CN109380674A - Add the Larimichthys crocea method for salting of leavening - Google Patents
Add the Larimichthys crocea method for salting of leavening Download PDFInfo
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L17/00—Food-from-the-sea products; Fish products; Fish meal; Fish-egg substitutes; Preparation or treatment thereof
- A23L17/65—Addition of, or treatment with, microorganisms or enzymes
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Abstract
The invention discloses a kind of Larimichthys crocea method for salting for adding leavening, include the following steps: to mix Nepal's staphylococcus culture fluid, staphylococcus xylosus culture solution, obtain complex microorganism bacterium solution；Fresh Larimichthys crocea removes internal organ, drains the water after flowing water cleaning, fish body after must handling；According to 106/ g inoculum concentration, complex microorganism bacterium solution is first uniformly sprayed be inoculated in fish body surface and abdominal cavity；Then divide 3 times plus salt is pickled.The present invention can not only improve the flavor of marinated rheum officinale fishery -ies product, moreover it is possible to improve its safety.
Description
Technical field
The invention belongs to food processing fields, and in particular to a kind of pickling process of Larimichthys crocea addition fermentative microorganism.
Background technique
Larimichthys crocea is the important marine economy fish in China, because its is full of nutrition, delicious flavour due to it is deep by the majority of consumers
Like.It promotes and comes from Larimichthys crocea artificial diet technique, the quantity of cultured large yellow croaker is growing day by day.Larimichthys crocea is mostly with chilled fish
Form sale, partially through degreasing be processed into freezing degreasing Larimichthys crocea, processing ratio it is lower.However, in face of diet diversification
The market demand and increasingly increased rheum officinale fish crop, exploitation type Larimichthys crocea fabricated product abundant can not only meet market
Demand, while the added value of Larimichthys crocea can be improved.Marinated is a kind of traditional processing method, microorganism and raw material in curing process
The collective effect of middle endogenous enzymes imparts the special flavor of product and quality, however since traditional pickling process process mostly uses nature to send out
The mode of ferment, fermentative microorganism is mainly from raw material and processing environment, if condition control is improper, easily causes product quality unstable
The growth of fixed or harmful microorganism causes the biohazard factor.
Leavening (Starter culture) refers to the culture of microorganism for fermented product production or is enriched fermentation
Some matrix (Holzapfel, 1997) of microorganism.The screening and addition of leavening decide the characteristic of fermented product.Currently,
The leavening (Selected starter cultures, SSC) of American-European countries's artificial screening fermented dairy product, ferment sausage,
A variety of fermented food processing industries such as grape wine, fermented vegetable are widely used (Cogan et al., 2007).Saccharomycete, cream
Many kinds in sour bacterium have been developed to food industry production leavening, and the microorganism of some other type also by
It develops (Gaggiano et al., 2007).Compared with spontaneous fermentation, the use of leavening is conducive to food-processing industry
It preferably controls technological parameter in process of producing product, the safety realized production mechanization, improve product, keep different batches
The consistency of product quality and ensure product quality.
In marinated fish, meat products production process, most of harmful microbes are grown under environment with high salt and are suppressed,
And be suitble in hypersaline environment the staphylococcus that grows that can then secrete significant quantities of fat enzyme and protease, and then by fat in raw material and
The macromolecules degradations such as protein are at the small molecules flavor substance such as fatty acid, amino acid.Stahnke is added to wood in sausage production
Sugared staphylococcus (Staphylococcus xylosus) and Staphylococcus carnosus (S.carnosus) are used as leavening, and GC-MS pairs
Product special flavour constituent analysis shows that it is big to protein and fat that most of flavor substance is all from addition Institute of Micro-biology secretion enzyme system
The degradation of molecule.
