Glucoamylase overexpression inAspergillus niger: Molecular genetic analysis of strains containing multiple copies of theglaA gene
Open Access
- 1 March 1993
- journal article
- Published by Springer Nature in Transgenic Research
- Vol. 2 (2) , 84-92
- https://doi.org/10.1007/bf01969381
Abstract
A strategy, based on the usage of the amdS selection marker and a cosmid vector containing four copies of the glucoamylase gene ( glaA ), was developed to obtain glucoamylase (GLA)-overproducing A. niger strains. With this strategy, fungal strains carrying up to 200 copies of the glaA gene could be isolated at a relatively high frequency. In each transformant analysed, integration occurred in a single chromosome. A significant increase in the extracellular GLA production was observed in most of the transformants carrying multiple copies of the glaA gene. Further analysis showed that the amount of GLA that is produced was not proportional to the number of glaA copies in these transformants. However, the level of GLA production clearly correlated with the amount of glaA mRNA produced in these transformants. From these results it is concluded that GLA production is limited at the level of transcription.Keywords
This publication has 28 references indexed in Scilit:
- Studies on transformation of Escherichia coli with plasmidsPublished by Elsevier ,2006
- Nucleotide sequence and expression of the glucoamylase-encoding gene (glaA) from Aspergillus oryzaeGene, 1991
- Growth MediaPublished by Elsevier ,1991
- Intracellular and extracellular production of proteins in Aspergillus under the control of expression signals of the highly expressed Aspergillus nidulans gpdA geneJournal of Biotechnology, 1991
- The pMTL nic− cloning vectors. I. Improved pUC polylinker regions to facilitate the use of sonicated DNA for nucleotide sequencingGene, 1988
- Transformation of Aspergillus based on the hygromycin B resistance marker from Escherichia coliGene, 1987
- TheamdS gene ofAspergillus nidulans: Control by multiple regulatory signalsBioEssays, 1986
- Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectorsGene, 1985
- Organization of the ribosomal RNA gene cluster in Aspergillus nidulansGene, 1982
- Low Repetitive DNA Content in Aspergillus nidulansScience, 1978