CN110982737A - Biofilm lactic acid bacteria agent for dogs and preparation method thereof - Google Patents

Biofilm lactic acid bacteria agent for dogs and preparation method thereof Download PDF

Info

Publication number
CN110982737A
CN110982737A CN201911219339.XA CN201911219339A CN110982737A CN 110982737 A CN110982737 A CN 110982737A CN 201911219339 A CN201911219339 A CN 201911219339A CN 110982737 A CN110982737 A CN 110982737A
Authority
CN
China
Prior art keywords
dogs
lactic acid
acid bacteria
biofilm
preparation
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.)
Pending
Application number
CN201911219339.XA
Other languages
Chinese (zh)
Inventor
陈则东
朱建平
刘蕾
马艳梅
卢炜
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Jiangsu Agri Animal Husbandry Vocational College
Original Assignee
Jiangsu Agri Animal Husbandry Vocational College
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Jiangsu Agri Animal Husbandry Vocational College filed Critical Jiangsu Agri Animal Husbandry Vocational College
Priority to CN201911219339.XA priority Critical patent/CN110982737A/en
Publication of CN110982737A publication Critical patent/CN110982737A/en
Pending legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N1/00Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
    • C12N1/20Bacteria; Culture media therefor
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23KFODDER
    • A23K10/00Animal feeding-stuffs
    • A23K10/10Animal feeding-stuffs obtained by microbiological or biochemical processes
    • A23K10/16Addition of microorganisms or extracts thereof, e.g. single-cell proteins, to feeding-stuff compositions
    • A23K10/18Addition of microorganisms or extracts thereof, e.g. single-cell proteins, to feeding-stuff compositions of live microorganisms
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23KFODDER
    • A23K50/00Feeding-stuffs specially adapted for particular animals
    • A23K50/40Feeding-stuffs specially adapted for particular animals for carnivorous animals, e.g. cats or dogs
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2400/00Lactic or propionic acid bacteria
    • A23V2400/11Lactobacillus

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Microbiology (AREA)
  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
  • Zoology (AREA)
  • Biotechnology (AREA)
  • Animal Husbandry (AREA)
  • Food Science & Technology (AREA)
  • Genetics & Genomics (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Wood Science & Technology (AREA)
  • Biomedical Technology (AREA)
  • Biochemistry (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Engineering & Computer Science (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Birds (AREA)
  • Medicinal Chemistry (AREA)
  • Virology (AREA)
  • Molecular Biology (AREA)
  • Physiology (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Fodder In General (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)

Abstract

The invention relates to the technical field of lactic acid bacteria, in particular to a biofilm-state lactic acid bacteria agent for dogs and a preparation method thereof, wherein the preparation method comprises the following steps: inoculating lactobacillus into an improved MRS culture medium for activated culture, transferring the culture solution, flatly spreading the culture solution into a cell culture plate, and standing for culture to obtain an enveloped bacterial solution; and preparing the tunica membranaceus bacterial liquid into a biofilm-state lactic acid bacteria agent for dogs. The film-coated lactic acid bacteria agent prepared by the preparation method can obviously improve the average daily gain of dogs, reduce the material-weight ratio and have obvious regulation effect on canine intestinal flora.

