Application of gene BnaCYP705a12 in brassinolide biosynthesis and transgenic plant production
A technology of brassinosteroids and transgenic plants, applied in the fields of application, plant products, genetic engineering, etc., to achieve the effects of increasing yield, increasing planting density and harvest index, and plant dwarfing
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Embodiment 1
[0038] Cloning of BnaCYP705a12 gene involved in brassinosteroid biosynthesis
[0039] The published French Brassica napus B.napus cv.'Darmor-bzh' genome (http: / / www.genoscope.cns.fr / brassicanapus / ) designed primers for amplifying genes involved in brassinosteroid biosynthesis , upstream primer P1: 5'-ATGGCAGCAATGATAGTTGA-3' and downstream primer P2: 5'-TTAAAGGCTGAGTCGAGAAA-3'; extract total RNA from fresh leaves of Brassica napus, and then use Reverse Transcription kit (Takara) to reverse Synthesize cDNA, and use the synthesized cDNA as a template to amplify the genes involved in the biosynthesis of brassinosteroids in rapeseed. After the reaction, perform 1% agarose gel electrophoresis detection on the PCR amplification products, and use AXYGEN spin column Type gel recovery kit, recover and purify, connect the recovered product into the vector pEasyBlunt Simple, and transform Escherichia coli (E.coli) DH5α competent cells by heat shock method. Positive clones were screened b...
Embodiment 2
[0043] Construction of Plant PFGC5941 Vector Containing BnaCYP705a12 Gene (RNAi-BnaCYP705a12)
[0044] Select interference fragment 170bp (SEQ ID NO.3) according to the conservative sequence of BnaCYP705a12 gene, add Asc I restriction endonuclease site at the upstream of SEQ ID NO.3 sequence, according to Asc I restriction endonuclease site and conservative Sequence design upstream primer, upstream primer P3:5'-TTACAATTACCATGGGGCGCGCCATCCCTCATCACACCATA-3', add Swa I restriction endonuclease site downstream of SEQID NO.3 sequence, according to Swa I restriction endonuclease site and conserved sequence Design downstream primers, downstream primer P4: 5'-TTAAATCATCGATTGGGCGCGCATCTACCAAACCTCCCTT-3'. The nucleotide sequence of SEQ ID NO.1 in the sequence listing cloned in Example 1 was amplified by PCR with primers P3 and P4, and the amplified product was the positive-sense strand of the BnaCYP705a12 gene. Add the Sma I restriction endonuclease site at the upstream of the SEQ ID N...
Embodiment 3
[0046] Obtaining RNAi-BnaCYP705a12 Transgenic Rapeseed
[0047] The plant RNAi-BnaCYP705a12 vector constructed in Example 2 was transformed into Agrobacterium EHA105 (Boerkin, NGC201-1) competent cells by the heat shock method, and coated on LB-resistant cells containing kanamycin and rifampicin. On the plate, culture at 28°C and 150rpm for 16 hours, pick out the single colony of Agrobacterium, screen the positive clones and sequence them, and re-inoculate the positive clones with correct sequencing in 20ml YEB liquid containing kanamycin and rifampicin In culture medium, cultivate 2 days under 28 ℃, 150rpm, then, inoculate bacterial liquid in the 300ml YEB liquid culture medium that contains kanamycin and rifampicin by volume ratio 2% inoculum again, at 28 Cultivate at 150 rpm for 18 hours until OD600=0.8-1.2. After the cultivation, the cells were collected by centrifugation at 5000 rpm for 20 minutes, and then the cells were suspended in 250 ml of a solution containing 5% s...
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