The Carboxylated Multi-walled Carbon Nanotubes/l-Asparaginase Doped Calcium-Alginate Beads: Structural and Biocatalytic Characterization

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dc.contributor.author Ulu, Ahmet
dc.contributor.author Karaman, Muhammet
dc.contributor.author Yapıcı, Fatma
dc.contributor.author Naz, Mehmet
dc.contributor.author Sayın, Selin
dc.contributor.author Saygılı, Eyüp İlker
dc.contributor.author Ateş, Burhan
dc.date.accessioned 2021-10-18T15:23:40Z
dc.date.available 2021-10-18T15:23:40Z
dc.date.issued 2020
dc.identifier.issn 1011-372X
dc.identifier.uri http://openaccess.sanko.edu.tr/xmlui/handle/20.500.12527/449
dc.description.abstract The calcium-alginate/multi-walled carbon nanotube hybrid beads (Ca-ALG/MWCNT-COOH) as a novel kind of matrix were fabricated and characterized in detailed. l-Asparaginase (l-ASNase), which is important chemotherapeutic enzyme-drug in leukemia, was immobilized on the Ca-ALG/MWCNT-COOH hybrid beads. To the best of our knowledge, this is the first study using Ca-ALG/MWCNT-COOH hybrid beads for l-ASNase immobilization. Our characterization investigations displayed that the hybridization between ALG and MWCNT-COOH caused significant changes on the surface morphology and structure. ALG of 0.5% (w/v), CaCl2 of 0.2 M concentration, enzyme of 187.5 U and bead size of 2 mm was found to be best with respect to enzyme loading efficiency. The enzyme was loaded a high yield (97.0%) on these hybrid beads. Remarkably, the tolerance of immobilized enzyme developed towards temperature and pH changes. The maximum activity for the free enzyme was observed at 35 degrees C, pH 7.5, whereas the immobilized enzyme showed maximum activity at 45 degrees C pH 8.5. After immobilization, storage stability of enzyme improved and retained more than 70% of its initial activity after 4 weeks at ~ 30 degrees C as compared with free enzyme which showed only 20% of residual activity. After immobilization, Km value decreased 1.27-fold compared to free counterpart, indicating increased the affinity between the substrate and enzyme. Moreover, immobilized enzyme maintained more than 36% of its original activity even after consecutive 14 reuse. As result, it is worthy of noting that this kind of hybrid materials may become a promising support material for the immobilization of commercial enzymes in areas such as industrial and medical. Graphic en_US
dc.language.iso English en_US
dc.publisher SPRINGERONE NEW YORK PLAZA, SUITE 4600 , NEW YORK, NY 10004, UNITED STATES en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Ca-alginate en_US
dc.subject Multi-walled carbon nanotubes en_US
dc.subject Hybrid beads en_US
dc.subject l-Asparaginase en_US
dc.subject Immobilization en_US
dc.subject Encapsulation en_US
dc.title The Carboxylated Multi-walled Carbon Nanotubes/l-Asparaginase Doped Calcium-Alginate Beads: Structural and Biocatalytic Characterization en_US
dc.type Article en_US
dc.relation.journal CATALYSIS LETTERS en_US
dc.identifier.issue 6 en_US
dc.identifier.startpage 1679 en_US
dc.identifier.endpage 1691 en_US
dc.identifier.volume 150 en_US
dc.contributor.authorID 0000-0002-4447-6233 : Ahmet Ulu en_US
dc.contributor.authorID 0000-0002-0102-4237 : Eyüp İlker Saygılı en_US
dc.contributor.authorID 0000-0001-6080-229X : Burhan Ateş en_US
dc.contributor.authorID 0000-0002-0155-3390 : Muhammet Karaman en_US
dc.contributor.authorID 0000-0002-4447-6233 : Ahmet Ulu en_US
dc.identifier.wos 000528850500014 en_US
dc.identifier.doi 10.1007/s10562-019-03069-y en_US
dc.contributor.sankoauthor Eyüp İlker Saygılı en_US
dc.contributor.sankoauthor Burhan Ateş en_US


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Gazimuhtar Paşa Bulvarı
No:36
27090
Şehitkamil / GAZİANTEP