The predicted 88, 123 and 99 amino acid (aa) sequences of Hyd1, Hyd2 and Hyd3, respectively, all contained a 60-65 aa core structure that contained the Cys residues. The conserved domain analysis of translated aa sequences using Simple Modular Architecture Research Tool (SMART) identified a single hydrophobin_2 domain (Pfam 06766) between aa positions 21-86, 21-85 and 30-91for Hyd1, Hyd2 and Hyd3, respectively. This structure was further confirmed by InterproScan and Conserved Domain Search (CDS) analyses. Signal P predicted 16-18 aa long

secretion signal peptides in the N-termini https://www.selleckchem.com/products/gsk1838705a.html of each C. rosea hydrophobin. The highest similarity of Hyd1 was with cerato-ulmin of Geosmithia spp. and Ophistoma nova-ulmi (e-value 3e-07; identity 33%), of Hyd2 with T. atroviride hydrophobin and spore related hydrophobin of T. viride (e-value 3e-10; identity 41%), and of Hyd3 with hydrophobin from Fusarium

spp. (e-value 3e-32; CCI-779 nmr identity 73%). In addition, aa similarity between Hyd1, Hyd2 and Hyd3 were below 20%. Hyd1 and Hyd2 contained eight Cys in their protein sequences, while Hyd3 contained only seven as the Cys residue closest to the C-terminus was replaced by a glutamine (Gln) (Figure 1). This replacement was similar to the T. harzianum hydrophobin QID3 that also contained seven Cys [30], although Hyd3 did not show the extended N-terminus of QID3. The Cys spacing of Hyd1, Hyd2 and Hyd3 conformed to the pattern of Class II (Figure 1). Furthermore, the hydropathy patterns of Hyd1, Hyd2 and Hyd3 were all indicative of class II hydrophobins (data not shown). Taken together, these analyses suggest that C. rosea Hyd1, Hyd2 and Hyd3 encode putative class II hydrophobins. Figure 1 Sequence alignment of C . rosea hydrophobins. Amino acid sequence alignment of C. rosea hydrophobins with class II hydrophobins from Trichoderma spp. and additional representatives of known class II hydrophobins. The amino acid sequences from first Cys to eight Cys residues were used for the alignment. Conserved residues in a column are indicated in white and boxed in black; two different

conserved residues in a column are highlighted by grey boxes; gaps are indicated by dashes. Conserved Cys residues are indicated G protein-coupled receptor kinase by asterisks. A phylogenetic tree was constructed with Hyd1, Hyd2 and Hyd3 together with class II hydrophobins from Trichoderma spp. and additional representatives of known class II hydrophobins (Additional file 1: Table S1). The result from the phylogenetic analysis click here showed that Hyd1, Hyd2 and Hyd3 do not represent recent gene duplicates as they clustered in different parts of the tree (Figure 2). Figure 2 Phylogenetic analysis of C . rosea hydrophobins. Phylogenetic analysis of class II hydrophobins using maximum likelihood methods implemented in PhyML-aBayes. Pleurotus ostreatus hydrophobins are used as out group.