The method of artificial screening leavening can not only guarantee the consistency between pickled products batch, while that adds has
Beneficial microorganism is able to suppress the safety that the self-contained harmful microbe of raw material breeds, improves product, also, the production filtered out
The excellent microorganism of enzyme ability can be fully hydrolyzed the macromoleculars such as protein and fat in curing process, improve the flavor of product
Quality.Currently, the preparation method for pickled fermented dose of Larimichthys crocea has not been reported.
Summary of the invention
The technical problem to be solved in the present invention is to provide a kind of Larimichthys crocea method for salting for adding leavening, the present invention passes through
Addition leavening improves the flavor of marinated rheum officinale fishery -ies product, improves its safety.
In order to solve the above technical problem, the present invention provides a kind of Larimichthys crocea method for salting for adding leavening, including such as
Lower step:
1), the activation of Staphylococcal fermentation bacterium；
Nepal staphylococcus, staphylococcus xylosus are activated respectively；
2), by after activation Nepal staphylococcus, staphylococcus xylosus respectively at improvement MSA fluid nutrient medium in expand
Big culture, until OD600nmIt is 0.6~0.8, to obtain Nepal's staphylococcus culture fluid, staphylococcus xylosus training respectively
Nutrient solution；
The improvement MSA fluid nutrient medium is that 7.5~8.5g (preferably 8g) is added in the MSA fluid nutrient medium of 100ml
NaCl is prepared and is obtained；
3), Nepal's staphylococcus culture fluid, staphylococcus xylosus culture solution are mixed, resulting composite microbial bacteria
The number of cells of the staphylococcic number of cells=staphylococcus xylosus of Ye Zhong Nepal；
4), fresh fish pre-treatment:
Fresh Larimichthys crocea goes internal organ (removing internal organs after splitting abdomen), drains the water after flowing water cleaning, fish body after must handling；
5), it is inoculated with composite ferment:
According to 106/ g inoculum concentration, complex microorganism bacterium solution is uniformly sprayed and is inoculated in fish body surface and abdominal cavity, and room temperature is quiet
Set 1.5~2.5h (preferably 2h), fish body after must being inoculated with；
Remarks explanation:
According to microorganism count, and calculate fish body weight；Above-mentioned 106The inoculum concentration of a (cell)/g (fish body after processing), refers to
The sum of the total amount of two kinds of bacterium, that is, Nepal staphylococcus is 0.5 × 106A/g, staphylococcus xylosus are also 0.5 × 106A/
g；
6), add salt for the first time:
Salt is uniformly applied to fish after inoculation by the salt for weighing fish body weight 4.5~5.5% (preferably 5%) after accounting for processing
Then body surface face covers fish body with preservative film, pickle 22~26 hours (preferably 22 DEG C, 24 hours) at 20~25 DEG C；?
Preliminary marinated rear fish body；
7), second plus salt:
The salt of fish body weight 9~11% (preferably 10%) after accounting for processing is weighed, preliminary marinated rear fish body is first drained into blood
Then salt is uniformly applied to abdomen and the surface of fish body by water；
Be vertically arranged and be placed in sterilized antistaling case in the way of upward by fish belly, imposed above fish fish body gross weight 35~
The pressure of 45% (preferably 40%), it is 4~6 days (preferably 22 DEG C, 5 days) marinated in 20~25 DEG C, obtain secondary marinated rear fish body；
8), third time plus salt:
The salt for weighing fish body weight 9~11% (preferably 10%) after accounting for processing, after salt to be uniformly applied to secondary pickle
The surface of fish body imposes the pressure of fish body gross weight 13~18% (preferably 15%) above fish, and 13 are pickled at 20~25 DEG C
~15d (preferably 22 DEG C, 14d).
Remarks explanation: above-mentioned steps 7) and step 8) in, " fish body gross weight " is calculated according to fish body weight after processing
's.
Fish body stacks the same step 7) of arrangement mode in step 8).
The improvement of Larimichthys crocea method for salting as addition leavening of the invention:
Nepal staphylococcus is Nepal staphylococcus L1-1；
Staphylococcus xylosus is staphylococcus xylosus S10-10.
