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Table 1 Oligonucleotide primers used in this study

From: Characterization of FsXEG12A from the cellulose-degrading ectosymbiotic fungus Fusarium spp. strain EI cultured by the ambrosia beetle

Primer

Gene

Nucleotide sequencea

DGGE analysis

 16S-f

16S rRNA

5′-CGCCCGGGGCGCGCCCCGGGCGGGGCGGGGGCACGGGGGGAACGCGAAGAACCTTAC-3′

 16S-r

16S rRNA

5′-CGGTATGTACAAGGCCCGGGAACG-3′

 18S-f

18S rRNA

5′-CGCCCGCCGCGCCCCGCGCCCGGCCCGCGGCCCCCGCCCCATTCCCCGTTACCCGTTG-3′

 18S-r

18S rRNA

5′-GTAGTCATATGCTTGTCTC-3′

 EF-f

EF-1α

5′-ATGGGTAAGGAAGACAAGAC-3′

 EF-r

EF-1α

5′-GGAAGTACCAGTGATCATG-3′

Cloning primers for the 25-kDa protein gene

 25-kDa-f

FsXEG_17404

5′-ATGAAGGGCTCTCTTGTCTTC-3′

 25-kDa-r

FsXEG_17404

5′-TTAGTTGACGTGAGCATTGAA-3′

Plasmid construction for recombinant protein production

 17404-f

FsXEG_17404

5′-AGAAAAGAGAGGCTGAAGCTGAATTCCAGTCTCTCTGCGACCAATA-3′

 17404-r

FsXEG_17404

5′-GACGGCCGGCTGGGCCACGTGAATTCTTAGTTGACGTGAGCATTGA-3′

  1. aGC-clamps are underlined. Primers for 16S rRNA and 18S rRNA were designed according to Muyzer et al. (1993) and May et al. (2001), respectively