Description

Biofilm lactic acid bacteria agent for dogs and preparation method thereof
Technical Field
The invention relates to the technical field of lactic acid bacteria, in particular to a biofilm-state lactic acid bacteria agent for dogs and a preparation method thereof.
Background
Dogs are one of the earliest domesticated animals and are currently the most prevalent companion animals in the world. The scale of feeding is extremely large worldwide. Such mass raising is due to great value of dogs, such as high intellectual level, social behavior, more developed sense organs than human, playing various roles in human society, often trained as working dogs, etc. Thus, the health of dogs is receiving increasing attention.
The health of canines is largely dependent on their gastrointestinal microorganisms, the composition and activity of their gut microflora being associated with several diseases. This microbial ecosystem plays a role in a variety of aspects, such as influencing the absorption and metabolism of nutrients, the nutrition and the protective function of the host. Any disturbance of the gastrointestinal flora may lead to the development of a number of diseases, such as diarrhoea, allergy, obesity and stress syndrome. Different treatments are being developed in order to balance the flora structure and to combat infections, among which probiotic therapy is of great interest.
Biofilm refers to a mass of bacterial biofilm-like material formed by bacteria adhering to a contact surface, secreting polysaccharide matrices, fibrin, lipoprotein, etc., and wrapping themselves around them. Microorganisms in the natural state often live in the form of a biofilm state, and have the advantages which are incomparable with the traditional culture state. At present, research on harmful microbial biofilms is more, research on probiotics, particularly lactobacillus biofilms is very rare, the probiotics and lactobacillus biofilms are suitable for dogs, average daily gain of dogs can be effectively improved, and no biofilm with an obvious regulation effect on canine intestinal flora is reported.
Disclosure of Invention
In view of the above, the present invention aims to provide a biofilm lactic acid bacterial agent for dogs and a preparation method thereof. The biomembrane state lactic acid bacteria agent provided by the invention can effectively improve the average daily gain of dogs and has an obvious regulation effect on canine intestinal flora.
In order to achieve the above purpose, the invention provides the following technical scheme:
the invention provides a preparation method of a biofilm lactic acid bacteria agent for dogs, which comprises the following steps:
inoculating lactobacillus into an improved MRS culture medium for activated culture, transferring the culture solution, flatly spreading the culture solution into a cell culture plate, and standing for culture to obtain an enveloped bacterial solution; preparing the tunicate bacteria liquid into a biofilm lactic acid bacteria agent for dogs;
the improved MRS culture medium comprises a liquid improved MRS culture medium and a solid improved MRS culture medium, wherein the liquid improved MRS culture medium comprises the following components: 10g/L of peptone, 5g/L of yeast extract, 2g/L of diammonium citrate, 20g/L of glucose and MgSO4·7H20.58g/L of O, 10g/L of beef extract and K2HPO4·3H2O2 g/L, sodium acetate 5g/L, Tween 801 g/L, MnSO4·4H2O0.25 g/L, 0.1-1% signal factor AI-2; the solid modified MRS culture medium consists of the components and agar of 16 g/L.
In some embodiments, the Lactobacillus is Lactobacillus plantarum LR-1.
In some embodiments, the liquid modified MRS medium consists of: 10g/L of peptone, 5g/L of yeast extract, 2g/L of diammonium citrate, 20g/L of glucose and MgSO4·7H20.58g/L of O, 10g/L of beef extract and K2HPO4·3H2O2 g/L, sodium acetate 5g/L, Tween 801 g/L, MnSO4·4H2O0.25 g/L, 0.5% signal factor AI-2; the solid modified MRS culture medium consists of the components and agar of 16 g/L.
In some embodiments, the activated culture is specifically that lactobacillus is inoculated in a solid modified MRS culture medium for streak culture, and then a single colony is taken to be cultured in a liquid modified MRS culture medium.
In some embodiments, the streaking culture is a three-zone streaking culture.
In some embodiments, the transferring is specifically: and adding the liquid modified MRS culture medium into the culture solution according to the volume ratio of 1: 100.
In some embodiments, the temperature of the static culture is 30-37 ℃, and the static culture is carried out until the viable count is more than or equal to 1 × 108CFU/mL. In some embodiments, the temperature of the static culture is 30 ℃, and the static culture is carried out until the viable count is 1 × 108CFU/mL。
In some embodiments, the preparation of the biofilm bacteria solution into the biofilm lactic acid bacteria agent for dogs specifically comprises: and (3) taking the membrane-state bacterium liquid, and performing refrigerated centrifugation, enrichment, heavy suspension and freeze drying to obtain the biofilm-state lactic acid bacteria agent for dogs.
Further, the temperature of the freezing centrifugation is 4-8 ℃, the time is 5-10 min, and the rotating speed is 4000-6000 g. In some embodiments, the temperature of the refrigerated centrifugation is 4 ℃, the time is 5min, and the rotation speed is 5000 g.
