CN108103156A - For detecting the specific primer of sunflower DNA and probe and real-time fluorescence quantitative PCR kit - Google Patents
For detecting the specific primer of sunflower DNA and probe and real-time fluorescence quantitative PCR kit Download PDFInfo
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Abstract
The present invention is provided to detect the specific primer of sunflower DNA and probe, the probe sequence is：5’‑ACGCTCTCCTCGCCAACAACAA‑3’；The specific primer be following sequences or be following sequences complementary strand sequence：Upstream primer sequence is 5 ' CAAATAGTCCGCCCACCACAA 3 '；Downstream primer sequence is 5 ' 5 ' TGGGAAGGGTTGTCAATGTTC 3 '.The present invention also provides corresponding real-time fluorescence quantitative PCR kits.The specific primer and probe and corresponding reagent box of the present invention can be used in real-time fluorescence quantitative PCR detection, and the method established has hypersensitivity and high specific, specificity can differentiate sunflower oil from a variety of oil crops such as peanut, flax, corn and soybean, potato, sesame, rape, walnut, sunflower, olive.
Description
Technical field
The present invention relates to molecular biology and external diagnosis reagent technical fields more particularly to a kind of sunflower DNA that is used for examine
The real-time fluorescent PCR reagent case of survey more particularly, to detects the specific primer and probe of sunflower DNA.
Background technology
The gene of detection edible oil DNA mass mainly has chloroplaset ATP, RBCL gene and species-specific gene.Design
Primer be derived from rbcL gene orders on chloroplaset.Chloroplaset is the important organelle of plant cell, and chloroplast DNA is extensive
For the research of phyletic evolution.Chloroplast gene has the conservative of height, and wherein rbcL genes are special just because of its evolution
It puts and is widely used in the research of botanical system generation.Rate is slower during evolution for its some code areas, than more conservative,
And evolutionary rate is than very fast between different species for some noncoding regions, with conservative in certain interspecific difference opposite sex and kind
Property, thus it is appropriate for species discriminating.It, can be to different by carrying out universal primer design to rbcL gene the preceding paragraphs sequence
Species are carried out at the same time amplification, and have interspecific difference different in nature simultaneously, and diversity ratio is larger between different species, are easy to carry out species
Differentiate.11S balls protein-2 genes are located on RBCL genes, are the key genes for synthesizing sunflower seed protein, have very high guard
Type.
Real-time fluorescence quantitative PCR (Fluorescence quantitative PCR) technology is stepped from Standard PCR qualitative detection
The step of upper quantization, its relatively conventional round pcr is advanced, it is easy to operate, can realize reality using Real-Time Fluorescent Quantitative PCR Technique
When monitoring, absolute quantitation and the purpose quickly detected, while there is high sensitivity, specific good, simple operation, therefore
It is very suitable for clinical detection.
Real-Time Fluorescent Quantitative PCR Technique has many branches, and quantitative manner is also different, is broadly divided into fluorescent dye insertion skill
Art, fluorescent probe technique and itself quenching fluorescence technology etc..Fluorescent dye embedded technology is to utilize the SYBR green I intercalations of DNA
Double-strand is the increased characteristic of fluorescence intensity, fluorescence signal is introduced double-stranded DNA, this method specificity is poor, is as a result subjected to and draws
The existing interference of object dimer and lead to problems such as false positive, therefore be not suitable for food and examine soon.And fluorescent probe technique
Such as Taqman technologies, molecular beacons technology are because it is specific than fluorescent dye embedded technology and itself quenching fluorescence technology
It is good, therefore it is more suitable for Food Inspection use.
The adulterated behavior of edible oil is frequently occurred currently on the market, and it is adulterated that Protocols in Molecular Biology is used to carry out edible oil
Detection, primarily on condition that extracting the DNA of suitable PCR amplification from grease.Due to table oil production need to pass through high temperature and
The processing such as high pressure, DNA degradation therein is fragment not of uniform size, and content is extremely low, this causes very big tired to DNA extractions
It is difficult.Thus there is an urgent need for building quick, easy, the accurate and efficient common adulterated molecular biology authentication technique system of edible oil, it is
Edible oil quality is supervised and control provides scientific method.
The content of the invention
It is a kind of for sunflower DNA inspections the present invention provides for detecting the specific primer of sunflower DNA and probe, also providing
The real-time fluorescent PCR reagent case of survey, have many advantages, such as it is quick, easy, accurate, efficient, have hypersensitivity and high specific.
First purpose of the present invention is to provide the specific primer and probe that detect sunflower DNA, the probe sequence
It is classified as：5’-ACGCTCTCCTCGCCAACAACAA-3’；
The specific primer be following sequences or be following sequences complementary strand sequence：
Upstream primer sequence is 5 '-CAAATAGTCCGCCCACCACAA-3 '；
Downstream primer sequence is 5 ' -5 '-TGGGAAGGGTTGTCAATGTTC-3 '.
