CN104450596A - Edwardsiella tarda ghost showing vibrio parahaemolyticus TDH and construction method - Google Patents
Edwardsiella tarda ghost showing vibrio parahaemolyticus TDH and construction method Download PDFInfo
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Abstract
The invention discloses an Edwardsiella tarda ghost showing vibrio parahaemolyticus TDH and a construction method and belongs to the field of genetic engineering. The method includes the steps that firstly, the phagocytosis PhiX174 bacteriolysis gene and the vibrio parahaemolyticus heat-resisting hemolysin gene tdh are cloned; secondly, a bacteriolysis plasmid vector p-E-tdh is constructed; thirdly, transforming and screening of the Edwardsiella tarda are conducted; fourthly, the ghost is obtained. According to the Edwardsiella tarda ghost showing vibrio parahaemolyticus TDH and the construction method, the constructed recombined Edwardsiella tarda vaccine for showing the vibrio parahaemolyticus heat-resisting hemolysin immune protection gene tdh has the common immune protection effect on the Edwardsiella and the vibrio parahaemolyticus.
Description
Technical field
The invention belongs to genetically engineered field, relate to a kind of restructuring Wdwardsiella tarda ghost and the construction process of showing the heat-resisting hemolysin TDH of Vibrio parahaemolyticus particularly.
Background technology
Bacterium ghost is the empty bacterial of acellular slurry and the fecundity formed by regulating and controlling the Lysis gene E of Phage PhiX174 and expressing in gram negative bacterium.Bacterium ghost not only can directly as vaccine use, but also can be used as submission heterologous antigen recombiant vaccine and as the nucleic acid vaccine even delivery vector of medicine.The present invention is intended to set up the method and immunoprotection application that Wdwardsiella tarda ghost prepared as the delivery vector of the heat-resisting hemolysin gene tdh of Vibrio parahaemolyticus.
Summary of the invention
The technical problem to be solved in the present invention is to provide a kind of Wdwardsiella tarda ghost and the construction process of showing the heat-resisting hemolysin gene tdh of Vibrio parahaemolyticus.
The invention provides a kind of restructuring Wdwardsiella tarda ghost showing the heat-resisting hemolysin gene tdh of Vibrio parahaemolyticus.
The invention provides a kind of construction process showing the restructuring Wdwardsiella tarda ghost of the heat-resisting hemolysin gene tdh of Vibrio parahaemolyticus, its step is as follows:
(1) clone phagocytosis PhiX174 bacteriolytic genes and the heat-resisting hemolysin gene tdh of Vibrio parahaemolyticus, described phagocytosis PhiX174 bacteriolytic genes is called for short E gene, and the heat-resisting hemolysin gene tdh of described Vibrio parahaemolyticus is called for short tdh gene;
(2) bacteriolyze plasmid vector p-E-tdh is built
According to the primers of Phage PhiX174 bacteriolytic genes and the heat-resisting hemolysin gene tdh of Vibrio parahaemolyticus, upstream and downstream prime end introduces restriction enzyme site EcoRI and BamHI respectively, and adds linker sequence in E downstream of gene primer and tdh upstream region of gene primer; And with the E gene of synthetic and tdh gene for template carries out pcr amplification respectively, reclaim object fragment, and with the object fragment after purifying for template, second time amplification is carried out with E upstream region of gene primer and tdh downstream of gene primer, E gene is connected together with tdh gene fragment, obtains fusion gene fragment E-tdh by kits PCR primer; With BamHI and EcoRI double digestion fusion gene fragment E-tdh, after 0.8% agarose gel electrophoresis, each fragment is reclaimed in rubber tapping, fragment after recovery connects with the pBV220 large fragment reclaimed through identical double digestion tapping rubber and transforms Top10 competent cell, after transforming with E upstream region of gene primer and tdh downstream of gene primer pair, the bacterium colony of incubation growth carries out PCR screening, after gained positive colony send company to carry out order-checking qualification correctly, bacteriolyze plasmid vector called after p-E-tdh, and carry p-E-tdh with plasmid extraction kit extraction bacteriolyze plasmid;
