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Fig. 2 | Fungal Biology and Biotechnology

Fig. 2

From: A genetic tool to express long fungal biosynthetic genes

Fig. 2

Determination of the full-length integration of the PterA:lpaA:TtrpC construct into the fwnA genomic locus of the A. niger recipient strain tLK01. A Schematic representation of the integration event of the five lpaA fragments into the genomic fwnA locus of A. niger tLK01. To mutate the SAM binding site in the C-methyltransferase domain of LpaA, the triplet GAC (pos. 4245–4247) encoding Asp1415 (probably binding the ribose moiety of SAM) was site-mutated into the triplet GCC encoding Ala1415. B An agarose gel of a PCR targeting the PterA promoter and the TtrpC terminator has been performed (oligonucleotides oMG370/oMG116). The expected amplicon size is indicated. Full length integration was evident for seven tLK04 (producing native LpaA) and three tLK05 transformants (producing LpaAD1415A). The genomic DNA of tLK07 (transformed with an empty vector) and the lpaA-encoding plasmid pPS03 [41] served as negative and positive controls, respectively

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