CN115322932A - Lactobacillus plantarum with capacity of dispelling effects of alcohol and sobering up and application thereof - Google Patents
Lactobacillus plantarum with capacity of dispelling effects of alcohol and sobering up and application thereof Download PDFInfo
- Publication number
- CN115322932A CN115322932A CN202211016608.4A CN202211016608A CN115322932A CN 115322932 A CN115322932 A CN 115322932A CN 202211016608 A CN202211016608 A CN 202211016608A CN 115322932 A CN115322932 A CN 115322932A
- Authority
- CN
- China
- Prior art keywords
- lactobacillus plantarum
- alcohol
- sobering
- alcoholism
- plantarum
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 title claims abstract description 90
- 240000006024 Lactobacillus plantarum Species 0.000 title claims abstract description 84
- 235000013965 Lactobacillus plantarum Nutrition 0.000 title claims abstract description 84
- 229940072205 lactobacillus plantarum Drugs 0.000 title claims abstract description 84
- 230000000694 effects Effects 0.000 title claims abstract description 44
- 108010081577 aldehyde dehydrogenase (NAD(P)+) Proteins 0.000 claims abstract description 14
- 210000004185 liver Anatomy 0.000 claims abstract description 12
- 238000004321 preservation Methods 0.000 claims abstract description 11
- 210000002966 serum Anatomy 0.000 claims abstract description 11
- 241001465754 Metazoa Species 0.000 claims abstract description 10
- 238000002474 experimental method Methods 0.000 claims abstract description 8
- 238000009629 microbiological culture Methods 0.000 claims abstract description 5
- 230000001580 bacterial effect Effects 0.000 claims description 25
- 239000003814 drug Substances 0.000 claims description 13
- 239000001963 growth medium Substances 0.000 claims description 10
- 230000015556 catabolic process Effects 0.000 claims description 7
- 238000006731 degradation reaction Methods 0.000 claims description 7
- 206010019133 Hangover Diseases 0.000 claims description 6
- 230000003472 neutralizing effect Effects 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- 238000012258 culturing Methods 0.000 claims description 4
- 235000013376 functional food Nutrition 0.000 claims description 4
- 230000003287 optical effect Effects 0.000 claims description 4
- 101710088194 Dehydrogenase Proteins 0.000 claims description 3
- 230000002265 prevention Effects 0.000 claims description 3
- 239000000825 pharmaceutical preparation Substances 0.000 claims 1
- 229940127557 pharmaceutical product Drugs 0.000 claims 1
- 238000004904 shortening Methods 0.000 claims 1
- 208000007848 Alcoholism Diseases 0.000 abstract description 23
- 201000007930 alcohol dependence Diseases 0.000 abstract description 23
- 230000035622 drinking Effects 0.000 abstract description 9
- 102000007698 Alcohol dehydrogenase Human genes 0.000 abstract description 8
- 108010021809 Alcohol dehydrogenase Proteins 0.000 abstract description 8
- 235000013305 food Nutrition 0.000 abstract description 8
- 230000001737 promoting effect Effects 0.000 abstract description 5
- 235000019441 ethanol Nutrition 0.000 description 63
- 241000699670 Mus sp. Species 0.000 description 21
- 241000894006 Bacteria Species 0.000 description 12
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 10
- 229940079593 drug Drugs 0.000 description 9
- 241000699666 Mus <mouse, genus> Species 0.000 description 6
- 239000006041 probiotic Substances 0.000 description 6
- 235000018291 probiotics Nutrition 0.000 description 6
- 230000028527 righting reflex Effects 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 5
- 230000002075 anti-alcohol Effects 0.000 description 5
- 230000000593 degrading effect Effects 0.000 description 5
- 239000004310 lactic acid Substances 0.000 description 5
- 235000014655 lactic acid Nutrition 0.000 description 5
- 241000186660 Lactobacillus Species 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 230000001154 acute effect Effects 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 210000004369 blood Anatomy 0.000 description 4
- 239000008280 blood Substances 0.000 description 4
- 230000006378 damage Effects 0.000 description 4
- 230000036541 health Effects 0.000 description 4
- 229940039696 lactobacillus Drugs 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000011160 research Methods 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 239000000284 extract Substances 0.000 description 3
- 230000002496 gastric effect Effects 0.000 description 3
- 230000012010 growth Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000009630 liquid culture Methods 0.000 description 3
- 230000004060 metabolic process Effects 0.000 description 3
- 244000005700 microbiome Species 0.000 description 3
- 230000000877 morphologic effect Effects 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 230000004622 sleep time Effects 0.000 description 3
- 108020004465 16S ribosomal RNA Proteins 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- 241000917009 Lactobacillus rhamnosus GG Species 0.000 description 2
- 239000001888 Peptone Substances 0.000 description 2
- 108010080698 Peptones Proteins 0.000 description 2
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
- 208000027418 Wounds and injury Diseases 0.000 description 2
- 210000001015 abdomen Anatomy 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 235000015278 beef Nutrition 0.000 description 2
- 229940041514 candida albicans extract Drugs 0.000 description 2
- ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 2
- 229910000396 dipotassium phosphate Inorganic materials 0.000 description 2
- 235000019797 dipotassium phosphate Nutrition 0.000 description 2
- 230000008034 disappearance Effects 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 238000000855 fermentation Methods 0.000 description 2
- 230000004151 fermentation Effects 0.000 description 2
- 235000021107 fermented food Nutrition 0.000 description 2
- 239000008103 glucose Substances 0.000 description 2
- 238000000338 in vitro Methods 0.000 description 2
- 238000001727 in vivo Methods 0.000 description 2
- 208000014674 injury Diseases 0.000 description 2
- 230000000968 intestinal effect Effects 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 229940059406 lactobacillus rhamnosus gg Drugs 0.000 description 2