Preferably, the fluorescent reporter group that 5 ' ends mark in probe is one kind in FAM, TET, JOE, HEX, VIC, 3 '
The fluorescent quenching group of end mark is one kind in TAMRA, DABCYL, BHQ.
Preferably, the sense primer and the anti-sense primer are to extend one to several bases to 5 ' ends and 3 ' extreme directions
Or delete a sequence obtained to several bases.
Second object of the present invention is to provide a kind of real-time fluorescence quantitative PCR kit for being used to detect sunflower DNA, institute
Stating real-time fluorescence quantitative PCR kit includes claim 1-3 any one of them specific primer and probe.
Preferably, in 10 μ l PCR reaction systems, the dosage of the sense primer is 0.1 μ l, the anti-sense primer
Dosage for 0.1 μ l, the dosage of the probe is 0.2 μ l.
Preferably, the real-time fluorescence quantitative PCR kit further includes series concentration standard items, positive control；It is described
Standard items are to be connected sunflower 11S RDNA genes with carrier, convert into competent cell induced expression, extract recombinant plasmid,
It is diluted after recombinant plasmid is quantified, obtains series concentration standard items.
Preferably, the nucleotides sequence of the standard items is classified as sequence 1 in sequence table.
Third object of the present invention is to provide above-mentioned specific primer and probe, real-time fluorescence quantitative PCR kit
It is following it is any in application：
(1) qualitatively or quantitatively detection or auxiliary detect sunflower DNA；
(2) product of qualitative or quantitative detection or auxiliary detection sunflower DNA are prepared；
(3) qualitatively or quantitatively whether sunflower oil is contained in detection or auxiliary detection vegetable oil；
(4) prepare in qualitative or quantitative detection or auxiliary detection vegetable oil whether the product containing sunflower oil.
Fourth object of the present invention be to provide it is a kind of detection or auxiliary detection vegetable oil in whether the side containing sunflower oil
Method respectively using standard items and sample to be tested DNA as template, carries out real-time fluorescence quantitative PCR using specific primer and probe, leads to
The Ct values for crossing standard curve and sample to be tested judge result；Preferably, the sample to be tested DNA is carried using freeze-drying
It takes.
Preferably, the reaction condition of the real-time fluorescence quantitative PCR is：94 DEG C of pre-degenerations 2 minutes, 94 DEG C 15 seconds, 60
DEG C 40s simultaneously collects fluorescence signal, 40 cycles.
The present invention has the following advantages compared with prior art：
1st, the present invention uses gene clone technology, and the 11S rDNA genetic fragments of sunflower are inserted into carrier pMD18-T,
The recombinant plasmid containing 11S DNA genetic fragments is obtained, in this, as standard items.It is compiled according to the genetic fragment of sunflower 11S rDNA
Code gene order designs and synthesizes a group-specific primers and probe, optimizes PCR reaction conditions, establishes and gathered with real time fluorescent quantitative
Synthase chain reaction is the detection method of platform, and the method to being established is assessed：The method established can be used in real time
Fluorescence quantitative PCR detection, and with hypersensitivity, (sensitivity is 1.00 × 10 to the method established2) and Gao Te copies/ml
The opposite sex (can be from a variety of oil crops such as peanut, flax, corn and soybean, potato, sesame, rape, walnut, sunflower, olive
Specificity differentiates sunflower oil).
2nd, the present invention is reachable in conjunction with real-time fluorescence quantitative PCR detection technique by extracting the DNA in detected sample
The purpose of sunflower oil DNA content into accurate quantitative analysis sample to be measured carries out sunflower oil DNA available in scientific research and Food Inspection
Qualitative and quantitative analysis is conducive to carry out edible oil Variety identification technical research, will be carried for the quality safety management of edible oil
For scientific method, be conducive to the specification of domestic edible oil market, high-end edible oil foreign trade being smoothed out and entirely eating
With the sound development of oily industry.
3rd, the present invention is quick, easy, accurate and efficient.
Description of the drawings
Attached drawing is used for providing a further understanding of the present invention, and a part for constitution instruction, the reality with the present invention
Example is applied together for explaining the present invention, is not construed as limiting the invention.In the accompanying drawings：
Fig. 1 is the result that sunflower oil 11S genes are compared with other plant oil base because carrying out blast.
Fig. 2-4 is 3 pairs of primed probe specific b LAST comparison results.
Fig. 5 is amplified production electrophoresis result after the optimal primer pair is expanded different templates using regular-PCR method.