In some embodiments, the resuspension is performed with skim milk powder. In some embodiments, the volume ratio of the skim milk powder to the enriched liquid in the enveloped state is 1: 10. In some embodiments, the number of viable bacteria after resuspension is greater than or equal to 1X 109CFU/mL. In some embodiments, the number of viable bacteria after resuspension is 1X 109CFU/mL。
In some embodiments, the temperature of the freeze drying is-80 ℃, and the time of the freeze drying is 36-48 h.
The invention also provides the biofilm state lactic acid bacteria agent for dogs prepared by the preparation method.
In some specific embodiments, the formulation of the biofilm lactic acid bacteria agent for dogs is freeze-dried powder.
The invention provides a dog biofilm lactic acid bacteria agent and a preparation method thereof, wherein the preparation method of the dog biofilm lactic acid bacteria agent comprises the following steps: inoculating lactobacillus into a solid modified MRS culture medium for streak culture, taking a single colony to culture in a liquid modified MRS culture medium, and then transferring and spreading a culture solution into a cell culture plate for standing culture to obtain an enveloped bacterial solution; and (3) taking the membrane-state bacteria liquid for freezing and centrifuging, enriching, resuspending and freeze-drying to obtain the biological membrane-state lactic acid bacteria agent for dogs. The invention adopts a specific process combined with an improved MRS culture medium to culture the lactobacillus, and the prepared tunica mucosa lactic acid bacteria agent can obviously improve the average daily gain of dogs, reduce the material-weight ratio and have obvious regulation effect on canine intestinal flora
Drawings
In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings used in the description of the embodiments or the prior art will be briefly described below.
FIG. 1 shows canine blood IgG content in example 3;
FIG. 2 shows canine blood sIgA in example 3;
FIG. 3 shows the blood IL-6 levels in dogs of example 3;
FIG. 4 shows the canine blood TNF- α levels in example 3;
FIG. 5 shows the blood SOD levels in dogs according to example 3;
FIG. 6 shows the malondialdehyde content in blood of dogs in example 3;
FIG. 7 shows the performance of the canine fecal microflora at the phylum level in example 4;
FIG. 8 shows the performance of the canine fecal microbiota at class level in example 4;
FIG. 9 shows the behavior of the canine fecal microbial flora at the genus level in example 4.
Detailed Description
The invention discloses a biofilm lactic acid bacteria agent for dogs and a preparation method thereof, and a person skilled in the art can use the content for reference and appropriately improve process parameters to realize the purpose. It is expressly intended that all such similar substitutes and modifications which would be obvious to one skilled in the art are deemed to be included in the invention. While the methods and applications of this invention have been described in terms of preferred embodiments, it will be apparent to those of ordinary skill in the art that variations and modifications in the methods and applications described herein, as well as other suitable variations and combinations, may be made to implement and use the techniques of this invention without departing from the spirit and scope of the invention.
The description of the disclosed embodiments is provided to enable any person skilled in the art to make or use the present invention. Various modifications to these embodiments will be readily apparent to those skilled in the art, and the generic principles defined herein may be applied to other embodiments without departing from the spirit or scope of the invention. Thus, the present invention is not intended to be limited to the embodiments shown herein but is to be accorded the widest scope consistent with the principles and novel features disclosed herein.
The invention is further illustrated by the following examples:
EXAMPLE 1 Lactobacillus plantarum LR-1 activation and preparation of biofilm-State lyophilized powder
Preparing a liquid modified MRS culture medium, a solid modified MRS culture medium and 0.85% of normal saline, sterilizing corresponding articles, drying and sterilizing an aseptic operation table.
The liquid modified MRS culture medium consists of the following components: 10g/L of peptone, 5g/L of yeast extract, 2g/L of diammonium citrate, 20g/L of glucose and MgSO4·7H20.58g/L of O, 10g/L of beef extract and K2HPO4·3H2O2 g/L, sodium acetate 5g/L, Tween 801 g/L, MnSO4·4H2O0.25 g/L, 0.5% signal factor AI-2; the solid modified MRS culture medium consists of the components and agar of 16 g/L.
Activated Lactobacillus plantarum LR-1: taking Lactobacillus plantarum LR-1 from a glycerol tube a little, standing and culturing at 30 ℃ until a single colony grows out, selecting the single colony in a liquid modified MRS culture medium, standing and culturing at 30 ℃ for 24h, then transferring the single colony with the liquid modified MRS culture medium according to the volume ratio of 1:100, and spreading the single colony in a cell culture plate, standing and culturing at 30 ℃ until the viable count reaches 108CFU/mL, biofilm formation.
Collecting 10mL of the bacterial liquid, centrifuging at 4 ℃ for 5min at 5000g, discarding the supernatant, washing with sterile physiological saline once, centrifuging to collect bacterial sludge, suspending in 1mL of sterile skim milk, placing in a sterile penicillin bottle, and sealing with sterile gauze. Placing the penicillin bottle containing the bacterial liquid and a vacuum freeze dryer tray together in a refrigerator at the temperature of 80 ℃ below zero for pre-freezing for 2 to 3 hours, and then placing the penicillin bottle and the vacuum freeze dryer tray into a vacuum freeze dryer for freeze drying for 36 hours to obtain bacterial powder, namely the biofilm peptide lactic acid bacteria agent.
