CN107028988A - Applications of the Lactobacillus plantarum YS1 in the food or medicine of prevention ulcerative colitis is prepared - Google Patents
Applications of the Lactobacillus plantarum YS1 in the food or medicine of prevention ulcerative colitis is prepared Download PDFInfo
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Classifications
-
- 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
- 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
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- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Medicinal Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Molecular Biology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
It is CCTCC NO the invention discloses deposit number:Applications of the M2016747 Lactobacillus plantarum YS1 (Lactobacillus plantarum YS1) in the food or medicine of prevention ulcerative colitis is prepared, not only expand Lactobacillus plantarum YS1 application, its application value is improved, and new hope is brought to the treatment or health care of ulcerative colitis.
Description
Technical field
The invention belongs to technical field of microbe application, it is related to a kind of Lactobacillus plantarum answering in food or medicine is prepared
With.
Background technology
Yak yogurt is a kind of spontaneous fermentation dairy products in Qinghai-Tibet Tibetan area, contains abundant nutritional ingredient, tool
There are anti-oxidant, reduction cholesterol, regulation immunity.Due to special spontaneous fermentation condition, including fermentation raw material breast, hair
Ferment temperature, fermentation time, fermentation vessel, particularly special fermentative microorganism composition, cause yak yogurt to have flavour
And quality.
Human ulcerative colitis is a kind of IBD of 2 type helper T lymphocyte (Th2) mediation, its cause of disease and hair
Interpretation of the cause, onset and process of an illness system is unclear, and therapeutic advance is slow and lacks specificity.The colitis of azolactone induction is a kind of Th2 of IL-4 mediations
Type inflammation, its histologic characteristics and inflammation are distributed similar human ulcerative colitis, the mouse Colon induced by Ci , azolactones
Scorching model can study and assess curative effect of medication or functional food physiological activity as Ulcerative Colitis
Beneficial instrument.
The content of the invention
It is an object of the invention to the mouse colitis model of Tong Guo azolactones induction, investigation is separated from yak yogurt
The Lactobacillus plantarum YS1 arrived is to the preventive effect of ulcerative colitis, to research and develop the food that can prevent ulcerative colitis
Or medicine.
Through research, the present invention provides following technical scheme:
Deposit number is CCTCC NO:M2016747 Lactobacillus plantarum YS1 (Lactobacillus plantarum
YS1) the application in the food or medicine of prevention ulcerative colitis is prepared.
Lactobacillus plantarum YS1 (Lactobacillus plantarum YS1) is the yak from Yushu district, Qinghai Tibetan autonomous prefecture
It is isolated in ox yogurt, it is preserved in China typical culture collection center (abbreviation CCTCC, address on December 14th, 2016:
No. 299 Wuhan Universitys of Wuhan City, Hubei Province Wuchang District Bayi Road), deposit number is CCTCC NO:M2016747.
After Shi azolactones induction BALB/c mouse colitis of the present invention, by determining, serum is related in colon to be referred to
Mark detection Lactobacillus plantarum YS1 colitis preventive effect.Experimental result shows that Lactobacillus plantarum YS1 can significantly reduce colon
The disease activity index (Disease activity index, DAI) of scorching mouse, suppresses the colon lengths contracting that colitis is caused
It is short, improve colon weight/colon lengths ratio;Can significantly reduce colitis mice colon myeloperoxidase (MPO),
NO, MDA content and raising GSH contents;IL-2 levels and reduction IL-10 water in colitis mice serum can also be significantly improved
It is flat.RT-PCR experimental results show that Lactobacillus plantarum YS1 can significantly raise nervous system type NOS in colitis mice colon
(nNOS), endothelium in type NOS (eNOS), c-Kit, SCF mRNA are expressed, and downward induces type NOS (iNOS), IL-8, CXCR2mRNA
Expression.As can be seen here, the mouse colitis of Lactobacillus plantarum YS1 Dui azolactones induction has good preventive effect, can be used for
Prepare the food or medicine of prevention ulcerative colitis.
The beneficial effects of the present invention are:Prevention ulcerative colitis is being prepared the invention provides Lactobacillus plantarum YS1
Food or medicine in application, not only expand Lactobacillus plantarum YS1 application, improve its application value, and
Treatment or health care to ulcerative colitis bring new hope.
