Disclosure of Invention
In order to solve the problems, the invention provides a compound proliferation agent capable of delaying the reduction of the viable count of lactobacillus plantarum fermented milk. The components of the compound proliferation agent comprise germinated brown rice powder, banana powder, hydrolyzed whey protein, oat extract, malt extract and fructo-oligosaccharide (the mass ratio of the germinated brown rice powder, the banana powder, the hydrolyzed whey protein, the oat extract, the malt extract and the fructo-oligosaccharide is 10-30: 5-15: 25-40: 20-80: 5-10); the compound proliferation agent is added into a milk-based system (the addition amount accounts for 5-10% of the total mass of the milk-based system), so that the technical problems that the lactobacillus plantarum grows slowly in the milk-based system and can not be curdled are solved, and the lactobacillus plantarum can rapidly produce acid and curdled in the milk-based system; the composite proliferation agent is used for fermenting the lactobacillus plantarum in a milk-based system, the fermentation end point (65-75 DEG T) can be reached only by 6-12 h, and at the moment, the viable count of the lactobacillus plantarum in the milk product obtained by fermentation can reach 1.2 multiplied by 109~1.6×109About CFU/g, the large-scale application of the lactobacillus plantarum in the fermented dairy product is greatly promoted; meanwhile, the inventor finds that the composite proliferation agent is used for fermenting the lactobacillus plantarum in a milk base system, so that the viable count of the lactobacillus plantarum in the fermented milk can be kept stable within 25 days of shelf life (after the 25 days of shelf life is finished, the viable count of the fermented milk is not less than 1.0 multiplied by 109CFU/g), which undoubtedly solves the problem that the viable count of fermented milk produced using solid malt extract decreases rapidly during shelf life.
The technical scheme of the invention is as follows:
the invention provides a compound proliferation agent capable of delaying reduction of viable count of lactobacillus plantarum fermented milk, which comprises components of germinated brown rice powder, banana powder, hydrolyzed whey protein, oat extract, malt extract and fructo-oligosaccharide.
The germinated brown rice powder is powder prepared by grinding germinated brown rice, which is a new individual through water absorption and swelling, germ germination, seed coat breaking and seed coat growing under the conditions of proper temperature, moisture and oxygen; the banana powder is a health-care food prepared by processing fresh bananas by an advanced technology, grinding the fresh bananas into powder, and carrying out pretreatment, mixing, inspection and packaging according to a certain proportion; the hydrolyzed whey protein is a product of concentrated whey protein or lactalbumin hydrolyzed by protease; the oat extract is a pure natural nutrient substance prepared by treating raw starch in oat by using a biological enzyme preparation (such as amylase and the like) and performing spray drying; the malt extract is a pure natural nutrient substance which is extracted from barley and/or malt by enzymolysis and is rich in maltose, fructose, amino acid, small molecular peptide, multiple vitamins, trace elements and multiple growth promoting factors.
In one embodiment of the present invention, the ratio of germinated brown rice powder, banana powder, hydrolyzed whey protein, oat extract, malt extract and fructo-oligosaccharide is (10 to 30): (10-30): (5-15): (25-40): (20-80): (5-10).
The invention provides a dairy product prepared by applying the compound proliferation agent capable of delaying the reduction of the number of viable lactobacillus plantarum fermented dairy bacteria.
In one embodiment of the invention, the dairy product comprises fermented milk.
The invention provides a preparation method of fermented milk rich in lactobacillus plantarum, which uses the compound proliferation agent capable of delaying the reduction of the viable count of the lactobacillus plantarum fermented milk.
In one embodiment of the present invention, the method comprises inoculating lactobacillus plantarum into raw milk to which the complex growth promoting agent for delaying the decrease in the viable count of lactobacillus plantarum fermented milk is added, and fermenting to obtain fermented milk.
In one embodiment of the invention, the raw milk is raw fresh milk and/or reconstituted milk.
The raw milk refers to raw milk extruded from the cow breast without any treatment; the reconstituted milk is prepared by concentrating and drying milk to obtain concentrated milk or milk powder, and adding appropriate amount of water to obtain emulsion with water and solid content ratio equivalent to that of original milk.
In one embodiment of the invention, the fat content in the raw milk is not less than 3.1% by weight of the total mass of the raw milk, the protein content is not less than 2.8% by weight of the total mass of the raw milk, and the solid content of nonfat milk is not less than 8.1% by weight of the total mass of the raw milk.
