Rapid fermentation method for shrimp paste based on combined strain fortification

US12089618B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12089618-B2
Application numberUS-202218572802-A
CountryUS
Kind codeB2
Filing dateDec 28, 2022
Priority dateMay 25, 2022
Publication dateSep 17, 2024
Grant dateSep 17, 2024

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Abstract

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A rapid fermentation method for shrimp paste based on combined strain fortification is provided. Cladosporium Z3 and Enterococcus faecalis X1 were deposited in the Chinese typical culture preservation center under preservation numbers CCTCC NO: M 2022487 and CCTCC NO: M 2022486, respectively. Two strains were employed to ferment the small hairy shrimp in two steps, utilizing each strain's properties, which enabled the fermentation capacity to be maximized to increase the fermentation speed and stabilize the quality. In addition, the pollution of miscellaneous bacteria is inhibited by strain-enhanced fermentation.

First claim

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What is claimed is: 1. A rapid fermentation method for shrimp paste based on combined strain fortification, comprising the following steps: (1) cutting hairy shrimps into a shrimp slurry, adding an edible salt at a predetermined ratio to the shrimp slurry, and mixing a resulting shrimp slurry well to obtain a shrimp pulp, wherein the edible salt is added in an amount of 5% to 10% by mass of the shrimp pulp; (2) inoculating Cladosporium Z3 in a yeast extract peptone dextrose (YPD) liquid medium for activation, and then applying a culture solution to a YPD solid medium for secondary incubation; subsequently, adding sterile saline to a plate and scraping a mycelium from a surface of the medium; then shaking and filtering a resulting solution to remove the mycelium, and diluting a filtrate with sterile saline to obtain a Cladosporium Z3 spore suspension, which is stored under a preservation number CCTCC NO: M 2022487; (3) inoculating Enterococcus faecalis X1 in a YPD liquid medium for activation and a seed solution is obtained after cultivation; subsequently, centrifuging the seed solution to obtain a bacterial sludge and resuspending the bacterial sludge in sterile saline to obtain an Enterococcus faecalis X1 spore suspension with a preservation number CCTCC NO: M 2022486; (4) inoculating the Cladosporium Z3 spore suspension prepared in the step (2) into the shrimp pulp prepared in the step (1) for one-step fermentation to obtain a fermentation primary product, wherein a dosage ratio of the Cladosporium Z3 spore suspension to the shrimp pulp is 1-6 mL: 100 g, a fermentation temperature is 20-25° C., and a fermentation time is 10-20 days; and (5) inoculating the Enterococcus faecalis X1 spore suspension prepared in the step (3) into a fermentation primary product prepared in the step (4) for two-step fermentation to obtain a rapidly fermented shrimp paste product, wherein a dosage ratio of the Enterococcus faecalis X1 spore suspension to the fermentation primary product is 1-6 mL:100 g, a fermentation temperature is 20-30° C., and a fermentation time is 2-15 days. 2. The rapid fermentation method for shrimp paste based on combined strain fortification according to claim 1 wherein, a time of the activation the Cladosporium Z3 in the step (2) is 2-4 days, a temperature is 20-30° C., and a speed is 100-170 rpm; a time of the secondary incubation of the YPD solid medium is 2-6 days, and a temperature is 20-30° C. 3. The rapid fermentation method for shrimp paste based on combined strain fortification according to claim 1 wherein, an amount of the sterile saline in the plate in the step (2) is sufficient to cover colonies on the surface of the medium, and a concentration of the Cladosporium Z3 spore suspension is 1×106−1×107 CFU/mL. 4. The rapid fermentation method for shrimp paste based on combined strain fortification according to claim 1 wherein, the YPD liquid medium in the step (2) or the step (3) has a formulation per 1 L of: yeast paste 10 g/L, tryptone 10 g/L, and glucose 10 g/L, and the YPD liquid medium is sterilized at 121° C. for 20 min. 5. The rapid fermentation method for shrimp paste based on combined strain fortification according to claim 1 wherein, the YPD solid medium (1 L) in the steps (2) has a formulation per 1 L of: yeast paste 10 g/L, tryptone 10 g/L, glucose 10 g/L, agar powder 10 g/L, and the YPD solid medium is sterilized at 121° C. for 20 min. 6. The rapid fermentation method for shrimp paste based on combined strain fortification according to claim 1 wherein, a time of the activation of the Enterococcus faecalis X1 in the step (3) is 24-48 h, a temperature is 20-30° C., and a speed is 100-170 rpm; a concentration of the Enterococcus faecalis X1 spore suspension is 1×107−1×108 CFU/mL; and the centrifugation is conducted at 4° C. and 6000-8000 rpm for 10-15 min. 7. A shrimp paste prepared by the method according to claim 1 . 8. A shrimp paste prepared by the method according to claim 2 . 9. A shrimp paste prepared by the method according to claim 3 . 10. A shrimp paste prepared by the method according to claim 4 . 11. A shrimp paste prepared by the method according to claim 5 . 12. A shrimp paste prepared by the method according to claim 6 .

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What does patent US12089618B2 cover?
A rapid fermentation method for shrimp paste based on combined strain fortification is provided. Cladosporium Z3 and Enterococcus faecalis X1 were deposited in the Chinese typical culture preservation center under preservation numbers CCTCC NO: M 2022487 and CCTCC NO: M 2022486, respectively. Two strains were employed to ferment the small hairy shrimp in two steps, utilizing each strain's prope…
Who is the assignee on this patent?
Univ Jiangsu
What technology area does this patent fall under?
Primary CPC classification A23L17/40. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Sep 17 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).