Brief description of the drawings
Fig. 1 is the agarose gel electrophoresis figure of Lactobacillus plantarum YS1 genomic DNA, and wherein M is λ DNA/Hind III
Marker, 1 is Lactobacillus plantarum YS1 genomic DNA.
Fig. 2 is Lactobacillus plantarum YS1 16S rDNA genetic fragment PCR amplifications, and wherein M is that DNA Marker, C are
Negative control, 1 is Lactobacillus plantarum YS1 16S rDNA genetic fragment pcr amplification products.
Fig. 3 is the influence that Lactobacillus plantarum YS1 is expressed mouse Colon tissue nNOS, eNOS and iNOS mRNA.
Fig. 4 is the influence that Lactobacillus plantarum YS1 is expressed mouse Colon tissue c-Kit and SCF mRNA.
Fig. 5 is the influence that Lactobacillus plantarum YS1 is expressed mouse Colon tissue IL-8 and CXCR2mRNA.
Fig. 3 is into Fig. 5, and LB represents lactobacillus bulgaricus, and LP-YS1 represents Lactobacillus plantarum YS1.
Embodiment
In order that the object, technical solutions and advantages of the present invention are clearer, below in conjunction with accompanying drawing to the excellent of the present invention
Embodiment is selected to be described in detail.
The separation and identification of embodiment 1, Lactobacillus plantarum YS1
First, lactic acid bacteria isolates and purifies
Pick up from 10 parts of the spontaneous fermentation yak yogurt sample of Yushu district, Qinghai Tibetan autonomous prefecture herdsman family, every part of sample nothing
After bacterium glass rod is fully stirred evenly, draw 50mL and be put into sterile centrifugation tube, be placed in food sampling box, take back laboratory, 4 DEG C of refrigerators
Preserve.
Every part of yak yogurt sample takes 1mL, and 10 times of gradient dilutions are made to 10 with sterile saline-7.Take 10-5、10-6、
10-7Each 1mL dilutions of three dilution factors respectively at equipped with 15mLMRS culture mediums (containing mass ratio be 5% CaCO3) plate
In, mix, put 30 DEG C of 72 ± 3h of insulating box culture.Each three, dilution factor work is parallel.After bacterium colony is formed, its form is observed special
Levy, the different bacterium colonies that picking has molten calcium circle are inoculated in degreasing milk medium respectively, put 30 DEG C of 24~48h of culture, treat that bacterial strain is given birth to
After length is good, streak inoculation puts 30 DEG C of culture 48h in MRS agar mediums;Above step is repeated at least three times, until obtaining
Pure bacterium colony.
2nd, the identification of Bacillus acidi lactici
Pure bacterial strain is rule on MRS solid mediums, 30 DEG C of culture 48h are put, with 10 times of amplification sem observation bacterium colony sizes,
The appearance features such as shape, carry out Gram's staining, and the typical bacterial strain of picking form carries out catalase test.By gram sun
Property, the negative meningitidis strains and bacillus strain of catalase test, fix tentatively as lactic acid bacteria.
Lactic acid bacillus mycopremna is carried out to growth temperature experiment (10 DEG C, 45 DEG C, 60 DEG C, 30min), the examination of pH value gradient respectively
Test, mobility test, catalase test, oxidase test, hydrogen sulfide production test, gelatin liquefaction experiment, nitrate reduction test, Yin
Diindyl experiment, the experiment of glucose aerogenesis, benzidine test, litmus milk tests, arginine production ammonia test, casein decomposition run and
Various sugar alcohol fermentation tests etc..
As a result isolated from 10 parts of yak yogurt samples and be purified into 20 plants of Bacillus acidi lacticis, be Gram-positive,
Catalase test is negative.By morphological observation and physiological and biochemical test, this 20 plants of bacterial strains are initially identified as 7 kinds of lactic acid
Bacillus, number consecutively is Lb1~Lb7, wherein, numbering is Lb4 Bacillus acidi lactici is initially identified as Lactobacillus plantarum
(Lactobacillus plantarum) (table 1).
The numbering of table 1 is LbThe morphological feature and physiological and biochemical test result of 4 Bacillus acidi lactici
Note:+, it is positive;-, it is negative;+ w, weakly positive.