Above-mentioned bacterial strains are in Microbiological Changes and Biodiversity of Cultivable
Indigenous Bacteria in Sanbao Larger Yellow Croaker(Pseudosciaena crocea),a
Chinese Salted and Fermented Seafood.Journal of Food Science.2015,80(4):M776
Have in~M781 and clearly informs.
The further improvement of Larimichthys crocea method for salting as addition leavening of the invention:
In the step 7), the part salt for accounting for 38~42% (preferably 40%) of salt gross weight is uniformly applied to fish body
Abdomen, remaining salt is uniformly applied to the surface of fish body.
The further improvement of Larimichthys crocea method for salting as addition leavening of the invention:
In the step 7), elder generation, which is vertically arranged in the way of upward by fish belly and then stacks (mounted on top) layer by layer, is placed on nothing
In bacterium antistaling box；It imposes above fish layer and is pickled after the pressure of fish body gross weight 35~45% (preferably 40%) after stacking；
At most stack 3 layers (that is, in the present invention, minimum 1 layer, up to 3 layers).
The further improvement of Larimichthys crocea method for salting as addition leavening of the invention:
The expansion of the step 2) is incubated in shaking table and carries out, and cultivation temperature is 29~31 DEG C (preferably 30 DEG C), shaking speed
For 80~120rpm (preferably 100rpm), culture is until OD600nmIt is 0.6~0.8.
It is carried out in general, being added the resulting activated bacterium solution of 4mL step 1) to 80mL improvement MSA fluid nutrient medium
Expand culture；According to above-mentioned condition, 48h is cultivated, OD can be made600nmIt is 0.6~0.8.
The further improvement of Larimichthys crocea method for salting as addition leavening of the invention:
The activation of the step 1) are as follows:
By be preserved in -80 DEG C Nepal staphylococcus, staphylococcus xylosus 30% glycerol bacterium solution do not walked as follows respectively
It is rapid:
It is to be restored to after room temperature, taking 500 μ L glycerol bacterium solutions to be added in 4mL improvement MSA fluid nutrient medium, 29~31 DEG C are (preferably
It is 30 DEG C) culture at least 48h.
Remarks explanation: when activating for the first time to the glycerol bacterium solution for being preserved in -80 DEG C, 30%, strain growth is slower,
Incubation time at least 48 extends incubation time to 72h in due course.
30% glycerol bacterium solution refers to the bacterium solution containing 30% (v/v) glycerol.
In the present invention, room temperature generally refers to 15~25 DEG C.
Microorganism used in the present invention separates arrogant yellow croaker curing process, belongs to endogenous in Larimichthys crocea pickling process
Microbial strains.Technique of the invention mainly includes the activation of Staphylococcal fermentation bacterial strain, the expansion culture of fermentation strain, determines again
It closes the cell quantity range of two kinds of bacterial strains in microbe leaven, fresh fish pre-treatment, inoculation composite ferment and adds for 3 times salted
System.
The present invention has studied the staphylococcus xylosus (S.xylosus) isolated from marinated Larimichthys crocea, saprophytic grape
Coccus (S.saprophyticus), Nepal staphylococcus (S.nepalensis), staphylococcus aureus (S.aureus),
Calf staphylococcus (S.vitulinus), Staphylococcus sciuri (S.sciuri), Staphylococcus equorum (S.equorum) and amber
8 kinds of staphylococcuses of amber staphylococcus (S.succinus), wherein staphylococcus aureus is pathogenic bacteria；And in remaining 7 kinds, calf
Staphylococcus (S.vitulinus), Staphylococcus sciuri (S.sciuri), Staphylococcus equorum (S.equorum) and amber Portugal
It is considerably less (each 2~3 plants) that grape coccus (S.succinus) separates quantity.The present invention is through experimental results demonstrate Nepal's grape balls
Bacterium, the resulting complex microorganism bacterium solution effect of staphylococcus xylosus compounding are best.