Described E upstream region of gene primer EcoRI-E-F:5 ' GAG
gAATTCaTGGTACGCTGGACTTTG-3 ',
Described E downstream of gene primer linker-E-R:5 '-CTGCCGCCACCGCCGCTTCCGCCACCGCCGCTTCCACCGCCACCCTCCTTCTGCAC GTA-3 ';
Described tdh upstream region of gene primer linker-tdh-F:5 '
GTGGCGGTGGAAGCGGCGGTGGCGGAAGCGGCG GTGGCGGCAG ATATCCATGTTGGCTGCA-3’，
Described tdh downstream of gene primer BamHI-tdh-R:5 '-TTAG
gGATCCcTAAAACGATTCTTTGTTGG-3 ';
(3) conversion of Wdwardsiella tarda and screening
Conventionally prepare Wdwardsiella tarda competent cell, ice bath Wdwardsiella tarda 10min, add bacteriolyze plasmid vector p-E-tdh 10 μ L, ice bath 30min, 42 DEG C of heat-shocked 90s, ice bath 1-2min, add 800 μ L not containing antibiotic pancreas peptone soybean broth medium liquid substratum, 28 DEG C of 80 ~ 100rpm/min shaking culture 45min-1h, 12, the centrifugal 1min of 000 × g, remove supernatant, the resuspended precipitation of residue 40-50 μ L supernatant liquor, it is on the trypticase soy broth agar culture medium flat plate of 100ug/ml penbritin that uniform liquid after resuspended precipitation is coated containing final concentration, 28 DEG C of overnight incubation, gained positive colony is namely containing the Wdwardsiella tarda of bacteriolyze plasmid vector p-E-tdh,
(4) acquisition that bacterium is de-
Being seeded in containing final concentration by the Wdwardsiella tarda containing bacteriolyze plasmid vector p-E-tdh after above-mentioned steps (3) transformation and selection is in the pancreas peptone soybean broth substratum of 100ug/ml penbritin, 28 DEG C, 180rpm spend the night concussion cultivate, then transfer in being in the pancreas peptone soybean broth substratum of 100ug/ml penbritin containing final concentration according to the volume ratio of 1:100,28 DEG C of concussions are cultured to the light absorption value OD of described nutrient solution
600nm carries out 42 DEG C of cultivations after reaching 0.3-0.4, to induce E gene and tdh genetic expression, cultivate induction after 5 hours for 42 DEG C, collected by centrifugation thalline also uses ddH
2the thalline that O, PBS washing is collected, i.e. ghost.
Further, the pcr amplification reaction system of described step (2) is:
Further, the pcr amplification condition of described step (2): 95 DEG C of 5min; 94 DEG C of 1min, 60 DEG C of 4min, totally 30 circulations; 72 DEG C of 10min; Be separated with 1% sepharose and reclaim corresponding object fragment, respectively getting 1 μ L and make template, carrying out second time amplification with E upstream region of gene primer and tdh downstream of gene primer, E gene is connected together with tdh gene fragment, and uses kits PCR primer.
The present invention also provides the bacterium constructed by a kind of aforesaid method to take off.
The present invention's beneficial effect compared with prior art:
Bacterium ghost vaccine (Bacterial ghosts vaccine) is the empty bacterial of being expressed in gram negative bacterium by regulation and control phage splitting gene E (lysisE) and being formed, and is a kind of desirable new generation vaccine and vaccine carrier.Prior art has proved a kind of ideal oral vaccine of Wdwardsiella tarda ghost vaccine; Vibrio parahaemolyticus (Vibrio Parahemolyticus) is a kind of pathogenic vibrio culture fishery being caused to significant damage, and the heat-resisting hemolysin gene tdh of this bacterium has immunoprotection antigenicity; Meanwhile, already reported that ghost vaccine was also a kind of ideal vaccine vector system.Therefore, the restructuring Wdwardsiella tarda ghost vaccine of the expression Vibrio parahaemolyticus heat-resisting hemolysin immunoprotection antigen gene tdh that the present invention builds, has the co-immunization protected effect to Wdwardsiella tarda and Vibrio parahaemolyticus.