3rd, the identification of Lactobacillus plantarum
It is L to take numberingbSupernatant is abandoned in the bacteria suspension of 4 Bacillus acidi lactici Liquid Culture, centrifugation, thalline is collected, according to bacterium base
Because a group DNA extraction kit (Beijing Suo Laibao scientific & technical corporation) methods described extracts genomic DNA, enter row agarose gel electrophoresis
(gel mass concentration ratio 0.8%, voltage 80V, electrophoresis 80min), after GelRed nucleic acid staining dyes, in gel imaging system
Middle observation (Fig. 1).The genomic DNA of extraction is diluted 200 times, concentration purity testing is carried out with ultraviolet specrophotometer.Using
Primer 2 7F:5 '-AGAGTTTGATCCTGGCTCAG-3 ' (SEQ ID No.1) and 1492R:5’-
GGCTACCTTGTTACGACTT-3 ' (SEQ ID No.2) enters performing PCR amplification (Fig. 2), amplification production to 16S rDNA genetic fragments
Thing is sequenced by Sangon Biotech (Shanghai) Co., Ltd. and Beijing Liuhe Huada Genomics Technology Co., Ltd, and will
Sequencing result (SEQ ID No.3) is compared with correlated series in Genbank.As a result show, numbering is Lb4 Bacillus acidi lactici
The similitude of 16S rDNA gene fragment orders and Lactobacillus plantarum strain NBRC 15891 reach
99%.
Therefore, numbering is Lb4 Bacillus acidi lactici is accredited as Lactobacillus plantarum (Lactobacillus plantarum), will
It is named as YS1, and is preserved in China typical culture collection center (abbreviation CCTCC, address on December 14th, 2016:Lake
No. 299 Wuhan Universitys of Bayi Road of Bei Sheng wuchang, wuhan area), deposit number is CCTCC NO:M2016747.
The prevention effect of embodiment 2, Lactobacillus plantarum YS1 Dui azolactone inducing mouse colitis
Main material, instrument and the experimental animal that the present embodiment is used are as follows:Lactobacillus plantarum YS1 (preserving numbers:CCTCC
NO:M2016747), lactobacillus bulgaricus (Chinese industrial Microbiological Culture Collection administrative center);Azolactone (U.S. Sigma
Company);MPO, NO, GSH, MDA, SOD determine kit (Bioengineering Research Institute is built up in Nanjing);IL-2, IL-10 serum cell
Factor determination kit (BioLegend companies of the U.S.);Trizol reagents, OligodT18, RNase, dNTP, MLV reverse transcriptase
(Invitrogen companies of the U.S.);(Japanese TAKARA is public by ROX reference Dye and SYBR Premix Ex Taq II
Department);RT-PCR primer (Beijing Tiangeng biochemical technology Co., Ltd).Biomate3S ultraviolet-visibles spectrophotometer,
The multi-functional ELIASA (Thermo Fisher Scientific companies of the U.S.) of A200PCR instrument, LUX;Tancon2500PCR coagulates
Glue imager (Shanghai Tian Neng Science and Technology Ltd.s);ICEN-24R high speed freezing centrifuges (Hangzhou Ao Sheng Instrument Ltd.).
SPF grades of BALB/c (body weight 25-30g) mouse of male 7 week old are purchased from Medical University Of Chongqing's animal experimental center (animal licensing
Number:SCXK (Chongqing) 2012-0001).