Compound microbial culture starter provided by the invention is answered salt tolerant, two kinds of microorganisms for having high protein enzymatic activity
Match, improves the percent hydrolysis of protein in salted fish production, increase the content of amino acid in pickled products, improve the wind of product
Taste.
Specific embodiment
The present invention is described further combined with specific embodiments below, but protection scope of the present invention is not limited in
This.
Embodiment 1, a kind of Larimichthys crocea method for salting for adding leavening, successively carry out following steps:
1), the activation of Staphylococcal fermentation bacterium；
Nepal staphylococcus L1-1, staphylococcus xylosus S10-10 are activated respectively；
Specifically:
The 30% glycerol bacterium solution (Nepal staphylococcus L1-1, staphylococcus xylosus S10-10) for being preserved in -80 DEG C is taken out
Afterwards, following steps are carried out respectively:
It is to be restored to after room temperature, taking 500 μ L glycerol bacterium solutions to be added in 4mL improvement MSA fluid nutrient medium, 30 DEG C of culture 48h；
Improvement MSA fluid nutrient medium is that 8g NaCl is added in the MSA culture medium of 100ml to prepare and obtain.
2) Nepal staphylococcus L1-1, the staphylococcus xylosus S10-10 after activation, are subjected to following expansion respectively
Culture:
Take the resulting activated culture of 4mL step 1) be added to 80mL improvement MSA fluid nutrient medium in, in shaking table into
Row expands culture；Cultivation temperature is 30 DEG C, shaking speed 100rpm；Culture is until OD600nmIt is 0.6~0.8；To respectively
Obtain Nepal staphylococcus L1-1 culture solution, staphylococcus xylosus S10-10 culture solution；
3), Nepal's staphylococcus L1-1 culture solution, staphylococcus xylosus S10-10 culture solution are mixed, it is resulting multiple
Close number of cells=staphylococcus xylosus S10-10 number of cells of Nepal staphylococcus L1-1 in microbial inoculum；
4), fresh fish pre-treatment:
Picking individual is complete, uniform fresh Larimichthys crocea, removes internal organs after splitting abdomen, with clean flowing water by fish body
Surface and cheek, abdominal cavity clean up, and drain the water, fish body after must handling；Weighing；
5), it is inoculated with composite ferment:
According to 106/ g inoculum concentration, complex microorganism bacterium solution is uniformly sprayed and is inoculated in fish body surface and abdominal cavity, and room temperature is quiet
Set 2h；Fish body after must being inoculated with；
Described 106/ g inoculum concentration refers to: fish body adapted contains 10 after every g processing6The complex microorganism bacterium solution of a bacterium；That is, Ni Bo
The inoculum concentration respectively 0.5 × 10 of that staphylococcus L1-1, staphylococcus xylosus S10-106A/g.
6), add salt for the first time:
Salt is uniformly applied to fish body surface after inoculation, then with fresh-keeping by the salt for weighing fish body weight 5% after accounting for processing
Film covers fish body, 24 hours marinated in 22 DEG C；Obtain tentatively marinated rear fish body；
7), second plus salt:
The salt of fish body weight 10% after accounting for processing is weighed, preliminary marinated rear fish body is first drained into watery blood, then will account for the salt
The part salt of the 40% of gross weight is uniformly applied to the abdomen of fish body, and remaining salt is uniformly applied to the surface of fish body；
That is, being fish belly according to salt ratio: salt is uniformly applied to fish belly chamber and body surface by fish table=2:3.
It is first vertically arranged in the way of upward by fish belly and then stacks (mounted on top) layer by layer and be placed in sterilized antistaling case,
Stack 3 layers；The pressure of fish body gross weight 40% after stacking is imposed above fish layer, it is 5 days marinated in 22 DEG C, obtain secondary marinated rear fish
Body.
8), third time plus salt:
Salt is uniformly applied to the surface of secondary marinated rear fish body, in fish by the salt for weighing fish body weight 10% after accounting for processing
Top imposes the pressure of fish body gross weight 15%, in 22 DEG C of marinated 14d.
