Myrothecium roridum A553 trichothecene synthase gene Tri5 promoter and application thereof
A technology of trichothecenes and Mycobacterium dew, applied in the field of genetic engineering, can solve the problem that the promoter has not yet been discovered
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Embodiment 1
[0025] Example 1 Obtaining the Trichothecene Synthase Gene Tri5 Promoter Sequence of Myrothecium roridum A553
[0026]Analysis of the expression level of trichothecene toxin biosynthetic genes: the endophytic fungus Myrothecium roridum A553 was inoculated on a YPD medium plate, cultured at 37°C for 72 hours, fresh mycelium was picked, and used Plant RNA Extraction Kit was used to extract RNA, and All-in-one RT Master Kit was used to reverse transcribe to obtain cDNA. Hiseq2000 was used for transcriptome sequencing, and primers for trichothecene biosynthesis-related genes Tri3, Tri4, Tri5, Tri6, Tri11, and Tri12 were designed based on the target gene sequence obtained by previous transcriptome sequencing. The primer sequence was: for the Tri3 gene (FP : 5′-ATGCTACTACAGGCAAATTTCAT-3′, RP: 5′-TCCGATATACGTCGCGAATCTAGC-3′), against the Tri4 gene (FP: 5′-ATGGATGCTCCGAAATCCAATG-3′, RP: 5′-GCCGATATATCTC GCATACCG-3′), against the Tri5 gene ( FP: 5′-ATGAGAGGACCAGACAGGAAGATCA-3′, RP: 5′...
Embodiment 2
[0031] Example 2 Functional verification of Tri5P in the core region of the Tri5 promoter
[0032] Insert Tri5P, the core region of the Tri5 promoter, into the yeast vector YEp352-TEF1-HYRB by homologous recombination (YEp352-TEF1-HYRB is an early constructed plasmid, carrying the hygromycin B resistance gene hph driven by the constitutive promoter TEF1 , is a known product in the prior art, and the vector map of YEp352-TEF1-HYRB is shown in image 3 A). Firstly, the upstream and downstream primers Tri5P-f0 (5'-AGCTCGGTACCCGGGGATCCCAATGTTCGCACTCTTAGTCAAG-3') and Tri5P-R (5'-GGTGAGTTCAGGCATCAGGGCTCAACTCAAGATCAAAGT-3') for the amplification of Tri5P (SEQ ID NO.1) in the core region of the Tri5 promoter were designed. Amplify the product. The vector YEp352-TEF1-HYRB was excised with BamH I and Xba I to excise TEF1 and recover the product, then the two products were recombined using ClonExpress II One Step Cloning Kit C112 (Vazyme) and transformed into DH5α to screen for positiv...
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