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Process optimization was conducted for the conversion of the aggragate-building substrate di-rhamnolipid to mono-rhamnolipid by Alpha-L-rhamnosidase from Penicillium decumbens and resulting in: (I) selection of optimal reaction conditions for enzyme activity and stability, (II) modeling of the reaction time course assuming mixed aggregates as a second phase, and (III) high mass diffusion resistances were completely overcome by the use of non-porous magnetic enzyme micro-carriers.
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Magario, I. 2009. Enzyme reaction engineering for the conversion of emulsified di-rhamnolipid by free and immobilized Naringinase. Karlsruhe: KIT Scientific Publishing. DOI: https://doi.org/10.5445/KSP/1000010067
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Veröffentlicht am 19. Februar 2009
Englisch
149
| Paperback | 978-3-86644-329-7 |