Probiotic fermented fruit and vegetable pulp composition containing active bacteria and preparation method thereof

Abstract

The present invention belongs to the technical field of beverages, and relates to a probiotic fermented fruit and vegetable puree composition containing active bacteria and its preparation method. The composition containing active bacteria is obtained by fermenting fruit and vegetable puree with Lactobacillus casei NCU215. The probiotic fermented fruit and vegetable puree has the following characteristics: the probiotic fermented fruit and vegetable puree may generate a natural mellow sour, effectively remove an astringency in fruit and a wild Artemisia flavor in vegetable, and neutralize an unpleasant sour in the fruit; with probiotic fermentation, the present invention may improve a content of amino acid in the fruit and vegetable by 20% or more, generate multiple aromatic substances, improve a flavor substance by 30% or more, and effectively improve a taste and a mouthfeel of the product; the present invention prolongs a shelf life of the product and prevents rot.

Claims

1. A probiotic fermented mango puree, produced by a method comprising: mixing 85 mass parts of a mango puree and 15 mass parts of glucose to form a starting mixture; sterilizing the starting mixture to form a pre-fermentation mixture; adding freeze-dried powder of L. casei NCU215 to the pre-fermentation mixture at a final concentration of 10.sup.6 cfu/ml to form a fermentation mixture; fermenting the fermentation mixture at 37° C. until a pH value of 3.0 is reached; then terminating fermentation to produce the fermented mango puree; wherein the probiotic is Lactobacillus casei NCU215 has a preservation number of CGMCC No. 18702 and a 16SrRNA sequence of SEQ ID NO:1; and wherein the fermented mango puree, comprises: a threonine content of 1.32 mg/ml, a glycine content of 0.027 mg/ml, a lysine content of 0.086 mg/ml, a vitamin C content of 92.24 mg/100 g, a Beta-carotene content of 0.77 mg/100 g, a total carotenoid content of 1.15 mg/100 g, a polyphenol content of 97.96 mg GAE/100 g, and a total flavones content of 75.08 mg DW/100 g; and wherein the fermented mango puree has increased antioxidant substances compared to an unfermented mango puree.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 shows a mycelial morphology of the strain NCU215.

(2) FIG. 2 shows a phylogenetic tree.

DESCRIPTION OF THE EMBODIMENTS

(3) In order to make the objectives, technical solutions and advantages of the present invention clearer, the present invention will be further described below in detail in combination with specific embodiments. It should be understood that the specific embodiments described herein are intended to explain the present invention but not limit the present invention.

(4) 1. A strain NCU215 used by the present invention has excellent fermentability, and a fast acid production speed in fruit and vegetable raw materials, and makes fermentation time shortened obviously as compared with other Lactobacillus casei. Taking carrot puree as a fermentation raw material to inoculate the NCU215, and Lactobacillus casei ATCC393 as a fermentation control strain, it is turned out that the strain NCU215 has a fast pH decreasing speed and a strong acid production capacity as compared with the ATCC393 strain. The pH value of the carrot puree is decreased to 3.8 or less after 8 h of fermentation of the strain NCU215 and decreased to 3.03 after 24 h, and the acidity is 4.34‰. However, the pH value of the carrot puree is 4.23 after 8 h of fermentation of the comparative strain and 3.56 after 24 h, and the acidity is only 3.15‰.

(5) 2. With the fermentation of the Lactobacillus casei NCU215, the fresh and sweet fragrance in the fruit and vegetable puree can be increased, and the bitterness can be reduced. With fermented mango puree and pumpkin puree as examples, compared with Lactobacillus casei ATCC393, CICC 6117 and ATCC334, amino acids of a sweet flavor, a fresh flavor and an aromatic flavor in the mango puree and pumpkin puree fermented by the Lactobacillus casei NCU215 are significantly improved, whereas an amino acid of a bitter flavor is significantly reduced, with a result shown in table 1 and table 2.

(6) Mango puree fermentation method: a fresh and unrotten mango was selected as a raw material, cleaned, peeled, denucleated and pulped; and puree was stirred uniformly according to components and a proportion (85 parts of mango puree and 15 parts of glucose), and sterilized for 9 min at 102° C. Upon sterilization, a feed liquid was cooled to 37° C.; freeze-dried powder of Lactobacillus casei NCU215, ATCC393, CICC 6117 and ATCC334 was respectively inoculated to the sterilized and cooled mango puree according to a proportion of 10.sup.6 cfu/mL; and fermentation was performed at 37° C., a pH value of 3.0 being a fermentation endpoint.

(7) Pumpkin puree fermentation method: a fresh and unrotten pumpkin was selected as a raw material, precooked and pulped; and puree was stirred uniformly according to components and a proportion (82 parts of pumpkin puree and 18 parts of white granulated sugar), and sterilized for 12 min at 100° C. Upon sterilization, a feed liquid was cooled to 38° C.; freeze-dried powder of Lactobacillus casei NCU215, ATCC393, CICC 6117 and ATCC334 was respectively inoculated to the sterilized and cooled pumpkin puree according to a proportion of 10.sup.6 cfu/mL; and fermentation was performed at 37° C., a pH value of 3.9 being a fermentation endpoint.