In one embodiment of the present invention, the lactobacillus plantarum is added in the raw milk in an amount of not less than 1.0 × 107~5.0×107CFU/mL。
In one embodiment of the invention, the lactobacillus plantarum comprises one or more of lactobacillus plantarum CGMCC No.8246, lactobacillus plantarum CGMCC No.8242, lactobacillus plantarum CGMCC No.8243, lactobacillus plantarum CGMCC No.6077, lactobacillus plantarum CGMCC No.5495, lactobacillus plantarum CGMCC No.5494, lactobacillus plantarum CGMCC No.5492, lactobacillus plantarum CGMCC No.4286, lactobacillus plantarum CCTCC No. m206032 or lactobacillus plantarum CCTCC No. m 206033.
In one embodiment of the invention, the amount of the composite proliferation agent added to the raw milk accounts for 5-10% of the total mass of the raw milk.
In one embodiment of the invention, lactobacillus plantarum is inoculated in raw milk added with the compound proliferation agent capable of delaying the reduction of the viable count of lactobacillus plantarum fermented milk, the thickening agent, the emulsifying agent, the sweet substance and the edible essence for fermentation to obtain fermented milk; the sweet substance refers to food material or food additive for imparting sweet taste to food.
In one embodiment of the invention, the addition amount of the thickener in the raw milk accounts for 0.5-1.5% of the total mass of the raw milk.
In one embodiment of the invention, the component of the thickener comprises one or more of pectin, carrageenan, xanthan gum, locust bean gum, agar, carboxymethyl cellulose, sodium alginate, Propylene Glycol Alginate (PGA), natural starch or modified starch.
In one embodiment of the invention, the ingredients of the thickener comprise pectin, agar, native starch and destructured starch.
In one embodiment of the invention, the pectin is a low ester pectin.
In one embodiment of the invention, the destructured starch comprises physically destructured starch as well as chemically destructured starch.
In one embodiment of the invention, the emulsifier is added in the raw milk in an amount of 0.05 to 0.15% by mass based on the total mass of the raw milk.
In one embodiment of the present invention, the ingredient of the emulsifier comprises a monoglyceride and/or diglyceride fatty acid ester.
In one embodiment of the present invention, the sweet substance is added to the raw milk in an amount of 0.0005 to 7.0% by mass based on the total mass of the raw milk.
In one embodiment of the invention, the ingredient of the sweetening substance comprises sugar and/or a sweetener.
In one embodiment of the invention, the sugar component comprises sucrose and/or beet sugar.
In one embodiment of the invention, the sugar is added to the raw milk in an amount of 3-7% by mass based on the total mass of the raw milk.
In one embodiment of the present invention, the sweetener is added to the raw milk in an amount of 0.0005 to 0.02% by mass based on the total mass of the raw milk.
In one embodiment of the invention, the sugar component comprises one or more of white sugar, soft white sugar, yellow granulated sugar, brown granulated sugar, polycrystalline rock sugar, single crystal rock sugar, cubic sugar bornyl sugar, high fructose syrup, honey or fructose.
In one embodiment of the invention, the ingredient of the sweetener comprises one or more of aspartame, acesulfame k, sucralose, or neotame.
In one embodiment of the invention, the addition amount of the edible essence in the raw milk accounts for 0.05-0.15% of the total mass of the raw milk.
In one embodiment of the invention, the method comprises the steps of mixing raw milk, a compound proliferation agent, a thickening agent, an emulsifier, a sweet substance, flavoring essence and water, and then stirring for the first time to obtain a feed liquid; homogenizing, sterilizing and cooling the obtained feed liquid to obtain treated feed liquid; inoculating lactobacillus plantarum in the treated feed liquid, and then stirring for the second time to obtain a fermentation raw material; and fermenting the fermentation raw material to obtain the fermented milk.
In one embodiment of the invention, the first stirring time is 15-30 min, the speed is 200-300 r/min, and the temperature is 40-55 ℃.
In one embodiment of the present invention, the homogenization is performed in two stages, the temperature of the first stage of homogenization is 60 to 70 ℃, and the pressure is 15 to 18MPa, and the temperature of the second stage of homogenization is 60 to 70 ℃, and the pressure is 2 to 5 MPa.
In one embodiment of the present invention, the sterilization temperature is 85-95 ℃ and the sterilization time is 5-10 min.
In one embodiment of the present invention, the cooling is performed to 30 to 37 ℃.
In one embodiment of the present invention, the time of the second stirring is 5 to 10min, and the speed is 100 to 200 r/min.