- 210000005228 liver tissue Anatomy 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 229940099596 manganese sulfate Drugs 0.000 description 2
- 239000011702 manganese sulphate Substances 0.000 description 2
- 235000007079 manganese sulphate Nutrition 0.000 description 2
- SQQMAOCOWKFBNP-UHFFFAOYSA-L manganese(II) sulfate Chemical compound [Mn+2].[O-]S([O-])(=O)=O SQQMAOCOWKFBNP-UHFFFAOYSA-L 0.000 description 2
- 208000030159 metabolic disease Diseases 0.000 description 2
- 239000002207 metabolite Substances 0.000 description 2
- 235000019319 peptone Nutrition 0.000 description 2
- 229920000136 polysorbate Polymers 0.000 description 2
- 239000013641 positive control Substances 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K potassium phosphate Substances [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- 239000001632 sodium acetate Substances 0.000 description 2
- 235000017281 sodium acetate Nutrition 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- 208000024891 symptom Diseases 0.000 description 2
- YWYZEGXAUVWDED-UHFFFAOYSA-N triammonium citrate Chemical compound [NH4+].[NH4+].[NH4+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O YWYZEGXAUVWDED-UHFFFAOYSA-N 0.000 description 2
- 239000001393 triammonium citrate Substances 0.000 description 2
- 235000011046 triammonium citrate Nutrition 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000012138 yeast extract Substances 0.000 description 2
- 229920001817 Agar Polymers 0.000 description 1
- 108020004414 DNA Proteins 0.000 description 1
- 208000004930 Fatty Liver Diseases 0.000 description 1
- 241000192125 Firmicutes Species 0.000 description 1
- 238000003794 Gram staining Methods 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- 206010067125 Liver injury Diseases 0.000 description 1
- 108091028043 Nucleic acid sequence Proteins 0.000 description 1
- 238000012408 PCR amplification Methods 0.000 description 1
- 241000589517 Pseudomonas aeruginosa Species 0.000 description 1
- 241000191967 Staphylococcus aureus Species 0.000 description 1
- 241000251539 Vertebrata <Metazoa> Species 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000003044 adaptive effect Effects 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 238000010171 animal model Methods 0.000 description 1
- 244000052616 bacterial pathogen Species 0.000 description 1
- 230000003385 bacteriostatic effect Effects 0.000 description 1
- 239000003833 bile salt Substances 0.000 description 1
- 238000010241 blood sampling Methods 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- 210000005252 bulbus oculi Anatomy 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 235000015872 dietary supplement Nutrition 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- PTKRHFQQMJPPJN-UHFFFAOYSA-N dipotassium;oxido-(oxido(dioxo)chromio)oxy-dioxochromium;sulfuric acid Chemical compound [K+].[K+].OS(O)(=O)=O.[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O PTKRHFQQMJPPJN-UHFFFAOYSA-N 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 238000003304 gavage Methods 0.000 description 1
- 230000008821 health effect Effects 0.000 description 1
- 231100000753 hepatic injury Toxicity 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 239000002054 inoculum Substances 0.000 description 1
- 230000035987 intoxication Effects 0.000 description 1
- 231100000566 intoxication Toxicity 0.000 description 1
- 230000006799 invasive growth in response to glucose limitation Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000013642 negative control Substances 0.000 description 1
- 238000011392 neighbor-joining method Methods 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 230000036542 oxidative stress Effects 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 206010036067 polydipsia Diseases 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000011514 reflex Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 235000021108 sauerkraut Nutrition 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000012163 sequencing technique Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 229940126680 traditional chinese medicines Drugs 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms, 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
- C12N1/20—Bacteria; Culture media therefor
- C12N1/205—Bacterial isolates
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/135—Bacteria or derivatives thereof, e.g. probiotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/66—Microorganisms or materials therefrom
- A61K35/74—Bacteria
- A61K35/741—Probiotics
- A61K35/744—Lactic acid bacteria, e.g. enterococci, pediococci, lactococci, streptococci or leuconostocs
- A61K35/747—Lactobacilli, e.g. L. acidophilus or L. brevis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P39/00—General protective or antinoxious agents
- A61P39/02—Antidotes
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
- C12R2001/00—Microorganisms ; Processes using microorganisms
- C12R2001/01—Bacteria or Actinomycetales ; using bacteria or Actinomycetales
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Abstract
The invention discloses a lactobacillus plantarum (Lactplantibibacillus plantarum) with the capacity of relieving alcoholism and sobering up, which is named as follows: LTJ30, category name: the lactobacillus plantarum has a preservation number of: cgmccno.25371, preservation date: 22/7/2022, depository: china general microbiological culture Collection center, west Lu No. 1 Hospital No. 3, beijing, chaoyang, the area of the republic of China. The lactobacillus plantarum belongs to a well-known safe strain which can be used for food; the health-care wine has the capability of relieving alcoholism and sobering up, and animal experiments prove that the health-care wine can reduce the alcoholism rate, obviously shorten the alcoholism time, reduce the ethanol content in serum and improve the activities of alcohol dehydrogenase and acetaldehyde dehydrogenase in liver when being taken one hour before drinking high-concentration white spirit, and has the obvious effects of preventing drunkenness and relieving alcoholism and promoting sobering up.
