## Abstract __Penicillium chrysogenum__ was immobilized in polyacrylamide gel prepared from 5% acrylamide monomers (85% acrylamide and 15% __N__,__N__β²βmethylene bisacrylamide). Penicillin produced from glucose by the immobilized mycelium was 17% of that produced by washed mycelium. However, the ac
Optimization of a pellicular biocatalyst for penicillin G production by Penicillium chrysogenum
β Scribed by William P. Flanagan; Herbert E. Klei; Donald W. Sundstrom; Carl W. Lawton
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 696 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0006-3592
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β¦ Synopsis
A previously developed immobilization technique involving latex coatings on solid particulate supports was investigated further for penicillin G production by Penicillium chrysogenum. Several modifications were found to decrease the germination lag time, including a higher spore concentration, a thinner latex layer, an increased latex porosity, and a decreased drying time. This approach enabled the development of immobilized mycelial pellets within 2-3 days from the onset of biocatalyst preparation and incubation.
A continuous immobilized-cell airlift bioreactor produced penicillin G in a series of r u n s in which the production phase lasted up to 30 days. The productivity of this system was 3-6 times greater than the productivity of the corresponding free-cell shake flask fermentation.
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