(8) TABLE-US-00001 TABLE 1 Change of amino acid before and after fermentation of mango puree Content (mg/g) After After After After fermentation fermentation fermentation fermentation Type of Before of of of of amino acid Flavor fermentation NCU215 ATCC393 CICC6117 ATCC334 Threonine Fresh 0.38 1.32 0.69 0.75 0.87 Aspartic acid Fresh 0.14 0.16 0.12 0.14 0.11 Serine Sweet 0.10 0.09 0.06 0.07 0.09 Methionine Bitter 0.005 0.004 0.008 0.006 0.007 Glutamic acid Fresh 0.16 0.18 0.13 0.13 0.15 Glycine Sweet 0.01 0.027 0.008 0.015 0.012 Alanine Sweet 0.28 0.31 0.14 0.25 0.29 Cysteine Aromatic 0.012 0.016 0.015 0.013 0.012 Valine Bitter 0.03 0.01 0.03 0.02 0.02 Histidine Sweet 0.033 0.035 0.025 0.031 0.033 Lysine Fresh 0.01 0.086 0.021 0.035 0.026 Proline Sweet 0.035 0.035 0.033 0.029 0.031 Arginine Bitter 0.15 0.14 0.16 0.15 0.15 Isoleucine Bitter 0.012 0 0.015 0.011 0.009 Leucine Bitter 0.01 0 0.012 0.011 0.007 Tyrosine Aromatic 0.015 0.022 0.017 0.016 0.019 Phenylalanine Aromatic 0.02 0.03 0 0.03 0.02

(9) TABLE-US-00002 TABLE 2 Change of amino acid before and after fermentation of pumpkin puree Content (mg/g) After After NCU215 fermentation fermentation ATCC334 Type of Before After of of After amino acid Flavor fermentation fermentation ATCC393 CICC6117 fermentation Threonine Fresh 0.47 1.79 0.65 0.58 0.66 Aspartic acid Fresh 0.19 0.33 0.21 0.20 0.29 Serine Sweet 1.24 2.84 1.57 1.98 1.75 Glutamic acid Fresh 0.45 0.99 0.44 0.48 0.86 Glycine Sweet 0.02 0.04 0.02 0.03 0.02 Alanine Sweet 0.27 0.47 0.23 0.39 0.31 Valine Bitter 0.21 0.18 0.20 0.19 0.20 Methionine Bitter 0.007 0.003 0.008 0.006 0.007 Isoleucine Bitter 0.08 0.07 0.07 0.06 0.08 Leucine Bitter 0.09 0.05 0.07 0.08 0.07 Cysteine Aromatic 0.033 0.057 0.035 0.049 0.038 Tyrosine Aromatic 0.10 0.05 0.07 0.08 0.07 Phenylalanine Aromatic 0.02 0.13 0.12 0.09 0.08 Histidine Sweet 0.17 0.19 0.16 0.17 0.18 Lysine Fresh 0.07 0.14 0.09 0.08 0.10 Arginine Bitter 0.19 0.13 0.19 0.18 0.17

(10) 3. Because of the fermentation of the Lactobacillus casei NCU215, the antioxidant substance in the fruit and vegetable puree is increased, the antioxidant capacity is enhanced, and the influence on a vitamin is relatively small. With the foregoing mango puree as an example, in the mango puree fermented by the Lactobacillus casei NCU215, such important antioxidant substances as polyphenol and flavone are increased, and the antioxidant capacity is enhanced. In the mango puree fermented by the comparative strains ATCC393, CICC 6117 and ATCC334, such important antioxidant substances as polyphenol and flavone and the antioxidant capacity are not increased significantly. For the mango puree fermented by all strains, a total content of vitamin C, beta-carotene and carotenoid is reduced to some extent. Nevertheless, compared with the comparative strains of Lactobacillus casei ATCC393, CICC 6117 and ATCC334, the total content of vitamin C, beta-carotene and carotenoid in the mango puree fermented by the Lactobacillus casei NCU215 is reduced minimally, with a result shown in table 3 and table 4.

(11) TABLE-US-00003 TABLE 3 Content of antioxidant substance before and after fermentation of mango puree After After After After Before fermenta- fermenta- fermenta- fermenta- Antioxidant fermenta- tion of tion of tion of tion of substance tion NCU215 ATCC393 CICC6117 ATCC334 Vitamin 97.61 92.24 90.58 91.32 90.87 C(mg/100 g) Beta- 0.87 0.77 0.59 0.67 0.59 carotene (mg/100 g) Total content 1.53 1.15 0.89 1.03 0.99 of carotenoid (mg/100 g) Polyphenol 88.58 97.96 87.23 89.73 88.52 (mg GAE/ 100 g) Total 71.61 75.08 70.01 70.69 71.79 flavones (mg DW/ 100 g)

(12) TABLE-US-00004 TABLE 4 Change of antioxidant capacity of mango puree before and after fermentation Equivalent After After After After weight of fermentation fermentation fermentation fermentation Determination antioxidant Before of of of of method substance fermentation NCU215 ATCC393 CICC6117 ATCC334 FRAP FeSO.sub.4 (mM) 5.22 5.96 5.01 5.23 5.55 ABTS V.sub.E (mM) 4.25 4.21 4.17 4.18 4.06 DPPH free radical V.sub.C (mg/100 mL) 20.39 21.86 19.73 20.56 20.74 scavenging rate Hydroxyl free V.sub.C (mg/mL) 0.44 0.54 0.42 0.51 0.49 radical scavenging rate

(13) 4. Thanks to the fermentation of the Lactobacillus casei NCU215, the storage stability is very good. Upon the completion of fermentation same as the foregoing mango puree fermentation method, by performing ultra-high temperature instantaneous sterilization for 3 s at 132° C., and filling in a sterile manner, a content of relevant substance is determinated.

