Vibrio alginolyticus Hfq gene knockout mutant strain and application thereof
1. The vibrio alginolyticus Hfq gene knockout mutant is characterized in that the preservation number of the vibrio alginolyticus Hfq gene knockout mutant is CCTCCNO: m2021539.
2. The vibrio alginolyticus Hfq gene knockout mutant strain of claim 1, wherein the pTargetF-Hfq recombinant plasmid targeting Hfq gene is constructed by the following method:
constructing a pTargetF-Hfq vector containing a 20bpHfq gene fragment by using the primer G2F/G2R with the pTargetF plasmid as a template;
wherein the primer G2F/G2R has the following sequence:
G2 F：5’-GCTACGTCGTGAGCGTATCCGTTTTAGAGCTAGAAATAGCA-3’；SEQ ID NO.2；
G2 R：5’-GGATACGCTCACGACGTAGCCTAGTATTATACCTAGGACTG-3’；SEQ ID NO.3；
the reaction system is as follows: taq enzyme 25. mu.L, ddH2O19. mu.L, 2. mu.L of pTargetF plasmid diluted 1000-fold, 2. mu.L each of the G2F/G2R primers;
the reaction procedure is as follows: the initial denaturation step was carried out at 94 ℃ for 5 minutes, followed by denaturation at 94 ℃ for 45 seconds in 35 cycles, annealing at 68 ℃ for 1 minute, extension at 72 ℃ for 1 minute, and final extension at 72 ℃ for 5 minutes.
3. The vibrio alginolyticus Hfq gene knockout mutant strain of claim 1, wherein the homology arms are constructed by the following method:
taking the genome of a vibrio alginolyticus wild strain as a template, respectively amplifying a front-segment gene fragment AB and a rear-segment gene fragment CD of a target gene by using primers AF/BR and CF/DR, after successful verification, amplifying by using the primers AF/DR by using the gene fragments AB and the gene fragment CD as the template, and splicing the two segments of genes to obtain a homologous arm;
wherein the sequences of the primers AF/BR and CF/DR are as follows:
AF：5’-TTTATCTCGGGCATTGGA-3’；SEQ ID NO.7；
BR：5’-AGGTGATTTGACGCTTGG-3’；SEQ ID NO.8；
CF：5’-CCAAGCGTCAAATCACCTACGCAAGAAGGTGAATGG-3’；SEQ ID NO.9；
DR：5’-TACGGTTGAAGAGTGTCG-3’；SEQ ID NO.10；
the reaction system is as follows: taq enzyme 25. mu.L, ddH2O18. mu.L, template AB 1. mu.L, template CD 2. mu.L, primer AF 2. mu.L, primer DR 2. mu.L;
the reaction procedure is as follows: the initial denaturation step was carried out at 94 ℃ for 5 minutes, followed by denaturation at 94 ℃ for 45 seconds in 35 cycles, annealing at 55 ℃ for 1 minute, extension at 72 ℃ for 1 minute, and final extension at 72 ℃ for 5 minutes.
4. Use of the vibrio alginolyticus Hfq gene knockout mutant strain of claim 1 for reducing the virulence of vibrio alginolyticus.
5. The use of the knock-out mutant of the Hfq gene of Vibrio alginolyticus according to claim 4, wherein the nucleotide sequence of the Hfq gene is represented by SEQ ID No. 1.
Background
The aquaculture industry develops rapidly in the global scope, and shellfish culture becomes the pillar industry of the aquaculture industry, and with the increase of the culture scale, vibriosis is frequent, so that a large amount of shellfish die, and huge economic loss is caused to the aquaculture industry. The vibrio alginolyticus is a gram-negative conditional pathogen which is common to human and livestock and is one of the most harmful bacterial pathogens in mariculture, can cause bacterial septicemia and parotitis ulceration of fishes and shellfishes, and brings serious threat to human health. Vibrio alginolyticus is often found as a pathogenic bacterium of fish, and in shellfish, Haliotis diversicolor and Philippine clam are mostly ill.
The bacteria have quorum sensing systems (QS) in vivo, and can respond to environmental signal changes in time. The regulation of small ribonucleic acids (SRNAs) in this system plays an important role in post-transcriptional regulation of gene expression and toxicity, and this process requires the involvement of the RNA chaperone protein Hfq. However, the research on the toxicity regulation of Hfq on scallop by Vibrio alginolyticus (vibrio algirolyticus) is not many at present, and based on the research, the deep research on the molecular pathogenesis of Vibrio alginolyticus is very important for preventing and controlling the outbreak of the vibrio alginolyticus disease of scallop.