In one embodiment of the invention, the fermentation temperature is 30-37 ℃, the fermentation time is 6-10 h, and the end point is acidity up to 65-75 DEG T.
In one embodiment of the invention, the method comprises the steps of mixing raw milk, a compound proliferation agent, a thickening agent, an emulsifier, a sweet substance, flavoring essence and water, and then stirring for the first time to obtain a feed liquid; homogenizing, sterilizing and cooling the obtained feed liquid to obtain treated feed liquid; inoculating lactobacillus plantarum in the treated feed liquid, and then stirring for the second time to obtain a fermentation raw material; fermenting the fermentation raw material to obtain fermented milk; and demulsifying the obtained fermented milk, and turning over the cylinder to obtain the treated fermented milk.
The demulsification is a process of converting the yogurt from a solidification state into a viscous liquid state by a mechanical stirring mode after the fermentation of the stirred yogurt is finished.
The cylinder turning is a process of conveying the stirred yoghurt from the fermentation tank to the tank to be filled through the volumetric pump after the fermentation is finished and the emulsion breaking is finished.
In one embodiment of the invention, the tilt cylinder is a back pressure tilt cylinder.
The back pressure cylinder turnover is a process of making the texture of the yoghourt more uniform and finer by carrying out certain back pressure treatment on the yoghourt in the cylinder turnover conveying process.
In one embodiment of the invention, the pressure of the back pressure turnover cylinder is 0.3-0.5 MPa.
In one embodiment of the invention, the pressure of the back pressure tilt cylinder is 0.4 MPa.
In one embodiment of the invention, the method comprises the steps of mixing raw milk, a compound proliferation agent, a thickening agent, an emulsifier, a sweet substance, flavoring essence and water, and then stirring for the first time to obtain a feed liquid; homogenizing, sterilizing and cooling the obtained feed liquid to obtain treated feed liquid; inoculating lactobacillus plantarum in the treated feed liquid, and then stirring for the second time to obtain a fermentation raw material; fermenting the fermentation raw material to obtain fermented milk; demulsifying the obtained fermented milk, and turning over the cylinder to obtain the treated fermented milk; and cooling, filling and after-ripening the treated fermented milk again to obtain a fermented milk finished product.
In one embodiment of the invention, the finished fermented milk product needs to be stored at 2-6 ℃.
The invention provides fermented milk prepared by the preparation method of the fermented milk rich in lactobacillus plantarum.
The invention provides a product containing the dairy product or the fermented milk.
Has the advantages that:
(1) the components of the composite proliferation agent comprise germinated brown rice powder, banana powder, hydrolyzed whey protein, oat extract, malt extract and fructo-oligosaccharide (the mass ratio of the germinated brown rice powder to the banana powder to the hydrolyzed whey protein to the oat extract to the malt extract to the fructo-oligosaccharide is 10-30: 5-15: 25-40: 20-80: 5-10), and the composite proliferation agent is added into a milk-based system (the addition amount accounts for 5-10% of the total mass of the milk-based system), so that the technical problems that lactobacillus plantarum grows slowly and cannot be subjected to milk coagulation in the milk-based system can be solved, and the lactobacillus plantarum can rapidly produce acid and milk coagulation in the milk-based system;
(2) the composite proliferation agent is used for fermenting the lactobacillus plantarum in a milk-based system, the fermentation end point (65-75 DEG T) can be reached only by 6-12 hours, and the viable count of the lactobacillus plantarum in the dairy product obtained by fermentation can reach 1.2 multiplied by 109~1.6×109About CFU/g, the large-scale application of the lactobacillus plantarum in the fermented dairy product is greatly promoted;
(3) the composite proliferation agent is used for fermenting the lactobacillus plantarum in a milk base system, so that the viable count of the lactobacillus plantarum in the fermented milk can be kept stable within 25 days of shelf life (the viable count in the fermented milk is not less than 1.0 multiplied by 10 after the 25 days of shelf life is finished)9CFU/g), which undoubtedly solves the problem that the viable count of the fermented milk produced by using the solid malt extract is reduced rapidly in the shelf life;
(4) the compound proliferation agent is used for fermenting the lactobacillus plantarum in a milk-based system, so that the problem of poor flavor (beany flavor or bitter taste) of a product generated when yeast powder, soybean protein, soybean peptone or hydrolyzed soybean protein is used for fermenting the lactobacillus plantarum in the milk-based system can be avoided, and the large-scale application of the lactobacillus plantarum in a fermented milk product is greatly promoted.
Detailed Description
The present invention will be further illustrated below with reference to specific examples and comparative examples.