(14) TABLE-US-00005 TABLE 5 Change of quality during storage of fermented mango puree Content of Sugar organic Crude Storage acidity Soluble content acid protein Vitamin C time/d pH g/kg solid/% mg/g mg/g g/100 g mg/100 g 0 3.41 10.16 ± 0.04 17.9 ± 0.02 95.32 ± 0.15 25.46 ± 0.04 0.57 ± 0.00 83.46 ± 0.25 30 3.42 10.19 ± 0.17   18 ± 0.10 94.68 ± 0.40 24.48 ± 0.55 0.56 ± 0.01 81.58 ± 0.39 60 3.4 10.21 ± 0.12 18.1 ± 0.04 94.32 ± 0.19 25.06 ± 0.36 0.57 ± 0.01 79.78 ± 1.00 90 3.41 10.17 ± 0.02 17.9 ± 0.12 93.38 ± 0.05 24.59 ± 0.28 0.54 ± 0.02 74.33 ± 0.84 120 3.43 10.12 ± 0.03   18 ± 0.05 92.27 ± 0.10 24.01 ± 0.07 0.54 ± 0.03   70 ± 0.45 150 3.43 10.12 ± 0.12 17.8 ± 0.01 93.11 ± 0.02 23.81 ± 0.02 0.52 ± 0.02 66.45 ± 1.24 180 3.44 10.09 ± 0.13 17.8 ± 0.03 92.34 ± 0.50 23.21 ± 0.04 0.53 ± 0.04 62.59 ± 0.69

(15) As can be seen from the above table, the contents of sugar and organic acid in the mango puree product fermented by the probiotic NCU215 change a little. At the 6th month, the preserving rates of the sugar and the organic acid are still very high, and are respectively 96.8% and 91.2%. For the content of protein, the preserving rate at the end of storage is up to 93%. The content of vitamin C tends to decline overall; and at the 6th month, it is determinated that the content is reduced by 35% as compared with an initial stage. The vitamin C is oxidized and decomposed easily, but compared with a change trend of the VC of a common mango beverage during storage, the preserving rate for the VC of the fermented mango puree is high.

(16) 5. The fermented fruit and vegetable puree provided by the present invention has the following functions compared with a common fruit and vegetable puree product: (1) the puree enhances immunity of a human body and prevents enteritis and intestinal cancer; (2) the puree may regulate blood fat and reduce cholesterol; (3) it moistens and relaxes the bowels; and (4) the probiotic fermented fruit and vegetable puree containing viable bacteria has an important regulation effect to a microecological balance of an intestinal tract of the human body.

(17) 6. The 16SrRNA sequence of the strain NCU215 is as follows (sequence table SEQ ID NO. 1):

(18) TABLE-US-00006 CGGCAGTGCGGGTGCTATACATGCAAGTCGAACGAGTTCTCGTTGATGAT CGGTGCTTGCACCGAGATTCAACATGGAACGAGTGGCGGACGGGTGAGTA ACACGTGGGTAACCTGCCCTTAAGTGGGGGATAACATTTGGAAACAGATG CTAATACCGCATAGATCCAAGAACCGCATGGTTCTTGGCTGAAAGATGGC GTAAGCTATCGCTTTTGGATGGACCCGCGGCGTATTAGCTAGTTGGTGAG GTAATGGCTCACCAAGGCGATGATACGTAGCCGAACTGAGAGGTTGATCG GCCACATTGGGACTGAGACACGGCCCAAACTCCTACGGGAGGCAGCAGTA GGGAATCTTCCACAATGGACGCAAGTCTGATGGAGCAACGCCGCGTGAGT GAAGAAGGCTTTCGGGTCGTAAAACTCTGTTGTTGGAGAAGAATGGTCGG CAGAGTAACTGTTGCCGGCGTGACGGTATCCAACCAGAAAGCCACGGCTA ACTACGTGCCAGCAGCCGCGGTAATACGTAGGTGGCAAGCGTTATCCGGA TTTATTGGGCGTAAAGCGAGCGCAGGCGGTTTTTTAAGTCTGATGTGAAA GCCCTCGGCTTAACCGAGGAAGCGCATCGGAAACTGGGAAACTTGAGTGC AGAAGAGGACAGTGGAACTCCATGTGTAGCGGTGAAATGCGTAGATATAT GGAAGAACACCAGTGGCGAAGGCGGCTGTCTGGTCTGTAACTGACGCTGA GGCTCGAAAGCATGGGTAGCGAACAGGATTAGATACCCTGGTAGTCCATG CCGTAAACGATGAATGCTAGGTGTTGGAGGGTTTCCGCCCTTCAGTGCCG CAGCTAACGCATTAAGCATTCCGCCTGGGGAGTACGACCGCAAAGGTTGA AACTCAAAGGAATTGACGGGGGCCCGCACAAGCGGTGGAGCATGTGGGTT TAATTCGAAGCAACGCGAAGAACCCTTACCAGGTCTTGACATCTTTTGAT CACCTGAGAGATCAGTTTTCCCCTTTCGGGGCAAAATGACAGGTGGTGCA TGATGTCGTCAGCCTCGTGTCGTGAGATGGTGGGGTAGGTCCCGCACGAG CGCACCTATGAACTAGTGCAGCATTAGTTGGTCACTCTAGTAGACTGCAG TGACGACCGGAGGCAACGTTGGAATGAACGGTTCAATTCATCAG.

(19) 7. Determination Method

(20) (1) A flavor substance is detected as follows:

(21) A static headspace-gas chromatography-mass spectrometry is used, and the flavor substance is detected by using an Agilent triple series quadrupole gas chromatograph-mass spectrometer, with conditions for gas chromatography and mass spectrometry as follows:

(22) Chromatographic column: HP-5 quartz capillary column (30 m*0.25 mm, 1 μm);

(23) Heating process: an initial temperature is 50° C. and is kept for 3 min, then is heated to 120° C. at 2° C./min, and at last is heated to 250° C. at 20° C./min and kept for 5 min; and a carrier gas (He) has a flow velocity of 1.0 mL/min, a pressure of 7.6522 psi, a sample size of 1 μL and no flow diversion.

(24) An electron ionization ion source has electron energy of 70 eV, a mass scanning range of 35-450 m/z and 20 scans/s, and a temperature of 230° C.

(25) The “-” in the flavor substance table denotes that the substance is undetected in the sample.