Fig. 6 is primer and probe system optimization experimental result of the present invention.Wherein, when 10 μ l systems are shown in figure, a representatives are drawn
(5 μM) of object adds in (5 μM) 0.2 μ l of addition of 0.1 μ l and probe；B represents (5 μM) of primer and adds in (5 μM) additions of 0.2 μ l and probe
0.1μl；C represents (5 μM) of primer and adds in (5 μM) 0.1 μ l of addition of 0.1 μ l and probe；D represents (5 μM) of primer and adds in 0.1 μ l and spy
(5 μM) 0.3 μ l of addition of pin；E represents (5 μM) of primer and adds in (5 μM) 0.2 μ l of addition of 0.3 μ l and probe；F represents (5 μM) of primer and adds
Enter (5 μM) 0.2 μ l of addition of 0.2 μ l and probe.
Fig. 7 is the standard curve of sunflower standard items of the present invention.
Fig. 8 is sensitivity experiment result of the present invention.Wherein A1 corresponds to plasmid concentration as 1.00 × 109Copies/ml, B1 are
1.00×108Copies/ml, C1 are 1.00 × 107Copies/ml, D1 are 1.00 × 106Copies/ml, E1 for 1.00 ×
105Copies/ml, F1 are 1.00 × 104Copies/ml, G1 are 1.00 × 103Copies/ml, H1 for 1.00 ×
102Copies/ml, I1 are 1.00 × 101Copies/ml and negative control.
Fig. 9 is specificity experiments result of the present invention.Wherein template is respectively：Peanut, flax, corn and soybean, potato, sesame
Fiber crops, rape, walnut, sunflower, olive, negative control.
Specific embodiment
Following embodiment facilitates a better understanding of the present invention, but does not limit the present invention.Experiment in following embodiments
Method is conventional method unless otherwise specified.The primer, probe and sequencing efforts used are by raw work biology work
Journey (Shanghai) limited company synthesizes and completes.
The preparation of 1 sunflower 11S rDNA gene standard items of embodiment
Establish real time fluorescence quantifying PCR method it may first have to which the external standards needed for preparation method, standard items should wrap
Containing highly conserved, special sequence, it is ensured that the high specific of reaction.The present invention is using sunflower 11S rDNA as target sequence.
The present embodiment mainly expands sunflower seed 11S rDNA genes using round pcr, and matter is connected to using gene recombination technology
In grain carrier pMD18-T, recombinant plasmid pMD18-T-11S is constructed, and carries out corresponding PCR identifications and sequencing identification, finally
Through quantitative as the standard items for treating method for building up, lay the foundation for the method and assessment of next step.
First, the preparation of template DNA
Sunflower seed genomic DNA is extracted, the template as the amplification of 11S rDNA gene PCRs.Using Shanghai life work biology
The Ezup pillar plant genome DNA extraction agent box kits of Technology Co., Ltd.'s production extract sunflower seed genome
DNA, specific extracting method are as follows：
Suitable plant tissue is taken to add in liquid nitrogen in mortar and is fully milled into subdivision.Transfer subdivision (fresh tissues of plants
It 100mg) to 1.5ml centrifuge tubes, not thaw, add in 550 μ l, 65 DEG C of preheating Buffer P1 and 4 μ l RNaseA and be acutely vortexed
It vibrates mixing 1 minute, is placed at room temperature for 10 minutes.The Buffer P2 of 130 μ l, abundant mixing are added in, 12000rpm is centrifuged 3 minutes.
Careful supernatant of drawing is careful not to be drawn onto boundary material, 12000rpm is centrifuged 1 minute, collects lower liquid to a splitter A.Add
The Buffer P3 for entering 1.5 times of volumes are softly vortexed at once, abundant mixing.Mixture obtained by previous step is added in into an adsorption column
In AC, (adsorption column is added in collecting pipe) 12000rpm is centrifuged 1 minute, outwells the waste liquid in collecting pipe.Add in 700 μ l rinsing liquids
WB, 12000rpm are centrifuged 1 minute, discard waste liquid.500 μ rinsing liquids WB, 12000rpm centrifugation 1 minute is added in, discards waste liquid.It will
Adsorption column AC is put back in sky collecting pipe, and 13000rpm is centrifuged 3-5 minutes, removes rinsing liquid as far as possible, is taken out adsorption column AC, is put into one
In a clean centrifuge tubes, 50 μ l elution buffer EB are added in the middle part of adsorption column, are placed at room temperature for 3-5 minutes,
12000rpm is centrifuged 1 minute and is collected DNA, can put -20 DEG C of preservations.
2nd, the PCR amplification of 11S rDNA genetic fragments
1st, the design and synthesis of primer
11S balls protein-2 genes are located on RBCL genes, are the key genes for synthesizing sunflower seed protein, have very high guarantor
Type is kept, therefore the present invention carries out design of primers on the basis of the gene.
The present invention to sunflower endogenous gene 11S rDNA complete sequences in ncbi database by carrying out bioinformatics comparison
Analysis is chosen and is suitble to the conservative fragments sequence for designing primer and probe for target, using 5 softwares of Primer Premier, if
One group of primer pair is counted.
The primer pair sequence is as follows：
Sense primer：11S1738F 5’-CAAATAGTCCGCCCACCACAA-3’
Anti-sense primer：11S1910R 5’-TGGGAAGGGTTGTCAATGTTC-3’.
