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Immobilization of Amylases via Adsorption on Agar-Coated Magnetic Nanoparticles

Year 2022, Issue: 34, 496 - 500, 31.03.2022
https://doi.org/10.31590/ejosat.1083196

Abstract

In this study, a new method for simultaneous synthesis and coating of magnetic iron oxide nanoparticles was employed, where ferric and ferrous ions were co-precipitated within an aqueous solution containing agar at room temperature under inert atmosphere. X-ray diffraction (XRD) analysis indicated that synthesized nanoparticles were pure Fe3O4 with a cubic structure and crystallite size ranging between 9.38 and 10.11 nm. The scanning electron microscope (SEM) images demonstrated the increasing surface roughness as concentration of surface coating material increased. The produced magnetic particles were used as a support for α−amylase immobilization by adsorption method. Effects of sonication, immobilization time (0.5; 1; 2; 4; 8; 16 h) concentration of surface coating material (0; 0.5; 1% w/v agar), immobilization pH (pH 3,4,5,6,7) on protein loading, enzyme activity and specific activity were investigated. Sonication did not enhance amylase immobilization. Based on the specific activity of the enzyme, the optimum adsorption was achieved at pH 4 and 5 after 4h-immobilization time, where, compared to the free α−amylase, a 3-fold increase in specific activity and 360% increase in relative activity was measured, respectively.

Supporting Institution

Eskişehir Teknik Üniversitesi, TÜBİTAK

Project Number

20ADP099, 20AG025

Thanks

Authors would like to thank the Anadolu University Plant Drug and Scientific Research Center (AUBIBAM) for the SEM images. This work was financially supported by Eskisehir Technical University (ESTU) research fund with project number 20ADP099 and TÜBİTAK — The Scientific and Technological Research Council of Turkey with the project no. TÜBİTAK 20AG025 under program no. TÜBİTAK 20AG001. Nihal Yılmaz was supported by TUBITAK-BIDEB 2210/C National Scholarship Program for MSc students.

References

  • Bai, H., Zhaoyang, L., Darren D.S., (2011). Highly water soluble and recovered dextran coated Fe3O4 magnetic nanoparticles for brackish water desalination. Separation and Purification Technology (81), 392-399. Technology (81), 392-399.
  • Bilal, M., Asgher, M., (2015). Sandal reactive dyes decolorization and cytotoxicity reduction using manganese peroxidase immobilized onto polyvinyl alcohol- alginate beads. Chemistry Central Journal (9)1, 47.
  • Bradford, M.M., (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein. Analytical Biochemistry, 248-254.
  • Datta, S., Christena, L.R., Rajaram, Y.R.S., (2012). Enzyme immobilization: an overview on techniques and support materials, 3 Biotech (3), 1-9.
  • Jiang, D., Long, S., Huang J., Xiao, H., Zhou, J., (2016). Immobilization of Pycnoporous sanguineus laccase on magnetic chitosan microsphere, Biochem Eng. (25), 15-23.
  • Junior, J.C.Q., Ferrazrezi, A.L., Borges, J.P., Brito, R.R., Gomes, E., Silva, R., Guisan, J.M., Boscolo, M., (2016). Hydrophobic adsorption in ionic medium improves the catalytic properties of lipases applied in the triacylglycerol hydrolysis by synergism. Bioprocess and Biosystems Engineering (39), 1933-1943.
  • Koeller, K.M., Wong, C.H., (2001). Enzymes for chemical synthesis. Nature (409), 232-240.
  • Li, X., Zhu, H., Feng, J., Zhang, X., Deng, B., Zhou, B., Zhang, H., Xue, D., Li, F., Mellors, N.J., Li, Y., Peng, Y., (2013). One-pot polyol synthesis of graphene decorated with size- and density-tunable Fe3O4 nanoparticles for porcine pancreatic lipase immobilization. Carbon (60), 488-497.
  • Liu, D.M., Chen, J., Shi, Y.P., (2018). Advances on methods and easy separated support materials for enzyme immobilization. TrAC Trends in Analytical Chemistry (102), 332-342.
  • Ranjbakhsh, E., Bordbar, A.K., Abbasi, M., Khosropour, A.R., Shams, E., (2012). Enhancement of stability and catalytic activity of immobilized lipaseon silica-coated modified magnetite nanoparticles. Chemical Engineering Journal (179), 272-276.
  • Sahutoglu, A.S., Akgul, C., (2015). Immobilization of Aspergillus oryzae alpha amylase and Aspergillus niger glucoamylase as cross-linked enzyme aggregates. Chemical Papers (69), 433-439.
  • Schmid, A., Dordick, J.S., Hauer, B., Kiener, A., Wubbolts, M., Witholt, B., (2001). Industrial biocatalysis today and tomorrow. Nature (409). 258-268.
  • Sohrabi, N., Rasouli, N., Torkzadeh, M., (2013). Enhanced stability and catalytic activity of immobilized α−amylase on modified Fe3O4 nanoparticles. Chemical Engineering Journal (240), 426-433.
  • Xiao, Z., Storms, R., Tsang, A., (2006). A quantitative starch-iodine method for measuring alpha-amylase and glucoamylase activities. Analytical Biochemistry (351). 146-148.
  • Zhu, Y.T., Ren, X.Y., Liu, Y.M., Wei, Y., Qing, L.S., Liao, X., (2014). Covalent immobilization of porcine pancreatic lipase on carboxyl-activated magnetic nanoparticles: Characterization and application for enzymatic inhibition assays. Material Science and Engineering: C (38).278-285.

