation, and then the chicken skin gelation was subjected to grinding with a No. 3 plate. 300 grams of the ground chicken breast and chicken skin were used to stuff 60 mm
casing. The sausage was cooked to an internal temperature of 90°C for 1 hour and cooled down to room temperature.
[0060] The texture analysis (using a TXA T2i texture analyzer) and taste evaluation were performed on the meat products obtained. The meat products were labeled P4, P5, P9, P10 and P11 , which were produced using seaweed meal samples S4, S5, S9, S10 and S11 , respectively. Seaweed meals S4, S5, and S11 all improved the hardness and chewiness of the meat products such that P4, P5, and P11 demonstrated a comparable texture to P10, which was obtained using commercially available carrageenan S10. All of these meat products had a better texture than P9, which was obtained using a commercially available seaweed meal S9.
Claims
1. A method of preparing a high quality seaweed meal suitable for food applications, comprising:
cleaning seaweed material with water, wherein the seaweed material is dry, fresh, or rehydrated seaweed material; and
pre-treating the seaweed with a salt under heat;
thereby to obtain the seaweed meal.
2. The method of claim 1 , further comprising bleaching the seaweed with a bleaching agent.
3. The method of claim 2, wherein the bleaching step is performed with a seaweed: bleaching solution ratio of between 1 :1 and 1 :3, between 1 :1 and 1 :5, between 1 :2 and 1 :5, or between 1 :1 and 1 :10.
4. The method of claim 2, wherein the bleaching step is performed with a concentration of available chlorine content of between 0.01 % and 5%, between 0.02% and 3%, between 0.05% and 2%, between 0.05% and 1 %, between 0.05% and 0.5%, or between 0.01 % and 0.1 % (wt%).
5. The method of claim 2, wherein the bleaching step is performed for a period of between 5 minutes and 240 minutes, between 10 minutes and 180 minutes, between 10 minutes and 120 minutes, between 10 minutes and 60 minutes, or between 20 minutes and 60 minutes.
6. The method of claim 2, wherein the bleaching agent is selected from the group consisting of hypochlorous acid, sodium hypochlorous, chlorine dioxide, and a combination thereof.
7. The method of claim 1 , further comprising treating the seaweed with an enzyme to improve mouthfeel of the seaweed meal, wherein the enzyme is cellulase.
8. The method of claim 7, wherein the enzyme treatment step is performed with a seaweed: enzyme ratio of between 1 : 1 and 1 :3, between 1 :2 and 1 :5, between 1 :1
and 1 :5, between 1 : 1 and 1 :6 or between 1 : 1 and 1 : 10.
9. The method of claim 7, wherein the enzyme treatment step is performed at a pH range of between 2.0 and 10.0, between 3.0 and 9.0, between 3.0 and 8.0, between 4.0 and 7.0, or between 5.0 and 6.0.
10. The method of claim 7, wherein the enzyme treatment step is performed at a concentration of the enzyme between 10 U/g and 500 U/g, between 20 U/g and 400 U/g, between 30 U/g and 300U/g, between 50 U/g and 200 U/g, or between 75 U/g and 150 U/g.
1 1 . The method of claim 7, wherein the enzyme treatment step is performed at a temperature of between 15°C and 100°C, between 20°C and 90°C, between 30°C and 80°C, between 20°C and 70°C, between 30°C and 60°C, or between 40°C and 50°C.
12. The method of claim 7, wherein the enzyme treatment step is performed for a period of between 0.5 hour and 12 hours, between 0.5 hour and 8 hours, between 0.5 hour and 6 hours, between 1 hour and 3 hours, or between 1 hour and 4 hours.
13. The method of claim 7, wherein the enzyme is selected from the group consisting of acid cellulase, neutral cellulase, alkali cellulase, and a combination thereof.
14. The method of claim 1 , further comprising drying and grinding the seaweed.
15. The method of claim 1 , wherein the pre-treated seaweed has an impurity of the red seaweed of less than 1 %, and a color of light brown to light yellow.
16. The method of claim 1 , wherein the seaweed material is red algae.
17. The method of claim 1 , wherein the seaweed material comprises Chondrus, Gigartina, Kappaphycus, Eucheuma, or a combination thereof.
18. The method of claim 1 , wherein the cleaning step is performed with a
fresh seaweed :water ratio of between 1 :1 and 1 :3, between 1 :1 and 1 :5, between 1 :2 and 1 :5, between 1 :1 and 1 :10, or between 1 :1 and 1 :15, or a dried seaweed:water ratio of between 1 :1 and 1 :40, between 1 :3 and 1 :30, between 1 :5 and 1 :25, between 1 :5 and 1 :20, between 1 :10 and 1 :20, or between 1 :5 and 1 :10.
19. The method of claim 1 , wherein the salt pre-treatment step is performed with a seaweed:salt solution ratio of between 1 :1 and 1 :3, between 1 :1 and 1 :5, between 1 :2 and 1 :5, or between 1 :1 and 1 :10.
20. The method of claim 1 , wherein the salt pre-treatment step is performed with a concentration of the salt solution between 1 % and 10%, between 5% and 15%, between 3% and 20%, between 5% and 25%, between 10% and 30%, or between 5% and 30% (wt%).
21. The method of claim 1 , wherein the salt pre-treatment step is performed at a temperature between 40°C and 80°C, between 50°C and 100°C, between 60°C and 90°C, or between 70°C and 120°C.
22. The method of claim 1 , wherein the salt pre-treatment step is performed for a period of between 0.5 hour and 24 hours, between 0.5 hour and 20 hours, between 0.5 hour and 15 hours, between 0.5 hour and 12 hours, between 0.5 hour and 8 hours, between 0.5 hour and 6 hours, between 1 hour and 4 hours, between 1.5 hours and 3 hours, or between 0.5 hour and 4 hours.
23. The method of claim 1 , wherein the salt is selected from the group consisting of sodium chloride, potassium chloride, sodium carbonate, sodium bicarbonate, potassium carbonate, potassium bicarbonate, sodium citrate, sodium tartaric acid, and a combination thereof.
24. A seaweed meal suitable for food applications produced by the method of claim 1.
25. The seaweed meal of claim 24, wherein the seaweed meal has a sulfate content of between 5% to 40%, a viscosity of at least 0.005 Pa-S, or a color of light
brown to light yellow.
26. A seaweed meal suitable for food applications produced by the method of claim 2.
27. The seaweed meal of claim 26, wherein the seaweed meal has a sulfate content of between 5% to 40%, a viscosity of at least 0.005 Pa-S, or a color of light brown to light yellow.
28. A seaweed meal suitable for food applications produced by the method of claim 7.
29. The seaweed meal of claim 28, wherein the seaweed meal has a sulfate content of between 5% to 40%, a viscosity of at least 0.005 Pa-S, or a color of light brown to light yellow.
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US201862781529P | 2018-12-18 | 2018-12-18 | |
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