(26) (2) An amino acid detection method is to determinate a type and content of amino acid in the sample by using an amino acid analyzer according to GB/T 5009.124-2003 Determination of Amino Acids in Foods.

(27) The present invention is further described below in combination with specific embodiments.

Embodiment 1: Probiotic Fermented Pear Puree

(28) For the probiotic fermented pear puree, a proportion of raw materials is as follows: 89.9 parts of pear puree, 10 parts of glucose and 0.1 parts of D-sodium isoascorbiate.

(29) A fresh and unrotten pear was selected as a raw material; sarcocarp was taken and pulped; and puree was stirred uniformly according to the above components and proportion, and sterilized for 2 min at 105° C. Upon sterilization, a feed liquid was cooled to 35° C., freeze-dried powder of Lactobacillus casei NCU215 was inoculated to the sterilized and cooled raw material according to a proportion of 10.sup.4 cfu/mL, and fermentation was performed for 72 h at 35° C., a pH value of 3.8 being a fermentation endpoint. Fermented pear puree was standardized in sweetness and sourness to obtain the probiotic fermented pear puree finished product. The standardized fermented pear puree was subjected to ultra-high temperature instantaneous sterilization for 3 s at 132° C., and filled in a sterile manner, a shelf life of the product at a room temperature being 18 months.

Embodiment 2: Probiotic Fermented Honey-Dew Melon Puree

(30) For the probiotic fermented honey-dew melon puree, a proportion of raw materials is as follows: 89.9 parts of honey-dew melon puree, 10 parts of malt syrup and 0.1 parts of D-sodium isoascorbiate.

(31) A fresh and unrotten honey-dew melon was selected as a raw material, cleaned, peeled, seeded and pulped; and puree was stirred uniformly according to the above components and proportion, and sterilized for 3 min at 100° C. Upon sterilization, a feed liquid was cooled to 40° C., inoculated with freeze-dried powder of Lactobacillus casei NCU215 according to a proportion of 10.sup.3 cfu/mL, and fermented for 90 h at 37° C., a pH value of 2.8 being a fermentation endpoint. Fermented honey-dew melon puree was standardized in sweetness and sourness to obtain the probiotic fermented honey-dew melon puree finished product. The standardized fermented honey-dew melon puree was put into a refrigerator at 0-4° C. for refrigeration, a shelf life of the product at 0-4° C. being 21 days.

Embodiment 3: Probiotic Fermented Peach Puree

(32) For the probiotic fermented peach puree, a proportion of raw materials is as follows: 89.9 parts of peach puree, 10 parts of erythritol and 0.1 parts of D-sodium isoascorbiate.

(33) A fresh and unrotten peach was selected as a raw material, cleaned, denucleated and pulped; and puree was stirred uniformly according to the above components and proportion, and sterilized for 8 min at 90° C. Upon sterilization, a feed liquid was cooled to 37° C., inoculated with freeze-dried powder of Lactobacillus casei NCU215 according to a proportion of 10.sup.6 cfu/mL, and fermented for 72 h at 37° C., a pH value of 3.1 being a fermentation endpoint. Fermented peach puree was standardized in sweetness and sourness to obtain the probiotic fermented peach puree finished product. The standardized fermented peach puree was subjected to ultra-high temperature instantaneous sterilization for 3 s at 132° C., and filled in a sterile manner, a shelf life of the product at a room temperature being 18 months.

Embodiment 4: Probiotic Fermented Bitter Gourd Puree

(34) For the probiotic fermented bitter gourd puree, a proportion of raw materials is as follows: 84.95 parts of bitter gourd puree, 5 parts of erythritol and 0.05 parts of D-sodium isoascorbiate.

(35) A fresh and unrotten bitter gourd was selected as a raw material, cleaned, seeded and pulped; and puree was stirred uniformly according to the above components and proportion, and sterilized for 2 s at 132° C. Upon sterilization, a feed liquid was cooled to 30° C., inoculated with freeze-dried powder of Lactobacillus casei NCU215 according to a proportion of 10.sup.4 cfu/mL, and fermented for 82 h at 32° C., a pH value of 3.0 being a fermentation endpoint. Fermented bitter gourd puree was standardized in sweetness and sourness to obtain the probiotic fermented bitter gourd puree finished product. The standardized fermented bitter gourd puree was put into a refrigerator at 0-4° C. for refrigeration, a shelf life of the product at 0-4° C. being 21 days.

Embodiment 5: Probiotic Fermented Celery Puree

(36) For the probiotic fermented celery puree, a proportion of raw materials is as follows: 80.95 parts of celery puree, 19 parts of erythritol and 0.05 parts of D-sodium isoascorbiate.

(37) A fresh and unrotten celery was selected as a raw material, cleaned and pulped; and puree was stirred uniformly according to the above components and proportion, and sterilized for 1 min at 112° C. Upon sterilization, a feed liquid was cooled to 42° C., inoculated with freeze-dried powder of Lactobacillus casei NCU215 according to a proportion of 10.sup.5 cfu/mL, and fermented for 54 h at 38° C., a pH value of 2.8 being a fermentation endpoint. Fermented celery puree was standardized in sweetness and sourness to obtain the probiotic fermented celery puree finished product. The standardized fermented celery puree was canned, sealed and sterilized for 30 min at 115° C., a shelf life of the product at a room temperature being 18 months.

Embodiment 6: Probiotic Fermented Blueberry Puree

(38) For the probiotic fermented blueberry puree, a proportion of raw materials is as follows: 82.1 parts of blueberry puree, 17.8 parts of glucose and 0.1 parts of D-sodium isoascorbiate.