2nd, PCR reaction systems and reaction condition
Using the sunflower DNA of extraction as template, using above-mentioned special primer sunflower 11S1738F/11S1910R as amplimer,
PCR amplification is carried out using following systems and reaction condition.
PCR system is as follows：
Wherein primer uses 11S1738F/11S1910R, and Taq enzyme wins day (BSA09M2) using Hangzhou, and PCR amplification instrument is
The grand PCR model MG96+ in Xi'an day.
Amplification program/reaction condition：94 DEG C of pre-degeneration 5min；94 DEG C of 30s, 55 DEG C of 30s, 72 DEG C of 1min, 35 Xun Huans；72
DEG C 10min takes 3 μ L amplified productions to carry out 1% agarose electrophoresis, detects PCR product size, is then produced using AXYGEN companies
The purifying of DNA gel QIAquick Gel Extraction Kit recycle remaining pcr amplification product.The sequence expanded using above-mentioned primer pair is：
5’-CAAATAGTCCGCCCACCACAAGACAGACGCTCTCCTCGCCAACAACAAGAGCAAGCGACGTCTCCT
CGCCAACAACAAGAGCAGCAGCAAGGCAGACGTGGCGGATGGAGCAACGGTGTGGAAGAAACCATCTGCAGCATGAA
GTTCAAAGTGAACATTGACAACCCTTCCCA-3’。
3rd, the structure of recombinant plasmid pMD18-T-11S rDNA and conversion
1st, coupled reaction：The pcr amplification product that above-mentioned purifying obtains and pMD18-T (Dalian treasured biotech firm) are connected
It connects, is prepared using following linked system：
Preparation completion is placed on 16 DEG C and carries out staying overnight coupled reaction.
2nd, the conversion of pMD18-T-11S plasmids and PCR identifications
1. taking out the DH5 α competent cells frozen from -70 DEG C of ultra low temperature freezer, being placed on ice chest makes it solve naturally
Freeze；
2. 10 μ L of connection product is taken to add in the DH5 α competent cells of 50 μ L, postposition ice bath is gently shaken up 30 minutes；
3. heat shock 90 seconds, puts cooled on ice 2min immediately in 42 DEG C of water-baths after heat shock；
After 4. LB fluid nutrient mediums (being free of ampicillin) mixing of the 400ml of precooling is added in into 1.5ml EP pipes,
37 DEG C of 200 revs/min of jog culture 1h；
5. 100 μ l is taken to be coated on the LB tablets containing Amp after above-mentioned culture solution is shaken up, face up and place 30min, treat
After bacterium solution is cultured base absorption completely, 37 DEG C of insulating box overnight incubations of culture dish are inverted；
6. next day is observed, picking white monoclonal diluting colonies draw 2 μ L conducts in 50 μ L sterile waters from tablet
Pcr template, remaining dilution bacterium solution are added in the LB culture mediums of 20ml expand and shake；
7. expanding above-mentioned dilution bacterium solution with carrier universal primer RV-M/M13-47, PCR product uses 1% Ago-Gel
Electrophoresis identifies positive transformant by detecting PCR product size.
Primer RV-M/M13-47 sequences are as follows：
Primer RV-M:5’-GAGCGGATAACAATTTCACACAGG-3’
Primer M13-47:5’-CGCCAGGGTTTTCCCAGTCACGAC-3’
PCR reaction systems are as follows：
Amplification program/reaction condition：94 DEG C of pre-degeneration 5min；94 DEG C of 30s, 55 DEG C of 30s, 72 DEG C of 1min, 35 Xun Huans；72
℃10min。
Positive recombinant plasmid pMD18-T-11S rDNA are extracted using the Plasmid Preparation kit of Axygen companies production, are surveyed
Determine concentration and purity, while draw a part of plasmid purification and supreme marine growth Engineering Co., Ltd is sent to be sequenced, determine insertion
The gene order of segment is consistent with aim sequence.
4th, the acquisition of standard items and quantitative
1st, by the 100 μ L transferred speciess of bacillus coli DH 5 alpha containing recombinant plasmid pMD18-T-11S rDNA that step 3 obtains in
The LB fluid nutrient mediums of 5mL, 37 DEG C of 200rpm shake training overnight；
2nd, the bacterium solution transferred speciess of 1ml overnight incubations is taken in 30ml LB fluid nutrient mediums, when 200rpm Zengjing Granules 2-3 is small, so
Afterwards using the Plasmid Preparation kit extraction plasmid of Axygen companies production；
3rd, the plasmid of extraction is measured using ultramicron ultraviolet-uisible spectrophotometer, measures A260、A280, according to
A260/A280The purity of plasmid is judged, according to A260Absorbance can calculate the content of Plasmid DNA in sample, i.e. 1OD values phase
When in 50 μ g/ml double-stranded DNAs.