Accompanying drawing explanation
Fig. 1 geneE electrophoresis result 1:geneE, M:Marker;
Fig. 2 gene tdh electrophoresis result (1:gene tdh, M:Marker);
Fig. 3 plasmid p-E-tdh structural representation;
Fig. 4 has turned Wdwardsiella tarda growth and the bacteriolyze process of bacteriolyze plasmid, and 0 is 42 DEG C of induction time openings, and in figure, numerical value represents the light absorption value under 600nm wavelength;
The Western blotting that Fig. 5 Wdwardsiella tarda ghost expresses the heat-resisting hemolysin gene tdh of Vibrio parahaemolyticus detects, M:Marker A: B after induction: before induction.
Embodiment
Come by reference to the accompanying drawings to be further explained technical solution of the present invention below by embodiment, but protection scope of the present invention is not by any pro forma restriction of embodiment.
A kind of construction process showing the Wdwardsiella tarda ghost of Vibrio parahaemolyticus TDH
, step is as follows:
(1) cloned phage PhiX174 bacteriolytic genes and the heat-resisting hemolysin gene tdh of Vibrio parahaemolyticus;
1) synthetic Phage PhiX174 bacteriolytic genes is also E gene.
According to GenBank pnagus medius PhiX174 bacteriolytic genes sequence, synthetic PhiX174 bacteriolytic genes, altogether 276bp, sequence is:
ATGGTACGCTGGACTTTGTGGGATACCCTCGCTTTCCTGCTCCTGTTGAGTTTATTGCTGCCGTCATTGCTTATTATGTTCATCCCGTCAACATTCAAACGGCCTGTCTCATCATGGAAGGCGCTGAATTTACGGAAAACATTATTAATGGCGTCGAGCGTCCGGTTAAAGCCGCTGAATTGTTCGCGTTTACCTTGCGTGTACGCGCAGGAAACACTGACGTTCTTACTGACGCAGAAGAAAACGTGCGTCAAAAATTACGTGCAGAAGGAGTGA。
Carry out electrophoresis after synthetic, size is 276bp (Fig. 1).Sequencing result shows that Phage PhiX174 bacteriolytic genes correctly synthesizes.
2) the heat-resisting hemolysin gene tdh of manual segmentation synthesis Vibrio parahaemolyticus is also tdh gene.
According to the gene order in GenBank, the gene order of the heat-resisting hemolysin gene tdh of Vibrio parahaemolyticus, altogether 570bp, sequence is:
ATGAAACACCAATATTTTGCAAAAAAATCATTTTTATTTATATCCATGTTGGCTGCATTCAAAACATCTGCTTTTGAGCTTCCATCTGTCCCTTTTCCTGCCCCCGGTTCTGATGAGATATTGTTTGTTGTTCGAGATACAACTTTTAATACCCAAGCTCCGGTCAATGTAAAGGTCTCTGACTTTTGGACAAACCGTAATGTAAAAAGAAAACCGTACGAAGATGTTTATGGTCAATCAGTATTCACAACGTCAGGTACTAAATGGTTGACATCCTACATGACTGTGAACATTAATGATAAAGACTATACAATGGCAGCGGTGTCTGGCTATAAGAGCGGTCATTCTGCTGTGTTCGTAAAATCAGATCAAGTACAACTTCAACATTCCTATAATTCTGTAGCTAACTTTGTTGGTGAAGATGAAGGTTCTATTCCAAGTAAAATGTATTTGGATGAAACTCCAGAATATTTTGTTAATGTAGAAGCATATGAGAGTGGTAGTGGTAATATATTGGTAATGTGTATATCCAACAAAGAATCGTTTTTTGAATATAAACATCAACAATAA。
After manual segmentation synthesis, round pcr connects, and through agarose electrophoresis, size is 570bp (Fig. 2).Sequencing result shows that tdh gene correctly synthesizes.