Therefore, it is an urgent problem to be solved by those skilled in the art to provide Hfq knockout mutants of Vibrio alginolyticus and applications thereof.
Disclosure of Invention
In view of the above, the invention provides a vibrio alginolyticus Hfq gene knockout mutant strain and application thereof.
In order to achieve the purpose, the invention adopts the following technical scheme:
the Vibrio alginolyticus Hfq gene knockout mutant strain has the preservation number of CCTCC NO: m2021539, deposited in China center for type culture Collection, CCTCC for short, address: wuhan university in Wuhan, China, with a preservation date of 2021, 05 month 17, was classified and named as vibrio algingomyticus HD-1(Hfq deleted).
Further, the pTargetF-Hfq recombinant plasmid targeting Hfq gene was constructed as follows:
constructing a pTargetF-Hfq vector containing a 20bp Hfq gene fragment by using a primer G2F/G2R by using the pTargetF plasmid as a template; because the forward and reverse primers have reverse complementary positions, the PCR product is a ring-forming structure, directly obtains a pTargetF-Hfq vector, and recovers the pTargetF-Hfq plasmid through a glue recovery process; 16S rRNA sequencing using G1F/G1R;
wherein the content of the first and second substances,
the G1F/G1R primer sequences are as follows:
G1 F：5’-CCCCTGATTCTGTGGATA-3’；SEQ ID NO.4；
G1 R：5’-TTCAAGTTGATAACGGACTA-3’；SEQ ID NO.5；
the primer G2F/G2R has the following sequence:
G2 F：5’-GCTACGTCGTGAGCGTATCCGTTTTAGAGCTAGAAATAGCA-3’；SEQ ID NO.2；
G2 R：5’-GGATACGCTCACGACGTAGCCTAGTATTATACCTAGGACTG-3’；SEQ ID NO.3；
the reaction system is as follows: taq enzyme 25. mu.L, ddH2O19. mu.L, 2. mu.L of pTargetF plasmid diluted 1000-fold, 2. mu.L each of the G2F/G2R primers;
the reaction procedure is as follows: the initial denaturation step was carried out at 94 ℃ for 5 minutes, followed by denaturation at 94 ℃ for 45 seconds in 35 cycles, annealing at 68 ℃ for 1 minute, extension at 72 ℃ for 1 minute, and final extension at 72 ℃ for 5 minutes.
G1F one-way sequencing results:
TGTCCTTGAGTGAGCTGATACCGCTCGCCGCAGCCGAACGACCGAGCGCAGCGAGTCAGTGAGCGAGGAAGCGGAAGAGCGCCTGATGCGGTATTTTCTCCTTACGCATCTGTGCGGTATTTCACACCGCATATGCTGGATCCTTGACAGCTAGCTCAGTCCTAGGTATAATACTAGGCTACGTCGTGAGCGTATCCGTTTTAGAGCTAGAAATAGCAAGTTAAAATAAGGCTAGTCCGTTATCAACTTGAA；SEQ ID NO.6；
the underlined part is the Hfq gene sequence inserted in the pTargetF plasmid.
Further, the construction method of the homology arm is as follows:
taking the genome of a vibrio alginolyticus wild strain as a template, respectively amplifying a front-segment gene fragment AB and a rear-segment gene fragment CD of a target gene by using primers AF/BR and CF/DR, performing 16srRNA gene sequencing, after the sequencing result is verified successfully, amplifying the gene fragment AB and the gene fragment CD by using the primers AF/DR, and splicing the two segments of genes to obtain a homology arm;
wherein the sequences of the primers AF/BR and CF/DR are as follows:
AF：5’-TTTATCTCGGGCATTGGA-3’；SEQ ID NO.7；
BR：5’-AGGTGATTTGACGCTTGG-3’；SEQ ID NO.8；
CF：5’-CCAAGCGTCAAATCACCTACGCAAGAAGGTGAATGG-3’；SEQ ID NO.9；
DR：5’-TACGGTTGAAGAGTGTCG-3’；SEQ ID NO.10；
the underlined sequence in CF is an additional terminal primer complementary to the BR reverse direction, so that the front end of the CD gene segment has a gene segment complementary to the terminal of the AB segment, and splicing is carried out through the coincident gene segments.