The lactobacillus plantarum used in the following examples was obtained from the food biotechnology center of south Jiangnan university; germinated brown rice powder is purchased from Yiwan biotechnology limited company in Zhejiang; banana powder was purchased from south beijing previ biotechnology limited; hydrolyzed whey protein was purchased from Shanghai Fuxin industries, Inc.; oat extract was obtained from xiamen glanbell biotechnology limited; malt extract was purchased from shanghai english united food and beverage limited; fructooligosaccharides were purchased from Shanghai Fuxin industries, Inc.
The detection methods referred to in the following examples are as follows:
the detection method of viable count comprises the following steps: the national standard GB 4789.35-2016 food safety national standard food microbiology detection of lactobacillus is adopted.
And (3) an acidity detection method: the national standard GB 431334-.
Sensory evaluation: fermented milk samples were taken and placed in tasting cups for sensory evaluation in a 500 population.
Sensory evaluation criteria: the sensory score is 1-5 points;
wherein, if the color of the fermented milk is milky white or yellowish, the fermented milk has the special texture of the fermented milk, the texture is compact, compact and uniform, the fermented milk has pleasant frankincense flavor and grain fragrance, and the flavor is coordinated, and the taste is sour and sweet, so the score is 5;
if the color of the fermented milk is milky white or yellowish, the fermented milk has the special texture of the fermented milk, the texture is compact, compact and uniform, the fermented milk has good milk fragrance and grain fragrance, the flavor is coordinated, and the taste is sour and sweet, which means 4 points;
if the color of the fermented milk is milky white or yellowish, the fermented milk has the special texture of the fermented milk, the texture is compact, compact and uniform, the fermented milk has better milk fragrance and grain fragrance, the flavor is more harmonious, and the taste is sour and sweet, so 3 minutes;
if the color of the fermented milk is milky white or yellowish, the fermented milk has the special texture of the fermented milk, loose and uniform texture, certain milk fragrance and grain fragrance, and certain bitterness and peculiar smell, the score is 2;
if the fermented milk is milky white or yellowish in color, does not have the texture peculiar to fermented milk, does not cause curd, does not have milk flavor and grain aroma, and has bitterness and foreign flavor, it can be said to be 1 point.
Example 1:
the method comprises the following specific steps:
(1) raw materials were taken as per table 1;
(2) premixing a sweet substance, a thickening agent, an emulsifier and a composite proliferation agent according to the proportion in a table 1, dissolving the obtained premix in raw milk at 40 ℃, slowly adding edible essence, stirring for 30min, and uniformly mixing to obtain a feed liquid A;
(3) homogenizing the material liquid A at a first-stage homogenizing pressure of 15MPa and a second-stage homogenizing pressure of 5MPa at a homogenizing temperature of 60 deg.C, sterilizing at 85 deg.C for 10min, and cooling to 30 deg.C to obtain material liquid B;
(4) inoculating Lactobacillus plantarum CGMCC No.5494 with an inoculum size of 2.5 × 10 in the feed liquid B7CFU/mL, the inoculation temperature is 30 ℃, after stirring and mixing for 5min at 200r/min, fermentation is carried out at 30 ℃ until the end-point acidity is 65-75 DEG T, and the fermentation time is 7-8 h, so as to obtain feed liquid C;
(5) in the fermentation process, 25g of the feed liquid C is sampled from the feed liquid C for viable bacteria counting and acidity measurement after 0h, 2h, 4h, 6h and 8h of fermentation respectively (the detection results are shown in Table 2).
(6) Back-pressing and turning over the feed liquid C to 0.3MPa, cooling to 20 ℃, filling at 20 ℃, and after-ripening the prepared fermented milk at 10 ℃ for 10 hours to obtain a fermented milk finished product;
(7) the fermented milk product is preserved at 4 ℃ for 25 days, and 25g of the fermented milk product is sampled respectively on days 1, 4, 12, 19 and 25 during the preservation process for viable bacteria counting and acidity determination (the detection results are shown in Table 2);
(8) a part of the fermented milk product was taken on day 25 of storage for sensory evaluation (see table 3 for evaluation results).
According to the table 2, the compound proliferation agent can enable fermented milk to reach the fermentation end point within 8h, the pH value and the titrated acidity are respectively 4.26 and 70 DEG T, and the viable count is kept at a high level (1.49 multiplied by 10)9CFU/g); after being preserved for 25 days, the viable count still keeps high level (1.31 multiplied by 10)9CFU/g),No significant drop occurred.
