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
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
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...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com