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Characterization of recombinant terrelysin, a hemolysin of Aspergillus terreus

Overview of Nayak AP et al.

AuthorsNayak AP  Blachere FM  Hettick JM  Lukomski S  Schmechel D  Beezhold DH  
AffiliationAllergy and Clinical Immunology Branch   Health Effects Laboratory Division   National Institute for Occupational Safety and Health   Centers for Disease Control and Prevention   1095 Willowdale Rd   Morgantown   WV 26505   USA.  
JournalMycopathologia
Year 2010

Abstract


Fungal hemolysins are potential virulence factors. Some fungal hemolysins belong to the aegerolysin protein family that includes cytolysins capable of lysing erythrocytes and other cells. Here, we describe a hemolysin from Aspergillus terreus called terrelysin. We used the genome sequence database to identify the terrelysin sequence based on homology with other known aegerolysins. Aspergillus terreus mRNA was isolated, transcribed to cDNA and the open reading frame for terrelysin amplified by PCR using specific primers. Using the pASK-IBA6 cloning vector, we produced recombinant terrelysin (rTerrelysin) as a fusion product in Escherichia coli. The recombinant protein was purified and using MALDI-TOF MS determined to have a mass of 16,428 Da. Circular dichroism analysis suggests the secondary structure of the protein to be predominantly β-sheet. Results from thermal denaturation of rTerrelysin show that the protein maintained the β-sheet confirmation up to 65°C. Polyclonal antibody to rTerrelysin recognized a protein of approximately 16.5 kDa in mycelial extracts from A. terreus.