The reaction system is as follows: taq enzyme 25. mu.L, ddH2O18. mu.L, template AB 1. mu.L, template CD 2. mu.L, primer AF 2. mu.L, primer DR 2. mu.L;
the reaction procedure is as follows: the initial denaturation step was carried out at 94 ℃ for 5 minutes, followed by denaturation at 94 ℃ for 45 seconds in 35 cycles, annealing at 55 ℃ for 1 minute, extension at 72 ℃ for 1 minute, and final extension at 72 ℃ for 5 minutes.
The AB gene fragment is located at 286-639bp upstream of the target gene, and the CD gene fragment is located at 93-687bp downstream of the target gene.
The nucleotide sequence of the Hfq gene is shown in SEQ ID NO. 1:
ATGGCTAAGGGGCAATCTCTACAAGACCCATTTCTAAACGCGCTACGTCGTGAGCGTATCCCGGTATCTATCTACCTTGTGAATGGTATTAAACTACAAGGTCAGATCGAATCATTCGATCAATTTGTGATCCTGCTGAAGAATACTGTTAACCAAATGGTGTACAAGCACGCGATCTCAACAGTTGTGCCGGCTCGTCCAGTGAGCCATCACAGCGGTGAACGTCCACAAGGTGAGCGTCCACAAGAGAAATCTGAAGATTAA；SEQ ID NO.1。
further, the Vibrio alginolyticus Hfq gene knockout mutant strain is applied to reduction of Vibrio alginolyticus virulence.
Further, the nucleotide sequence of the Hfq gene is shown as SEQ ID NO. 1.
Further, the application of the Hfq gene knockout mutant strain of the vibrio alginolyticus in reducing the toxicity of the vibrio alginolyticus and reducing the pathogenicity to scallops.
According to the technical scheme, compared with the prior art, the invention discloses and provides the Hfq gene knockout mutant strain of the vibrio alginolyticus and the application thereof, the CRISPR/Cas system is widely existed in genomes of bacteria and archaea, the high efficiency and the accuracy of the system are utilized to construct the mutant strain of the vibrio alginolyticus, the important effect of Hfq on the toxicity of the vibrio alginolyticus is proved by comparing the pathogenicity of the mutant strain and a wild strain on chlamys farreri, and the pathogenic mechanism of the vibrio alginolyticus is further researched. These findings lay the foundation for further research of vibriosis.
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, it is obvious that the drawings in the following description are only embodiments of the present invention, and for those skilled in the art, other drawings can be obtained according to the provided drawings without creative efforts.
FIG. 1 is a drawing showing the results of resistance of a Vibrio alginolyticus wild-type strain to spectinomycin and kanamycin;
wherein, 1, does not contain a resistant 2216E culture medium; 2, 2216E medium containing 50 μ g/ml kanamycin; 3, 2216E medium containing 150 μ g/ml kanamycin; 4, no resistant 2216E medium; 5, 2216E medium containing 50 μ g/ml spectinomycin; 6, 2216E medium containing 150. mu.g/ml spectinomycin;
FIG. 2 is a diagram showing the result of electrophoresis for verifying positive clones according to the present invention;
wherein, M: DNA marker (50-500 bp); 1-8 are negative clones; 9 is positive clone;
FIG. 3 is a transmission electron micrograph of a strain according to the present invention;
wherein, 1, wild type strains; mutant strains (Vibrio alginolyticus v. DELTA. Hfq-).
Detailed Description
The technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the drawings in the embodiments of the present invention, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
The pCas plasmid contains the kanamycin resistance gene and the pTargetF plasmid contains the spectinomycin resistance gene. The primers used in the invention are synthesized by Shanghai bioengineering GmbH.
Example 1 construction of Vibrio alginolyticus v. DELTA. Hfq-
(1) Resistance test
The research institute screens and identifies diseased chlamys farreri to obtain vibrio alginolyticus wild strain.
An antibiotic experiment was performed on a Vibrio alginolyticus wild-type strain, and 100. mu.l of the strain (OD ═ 1.0) was applied to a 2216E medium plate containing no resistance, a 2216E medium plate containing 50. mu.g/ml spectinomycin, a 2216E medium plate containing 150. mu.g/ml spectinomycin, a 2216E medium plate containing 50. mu.g/ml kanamycin, and a 2216E medium plate containing 150. mu.g/ml kanamycin, respectively, and the strain was cultured in an incubator at 28 ℃ for 24 hours to observe the growth of the wild-type strain, and the results are shown in FIG. 1.
