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Termofilik Geobacillus sp. TF14’ten saflaştırılan α-Amilaz enziminin Kitosan boncuklara kovalent immobilizasyonu

Year 2017, Volume: 21 Issue: 6, 1342 - 1348, 01.12.2017
https://doi.org/10.16984/saufenbilder.293313

Abstract

Bu çalışmada, daha önce Geobacillus sp. TF14den saflaştırılmış
α-amilaz enzimi, kitosan boncuklara kovalent olarak immobilize edildi. Kitosan
boncuklar, toz haldeki kitosanın % 5’lik asetik asit çözeltisinde çözülmesi ve
1 M NaOH çözeltisine damla damla eklenmesiyle elde edildi. Daha sonra boncuklar
NaOH'in fazlasının giderilmesi için ard arda saf su ile yıkandı. İmmobilizasyon
iki aşamada gerçekleştirildi. Öncelikle, % 2,5 Gluteraldehit çözeltisi ile
reaksiyona sokularak kitosan boncuklar aktive edildi. Aktive edilmiş kitosan
boncuklar immobilizasyonun tamamlanması için enzim çözeltisi ile karıştırıldı.
İmmobilize edilen α-amilazın biyokimyasal karakterizasyonu da gerçekleştirildi.
İmmobilize α-amilazın pH 9,00'da maksimum aktiviteye ulaştığı ve enzimin 48 saatlik
bir sürede bu pH'da oldukça kararlı olduğu tespit edildi. İmmobilize enzimin
optimum sıcaklık değeri 95 °C olarak belirlendi. Enzimin, bu sıcaklıkta 48 saat
inkübasyon işleminden sonra başlangıçtaki aktivitesinin % 50'sini koruduğu
tespit edildi. Mn2+, Co2+ ve EDTA’nın immobilize enzim
aktivitesini neredeyse tamamen inhibe ettiği, diğer metal iyonlarının farklı
oranlarda inhibisyona neden olduğu belirlendi. Bazı deterjanlar varlığında
enzimin aktivitesini koruduğu tespit edildi. İmmobilize edilen α-amilazın
nişasta esaslı birçok sanayi alanında kullanılabileceği sonucuna varılabilir.

