gloeosporioides [25, 26]. Despite N-glycosylation is common in pectinolytic enzymes and has been reported in several fungal pectin lyases al similar positions, little is known about the function of this posttranslational modification. Although it is believed that it affect enzyme stability and activity MAPK Inhibitor Library high throughput [60, 61]. Southern blot analysis The genomic organization of the Clpnl2 gene was investigated by Southern blot analysis. Total DNA was digested with the restriction endonucleases BamHI, EcoRI, Hind III, XhoI, EcoRI/BamHI and Hind III/XhoI. The digested DNA was fractionated on a 0.8% agarose gel and hybridized to

the 32P-radiolabeled Clpnl2 probe. As depicted in Figure 2, commonly a single hybridization product was detected. In addition, a very faint signal probably resulting from hybridization with another gene of low similarity was observed. These results suggest CP-673451 purchase that the C. lindemuthianum genome contains a single copy of the Clpnl2 gene, as does C. gloeosporioides [26]. Figure 2 Southern blot analysis of total DNA from C. lindemuthianum. Total DNA was digested with BamHI (1), EcoRI

(2), HindIII (3), XhoI (4), EcoRI/BamHI (5), or HindIII/XhoI (6), analyzed on a 0.8% agarose gel, transferred to nylon membrane and hybridized with a 32P-radiolabeled Clpnl2 fragment. Protein homology modeling The tertiary structure of Clpnl2 predicted by homology modeling coincided with the typical topology of the parallel β-helix of PNLs (Figure 3). After energy minimization, the energy value was -17418.428 kJ/mol, and the quality of the model generated was assessed by plating dihedrals Φ and Ψ onto Ramachandran plots (SPDBV v. 4.01) [49]. The results are in agreement with the requirements for preferred and allowed regions, except for 3 non-glycine residues (0.8%). Figure 3 Three-dimensional structure of Clpnl2 from C. lindemuthianum showing highly conserved residues involved in catalysis. Phylogenetic analyses To elucidate the relationship of Clpnl2 from C. lindemuthianum with bacterial, oomycete and fungal pectin lyases,

sequences reported in databases were analyzed. Protein or deduced amino acid PNL sequences from Etomidate 14 fungal species including: basidiomycetes, ascomycetes and one oomycete species, three bacterial species, and a pectate lyase sequence from A. thaliana as an external group, were used to generate phylogenetic trees. Clustal alignment used for phylogenetic analysis (Figure 4) allowed to determine the location of amino acids expected to have a catalytic role in the PNLs [4, 13]. Asp154 and Arg176 (numbered from A. niger PELA) are conserved in fungi and oomycetes, although Arg176 could not be located in P. griseoroseum [GenBank: AF502280], and Arg 236 is conserved in all analyzed sequences. Additionally, several conserved domains among the sequences of fungi and oomycetes were observed, and some of these were shared with bacterial amino acid sequences.