Cordyceps militaris glyceraldehyde-3-phosphate dehydrogenase gene promoter
A technology of Cordyceps sinensis glycerin and phosphate dehydrogenase, applied in the direction of microorganism-based methods, DNA/RNA fragments, microorganisms, etc., to achieve high activity and change the effect of resource scarcity
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Embodiment 1
[0015] Step 1, cloning of the promoter of the glyceraldehyde-3-phosphate dehydrogenase gene of Cordyceps militaris
[0016] 1. The cultivation of Cordyceps militaris
[0017] Put the Cordyceps militaris strain preserved on the slant of the test tube (Cordyceps militaris number: 51534, derived from the Culture Collection Center of the Chinese Academy of Agricultural Sciences) to 28°C for activation for 24 hours, pick the mycelium of the strain on the slant of the test tube and connect it to the comprehensive medium containing potato ( Potato Dextrose Agar, PDA) plate, 28 ° C constant temperature culture for 7 days. 1cm 2 The left and right strains grown on the PDA plate were inoculated into the PDA liquid medium, and cultured at 28° C. and 120 rpm for 5 days.
[0018] 2. Isolation of Cordyceps militaris DNA
[0019] Genomic DNA was extracted by high-salt and low-pH method, including the following steps:
[0020] (1) Put about 1 g of the sample ground by liquid nitrogen into t...
Embodiment 2
[0101] Step 1, PCR amplification of the missing promoter fragment
[0102] (1) Synthesis of primers
[0103] According to the full-length sequence of the Cordyceps militaris glyceraldehyde-3-phosphate dehydrogenase gene, a sequence (501-2515 nucleotides in SEQ ID NO.1) capable of amplifying a 2000 bp promoter region is designed. The primer sequence is: upstream primer: 5'-AGACGGCTTTGGGCGGCTGCTTGC-3'; downstream primer: 5'-TGTTCTTGATTAGAAAAGTGAGGTG-3';
[0104] (2) PCR amplification
[0105] Using the Cordyceps militaris genomic DNA as a template, using the primers described in step (1), after PCR amplification, the partial sequence (about 2000bp) of the 5' flank of the Cordyceps militaris glyceraldehyde-3-phosphate dehydrogenase gene was cloned into Intermediate vector (such as pMD 18-T vector), the sequencing result is compared with the 5' flanking sequence of the obtained 2515bp CmGDP1P, and the identity with the 501-2515th nucleotide in SEQ ID NO.1 is 100%, indicating tha...
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