CN106399173B - A kind of cheese leavening and preparation method thereof - Google Patents

A kind of cheese leavening and preparation method thereof Download PDF

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CN106399173B
CN106399173B CN201610840580.4A CN201610840580A CN106399173B CN 106399173 B CN106399173 B CN 106399173B CN 201610840580 A CN201610840580 A CN 201610840580A CN 106399173 B CN106399173 B CN 106399173B
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cgmcc
lactococcus lactis
lactis subsp
lactis
culture
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CN106399173A (en
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焦晶凯
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Bright Dairy and Food Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N1/00Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
    • C12N1/20Bacteria; Culture media therefor
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23CDAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING THEREOF
    • A23C19/00Cheese; Cheese preparations; Making thereof
    • A23C19/02Making cheese curd
    • A23C19/032Making cheese curd characterised by the use of specific microorganisms, or enzymes of microbial origin
    • A23C19/0323Making cheese curd characterised by the use of specific microorganisms, or enzymes of microbial origin using only lactic acid bacteria, e.g. Pediococcus and Leuconostoc species; Bifidobacteria; Microbial starters in general
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2400/00Lactic or propionic acid bacteria
    • A23V2400/11Lactobacillus
    • A23V2400/157Lactis
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2400/00Lactic or propionic acid bacteria
    • A23V2400/11Lactobacillus
    • A23V2400/169Plantarum

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Abstract

The invention discloses a kind of cheese leavenings and preparation method thereof.The leavening includes lactococcus lactis subsp CGMCC No.10746, can also include one of Lactococcus lactis subsp. lactis CGMCC No.10744, Lactococcus lactis subsp. lactis CGMCC No.10745 and lactobacillus plantarum CGMCC No.10747 or a variety of.The viable count ratio of the sum of lactis subsp. cremoris CGMCC No.10746 and Lactococcus lactis subsp. lactis CGMCC No.10744, Lactococcus lactis subsp. lactis CGMCC No.10745 and lactobacillus plantarum CGMCC No.10747 three are greater than 1.The cheese leavening, which can be used for industrialized production, pleasant aroma, excellent flavor, the reasonable cheese of texture.

Description

A kind of cheese leavening and preparation method thereof
Technical field
The present invention relates to dairy product processing fields, and in particular to a kind of cheese leavening and preparation method thereof.
Background technique
The preservation that the invention of cheese keeps milk long-term, and different cheese has diversified flavor, texture And character, be one of advantage source of protein, fat and minerals, wherein also containing essential amino acid and vitamin such as VA, VB2, VB6 and VB12.Aged cheese is that the milk acidification that a kind of hard, semi-rigid form protein cross by renin is dense Contracting product.Cheese is one of optimal selection of balanced diet.
One of an important factor for cheesy flavor is the selection of influence consumer spending and acceptance, many western countries receive greatly vigorously The cheese varieties met but rarely have in China makes inquiries.Cheesy flavor depends on the chemical component of cheese complexity itself and by wherein micro- The influence of biology is very big.The formation of cheesy flavor is by a series of complex microorganism, biochemistry and chemical action process.Though Environment of the right cheese microorganism group at major part from local milk supply and locality, but enterprise's production cheese is new there is still a need for adding Strain adjust the flavor of cheese to adapt to the needs of consuming public, therefore contribute cheesy flavor excellent bacterial strain screening It is imperative.
China is more rare to the research of novel species fermented cheese at present, and research and development are suitable for Chinese taste, special with China The Flavor Cheese of color is the historic responsibility of the Chinese government, researcher and Dairy Enterprise.
Summary of the invention
Technical problem to be solved by the present invention lies in prior art blank is filled up, provide a kind of cheese leavening and its Preparation method.
Technical solution of the present invention first is that: a kind of cheese leavening comprising lactococcus lactis subsp (Lactococcus lactis subsp.cremoris)CGMCC No.10746。
In the present invention, lactococcus lactis subsp CGMCC No.10746 is isolated from the city Inner Mongolia Autonomous Region Lun Beier The self-control dairy products of the black bead bush in Chenbarhu Banner east, the well-grown in cream, acid production speed is moderate, for producing cheese Excellent flavor, yield are high.The bacterial strain is identified, result is lactococcus lactis subsp (Lactococcus lactis Subsp.cremoris), it is named as E11.The bacterial strain is preserved in Chinese microorganism strain preservation management on April 27th, 2015 Committee's common micro-organisms center, and receive collection and register on the books number CGMCC No.10746.
Preferably, the cheese starter further includes Lactococcus lactis subsp. lactis (Lactococcus lactis Subsp.lactis) CGMCC No.10744 (C24), Lactococcus lactis subsp. lactis (Lactococcus lactis Subsp.lactis) CGMCC No.10745 (C45) and lactobacillus plantarum (Lactobacillus plantarum) CGMCC One of No.10747 (G42) or a variety of.