According to the table 3, the flavor and the mouthfeel of the product are both good, and 500 people feel that the evaluation result is averagely divided into 46 points, reach the favorite level and are close to the favorite level.
TABLE 1 raw material formulation
TABLE 2 Lactobacillus plantarum CGMCC No.5494 viable count and acidity change during fermentation and preservation
Time
|
pH
|
Acidity (° T) is titrated
|
Viable count (. times.10)7CFU/g)
|
0h
|
6.27
|
21
|
2.58
|
2h
|
6.15
|
23
|
3.23
|
4h
|
5.60
|
32
|
11.9
|
6h
|
4.83
|
49
|
95
|
8h
|
4.25
|
69
|
147
|
1d
|
4.26
|
70
|
149
|
4d
|
4.10
|
90
|
142
|
12d
|
3.89
|
102
|
162
|
19d
|
3.93
|
106
|
145
|
25d
|
4.00
|
102
|
131 |
Example 2:
the method comprises the following specific steps:
(1) raw materials were taken as per table 4;
(2) premixing the sweet substance, the thickening agent, the emulsifying agent and the composite proliferation agent according to the proportion in the table 4, dissolving the obtained premix in raw milk at 55 ℃, slowly adding the premix and edible essence, stirring for 15min, and uniformly mixing to obtain feed liquid A;
(3) homogenizing the material liquid A at a first-stage homogenizing pressure of 18MPa and a second-stage homogenizing pressure of 2MPa at a homogenizing temperature of 70 deg.C, sterilizing at 95 deg.C for 5min, and cooling to 37 deg.C to obtain material liquid B;
(4) inoculating Lactobacillus plantarum CGMCC No.6077 with an inoculum size of 1.0 × 10 in the feed liquid B7CFU/mL, the inoculation temperature is 37 ℃, the mixture is stirred and mixed for 10min at 100r/min, and then the mixture is fermented at 37 ℃ until the final acidity is 65-75 DEG T, the fermentation time is 10h, and feed liquid C is obtained;
(5) in the fermentation process, 25g of the feed liquid C is sampled from the feed liquid C for viable bacteria counting and acidity measurement after 0h, 2h, 4h, 6h and 8h of fermentation respectively (the detection results are shown in Table 5).
(6) Back-pressing and turning over the feed liquid C to 0.5MPa, cooling to 25 ℃, filling at 25 ℃, and after-ripening the prepared fermented milk for 15h at 2 ℃ to obtain a fermented milk finished product;
(7) the fermented milk product is preserved at 4 ℃ for 25 days, and 25g of the fermented milk product is sampled respectively on days 1, 4, 12, 19 and 25 during the preservation process for viable bacteria counting and acidity determination (the detection results are shown in Table 5);
(8) a part of the fermented milk product was taken on day 25 of storage for sensory evaluation (see table 3 for evaluation results).
According to the table 5, the compound proliferation agent can enable fermented milk to reach the fermentation end point within 8h, the pH value and the titrated acidity are respectively 4.34 and 75 DEG T, and the viable count is kept at a high level (1.60 multiplied by 10)9CFU/g); after being preserved for 25 days, the viable count still keeps high level (1.31 multiplied by 10)9CFU/g) no significant drop occurred.
According to the table 3, the flavor and the mouthfeel of the product are good, 500 people feel that the evaluation result is averagely divided into 48 points, the favorable level is reached, and the preference is close to the extreme preference.
TABLE 4 raw material formulation
TABLE 5 Lactobacillus plantarum CGMCC No.6077 viable count and acidity change during fermentation and preservation
Time
|
pH
|
Acidity (° T) is titrated
|
Viable count (. times.10)7CFU/g)
|
0h
|
6.37
|
16
|
0.8
|
2h
|
6.06
|
26
|
1.36
|
4h
|
5.56
|
33
|
85
|
6h
|
4.84
|
56
|
105
|
8h
|
4.34
|
75
|
160
|
1d
|
4.32
|
76
|
161
|
4d
|
3.98
|
95
|
183
|
12d
|
3.80
|
112
|
199
|
19d
|
3.76
|
116
|
125
|
25d
|
4.0
|
110
|
120 |
Example 3:
the method comprises the following specific steps:
(1) raw materials were taken as per table 6;
(2) premixing the sweet substance, the thickening agent, the emulsifying agent and the composite proliferation agent according to the proportion in the table 6, dissolving the obtained premix in raw milk at 55 ℃, slowly adding the premix and edible essence, stirring for 15min, and uniformly mixing to obtain feed liquid A;
(3) homogenizing the material liquid A at a first-stage homogenizing pressure of 18MPa and a second-stage homogenizing pressure of 2MPa at a homogenizing temperature of 70 deg.C, sterilizing at 95 deg.C for 5min, and cooling to 35 deg.C to obtain material liquid B;
(4) inoculating Lactobacillus plantarum CGMCC No.5492 with the inoculum size of 4.0 × 10 in the feed liquid B7CFU/mL, the inoculation temperature is 35 ℃, the mixture is stirred and mixed for 10min at 100r/min, and then the mixture is fermented at 35 ℃ until the final acidity is 65-75 DEG T, the fermentation time is 8h, and feed liquid C is obtained;
(5) in the fermentation process, 25g of the feed liquid C is sampled for viable count and acidity determination in 0h, 2h, 4h, 6h, 8h, 10h and 12h of fermentation respectively (the detection results are shown in Table 7).