4th, plasmid pMD18-T-11S rDNA concentration (copy number) calculates
(1) molecular weight=2865bp × 660 (average molecular weight of each pair base) of plasmid
(2) plasmid concentration is measured as 136.5 μ g/ul.Cause is when carrying out real-time fluorescence quantitative PCR, it is necessary to " copy number "
For unit, it is therefore desirable to by Conversion of measurement unit into copies/ml.
Plasmid copies/ml=Avgadro constants × plasmid molal quantity
Wherein Avgadro constant=6.02 × 1023copies/mol。
Therefore plasmid concentration copies/ml=136.5 μ g/ml × 10 of extraction-9×6.02×1023copies/mol÷
(2865bp × 660g/bpmol)=4.34 × 1010copies/ml
The sterile water of+33.4 μ l of 10 μ l plasmids just obtains concentration as 1.00 × 1010The plasmid of copies/ml, then by the matter
Grain carries out 10 doubling dilutions and just can obtain a series of plasmid of concentration, and is saved backup in -20 DEG C.
2 real-time fluorescence quantitative PCR kit of embodiment
First, the design and synthesis of specific primer and probe
Using the conservative fragments of the 11S rDNA genes of the sunflower of above-mentioned selection as target, using Primer Premier 5
Software devises one group of real-time fluorescence quantitative PCR primer and probe.
In order to distinguish the frequently seen plants such as sunflower and peanut, corn and soybean, potato, sesame, rape, flax, walnut and olive
Oil, the sunflower oil detection zone chosen in of the invention are the 11S ball protein-2 genes on RBCL genes, which is synthesis sunflower seed
The key gene of protein has very high conservative.Sunflower oil 11S genes are subjected to blast comparisons in NCBI, as a result such as
Fig. 1.
Comparison result shows that sunflower 11S ball protein-2 genes conservatives are very high, in the chromosome 1 belonged in Burkholderia, splits a silk ribbon
There is presence in the genome of Eimeria, there is Homoeology.With Vegetable Oils such as peanut oil Arah1 genes, corn oil corn alcohol
Molten albumen Zein genes, soybean oil Lectin genes, sesame oil Zein rDNA bases, siritch FAD3a without any homology, because
This can design primed probe for detecting sunflower oil on this gene.
Sunflower 11S ball protein-2 genes are downloaded on NCBI, pass through Primer Premier 5 and Becon Designer softwares
Multipair 11S balls protein-2 genes primer and probe is devised, and passes through the progress primer specificity verifications of the BLAST in NCBI and thinks wherein
There are three pairs of primer specificities all very high.Comparison result is shown in Fig. 2-Fig. 4.
Fig. 2-4 is 3 pairs of primed probe specific b LAST comparison results.
Every pair of primers of sunflower is subjected to primer specificity screening by regular-PCR, the template of selection is：Sunflower, greatly
Beans, flax, peanut, rape, corn, sesame, olive, walnut, potato, using water as feminine gender, amplified band runs glue, in three pairs of primers
There are the PCR specificity highests of pair of primers, the nucleotides sequence of the primer pair is classified as：
Sense primer：11S1738F 5’-CAAATAGTCCGCCCACCACAA-3’
Anti-sense primer：11S1910R 5’-TGGGAAGGGTTGTCAATGTTC-3’.
Fig. 5 is amplified production electrophoresis result after the optimal primer pair is expanded different templates using regular-PCR method.Its
In, from left to right it is followed successively by：Mark, soybean, sunflower, flax, peanut, rape, corn, sesame, olive, walnut, potato, water.
Fluorescence quantification PCR primer specificity screening is carried out using the primer and probe, experimental result is that the primed probe is true
Specific requirements can be met in fact.It is specific as follows：
As the core of the present invention, one group of primer and probe nucleotide sequence for sunflower real time fluorescent PCR detection method is such as
Under：
Sense primer：11S1738F 5’-CAAATAGTCCGCCCACCACAA-3’
Anti-sense primer：11S1910R 5’-TGGGAAGGGTTGTCAATGTTC-3’
Probe：5’-FAM-ACGCTCTCCTCGCCA ACAACAA-TAMRA-3’；
The fluorescent reporter group of 5 ' end marks is one kind in FAM, TET, JOE, HEX, VIC in probe, 3 ' end marks
Fluorescent quenching group is one kind in TAMRA, DABCYL, BHQ.
The primer and probe expands Target Nucleotide Sequence：
5’-CAAATAGTCCGCCCACCACAAGACAGACGCTCTCCTCGCCAACAACAAGAGCAAGCGACGTCTCCT
CGCCAACAACAAGAGCAGCAGCAAGGCAGACGTGGCGGATGGAGCAACGGTGTGGAAGAAACCATCTGCAGCATGAA
GTTCAAAGTGAACATTGACAACCCTTCCCA-3’。
2nd, the preparation of sample to be tested
The present invention extracts vegetable oil DNA using freeze-drying, ensures the purity and concentration of vegetable oil DNA extractions.