Example 2 Effect of the biofilm-state lactic acid bacteria agent of the present invention on body weight and digestibility
1. Feeding with lactobacillus
Lactic acid prepared in example 1The microbial inoculum is diluted by 1mL of sterile normal saline, and the total bacterial count is 109CFU/mL, the total volume is 1mL, a 4-month-old beagle dog is fed by adopting an injector, 5 dogs in a control group, a floating state treatment group and a capsule state treatment group respectively and a floating state treatment group are adopted, and the preparation method of the floating state is as follows: inoculating lactobacillus into a solid modified MRS culture medium for streak culture, taking a single colony to culture in a liquid modified MRS culture medium, transferring a culture solution into a test tube, and performing shake culture at 30-37 ℃ until the viable count is at least 108CFU/mL to obtain planktonic bacteria liquid; taking the floating state bacterial liquid for refrigerated centrifugation, enrichment, heavy suspension and freeze drying until the viable count is at least 109CFU/mL, which is the planktonic lactic acid bacteria agent for dogs. The control group was fed the same volume of sterile normal saline.
2. Body weight determination
The body weights of the tested dogs are detected and recorded, and the average daily gain and the material weight ratio are calculated, and the results are shown in table 1.
TABLE 1
Figure BDA0002300372580000051
Note: the different letters of the shoulder marks in the same row show significant differences (P < 0.05).
From the results in table 1, it can be seen that the modal treated group of the invention significantly increased the average daily gain of dogs (P <0.05) and significantly decreased the feed-to-weight ratio (P <0.05) compared to the control group and the planktonic treated group.
3. Determination of digestibility
Dog faeces of the control and test groups were collected at 50g per sample and 7 items of moisture, crude protein, crude fat, crude fibre, calcium, total phosphorus and ash were measured separately and the total raw composition of the feed was compared to calculate the digestibility of 6 of these items as shown in table 2.
TABLE 2
Figure BDA0002300372580000061
Note: the shoulder marks in the same row show significant differences (P <0.05) in different lower case letters, and show significant differences (P < 0.01) in different upper case letters.
As can be seen from Table 2, the biofilm freeze-dried lactic acid bacteria for dogs can remarkably improve the digestibility of crude protein, crude fat, crude fiber and total phosphorus, and has a remarkable difference (P is less than 0.05) compared with the planktonic treatment group; significant difference in crude protein digestibility compared to the control group (P < 0.05); the total phosphorus digestibility of the fat, the fiber and the phosphorus were significantly different from that of the control group (P < 0.05).
Example 3 Effect of the biofilm lactic acid bacteria agent of the present invention on blood indices
1. Feeding with lactobacillus
The same procedure as in example 2 was used for feeding the lactic acid bacteria.
2. Blood index measurement
ELISA kit is used for detecting the content of IgG, sIgA, IL-6 and TNF- α in the canine serum, and biochemical index detection kit is used for detecting the content of SOD and malondialdehyde.
The results are shown in FIGS. 1 to 6, which indicate that the mean IgG content of the treated group was increased.
Example 4 microbial diversity in feces after dogs received biofilm lactic acid bacteria
1. Feeding with lactobacillus
The same procedure as in example 2 was used for feeding the lactic acid bacteria.
2. Feces collection
Feces were collected at 28 days after feeding, 50g of each sample, and frozen in liquid nitrogen.
3. Genome extraction and library construction
And extracting a genome of the collected sample, constructing a library of the qualified sample for detection, performing cluster preparation and sequencing on the qualified library, and performing corresponding biological information analysis on data obtained by off-machine analysis.
4. Data analysis
The data of the off-line terminal is filtered to remove low-quality reads and leave high-quality Clean data; sample species complex analysis as well as inter-group species difference analysis were performed based on OUT and species annotation results. Diversity was determined based on the sequence of the 16SrDNA variable region. The results are shown in FIGS. 7 to 9. As can be seen from the graphs in FIGS. 7 to 9, the microbial diversity in the dog feces of the membrane-state treated group is remarkably changed, wherein the content of lactobacillus is remarkably increased, which indicates that the lactobacillus of the membrane-state treated group has more field planting numbers, and thus the membrane-state treated group has a better regulation effect on dog intestinal flora.
The foregoing is only a preferred embodiment of the present invention, and it should be noted that, for those skilled in the art, various modifications and decorations can be made without departing from the principle of the present invention, and these modifications and decorations should also be regarded as the protection scope of the present invention.