In the present invention, Lactococcus lactis subsp. lactis CGMCC No.10744 is isolated from the city Inner Mongolia Autonomous Region Lun Beier The white oil cream dairy products in haji area, the well-grown in cream, acid production speed is moderate, good for producing cheesy flavor, obtains Rate is high.The bacterial strain is identified, result is Lactococcus lactis subsp. lactis (Lactococcus lactis Subsp.lactis), it is named as C24.The bacterial strain has been preserved in Chinese microorganism strain preservation management committee on April 27th, 2015 Member can common micro-organisms center, and receive collection and register on the books number CGMCC No.10744.
In the present invention, Lactococcus lactis subsp. lactis CGMCC No.10745 is isolated from the city Inner Mongolia Autonomous Region Lun Beier The manual cheese in haji area, the well-grown in cream, acid production speed is moderate, good for producing cheesy flavor, and yield is high. The bacterial strain is identified, result is Lactococcus lactis subsp. lactis (Lactococcus lactis subsp.lactis), life Entitled C45.The bacterial strain is preserved in China Committee for Culture Collection of Microorganisms's common micro-organisms on April 27th, 2015 The heart, and receive collection and register on the books number CGMCC No.10745.
In the present invention, lactobacillus plantarum CGMCC No.10747 is isolated from the western Wu Zhuer in the city Inner Mongolia Autonomous Region Lun Beier The self-control dairy products in area, the well-grown in cream, acid production speed is moderate, good for producing cheesy flavor, and yield is high.It is right The bacterial strain is identified that result is lactobacillus plantarum (Lactobacillus plantarum), is named as G42.The bacterial strain in On April 27th, 2015 is preserved in China Committee for Culture Collection of Microorganisms's common micro-organisms center, and receives collection Number of registering on the books CGMCC No.10747.
In the present invention, in the cheese starter, the lactis subsp. cremoris CGMCC No.10746 is main leavening, Lactococcus lactis subsp. lactis CGMCC No.10744, Lactococcus lactis subsp. lactis CGMCC No.10745 and plant cream One of bacillus CGMCC No.10747 or a variety of is adjunct culture.Preferably, the main fermentation agent and the attached hair The viable count ratio of ferment agent is greater than 1;It is more preferably 1:1~10:1.Most preferably, in the cheese starter, the Lactococcus lactis It is bacterium lactic acid subspecies CGMCC No.10746 (E11), the Lactococcus lactis subsp. lactis CGMCC No.10744 (C24), described The work of Lactococcus lactis subsp. lactis CGMCC No.10745 (C45) and the lactobacillus plantarum CGMCC No.10747 (G42) Bacterium number ratio is 20:1:2:2 or 5:2:1:2.
Preferably, the cheese starter further includes auxiliary material.The auxiliary material is the auxiliary material of this field routine, for doing The preparation of junket leavening.Be preferably comprised water, lactose, sucrose, maltodextrin, sodium glutamate, gelatin, glycerol, sorbierite, One of trehalose, yeast extract and beta-cyclodextrin are a variety of.
The form of the cheese starter is the form of this field routine, preferably liquid starter, frozen fermented Agent or throw type leaven are more preferably throw type leaven, i.e., the cheese starter is without activating it, expanding Culture etc. pre-treatment steps and direct plunge into fermentation substrate use.
Technical solution of the present invention second is that: a kind of preparation method of the cheese leavening comprising step below It is rapid:
(1) lactococcus lactis subsp CGMCC No.10746 is inoculated in culture medium, obtains culture.
Step (1) are as follows: lactococcus lactis subsp CGMCC No.10746 is inoculated in culture medium, is cultivated Object.Wherein, the culture medium is the culture medium of this field routine, can grow the lactococcus lactis subsp CGMCC No.10746, preferably MRS culture medium, M17 culture medium, degreasing milk medium or culture medium A;More preferably it is Culture medium A, the culture medium A is by glucose 23g/L, soy peptone 11g/L, beef extract 11g/L, tryptone 5g/L, second Sour sodium 1.8g/L, K2HPO41.2g/L, sodium citrate 1.2g/L, MgSO4·7H2O 0.4g/L、MnSO4·5H2O54mg/L、L- Cysteine hydrochloride 0.5g/L and Tween 80 1g/L composition, pH 7.
In the present invention, the MRS culture medium be this field routine MRS culture medium, preferably, its by peptone 10g/L, Beef extract 10g/L, yeast extract 5g/L, citric acid hydrogen diamine 2g/L, glucose 20g/L, tween 1ml/L, sodium acetate 5g/L, phosphoric acid Hydrogen dipotassium 2g/L, magnesium sulfate 0.58g/L and manganese sulfate 0.25g/L composition, pH6.6.
In the present invention, the M17 culture medium is the M17 culture medium of this field routine, preferably, it is by phytone 5g/L, yeast powder 5g/L, polyprotein peptone 5g/L, ascorbic acid 0.5g/L, beef extract 2.5g/L, MgSO4·7H2O 0.01g/L and Phosphoglycerol disodium 19g/L composition, pH7.
In the present invention, the degreasing milk medium be this field routine degreasing milk medium, preferably 10~14% Degreasing milk medium.Skimmed milk powder is dissolved in the water and is mixed up to the degreasing milk medium, the percentage is described de- Fat milk powder accounts for the mass percent of the skimmed milk powder and the water gross mass.