FIG. 1 shows the results of resistance experiments, that the Vibrio alginolyticus wild-type strain has no resistance or very low resistance to kanamycin and spectinomycin at 150. mu.g/ml.
(2) Construction of pTargetF-Hfq recombinant plasmid
Using pTargetF plasmid (Jiang Yu, Chen Biao, Duan Chunlan, Sun Bingbig, Yang Junjie, Yang Sheng. multigene editing in the Escherichia coli genome via the CRISPR-Cas9 system. [ J ]. Applied and environmental microbiology, 352015, 81(7).) as template, pTargetF-Hfq vector containing 20bp Hfq gene fragment was constructed using primer G2F/G2R, thus obtaining pTargetF-Hfq recombinant plasmid targeting Hfq gene. Wherein the primer G2F/G2R has the following sequence:
G2 F：5’-GCTACGTCGTGAGCGTATCCGTTTTAGAGCTAGAAATAGCA-3’；SEQ ID NO.2；
G2 R：5’-GGATACGCTCACGACGTAGCCTAGTATTATACCTAGGACTG-3’；SEQ ID NO.3；
among them, the underlined part is a 20bp Hfq gene fragment.
The reaction system is as follows: taq enzyme 25. mu.L, ddH2O19. mu.L, 2. mu.L of pTargetF plasmid diluted 1000-fold, 2. mu.L each of the G2F/G2R primers.
The reaction procedure is as follows: the initial denaturation step was carried out at 94 ℃ for 5 minutes, followed by denaturation at 94 ℃ for 45 seconds in 35 cycles, annealing at 68 ℃ for 1 minute, extension at 72 ℃ for 1 minute, and final extension at 72 ℃ for 5 minutes.
The pTargetF-Hfq vector is recovered by a gel recovery kit, and whether the pTargetF-Hfq vector is correctly inserted into the sequence of the Hfq gene fragment is verified by PCR amplification by using a G1F/G1R primer.
Wherein the primer sequences of G1F/G1R are as follows:
G1 F：5’-CCCCTGATTCTGTGGATA-3’；SEQ ID NO.4；
G1 R：5’-TTCAAGTTGATAACGGACTA-3’；SEQ ID NO.5；
G1F one-way sequencing results:
TGTCCTTGAGTGAGCTGATACCGCTCGCCGCAGCCGAACGACCGAGCGCAGCGAGTCAGTGAGCGAGGAAGCGGAAGAGCGCCTGATGCGGTATTTTCTCCTTACGCATCTGTGCGGTATTTCACACCGCATATGCTGGATCCTTGACAGCTAGCTCAGTCCTAGGTATAATACTAGGCTACGTCGTGAGCGTATCCGTTTTAGAGCTAGAAATAGCAAGTTAAAATAAGGCTAGTCCGTTATCAACTTGAA；SEQ ID NO.6；
the underlined part is the Hfq gene sequence inserted in the pTargetF plasmid.
The pTargetF-Hfq vector verified to be correct was transformed into DH 5. alpha. competence by chemical transformation, cultured in LB medium, and pTargetF-Hfq recombinant plasmid was extracted using plasmid extraction cassette and stored at-20 ℃.
(3) Construction of homology arms
And (2) taking the genome of the vibrio alginolyticus wild strain as a template, amplifying the front-segment gene fragment AB and the back-segment gene fragment CD of the target gene by using primers AF/BR and CF/DR respectively, after successful verification, amplifying by using the primers AF/DR by using the gene fragment AB and the gene fragment CD as templates, and splicing the two segments of genes to obtain the homologous arm.
Wherein the sequences of the primers AF/BR and CF/DR are as follows:
AF：5’-TTTATCTCGGGCATTGGA-3’；SEQ ID NO.7；
BR：5’-AGGTGATTTGACGCTTGG-3’；SEQ ID NO.8；
CF：5’-CCAAGCGTCAAATCACCTACGCAAGAAGGTGAATGG-3’；SEQ ID NO.9；
DR：5’-TACGGTTGAAGAGTGTCG-3’；SEQ ID NO.10；
the reaction system is as follows: taq enzyme 25. mu.L, ddH2O18. mu.L, template AB 1. mu.L, template CD 2. mu.L, primer AF 2. mu.L, primer DR 2. mu.L.
