Application of SBP-box type transcription factors of switchgrass in aspect of increasing plant biomass and fermentable sugar yields
A transcription factor, sbp-box technology, applied in the field of plant genetic engineering, can solve problems such as unclear mechanism, and achieve the effect of increasing biomass and fermentable sugar production
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Embodiment 1
[0025] Example 1: Cloning and sequence determination of PvSPL2 gene
[0026] Take the tender stem parts of lowland switchgrass Alamo, extract the total RNA from tender stems with TriZolReagent (Invitrogen, Cat. For the reverse transcription reaction, the reverse transcriptase used was M-MLV (Promega, Cat. No. M1701). For the steps of the reverse transcription reaction, refer to the instructions for use of the reverse transcriptase. Using the first-strand cDNA synthesized by reverse transcription reaction as a template, use primers:
[0027] 5'-ATGGGTTCATTTGGGATGGAC-3'
[0028] 5'-AAGCGTCAGTGCATCAGGTCATAG-3'
[0029]Carry out routine PCR amplification; PCR reaction system: 2 μL cDNA, 5 μL 10×Buffer, 4 μL dNTP (2.5 mM), forward / reverse primer (10 μM) 1 μL each, 0.5 μL Taq enzyme (5U / μL) and 36.5 μL ddH 2 O. Mix well after adding the sample on ice. The PCR reaction conditions are: 94 o C5min; 94 o C30sec, 56 o C30sec; 72 o C90sec, 32 cycles; 72 o C10min. A fragment of ...
Embodiment 2
[0030] Example 2: Construction and genetic transformation of chimeric suppressor silencing expression vector of PvSPL2 gene
[0031] The negative regulatory factor used in the chimeric suppressor silencing expression vector used in the present invention is a kind of EAR-like motif transcriptional suppressor SRDX (LDLDLELRLGFA). The coding sequence of this motif was fused by PCR reaction before the stop codon (TGA) of PvSPL2 using primers:
[0032] 5'-CACCATGGGTTCATTTGGGATGGAC-3';
[0033] 5'-TCATTAAGCGAAACCCAAACGGAGTTCTAGATCCAGATCCAGGTGCATCAGGTCATAGTG-3'
[0034] Perform PCR amplification, and the amplification template is the above-mentioned PvSPL2-pMD18T recombinant plasmid. The PCR reaction system is: 2 μL template, 5 μL 10×Buffer, 4 μL dNTP (2.5 mM), 1 μL forward / reverse primer (10 μM), 0.5 μL Taq enzyme (5U / μL) and 36.5 μL ddH 2 O. The PCR reaction conditions are: 94 o C5min; 94 o C30sec, 56 o C30sec; 72 o C90sec, 32 cycles; 72 o C10min. A fragment of about 1.4 ...
Embodiment 3
[0036] Example 3: Molecular Identification of Transgenic Plants
[0037] Take the tender stem tissue of the positive transgenic plants identified above, use the TriZol (Invitrogen Company, product number 15596026) method to extract total RNA, reverse transcriptase (Promega Company, product number M1701) to synthesize the first-strand cDNA, and switchgrass Ubiquitin gene as an internal reference gene. Primers PvSPL2-qF1 / qR1 and PvSPL2-qF2 / qR2 detect the expression of endogenous and total PvSPL2 genes in positive transgenic plants ( image 3 ), the primer sequences are as follows:
[0038] PvUbiquitin-qF:5'-TTCGTGGTGGCCAGTAAG-3'
[0039] PvUbiquitin-qR:5'-AGAGACCAGAAGACCCAGGTACAG-3'
[0040] PvSPL2-qF1:5'-GCGCGGTTTCAGGCTCTCG-3'
[0041] PvSPL2-qR1:5-CCTCGCAACCGGACAATGGA-3'
[0042] PvSPL2-qF2:5'-GTGTGGAGCGGCGGTTTT-3'
[0043] PvSPL2-qR2:5'-TCCGTCTGCGGGCATTGT-3'
[0044] Such as image 3 As shown, the expression level of endogenous PvSPL2 in transgenic plants (marked as TS...
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