References

  • Jose L.Adrio and Arnold. L. Demain, «Microbial Enzymes: Tools for Biotechnological Processes,» Biomolecules, cilt 4, no. 1, pp. 117-139, 2014.
  • Adler-Nissen Jens, «Limited Enzymatic Degredation of proteins: A new aproach in the industrial application of hydrolases,» Journal of Chemical Technology and Biotechnology, cilt 32, no. 1, pp. 138-156, 1982.
  • Archana Sharma and T. Satyanarayana, «Microbial Acid Stable α-amylases: Characteristics, Genetic Engineering and Aplications,» Process Biochemistry, cilt 48, no. 2, pp. 201-211, 2013.
  • Cesar Mateo, Jose M. Palomo, Gloria Fernandez-Lorente, Jose M. Guisan and Roberto Fernandez-Lafuente, «Improvement of enzyme activity, stability and selectivity via immobilization techniques,» Enzyme and Microbial Technology, cilt 40, no. 6, pp. 1451-1463, 2007.
  • Singh K, Srivastava G, Talat M, Srivastava O. N. and Kayastha A. M., «α-Amylase immobilization onto functionalized graphene nanosheets as scaffolds: Its characterization, kinetics and potential applications in starch based industries,» Biochemistry and Biophysics, cilt 3, pp. 18-25, 2015.
  • Şaban KESKİN, Termofilik Geobacillus sp.TF14'ten Endüstriyel Öneme Sahip α-Amilazın Saflaştırılması, İmmobilizasyonu ve Karakterizasyonu, Doktora tezi, Trabzon: Fen Bilimleri Enstitüsü, Karadeniz Teknik Üniversitesi, 2015.
  • Rodrigues D. S., Mendes A. A., Adriano W. S., Gonçalves L. R. B. and Giordano R. L.C., «Multipoint covalent immobilization of microbial lipase on chitosan and agarose activated by different methods,» Journal of Molecular Catalysis B: Enzymatic, cilt 51, pp. 100-109, 2008.
  • Lorena B., Fernando L-G., Aurelio H., Noelia A-M., Gisela D-O. C. M., Roberto F-L. and Jose M.G., «Different mechanisms of protein immobilization on glutaraldehyde activated support: Effect of support activation and immobilization conditions,» Enzyme and Microbial Technology, cilt 39, pp. 877-882, 2006.
  • M. M. Bradford, «Rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding,» Analitical Biochemistry, cilt 72, pp. 248-254, 1976.
  • Kapish G., Asim K. J., Sandeep K. and Mithu M., «Immobilization of α-amylase and amyloglucosidase onto ion-exchange resin beads and hydrolysis of natural starch at high concentrations,» Bioprocess Biosyst Eng, cilt 36, pp. 1715-1724, 2013.
  • Lineweaver H. and Burk D., «The Determination of Enzyme Dissociation Constants,» Journal of the American Chemical Society, cilt 56, no. 3, pp. 658-666, 1934.
  • Hasirci N., Aksoy S. and Tumturk H., «Activation of poly(dimer acid-co-alkyl polyamine) particles for covalent immobilization of α-amylase,» Reactive & Functional Polymers, cilt 66, pp. 1546-1551, 2006.
  • Zhongjie W., Wei Q., Mengfan W., Yuefei W., Rongxin S. and Zhimin H., «Chelate immobilization of amylase on metal ceramic powder : Preparation, characterization and application,» Biochemical Engineering Journal, cilt 77, pp. 190-197, 2013.
  • Gashtasbi F., Ahmadian G. and Noghab K. A., «New insights into the effectiveness of α-amylase enzyme presentation on the Bacillus subtilis spore surface by adsorption and covalent immobilization,» Enzyme and Microbial Technology, cilt 64, no. 65, pp. 17-23, 2014.
  • Sachin Talekar and Sandeep Chavare, «Optimization of immobilization of α-amylase in alginate gel and its comparative biochemical studies with free α-amylase,» Recent Research in Science and Technology, cilt 4, no. 2, pp. 01-05, 2012.
  • Padma V. I. and Laxmi A., «Enzyme stability and stabilization Aqueous and non-aqueous environment,» Process Biochemistry, cilt 43, pp. 1019-1032, 2008.
  • Chen J. P., Chu D. H. and Sun Y. M., «Immobilization of α-Amylase to Temperature Responsive Polymers by Single or Multiple Point Attachments,» Journal of Chemical Technology& Biotechnology, cilt 69, pp. 421-428, 1997.
  • Manu Sharma, Vinay Sharma and Dipak K. Majumdar, «Entrapment of -Amylase in Agar Beads for Biocatalysis of Macromolecular Substrate,» International Scholarly Research Notices, cilt vol. 2014, p. 8 pages, 2014.

Covalent Immobilization of α-Amylase from Thermophilic Geobacillus sp. TF14 on Chitosan Beads

Year 2017, Volume: 21 Issue: 6, 1342 - 1348, 01.12.2017
https://doi.org/10.16984/saufenbilder.293313

Abstract

In this
study, α-amylase formerly purified from Geobacillus
sp.
TF14 strain was covalently immobilized onto chitosan beads. Chitosan
beads were prepared by dissolving chitosan powder in 5% acetic acid solution
and by addition dropwise to 1 M NaOH solution. The consisted beads were washed
to remove excessive amount of NaOH. Immobilization was carried out in two
steps. Firstly, chitosan beads were activated by reacting with 2.5%
Glutaraldehyde solution. Next, activated chitosan beads were mixed with enzyme
solution to complete immobilization. Biochemical characterization of
immobilized α-amylase was also carried out. It was found that immobilized
α-amylase achieved maximum activity at pH 9.00 and the enzyme was quite stable
at this pH over a period of 48 h. Temperature optimum of the enzyme was
determined as 95 °C. It was also determined that the enzyme protected 50% of
its initial activity after incubation of 48 h at this temperature. While Mn2+,
Co2+ and EDTA almost completely inhibited the enzyme, other metal
ions showed inhibitory effects at different ratio. In the presence of some
detergents the enzyme conserved its initial activity. It can be concluded that
the immobilized α-amylase may find application in many fields of starch based
industries.