The reaction procedure is as follows: the initial denaturation step was carried out at 94 ℃ for 5 minutes, followed by denaturation at 94 ℃ for 45 seconds in 35 cycles, annealing at 55 ℃ for 1 minute, extension at 72 ℃ for 1 minute, and final extension at 72 ℃ for 5 minutes.
(4) Gene knockout
Taking a vibrio alginolyticus wild strain as a knockout object, firstly preparing a competent cell of the vibrio alginolyticus wild strain, transferring a pCas plasmid into the competent cell of the vibrio alginolyticus wild strain by using an electroporation transformation method, and sequencing to obtain a positive monoclonal containing the pCas plasmid; after successful verification, the vibrio alginolyticus containing the pCas plasmid is continuously prepared into a competent cell v. delta pCas +, the pTargetF-Hfq recombinant plasmid and a homologous arm are simultaneously transformed into the competent cell V. delta pCas + by an electroporation transformation method, a bacterial solution recovered in a 2216E culture medium is coated on a 2216E plate simultaneously containing 150 mu g/ml kanamycin and 150 mu g/ml spectinomycin, the culture is carried out at 28 ℃, and a single colony is picked for nucleic acid gel electrophoresis and 16SrRNA identification.
Positive monoclonal sequencing results with pCas plasmid:
GGGGATCCGTGAGGTTGAGTAGTGCCACACAGCATAAAATTAGCTTGGTTTCATGCTCCGTTAAGTCATAGCGACTAATCGCTAGTTCATTTGCTTTGAAAACAACTAATTCAGACATACATCTCAATTGGTCTAGGTGATTTTAATCACTATACCAATTGAGATGGGCTAGTCAATGA；SEQ ID NO.11；
the pCas plasmid is successfully transferred into the competent cell of the vibrio alginolyticus wild strain.
In order to identify whether the Hfq gene of the monoclonal colony is successfully knocked out, the genome of the selected monoclonal colony is subjected to PCR amplification by using HfqF/Hfq R primers. 16S rRNA sequencing was performed using Hfq-1F/Hfq-1R.
The HfqF/HfqR primer sequence is as follows:
Hfq F：5’-TTTGCATTGCACCACTAG-3’；SEQ ID NO.12；
Hfq R：5’-CTCACCGGATTCATAACG-3’；SEQ ID NO.13；
Hfq-1F：5’-TCCATACGATGCGTCGGTTA-3’；SEQ ID NO.14；
Hfq-1R：5’-CAGGAGAGAGGGCGTGATTA-3’；SEQ ID NO.15；
the PCR products were analyzed by 1.1% agarose gel electrophoresis, and the results are shown in FIG. 2. FIG. 2 shows that the monoclonal strain No. 9 is a positive clone, and no band of the Hfq gene fragment is detected; meanwhile, the sequencing result of 16S rRNA shows that the Hfq gene segment of the strain is deleted. Indicating that the vibrio alginolyticus which lacks Hfq gene segment is obtained v.
And (3) sequencing results:
ATCAGCCAGTATTTAGATGGGGAGTGTACACGTGACGAAGCGGTATTTCGTGGCGTATGCGCGACTCGTCAATTGGCCAAGCGTCAAATCACCTCGCAAGAAGGTGAATGGGAAGATCTGGCTGAGTTCGAAATGCTGGTTTCTTCTGCTGGGGTAGAGGCGCTACAAGTGGTAACTGGTAGTCGTCAATCCCCACACCCGAAATACTATGTCGGAGAGGGTAAGGCCCAAGAGATTGCTACAGCGGTACAATCAACGGGTGCCGAAATTGTGATTTTTAA；SEQ ID NO.16；
sequencing results show that the target gene is knocked out.
The wild type and mutant strains were inoculated into 2216E plates and cultured at 28 ℃ for 24 hours, respectively, and the colony characteristics were observed under a transmission electron microscope (JEM-1200EX, JOEL, Tokyo, Japan). As shown in FIG. 3, both the wild type and mutant strains showed an oval shape, the wild type strain had periphytic flagella and terminal flagella, and the mutant strain had periphytic flagella shed and only terminal flagella grew.