Description
Technical Field
The invention belongs to the technical field of microorganisms, and particularly relates to lactobacillus plantarum with the capacity of dispelling effects of alcohol and sobering up and application thereof.
Background
Probiotics are a microbial supplement and have various physiological effects on the human body which are incomparable with other normal physiological flora. They can improve the balance of intestinal microorganisms. Lactic acid bacteria are the most important types of probiotics, and the addition of lactic acid bacteria in the fermentation process can improve not only the functions of the probiotics but also the flavor. Lactobacillus plantarum is a gram-positive bacterium widely found in food, feed, plants, vertebrates and invertebrates and in human-related nutritionally rich habitats. Lactobacillus plantarum is of great economic importance for its application in food, biotechnology and therapy. Lactobacillus plantarum is an important member of lactic acid bacteria, and is widely distributed in traditional fermented foods. Due to their health promoting effect, more and more lactobacillus plantarum strains are widely used as probiotics in food products and dietary supplements.
Alcoholism refers to the symptom that the body of a drinker is changed from a nervous central excitation state to an inhibition state due to excessive drinking of alcohol by a human or an animal, and the serious drinker usually can cause symptoms such as acute gastrorrhagia and even die, so that the alcoholism has great harm to the body of the drinker. In recent years, with the improvement of the living standard of people, people pay more attention to their health and the health care awareness is gradually enhanced, so the demand of anti-alcohol products is also increased. The core of the anti-alcohol medicine is to reduce the concentration of ethanol and harmful metabolites thereof in the human body, relieve the damage of the ethanol and the harmful metabolites thereof to various organs, and regulate the metabolic disorder in the human body caused by alcohol metabolism. The antialcoholism can be performed from the aspects of delaying the absorption of alcohol, promoting alcohol metabolism, regulating in-vivo metabolic disorders caused by alcohol metabolism, removing free radicals and the like. At present, the antialcoholic drugs mainly focus on the aspects of compound and initial extract of traditional Chinese medicines, and probiotics (lactic acid bacteria) are rarely used for antialcoholic study.
Therefore, the research on the probiotics with the capacity of relieving alcoholism and sobering up has important significance on the research and development of health-care products for relieving alcoholism and further on the health of human bodies.
Through searching, the following patent publications related to the patent application of the invention are found:
1. the application of lactobacillus plantarum LP45 in preparing food for relieving body injury after drinking (CN 110192654A) belongs to the technical field of microorganisms, and has very wide application prospects in relieving body discomfort caused by drinking and protecting liver health after drinking.
2. A Lactobacillus plantarum producing acetaldehyde dehydrogenase and application thereof (CN 107760624A), the Lactobacillus plantarum is named as Lactobacillus plantarum FCJX 102 (Lactobacillus plantarum FCJX 102), and is preserved in China center for type culture Collection in 6 months and 16 days in 2017, and the preservation number is CCTCC NO: M2017340. The Lactobacillus plantarum FCJX 102 (Lactobacillus plantarum FCJX 102) has the advantages that acetaldehyde dehydrogenase can be produced in a high yield under the induction of ethanol, and the Lactobacillus plantarum FCJX 102 has a wide application prospect in the aspects of anti-alcohol and liver-protecting medicines and foods.
3. The invention discloses a lactobacillus plantarum P101 with high antioxidant activity and application thereof (CN 114196593A). The lactobacillus plantarum P101 is separated from sauerkraut prepared by farmers in Jian city in Jiangxi province, and the preservation number is CCTCC M2021108. The lactobacillus plantarum P101 has good bacteriostatic activity, and can remarkably inhibit the activity of intestinal pathogenic bacteria such as staphylococcus aureus, pseudomonas aeruginosa and the like; the lactobacillus plantarum P101 has strong antioxidant activity, in vitro experimental results show that the clearance rate of 1,1 diphenyl-2-trinitrophenylhydrazine (DPPH) and hydroxyl free radicals by the lactobacillus plantarum P101 is remarkably higher than that of lactobacillus rhamnosus GG (LGG), in vivo experimental results show that the lactobacillus plantarum P101 can effectively weaken alcohol-induced oxidative stress injury and inhibit organism inflammatory reaction. The survival rate of the lactobacillus plantarum P101 in an acidic or high-bile-salt environment is remarkably higher than that of the lactobacillus plantarum ZDY2013, and in addition, the lactobacillus plantarum P101 has remarkable benefit in relieving alcohol-induced steatohepatitis.
The patent publications mainly show the research on in vitro functions and the alleviation of long-term alcoholic liver injury, while the patent application of the invention shows a lactobacillus plantarum strain with the capacity of relieving alcoholism and sobering up and application, so by contrast, the patent application of the invention is fundamentally different from the patent publications.
Disclosure of Invention
The invention aims to overcome the defects of the prior art and provides lactobacillus plantarum with the capacity of dispelling effects of alcohol and application.