Wherein, the temperature of the culture is the temperature of this field routine, and it is sub- can to grow the Lactococcus lactis butterfat Kind CGMCC No.10746, preferably 26~34 DEG C, be more preferably 30 DEG C.The time of the culture is that this field is conventional Time, preferably 12~48 hours, be more preferably 48 hours.The pH of the culture is the pH, Neng Gousheng of this field routine Lactococcus lactis subsp CGMCC No.10746 described in length, preferably 7.
In the present invention, preferably, the preparation method include the steps that it is following,
(2) by Lactococcus lactis subsp. lactis CGMCC No.10744, Lactococcus lactis subsp. lactis CGMCC One of No.10745 and lactobacillus plantarum CGMCC No.10747 or a variety of be inoculated in culture medium are cultivated, and are cultivated Object;
(3) the resulting culture of step (1) and the resulting culture of step (2) are mixed.
In the present invention, the condition of culture described in step (2) is the condition of this field routine, can make the Lactococcus lactis Bacterium lactic acid subspecies CGMCC No.10744, Lactococcus lactis subsp. lactis CGMCC No.10745 and lactobacillus plantarum CGMCC One of No.10747 or a variety of normal growths are simultaneously proliferated.
In the present invention, preferably, by the resulting culture of the step (1) and step (2) resulting culture according to cream Yogurt coccus lactic acid subspecies CGMCC No.10746 and Lactococcus lactis subsp. lactis CGMCC No.10744, Lactococcus lactis One of bacterium lactic acid subspecies CGMCC No.10745 and lactobacillus plantarum CGMCC No.10747 three or a variety of viable counts Ratio of the ratio greater than 1 mixes.More preferably, according to Lactococcus lactis subsp. lactis CGMCC No.10746, lactic acid cream Coccus lactic acid subspecies CGMCC No.10744, Lactococcus lactis subsp. lactis CGMCC No.10745 and lactobacillus plantarum CGMCC The ratio that No.10747 viable count is 20:1:2:2 or 5:2:1:2 mixes.
In the present invention, more preferably, the preparation method include thes steps that following: auxiliary material, mixing is added.
Wherein, the auxiliary material is the auxiliary material of this field routine, is preferably comprised water, lactose, sucrose, maltodextrin, paddy One of propylhomoserin sodium, gelatin, glycerol, sorbierite, trehalose, yeast extract and beta-cyclodextrin are a variety of.
Technical solution of the present invention third is that: one kind described in cheese leavening preparing the application in cheese.
The cheese is the cheese of this field routine, preferably Gouda cheese, Cheddar and Pa Masen cheese.More It goodly is Gouda cheese.
On the basis of common knowledge of the art, above-mentioned each optimum condition, can any combination to get each preferable reality of the present invention Example.
The reagents and materials used in the present invention are commercially available.
The positive effect of the present invention is that: cheese leavening of the present invention can prepare cheese, made Cheese sensory evaluation, in terms of with to be commercialized cheese obtained by commercially available leavening very nearly the same, it is satisfactory. The cheese passes through the proportionate relationship selected between suitable fermentation strain and fermentation strain with leavening simultaneously, so that The cheese leavening, which can be used for industrialized production, pleasant aroma, excellent flavor, the reasonable cheese of texture.
Biomaterial preservation information
Lactococcus lactis subsp E11 of the invention has been deposited in Chinese microorganism strain guarantor on April 27th, 2015 It hides administration committee's common micro-organisms center (CGMCC), preservation address: Yard 1, BeiChen xi Road, Chaoyang District, Beijing City 3, postcode: 100101, deposit number are as follows: CGMCC No.10746, culture title are lactococcus lactis subsps, and classification naming is Lactococcus lactis subsp.cremoris。
Lactococcus lactis subsp. lactis C24 of the invention has been deposited in Chinese microorganism strain guarantor on April 27th, 2015 It hides administration committee's common micro-organisms center (CGMCC), preservation address: Yard 1, BeiChen xi Road, Chaoyang District, Beijing City 3, postcode: 100101, deposit number are as follows: CGMCC No.10744, culture title are Lactococcus lactis subsp. lactis, and classification naming is Lactococcus lactis subsp.lactis。
Lactococcus lactis subsp. lactis C45 of the invention has been deposited in Chinese microorganism strain guarantor on April 27th, 2015 It hides administration committee's common micro-organisms center (CGMCC), preservation address: Yard 1, BeiChen xi Road, Chaoyang District, Beijing City 3, postcode: 100101, deposit number are as follows: CGMCC No.10745, culture title are Lactococcus lactis subsp. lactis, and classification naming is Lactococcus lactis subsp.lactis。
Lactobacillus plantarum G42 of the invention has been deposited in Chinese microorganism strain preservation management committee on April 27th, 2015 Member's meeting common micro-organisms center (CGMCC), preservation address: Yard 1, BeiChen xi Road, Chaoyang District, Beijing City 3, postcode: 100101, Deposit number are as follows: CGMCC No.10747, culture title are lactobacillus plantarums, and classification naming is Lactobacillus plantarum。
Detailed description of the invention
Fig. 1 is the radar map of 2 gained cheese of Application Example fermentation later period main flavor.