Claims (10)

1. A preparation method of a biofilm lactic acid bacteria agent for dogs is characterized by comprising the following steps:
inoculating lactobacillus into an improved MRS culture medium for activated culture, transferring the culture solution, flatly spreading the culture solution into a cell culture plate, and standing for culture to obtain an enveloped bacterial solution; preparing the tunicate bacteria liquid into a biofilm lactic acid bacteria agent for dogs;
the improved MRS culture medium comprises a liquid improved MRS culture medium and a solid improved MRS culture medium, wherein the liquid improved MRS culture medium comprises the following components: 10g/L of peptone, 5g/L of yeast extract, 2g/L of diammonium citrate, 20g/L of glucose and MgSO4·7H20.58g/L of O, 10g/L of beef extract and K2HPO4·3H2O2 g/L, sodium acetate 5g/L, Tween 801 g/L, MnSO4·4H2O0.25 g/L, 0.1-1% signal factor AI-2; the solid modified MRS culture medium consists of the components and agar of 16 g/L.
2. The method according to claim 1, wherein the lactobacillus is Lactobacillus plantarum LR-1.
3. The preparation method according to claim 1, wherein the liquid MRS medium consists of the following components: 10g/L of peptone, 5g/L of yeast extract and 2g of diammonium citrateL, glucose 20g/L, MgSO4·7H20.58g/L of O, 10g/L of beef extract and K2HPO4·3H2O2 g/L, sodium acetate 5g/L, Tween 801 g/L, MnSO4·4H2O0.25 g/L, 0.1-1% signal factor AI-2; the solid modified MRS culture medium consists of the components and agar of 16 g/L.
4. The preparation method according to claim 1, wherein the activated culture is specifically that lactobacillus is inoculated in a solid modified MRS culture medium for streak culture, and then a single colony is taken to be cultured in a liquid modified MRS culture medium.
5. The preparation method according to claim 1, wherein the switching is specifically to add the liquid modified MRS medium to the culture solution according to a volume ratio of 1: 100.
6. The method according to claim 1, wherein the temperature of the static culture is 30 to 37 ℃ and the static culture is carried out until the viable count is not less than 1X 108CFU/mL。
7. The preparation method according to claim 1, wherein the preparation of the tunicates into the biofilm-state lactic acid bacteria for dogs specifically comprises: and (3) taking the membrane-state bacterium liquid, and performing refrigerated centrifugation, enrichment, heavy suspension and freeze drying to obtain the biofilm-state lactic acid bacteria agent for dogs.
8. The preparation method according to claim 7, wherein the temperature of the refrigerated centrifugation is 4-8 ℃, the time is 5-10 min, and the rotating speed is 4000-6000 g; the number of the live bacteria after heavy suspension is more than or equal to 1 multiplied by 109CFU/mL; the temperature of the freeze drying is-80 ℃, and the time is 36-48 h.
9. Biofilm-state lactic acid bacteria agent for dogs prepared by the preparation method as described in any one of claims 1 to 8.
10. The biofilm lactic acid bacteria agent for dogs as claimed in claim 9, wherein the dosage form of the biofilm lactic acid bacteria agent for dogs is freeze-dried powder.
CN201911219339.XA 2019-12-03 2019-12-03 Biofilm lactic acid bacteria agent for dogs and preparation method thereof Pending CN110982737A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201911219339.XA CN110982737A (en) 2019-12-03 2019-12-03 Biofilm lactic acid bacteria agent for dogs and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201911219339.XA CN110982737A (en) 2019-12-03 2019-12-03 Biofilm lactic acid bacteria agent for dogs and preparation method thereof

Publications (1)

Publication Number Publication Date
CN110982737A true CN110982737A (en) 2020-04-10

Family

ID=70089673

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201911219339.XA Pending CN110982737A (en) 2019-12-03 2019-12-03 Biofilm lactic acid bacteria agent for dogs and preparation method thereof

Country Status (1)

Country Link
CN (1) CN110982737A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113632762A (en) * 2021-07-06 2021-11-12 云南农业大学 Method for improving working performance of Kunming dog puppy by using fecal strain transplantation

