Bergquist Peter L, Te'o V S Junior, Gibbs Moreland D, Cziferszky Angela C E, De Faria Fabricia P, Azevedo Maristela O, Nevalainen K M Helena
Department of Biological Sciences, Macquarie University, Sydney, NSW, Australia.
Appl Biochem Biotechnol. 2002 Spring;98-100:165-76. doi: 10.1385/abab:98-100:1-9:165.
Cost-effective production of enzymes for industrial processes makes the appropriate selection of the host-vector expression system critical. We have developed two systems for the bulk production of bleaching enzymes from thermophiles. Kluyveromyces lactis has been developed as a secretion host employing expression vectors based on the 2mu-like plasmid pKD1 of Kluyveromyces drosophilarium. Our second system involves the filamentous fungus Trichoderma reesei. Fusion and nonfusion vectors have been constructed using the strong cellobiohydrolase 1 (cbh1) promoter. The KEX2 protease cleavage site and a 6 x HIS-tag have been incorporated to facilitate both cleavage and purification of the mature foreign proteins.