50 BALB/c mouses are randomly divided into 5 groups, are normal group, model control group respectively, at lactobacillus bulgaricus
Reason group, Lactobacillus plantarum YS1 low concentrations treatment group and high concentration treatment group, every group 10.Normal group and model control group are normal
Freely take in diet and drink water 2 weeks;During this is 2 weeks except it is normal freely take in diet and drinks water in addition to, at lactobacillus bulgaricus
The 1.0 × 10 of the daily every gavage 2mL of reason group mouse9At CFU/mL lactobacillus bulgaricus, Lactobacillus plantarum YS1 low concentrations
The 1 × 10 of reason group and the daily every difference gavage 2mL of high concentration treatment group mouse8CFU/mL Lactobacillus plantarum YS1 and 1 ×
109CFU/mL Lactobacillus plantarum YS1.The belly of the 1st day all mouse carries out shaving, normal group with 2 × 2cm areas after 2 weeks
Mouse web portion smears 0.2mL ethanol;It is that (ethanol is 3% azolactones solution that other each group mouse web portions, which smear 0.2mL mass ratioes,
Solvent).Implement within 5th day fasting to mouse, but allow mouse freely to take in after drinking-water, fasting 24h that mouse implementation is anaesthetized
(0.1mL/10g chloraldurate), then carries out bowel lavage:With silicone tube it is blunt nosed from mouse anus insert enteron aisle depth 3.5cm, normally
The ethanol solution that group mouse injection 0.15mL volume ratios are 50%, other each group mouse injection 0.15mL mass ratioes are 1% Evil
Conduit is extracted after oxazolone solution (ethanol solution that volume ratio is 50% is solvent), 20s, while mouse is inverted into 30s.Bowel lavage 7
The neck that breaks after it puts to death whole mouse, collects mice plasma and colon is standby.
1st, influences of the Lactobacillus plantarum YS1 to colitis symptoms
(the 20th day), 3 days (the 22nd day), 6 days (the 25th day) the DAI standards of grading calculating as described in table 2 respectively 1 day after bowel lavage
DAI values, DAI=(Body weight loss fraction+stool fraction+fraction of having blood in stool)/3.Colitis can cause body weight loss simultaneously
There is diarrhoea and the symptom such as bleeding, can be as measurement colitis using body weight, stool and the DAI having blood in stool as score standard
The standard of degree.
Table 2DAI standards of grading
The DAI value result of calculations of each group mouse are shown in Table 3, and DAI value of the normal group mouse in whole experimental period is remained
0.00 ± 0.00, DAI values increase and keep highest in each group always always after model control group mouse azolactone bowel lavage, protect
Plus the DAI values of Leah lactobacillus and Lactobacillus plantarum YS1 gavage Hou azolactone inducing colitis mouse are aobvious compared with model control group
Write and decline (p<0.05), wherein Lactobacillus plantarum YS1 high concentrations treatment group is reduced by up to.
The DAI values of each group mouse of table 3
Note:Alphabetical different expression group differences are significantly (P < 0.05).
Mouse Colon tissue is taken, the weight and length of colon is determined, colon weight/colon lengths ratio is calculated.Colon is long
Degree and colon weight/colon lengths ratio also weigh the standard of colitis degree, and compared with normal mouse, colitis is small
The colon lengths of mouse are shorter, colon weight/colon lengths ratio is lower.
The colon lengths and colon weight of each group mouse/colon lengths ratio are shown in Table 4, and the colon of model control group mouse is long
Degree and colon weight/colon lengths ratio are minimum, normal group mouse highest, and Lactobacillus plantarum YS1 high concentration treatment groups are small
The colon lengths and colon weight of mouse/colon lengths ratio are closest to normal group.
The colon lengths and colon weight/colon lengths ratio of each group mouse of table 4
Note:Alphabetical different expression group differences are significantly (P < 0.05).
The mouse colitis symptom of low azolactone induction can drop in above-mentioned experimental result explanation, Lactobacillus plantarum YS1, and with
The increase effect for concentration becomes apparent, and its effect is better than the lactobacillus bulgaricus with concentration.
2nd, influences of the Lactobacillus plantarum YS1 to mouse Colon tissue MPO, NO, GSH and MDA content
The physiological saline of 9 times of quality is added in clean mouse Colon, is homogenized colon using Ultrasonic Pulverization, so
MPO, NO, GSH and MDA content in mouse Colon tissue are measured by kit specification afterwards.Contents of the MPO in colon
Raising means that stream enters colon in neutrophil leucocyte, is the performance of neutrophil accumulation reduction in Inflamed tissue.
INOS generates the damage that NO aggravates colon during colitis, while increasing MPO with NO content in colon
Activity also strengthens therewith, inflammation aggravation.Colitis may further result in ROS (active oxygen) and RNS (active nitrogen) largely generations, make group
Knit cell and occur toxic reaction, colon is inflamed damage.The ROS a large amount of generations after reacting that are inflamed will destroy machine
GSH content in body oxidation/anti-oxidant balance, reduction colon, substantial amounts of peroxidatic reaction of lipid aggravates lipid peroxidation
End-product MDA generation.