Remarks explanation: above-mentioned steps 7) and step 8) in, " fish body gross weight " is calculated according to fish body weight after processing
's.Fish body stacks the same step 7) of arrangement mode in step 8).
Comparative example 1, tradition marinated Larimichthys crocea with high salt
Using chilled Larimichthys crocea as raw material, successively follow the steps below:
1) picking individual is complete, uniform fresh Larimichthys crocea, is cleaned fish body surface and cheek with clean flowing water dry
Only, it drains the water, weighs；
2) add salt for the first time: weighing the salt of 10% fish body weight in wet base, be uniformly applied to fish body surface, cover fish body with preservative film,
30 DEG C are pickled for 24 hours.
3) second plus salt: draining watery blood, be fish belly: fish table=4:5 according to salt ratio, with the wooden chopsticks by salt from the fish gill
Place is passed through in Larimichthys crocea fish belly, and fish belly upward, is arranged in sterile guarantor with being had levels after remaining salt is applied to fish body surface
(number of plies being stacked with 3 layers of embodiment 1) in fresh case, the pressure that fish body weighs 40% being imposed above fish layer, 30 DEG C of marinated 5d (add salt
Amount is the 20% of fish body weight in wet base).
4) third time plus salt: salt is applied to fish body surface, upper layer applies 40% pressure of fish weight, and in temperature 30
14d is pickled at DEG C (salt adding amount is the 20% of fish body weight in wet base).
Comparative example 2, the Larimichthys crocea for not adding microbe leaven are marinated:
For embodiment 1, cancellation step 1)~step 3) and step 5), that is, by fish after the resulting processing of step 4)
Body directly carries out first time described in step 6) and adds salt, remaining is equal to embodiment 1.
Comparative example 3-1, the use for cancelling staphylococcus xylosus S10-10, meet Nepal staphylococcus L1-1 in step 5)
Kind amount is 106/ g (that is, total bacterium amount is still with embodiment 1)；Remaining is equal to embodiment 1.
Comparative example 3-2, the use for cancelling Nepal staphylococcus L1-1, make staphylococcus xylosus S10-10 in step 5)
Inoculum concentration is 106/ g (that is, total bacterium amount is still with embodiment 1)；Remaining is equal to embodiment 1.
Comparative example 3-3, staphylococcus xylosus S10-10 is changed to bacterium staphylococcus saprophyticus S5-8, remaining is equal to embodiment
1。
Comparative example 3-4, Nepal staphylococcus L1-1 is changed to bacterium staphylococcus saprophyticus S5-8, remaining is equal to embodiment
1。
Comparative example 3-5, staphylococcus xylosus S10-10 is changed to bacterium calf staphylococcus SX8, remaining is equal to embodiment
1。
Comparative example 3-6, Nepal staphylococcus L1-1 is changed to calf staphylococcus SX8, remaining is equal to embodiment 1.
Comparative example 3-7, by complex microorganism bacterium solution, the number of cells of Nepal staphylococcus L1-1: xylose grape ball
The number of cells of bacterium S10-10 is changed to 1.5:1 by 1:1；Total inoculum concentration remains unchanged, and is still 106/g；Remaining is equal to implementation
Example 1.
Comparative example 3-8, by complex microorganism bacterium solution, the number of cells of Nepal staphylococcus L1-1: xylose grape ball
The number of cells of bacterium S10-10 is changed to 1:1.5 by 1:1；Total inoculum concentration remains unchanged, and is still 106/g；Remaining is equal to implementation
Example 1.
Salt ratio in the step 7) of embodiment 1 is changed to by " fish belly: fish table=2:3 " such as routine techniques by comparative example 4
" fish belly: fish table=4:5 ", remaining is equal to embodiment 1.
Measurement to the total amino acid content of above-mentioned different curing condition products, saliferous rate and histamine content.Measurement result is shown in
Table 1.
