[en] Production of xylanases by Penicillium canescens 10-10c is the research object in Walloon Center of Industrial Biology. Previous works used submerged or liquid fermentation. The actual works are oriented more and more towards solid fermentation from agricultural or agro-alimentary residues. In addition to the valorization of these residues, solid-state fermentation reaches an increasingly significant interest in various other fields like the biological breakdown of the solid residues, the bioremediation of the organic pollutants in the grounds and the reduction of the air pollution by the biofiltration. Xylanase is an industrial enzyme used in general in extraction and clarification processes. P. canescens can produce an activity of it, particularly in its balanced forms of xylanases, beta-xylosidase and arabinosidase, and not contaminated by cellulolytic and amylolytic activities. It is a hyper producing strain of xylanase. The production rate is one of the highest in literature (535 U.ml-1 and 9,632 U.g-1 in Erlenmeyer flasks, in submerged and solid state fermentation, respectively). The biobleaching
activity of the cellulose pulp by the purified enzyme is higher than a commercial preparation of xylanases from Trichoderma longibrachiatum used industrially. It has a complete hydrolysis degree of 40% (on glucuronoxylan) and 35% (on arabinoxylan) at 55°C and at pH of 5.9. These characteristics lead to many industrial applications of this enzyme. That is why the optimization of its production by the solid-state fermentation at the laboratory scale in order to define a policy for the industrial transposition later is carried out. This article presents a summary of the scientific literature on this subject.
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Bakri Y., Jacques Ph. & Thonart Ph., 2003. Xylanase production by Penicillium canescens 10-10c in solid-state fermentation. Appl. Biochem. Biotechnol., 108, 737-748.
Bellon-Maurel V., Orliac O. & Christen P., 2003. Sensors and measurements in solid-state fermentation: a review. Process Biochem., 38, 881-896.
Chavez R., Bull P. & Ey Zaguirre J., 2006. The xylanolytic enzyme system from the genus Penicillium. J. Biotechnol., 1(2), 64-66.
Crépy H., 2000. Mise en évidence et dosage de l'ergostérol, biomarqueur de moisissures retrouvées dans les lieux de travail. Mémoire: Faculté universitaire des Sciences agronomiques de Gembloux (Belgique).
Durand A., 2003. Bioreactor designs for solid-state fermentation. Biochem. Eng. J., 13, 113-125.
Gaspar A., Cosson T., Roques C. & Thonart Ph., 1997. Study on the production of a xylanolytic complex from Penicillium canescens 10-10c. Appl. Biochem. Biotechnol., 67, 45-58.
Gaspar A., 1999. Étude des interactions entre les paramètres biologiques et les grandeurs physiques liées à l'agitation et à l'aération lors de la production de xylanases par Penicillium canescens. Thèse de doctorat: Faculté universitaire des Sciences agronomiques de Gembloux (Belgique).
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Mathot P., 1996. Modélisation d'un réacteur simplifié pour la fermentation solide de produits et sous-produits agricoles. Valorisation de l'aliment fermenté par le porc. Thèse de doctorat: Faculté universitaire des Sciences agronomiques de Gembloux (Belgique).
Nikolaev I.V. & Vinetski Y.P., 1998. L-arabinose induces synthesis of secreted ββ-galactosidase in the filamentous fungus Penicillium canescens. Biochemistry, 63(11), 1294-1298.
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Sinitsyna O.A. et al., 2003a. Isolation and properties of major components of Penicillium canescens extracellular enzyme complex. Biochemistry, 68(11), 1200-1209.
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Yang S.Q. et al., 2006. High-level of xylanase production by the thermophilic Paecilomyces themophila J18 on wheat straw in solid-state fermentation. Bioresour. Technol., 97(15), 1794-1800.