(39) A fresh and unrotten blueberry was selected as a raw material, cleaned and pulped; and puree was stirred uniformly according to the above components and proportion, and sterilized for 10 min at 85° C. Upon sterilization, a feed liquid was cooled to 35° C., inoculated with freeze-dried powder of Lactobacillus casei NCU215 according to a proportion of 10.sup.9 cfu/mL, and fermented for 72 h at 35° C., a pH value of 2.5 being a fermentation endpoint. Fermented blueberry puree was standardized in sweetness and sourness to obtain the probiotic fermented blueberry puree finished product. The standardized fermented blueberry puree was put into a refrigerator at 0-4° C. for refrigeration, a shelf life of the product at 0-4° C. being 21 days.

Embodiment 7: Probiotic Fermented Tomato Puree

(40) For the probiotic fermented tomato puree, a proportion of raw materials is as follows: 85.3 parts of tomato puree, 14.6 parts of maltitol and 0.1 parts of D-sodium isoascorbiate.

(41) A fresh and unrotten tomato was selected as a raw material, cleaned and pulped; and after peel was filtered, puree was stirred uniformly according to the above components and proportion, and sterilized for 2 min at 105° C. Upon sterilization, a feed liquid was cooled to 37° C., inoculated with freeze-dried powder of Lactobacillus casei NCU215 according to a proportion of 10.sup.5 cfu/mL, and fermented for 72 h at 38° C., a pH value of 2.8 being a fermentation endpoint. Fermented tomato puree was standardized in sweetness and sourness to obtain the probiotic fermented tomato puree finished product. The standardized fermented tomato puree was subjected to ultra-high temperature instantaneous sterilization for 3 s at 132° C., and filled in a sterile manner, a shelf life of the product at a room temperature being 18 months.

Embodiment 8: Probiotic Fermented Ginger Puree

(42) For the probiotic fermented ginger puree, a proportion of raw materials is as follows: 84.07 parts of ginger puree, 15.9 parts of starch syrup and 0.03 parts of D-sodium isoascorbiate.

(43) A fresh and unrotten ginger was selected as a raw material, cleaned, peeled and pulped; and puree was stirred uniformly according to the above components and proportion, and sterilized for 10 min at 85° C. Upon sterilization, a feed liquid was cooled to 38° C., inoculated with freeze-dried powder of Lactobacillus casei NCU215 according to a proportion of 10.sup.7 cfu/mL, and fermented for 96 h at 32° C., a pH value of 2.7 being a fermentation endpoint. Fermented ginger puree was standardized in sweetness and sourness to obtain the probiotic fermented ginger puree finished product. The standardized fermented ginger puree was subjected to ultra-high temperature instantaneous sterilization for 3 s at 132° C., and filled in a sterile manner, a shelf life of the product at a room temperature being 18 months.

Embodiment 9: Probiotic Fermented Sweet Potato Puree

(44) For the probiotic fermented sweet potato puree, a proportion of raw materials is as follows: 85.09 parts of sweet potato puree, 14.9 parts of malt syrup and 0.01 parts of D-sodium isoascorbiate.

(45) A fresh and unrotten sweet potato was selected as a raw material, precooked, peeled and pulped; and puree was stirred uniformly according to the above components and proportion, and sterilized for 3 min at 101° C. Upon sterilization, a feed liquid was cooled to 40° C., inoculated with freeze-dried powder of Lactobacillus casei NCU215 according to a proportion of 10.sup.4 cfu/mL, and fermented for 50 h at 37° C., a pH value of 2.6 being a fermentation endpoint. Fermented sweet potato puree was standardized in sweetness and sourness to obtain the probiotic fermented sweet potato puree finished product. The standardized fermented sweet potato puree was canned, sealed and sterilized for 30 min at 115° C., a shelf life of the product at a room temperature being 18 months.

Embodiment 10: Probiotic Fermented Banana Puree

(46) For the probiotic fermented banana puree, a proportion of raw materials is as follows: 87.99 parts of banana puree, 12 parts of starch syrup and 0.01 parts of D-sodium isoascorbiate.

(47) A fresh and unrotten banana was selected as a raw material, peeled and pulped; and puree was stirred uniformly according to the above components and proportion, and sterilize for 10 min at 85° C. Upon sterilization, a feed liquid was cooled to 40° C., inoculated with freeze-dried powder of Lactobacillus casei NCU215 according to a proportion of 10.sup.7 cfu/mL, and fermented for 60 h at 34° C., a pH value of 3.0 being a fermentation endpoint. Fermented banana puree was standardized in sweetness and sourness to obtain the probiotic fermented banana puree finished product. The standardized fermented banana puree was canned, sealed and sterilized for 30 min at 115° C., a shelf life of the product at a room temperature being 18 months.

Embodiment 11: Probiotic Fermented Pineapple Puree

(48) For the probiotic fermented pineapple puree, a proportion of raw materials is as follows: 84.95 parts of pineapple puree, 5 parts of isomaltooligosaccharide and 0.05 parts of D-sodium isoascorbiate.

(49) A fresh and unrotten pineapple was selected as a raw material, peeled and pulped; and puree was stirred uniformly according to the above components and proportion, and sterilized for 2 s at 132° C. Upon sterilization, a feed liquid was cooled to 32° C., inoculated with freeze-dried powder of Lactobacillus casei NCU215 according to a proportion of 10.sup.5 cfu/mL, and fermented for 48 h at 32° C., a pH value of 2.8 being a fermentation endpoint. Fermented pineapple puree was standardized in sweetness and sourness to obtain the probiotic fermented pineapple puree finished product. The standardized fermented pineapple puree was put into a refrigerator at 0-4° C. for refrigeration, a shelf life of the product at 0-4° C. being 21 days.

Embodiment 12: Probiotic Fermented Wolfberry Puree

(50) For the probiotic fermented wolfberry puree, a proportion of raw materials is as follows: 81.97 parts of wolfberry puree, 18 parts of erythritol and 0.03 parts of D-sodium isoascorbiate.