Table 1
As can be drawn from Table 1, traditional handicraft, which pickles Larimichthys crocea, is completed under the conditions of 30 DEG C of (50%) with high salt, although high
Microorganism producing enzyme and the endogenous enzyme activity of fish body are higher under the conditions of temperature, and promote fish protein is degraded to flavour amino abundant
Sour small molecule, but conventional high-temperature, marinated the shortcomings that also making product (35.61%) excessively high there are salt content with high salt.In addition, traditional work
Hot conditions in skill are marinated, although obtaining the product of better flavor, it is raised also to bring product histamine content simultaneously
Defect.In comparative example 1, histamine content is up to 91.67mg/kg, and histamine must not surpass in the import aquatic products required higher than U.S. FDA
The limitation of 50mg/kg is crossed, and histamine content must not be higher than the limitation upper limit of 100mg/kg close in aquatic products as defined in European Union.Fish
With the histamine in fish product is exceeded may cause food poisoning, and the histamine of high concentration can lead to the allergy of human body sensitivity constitution
Shape.The accumulation that histamine in product can be effectively reduced using the method for controlling marinated temperature, is can simultaneously be effectively reduced and is salted down
The usage amount of salt during system.However, under the conditions of low-temperature salting, from the endogenous enzyme activity of microorganism and fish body itself in raw material
Power is lower, and fish protein hydrolysis degree is far away from conventional high-temperature pickling process.It is such as added during low-temperature salting and produces protease
The stronger compound microbial culture starter of vigor, fish protein can be fermented agent Institute of Micro-biology and produce protease in raw material decomposes step by step,
And then amino acid is promoted largely to accumulate (24.75g/100g is shown in embodiment 1).
According to above-mentioned comparative example, we are learnt: different zymogenic selections, total amino acid content to products therefrom and
Histamine content has large effect.Meanwhile individually addition staphylococcus xylosus S10-10 or individually addition Nepal's grape ball
Bacterium L1-1 carries out salted fish production, and product amino acid content is below the effect of the two equal proportion addition (embodiment 1)；And with corruption
When raw staphylococcus S-8 or calf staphylococcus SX8 replace two plants of strains testeds in the present invention respectively, the amino acid of product is total
Amount is below embodiment 1, and histamine content is much higher than the obtained product of embodiment 1.
The above list is only a few specific embodiments of the present invention for finally, it should also be noted that.Obviously, this hair
Bright to be not limited to above embodiments, acceptable there are many deformations.Those skilled in the art can be from present disclosure
All deformations for directly exporting or associating, are considered as protection scope of the present invention.
Claims (6)
1. add leavening Larimichthys crocea method for salting, it is characterized in that include the following steps: 1), the work of Staphylococcal fermentation bacterium
Change；Nepal staphylococcus, staphylococcus xylosus are activated respectively；2), by the Nepal staphylococcus after activation, wood
Sugared staphylococcus expands culture respectively in improvement MSA fluid nutrient medium, until OD600nmIt is 0.6~0.8, thus point
It Huo get not Nepal's staphylococcus culture fluid, staphylococcus xylosus culture solution；The improvement MSA fluid nutrient medium be
7.5~8.5gNaCl is added in the MSA fluid nutrient medium of 100ml to prepare and obtain；3), by Nepal's staphylococcus culture fluid, wood
Sugared staphylococcus culture fluid is mixed, the staphylococcic number of cells=wood of Nepal in resulting complex microorganism bacterium solution
The staphylococcic number of cells of sugar；4), fresh fish pre-treatment: fresh Larimichthys crocea removes internal organ, drains the water, must handle after flowing water cleaning
Fish body afterwards；5), it is inoculated with composite ferment: according to 106/ g inoculum concentration, complex microorganism bacterium solution is uniformly sprayed and is inoculated in fish body
Surface and abdominal cavity, are stored at room temperature 1.5~2.5h, fish body after must being inoculated with；6), add salt for the first time: weighing fish after accounting for processing
Salt is uniformly applied to fish body surface after inoculation, then covers fish body with preservative film by the salt of body weight 4.5~5.5%,
It is pickled 22~26 hours at 20~25 DEG C；Obtain tentatively marinated rear fish body；7), second plus salt: fish body after accounting for processing is weighed
Preliminary marinated rear fish body is first drained watery blood, then salt is uniformly applied to the abdomen of fish body by the salt of weight 9~11%
The surface and；Be vertically arranged and be placed in sterilized antistaling case in the way of upward by fish belly, imposed above fish fish body gross weight 35~
45% pressure, it is 4~6 days marinated in 20~25 DEG C, obtain secondary marinated rear fish body；8) it, third time plus salt: weighs and accounts for processing
Salt is uniformly applied to the surface of secondary marinated rear fish body, fish is imposed above fish by the salt of fish body weight 9~11% afterwards
The pressure of body gross weight 13~18% pickles 13~15d at 20~25 DEG C.