References

  • Jose L.Adrio and Arnold. L. Demain, «Microbial Enzymes: Tools for Biotechnological Processes,» Biomolecules, cilt 4, no. 1, pp. 117-139, 2014.
  • Adler-Nissen Jens, «Limited Enzymatic Degredation of proteins: A new aproach in the industrial application of hydrolases,» Journal of Chemical Technology and Biotechnology, cilt 32, no. 1, pp. 138-156, 1982.
  • Archana Sharma and T. Satyanarayana, «Microbial Acid Stable α-amylases: Characteristics, Genetic Engineering and Aplications,» Process Biochemistry, cilt 48, no. 2, pp. 201-211, 2013.
  • Cesar Mateo, Jose M. Palomo, Gloria Fernandez-Lorente, Jose M. Guisan and Roberto Fernandez-Lafuente, «Improvement of enzyme activity, stability and selectivity via immobilization techniques,» Enzyme and Microbial Technology, cilt 40, no. 6, pp. 1451-1463, 2007.
  • Singh K, Srivastava G, Talat M, Srivastava O. N. and Kayastha A. M., «α-Amylase immobilization onto functionalized graphene nanosheets as scaffolds: Its characterization, kinetics and potential applications in starch based industries,» Biochemistry and Biophysics, cilt 3, pp. 18-25, 2015.
  • Şaban KESKİN, Termofilik Geobacillus sp.TF14'ten Endüstriyel Öneme Sahip α-Amilazın Saflaştırılması, İmmobilizasyonu ve Karakterizasyonu, Doktora tezi, Trabzon: Fen Bilimleri Enstitüsü, Karadeniz Teknik Üniversitesi, 2015.
  • Rodrigues D. S., Mendes A. A., Adriano W. S., Gonçalves L. R. B. and Giordano R. L.C., «Multipoint covalent immobilization of microbial lipase on chitosan and agarose activated by different methods,» Journal of Molecular Catalysis B: Enzymatic, cilt 51, pp. 100-109, 2008.
  • Lorena B., Fernando L-G., Aurelio H., Noelia A-M., Gisela D-O. C. M., Roberto F-L. and Jose M.G., «Different mechanisms of protein immobilization on glutaraldehyde activated support: Effect of support activation and immobilization conditions,» Enzyme and Microbial Technology, cilt 39, pp. 877-882, 2006.
  • M. M. Bradford, «Rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding,» Analitical Biochemistry, cilt 72, pp. 248-254, 1976.
  • Kapish G., Asim K. J., Sandeep K. and Mithu M., «Immobilization of α-amylase and amyloglucosidase onto ion-exchange resin beads and hydrolysis of natural starch at high concentrations,» Bioprocess Biosyst Eng, cilt 36, pp. 1715-1724, 2013.
  • Lineweaver H. and Burk D., «The Determination of Enzyme Dissociation Constants,» Journal of the American Chemical Society, cilt 56, no. 3, pp. 658-666, 1934.
  • Hasirci N., Aksoy S. and Tumturk H., «Activation of poly(dimer acid-co-alkyl polyamine) particles for covalent immobilization of α-amylase,» Reactive & Functional Polymers, cilt 66, pp. 1546-1551, 2006.
  • Zhongjie W., Wei Q., Mengfan W., Yuefei W., Rongxin S. and Zhimin H., «Chelate immobilization of amylase on metal ceramic powder : Preparation, characterization and application,» Biochemical Engineering Journal, cilt 77, pp. 190-197, 2013.
  • Gashtasbi F., Ahmadian G. and Noghab K. A., «New insights into the effectiveness of α-amylase enzyme presentation on the Bacillus subtilis spore surface by adsorption and covalent immobilization,» Enzyme and Microbial Technology, cilt 64, no. 65, pp. 17-23, 2014.
  • Sachin Talekar and Sandeep Chavare, «Optimization of immobilization of α-amylase in alginate gel and its comparative biochemical studies with free α-amylase,» Recent Research in Science and Technology, cilt 4, no. 2, pp. 01-05, 2012.
  • Padma V. I. and Laxmi A., «Enzyme stability and stabilization Aqueous and non-aqueous environment,» Process Biochemistry, cilt 43, pp. 1019-1032, 2008.
  • Chen J. P., Chu D. H. and Sun Y. M., «Immobilization of α-Amylase to Temperature Responsive Polymers by Single or Multiple Point Attachments,» Journal of Chemical Technology& Biotechnology, cilt 69, pp. 421-428, 1997.
  • Manu Sharma, Vinay Sharma and Dipak K. Majumdar, «Entrapment of -Amylase in Agar Beads for Biocatalysis of Macromolecular Substrate,» International Scholarly Research Notices, cilt vol. 2014, p. 8 pages, 2014.
There are 18 citations in total.