Agar-Kaplı Manyetik Nanopartiküller Üzerine Adsorpsiyon ile Amilaz İmmobilizasyonu

Year 2022, Issue: 34, 496 - 500, 31.03.2022
https://doi.org/10.31590/ejosat.1083196

Abstract

Bu çalışmada, inert atmosfer altında oda sıcaklığında agar içeren sulu bir çözelti içinde ferrik ve ferröz iyonlarının birlikte çökeltildiği, manyetik demir oksit nanopartiküllerin eşzamanlı sentezi ve kaplanması için yeni bir yöntem kullanıldı. X-ışını kırınımı (XRD) analizi, sentezlenen nanopartiküllerin kübik yapıya ve 9.38 ile 10.11 nm arasında değişen kristalit boyutuna sahip saf Fe3O4 olduğunu gösterdi. Taramalı elektron mikroskobu (SEM) görüntüleri, yüzey kaplama malzemesi konsantrasyonu arttıkça artan yüzey pürüzlülüğünü gösterdi. Üretilen manyetik partiküller adsorpsiyon yöntemiyle α-amilaz immobilizasyonu için destek olarak kullanıldı. Sonikasyon, immobilizasyon süresi (0,5; 1; 2; 4; 8; 16 saat), yüzey kaplama malzemesi konsantrasyonu (0; 0,5; %1 w/v agar), immobilizasyon pH'ının (pH 3,4,5,6, 7) protein yüklemesi, enzim aktivitesi ve spesifik aktivite üzerine etkileri araştırıldı. Sonikasyon, amilaz immobilizasyonunu arttırmadı. Enzimin spesifik aktivitesine dayalı olarak, optimum adsorpsiyon pH 4 ve 5'te 4 saatlik immobilizasyon süresinde elde edildi; bu koşullarda serbest α−amilaza kıyasla spesifik aktivitede 3 kat artış ve bağıl aktivitede %360 artış ölçüldü.