Specific embodiment
The present invention is further illustrated below by the mode of embodiment, but does not therefore limit the present invention to the reality It applies among a range.In the following examples, the experimental methods for specific conditions are not specified, according to conventional methods and conditions, or according to quotient The selection of product specification.
The preparation of 1 leavening of embodiment
Lactococcus lactis subsp E11 is inoculated in the skimmed milk of 12% (w/v) sterilizing by the inoculum concentration of 2% (v/v) In culture medium (cooperating dairy industry Co., Ltd purchased from New Zealand Westland), 30 DEG C of constant incubator cultures 24 hours are placed in, it is living Changed for 2 generations, obtains the bacterial strain of activation.The bacterial strain of activation is inoculated in the skimmed milk of 12% (w/v) sterilizing by the inoculum concentration of 2% (v/v) In culture medium, it is placed in 30 DEG C of constant incubator cultures and expands culture for 24 hours, be repeated 3 times to get the leavening containing E11 1。
The preparation of 2 leavening of embodiment
(1), lactococcus lactis subsp E11, Lactococcus lactis subsp. lactis C24 are connect by the inoculum concentration of 2% (v/v) Kind is placed in 30 in the degreasing milk medium (cooperating dairy industry Co., Ltd purchased from New Zealand Westland) that 12% (w/v) sterilizes It DEG C constant incubator culture 24 hours, activated for 2 generations, obtains the bacterial strain of activation.The bacterial strain of activation is connect by the inoculum concentration of 2% (v/v) Kind is placed in 30 DEG C of constant incubator cultures and expands culture for 24 hours in the degreasing milk medium that 10% (w/v) sterilizes, weight It is 3 times multiple.
(2), lactococcus lactis subsp E11, the Lactococcus lactis obtained the resulting culture of step (1) is sub- Kind C24, the ratio that the viable count according to the lactococcus lactis subsp E11, Lactococcus lactis subsp. lactis C24 is 1:1 Mixing, adds suitable lactose to get the leavening 2 containing E11 and C24.
The preparation of 3 leavening of embodiment
(1), lactococcus lactis subsp E11, Lactococcus lactis subsp. lactis C45 are connect by the inoculum concentration of 2% (v/v) Kind is placed in 30 in the degreasing milk medium (cooperating dairy industry Co., Ltd purchased from New Zealand Westland) that 12% (w/v) sterilizes It DEG C constant incubator culture 24 hours, activated for 2 generations, obtains the bacterial strain of activation.The bacterial strain of activation is connect by the inoculum concentration of 2% (v/v) Kind is placed in 30 DEG C of constant incubator cultures and expands culture for 24 hours in the degreasing milk medium that 10% (w/v) sterilizes, weight It is 3 times multiple.
(2), lactococcus lactis subsp E11, the Lactococcus lactis obtained the resulting culture of step (1) is sub- Kind C45, the ratio that the viable count according to the lactococcus lactis subsp E11, Lactococcus lactis subsp. lactis C45 is 1:1 Mixing, adds suitable glycerol and yeast extract to get the leavening 3 containing E11 and C45.
The preparation of 4 leavening of embodiment
(1), lactococcus lactis subsp E11, lactobacillus plantarum G42 are inoculated in 12% by the inoculum concentration of 2% (v/v) (w/v) in the degreasing milk medium (cooperating dairy industry Co., Ltd purchased from New Zealand Westland) to sterilize, 30 DEG C of constant temperature trainings are placed in It supports case culture 24 hours, activated for 2 generations, obtain the bacterial strain of activation.The bacterial strain of activation is inoculated in 10% by the inoculum concentration of 2% (v/v) (w/v) in the degreasing milk medium to sterilize, 30 DEG C of constant incubator cultures is placed in and are expanded culture within 24 hours, are repeated 3 times.
(2), lactococcus lactis subsp E11, the lactobacillus plantarum G42 for obtaining the resulting culture of step (1), is pressed The ratio that viable count according to the lactococcus lactis subsp E11, lactobacillus plantarum G42 is 1:1 mixes to contain E11 With the leavening 4 of G42.
The preparation of 5 leavening of embodiment
(1), by lactococcus lactis subsp E11, Lactococcus lactis subsp. lactis C24 and Lactococcus lactis subsp. lactis The degreasing milk medium that C45 is inoculated in 12% (w/v) sterilizing by the inoculum concentration of 2% (v/v) (is cooperated purchased from New Zealand Westland Dairy industry Co., Ltd) in, 30 DEG C of constant incubator cultures 24 hours are placed in, activated for 2 generations, obtains the bacterial strain of activation.By the bacterium of activation Strain is inoculated in the degreasing milk medium of 10% (w/v) sterilizing by the inoculum concentration of 2% (v/v), is placed in 30 DEG C of constant incubator trainings It supports 24 hours and expands culture, be repeated 3 times.
(2), lactococcus lactis subsp E11, the Lactococcus lactis obtained the resulting culture of step (1) is sub- Kind C24 and Lactococcus lactis subsp. lactis C45, according to the lactococcus lactis subsp E11, Lactococcus lactis subsp. lactis The ratio that the viable count of C24 and Lactococcus lactis subsp. lactis C45 are 6:2:4 mixes to get the hair containing E11, C24 and C45 Ferment agent 5.