As shown in Table 5, MPO, NO, MDA content highest in model control group mouse Colon tissue, GSH contents are minimum;Just
Often the colon of group mouse shows opposite trend, and MPO, NO, MDA content are minimum, GSH content highests;Relative to model
Control group, lactobacillus bulgaricus and Lactobacillus plantarum YS1 can reduce MPO in colitis mice colon, NO,
MDA contents and raising GSH contents, but Lactobacillus plantarum YS1 effect is stronger.
MPO, NO, GSH and MDA content of each group mouse Colon tissue of table 5
Note:Alphabetical different expression group differences are significantly (P < 0.05).
3rd, influences of the Lactobacillus plantarum YS1 to mice serum cell factor IL-2 and IL-10 level
Mice serum is taken, IL-2 and IL-10 cell factors in mice serum are determined by kit specification using ELISA method
Content.The colitis of azolactone induction is a kind of cell-mediated inflammation of Th2, and the mechanism that inflammation is produced is between Th2/Th1
Immunological network it is unbalance cause colitis, IL-10 is the cell factor that a kind of Th2 cells are produced, and IL-2 is that Th1 cells are produced
Cell factor, all directly related with colitis, too low IL-2 levels and too high IL-10 levels can mean that colitis degree
Deepen.
As shown in Table 6, normal group mice serum cell factor IL-2 is significantly higher than other group of mouse (p<0.05), IL-
10 levels are substantially less than other group of mouse (p<0.05);Compared with other each groups, Lactobacillus plantarum YS1 high concentration treatment group mouse
The closest normal group of serum cytokines IL-2 and IL-10 level.
The influence of each group mice serum cell factor IL-2 and the IL-10 level of table 6
Note:Alphabetical different expression group differences are significantly (P < 0.05).
4th, influences of the Lactobacillus plantarum YS1 to mouse Colon tissue correlated expression
The colon of mouse is taken, colon's total serum IgE is extracted with RNAzol after crushing, is diluted to 1 μ g/ μ L;Take 2 μ L dilute
Total RNAs extraction liquid after releasing, sequentially adds 1 μ L oligodT18, RNase, dNTP, MLV enzyme and 10 μ L 5 × buffer, 37
DEG C 120min, 99 DEG C of 4min, 4 DEG C of 3min synthesis cDNA;Then use primer described in table 7, RT-PCR amplification nNOS, eNOS,
INOS, c-Kit, SCF, IL-8 and CXCR2 mRNA expression, internal reference is used as using housekeeping gene GAPDH;Finally with containing mass ratio
Agar electrophoresis for 1% ethidium bromide checks pcr amplification product, and carries out semi-quantitative analysis with Image1.44 softwares.
Table 7RT-PCR primer sequences
(1) influence that Lactobacillus plantarum YS1 is expressed mouse Colon tissue nNOS, eNOS and iNOS mRNA
NOS points are nNOS, eNOS and iNOS, and research confirms that the NO that eNOS is produced has crucial work to the damage of control colon
With the excessive NO that iNOS is produced then accelerates colitis to damage, and nNOS, which is lowered, also makes iNOS expression strengthen a large amount of release NO simultaneously.
From Fig. 3 and table 8, nNOS, eNOS mRNA expression highests of normal group mouse Colon tissue, and iNOSmRNA
Expression it is minimum;NNOS, eNOSmRNA of model control group mouse express minimum, iNOSmRNA expression highest;Relative to mould
Type control group, lactobacillus bulgaricus and Lactobacillus plantarum YS1 can significantly raise nNOS in colitis mice colon,
ENOS mRNA expression and the expression (p for lowering iNOSmRNA<0.05), but Lactobacillus plantarum YS1 effect it is stronger.
Semi-quantitative analysis (the phase that the Lactobacillus plantarum YS1 of table 8 is expressed mouse Colon tissue nNOS, eNOS and iNOS mRNA
Multiple is expressed to control group)
Note:Alphabetical different expression group differences are significantly (P < 0.05).
