P. AZD1480 pastoris was grown in YPD medium (10 g L-1 yeast extract,

20 g L-1 peptone, 20 g L- 1 glucose) at 30°C for 3 days with shaking at 250 rpm. When required, the final antibiotics concentration for ampicillin was 100 μg mL-1 while for zeocin it was either 30, 50 or 100 μg mL-1. Plasmid pGAPZα-A (Invitrogen, Darmstadt, Germany) was used as the cloning and expression vector. Table 1 shows the plasmids and strains used in this study. Table 1 List of microorganisms and plasmids used in this study Strain or plasmid Genotype Reference Strains     Escherichia Nutlin-3a chemical structure coli TOP10 F- mcrA Δ(mrr-hsdRMS-mcrBC) φ80lacZΔM15 ΔlacX74 recA1 araD139 Δ(ara-leu) 7697 galU galK rpsL (StrR) endA1 nupG 10 Pichia pastoris     X-33 Wild type Invitrogen Mucor circinelloides     DSM 2183 Wild type German resource centre for biological material Plasmids     pGAPZα-A The pGAPZα-A vector use the GAP promoter to constitutively express recombinant proteins in Pichia pastoris. Contains the zeocin resistance gene (Sh ble). Invitrogen pGAPZα+MCAP pGAPZα-A derivative carrying the whole MCAP gene1. This work pGAPZα+MCAP-2 pGAPZα-A derivative carrying the MCAP gene without an intron1. This work pGAPZα+MCAP-3 pGAPZα-A

derivative carrying the MCAP gene without an intron2. This work pGAPZα+MCAP-5 pGAPZα-A derivative carrying the MCAP gene without a signal sequence and without an intron2. This work pGAPZα+MCAP SP-1 pGAPZα-A derivative carrying from PCI-32765 order the amino acid sequence number 67 to 394 of the MCAP gene without an intron1. This work pGAPZα+SyMCAP-6 pGAPZα-A derivative carrying the MCAP gene without signal sequence and without intron. The original MCAP gene was adapted to the optimal codon usage of P. pastoris. The insert was cloned flush with the Kex2 cleavage site and in frame of the α- factor signal sequence AMP deaminase and in frame with the C-terminal polyhistidine tag into the XhoI and NotI site of the pGAPZα-A. This work 1The insert was cloned in frame with the α-factor signal sequence and in frame with the C-terminal polyhistidine

tag into the EcoRI and NotI sites of the pGAPZα-A. 2The insert was cloned flush with the Kex2 cleavage site and in a frame of the α-factor signal sequence and in a frame with the C-terminal polyhistidine tag into the XhoI and NotI site of the pGAPZα-A. Genomic DNA extraction For genomic DNA extraction, M. circinelloides DSM 2183 spores (1 × 105 spores) were inoculated into potato dextrose agar plates (PDA) which were incubated at 24°C for 3 days. The PDA medium was prepared according to the supplier’s protocol (Difco, Detroit, MI, USA). About 250 mg of fresh mycelium were collected with tweezers in a 1.5 mL vial. The mycelium were washed with sterile water and centrifuged at 5000 g for 2 min. The spores were lysed in 466 μL TE buffer (10 mM Tris-Cl, pH 8.0, 1 mM EDTA) with 3 μL Proteinase K (20 mg mL-1), 1 μL RNAse (10 mg mL-1) and 30 μL SDS (100 mg mL-1).