(2) bacteriolyze plasmid vector p-E-tdh is built
According to the primers of Phage PhiX174 bacteriolytic genes and the heat-resisting hemolysin gene tdh of Vibrio parahaemolyticus, upstream and downstream prime end introduces restriction enzyme site EcoRI and BamHI respectively, and linker sequence (underscore) is added in E downstream of gene primer and Vibrio parahaemolyticus tdh upstream region of gene primer, synthesized by company.And with the E gene of corresponding synthetic and tdh gene for template carries out pcr amplification.
E upstream region of gene primer EcoRI-E-F:
5’-GAG
GAATTCATGGTACGCTGGACTTTG-3’，
E downstream of gene primer l inker-E-R:
5’-CTGCCGCCACCGCCGCTTCCGCCACCGCCGCTTCCACCGCCA
CCCTCCTTCTGCACGTA-3’；
Tdh upstream region of gene primer l inker-tdh-F:
5’-GTGGCGGTGGAAGCGGCGGTGGCGGAAGCGGCGGTGGCGGCAGATATCCATGTTGGCTGCA-3’
Tdh downstream of gene primer BamHI-tdh-R:
5’-TTAG
GGATCCCTAAAACGATTCTTTGTTGG-3’；
The preparation of fusion gene E-tdh: with primer EcoRI-E-F, linker-E-R, linker-tdh-F, BamHI-tdh-R carry out pcr amplification respectively.Pcr amplification reaction system is:
Amplification condition: 95 DEG C of 5min; 94 DEG C of 1min, 60 DEG C of 4min, totally 30 circulations; 72 DEG C of 10min.Be separated with 1% sepharose and reclaim corresponding object fragment, respectively get 1 μ L and make template, second time amplification is carried out with E upstream region of gene primer and tdh downstream of gene primer, E gene is connected together with tdh gene fragment, obtain fusion gene fragment E-tdh, and with kits fusion gene fragment E-tdh.
With BamHI and EcoRI double digestion fusion gene fragment E-tdh, after 0.8% agarose gel electrophoresis, each fragment is reclaimed in rubber tapping, and the fragment after recovery connects with the pBV220 large fragment that reclaims of also tapping rubber through identical BamHI and EcoRI double digestion and transforms Top10 competent cell.After transforming with E upstream region of gene primer and tdh downstream of gene primer pair, the bacterium colony of growth carries out PCR screening, after gained positive colony send company to carry out order-checking qualification correctly, called after bacteriolyze plasmid vector p-E-tdh (see Fig. 3), and extract bacteriolyze plasmid vector p-E-tdh with plasmid extraction kit.
(3) Wdwardsiella tarda transforms and screening
Conventionally prepare Wdwardsiella tarda competent cell, ice bath delays Edwardsiella 10min, add plasmid vector p-E-tdh10 μ L, ice bath 30min, 42 DEG C of heat-shocked 90s, ice bath 1-2min, add 800 μ L not containing antibiotic pancreas peptone soybean broth substratum (TSB) liquid nutrient medium, 28 DEG C of 80 ~ 100rpm/min shaking culture 45min-1h, 12, the centrifugal 1min of 000 × g, remove supernatant, the resuspended precipitation of residue about 50 μ L liquid, being spread evenly across containing final concentration is on trypticase soy broth agar substratum (TSA) flat board of 100ug/ml penbritin (Amp), 28 DEG C of overnight incubation.
The single bacterium colony of picking from the flat board of above-mentioned incubated overnight, being inoculated in 3mL containing final concentration is in the TSB liquid nutrient medium of 100ug/mlAmp, and 28 DEG C jolt overnight incubation, extracts plasmid and carries out PCR qualification.
Carry out pcr amplification to the Wdwardsiella tarda proceeding to bacteriolyze plasmid vector p-E-tdh, clip size is consistent with expection band, and conform to theoretic conclusion, preliminary proof is positive recombinant plasmid.
