Generating expression construct Amplification of DNA by PCR was performed using proof-reading PfuTurbo® Cx Hotstart polymerase selleck screening library (Stratagene) in 50 μl according to the manufacturer’s instructions. The reaction

mixtures were heated to 95°C for 2 min followed by 30 cycles at 95°C for 30 s, 58°C for 30 s, and 72°C for 3 min. A fragment containing the fungal selection marker argB was amplified from the expression vector pU1111 [18] with primers BGHA71 and BGHA72 and cloned into MfeI/SbfI digested expression vector pU0002 [18] resulting in construct pHC1. A 2689 bp fragment containing mpaF including mpaF promoter and terminator was amplified using primers BGHA125 and BGHA132 from P. brevicompactum IBT 23078 gDNA and cloned into the KpnI/AsiSI site of pHC1 resulting in pHC2. The flanking regions of imdA (AN10476, A. nidulans Androgen Receptor Antagonist concentration IMPDH) were amplified using primer pairs BGHA168/BGHA169 and BGHA170/BGHA171. pHC3 was created by USER cloning these fragments into pHC2 following the USER cloning method previously described [18, 20]. All plasmids

were propagated in Escherichia coli strain DH5α. All primers used in this study are listed in Table 2. Table 2 List of primers Name Sequence (5′ → 3′) BGHA236 HC ATGCCIATYNCCRMCGGIGAYKC BGHA246 HC CRGCCTTCTTRTCCTCCATGG BGHA240 HC ATGGTCGADRTYCWGGAYTAYACC BGHA241 HC GARGCRCCRGCGTTMTTG BGHA343 GAGCGYATGARYGTYTAYTTCA BGHA344 GTGAACTCCATCTCRTCCATACC BGHA70 TTAACACAATTGCGCGGTTTTTTGGGGTAGTCATC Buspirone HCl MfeI BGHA71 TTAACACCTGCAGGCGCGGTTTTTTGGGGTAGTCATC SbfI BGHA125 TTAACAGGGTACCAAGTCAATTTTCACCAATCAAGC KpnI BGHA132 TGGTATGCGATCGCGTCAGAGTCAAACAAAGCCAGA AsiSI BGHA168 GGGTTTAAUACAGACGAAAGGGTTGTTGG BGHA169 GGACTTAAUGTCTCTATCAGGACACGCAGA BGHA170 GGCATTAAUTGGCTTTCTTTTCGTTTCTTG BGHA171 GGTCTTAAUTGCTTCTGCAATTTCGACAC BGHA98 GGTTTCGTTGTCAATAAGGGAA BGHA256 HC CATGGAGGGCTTCCAGAATA BGHA255 HC TTTTGCTGTGCTGTAGTCGTG

BGHA225 CCAGTTATCTGGGCAAACCAAAAG A. nidulans strain construction Protoplasting and gene-targeting procedures were performed as described previously [21, 22]. 5 μg pHC3 was digested with NotI to liberate the gene targeting substrate, which was used for transformation of NID3 [23]. Transformants containing the desired gene targeting event were verified by PCR with primer-pairs BGHA98/BGHA256HC and BGHA255HC/BGHA225 using Taq-polymerase (Sigma-Aldrich) on genomic DNA obtained from streak purified transformants extracted using the FastDNA® SPIN for Soil Kit (MP Biomedicals, LLC). MPA treatment of fungi Spores from A. nidulans NID191 and A. nidulans NID495 were harvested. 10-fold dilution series was performed on freshly made MM-plates with 0, 5, 25, 100, 200 μg MPA/ml (Sigma). All plates contained 0.8% (v/v) methanol. Relative growth of the strains was assessed by visual inspection. Degenerate PCR An alignment with the DNA sequence (including introns) of the genes encoding P. brevicompactum IMPDH-B, A. nidulans IMPDH-A, P. chrysogenum IMPDH-A, P.