The application of L-amino acid oxidase (L-ASOD) for monitoring of amino acids during the cultivation of the recombinant insect cell line, Spodopteru frugiperda, and the production of Pgalactosidase as well as the application of L-lactate monooxidase (L-LMO) for the monitoring of the lactate concent
Development of enzyme cartridge flow-injection analysis for industrial process monitoring. Part II. Application for monitoring of microorganism cultivations
✍ Scribed by H. Jürgens; L. Brandes; R. Joppien; M. Siebold; J. Schubert; X. Wu; G. Kretzmer; K. Schügerl
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 615 KB
- Volume
- 302
- Category
- Article
- ISSN
- 0003-2670
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✦ Synopsis
Five cartridges with immobilized glucose oxydase, alcohol oxydase, pyranose oxydase, L-amino acid oxydase and t_-lactate-2-monooxigenase, respectively, were integrated into a flow injection analysis (FIA) system and applied to the monitoring of medium components: glucose and ethanol during the cultivation of Saccharomyces cereuisiae, L-amino acids during the production of the fusion protein EcoRI::SPA by recombinant Escherichiu coli, and lactate during the production of lactic acid by Luctobucillus saliuurius var. saliuurius. The developed enzyme cartridge-FIA systems show a reproducible operation, low pressure drop and long-range enzyme activities and are well suited for on-line monitoring of microbial cultivation processes.
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The preparation of cartridges with five different enzymes: glucose oxidase (GOD), pyranose oxidase (PyOD), alcohol oxidase ( AOD) , L-amino acid oxidase ( t-ASOD) and L-lactate-2-monooxigenase (LMO) immobilized on VA-Epoxy Biosynth carrier were optimized and standardized. The enzyme cartridges were
An ion-exchange chromatographic method was developed for measuring chloride, phosphate, nitrate, and sulfate anions in model media, and chloride, phosphate and sulfate anions in industrial cultivation medii of microorganisms. By optimisation, an analysis time of 14 min was obtained. An ion-exclusion
Enzymes were (co)hnmobilized on the pH-sensitive gates of an eightchannel field-effect transistor @ET). Glucose was analysed with a glucose dehydrogenase (GDH) FET, maltose with a coimmobilized maltase (MAL)/GDH FET, sucrose with a cohnmobilized invertase (INV)/GDH FET, lactose with a /3-galactosid