(2) influence that Lactobacillus plantarum YS1 is expressed mouse Colon tissue c-Kit and SCF mRNA
Ulcerative colitis not only shows to suffer from diarrhoea and have blood in stool, while also there is colonic motor disorder.Research has shown that ICC
(Cajal interstitial cells) is relevant with colonic activity, directly participates in colitis process.When there is IBD, SCF is to maintaining
ICC quantity and function have direct effect, and SCF is c-Kit natural ligand, ICC increasing after SCF/Kit signal pathways sustain damage
Growing and breaking up can decline, so as to aggravate colitis.
From Fig. 4 and table 9, relative to model control group, lactobacillus bulgaricus and Lactobacillus plantarum YS1 can show
Write the expression (p of c-Kit and SCF mRNA in up-regulation colitis mice colon<0.05), but Lactobacillus plantarum YS1 effect
It is stronger.
The semi-quantitative analysis that the Lactobacillus plantarum YS1 of table 9 is expressed mouse Colon tissue c-Kit and SCF mRNA is (relatively right
According to a group expression multiple)
Note:Alphabetical different expression group differences are significantly (P < 0.05).
(3) influence that Lactobacillus plantarum YS1 is expressed mouse Colon tissue IL-8 and CXCR2mRNA
IL-8 has inflammatory activity and chemotaxis, and CXCR is IL-8 acceptors, and the morbidity of IL-8 and CXCR2 with colon cancer has
Close, document also reports the high expression that IL-8 and CXCR2 occurs under colon cancer state.
From Fig. 5 and table 10, relative to model control group, lactobacillus bulgaricus and Lactobacillus plantarum YS1 can
Significantly lower the expression (p of IL-8 and CXCR2mRNA in colitis mice colon<0.05), but Lactobacillus plantarum YS1 work
With stronger.
The semi-quantitative analysis that the Lactobacillus plantarum YS1 of table 10 is expressed mouse Colon tissue IL-8 and CXCR2mRNA is (relatively right
According to a group expression multiple)
Note:Alphabetical different expression group differences are significantly (P < 0.05).
Finally illustrate, the above embodiments are merely illustrative of the technical solutions of the present invention and it is unrestricted, although pass through ginseng
According to the preferred embodiments of the present invention, invention has been described, it should be appreciated by those of ordinary skill in the art that can
So that various changes are made to it in the form and details, the present invention limited without departing from appended claims
Spirit and scope.
<110>The college of education of Chongqing second;Tan Fang
<120>Applications of the Lactobacillus plantarum YS1 in the food or medicine of prevention ulcerative colitis is prepared
<160> 19
<210> 1
<211> 20
<212> DNA
<213>Artificial sequence
<220>
<223>Primer 2 7F
<400> 1
agagtttgat cctggctcag 20
<210> 2
<211> 19
<212> DNA
<213>Artificial sequence
<220>
<223>Primer 1492R
<400> 2
ggctaccttg ttacgactt 19
<210> 3
<211> 1472
<212> DNA
<213>Lactobacillus plantarum YS1(Lactobacillus plantarum YS1)
<220>
<223>16S rDNA genetic fragments
<400> 3
gacgaacgct ggcggcgtgc ctaatacatg caagtcgaac gaactctgga ttgattggtg 60
cttgcatcat gatttacatt tgagtgagtg gcgaactggt gagtaacacg tgggaaacct 120
gcccagaagc gggggataac acctggaaac agatgctata ccgcataaca acttggaccg 180
catggtccga gnttgaaaga tggcttcggc tatcactttt ggatggtccc gcggcgtatt 240
agctagatgg tggggtaacg gctcaccatg gcaatgatac gtagccgacc tgagagggta 300
atcggccaca ttgggactga gacacggcca aactcctacg ggaggcagca gtagggaatc 360
ttccacaatg gacgaagtct gatggagcaa cgccgcgtga gtgaaaaggg tttcggctcg 420
taaactctgt tgttaaagaa gaacatatct gagagtaact gttcaggtat tgacggtatt 480
taacagaaag ccacggctaa ctacgtgcca gcagccgcgg taatacgtag gtggcaagcg 540
ttgtccggat ttattgggcg taaagcgagc gcaggcggtt ttttaagtct gatgtgaaag 600
