A recombinant strain of Aspergillus niger (B1-D), engineered to produce the marker protein hen egg white lysozyme, was investigated with regard to its susceptibility to "oxidative stress" in submerged culture in bioreactor systems. The culture response to oxidative stress, produced either by additio
Optimization of catalase biosynthesis in submerged cultures of Aspergillus niger mutant
β Scribed by A. Gromada; Dr. hab. J. Fiedurek
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 492 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0233-111X
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β¦ Synopsis
Abstract
The effect of some medium components, viscous substances and metabolic inhibitors, on catalase production by mutant Aspergillus niger has been studied in shake culture. Altering the composition of the basal medium, particularly substituting NaNO~3~ for KNO~3~, and peptone for yeast extract brought an increase in extraβ and intracellular catalase activity by 1.5β and 3βfold, respectively. The addition of 2.0β6.0 mg sodium alginate or pectin/ml as viscous additive to the medium, containing glucose as carbon source, increased the medium viscosity and catalase production in shake culture by about 2.8β to 3.0βfold. The highest yield of extracellular catalase activity of A. niger was obtained in the presence of sodium orthovanadate and Triton Xβ100, which improved the activity of this enzyme by about 1.5β2.2βfold. A significant increase in intracellular catalase activity was observed in the presence of hematin, Tween 80 and sodium orthovanadate (1.7β, 1.6β and 1.4βfold respectively). The time course of growth and enzyme production by A. niger in the optimized medium is also reported.
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