(51) A fresh and unrotten wolfberry was selected as a raw material, cleaned and pulped; and puree was stirred uniformly according to the above components and proportion, and sterilized for 1 min at 112° C. Upon sterilization, a feed liquid was cooled to 37° C., inoculated with freeze-dried powder of Lactobacillus casei NCU215 according to a proportion of 10.sup.6 cfu/mL, and fermented for 46 h at 37° C., a pH value of 2.7 being a fermentation endpoint. Fermented wolfberry puree was standardized in sweetness and sourness to obtain the probiotic fermented wolfberry puree finished product. The standardized fermented wolfberry puree was canned, sealed and sterilized for 30 min at 115° C., a shelf life of the product at a room temperature being 18 months.

Embodiment 13 Standard on Evaluation of Shelf Life

(52) The shelf life of the present invention is determined by means of the following indicators:

(53) Change in sensory quality and number of bacteria during storage of unsterilized fermented fruit and vegetable puree at 0-4° C.

(54) TABLE-US-00007 Number of bacteria Sensory quality Total Retention Tissue bacterial time/days Color Odor Taste state count Coliform 0 Unchanged Unchanged Unchanged Unchanged ≥10.sup.9 cfu/mL Undetected 7 Unchanged Unchanged Unchanged Unchanged ≥10.sup.9 cfu/mL Undetected 14 Unchanged Unchanged Unchanged Unchanged ≥10.sup.9 cfu/mL Undetected 21 Unchanged Unchanged Unchanged Unchanged ≥10.sup.9 cfu/mL Undetected 28 Unchanged Unchanged Souring Unchanged ≥10.sup.9 cfu/mL >1 cfu/mL

(55) Change in sensory quality and number of bacteria during storage of sterilized fermented puree at room temperature

(56) TABLE-US-00008 Number of bacteria Sensory quality Total Retention Tissue bacterial time/months Color Odor Taste state count Coliform 0 Unchanged Unchanged Unchanged Unchanged 0 Undetected 6 Unchanged Unchanged Unchanged Unchanged 0 Undetected 12 Unchanged Unchanged Unchanged Unchanged 0 Undetected 18 Unchanged Unchanged Unchanged Unchanged 0 Undetected 20 Unchanged Unchanged Unchanged Unchanged >100 cfu/mL >1 cfu/mL

Embodiment 15 Determination of Physiological-Biochemical Characteristics of NCU215

(57) {circle around (1)} Test on Acid Resistance—with 2-h Treatment in a PBS at a pH of 2.0, the Survival Rate is 78.98%.

(58) A selected NCU215 was activated twice by using an MRS liquid culture medium, and cultured for 24 h at 37° C. according to 2% (v/v) of inoculum size; and 10000 g was centrifuged for 5 min to collect a thallus. The thallus was re-suspended with a sterile PBS having a pH of 2.0, the concentration of viable bacteria was regulated to 10.sup.8 CFU/m, incubation was performed for 2 h at 37° C., and a dilution spread method was used to determinate the number of viable bacteria before and after the incubation, thus determining the survival rate. The survival rate was calculated as per the following formula.

(59) $\mathrm{Survival}\mathrm{rate}\left(\%\right)=\frac{\log N_1}{\log N_0}\times 100$

(60) Where, the N.sub.1 is the number of survival viable bacteria after the incubation and the No is the initial number of bacteria.

(61) {circle around (2)} Test on Cholate Resistance—with 4-h Treatment in an Environment Containing 0.5% of Cholate, the Survival Rate is 84.89%.

(62) 10000 g of NCU215 that was cultured for 24 h was centrifuged for 5 min at 4° C. to collect a thallus; the obtained thallus was re-suspended with a sterile PBS containing 0.5% of cholate, the concentration of viable bacteria was regulated to 10.sup.8 CFU/m, incubation was performed for 4 h at 37° C., and a dilution spread method was used to determinate the number of viable bacteria to evaluate the cholate resistance of the NCU215. The survival rate of the NCU215 was calculated according to the following formula.

(63) $\mathrm{Survival}\mathrm{rate}\left(\%\right)=\frac{\log N_1}{\log N_0}\times 100$

(64) Where, the N.sub.1 is the number of survival viable bacteria and the No is the initial number of bacteria.

(65) {circle around (3)} Tolerance in Simulated Gastric and Intestinal Fluid

(66) 10000 g of NCU215 that was cultured for 24 h was centrifuged for 5 min at 4° C. to collect a thallus, and the thallus was cleaned twice with a sterile PBS; thereafter, the thallus was re-suspended in a simulated gastric fluid having a pH of 3.0 to incubate for 3 h at 37° C., and the number of viable bacteria was determinated at 0 h, 1 h, 2 h, and 3 h; and then, 1 mL of culture was added to 9 mL of simulated intestinal fluid to incubate for 8 h at 37° C., and the number of viable bacteria in the culture was determinated at 0 h, 2 h, 4 h and 8 h. The survival rate of the NCU215 was calculated according to the following formula.

(67) $\mathrm{Survival}\mathrm{rate}\left(\%\right)=\frac{\log N_1}{\log N_0}\times 100$

(68) Where, the N.sub.1 is the number of survival viable bacteria and the No is the initial number of bacteria.

(69) It is turned out that by digesting for 3 h in a simulated gastric fluid having a pH of 3.0 and then transferring to a simulated intestinal fluid having a pH of 8.0 to digest for 8 h, the vitality is not significantly reduced; with 3-h treatment in the simulated gastric fluid, the survival rate is 101.52±1.67%; and with 8-h treatment in the simulated intestinal fluid, the survival rate is 100.27±2.05%.