ccttcggctc aaccgaagaa gtgcatcgga aatgggaaac ttgagtgcag aagaggacag 660
tggaactcca ttgtagcggt gaaatgcgta gatatatgga agaacaccag tggcgaaggc 720
gctgtctggt ctgtaactga cgctgaggct cgaaagtatg gtagcaaaca ggattagata 780
ccctggtatc cataccgtaa acgatgaatg ctaagtgttg gagggtttcc gcccttcagt 840
gctgcagcta acgcattaag cattccgcct ggggagtacg gccgcaaggc tgaaactcaa 900
aggaattacg ggggcccgca caagcggtgg agcatgtggt ttaattcgaa gctacgcgaa 960
gaaccttacc aggtcttgac atactatgca aatctaagag attagacgtt cccttcgggg 1020
acatggatac aggtggtgca tggttgtcgt cagctcgtgt cgtgagatgt tgggttagtc 1080
ccgcacgagc gcaaccctta ttatcagttg ccagcattaa gttgggcact ctggtgagac 1140
tgccggtgac aaacggagga aggtggggat gacgtcaaat catcatgccc cttatgacct 1200
gggctacaca cgtgctacaa tggatggtac aacagttgcg aactcgcgag agtaagctaa 1260
tctcttaaag ccattctcag ttcggattgt aggctgcaac tcgcctacat gaagtcggaa 1320
tcgctagtaa tccggatcag catgccgcgg tgaatacgtt cccgggcctt gacacaccgc 1380
ccgtcacacc atgagagttt gtaacaccca aagtcggtgg ggtaaccttt taggaaccag 1440
ccgcctaagg gggacagatg attagggtga ag 1472
<210> 4
<211> 23
<212> DNA
<213>Artificial sequence
<220>
<223>The sense primer of RT-PCR amplification nNOS mRNA expression
<400> 4
gaataccagc ctgatccatg gaa 23
<210> 5
<211> 26
<212> DNA
<213>Artificial sequence
<220>
<223>The anti-sense primer of RT-PCR amplification nNOS mRNA expression
<400> 5
tcctccagga gggtgtccac cgcatg 26
<210> 6
<211> 20
<212> DNA
<213>Artificial sequence
<220>
<223>The sense primer of RT-PCR amplification eNOS mRNA expression
<400> 6
ggagaggctg catgacattg 20
<210> 7
<211> 22
<212> DNA
<213>Artificial sequence
<220>
<223>The anti-sense primer of RT-PCR amplification eNOS mRNA expression
<400> 7
ggtagagcca tagtggaatg ac 22
<210> 8
<211> 18
<212> DNA
<213>Artificial sequence
<220>
<223>The sense primer of RT-PCR amplification iNOS mRNA expression
<400> 8
agagagatcg ggttcaca 18
<210> 9
<211> 18
<212> DNA
<213>Artificial sequence
<220>
<223>The anti-sense primer of RT-PCR amplification iNOS mRNA expression
<400> 9
cacagaactg agggtaca 18
<210> 10
<211> 16
<212> DNA
<213>Artificial sequence
<220>
<223>The sense primer of RT-PCR amplification c-Kit mRNA expression
<400> 10
agaccgaacg caactt 16
<210> 11
<211> 16
<212> DNA
<213>Artificial sequence
<220>
<223>The anti-sense primer of RT-PCR amplification c-Kit mRNA expression
<400> 11
ggtgccatcc acttca 16
<210> 12
<211> 16
<212> DNA
<213>Artificial sequence
<220>
<223>The sense primer of RT-PCR amplification SCF mRNA expression
<400> 12
aaactggtgg cgaatc 16
<210> 13
<211> 16
<212> DNA
<213>Artificial sequence
<220>
<223>The anti-sense primer of RT-PCR amplification SCF mRNA expression
<400> 13
cacgggtagc aagaac 16
<210> 14
<211> 21
<212> DNA
<213>Artificial sequence
<220>
<223>The sense primer of RT-PCR amplification IL-8 mRNA expression
<400> 14
agaagcatgg cccagaaatc a 21
<210> 15
<211> 20
<212> DNA
<213>Artificial sequence
<220>
<223>The anti-sense primer of RT-PCR amplification IL-8 mRNA expression
<400> 15
ggccttgtag acaccttggt 20
<210> 16
<211> 18
<212> DNA
<213>Artificial sequence
<220>
<223>The sense primer of RT-PCR amplification CXCR2 mRNA expression
<400> 16
gaacaaaggc aaggctaa 18
<210> 17
<211> 20
<212> DNA
<213>Artificial sequence
<220>
<223>The anti-sense primer of RT-PCR amplification CXCR2 mRNA expression
<400> 17
aacataacaa catctgggca 20
<210> 18
<211> 20
<212> DNA
<213>Artificial sequence
<220>
<223>The sense primer of RT-PCR amplification GAPDH mRNA expression
<400> 18
cggagtcaac ggatttggtc 20
<210> 19
<211> 20
<212> DNA
<213>Artificial sequence
<220>
<223>The anti-sense primer of RT-PCR amplification GAPDH mRNA expression
<400> 19
agccttctcc atggtcgtga 20
Claims (1)
1. deposit number is CCTCC NO:M2016747 Lactobacillus plantarum YS1 (Lactobacillus plantarum YS1)
Application in the food or medicine of prevention ulcerative colitis is prepared.
