Citrus fruit fly odorant binding protein-based attractant screening method
An odor-binding protein and Bactrocera dorsalis technology, applied in the field of bioengineering, can solve problems such as complex volatile components
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Embodiment 1
[0026] Example 1: Collection of Bacteralis dorsalis antennal total RNA and gene cloning of odorant binding protein OBP
[0027] 1 Cloning of Bacteralis dorsalis odorant-binding protein BdorOBP2
[0028] 1.1 Extraction of Bacteralis dorsalis total RNA
[0029] The total RNA of Bactrocera dorsalis was extracted with Trizol reagent, and the specific operation steps were as follows:
[0030] 1) Take out the preserved Bactrocera dorsalis sample from -80 ℃, put it into a mortar pre-cooled with liquid nitrogen, add liquid nitrogen to grind quickly, this step is performed on ice, and after being ground into powder, weigh 100 mg tissue sample into a 1.5 mL centrifuge tube, then add 1 ml Trizol reagent, and mix on a vortex mixer;
[0031] 2) Let the sample stand at room temperature for 5 minutes to completely separate the nucleic acid-protein complex;
[0032] 3) Centrifuge at 12 000×g for 5 minutes at 4°C;
[0033] 4) Transfer the supernatant to a new centrifuge tube (do not suck t...
Embodiment 2
[0064] Example 2: Bacteralis dorsalis odorant binding protein BdorOBP2 expression vector construction
[0065] 2.1 PCR amplification of BdorOBP2 gene
[0066] The total RNA of Bactrocera dorsalis was extracted, the first strand of cDNA obtained by reverse transcription was used as a template, and the front and back primers of BdorOBP2 designed and synthesized were used for PCR reaction, and the PCR results were electrophoresed on agarose gel, as shown in figure 1 As shown in , the target fragment of about 447bp was obtained, which was consistent with the expected fragment length.
[0067] 2.2 Identification of bacterial liquid PCR
[0068] The target fragment obtained by PCR amplification of the BdorOBP2 gene was recovered and purified by gel, connected with pMD?18-T Vector and transformed, after blue-white and ampicillin identification, the selected white clone was identified as a positive clone, and the PCR verification results were as follows figure 2 As shown, the targ...
Embodiment 3
[0088] Example 3: Induced expression of Bacteralis dorsalis odorant binding protein BdorOBP2
[0089] After verification, the single colonies were cultured in 3 mL LB medium containing 100 μg / mL ampicillin with shaking at 37°C overnight, and inoculated into 20 mL LB medium at an inoculation volume of 1% (V / V) for expansion on the next day When the OD600 is around 0.5, add IPTG to a final concentration of 1 mmol / L and start to induce expression at 30°C and 200 rpm. Take out 1 mL of bacterial liquid every 1 h, induce 5 h in total, and use uninduced bacterial liquid as a negative control. After the induction, the bacterial liquid collected every hour is centrifuged at 8000 rpm for 10 min to precipitate, and washed with ddH 2 0 were resuspended and centrifuged at 5000rpm for 10 minutes to collect the bacteria, and 150 μl of 1×SDS sample buffer was added to suspend the bacteria pellet, and boiled at 100°C for 10 minutes to fully lyse the bacteria, and then the samples in each tube ...
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