The technical scheme adopted by the invention for solving the technical problems is as follows:
lactobacillus plantarum (Lactplantibibacillus plantarum) with the capacity of relieving or neutralizing the effect of alcohol is named as follows: LTJ30, category name: the lactobacillus plantarum has a preservation number of: CGMCC No.25371, preservation date: 22/7/2022, depository: china general microbiological culture Collection center, west Lu No. 1 Hospital No. 3, beijing, chaoyang, the area of the republic of China.
Further, the lactobacillus plantarum is separated from fermented grains of white spirit and is the dominant strain in the fermented grains.
Furthermore, the bacterial colony and thallus characteristics of the lactobacillus plantarum are as follows: culturing for 24 hours on an MRS culture medium, wherein the bacterial colony is white, opaque, protruding, moist, flat in edge and glossy, and the diameter of the bacterial colony is 0.8-1.0 mm; observing the cell morphology under an optical microscope, wherein the gram stain shows G + The thallus is in the shape of a small short rod.
Further, the lactobacillus plantarum can produce degradation effect on alcohol after being cultured in the presence of the alcohol.
Furthermore, animal experiments prove that the lactobacillus plantarum can reduce the drunkenness rate, remarkably shorten the drunkenness time, reduce the ethanol content in serum, improve the activity of ethanol dehydrogenase and acetaldehyde dehydrogenase in liver and has remarkable effects of preventing drunkenness and dispelling the effects of alcohol and promoting sobering up when being taken in the first hour before drinking high-concentration white spirit.
Further, the high-concentration white spirit is 56% white spirit.
The lactobacillus plantarum is applied to the aspect of relieving alcoholism.
The lactobacillus plantarum is applied to functional foods and medicines.
The lactobacillus plantarum is applied to the preparation of anti-alcoholism medicines.
The invention has the advantages and positive effects that:
1. the lactobacillus plantarum (Lactplantibibacillus plantarum) is derived from fermented grains in the traditional fermentation process of fermented food white spirit, and belongs to a well-known and safe strain which can be used for food. The lactobacillus plantarum has the capacity of degrading alcohol, is the dominant strain in fermented grains of white spirit, and has the capacity of dispelling the effects of alcohol.
2. The lactobacillus plantarum (Lactplantibibacillus plantarum) has certain capacity of degrading alcohol after being cultured under the condition of containing alcohol.
3. Animal experiments prove that the lactobacillus plantarum (Lactplantibibacillus plantarum) can reduce the drunkenness rate, remarkably shorten the drunkenness time, reduce the ethanol content in serum and improve the activity of alcohol dehydrogenase and acetaldehyde dehydrogenase in liver when being taken in the first hour before drinking high-concentration white spirit, has remarkable effects of preventing drunkenness and dispelling the effects of alcohol and promoting sobering, and can be used in the fields of food, medicine and the like, such as development of related functional food and medicines (dispelling the effects of alcohol).
Drawings
FIG. 1 is a colony morphology (left) and a cell morphology (right) of Lactobacillus plantarum CGMCC No.25371 in the present invention;
FIG. 2 is a 16S rDNA phylogenetic tree diagram of Lactobacillus plantarum CGMCC No.25371 in the present invention;
FIG. 3 shows the concentration of the lactobacillus plantarum CGMCC No.25371 capable of degrading alcohol under the alcohol treatment of different concentrations.
Detailed Description
The present invention is further illustrated by the following examples, which are intended to be illustrative, not limiting and are not intended to limit the scope of the invention.
The raw materials used in the invention are all conventional commercial products if no special description is provided, the method used in the invention is all conventional methods in the field if no special description is provided, and the mass of all the materials used in the invention is the conventional use mass.
Lactobacillus plantarum (Lactplantibibacillus plantarum) with the capacity of relieving or neutralizing the effect of alcohol is named as follows: LTJ30, category name: the lactobacillus plantarum has a preservation number of: CGMCC No.25371, preservation date: 22/7/2022, depository: china general microbiological culture Collection center, west Lu No. 1 Hospital No. 3, beijing, chaoyang, the area of the republic of China.
Preferably, the lactobacillus plantarum is separated from fermented grains of white spirit and is the dominant strain in the fermented grains.
Preferably, the bacterial colony and thallus characteristics of the lactobacillus plantarum are as follows: culturing for 24h on an MRS culture medium, wherein the bacterial colony is white, opaque, prominent, moist, flat in edge and glossy, and the diameter of the bacterial colony is 0.8-1.0 mm; observing the cell morphology under an optical microscope, wherein the gram stain shows G + The thallus is in the shape of a small short rod.
Preferably, the lactobacillus plantarum can degrade alcohol after being cultured in the presence of the alcohol.
Preferably, animal experiments prove that the lactobacillus plantarum can reduce the drunkenness rate, remarkably shorten the drunkenness time, reduce the ethanol content in serum and improve the activity of ethanol dehydrogenase and acetaldehyde dehydrogenase in liver when being taken in the first hour before drinking high-concentration white spirit, and has remarkable drunkenness prevention, alcohol effect dispelling and wakening promotion effects.
Preferably, the high-concentration white spirit is 56% white spirit.
The lactobacillus plantarum is applied to the aspect of relieving alcoholism.
The lactobacillus plantarum is applied to functional foods and medicines.