(6) Back-pressing and turning over the feed liquid C to 0.4MPa, cooling to 20 ℃, filling at 20 ℃, and after-ripening the prepared fermented milk at 4 ℃ for 15h to obtain a fermented milk finished product;
(7) the fermented milk product is preserved at 4 ℃ for 25 days, and 25g of the fermented milk product is sampled at 1 st day, 4 th day, 12 th day, 19 th day and 25 th day for viable bacteria count and acidity determination during the preservation process (the detection results are shown in Table 7);
(8) a part of the fermented milk product was taken on day 25 of storage for sensory evaluation (see table 3 for evaluation results).
According to the table 7, the compound proliferation agent can enable fermented milk to reach the fermentation end point within 12h, the pH value and the titrated acidity are respectively 4.43 and 65 DEG T, and the viable count is kept at a high level (1.22 multiplied by 10)9CFU/g); after being preserved for 25 days, the viable count still keeps high level (1.05X 10)9CFU/g) no significant drop occurred.
According to the table 3, the flavor and the mouthfeel of the product are good, and 500 people feel that the evaluation result is averagely divided into 45 points, so that the favorite level is reached and the favorite level is close to the favorite level.
TABLE 6 raw material formulation
TABLE 7 Lactobacillus plantarum CGMCC No.5492 viable count and acidity change during fermentation and preservation
Time
|
pH
|
Acidity (° T) is titrated
|
Viable count (. times.10)7CFU/g)
|
0h
|
6.31
|
17
|
3.9
|
2h
|
6.05
|
23
|
4.5
|
4h
|
5.45
|
31
|
33
|
6h
|
5.09
|
40
|
54
|
8h
|
4.96
|
46
|
66
|
10h
|
4.86
|
56
|
82
|
12h
|
4.43
|
64
|
122
|
1d
|
4.43
|
65
|
120
|
4d
|
4.01
|
89
|
140
|
12d
|
3.91
|
100
|
139
|
16d
|
3.86
|
104
|
121
|
20d
|
3.81
|
107
|
115
|
25d
|
3.91
|
103
|
105 |
Example 4:
the method comprises the following specific steps:
(1) raw materials were taken as per table 8;
(2) premixing the sweet substance, the thickening agent, the emulsifying agent and the composite proliferation agent according to the proportion in the table 8, dissolving the obtained premix in raw milk at 55 ℃, slowly adding the premix and edible essence, stirring for 15min, and uniformly mixing to obtain feed liquid A;
(3) homogenizing the material liquid A at a first-stage homogenizing pressure of 18MPa and a second-stage homogenizing pressure of 2MPa at a homogenizing temperature of 70 deg.C, sterilizing at 95 deg.C for 5min, and cooling to 35 deg.C to obtain material liquid B;
(4) inoculating Lactobacillus plantarum CGMCC No.5494 with an inoculum size of 2.5 × 10 in the feed liquid B7CFU/mL, the inoculation temperature is 35 ℃, the mixture is stirred and mixed for 10min at 100r/min, and then the mixture is fermented at 35 ℃ until the final acidity is 65-75 DEG T, and the fermentation time is 6-7 h, so that feed liquid C is obtained;
(5) in the fermentation process, 25g of the feed liquid C is sampled from the feed liquid C for viable bacteria counting and acidity measurement after 0h, 2h, 4h, 6h and 8h of fermentation respectively (the detection results are shown in Table 9).