Carry out plasmid sequence mensuration to the doubtful Wdwardsiella tarda proceeding to bacteriolyze plasmid vector p-E-tdh, sequencing result shows that restructuring bacteriolyze plasmid vector p-E-tdh meets completely with design.Sequencing result is as follows:
GATACGAAACGAAGCATTGGTTAAAAATTAAGGAGGAATTCATGGTACGCTGGACTTTGTGGGATACCCTCGCTTTCCTGCTCCTGTTGAGTTTATTGCTGCCGTCATTGCTTATTATGTTCATCCCGTCAACATTCAAACGGCCTGTCTCATCATGGAAGGCGCTGAATTTACGGAAAACATTATTAATGGCGTCGAGCGTCCGGTTAAAGCCGCTGAATTGTTCGCGTTTACCTTGCGTGTACGCGCAGGAAACACTGACGTTCTTACTGACGCAGAAGAAAACGTGCGTCAAAAATTACGTGCAGAAGGAGGGTGGCGGTGGAAGCGGCGGTGGCGGAAGCGGCGGTGGCGGCAGCAAACACCAATATTTTGCAAAAAAATCATTTTTATTTATATCCATGTTGGCTGCATTCAAAACATCTGCTTTTGAGCTTCCATCTGTCCCTTTTCCTGCCCCCGGTTCTGATGAGATATTGTTTGTTGTTCGAGATACAACTTTTAATACCCAAGCTCCGGTCAATGTAAAGGTCTCTGACTTTTGGACAAACCGTAATGTAAAAAGAAAACCGTACGAAGATGTTTATGGTCAATCAGTATTCACAACGTCAGGTACTAAATGGTTGACATCCTACATGACTGTGAACATTAATGATAAAGACTATACAATGGCAGCGGTGTCTGGCTATAAGAGCGGTCATTCTGCTGTGTTCGTAAAATCAGATCAAGTACAACTTCAACATTCCTATAATTCTGTAGCTAACTTTGTTGGTGAAGATGAAGGTTCTATTCCAAGTAAAATGTATTTGGATGAAACTCCAGAATATTTTGTTAATGTAGAAGCATATGAGAGTGGTAGTGGTAATATATTGGTAATGTGTATATCCAACAAAGAATCGTTTTAGGGATCCCTAA。
(4) acquisition that recombinant bacterium is de-
Containing final concentration at 5mL is the Wdwardsiella tarda competent cell that in the TSB of 100ug/ml penbritin (Amp), inoculation contains bacteriolyze plasmid vector p-E-tdh, (180rpm) is cultivated in 28 DEG C of concussions of spending the night, then transfer 2mL in 200mL containing in the TSB of 100ug/ml penbritin, 28 DEG C of concussions are cultured to OD
60042 DEG C of cultivations are carried out, to induce E gene and tdh genetic expression after nm reaches about 0.4.The each culture OD of sampling Detection after 0.5 hour
600nm.Result shows, and induces after 0.5 hour, the OD of bacterium liquid
600nmslightly raise, induce after 1 hour, due to the degraded of bacterium, the OD of bacterium liquid
600nmstart to decline rapidly, after arriving Schwellenwert after 5 hours basicly stable constant (Fig. 4), show to obtain ghost.
(5) Wdwardsiella tarda ghost expresses the qualification of the heat-resisting hemolysin gene tdh of Vibrio parahaemolyticus
After induction bacteriolyze, ultrasonic grinding Wdwardsiella tarda ghost, protein electrophorese, and the electrotransfer carrying out product: after SDS-PAGE terminates, take out gel, prepare polyacrylamide gel-film " sandwich " by having structure level: one deck filter paper-gel-pvdf membrane-one deck filter paper.Gel-film " sandwich " is rolled across gently, to remove the bubble between each layer with a clean small test tube.Filter paper, nitrocellulose (NC) film balance 15-20min in advance in transfering buffering liquid.Gel-the film " sandwich " fixed is transferred in electrotransfer instrument, gel side towards negative pole, NC film side towards positive pole, with 0.8mA/cm
2current transfer 90 minutes.
Close: pvdf membrane 5% skim-milk room temperature is closed and spent the night for 2 hours or 4 DEG C.
Wash film I: discard confining liquid, slowly shake with PBST and wash film 3 times, each 10min.