Because refined oil is less by complicated processing rear impurity, therefore how effectively the emphasis that DNA is extracted in refined oil is
Enriching plant oil in minim DNA.The process as a concentration is freeze-dried, DNA concentration can be made to be increased to precipitation and made
In the range of, prepare for subsequent precipitation, ensure the purity and concentration of vegetable oil DNA extractions.
1. sample pre-treatments
1) sunflower oil 20ml is taken in 50ml centrifuge tubes, adds 20ml sterile waters, vibrates 30min；
2) 5000r/min centrifuges 30min, is carefully mutually transferred to water in culture dish；
3) culture dish is put in -80 DEG C of freeze overnights, culture dish then is gone to vacuum drying machine steams completely to moisture
Hair.
2. cracking is with separating
1) plus 1-2ml CTAB Extraction buffers (in 1000ml water dissolve CTAB 20g, Tris 12.1114g,
NaCl81.1816g, Na2EDTA7.4144g, high pressure sterilization) into culture dish, 65 DEG C of warm bath 10min；
2) culture dish is rinsed repeatedly with CTAB Extraction buffer carefuls, buffer solution is transferred to 1.5ml centrifuge tubes
In；
3) 400 μ L/ are managed, and add 1 μ L2.5% linear acrylamides, 3mol/l NaAc, the 1ml absolute ethyl alcohols of 1/10 volume,
Mixing, -20 DEG C of placement 1h；
4) 15000r/min centrifuges 10min removal supernatants, and 70% ethyl alcohol is washed precipitation 1 time, dried；
5) plus 100 μ L sterile waters fully dissolve precipitation, -20 DEG C of preservations.
3rd, real-time fluorescence quantitative PCR condition optimizing
Using concentration as 1.00 × 106The positive plasmid of copies/ml be template, using hundred Imtech production 2 ×
Real-time PCR Premixture (probe) real-time fluorescence quantitative PCR kit is tested, and tests the real-time glimmering of use
Fluorescent Quantitative PCR instrument is Suzhou Bai Yuan gene technology Co., Ltd ASA-4800 real-time fluorescence quantitative PCRs.
Reaction system uses 10 μ l systems, and the wherein amount of primer and probe is reacted using the combination of table 1.
Table 1
Reaction condition：94 DEG C of pre-degenerations 2 minutes, 94 DEG C 15 seconds, 60 DEG C of 40s and collect fluorescence signal, 40 cycles.As a result
Reference Fig. 1, when data show 10 μ l systems, when primer (5 μM) is separately added into (5 μM) 0.2 μ l of addition of 0.1 μ l and probe, Ct values
Minimum, fluorescence signal are most strong.
Fig. 6 is primer and probe system optimization experimental result of the present invention.Wherein, when 10 μ l systems are shown in figure, a representatives are drawn
(5 μM) of object adds in (5 μM) 0.2 μ l of addition of 0.1 μ l and probe；B represents (5 μM) of primer and adds in (5 μM) additions of 0.2 μ l and probe
0.1μl；C represents (5 μM) of primer and adds in (5 μM) 0.1 μ l of addition of 0.1 μ l and probe；D represents (5 μM) of primer and adds in 0.1 μ l and spy
(5 μM) 0.3 μ l of addition of pin；E represents (5 μM) of primer and adds in (5 μM) 0.2 μ l of addition of 0.3 μ l and probe；F represents (5 μM) of primer and adds
Enter (5 μM) 0.2 μ l of addition of 0.2 μ l and probe.4th, the foundation of real-time fluorescence quantitative PCR kit
1st, real-time fluorescence quantitative PCR kit includes following components：
2 × premix, final concentration of 5 μM of sense primer, final concentration of 5 μM of anti-sense primer, final concentration of 5 μM of spy
11S rDNA gene series concentration standards (1.00 × 10 prepared by pin, embodiment 18copies/ml、1.00×107copies/
ml、1.00×106copies/ml、1.00×105copies/ml、1.00×104Copies/ml), (concentration is positive control
1.00×10711S rDNA recombinant plasmid pMD18-T-11S rDNA prepared by the embodiment 1 of copies/ml) and ddH2O,
ddH2O is used as reagent and negative control.
Sense primer：11S1738F 5’-CAAATAGTCCGCCCACCACAA-3’
Anti-sense primer：11S1910R 5’-TGGGAAGGGTTGTCAATGTTC-3’
Probe：5’-FAM-ACGCTCTCCTCGCCA ACAACAA-TAMRA-3’；
The fluorescent reporter group of 5 ' end marks is one kind in FAM, TET, JOE, HEX, VIC in probe, 3 ' end marks
Fluorescent quenching group is one kind in TAMRA, DABCYL, BHQ.