(70) {circle around (4)}-1 Test on Auto-Aggregation Capacity

(71) 10000 g of Lactobacillus cultured for overnight was centrifuged for 5 min to collect a thallus, and the thallus was cleaned twice with a sterile PBS buffer solution. Thereafter, the obtained thallus cell was re-suspended with a sterile PBS, regulated to A.sub.600=0.6±0.05 (A.sub.0), and incubated for 24 h at 37° C. after 10 s of vortex oscillation. An upper layer of bacterial suspension was taken at 0 h, 2 h, 4 h, 6 h, 12 h and 24 h, and the absorbancy (A.sub.t) was determinated at 600 nm, three parallels were determinated at each time, and the test was repeated for three times. The auto-aggregation capacity of the bacteria was calculated according to the following formula.

(72) $\mathrm{Percentage}\mathrm{of}\mathrm{auto}\text{-}\mathrm{aggregation}\mathrm{of}\mathrm{bacteria}=\left(1-\frac{A_t}{A_0}\right)\times 100\%$

(73) Where, the A.sub.0 denotes an initial absorbance of the thallus, and the A.sub.t denotes an absorbance of the upper layer of bacterial solution at a t moment.

(74) It is turned out that the auto-aggregation rate of the strain within 24 h is 64.32%.

(75) {circle around (4)}-2 Test on Surface Hydrophobicity

(76) A Bacteria Adhesion To Hydrocarbons (BATH) method was used to determinate the surface hydrophobicity of Lactobacillus. First of all, 10000 g of Lactobacillus cultured for overnight was centrifuged for 5 min to collect a thallus cell, and the thallus cell was cleaned twice with a sterile PBS buffer solution; thereafter, the obtained thallus cell was re-suspended with 0.1 mol/L KNO.sub.3 and regulated to A.sub.600=0.6±0.05 (A.sub.0). Then, 1 mL of xylene was taken, and added to 3 mL of thallus cell suspension having a well regulated concentration; and after mixing, the mixed solution was pre-incubated for 10 min at a room temperature, subjected to vortex oscillation for 2 min, and then incubated for 30 min at the room temperature for layering; an aqueous phase was absorbed carefully; and with a sterile PBS as a blank, an OD600 value (A) was determinated. The hydrophobicity of the bacteria was calculated according to the following formula.

(77) $\mathrm{Hydrophobic}\mathrm{rate}\left(\%\right)=\left(1-\frac{A_0}{A}\right)\times 100\%$

(78) Where, the A.sub.0 denotes an initial absorbance of the thallus, and the A is an absorbance for a lower layer of aqueous phase after treatment of xylene. It is turned out that the surface hydrophobic rate of the strain is 23.15%.

(79) {circle around (4)}-3 Test on Adhesion

(80) A cultured Caco-2 cell was digested with a pancreatin-EDTA digestive fluid, then a cell concentration was regulated to 1.0*10.sup.5 pcs/mL with a DMEM complete culture solution, the solution was put into a 6-pore tissue culture plate, 2 mL for each pore, and incubated at 37° C. in a CO.sub.2 incubator (5% of CO.sub.2 and 95% of air) till the cell was grown to a differentiated single layer, and the solution was changed once every 2 days. The DMEM culture solution in each pore of the tissue culture plate was removed, the culture plate was cleaned twice with a sterile PBS buffer solution, 1 mL of Lactobacillus suspension (10.sup.8 CFU/mL, OD=1) (Caco-2 cell: number of bacteria≥1:100) re-suspended by a DMEM incomplete culture solution was added, and incubation was performed for 2 h at 37° C. Upon the completion of the incubation, a mixed solution in each pore of the tissue culture plate was removed, and the sterile PBS buffer solution was used for cleaning for 5 times to remove an unadhered thallus cell. 0.5 mL of 0.25% pancreatin was added to incubate for 5 min at 37° C. to digest the cell, and then a cell digestive fluid was subjected to gradient dilution and spread on an MRS solid plate to calculate the number of adhered bacteria. The adhesion was calculated by using the following formula.
Adhesion rate (%)=N.sub.t/N.sub.0×100

(81) Where, the N.sub.t denotes the number of bacteria adhered on the Caco-2 cell, and the No denotes the number of total bacteria in the added NCU215. It is turned out that the adhesion rate of the strain to a human colon cancer cell Caco-2 is 7.47%.

(82) {circle around (5)} Test on Antioxidant Activity (the NCU215 Sample Solution has a Thallus Concentration of 10.sup.9 CFU/mL)

(83) DPPH Free Radical Scavenging Capacity

(84) 1.0 mL of NCU215 sample solution was added to 1 mL of ethanol DPPH free radical solution (0.1 mM), mixed uniformly and incubated for 30 min in a dark environment at a room temperature. After 8000 g was centrifuged for 10 min, with PBS and DPPH solutions as controls and an ethanol solution and an NCU215 sample as blanks, the absorbancy of the obtained solution was determinated at 517 nm. The scavenging capacity was represented by the following formula.

(85) $\mathrm{Scavenging}\mathrm{rate}\left(\%\right)=\left(1-\frac{A_s-A_b}{A_c}\right)\times 100\%$

(86) Where, the A.sub.s is the absorbancy of the sample at 517 nm, the A.sub.b is the absorbancy of the blank at 517 nm, and the A.sub.c is the absorbancy of the control at 517 nm.

(87) Hydroxyl Free Radical Scavenging Capacity

(88) 1 mL of 2.5 mM phenanthroline, 1 mL of PBS (having a pH of 7.4), 1 mL of 2.5 mM FeSO.sub.4 and 1 mL of NCU215 sample were mixed simply. By means of adding 1 mL of 20 mM H.sub.2O.sub.2 and incubating for 90 min at 37° C., a reaction started. The absorbancy of a mixture was determinated at 536 nm, and a hydroxyl free radical scavenging activity was calculated according to the following formula.