2. the Larimichthys crocea method for salting of addition leavening according to claim 1, it is characterized in that: Nepal staphylococcus
For Nepal staphylococcus L1-1；Staphylococcus xylosus is staphylococcus xylosus S10-10.
3. the Larimichthys crocea method for salting of addition leavening according to claim 2, it is characterized in that: in the step 7),
38~42% part salt for accounting for salt gross weight is uniformly applied to the abdomen of fish body, remaining salt is uniformly applied to
The surface of fish body.
4. the Larimichthys crocea method for salting of any addition leavening according to claim 1~3, it is characterized in that: the step
It is rapid 7) in, be first vertically arranged in the way of upward by fish belly and then stack be placed in sterilized antistaling case layer by layer；Above fish layer
It is pickled after imposing the pressure for stacking rear fish body gross weight 35~45%；At most stack 3 layers.
5. the Larimichthys crocea method for salting of any addition leavening according to claim 1~3, it is characterized in that: the step
Rapid expansion 2), which is incubated in shaking table, to be carried out, cultivation temperature be 29~31 DEG C, shaking speed be 80~120rpm, culture until
OD600nmIt is 0.6~0.8.
6. the Larimichthys crocea method for salting of any addition leavening according to claim 1~3, it is characterized in that: the step
Rapid activation 1) are as follows: Nepal staphylococcus, the 30% glycerol bacterium solution of staphylococcus xylosus of being preserved in -80 DEG C is respectively other
Carry out following steps: it is to be restored to after room temperature, taking 500 μ L glycerol bacterium solutions to be added in 4mL improvement MSA fluid nutrient medium, 29
~31 DEG C (preferably 30 DEG C) culture at least 48h.
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN112408607A (en) * | 2020-12-07 | 2021-02-26 | 山东卓苒生物科技有限公司 | Application of staphylococcus nepalensis in degradation of residual sugar in fermentation industrial organic wastewater |
| CN113826837A (en) * | 2021-09-22 | 2021-12-24 | 成都大学 | Fermented flavored preserved meat and preparation method thereof |
| CN114209027A (en) * | 2021-11-23 | 2022-03-22 | 集美大学 | Preparation method of canned fatty fish |
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2018
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN112408607A (en) * | 2020-12-07 | 2021-02-26 | 山东卓苒生物科技有限公司 | Application of staphylococcus nepalensis in degradation of residual sugar in fermentation industrial organic wastewater |
| CN112408607B (en) * | 2020-12-07 | 2021-08-13 | 山东卓苒生物科技有限公司 | Application of staphylococcus nepalensis in degradation of residual sugar in fermentation industrial organic wastewater |
| CN113826837A (en) * | 2021-09-22 | 2021-12-24 | 成都大学 | Fermented flavored preserved meat and preparation method thereof |
| CN114209027A (en) * | 2021-11-23 | 2022-03-22 | 集美大学 | Preparation method of canned fatty fish |
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