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019085521A1 (en) * | 2017-11-03 | 2019-05-09 | 江南大学 | Lactobacillus plantarum with colorectal cancer inhibition function, and use thereof |
CN110692726A (en) * | 2018-07-10 | 2020-01-17 | 重庆第二师范学院 | Lactobacillus plantarum CQPC01 and application thereof in preparation of food for improving constipation |
CN113234612A (en) * | 2021-02-05 | 2021-08-10 | 重庆第二师范学院 | Lactobacillus fermentum ZS40 having preventive effect on colitis |
CN114990014A (en) * | 2022-05-31 | 2022-09-02 | 成都医学院 | Lactobacillus plantarum for preventing and treating inflammatory enteritis and application thereof |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014193014A1 (en) * | 2013-05-29 | 2014-12-04 | 바이오제닉스코리아 주식회사 | Nano-sized kimchi lactic acid bacteria |
CN105106246A (en) * | 2015-08-20 | 2015-12-02 | 江南大学 | Lactobacillus plantarum ZS2058 and application thereof |
CN105343133A (en) * | 2015-12-08 | 2016-02-24 | 东北农业大学 | Compound probiotics and drug for treating ulcerative colitis and preparation method thereof |
-
2017
- 2017-04-25 CN CN201710279022.XA patent/CN107028988A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014193014A1 (en) * | 2013-05-29 | 2014-12-04 | 바이오제닉스코리아 주식회사 | Nano-sized kimchi lactic acid bacteria |
CN105106246A (en) * | 2015-08-20 | 2015-12-02 | 江南大学 | Lactobacillus plantarum ZS2058 and application thereof |
CN105343133A (en) * | 2015-12-08 | 2016-02-24 | 东北农业大学 | Compound probiotics and drug for treating ulcerative colitis and preparation method thereof |
Non-Patent Citations (2)
Title |
---|
叶胜青等: "植物乳杆菌对2,4,6-三硝基苯磺酸诱导的小鼠结肠炎的治疗作用", 《世界华人消化杂志》 * |
孙鹏等: "植物乳杆菌YS1对恶唑酮诱导BALB/c小鼠结肠炎的预防作用", 《食品工业科技》 * |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019085521A1 (en) * | 2017-11-03 | 2019-05-09 | 江南大学 | Lactobacillus plantarum with colorectal cancer inhibition function, and use thereof |
CN110692726A (en) * | 2018-07-10 | 2020-01-17 | 重庆第二师范学院 | Lactobacillus plantarum CQPC01 and application thereof in preparation of food for improving constipation |
CN113234612A (en) * | 2021-02-05 | 2021-08-10 | 重庆第二师范学院 | Lactobacillus fermentum ZS40 having preventive effect on colitis |
CN114990014A (en) * | 2022-05-31 | 2022-09-02 | 成都医学院 | Lactobacillus plantarum for preventing and treating inflammatory enteritis and application thereof |
CN114990014B (en) * | 2022-05-31 | 2023-05-23 | 成都医学院 | Lactobacillus plantarum for preventing and treating inflammatory enteritis and application thereof |
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