Primary antibodie: discard PBST, adds rabbit anti-tdh polyclonal antibody IgG (1:5000 is diluted in PBS solution), and 37 DEG C of slow jolting effect at least 1h, spend the night and can strengthen sensitivity.
Wash film II: discard primary antibodie, wash film 3 times with PBST, each 10min.
Two resist: discard PBST, add the goat-anti rabbit ELIAS secondary antibody being diluted in PBS solution by 1:5000,37 DEG C of slow jolting effects at least 1h or spend the night.
Wash film III: discard ELIAS secondary antibody, wash film 3 times with TBS, each 10min.
Colour developing: take 6mg DAB powder, be dissolved in 10mLPBS, add 10 μ L30%H
2o
2rear filtration.Pvdf membrane is placed in nitrite ion, colour developing 3 ~ 5min, after specific reaction band to appear, washes the reaction of film color development stopping with distilled water.
After induction bacteriolyze, ultrasonic grinding, protein electrophorese and westernblot analyze display, the heat-resisting hemolysin gene tdh (Fig. 5) of Wdwardsiella tarda successful presentation Vibrio parahaemolyticus.
(6) immunoprotection and challenge trial
120 tail zebra fishs are divided into 4 groups at random: ghost group (A group), ghost group (B group) and PBS control group 2 groups (C group, D group), often organize 30 tails.Immunization method is abdominal injection, and first anaesthetize zebra fish with the MSS of 100mg/L, then use syringe special used for insulin U-100 abdominal injection vaccine and PBS, before immunity, 24h stops feeding, and immunizing dose is 1 × 10
6cFU/10 μ L/ tail, PBS group 10 μ L/ tail, each group uses same treatment booster immunization once all after 2 weeks.
After ghost and PBS immunity, have no zebra fish and occur any Behavioral change and disease symptoms.Observe 2 weeks after attacking poison, record death condition, calculates protection ratio (see table 1).
The immune protective rate after poison attacked by table 1
The immunity of A ghost, Wdwardsiella tarda attacks poison
The immunity of B ghost, Vibrio parahaemolyticus attacks poison
C PBS immunity, Wdwardsiella tarda attacks poison
D PBS immunity, Vibrio parahaemolyticus attacks poison.
Claims (5)
1. show the restructuring Wdwardsiella tarda ghost of the heat-resisting hemolysin gene tdh of Vibrio parahaemolyticus for one kind.
2. a kind of construction process showing the restructuring Wdwardsiella tarda ghost of the heat-resisting hemolysin gene tdh of Vibrio parahaemolyticus according to claim 1, is characterized in that its step is as follows:
(1) clone phagocytosis PhiX174 bacteriolytic genes and the heat-resisting hemolysin gene tdh of Vibrio parahaemolyticus, described phagocytosis PhiX174 bacteriolytic genes is called for short E gene, and the heat-resisting hemolysin gene tdh of described Vibrio parahaemolyticus is called for short tdh gene;
(2) bacteriolyze plasmid vector p-E-tdh is built
According to the primers of Phage PhiX174 bacteriolytic genes and the heat-resisting hemolysin gene tdh of Vibrio parahaemolyticus, upstream and downstream prime end introduces restriction enzyme site EcoRI and BamHI respectively, and adds linker sequence in E downstream of gene primer and tdh upstream region of gene primer; And with the E gene of synthetic and tdh gene for template carries out pcr amplification respectively, reclaim object fragment, and with the object fragment after purifying for template, second time amplification is carried out with E upstream region of gene primer and tdh downstream of gene primer, E gene is connected together with tdh gene fragment, obtains fusion gene fragment E-tdh by kits PCR primer; With BamHI and EcoRI double digestion fusion gene fragment E-tdh, after 0.8% agarose gel electrophoresis, each fragment is reclaimed in rubber tapping, fragment after recovery connects with the pBV220 large fragment reclaimed through identical double digestion tapping rubber and transforms Top10 competent cell, after transforming with E upstream region of gene primer and tdh downstream of gene primer pair, the bacterium colony of incubation growth carries out PCR screening, after gained positive colony send company to carry out order-checking qualification correctly, bacteriolyze plasmid vector called after p-E-tdh, and carry p-E-tdh with plasmid extraction kit extraction bacteriolyze plasmid;