The preparation of 6 leavening of embodiment
(1), lactococcus lactis subsp E11, Lactococcus lactis subsp. lactis C24 and lactobacillus plantarum G42 are pressed 2% (v/v) degreasing milk medium that inoculum concentration is inoculated in 12% (w/v) sterilizing is (limited purchased from New Zealand Westland cooperation dairy industry Company) in, 30 DEG C of constant incubator cultures 24 hours are placed in, activated for 2 generations, obtains the bacterial strain of activation.The bacterial strain of activation is pressed 2% (v/v) inoculum concentration is inoculated in the degreasing milk medium of 10% (w/v) sterilizing, is placed in 30 DEG C of constant incubator cultures 24 hours It expands culture, is repeated 3 times.
(2), lactococcus lactis subsp E11, the Lactococcus lactis obtained the resulting culture of step (1) is sub- Kind C24 and lactobacillus plantarum G42, according to the lactococcus lactis subsp E11, Lactococcus lactis subsp. lactis C24 and plant The ratio that the viable count of object lactobacillus G42 is 2:1:1 mixes to get the leavening 6 containing E11, C24 and G42.
The preparation of 7 leavening of embodiment
(1), lactococcus lactis subsp E11, Lactococcus lactis subsp. lactis C45 and lactobacillus plantarum G42 are pressed 2% (v/v) degreasing milk medium that inoculum concentration is inoculated in 12% (w/v) sterilizing is (limited purchased from New Zealand Westland cooperation dairy industry Company) in, 30 DEG C of constant incubator cultures 24 hours are placed in, activated for 2 generations, obtains the bacterial strain of activation.The bacterial strain of activation is pressed 2% (v/v) inoculum concentration is inoculated in the degreasing milk medium of 10% (w/v) sterilizing, is placed in 30 DEG C of constant incubator cultures 24 hours It expands culture, is repeated 3 times.
(2), lactococcus lactis subsp E11, the Lactococcus lactis obtained the resulting culture of step (1) is sub- Kind C45 and lactobacillus plantarum G42, according to the lactococcus lactis subsp E11, Lactococcus lactis subsp. lactis C45 and plant The ratio that the viable count of object lactobacillus G42 is 3:1:1 mixes to get the leavening 7 containing E11, C45 and G42.
The preparation of 8 leavening of embodiment
(1), by lactococcus lactis subsp E11, Lactococcus lactis subsp. lactis C24, Lactococcus lactis subsp. lactis C45 and lactobacillus plantarum G42 is inoculated in the degreasing milk medium of 12% (w/v) sterilizing by the inoculum concentration of 2% (v/v) (purchased from new West orchid Westland cooperates dairy industry Co., Ltd) in, 30 DEG C of constant incubator cultures 24 hours are placed in, activated for 2 generations, obtains activation Bacterial strain.The bacterial strain of activation is inoculated in the degreasing milk medium of 10% (w/v) sterilizing by the inoculum concentration of 2% (v/v), is placed in 30 It DEG C expands culture within constant incubator culture 24 hours, is repeated 3 times.
(2), lactococcus lactis subsp E11, the Lactococcus lactis obtained the resulting culture of step (1) is sub- Kind C24, Lactococcus lactis subsp. lactis C45 and lactobacillus plantarum G42, according to the lactococcus lactis subsp E11, lactic acid The viable count of galactococcus lactic acid subspecies C24, Lactococcus lactis subsp. lactis C45 and lactobacillus plantarum G42 are the ratio of 20:1:2:2 Example mixing is to get the leavening 8 containing E11, C24, C45 and G42.
The preparation of 9 leavening of embodiment
(1), by lactococcus lactis subsp E11, Lactococcus lactis subsp. lactis C24, Lactococcus lactis subsp. lactis C45 and lactobacillus plantarum G42 is inoculated in the degreasing milk medium of 12% (w/v) sterilizing by the inoculum concentration of 2% (v/v) (purchased from new West orchid Westland cooperates dairy industry Co., Ltd) in, 30 DEG C of constant incubator cultures 24 hours are placed in, activated for 2 generations, obtains activation Bacterial strain.The bacterial strain of activation is inoculated in the degreasing milk medium of 10% (w/v) sterilizing by the inoculum concentration of 2% (v/v), is placed in 30 It DEG C expands culture within constant incubator culture 24 hours, is repeated 3 times.
(2), lactococcus lactis subsp E11, the Lactococcus lactis obtained the resulting culture of step (1) is sub- Kind C24, Lactococcus lactis subsp. lactis C45 and lactobacillus plantarum G42, according to the lactococcus lactis subsp E11, lactic acid The viable count of galactococcus lactic acid subspecies C24, Lactococcus lactis subsp. lactis C45 and lactobacillus plantarum G42 are the ratio of 5:2:1:2 Mixing is to get the leavening 9 containing E11, C24, C45 and G42.