EXAMPLE 2 determination of LD50
Culturing wild strain and mutant strain in 2216E culture medium at 28 deg.C, centrifuging, and filtering with 0.45 μm filter membrane to obtain seawater (strong aquatic product)Wholesale, Qingdao) to 1 × 108、1×107、1×106、1×105、1×104CFU/mL, 5 concentration gradients in total, divided into three groups (wild type, mutant strain, filtered seawater control group), selecting scallops with good activity, ensuring the consistent number of the experimental objects of each gradient, adopting a 20 ℃ soaking and dip dyeing mode, recording the death condition every 24h, calculating LD50 by using regression analysis in SPSS.22, and the results are shown in Table 1.
TABLE 1
The results in Table 1 show that the LD50 of the mutant strain is 2.98X 10 after soaking and dip dyeing for 2 days at 20 DEG C6CFU/mL, LD50 of wild strain 1.09X 105CFU/mL, LD50 concentration increased to 27 times.
The previous 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.
Sequence listing
<110> department of natural resources first oceanographic institute
<120> vibrio alginolyticus Hfq gene knockout mutant strain and application thereof
<160> 15
<170> SIPOSequenceListing 1.0
<210> 1
<211> 264
<212> DNA
<213> Artificial Sequence
<400> 1
atggctaagg ggcaatctct acaagaccca tttctaaacg cgctacgtcg tgagcgtatc 60
ccggtatcta tctaccttgt gaatggtatt aaactacaag gtcagatcga atcattcgat 120
caatttgtga tcctgctgaa gaatactgtt aaccaaatgg tgtacaagca cgcgatctca 180
acagttgtgc cggctcgtcc agtgagccat cacagcggtg aacgtccaca aggtgagcgt 240
ccacaagaga aatctgaaga ttaa 264
<210> 2
<211> 41
<212> DNA
<213> Artificial Sequence
<400> 2
gctacgtcgt gagcgtatcc gttttagagc tagaaatagc a 41
<210> 3
<211> 41
<212> DNA
<213> Artificial Sequence
<400> 3
ggatacgctc acgacgtagc ctagtattat acctaggact g 41
<210> 4
<211> 18
<212> DNA
<213> Artificial Sequence
<400> 4
cccctgattc tgtggata 18
<210> 5
<211> 20
<212> DNA
<213> Artificial Sequence
<400> 5
ttcaagttga taacggacta 20
<210> 6
<211> 252
<212> DNA
<213> Artificial Sequence
<400> 6
tgtccttgag tgagctgata ccgctcgccg cagccgaacg accgagcgca gcgagtcagt 60
gagcgaggaa gcggaagagc gcctgatgcg gtattttctc cttacgcatc tgtgcggtat 120
ttcacaccgc atatgctgga tccttgacag ctagctcagt cctaggtata atactaggct 180
acgtcgtgag cgtatccgtt ttagagctag aaatagcaag ttaaaataag gctagtccgt 240
tatcaacttg aa 252
<210> 7
<211> 18
<212> DNA
<213> Artificial Sequence
<400> 7
tttatctcgg gcattgga 18
<210> 8
<211> 18
<212> DNA
<213> Artificial Sequence
<400> 8
aggtgatttg acgcttgg 18
<210> 9
<211> 36
<212> DNA
<213> Artificial Sequence
<400> 9
ccaagcgtca aatcacctac gcaagaaggt gaatgg 36
<210> 10
<211> 18
<212> DNA
<213> Artificial Sequence
<400> 10
tacggttgaa gagtgtcg 18
<210> 11
<211> 179
<212> DNA
<213> Artificial Sequence
<400> 11
ggggatccgt gaggttgagt agtgccacac agcataaaat tagcttggtt tcatgctccg 60
ttaagtcata gcgactaatc gctagttcat ttgctttgaa aacaactaat tcagacatac 120
atctcaattg gtctaggtga ttttaatcac tataccaatt gagatgggct agtcaatga 179
<210> 12
<211> 18
<212> DNA
<213> Artificial Sequence
<400> 12
tttgcattgc accactag 18
<210> 13
<211> 18
<212> DNA
<213> Artificial Sequence
<400> 13
ctcaccggat tcataacg 18
<210> 14
<211> 20
<212> DNA
<213> Artificial Sequence
<400> 14
tccatacgat gcgtcggtta 20
<210> 15
<211> 20
<212> DNA
<213> Artificial Sequence
<400> 15
caggagagag ggcgtgatta 20