2nd, using the standard curve of real-time fluorescence quantitative PCR kit measurement standard items
The 11S rDNA gene series concentration standards (1.00 × 10 prepared with embodiment 18copies/ml、1.00×
107copies/ml、1.00×106copies/ml、1.00×105copies/ml、1.00×104Copies/ml it is) template,
Using the primer and probe in kit, fluorescent quantitative PCR is carried out, while positive control and negative control are set.
PCR reaction systems are as follows：
Reaction condition：94 DEG C of pre-degenerations 2 minutes, 94 DEG C 15 seconds, 60 DEG C of 40s and collect fluorescence signal, 40 cycles.
The preparation method of standard curve：Using the logarithm of the plasmid concentration of standard items as abscissa, obtained using ct values as ordinate
To standard curve, as a result with reference to figure 7.Standard curve original equation is y=a+bx, and the equation of this standard curve is y=
38.57-3.13x。
Fig. 7 is the standard curve of sunflower standard items of the present invention.As shown in Figure 7, standard items standard curve is smooth, related coefficient
Height is specially R2=0.9987, meet the requirement of real-time fluorescence quantitative PCR detection.
3 real-time fluorescence quantitative PCR kit of embodiment is to the quantitative detecting method of sample to be tested
Prepared respectively with sample to be tested DNA and embodiment 1 11S rDNA gene series concentration standards (1.00 ×
108copies/ml、1.00×107copies/ml、1.00×106copies/ml、1.00×105copies/ml、1.00×
104Copies/ml it is) template, using the primer and probe in kit, carries out fluorescent quantitative PCR, while the positive is set
Control and negative control.
PCR reaction systems are as follows：
Reaction condition：94 DEG C of pre-degenerations 2 minutes, 94 DEG C 15 seconds, 60 DEG C of 40s and collect fluorescence signal, 40 cycles.Pass through
The Ct values of standard curve and sample to be tested carry out Quantitative detection.
The performance test of 4 real-time fluorescence quantitative PCR kit of embodiment
1st, sensitivity experiment
The above-mentioned plasmid being prepared is subjected to 10 doubling dilutions and obtains a series of plasmid of concentration, it is 1.00 to choose concentration
×109copies/ml、1.00×108copies/ml、1.00×107copies/ml、1.00×106copies/ml、1.00×
105copies/ml、1.00×104copies/ml、1.00×103copies/ml、1.00×102copies/ml、1.00×
101Copies/ml etc. is used as gradient template.Reaction system is as follows：
Reaction condition：94 DEG C of pre-degenerations 2 minutes, 94 DEG C 15 seconds, 60 DEG C of 40s and collect fluorescence signal, 40 cycles.According to
Fluorescence signal detected by instrument obtains fluorescence curve through software processing, observes the signal of fluorescence curve, is as a result shown (see Fig. 8)
Show when plasmid concentration reaches 1.00 × 102Fluorescence signal can be still detected during copies/ml, when plasmid concentration reaches 1.00 ×
101It can't detect fluorescence signal during copies/ml, therefore the sensitivity of this method is 1.00 × 102copies/ml。
Fig. 8 is sensitivity experiment result of the present invention.Wherein A1-I 1 correspond to plasmid concentration be respectively 1.00 ×
109copies/ml、1.00×108copies/ml、1.00×107copies/ml、1.00×106copies/ml、1.00×
105copies/ml、1.00×104copies/ml、1.00×103copies/ml、1.00×102copies/ml、1.00×
101Copies/ml and negative control.
2nd, specificity experiments
In order to confirm specificity of the present invention to sunflower detection, we have chosen other oil crops and do specificity experiments,
The oil crops of selection include：Peanut, flax, corn and soybean, potato, sesame, rape, walnut, sunflower, olive.
Wherein peanut, flax, corn and soybean, potato, sesame, rape, walnut, sunflower, olive etc. use hundred Tyke of Beijing
New quick-speed plant tissue gene group DNA extraction kit (DP3111) extracts DNA.Using hundred Imtech production 2 ×
Real-time PCR Premixture (probe) real-time fluorescence quantitative PCR kit is tested, and reaction system is as follows：
Reaction condition：94 DEG C of pre-degenerations 2 minutes, 94 DEG C 15 seconds, 60 DEG C of 40s and collect fluorescence signal, 40 cycles.According to
Fluorescence signal detected by instrument obtains fluorescence curve through software processing, observes the signal of fluorescence curve, analysis specificity.Knot
Fruit is feminine gender for only sunflower test positive, remaining oil crops with reference to figure 9, concrete outcome, and it is fine to show that the present invention has
Specificity (Ct values>36 be feminine gender).Testing result such as table 2.