Effect example 1
(1) 50L raw milk (being purchased from Kingsoft pasture) is filtered, is stirred evenly, it is cooling after 72 DEG C, 2min pasteurize To 31 DEG C.Leavening 1 made from embodiment 1 is poured into the raw milk after pasteurize, the dense of the leavening 1 in raw milk is made Degree is 2%, and the percentage is percent by volume.0.5g/50L renin (Fromase is added while leavening is added 750XLG is purchased from Chr. Hansen A/S), it cultivates under 31 DEG C of constant temperature to pH 6.5.
It 2) is 1cm at volume by curd cutting made from step 1)3Grumeleuse, all creams are discharged after being slowly stirred 10min Clearly;It is added salt salt marsh 20 hours of 2.5%, the percentage is mass percent.Enter square dies later, is put on mold One keg water (about 1.0 kilograms) is simultaneously periodically overturn, and the time continues 12h.It is 10 DEG C later, 4 months mature, obtain Cheddar.
Effect example 2
(1) 50L raw milk is filtered, is stirred evenly, 28 DEG C are cooled to after 75 DEG C, 2min pasteurize.It will implement Leavening 5 made from example 5 pours into the raw milk after pasteurize, makes the concentration 1% of the leavening 5 in raw milk, described Percentage is percent by volume.0.8g/50L renin is added while leavening is added, and (Fromase 750XLG, is purchased from Chr. Hansen A/S), it cultivates under 28 DEG C of constant temperature to pH 6.5.
It 2) is 1.2cm at volume by curd cutting made from step 1)3Grumeleuse, be slowly stirred 20min.Then exist In 45min, temperature is increased to 40 DEG C from 28 DEG C.It is then discharged out all whey;It is added salt salt marsh 20 hours of 2%, it is described Percentage is mass percent.Enter square dies later, a keg water (about 1.0 kilograms) is put on mold and periodically overturns, when Between continue 15 hours.Then 15 DEG C, 3 months mature, obtain Ida nurse cheese.
Effect example 3
(1) 50L raw milk is filtered, is stirred evenly, 32 DEG C are cooled to after 75 DEG C, 3min pasteurize.It will implement Leavening 8 made from example 8 pours into the raw milk after pasteurize, makes the concentration 1% of the leavening 8 in raw milk, described Percentage is percent by volume.0.3g/50L renin is added while leavening is added, and (Fromase 750XLG, is purchased from Chr. Hansen A/S), it cultivates under 32 DEG C of constant temperature to pH 6.5.
It 2) is 1.4cm at volume by curd cutting made from step 1)3Grumeleuse, be slowly stirred 20min.Water is used at 35 DEG C Grumeleuse is washed, and is kept stirring 25min.It is then discharged out all whey.Square dies are added, squeeze 75min, are acidified 1h.Again plus Enter 2% salt salt marsh 4 days, the percentage is mass percent.Then 12 DEG C, 6 months mature, obtain Cheddar.
Effect example 4
(1) 50L raw milk is filtered, is stirred evenly, 30 DEG C are cooled to after 73 DEG C, 3min pasteurize.It will implement Leavening 9 made from example 9 pours into the raw milk after pasteurize, makes the concentration 1% of the leavening 9 in raw milk, described Percentage is percent by volume.0.7g/50L renin is added while leavening is added, and (Fromase 750XLG, is purchased from Chr. Hansen A/S), it cultivates under 30 DEG C of constant temperature to pH 6.5.
It 2) is 1.0cm at volume by curd cutting made from step 1)3Grumeleuse.Then in 30min, by temperature from 30 DEG C 39 DEG C are increased to, and is kept stirring 1 hour.It is then discharged out all whey.Square dies, dry salt salt marsh 2 days is added.Then 12 DEG C, it is 5 months mature, obtain Gouda cheese.
Comparative example 1
Cheddar is made using commercial fermentation agent CHOOZITTM RM 32 (DANISCO company).Contain in the leavening Lactococcus lactis subsp, lactococcus lactis subsp, Lactococcus lactis biacetyl subspecies and streptococcus thermophilus.
Remaining preparation method is identical with the preparation method of effect example 1.
Comparative example 2
Ida nurse cheese is made using commercial fermentation agent FD-DVS R-704 (Chr. Hansen A/S).In the leavening Contain lactococcus lactis subsp and lactococcus lactis subsp.
Remaining preparation method is identical with the preparation method of effect example 2.
Comparative example 3
Commercial fermentation agent FD-DVS CHN-22 (Chr. Hansen A/S) makes Cheddar.Contain in the leavening Lactococcus lactis subsp, lactococcus lactis subsp, Lactococcus lactis biacetyl subspecies and leukonid.
Remaining preparation method is identical with the preparation method of effect example 3.
Comparative example 4
(1) by Lactococcus lactis subsp. lactis BD164 (deposit number are as follows: CGMCC No.10751), Lactococcus lactis cream Sour subspecies BD2263 (deposit number are as follows: CGMCC No.10749), Lactococcus lactis subsp. lactis BD401 (deposit number are as follows: CGMCC No.10752) and Leuconostoc mesenteroides LM79 (deposit number are as follows: CGMCC No.10750) press 2% (v/v) inoculation Amount is inoculated in the degreasing milk medium (cooperating dairy industry Co., Ltd purchased from New Zealand Westland) of 10% (w/v) sterilizing, is set In 30 DEG C constant incubator culture 24 hours, activate 2 generations, obtain the bacterial strain of activation.The bacterial strain of activation is pressed to the inoculation of 2% (v/v) Amount is inoculated in the degreasing milk medium of 10% (w/v) sterilizing, is placed in 30 DEG C of constant incubator cultures and is carried out expansion training in 24 hours It supports, is repeated 3 times, obtain culture.
