A kind of bdref2 gene that regulates the synthesis and metabolism of plant ferulic acid and its application
A technology of synthetic metabolism and ferulic acid, applied in the field of genetic engineering, can solve the problems that have not been reported in the research and affect the degradability of plant biomass, and achieve the effect of improving the degradation efficiency
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0027] Example 1: BdREF2 gene segregation
[0028] (1) PCR amplification of gene fragments: using the In-Fusion SMARTer Directional cDNA LibraryConstruction Kit (TaKaRa product), the mRNA of Brachypodium distachydium (provided by the School of Life Sciences, Shandong Agricultural University, Tai'an, Shandong) was extracted by conventional methods, and the construction of the two panicle Brachypodium cDNA library. Using the library cDNA as a template, the following primer pairs were used for PCR amplification:
[0029] Forward primer sequence REF2-F: 5′-CCATCTTCTTTCAGCCAAGC-3′ (SEQ.ID.NO.3)
[0030] Reverse primer sequence REF2-R: 5′-TACGCAAGGAGCACTCAG-3′ (SEQ.ID.NO.4)
[0031]RT-PCR amplification uses KOD-Plus-Neo high-fidelity DNA polymerase system (TOYOBO product), the reaction system is: 10×PCR Buffer 5μL, 2mM dNTPs 5μL, 25mM MgSO 4 3 μL, 1.5 μL each of 10 μM forward and reverse primers, 1 μL of cDNA template, 1 U of KOD-Plus-Neo enzyme, with sterile dH 2 O to make up...
Embodiment 2
[0034] Example 2: BdREF2 Gene expression patterns in Brachypodium distachyon
[0035] (1) Preparation of total RNA from different tissues and organs of Brachypodium distachyon: young leaves, mature leaves, young stems, mature stems, young ears and roots of Brachypodium distachyon were collected from six different tissues and organs, respectively, about 20 days after heading. 0.1 g of each tissue material was used to prepare total RNA samples using MiniBEST Plant RNA Extraction Kit (TaKaRa product), and then the integrity and concentration of RNA samples were detected by 1% agarose gel electrophoresis and UV spectrophotometer respectively.
[0036] (2) mRNA reverse transcription reaction: 1 μg total RNA was used as the starting material for the reverse transcription reaction, and the reaction volume was 20 μL according to the steps introduced in the instruction manual of PrimeScript™ RTreagent Kit (TaKaRa product). The synthesized cDNA was used as a template for real-time fluo...
Embodiment 3
[0044] Example 3: BdREF2 prokaryotic expression of genes
[0045] (1) BdREF1 Construction of gene prokaryotic expression vector: based on the cloned BdREF2 Gene sequence, using Primer Premier 6.0 to design specific PCR primers for amplification BdREF2 ORF region sequence without terminator.
[0046] The primer sequences are as follows:
[0047] REF2-OF: 5′-AG CATATG GGAAGCAACGAGGGAGG-3' (SEQ ID NO.9), the underlined part is Nde I digestion recognition site.
[0048] REF2-OR: 5′-AA GCGGCCGC ATACCAAGGCGAGTCAGGGA-3' (SEQ ID NO.10), the underlined part is not I digestion recognition site.
[0049] With the pTA2- obtained in step (2) of Example 1 BdREF2 Plasmid DNA (cloning the PCR product into the pTA2 vector) was used as a template, and the KOD-Plus-Neo high-fidelity DNA polymerase system (TOYOBO product) was used to amplify the ORF region of the gene. The PCR product was first purified with the SanPrep Column PCR Product Purification Kit (Shanghai Sangong Product...
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