The lactobacillus plantarum is applied to the preparation of anti-alcoholism medicines.
Specifically, the following examples illustrate the technical solutions of the present invention from the characteristics of the separation and identification of the strains, the ability of degrading alcohol under alcohol treatment of different concentrations, and the anti-hangover effect of the strains on acute alcoholism mice in animal experiments, respectively, and specifically include the following contents.
Example 1 isolation and identification of lactic acid bacteria
The following experiments were all performed under sterile conditions.
1. Enrichment of strains
Weighing 25g of fermented grains in the liquor making process, adding 225mL of sterile normal saline, mixing uniformly, diluting the obtained bacterial liquid by 10 percent 3 ~10 5 After doubling, 100 mu L of the suspension was spread on an MRS plate, and the suspension was cultured in an inverted state at 37 ℃ for 24 hours to observe the growth of colonies.
The preparation method of the MRS solid culture medium comprises the following steps: 10g of peptone, 5g of beef extract powder, 80 mL of Tween, 2g of dipotassium phosphate, 4g of yeast extract powder, 0.2g of magnesium sulfate, 2g of triammonium citrate, 20g of glucose, 0.05g of manganese sulfate, 5g of sodium acetate, 20g of agar, 1L of distilled water, pH 6.2 +/-0.2, and sterilization at 121 ℃ for 20min for later use.
2. Isolation of the Strain
And (3) selecting the bacterial colony obtained in the step (1), performing microscopic examination by using a gram staining method, observing morphological characteristics of the bacterial colony, and selecting gram-positive bacteria as target strains.
3. Purification of the strains
And (3) selecting the bacterial colonies obtained in the step (2), streaking on an MRS plate, repeatedly purifying until no other mixed bacteria exist, and recording the states of different bacterial colonies.
4. Identification of the strains
The bacterial genome DNA rapid extraction kit is adopted to extract the lactobacillus strain genome, and the lactobacillus strain genome is used as a template for PCR amplification. And sequencing the successfully amplified PCR products, splicing to obtain a DNA sequence, and comparing and analyzing sequence homology by using a BLAST retrieval system of NCBI. The known strains with the highest similarity were selected and analyzed for similarity. Phylogenetic trees were created using the Neighbor-Joining method in MEGA 5 software (NJ).
Physiological and biochemical experimental research is carried out on the pure bacteria obtained in the step 3, the bacterial strain is found to have certain capacity of degrading alcohol, the bacterial strain is cultured on an MRS culture medium for 24 hours, bacterial colonies are white and opaque, bacterial colonies are protruded, moist, smooth in edge and glossy, the diameter of the bacterial colonies is 0.8-1.0 mm, the cell morphology of the bacterial colonies is observed under an optical microscope, and gram stain is G + The cells were in the form of small short rods (as shown in FIG. 1).
The result is shown in figure 2 by using BLAST software through homology comparison, and the result is determined to be a new plant lactobacillus (Lactplantibacillus plantarius) in lactobacillus by combining the colony morphological characteristics, the cell morphological characteristics and the 16S rDNA gene sequence result, the strain is preserved in China general microbiological culture Collection center (CGMCC) in 2022, 7 and 22 months, the preservation number is CGMCC No.25371, the address: xilu No. 1 Hospital No. 3, beijing, chaoyang, north.
Example 2 the capacity of Lactobacillus plantarum CGMCC No.25371 to degrade alcohol under different alcohol concentrations
Selecting strains at the last logarithmic growth stage, adding 2% of inoculum size into MRS liquid culture medium with different contents (volume fraction is 4%,6%,8%,10%, 12%) of alcohol, and performing alcohol treatment in an incubator at 37 ℃ for 12h, wherein an alcohol-free MRS culture medium culture group is used as a negative control. And after the alcohol treatment, determining the residual amount of the alcohol in the culture medium by using a potassium dichromate-sulfuric acid method, calculating the degraded alcohol concentration, and analyzing the alcohol degradation capability of each strain.
The preparation method of the MRS liquid culture medium comprises the following steps: 10g of peptone, 5g of beef extract powder, 80 mL of Tween, 2g of dipotassium phosphate, 4g of yeast extract powder, 0.2g of magnesium sulfate, 2g of triammonium citrate, 20g of glucose, 0.05g of manganese sulfate, 5g of sodium acetate, 1L of distilled water, pH 6.2 +/-0.2, and sterilization at 121 ℃ for 20min for later use.
The pure bacteria obtained in example 1 were subjected to alcohol treatment with different concentrations, the alcohol degradation ability of lactobacillus plantarum CGMCC No.25371 was substantially decreased with the increase of alcohol concentration, and the alcohol degradation concentrations (volume fraction) were 2.27%, 0.68%, 0.70%, 0.10%, 0.33% in order under the alcohol treatment of 4%,6%,8%,10%,12% (volume fraction), and had a certain alcohol degradation ability, especially a higher alcohol degradation ability at low alcohol concentration (as shown in fig. 3).
Example 3 anti-hangover Effect of Lactobacillus plantarum CGMCC No.25371 on acute alcoholism mice
1. Preparation of bacterial liquid
Selecting strain at late logarithmic growth stage, adding 2% of strain into MRS liquid culture medium, culturing at 37 deg.C in incubator for 10min, centrifuging at 5000r/min for 10min, washing the strain twice with sterile normal saline, and adjusting concentration of bacterial liquid to 10 10 CFU/mL, stored at 4 ℃ until use.