(2) the resulting culture of step (1) is obtained into Lactococcus lactis subsp. lactis BD164, Lactococcus lactis Asia Kind BD2263, Lactococcus lactis subsp. lactis BD401 and Leuconostoc mesenteroides LM79, then according to the Lactococcus lactis Subspecies BD401, the Lactococcus lactis subsp. lactis BD2263, the Lactococcus lactis subsp. lactis BD164 and the goldbeater's skin The ratio that the viable count of leukonid LM79 is 1:1:1:1 mixes, and obtains leavening A.
(3) Cheddar is made using leavening A.The complete phase of preparation method of remaining preparation method and effect example 1 Together.
Comparative example 5
(1), by lactococcus lactis subsp E11, Lactococcus lactis subsp. lactis C24, Lactococcus lactis subsp. lactis C45 and lactobacillus plantarum G42 is inoculated in the degreasing milk medium of 12% (w/v) sterilizing by the inoculum concentration of 2% (v/v) (purchased from new West orchid Westland cooperates dairy industry Co., Ltd) in, 30 DEG C of constant incubator cultures 24 hours are placed in, activated for 2 generations, obtains activation Bacterial strain.The bacterial strain of activation is inoculated in the degreasing milk medium of 10% (w/v) sterilizing by the inoculum concentration of 2% (v/v), is placed in 30 It DEG C expands culture within constant incubator culture 24 hours, is repeated 3 times.
(2), lactococcus lactis subsp E11, the Lactococcus lactis obtained the resulting culture of step (1) is sub- Kind C24, Lactococcus lactis subsp. lactis C45 and lactobacillus plantarum G42, according to the lactococcus lactis subsp E11, lactic acid The viable count of galactococcus lactic acid subspecies C24, Lactococcus lactis subsp. lactis C45 and lactobacillus plantarum G42 are the ratio of 1:1:1:1 Mixing is to get the leavening B containing E11, C24, C45 and G42.
(3) Cheddar is made using leavening B.The complete phase of preparation method of remaining preparation method and effect example 1 Together.
The measurement of flavor substance in 1 cheese of Application Example
Using low-polarity components (GC-MS), (referring to Wu Gu equality, gas chromatograph-mass spectrometer method measures amino first in 7 in vegetables 1999,15 (6): ester pesticide, Chinese public health 534), measure effect example 1,4 and comparative example 1,4 are made The flavor substance of standby cheese.As a result as shown in table 1 and Fig. 1.
1 cheese of table fermentation initial stage main flavor and its content
Wherein, the meaning of "-" indicates that content down under minimum detection value, can be estimated without containing the substance.It can by table 1 It is compared, the spy that the present invention selects with finding out with the Ida cheese of commercial fermentation agent preparation (i.e. the cheese of the preparation of comparative example 1) The aged cheese of the different resulting leavening production of bacterial strain has special aromatic substance isoamyl alcohol at fermentation initial stage, and isoamyl alcohol is main There are calvados fragrance and acid.And other key aroma ingredients content compared with Ida cheese prepared by commercial fermentation agent With significant difference.
Application Example 2
Using low-polarity components (GC-MS), measures and done prepared by effect example 2,3 and comparative example 2,4,5 The aromatic substance of junket.As a result as shown in Table 2 and Fig. 1.
The measurement of aromatic substance content in 2 cheese of table
Wherein, the meaning of "-" indicates that content down under minimum detection value, can be estimated without containing the substance.It can by table 2 Butyric acid, 1,2,4- trimethylbenzene, amylalcohol, cyclohexanone, ethyl -2 1- are also detected in cheese to find out effect example preparation, 3 dimethyl benzenes, 3- methyltridec, 2,6,10- trimethyldodecane, acrylic acid-2-ethyl caproite, longifolene, O-phthalic Dibutyl phthalate, and above-mentioned substance is not detected in the cheese of comparative example preparation.
Application Example 3
It is using Texture instrument (being purchased from Britain Stable Micro Systems company), effect example 1,2 and comparison is real Apply the measurement that cheese prepared by example 3,5 carries out texture characteristic.Wherein, measurement method is to push, test speed 5.00mm/ seconds; Testing time is 5 seconds;Probe type is P/5 probe, and every group of sample is measured in parallel 5 times.The results are shown in Table 3.
The measurement of 3 cheese texture characteristic of table
Embodiment Hardness/g Viscosity Elasticity
Effect example 1 1301.66±38.32 -40.00±7.64 0.25±0.04
Effect example 2 1206.85±55.36 -39.74±5.46 0.32±0.08
Comparative example 3 1026.34±215.84 -40.50±6.76 0.21±0.06
Comparative example 5 1055.64±123.87 -40.22±6.11 0.18±0.04
The elasticity of comparative example 3 and 5 is obvious poor it can be seen from texture characteristic, and hardness is lower, illustrates that inoculating proportion is wanted In a certain proportion, otherwise production cheese is ineffective.
