Abstract
The filamentous fungus Aspergillus niger produces two glycosylated forms of the sucrose-hydrolysing enzyme, invertase. In contrast, some Trichoderma species lack invertase and are unable to utilise sucrose as a sole carbon source. Using an A. niger genomic library constructed in a cosmid vector containing the ura5 gene of Podospora anserina as a selectable marker, and the T. reesei ura5- strain as a sucrose-minus recipient strain, an A. niger invertase gene (suc1) has been cloned by a sib selection procedure. PAGE and enzyme analysis confirmed that transformants had acquired invertase activity. The cloned gene contained DNA sequences which were complementary to the amino-acid sequences of tryptic peptides found in invertase purified from A. niger. The suc1 invertase gene can be used as a dominant selectable marker for the transformation of Trichoderma strains.
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Communicated by P. P. Slonimski
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Bergès, T., Barreau, C., Peberdy, J.F. et al. Cloning of an Aspergillus niger invertase gene by expression in Trichoderma reesei . Curr Genet 24, 53–59 (1993). https://doi.org/10.1007/BF00324665
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DOI: https://doi.org/10.1007/BF00324665