(6) Back-pressing and turning over the feed liquid C to 0.4MPa, cooling to 20 ℃, filling at 20 ℃, and after-ripening the prepared fermented milk at 4 ℃ for 15h to obtain a fermented milk finished product;
(7) the fermented milk product is preserved at 4 ℃ for 25 days, and 25g of the fermented milk product is sampled respectively on days 1, 4, 12, 19 and 25 during the preservation process for viable count and acidity determination (the detection results are shown in Table 9);
(8) a part of the fermented milk product was taken on day 25 of storage for sensory evaluation (see table 3 for evaluation results).
According to the table 9, the compound proliferation agent can enable the fermented milk to exceed the fermentation end point after 8h, and the pH value and the titrated acidity of the fermented milk are respectively higher4.40 and 66 DEG T, the viable count remains high (1.43X 10)9CFU/g); after being preserved for 25 days, the viable count still keeps high level (1.09X 10)9CFU/g) no significant drop occurred.
According to the table 3, the flavor and the mouthfeel of the product are both good, 500 people feel that the evaluation result is averagely divided into 47 points, the favorite level is reached, and the taste is close to a very favorite level.
TABLE 8 raw material formulation
TABLE 9 Lactobacillus plantarum CGMCC No.5494 viable count and acidity change during fermentation and preservation
Time
|
pH
|
Acidity (° T) is titrated
|
Viable count (. times.10)7CFU/g)
|
0h
|
6.36
|
18
|
2.5
|
2h
|
6.26
|
19
|
3.7
|
4h
|
5.60
|
35
|
46
|
6h
|
4.96
|
46
|
85
|
8h
|
4.40
|
66
|
145
|
1d
|
4.40
|
67
|
143
|
4d
|
4.05
|
85
|
161
|
12d
|
3.90
|
110
|
145
|
16d
|
3.85
|
112
|
132
|
20d
|
3.80
|
115
|
115
|
25d
|
3.85
|
111
|
109 |
Comparative example 1:
the method comprises the following specific steps:
(1) raw materials were taken as per table 10;
(2) premixing the sweet substance, the thickening agent, the emulsifying agent and the composite proliferation agent according to the proportion in the table 10, dissolving the obtained premix in raw milk at 55 ℃, slowly adding the premix and edible essence, stirring for 15min, and uniformly mixing to obtain feed liquid A;
(3) homogenizing the material liquid A, wherein the primary homogenizing pressure is 18MPa, the secondary homogenizing pressure is 2MPa, the homogenizing temperature is 70 deg.C, sterilizing at 85 deg.C for 10min, and cooling to 35 deg.C to obtain material liquid B;
(4) inoculating Lactobacillus plantarum CGMCC No.5494 with an inoculum size of 2.5 × 10 in the feed liquid B7CFU/mL, the inoculation temperature is 35 ℃, the mixture is stirred and mixed for 10min at 100r/min, and then the mixture is fermented at 35 ℃ until the final acidity is 65-75 DEG T, and the fermentation time is 8-12 h, so that feed liquid C is obtained;
(5) in the fermentation process, 25g of the feed liquid C is sampled from the feed liquid C for viable count and acidity measurement after 0h, 4h, 8h, 12h and 24h of fermentation respectively (the detection results are shown in Table 11).
(6) Back-pressing and turning over the feed liquid C to 0.4MPa, cooling to 20 ℃, filling at 20 ℃, and after-ripening the prepared fermented milk at 4 ℃ for 15h to obtain a fermented milk finished product;
(7) part of the fermented milk product was subjected to sensory evaluation (see table 3 for evaluation results).
According to the table 11, the compound proliferation agent can ensure that the pH and the titration acidity of the product are respectively 4.25 and 80 DEG T at 12h, and the viable count is kept at a high level (9.3 multiplied by 10)8CFU/g), the time required for reaching the fermentation end point (65-75 DEG T) is 8-12 h; compared with comparative example 2, the lactobacillus plantarum acid production is promoted faster, the proliferation effect is obvious, the viable bacteria are high, but the effect is obviously not as good as the real oneExamples 1 to 4.
According to table 3, the product had very poor flavor and mouthfeel, had a pronounced beany flavor and bitterness, and 500 people were rated on average 17 points on a sensory scale, on a very dislike and dislike scale.