Application Example 4
Subjective appreciation experiment
This subjective appreciation personnel include 12 personnel for being engaged in food research, are familiar with subjective appreciation points for attention and comment Minute mark is quasi-.Total score is 50 points, and score is evaluated in accordance with table 4.Each assessment officer independently evaluates, and uses clear water when replacing sample every time It gargles, the results are shown in Table 5.
4 cheese subjective appreciation method of table
5 cheese results of sensory evaluation of table
The result of table 5 illustrates, cheese produced by the present invention characteristic odor, in terms of be substantially better than comparison and implement Cheese obtained by example, whole scoring are also relatively high.
It should be understood that those skilled in the art can make the present invention various after having read above content of the invention Change or modification, these equivalent forms also fall within the scope of the appended claims of the present application.

Claims (13)

1. a kind of cheese leavening, which is characterized in that it include lactococcus lactis subsp (Lactococcus lactis subsp.cremoris)CGMCC No.10746。
2. cheese leavening as described in claim 1, which is characterized in that it further includes Lactococcus lactis subsp. lactis (Lactococcus lactis subsp.lactis) CGMCC No.10744, Lactococcus lactis subsp. lactis (Lactococcus lactis subsp.lactis) CGMCC No.10745 and lactobacillus plantarum (Lactobacillus plantarum) one of CGMCC No.10747 or a variety of.
3. cheese leavening as claimed in claim 2, which is characterized in that the lactis subsp. cremoris CGMCC No.10746 is main leavening, Lactococcus lactis subsp. lactis CGMCC No.10744, Lactococcus lactis subsp. lactis One of CGMCC No.10745 and lactobacillus plantarum CGMCC No.10747 or a variety of are adjunct culture, the main fermentation The viable count ratio of agent and the adjunct culture is greater than 1.
4. cheese leavening as claimed in claim 3, which is characterized in that the main fermentation agent and the adjunct culture Viable count ratio is 1:1~10:1.
5. cheese leavening as claimed in claim 3, which is characterized in that the Lactococcus lactis subsp. lactis CGMCC No.10746, Lactococcus lactis subsp. lactis CGMCC No.10744, Lactococcus lactis subsp. lactis CGMCC No.10745 and Lactobacillus plantarum CGMCC No.10747 viable count ratio is 20:1:2:2 or 5:2:1:2.
6. such as cheese leavening according to any one of claims 1 to 5, which is characterized in that the cheese starter is also Including auxiliary material.
7. a kind of preparation method of cheese leavening, which is characterized in that it includes the following steps:
(1) Lactococcus lactis subsp. lactis CGMCC No.10746 is inoculated in culture medium, obtains culture.
8. preparation method as claimed in claim 7, which is characterized in that culture medium described in step (1) be MRS culture medium, M17 culture medium, degreasing milk medium or culture medium A, the culture medium A is by glucose 23g/L, soy peptone 11g/L, beef Cream 11g/L, tryptone 5g/L, sodium acetate 1.8g/L, K2HPO41.2g/L, sodium citrate 1.2g/L, MgSO4·7H2O 0.4g/L、MnSO4·5H2O 54mg/L, L-cysteine hydrochloride 0.5g/L and Tween 80 1g/L composition, pH7;The culture Temperature be 26~34 DEG C;And/or the time of the culture is 12~48 hours.
9. preparation method as claimed in claim 7, which is characterized in that it include thes steps that following:
(2) by Lactococcus lactis subsp. lactis CGMCC No.10744, Lactococcus lactis subsp. lactis CGMCC No.10745 and One of lactobacillus plantarum CGMCC No.10747 or a variety of be inoculated in culture medium are cultivated, and culture is obtained;
(3) the resulting culture of step (1) and the resulting culture of step (2) are mixed.
10. preparation method as claimed in claim 9, which is characterized in that by the resulting culture of the step (1) and step (2) resulting culture is according to Lactococcus lactis subsp. lactis CGMCC No.10746 and the Lactococcus lactis subsp. lactis CGMCC No.10744, Lactococcus lactis subsp. lactis CGMCC No.10745 and lactobacillus plantarum CGMCC No.10747 three One of or a variety of viable count ratios greater than 1 ratio mix.
11. preparation method as claimed in claim 10, which is characterized in that by the resulting culture of the step (1) and step (2) resulting culture is according to Lactococcus lactis subsp. lactis CGMCC No.10746, Lactococcus lactis subsp. lactis CGMCC No.10744, Lactococcus lactis subsp. lactis CGMCC No.10745 and lactobacillus plantarum CGMCC No.10747 viable bacteria The ratio that number is 20:1:2:2 or 5:2:1:2 mixes.
12. the preparation method as described in any one of claim 7~10, which is characterized in that it include thes steps that following: adding Enter auxiliary material, mixes.
13. a kind of cheese leavening as claimed in any one of claims 1 to 5 is preparing the application in cheese.
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