Enhanced enzyme production with the pelleted form of D. squalens in laboratory bioreactors using added natural lignin inducer

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Abstract

White-rot fungi are extensively used in various submerged biotechnology processes to produce ligninolytic enzymes. Transfer of the process from the laboratory to the industrial level requires optimization of the cultivation conditions on the laboratory scale. An interesting area of optimization is pellet growth since this morphological form solves problems such as the decreased oxygen concentration, limited heat, and nutrient transport, which usually occur in dispersed mycelium cultures. Many submerged fermentations with basidiomycetes in pellet form were done with Phanerochaete, Trametes, and Bjerkandera species, among others. In our study, another promising basidiomycete, D. squalens, was used for ligninolytic enzyme production. With the addition of wood particles (sawdust) as a natural inducer and optimization of mixing and aeration conditions in laboratory stirred tank (STR) and bubble column (BCR) reactors on pellet growth and morphology, the secretion of laccase and the manganese-dependent peroxidase into the medium was substantially enhanced. The maximum mean pellet radius was achieved after 10 days in the BCR (5.1 mm) where pellets were fluffy and 5 days in the STR (3.5 mm) where they were round and smooth. The maximum Lac activity (1,882 U l -1 ) was obtained after 12 days in the STR, while maximum MnP activity (449.8 U l -1 ) occurred after 18 days in the BCR. The pellet size and morphology depended on the agitation and aeration conditions and consequently influenced a particular enzyme synthesis. The enzyme activities were high and comparable with the activities found for other investigations in reactors with basidiomycetes in the form of pellets. © 2011 Society for Industrial Microbiology and Biotechnology.

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Babič, J., & Pavko, A. (2012). Enhanced enzyme production with the pelleted form of D. squalens in laboratory bioreactors using added natural lignin inducer. Journal of Industrial Microbiology and Biotechnology, 39(3), 449–457. https://doi.org/10.1007/s10295-011-1036-2

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