134 research outputs found
Role of enzyme immobilization in the formulation of enzymes for single use
Immobilized enzymes find application in diverse areas of biosciences as biofuels, biosensors and biocatalysis. Development of a immobilization for an enzyme implies a careful selection and optimization of different parameters that have a critical influence on the final properties, e.g. activity, stability [1,2]. Enzyme stabilization via immobilization is a common target and it is achievable when properly performed [2]. There is the general idea that the use of enzyme in free soluble form is associated to single use due to the simplicity and significant lower cost, whereas the use of immobilized preparations is generally associated to facilitate retention, recycling or continuous use. Nevertheless, there are some constraints where immobilization is a fundamental tool to enable the single use of the enzyme under conditions otherwise not-applicable. Among others, these conditions involve the preservation of enzyme activity during extraction, purification, storage and transport, stabilization under condition of use and easy separation from the medium where it is applied. This communication presents some examples of immobilization strategies and benefits for the application of oxidative enzymes. Glucose oxidase and D-amino acid oxidase were immobilized into porous materials made from natural organic polymers or synthetic organic polymers [3,4]. Under the conditions of use, that involves diluted application and existence of gas-liquid interfaces, the free enzymes have half-lifetime lower than 5 min whereas proper immobilized preparations within porous materials did not show decrease of activity during a time span of observation of 40 h. The storage of the enzyme formulation was also facilitated, immobilized enzymes were stable under simple storage conditions whereas free enzymes required prevention microbiological contamination and tuning of buffer conditions to avoid protein precipitation. Among different strategies, the use of reversible immobilization was evaluated to enable the reuse of support and facilitate an immobilization on/off character. The development reversible one step purification-immobilization simplified the production and application of the immobilizate format compared with the soluble counterpart [3]. Finally, the immobilization was used as a compartmentalization strategy, two enzymes (oxidase-catalase, oxidase-peroxidase) or a pair of oxidase - oxygen probe can be used when they are confined into solid materials compared to incompatible conditions of use in soluble format [5]. Co-joined design of polymeric materials and immobilization strategies is recognized as important for the efficient cost-effective formulation of enzyme immobilizates. [1] Bolivar, J.M., Eisl, I., Nidetzky, B.(2016) Catalysis Today, 259, pp. 66-80. [2] Rodrigues, R.C., Ortiz, C., Berenguer-Murcia, A., Torres, R., Fernández-Lafuente, R. (2013) Chemical Society Reviews, 42 (15), pp. 6290-6307. [3] Wiesbauer, J., Bolivar, J.M., Mueller, M., Schiller, M., Nidetzky, B. (2011) ChemCatChem, 3 (8), pp. 1299-1303. [5] Bolivar, J.M., Consolati, T., Mayr, T., Nidetzky, B. (2013) Biotechnology and Bioengineering, 110 (8), pp. 2086-2095. [4] Bolivar, J.M., Consolati, T., Mayr, T., Nidetzky, B. (2013) Trends in Biotechnology, 31 (3), pp. 194-20
Cellulose hydrolysis by the cellulases from Trichoderma reesei: adsorptions of two cellobiohydrolases, two endocellulases and their core proteins on filter paper and their relation to hydrolysis
Oscillatory Flow Bioreactor (OFB) Applied in Enzymatic Hydrolysis at High Solid Loadings
Within this study, an enzymatic hydrolysis process using α-cellulosic feedstock was performed in a specially designed plug-flow reactor, referred to as an Oscillatory Flow Bioreactor (OFB). The aims of this approach were to achieve intensification in terms of realising a more energy- and resource-efficient enzymatic hydrolysis, as well as to set the basis for continuous processes in such a reactor. The OFB performance was evaluated for high solid loadings of up to 15 %, and compared to the performance of a Stirred Tank Reactor (STR). Experimental results of the OFB operating at an oscillation frequency of
2 Hz and an oscillation amplitude of 10 mm exhibit better conversion efficiencies (+ 6.7 %) than the STR after 24 h, while requiring only 7 % of the STR power density (W m–3). Therefore, the OFB enables efficient, uniform mixing at lower power densities than STRs for applications with high solid loadings.
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From wheat straw to bioethanol: integrative analysis of a separate hydrolysis and co-fermentation process with implemented enzyme production
From an electrophoretic mobility shift assay to isolated transcription factors: a fast genomic-proteomic approach
The micromorphology of Trichoderma reesei analyzed in cultivations on lactose and solid lignocellulosic substrate, and its relationship with cellulase production
Optimization of cellulolytic enzyme components through engineering Trichoderma reesei and on-site fermentation using the soluble inducer for cellulosic ethanol production from corn stover
Functional characterization of the native swollenin from Trichoderma reesei: study of its possible role as C1 factor of enzymatic lignocellulose conversion
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