(89) $\mathrm{Scavenging}\mathrm{activity}\left(\%\right)=\frac{\left(A_{\mathrm{sample}}-A_{\mathrm{blank}}\right)}{\left(A_{\mathrm{control}}-A_{\mathrm{blank}}\right)}\times 100\%$

(90) Where, the A.sub.sample is the absorbancy in the presence of the sample and the H.sub.2O.sub.2, the A.sub.control is the absorbancy in the absence of the sample and the H.sub.2O.sub.2, and the A.sub.blank is the absorbancy of the control in the absence of the sample and the H.sub.2O.sub.2.

(91) ABTS Free Radical Scavenging Capacity

(92) An ABTS working mother solution was prepared according to a specification of an ABTS free radical detection kit (Beyotime), and placed for 16 h away from light at a room temperature; and then, a PBS was used to regulate the absorbance A.sub.734=0.7±0.01 (ABTS working solution). 200 μL of ABTS working solution was added to each detection pore of a 96-pore plate. 10 μL of PBS was added to a blank control pore; 10 μL of Trolox standard solution having 0.15 mM, 0.3 mM, 0.6 mM, 0.9 mM, 1.2 mM and 1.5 mM was respectively added to a standard curve detection pore; and 10 μL of NCU215 sample was added to a sample detection pore and mixed uniformly and slightly. Upon 6 min of incubation away from the light at the room temperature, A.sub.734 was determinated. The total antioxidant capacity of the sample was calculated according to a standard curve.

(93) Total Reducing Capacity

(94) An FRAP working solution was prepared according to a specification of an FRAP total reducing capacity detection kit (Beyotime). A solution having 0.15 mM, 0.3 mM, 0.6 mM, 0.9 mM, 1.2 mM and 1.5 mM was prepared newly. 180 μL of FRAP working solution was added to each detection pore of a 96-pore plate; 5 μL of PBS solution was added to a blank control pore; 5 μL of newly prepared FeSO.sub.4 standard solution having 0.15 mM, 0.3 mM, 0.6 mM, 0.9 mM, 1.2 mM and 1.5 mM was added to a standard curve detection pore; and 5 μL of NCU215 sample was added to a sample detection pore, and mixed uniformly and slightly. Upon 5 min of incubation at 37° C., A.sub.593 was determinated. The total antioxidant capacity of the sample was calculated according to a standard curve.

(95) It is turned out that the strain has a good antioxidant activity: the DPPH free radical scavenging rate is 11.91%, the hydroxyl free radical scavenging rate is 10.85%, the total antioxidant capacity is equivalent to 95.90 μmol of Trolox, and the total reducing capacity is equivalent to 0.28 mM FeSO.sub.4.

(96) {circle around (6)}-1 Test on Antibacterial Activity

(97) NCU215 was cultured for 24 h at 37° C. in an MRS culture medium, and 10000 g of NCU215 was centrifuged for 10 min at 4° C. A fermentation supernate was filtered by a 0.22 μm filter membrane to remove bacteria to obtain a Cell-Free Supernate (CFS) and the CFS was stored at −80° C. for later use. An antibacterial activity of the NCU215 CFS to pathogenic bacteria was determinated in a punching method, that was, 200 μL of NCU215 CFS was taken, added to an LB plate pore coated by Escherichia coli, salmonella, Listeria monocytogenes, Pseudomonas aeruginosa, Enterobacter sakazakii, Bacillus cereus and Staphylococcus aureus, and incubated for 12 h at 37° C. to determinate a diameter of a bacterial inhibition ring.

(98) {circle around (6)}-2 Test on Hemolytic Activity

(99) A single colony of a test strain was selected, scratched to a Columbia blood agar plate, and cultured for 48 h at 37° C. to determine a hemolytic activity. With Lactobacillus fermenti CECT5716 as a positive control and Staphylococcus aureus as a negative control, the test was repeated for three times.

(100) {circle around (6)}-3 Test on Antibiotic Sensitivity

(101) K-B (drug sensitive disc agar diffusion test) was used to perform a drug sensitive test, thus evaluating antibiotic resistance of the strain. A thallus concentration of a Lactobacillus fermentation broth that was cultured for overnight was regulated to 10.sup.8 CFU/mL, and 100 μL was absorbed and spread on an MRS plate. Drug sensitive discs of streptomycin (10 mg/mL), ampicillin (10 mg/mL), erythromycin (15 mg/mL), tetracycline (30 mg/mL), gentamicin (gentamicin), kanamycin (30 mg/mL), penicillin (10 mg/mL), cefalotin (15 mg/mL), ciprofloxacin (5 mg/mL) and amoxicillin (30 mg/mL) were respectively and slightly placed on the MRS plate coated by a Lactobacillus bacterial solution, and cultured for 24 h at 37° C.; and a vernier caliper was used to determinate a diameter of a bacterial inhibition ring, thus determining the sensitivity of the Lactobacillus to the above antibiotics.

(102) It is turned out that a 24-h fermented supernate of the strain has an excellent antibacterial activity to common food-borne pathogenic bacteria, and particularly has the best inhibitory activity to Listeria monocytogenes and Staphylococcus aureus, with diameters of bacterial inhibition rings respectively being 23.18 mm and 24.42 mm. Additionally, a test on a hemolytic activity of the strain turns out that the strain is not hemolytic; and a test on an antibiotic sensitivity turns out that the strain is sensitive to tetracycline, ampicillin, amoxicillin, cefalotin, erythromycin and penicillin and tolerant to kanamycin, ciprofloxacin, streptomycin and gentamicin.

(103) The above embodiments only describe several implementation manners of the present invention. The description is specific and detailed, but cannot be understood as a limit to a scope of the present invention accordingly. It should be pointed out that the person of ordinary skill in the art may further make multiple changes, combinations and improvement to the above implementation manners without departing from a concept of the present invention and those also belong to the protection scope of the present invention. Therefore, the protection scope of the present invention shall be subjected to the claims.