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105624097A (en) * 2016-03-16 2016-06-01 中国农业大学 Application of AI-2 in improving bacteria acid resistance and/or oxygen resistance and method for improving bacteria acid resistance and/or oxygen resistance
CN109517764A (en) * 2019-01-10 2019-03-26 西华大学 A kind of biofilm state lactobacillus-fermented microbial inoculum and preparation method thereof
CN110193030A (en) * 2019-04-29 2019-09-03 山东苏柯汉生物工程股份有限公司 A kind of dog probiotics and preparation method thereof
CN110507673A (en) * 2019-09-17 2019-11-29 江苏农牧科技职业学院 A kind of dog is with lactic acid bacteria and signaling molecule combination preparation and preparation method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105624097A (en) * 2016-03-16 2016-06-01 中国农业大学 Application of AI-2 in improving bacteria acid resistance and/or oxygen resistance and method for improving bacteria acid resistance and/or oxygen resistance
CN109517764A (en) * 2019-01-10 2019-03-26 西华大学 A kind of biofilm state lactobacillus-fermented microbial inoculum and preparation method thereof
CN110193030A (en) * 2019-04-29 2019-09-03 山东苏柯汉生物工程股份有限公司 A kind of dog probiotics and preparation method thereof
CN110507673A (en) * 2019-09-17 2019-11-29 江苏农牧科技职业学院 A kind of dog is with lactic acid bacteria and signaling molecule combination preparation and preparation method thereof

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
刘蕾等: "tuf基因同源超表达对植物乳杆菌LR-1生理行为的影响", 《食品科学》 *
刘蕾等: "基于AI-2介导的类植物乳杆菌生物被膜态与浮游态抗胁迫能力比较与分析", 《食品科学》 *
刘蕾等: "类植物乳杆菌L-ZS9生物被膜态的黏附能力及形成影响因素", 《食品科学》 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113632762A (en) * 2021-07-06 2021-11-12 云南农业大学 Method for improving working performance of Kunming dog puppy by using fecal strain transplantation

Similar Documents

Publication Publication Date Title
CN111235070B (en) Breast milk infant source lactobacillus plantarum BF _15 and application thereof
CN102533618B (en) Lactobacillus plantarum CCFM8724 and application thereof
CN102747003B (en) Screening and application of probiotic Enterococcus faecium
CN1186440C (en) New bifidobacteria preventing diarrhea caused by pathogenic bacteria
CN113088463B (en) Lactobacillus acidophilus with probiotic characteristics and application thereof
CN112195139B (en) Lactobacillus plantarum strain LDVS007 and application thereof
CN109481476B (en) Application of lactobacillus fermentum CQPC04 in preparing food or medicine for improving ulcerative colitis
CN108384735A (en) Lactobacillus plantarum CCFM1019, its fermented food and its application in medicine preparation
CN112094790B (en) Lactobacillus plantarum LP45 live bacterium preparation for regulating intestinal flora and application thereof
CN103911306B (en) Lactobacillus gasseri bacterial strain and application thereof
CN103911305B (en) Lactobacillus crispatus bacterial strain and uses thereof
CN103911309B (en) Lactobacillus gasseri bacterial strain and application thereof
CN103911308A (en) Lactobacillus crispatus strain and its uses
CN112239739B (en) Lactobacillus plantarum capable of relieving ETEC (enterotoxigenic enterobacteria) induced diarrhea and application thereof
CN108018248B (en) Lactobacillus casei capable of regulating flora structural disorder caused by antibiotics
CN112574924B (en) Bacillus subtilis strain, microecological preparation and application thereof
CN109652334A (en) A kind of complex microbial inoculum and its preparation method and application
CN103911307B (en) Lactobacillus crispatus bacterial strain and uses thereof
CN110982737A (en) Biofilm lactic acid bacteria agent for dogs and preparation method thereof
CN114908009B (en) Lactobacillus mucilaginosus PR63 and application thereof
CN112538441B (en) Lactobacillus reuteri CCFM1144 for relieving diarrhea caused by ETEC and application thereof
CN109619183B (en) Application of lactobacillus plantarum CQPC03 in preparation of medicine for preventing oxidative damage of liver
JP2017012163A (en) Lactobacillus plantarum llp5193 with high acid- and bile-resistance and high cell attaching ability and products containing it as the effective ingredient
CN104694441A (en) Lactobacillus plantarum suitable for being made into freeze-dried powder
CN116694503B (en) Lactobacillus plantarum Lp-HZ55 with bowel relaxing and immunity improving functions

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