Details

Subjects Chemical Engineering
Journal Section Research Articles
Authors

Şaban Keskin

Nagihan Sağlam Ertunga

Kadriye İnan Bektaş This is me

Publication Date December 1, 2017
Submission Date February 22, 2017
Acceptance Date August 1, 2017
Published in Issue Year 2017 Volume: 21 Issue: 6

Cite

APA Keskin, Ş., Sağlam Ertunga, N., & İnan Bektaş, K. (2017). Covalent Immobilization of α-Amylase from Thermophilic Geobacillus sp. TF14 on Chitosan Beads. Sakarya University Journal of Science, 21(6), 1342-1348. https://doi.org/10.16984/saufenbilder.293313
AMA Keskin Ş, Sağlam Ertunga N, İnan Bektaş K. Covalent Immobilization of α-Amylase from Thermophilic Geobacillus sp. TF14 on Chitosan Beads. SAUJS. December 2017;21(6):1342-1348. doi:10.16984/saufenbilder.293313
Chicago Keskin, Şaban, Nagihan Sağlam Ertunga, and Kadriye İnan Bektaş. “Covalent Immobilization of α-Amylase from Thermophilic Geobacillus Sp. TF14 on Chitosan Beads”. Sakarya University Journal of Science 21, no. 6 (December 2017): 1342-48. https://doi.org/10.16984/saufenbilder.293313.
EndNote Keskin Ş, Sağlam Ertunga N, İnan Bektaş K (December 1, 2017) Covalent Immobilization of α-Amylase from Thermophilic Geobacillus sp. TF14 on Chitosan Beads. Sakarya University Journal of Science 21 6 1342–1348.
IEEE Ş. Keskin, N. Sağlam Ertunga, and K. İnan Bektaş, “Covalent Immobilization of α-Amylase from Thermophilic Geobacillus sp. TF14 on Chitosan Beads”, SAUJS, vol. 21, no. 6, pp. 1342–1348, 2017, doi: 10.16984/saufenbilder.293313.
ISNAD Keskin, Şaban et al. “Covalent Immobilization of α-Amylase from Thermophilic Geobacillus Sp. TF14 on Chitosan Beads”. Sakarya University Journal of Science 21/6 (December 2017), 1342-1348. https://doi.org/10.16984/saufenbilder.293313.
JAMA Keskin Ş, Sağlam Ertunga N, İnan Bektaş K. Covalent Immobilization of α-Amylase from Thermophilic Geobacillus sp. TF14 on Chitosan Beads. SAUJS. 2017;21:1342–1348.
MLA Keskin, Şaban et al. “Covalent Immobilization of α-Amylase from Thermophilic Geobacillus Sp. TF14 on Chitosan Beads”. Sakarya University Journal of Science, vol. 21, no. 6, 2017, pp. 1342-8, doi:10.16984/saufenbilder.293313.
Vancouver Keskin Ş, Sağlam Ertunga N, İnan Bektaş K. Covalent Immobilization of α-Amylase from Thermophilic Geobacillus sp. TF14 on Chitosan Beads. SAUJS. 2017;21(6):1342-8.