Described E upstream region of gene primer E upstream region of gene primer EcoRI-E-F:5 ' GAG
gAATTCaTGGTACGCTGGACTTTG-3 ',
Described E downstream of gene primer linker-E-R:5 '-CTGCCGCCACCGCCGCTTCCGCCACCGCCGCTTCCACCGCCACCCTCCTTCTGCAC GTA-3 ';
Described tdh upstream region of gene primer linker-tdh-F:5 '
GTGGCGGTGGAAGCGGCGGTGGCGGAAGCGGCG GTGGCGGCAG ATATCCATGTTGGCTGCA-3’，
Described tdh downstream of gene primer BamHI-tdh-R:5 '-TTAG
gGATCCcTAAAACGATTCTTTGTTGG-3 ';
(3) conversion of Wdwardsiella tarda and screening
Conventionally prepare Wdwardsiella tarda competent cell, ice bath Wdwardsiella tarda 10min, add bacteriolyze plasmid vector p-E-tdh 10 μ L, ice bath 30min, 42 DEG C of heat-shocked 90s, ice bath 1-2min, add 800 μ L not containing antibiotic pancreas peptone soybean broth medium liquid substratum, 28 DEG C of 80 ~ 100rpm/min shaking culture 45min-1h, 12, the centrifugal 1min of 000 × g, remove supernatant, the resuspended precipitation of residue 40-50 μ L supernatant liquor, it is on the trypticase soy broth agar culture medium flat plate of 100ug/ml penbritin that uniform liquid after resuspended precipitation is coated containing final concentration, 28 DEG C of overnight incubation, gained positive colony is namely containing the Wdwardsiella tarda of bacteriolyze plasmid vector p-E-tdh,
(4) acquisition that bacterium is de-
Being seeded in containing final concentration by the Wdwardsiella tarda containing bacteriolyze plasmid vector p-E-tdh after above-mentioned steps (3) transformation and selection is in the pancreas peptone soybean broth substratum of 100ug/ml penbritin, 28 DEG C, 180rpm spend the night concussion cultivate, then transfer in being in the pancreas peptone soybean broth substratum of 100ug/ml penbritin containing final concentration according to the volume ratio of 1:100,28 DEG C of concussions are cultured to the light absorption value OD of described nutrient solution
600nm carries out 42 DEG C of cultivations after reaching 0.3-0.4, to induce E gene and tdh genetic expression, cultivate induction after 5 hours for 42 DEG C, collected by centrifugation thalline also uses ddH
2the thalline that O, PBS washing is collected, i.e. ghost.
3. a kind of construction process showing the restructuring Wdwardsiella tarda ghost of the heat-resisting hemolysin gene tdh of Vibrio parahaemolyticus according to claim 2, is characterized in that the pcr amplification reaction system of described step (2) is:
。
4. a kind of construction process showing the restructuring Wdwardsiella tarda ghost of the heat-resisting hemolysin gene tdh of Vibrio parahaemolyticus according to claim 2, is characterized in that the pcr amplification condition of described step (2): 95 DEG C of 5min; 94 DEG C of 1min, 60 DEG C of 4min, totally 30 circulations; 72 DEG C of 10min; Be separated with 1% sepharose and reclaim corresponding object fragment, respectively getting 1 μ L and make template, carrying out second time amplification with E upstream region of gene primer and tdh downstream of gene primer, E gene is connected together with tdh gene fragment, and uses kits PCR primer.
5. the bacterium that claim 2-4 method described in any one builds takes off.
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110283770A (en) * | 2019-07-30 | 2019-09-27 | 浙江农林大学 | Show the vibrio parahaemolytious bacterium shadow vaccine preparation of vibrio parahaemolytious VP1667 and VP2369 albumen |
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| CN112481221A (en) * | 2019-09-10 | 2021-03-12 | 宁波大学 | Edwardsiella tarda efficient lytic phage vB _ EtaM-IME523 and application thereof |
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