Table 2
| Oil crops title | Ct values | Sentence read result |
| Peanut | Nothing | It is negative |
| Flax | Nothing | It is negative |
| Corn | Nothing | It is positive |
| Soybean | Nothing | It is negative |
| Potato | Nothing | It is negative |
| Semen sesami nigrum | Nothing | It is negative |
| Rape | Nothing | It is negative |
| Walnut | Nothing | It is negative |
| Sunflower | 20.05 | It is positive |
| Olive | Nothing | It is negative |
| Blank control | Nothing | It is negative |
Fig. 9 is specificity experiments result of the present invention.Wherein template is respectively：Peanut, flax, corn and soybean, potato, sesame
Fiber crops, rape, walnut, sunflower, olive, negative control.
Finally it should be noted that：The foregoing is only a preferred embodiment of the present invention, is not intended to limit the invention,
Although the present invention is described in detail with reference to the foregoing embodiments, for those skilled in the art, still may be used
To modify to the technical solution recorded in foregoing embodiments or carry out equivalent substitution to which part technical characteristic.
Within the spirit and principles of the invention, any modifications, equivalent replacements and improvements are made should be included in the present invention's
Within protection domain.
Sequence table
<110>Suzhou Bai Yuan gene technology Co., Ltd
<120>For detecting the specific primer of sunflower DNA and probe and real-time fluorescence quantitative PCR kit
<160> 1
<170> SIPOSequenceListing 1.0
<210> 1
<211> 173
<212> DNA
<213> 11S rDNA(11S rDNA)
<400> 1
caaatagtcc gcccaccaca agacagacgc tctcctcgcc aacaacaaga gcaagcgacg 60
tctcctcgcc aacaacaaga gcagcagcaa ggcagacgtg gcggatggag caacggtgtg 120
gaagaaacca tctgcagcat gaagttcaaa gtgaacattg acaacccttc cca 173
Claims (10)
1. for detecting the specific primer and probe of sunflower DNA, it is characterised in that：The probe sequence is：5’-
ACGCTCTCCTCGCCAACAACAA-3’；
The specific primer be following sequences or be following sequences complementary strand sequence：
Upstream primer sequence is 5 '-CAAATAGTCCGCCCACCACAA-3 '；
Downstream primer sequence is 5 ' -5 '-TGGGAAGGGTTGTCAATGTTC-3 '.
2. specific primer according to claim 1 and probe, it is characterised in that：The fluorescence report of 5 ' end marks in probe
Group is one kind in FAM, TET, JOE, HEX, VIC, and the fluorescent quenching group of 3 ' end marks is in TAMRA, DABCYL, BHQ
One kind.
3. specific primer according to claim 1 and probe, it is characterised in that：The sense primer and the downstream are drawn
Object is to 5 ' ends and 3 ' extreme directions extension one to several bases or deletes a sequence obtained to several bases.
4. a kind of real-time fluorescence quantitative PCR kit for being used to detect sunflower DNA, it is characterised in that：The real time fluorescent quantitative
PCR kit includes claim 1-3 any one of them specific primer and probe.
5. real-time fluorescence quantitative PCR kit according to claim 4, it is characterised in that：In 10 μ l PCR reaction systems
In, the dosage of the sense primer is 0.1 μ l, and the dosage of the anti-sense primer is 0.1 μ l, and the dosage of the probe is 0.2 μ l.
6. real-time fluorescence quantitative PCR kit according to claim 4 or 5, it is characterised in that：The real time fluorescent quantitative
PCR kit further includes series concentration standard items, positive control；The standard items are to connect sunflower 11S RDNA genes and carrier
It connects, converts into competent cell induced expression, extract recombinant plasmid, diluted after recombinant plasmid is quantified, obtain series concentration
Standard items.
7. real-time fluorescence quantitative PCR kit according to claim 6, it is characterised in that：The nucleotide of the standard items
Sequence is sequence 1 in sequence table.
8. any specific primers of claim 1-3 and any real time fluorescent quantitative of probe, claim 4-6
PCR kit it is following it is any in application：
(1) qualitatively or quantitatively detection or auxiliary detect sunflower DNA；
(2) product of qualitative or quantitative detection or auxiliary detection sunflower DNA are prepared；
(3) qualitatively or quantitatively whether sunflower oil is contained in detection or auxiliary detection vegetable oil；
(4) prepare in qualitative or quantitative detection or auxiliary detection vegetable oil whether the product containing sunflower oil.
9. it is a kind of detection or auxiliary detection vegetable oil in whether the method containing sunflower oil, it is characterised in that：Respectively with standard items
It is template with sample to be tested DNA, carries out real-time fluorescence quantitative PCR using specific primer and probe, by standard curve and treat
The Ct values of sample judge result；Preferably, the sample to be tested DNA is extracted using freeze-drying.
10. according to the method described in claim 9, it is characterized in that：The reaction condition of the real-time fluorescence quantitative PCR is：94
DEG C pre-degeneration 2 minutes, 94 DEG C 15 seconds, 60 DEG C of 40s and collect fluorescence signal, 40 cycles.
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110846410A (en) * | 2019-12-20 | 2020-02-28 | 西北民族大学 | Method for detecting walnut allergens in food by real-time fluorescent quantitative PCR |
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