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Table 1 Primers used in this study

From: Production of highly efficient cellulase mixtures by genetically exploiting the potentials of Trichoderma reesei endogenous cellulases for hydrolysis of corncob residues

Primers

Sequences (5′–3′)

Employment

CBH2-1183UF

TGAAACCCCTCACTACTGCCAT

cbh2 overexpression strain construction

CBH2-2817DR

CTAATGCCTCGGGCTGGGACAACGAAATGGTAGGGTACGGTCAG

cbh2 overexpression strain construction

EG2-1524UF

GACAAGAAATCGGGTGTTTAGGT

egl2 overexpression strain construction

EG2-1813DR

CTAATGCCTCGGGCTGGGACAAATAAGAATGCGGCCGCGTGGGCTGGGTAGGGTTTG

egl2 overexpression strain construction

PyrG-S

CTTCCTAATACCGCCTAGTCAT

PyrG markers amplification

PyrG-A

AGCCGCTGGTCAATGTTATC

PyrG markers amplification

DR-S

TTGTCCCAGCCCGAGGCATTAG

PyrG markers amplification

CBH2-1179UF

ACCCCTCACTACTGCCATTTAT

cbh2 overexpression strain construction

pyrG-1172DR

TATCAATCTGGGGTAACGGACG

cbh2/egl2 overexpression strain construction

Y-cbh2-F1

TTCACCTCCTCTTAGTGCAG

cbh2 overexpression strain verification

Y-PyrG-R1

TACGGTCGCATAGCAGTG

cbh2/egl2 overexpression strain verification

Y-egl2-F1

GCATATGTCAAATTTGGAGCGG

egl2 overexpression strain verification

Y1

GCCAGGGATGCTTGAGTGTA

bgl1 overexpression strain verification

Y2

CCCAGCCACAGGACCAAGTATG

bgl1 overexpression strain verification

real-cbhl-Sl

GGTGGCGTGAGCAAGTATCC

Used for RT-PCR

real-cbhl-Al

TGTCCTCCAATGCCCGTGTT

Used for RT-PCR

real-cbh2-S

CTGGTCCAACGCCTTCTTCA

Used for RT-PCR

real-cbh2-A

GACCCAGACAAACGAATCCAG

Used for RT-PCR

real-actin-S

CCCAAGTCCAACCGTGAGA

Used for RT-PCR

real-actin-A

CAATGGCGTGAGGAAGAGC

Used for RT-PCR

real-egl1-S1

GGCTCGCTCTACCTGTCTCA

Used for RT-PCR

real-egl1-A1

GGGTGCCGTTCCTCCAT

Used for RT-PCR

real- egl2 -S1

ACGAGCCTTTGGTCGCAGTT

Used for RT-PCR

real- egl2-A1

GGCAGCCCAGGTGTTGATGT

Used for RT-PCR