2. Laboratory animal
Kunming male mice 6 weeks old. A breeding environment: the temperature of the animal raising room is kept at 22-24 ℃, the relative humidity is 40% -60%, the air is ventilated at regular time, and the natural light and shade period is 12h (turning on a lamp 8. Constant temperature and humidity, standard feed and free drinking water. Adaptive feeding for 1 week.
3. Drunkenness prevention test
Taking 72 male mice, randomly dividing the mice into 4 groups, wherein each group comprises 18 mice, and the 4 groups are respectively named as: normal control group (NC), model group (M), positive control group (PC) and lactobacillus plantarum CGMCC No.25371 group (L30). Before the test, the mice are fasted for 12 hours, and then the normal control group, the model group, the positive control group and the lactobacillus plantarum CGMCC No.25371 group are respectively infused with gastric sterile normal saline, an anti-alcoholism drug (Haiwang Jinzun tablets) and bacterial suspension according to the dose of 5mL/kg, 3 groups of test groups except the normal control group require that the gastric sterile normal saline, the anti-alcoholism drug and the bacterial suspension are infused with gastric white spirit (56% Hongxing Erguotou) according to the dose of 13mL/kg after 1 hour, and the normal control group replaces the white spirit with the sterile normal saline. The sobering index is that the righting reflex of the mouse disappears, the mouse creeps unstably, the rear abdomen drags the ground, the hair is loose and turns round, and the sobering index is that the righting reflex recovers, the activity is free, flexible, spiritual and smooth. And (5) observing the activity of the mice in the gavage liquor group, and recording the number of drunk mice, the number of dead mice, the time for giving liquor, the disappearance time of righting reflex and the recovery time of righting reflex. Intoxication latency = righting reflex disappearance-time to give alcohol; sleep time = righting reflex recovery time-righting reflex disappearance time; sobering-up time = righting recovery time-drunken time.
4. Determination of blood alcohol concentration in mice
Modeling is carried out according to the anti-intoxication test, after each group of mice is modeled, eyeball blood sampling is carried out at the time node of 2.5h, the collected blood is placed at 37 ℃ for 1h and 4 ℃ for 1h, centrifugation is carried out at 3000r/min for 10min, the upper layer serum is taken, and the serum is transferred to a 1.5mL EP tube. And (3) measuring the blood ethanol concentration of the mouse by adopting a blood ethanol measuring kit.
5. Determination of mouse liver alcohol dehydrogenase and acetaldehyde dehydrogenase Activity
The mice were sacrificed by dislocation, the abdomen was dissected, the liver tissue was separated, 0.5g of the right lobe tissue of the liver was cut and placed in 4.5mL of ice-precooled physiological saline, and the homogenate was sufficiently made by a homogenizer to prepare a 10% liver tissue homogenate. The alcohol dehydrogenase test kit and the acetaldehyde dehydrogenase test kit are adopted to measure the activity of the alcohol dehydrogenase and the acetaldehyde dehydrogenase of the liver of the mouse.
TABLE 1 influence of Lactobacillus plantarum CGMCC No.25371 on drunkenness in mice
As can be seen from Table 1, the study on the effect of Lactobacillus plantarum CGMCC No.25371 on drunkenness of mice shows that the strain can reduce drunkenness rate from 83.33% to 66.67%.
TABLE 2 drunkenness treating effect of Lactobacillus plantarum CGMCC No.25371 on mice
M | PC | L30 | |
Latent period of drunk (min) | 19±16 | 20±18 | 30±29 |
Sleep time (min) | 283±42 | 178±70* | 145±84** |
Time to sober up (min) | 302±35 | 197±66* | 175±91** |
As can be seen from the table 2, the research on the drunkenness treatment effect of the lactobacillus plantarum CGMCC No.25371 on mice shows that the bacterium prolongs the drunkenness latent period from 19min to 30min, obviously shortens the sleep time from 283min to 145min, obviously shortens the sobering time, shortens the total time from 302min to 175min, and has the sobering effect superior to that of a sobering medicine set.
TABLE 3 influence of Lactobacillus plantarum CGMCC No.25371 on the concentration of ethanol in serum 2.5h after drinking alcohol
As can be seen from Table 3, the determination of the concentration of ethanol in the serum of 2.5h after the mice are drunk by the Lactobacillus plantarum CGMCC No.25371 shows that the Lactobacillus plantarum reduces the ethanol content in the serum of the mice from 1.86mg/mL to 1.50mg/mL.
TABLE 4 influence of Lactobacillus plantarum CGMCC No.25371 on the activity of alcohol dehydrogenase and acetaldehyde dehydrogenase in the liver 2.5h after drinking alcohol in mice
As can be seen from Table 4, the lactobacillus plantarum CGMCC No.25371 has the advantages that the activity of alcohol dehydrogenase and acetaldehyde dehydrogenase in the liver of a mouse is improved by the lactobacillus plantarum CGMCC No.25371 after drinking wine for 2.5h, and the activity of the acetaldehyde dehydrogenase is obviously improved and is obviously improved from 24.73U/mg to 34.21U/mg.