TABLE 10 raw material formulation
TABLE 11 Lactobacillus plantarum CGMCC No.5494 viable count and acidity change during fermentation and preservation
Time
|
pH
|
Acidity (° T) is titrated
|
Viable count (. times.10)7CFU/g)
|
0h
|
6.45
|
29
|
2.5
|
4h
|
5.35
|
42
|
42
|
8h
|
4.65
|
60
|
78
|
12h
|
4.25
|
85
|
93
|
24h
|
3.98
|
105
|
121
|
1d
|
3.97
|
106
|
120
|
7d
|
3.90
|
108
|
12
|
10d
|
3.89
|
108
|
6.7
|
14d
|
3.86
|
112
|
1.2 |
Comparative example 2:
the method comprises the following specific steps:
(1) raw materials were taken as per table 14;
(2) according to the proportion in the table 14, firstly premixing the sweet substance, the thickening agent, the emulsifying agent and the composite proliferation agent, dissolving the obtained premix in raw milk at 55 ℃, slowly adding the premix and the edible essence, stirring for 15min, and uniformly mixing to obtain feed liquid A;
(3) homogenizing the material liquid A, wherein the primary homogenizing pressure is 18MPa, the secondary homogenizing pressure is 2MPa, the homogenizing temperature is 70 deg.C, sterilizing at 85 deg.C for 10min, and cooling to 35 deg.C to obtain material liquid B;
(4) inoculating Lactobacillus plantarum CGMCC No.5494 with an inoculum size of 2.5 × 10 in the feed liquid B7CFU/mL, the inoculation temperature is 35 ℃, the mixture is stirred and mixed for 10min at 100r/min, and then the mixture is fermented at 35 ℃ until the final acidity is 65-75 DEG T, the fermentation time is 10h, and feed liquid C is obtained;
(5) in the fermentation process, 25g of the feed liquid C is sampled from the feed liquid C for viable bacteria counting and acidity measurement after fermentation for 0h, 2h, 4h, 6h, 8h and 10h respectively (the detection results are shown in Table 13).
(6) Back-pressing and turning over the feed liquid C to 0.4MPa, cooling to 20 ℃, filling at 20 ℃, and after-ripening the prepared fermented milk at 4 ℃ for 15h to obtain a fermented milk finished product;
(7) the fermented milk product was preserved at 4 ℃ for 25 days, and 25g of the fermented milk product was sampled for viable cell count and acidity determination on days 1, 4, 8, 12, 16, 20 and 25 during the preservation process (see table 15 for the test results);
(8) a part of the fermented milk product was taken on day 25 of storage for sensory evaluation (see table 3 for evaluation results).
According to the table 15, the compound proliferation agent can enable fermented milk to reach the fermentation end point within 10h, the pH value and the titrated acidity are respectively 4.37 and 74 DEG T, and the viable count is kept at a high level (1.08 multiplied by 10)9CFU/g); the compound proliferation agent can ensure that the acidity of the fermented milk is not obviously increased within 25 days of shelf life, but the viable count is obviously reduced.
According to the table 3, the flavor and the mouthfeel of the product are good, 500 people feel that the evaluation result is averagely divided into 48 points, the favorable level is reached, and the preference is close to the extreme preference.
TABLE 14 raw material formulation
Components
|
Amount (mass%/%)
|
White granulated sugar
|
7.0
|
Solid malt extract
|
7.5
|
Plant lactobacillus CGMCC No.6077 bacterial powder
|
0.00625
|
Thickening agent
|
1.5
|
Emulsifier
|
0.15
|
Edible essence
|
0.15
|
Raw milk
|
Supplement to 100 |
TABLE 15 Lactobacillus plantarum CGMCC No.5494 viable count and acidity change during fermentation and preservation
Time
|
pH
|
Acidity (° T) is titrated
|
Viable count (. times.10)7CFU/g)
|
0h
|
6.19
|
26
|
2.5
|
2h
|
6.12
|
26
|
3.3
|
4h
|
5.73
|
32
|
8
|
6h
|
5.26
|
44
|
32
|
8h
|
4.66
|
64
|
74
|
10h
|
4.37
|
74
|
108
|
1d
|
4.45
|
72
|
99
|
4d
|
4.26
|
83
|
51
|
8d
|
4.11
|
86
|
36
|
12d
|
4.07
|
88
|
31
|
16d
|
4.07
|
91
|
20
|
20d
|
4.08
|
90
|
12
|
25d
|
4.15
|
88
|
2.8 |
TABLE 3 sensory evaluation results
Numbering
|
Score of
|
Example 1
|
46
|
Example 2
|
48
|
Example 3
|
45
|
Example 4
|
47
|
Comparative example 1
|
17
|
Comparative example 2
|
48 |
Although the present invention has been described with reference to the preferred embodiments, it should be understood that various changes and modifications can be made therein by those skilled in the art without departing from the spirit and scope of the invention as defined in the appended claims.