Gene related to drought resistance of oilseed rape, overexpression vector, cell line, host bacterium and application of gene, overexpression vector, cell line and host bacterium
A drought resistance, genetic technology, applied in application, genetic engineering, plant genetic improvement, etc., can solve problems such as yield reduction or no harvest, economic loss, etc.
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Embodiment 1
[0028] Embodiment 1, the cloning of Brassica napus BnWRKY255 gene
[0029] Use RNA extraction and separation reagent (Trizol, Invitrogen) to extract the total RNA of Brassica napus seedlings. The specific method is: collect about 80-150 mg of Brassica napus seedlings, put them into the correspondingly labeled EP tube, then add 1ml Trizol reagent, and mix quickly Place on ice for 8-10min; add 0.2ml chloroform, gently invert up and down for 15-30s at a uniform speed, and let stand on ice for 5-8min; centrifuge at 12000rpm at 4°C for 15-20min; transfer the supernatant to a new RNase free EP tube Add 0.5ml of pre-cooled isopropanol and mix gently, let stand for 3-5min, and centrifuge at 12,000g for 20min at 4°C to precipitate RNA; wash the RNA pellet with 1ml of 75% ethanol, let it dry for 5min, dissolve in an appropriate amount of DEPC-treated Store in water at -80°C for later use.
[0030] The gene overexpression vector was constructed according to Gateway recombination technol...
Embodiment 2
[0039] Embodiment 2, the acquisition of transgenic Arabidopsis plants of BnWRKY255
[0040] In order to study the role of BnWRKY255, transgenic plants overexpressing BnWRKY255 were constructed in Arabidopsis, and the transgenic lines were identified, according to the semi-quantitative results as follows: figure 2 As shown, three independent homozygous T3 transgenic lines highly expressing BnWRKY255 were randomly selected for further phenotypic analysis.
[0041] 1. Construction of an overexpression vector for Brassica napus BnWRKY255 transgenic plants: the sequence-verified fragment obtained in Example 1 was recombined into the pDONR207 vector through the BP reaction (BP Clonase II EnzymeMix, Invitrogen) using the Gateway technology of Invitrogen Company, and transformed into Escherichia coli DH5α In the competent cells, the entry clone was obtained by screening with 50mg / L Qingda, and then the plasmid was extracted and recombined the BnWRKY255 gene into the pEarleyGate103-RF...
Embodiment 3
[0044] Example 3, Determination of Drought Sensitivity of Transgenic BnWRKY255 Arabidopsis
[0045] To study the effect of mannitol on the root growth of transgenic BnWRKY255 Arabidopsis thaliana, the method is as follows: Transgenic and wild-type Arabidopsis seeds harvested at the same time after disinfection and cleaning were sown in 1 / 2MS solid medium, and vernalized at 4°C for 2 days Place them in a long-day culture room (22°C, light for 16 hours, and darkness for 8 hours). After 3 days of germination, move the seedlings in the same growth state to 1 / 2 MS solid medium containing 200 mM and 300 mM mannitol in the ultra-clean workbench. , put into the long-day cultivation room, place vertically, count the root length and take pictures after cultivating for 7 days. The experimental results showed that: under the influence of mannitol, the root growth of the BnWRKY255 overexpression line was significantly inhibited. The root length of the overexpression line was statistically...
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