The pure bacteria obtained in example 1 were subjected to animal experiments to study the hangover alleviating effect of acute alcoholism mice. The bacterium is found to have stronger capacity of relieving alcoholism and sobering up, can reduce the alcoholism rate, obviously shorten the alcoholism time, reduce the ethanol content in serum and improve the activities of alcohol dehydrogenase and acetaldehyde dehydrogenase in liver when being taken one hour before drinking high-concentration white spirit, and has obvious effects of preventing drunkenness and relieving alcoholism and promoting sobering up.
Although the embodiments of the present invention have been disclosed for illustrative purposes, those skilled in the art will appreciate that: various substitutions, alterations and modifications are possible without departing from the spirit and scope of this disclosure and appended claims, and accordingly, the scope of this disclosure is not limited to the embodiments disclosed.
Claims (9)
1. Lactobacillus plantarum (Lactplantibibacillus plantarum) with capacity of dispelling effects of alcohol, and is characterized in that: the lactobacillus plantarum is named as follows: LTJ30, category name: the lactobacillus plantarum has a preservation number of: CGMCC No.25371, preservation date: 22/7/2022, depository: china general microbiological culture Collection center, west Lu No. 1 Hospital No. 3, beijing, chaoyang, the area of the republic of China.
2. A lactobacillus plantarum having anti-hangover capabilities according to claim 1, characterized in that: the lactobacillus plantarum is separated from fermented grains of white spirit and is a dominant strain in the fermented grains.
3. The lactobacillus plantarum capable of alleviating or neutralizing the effect of alcohol according to claim 1, wherein: the bacterial colony and the thallus characteristics of the lactobacillus plantarum are as follows: culturing for 24 hours on an MRS culture medium, wherein the bacterial colony is white, opaque, protruding, moist, flat in edge and glossy, and the diameter of the bacterial colony is 0.8-1.0 mm; observing the cell morphology under an optical microscope, wherein the gram stain shows G + The thallus is in the shape of a small short rod.
4. The lactobacillus plantarum capable of alleviating or neutralizing the effect of alcohol according to claim 1, wherein: the lactobacillus plantarum can produce degradation effect on alcohol after being cultured in the presence of the alcohol.
5. Lactobacillus plantarum having the capacity for neutralizing the effect of alcohol according to any of claims 1 to 4, characterized by: animal experiments prove that the lactobacillus plantarum is capable of reducing the drunkenness rate, remarkably shortening drunkenness time, reducing the ethanol content in serum and improving the activities of ethanol dehydrogenase and acetaldehyde dehydrogenase in liver when being taken in the first hour before high-concentration white spirit is drunk, and has remarkable drunkenness prevention, alcohol effect dispelling and awakening promotion effects.
6. The lactobacillus plantarum capable of alleviating or neutralizing the effect of alcohol according to claim 5, wherein: the high-concentration white spirit is 56% white spirit.
7. Use of lactobacillus plantarum as claimed in any one of claims 1-6 for alleviating hangover.
8. Use of the Lactobacillus plantarum of any one of claims 1-6 in functional food, pharmaceutical products.
9. Use of the lactobacillus plantarum as defined in any one of claims 1-6 for the preparation of a medicament for alleviating hangover.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202211016608.4A CN115322932B (en) | 2022-08-24 | 2022-08-24 | Lactobacillus plantarum with anti-alcohol and sobering-up capabilities and application thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202211016608.4A CN115322932B (en) | 2022-08-24 | 2022-08-24 | Lactobacillus plantarum with anti-alcohol and sobering-up capabilities and application thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
CN115322932A true CN115322932A (en) | 2022-11-11 |
CN115322932B CN115322932B (en) | 2023-11-28 |
Family
ID=83926774
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202211016608.4A Active CN115322932B (en) | 2022-08-24 | 2022-08-24 | Lactobacillus plantarum with anti-alcohol and sobering-up capabilities and application thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN115322932B (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN116622559A (en) * | 2023-05-10 | 2023-08-22 | 江苏新申奥生物科技有限公司 | Lactobacillus casei for producing acetaldehyde dehydrogenase, anti-alcohol probiotic composition and preparation method thereof |
CN117099850A (en) * | 2023-10-24 | 2023-11-24 | 新益(天津)生物科技有限责任公司 | Fermented plant-based yoghourt capable of dispelling effects of alcohol, protecting liver and reducing uric acid as well as preparation method and application thereof |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106867930A (en) * | 2016-12-29 | 2017-06-20 | 大连医科大学 | Lactobacillus plantarum PLH1405 and the application in treatment acute alcoholism medicine is prepared |
CN107760624A (en) * | 2017-11-08 | 2018-03-06 | 南昌大学 | A kind of Lactobacillus plantarum for producing acetaldehyde dehydrogenase and its application |
CN111944712A (en) * | 2020-07-13 | 2020-11-17 | 天津科技大学 | Lactobacillus plantarum with excellent alcohol tolerance and application thereof |