Project Number

20ADP099, 20AG025

References

  • Bai, H., Zhaoyang, L., Darren D.S., (2011). Highly water soluble and recovered dextran coated Fe3O4 magnetic nanoparticles for brackish water desalination. Separation and Purification Technology (81), 392-399. Technology (81), 392-399.
  • Bilal, M., Asgher, M., (2015). Sandal reactive dyes decolorization and cytotoxicity reduction using manganese peroxidase immobilized onto polyvinyl alcohol- alginate beads. Chemistry Central Journal (9)1, 47.
  • Bradford, M.M., (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein. Analytical Biochemistry, 248-254.
  • Datta, S., Christena, L.R., Rajaram, Y.R.S., (2012). Enzyme immobilization: an overview on techniques and support materials, 3 Biotech (3), 1-9.
  • Jiang, D., Long, S., Huang J., Xiao, H., Zhou, J., (2016). Immobilization of Pycnoporous sanguineus laccase on magnetic chitosan microsphere, Biochem Eng. (25), 15-23.
  • Junior, J.C.Q., Ferrazrezi, A.L., Borges, J.P., Brito, R.R., Gomes, E., Silva, R., Guisan, J.M., Boscolo, M., (2016). Hydrophobic adsorption in ionic medium improves the catalytic properties of lipases applied in the triacylglycerol hydrolysis by synergism. Bioprocess and Biosystems Engineering (39), 1933-1943.
  • Koeller, K.M., Wong, C.H., (2001). Enzymes for chemical synthesis. Nature (409), 232-240.
  • Li, X., Zhu, H., Feng, J., Zhang, X., Deng, B., Zhou, B., Zhang, H., Xue, D., Li, F., Mellors, N.J., Li, Y., Peng, Y., (2013). One-pot polyol synthesis of graphene decorated with size- and density-tunable Fe3O4 nanoparticles for porcine pancreatic lipase immobilization. Carbon (60), 488-497.
  • Liu, D.M., Chen, J., Shi, Y.P., (2018). Advances on methods and easy separated support materials for enzyme immobilization. TrAC Trends in Analytical Chemistry (102), 332-342.
  • Ranjbakhsh, E., Bordbar, A.K., Abbasi, M., Khosropour, A.R., Shams, E., (2012). Enhancement of stability and catalytic activity of immobilized lipaseon silica-coated modified magnetite nanoparticles. Chemical Engineering Journal (179), 272-276.
  • Sahutoglu, A.S., Akgul, C., (2015). Immobilization of Aspergillus oryzae alpha amylase and Aspergillus niger glucoamylase as cross-linked enzyme aggregates. Chemical Papers (69), 433-439.
  • Schmid, A., Dordick, J.S., Hauer, B., Kiener, A., Wubbolts, M., Witholt, B., (2001). Industrial biocatalysis today and tomorrow. Nature (409). 258-268.
  • Sohrabi, N., Rasouli, N., Torkzadeh, M., (2013). Enhanced stability and catalytic activity of immobilized α−amylase on modified Fe3O4 nanoparticles. Chemical Engineering Journal (240), 426-433.
  • Xiao, Z., Storms, R., Tsang, A., (2006). A quantitative starch-iodine method for measuring alpha-amylase and glucoamylase activities. Analytical Biochemistry (351). 146-148.
  • Zhu, Y.T., Ren, X.Y., Liu, Y.M., Wei, Y., Qing, L.S., Liao, X., (2014). Covalent immobilization of porcine pancreatic lipase on carboxyl-activated magnetic nanoparticles: Characterization and application for enzymatic inhibition assays. Material Science and Engineering: C (38).278-285.
There are 15 citations in total.

Details

Primary Language English
Subjects Engineering
Journal Section Articles
Authors

Nihal Yılmaz 0000-0001-6682-3745

Suzan Biran Ay 0000-0002-2968-4982

Project Number 20ADP099, 20AG025
Early Pub Date January 30, 2022
Publication Date March 31, 2022
Published in Issue Year 2022 Issue: 34

Cite

APA Yılmaz, N., & Biran Ay, S. (2022). Immobilization of Amylases via Adsorption on Agar-Coated Magnetic Nanoparticles. Avrupa Bilim Ve Teknoloji Dergisi(34), 496-500. https://doi.org/10.31590/ejosat.1083196