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Magnetically modified bacterial cellulose: A promising carrier for immobilization of affinity ligands, enzymes, and cells

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    SYSNO ASEP0474812
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleMagnetically modified bacterial cellulose: A promising carrier for immobilization of affinity ligands, enzymes, and cells
    Author(s) Baldíková, E. (CZ)
    Pospíšková, K. (CZ)
    Ladakis, D. (GR)
    Kookos, I.K. (GR)
    Koutinas, A.A. (GR)
    Šafaříková, Miroslava (BC-A) RID
    Šafařík, Ivo (BC-A) RID, ORCID
    Source TitleMaterials Science & Engineering C-Materials for Biological Applications. - : Elsevier - ISSN 0928-4931
    Roč. 71, February (2017), s. 214-221
    Number of pages8 s.
    Languageeng - English
    CountryNL - Netherlands
    Keywordsbacterial cellulose ; Komagataeibacter sucrofermentans ; copper phthalocyanine ; crystal violet ; yeast cells ; trypsin
    Subject RIVEI - Biotechnology ; Bionics
    OECD categoryBioproducts (products that are manufactured using biological material as feedstock) biomaterials, bioplastics, biofuels, bioderived bulk and fine chemicals, bio-derived novel materials
    Institutional supportBC-A - RVO:60077344
    UT WOS000390967200027
    EID SCOPUS84991730101
    DOI10.1016/j.msec.2016.10.009
    AnnotationBacterial cellulose (BC) produced by Komagataeibacter sucrofermentans was magnetically modified using perchloric acid stabilized magnetic fluid. Magnetic bacterial cellulose (MBC) was used as a carrier for the immobilization of affinity ligands, enzymes and cells. MBC with immobilized reactive copper phthalocyanine dye was an efficient adsorbent for crystal violet removal, the maximum adsorption capacity was 388 mg/g. Kinetic and thermodynamic parameters were also determined. Model biocatalysts, namely bovine pancreas trypsin and Saccharomyces cerevisiae cells were immobilized on MBC using several strategies including adsorption with subsequent cross-linking with glutaraldehyde and covalent binding on previously activated MBC using sodium periodate or 1,4-butanediol diglycidyl ether. Immobilized yeast cells retained approximately 90% of their initial activity after 6 repeated cycles of sucrose solution hydrolysis. Trypsin covalently bound after MBC periodate activation was very stable during operational stability testing, it could be repeatedly used for ten cycles of low molecular weight substrate hydrolysis without loss of its initial activity.
    WorkplaceBiology Centre (since 2006)
    ContactDana Hypšová, eje@eje.cz, Tel.: 387 775 214
    Year of Publishing2018
Number of the records: 1  

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