CN112143667A (en) * | 2020-09-07 | 2020-12-29 | 安徽农业大学 | Acid-resistant lactobacillus plantarum with high acetaldehyde dehydrogenase expression and application thereof |
CN114591854A (en) * | 2022-03-07 | 2022-06-07 | 天津小薇生物科技有限公司 | Lactobacillus plantarum LZ026 with function of degrading plant fat and application thereof |
CN114672443A (en) * | 2022-05-07 | 2022-06-28 | 山东百沃生物科技有限公司 | Lactobacillus plantarum with function of preventing or improving facial redness and type I rosacea |
-
2022
- 2022-08-24 CN CN202211016608.4A patent/CN115322932B/en active Active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106867930A (en) * | 2016-12-29 | 2017-06-20 | 大连医科大学 | Lactobacillus plantarum PLH1405 and the application in treatment acute alcoholism medicine is prepared |
CN107760624A (en) * | 2017-11-08 | 2018-03-06 | 南昌大学 | A kind of Lactobacillus plantarum for producing acetaldehyde dehydrogenase and its application |
CN111944712A (en) * | 2020-07-13 | 2020-11-17 | 天津科技大学 | Lactobacillus plantarum with excellent alcohol tolerance and application thereof |
CN112143667A (en) * | 2020-09-07 | 2020-12-29 | 安徽农业大学 | Acid-resistant lactobacillus plantarum with high acetaldehyde dehydrogenase expression and application thereof |
CN114591854A (en) * | 2022-03-07 | 2022-06-07 | 天津小薇生物科技有限公司 | Lactobacillus plantarum LZ026 with function of degrading plant fat and application thereof |
CN114672443A (en) * | 2022-05-07 | 2022-06-28 | 山东百沃生物科技有限公司 | Lactobacillus plantarum with function of preventing or improving facial redness and type I rosacea |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN116622559A (en) * | 2023-05-10 | 2023-08-22 | 江苏新申奥生物科技有限公司 | Lactobacillus casei for producing acetaldehyde dehydrogenase, anti-alcohol probiotic composition and preparation method thereof |
CN116622559B (en) * | 2023-05-10 | 2023-12-01 | 江苏新申奥生物科技有限公司 | Lactobacillus casei for producing acetaldehyde dehydrogenase, anti-alcohol probiotic composition and preparation method thereof |
CN117099850A (en) * | 2023-10-24 | 2023-11-24 | 新益(天津)生物科技有限责任公司 | Fermented plant-based yoghourt capable of dispelling effects of alcohol, protecting liver and reducing uric acid as well as preparation method and application thereof |
CN117099850B (en) * | 2023-10-24 | 2024-03-12 | 新益(天津)生物科技有限责任公司 | Fermented plant-based yoghurt and preparation method and application thereof |
Also Published As
Publication number | Publication date |
---|---|
CN115322932B (en) | 2023-11-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN110835616B (en) | Active substance of lactobacillus paracasei GKS6, composition containing same and application of active substance in promoting longevity | |
CN115322932B (en) | Lactobacillus plantarum with anti-alcohol and sobering-up capabilities and application thereof | |
CN114276967B (en) | Lactobacillus plantarum HL-16 and application thereof | |
CN113755409B (en) | Bifidobacterium longum for relieving insulin resistance and application thereof | |
CN110577912A (en) | lactobacillus gasseri and application thereof in preparing fermented milk | |
CN110833565B (en) | Active substance of lactobacillus plantarum GKM3, composition containing same and application of active substance in promoting longevity | |
CN115287240A (en) | Lactobacillus plantarum with hyperuricemia and gout prevention and treatment effects and application thereof | |
CN102174421A (en) | Glycerol-producing saccharomyces cerevisiae NAU-ZH-GY1 and application thereof | |
US20230364166A1 (en) | Application of postbiotics of inactivated lactobacillus casei iob-p9 in blood glucose reducing | |
CN115895966B (en) | Bifidobacterium bifidum BL002 for assisting in relieving gout and application thereof | |
CN105624071A (en) | Lactobacillus salivarius XJP2 and application thereof | |
CN113439838B (en) | Fermentation method, fermentation product and kit containing fermentation product | |
CN114836349A (en) | Lactobacillus acidophilus LA16 for antagonizing helicobacter pylori and application thereof | |
CN111154694A (en) | Microbial fermentation inoculant and preparation method and application thereof | |
CN111961602A (en) | Saccharomyces cerevisiae and application thereof in feed for lactating calves | |
CN116376770B (en) | Application of lactobacillus rhamnosus RH0121 in preparation of hypoglycemic products | |
CN116622559B (en) | Lactobacillus casei for producing acetaldehyde dehydrogenase, anti-alcohol probiotic composition and preparation method thereof | |
CN116622593B (en) | Lactobacillus paracasei for fermentation and fermentation process for preparing wind-resistant acid-discharging ferment by same | |
CN117511825B (en) | Application of segment fermentation inoculant of Wittman coagulans IOB502 in alcoholic liver injury | |
CN117264850B (en) | Pediococcus pentosaceus SW006 with auxiliary treatment of colpitis and immunity enhancing functions and application thereof | |
CN114591863B (en) | Tibetan pig source fungicide combination for improving growth performance and immune function of weaned piglets | |
CN116970536A (en) | Pediococcus pentosaceus with uric acid reducing function and metaplasia and application thereof | |
CN115478028A (en) | Lactobacillus acidophilus F02 and preparation prepared by same and application thereof | |
CN117568201A (en) | Lactobacillus rhamnosus YFA-012 with high tolerance and application thereof | |
CN115997860A (en) | Microecological preparation for improving intestinal health of dogs as well as preparation method and application thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |