Immobilized metal ion affinity nanospheres for α-amylase immobilization

Immobilized metal ion affinity nanospheres for α-amylase immobilization

Immobilized metal chelate affinity chromatography (IMAC) support was practiced for α -amylase immo- 2+ 2+bilization. Poly(hydroxyethylmethacrylate-methacryloylamidotryptophan)-Ni [p(HEMA-MAT)-Ni ] nanospheres, average diameter 100 nm, were produced by surfactant free emulsion polymerization. Characterizations of p(HEMA- MAT)-Ni 2+ nanospheres were carried out by Fourier transform infrared (FTIR) spectroscopy and scanning electron microscope (SEM). In addition, average particle size, size distribution, and surface charge were specified. The amount of N-methacryloylamidotryptophan (MAT) incorporated to polymer was determined as 1.95 mmol/g polymers by using nitrogen stoichiometry. The specific surface areas of poly(hydroxyethylmethacrylate) [p(HEMA)] and p(HEMA-MAT) 2 2nanospheres were calculated as 1856 m /g and 1914 m /g, respectively. Protein adsorption increased with increasing initial protein concentration and maximum α -amylase adsorption on p(HEMA-MAT)-Ni 2+ nanospheres was observed at pH 4.0. Both free and immobilized α -amylase showed pH optimum at pH 7.0. It was determined that the immobilized α -amylase had better thermostability than the free one. Immobilization of the enzyme did not significantly change the kinetic parameters. The storage stability of α -amylase increased upon immobilization. It was also observed that 2+p(HEMA-MAT)-Ni nanospheres can be repeatedly used for α -amylase immobilization.

___

  • Schenck, F. W.; Hebeda, R. E. Starch Hydrolysis Products: Worldwide Technology, Production and Applications, VCH, New York, 1992.
  • Windish, W. W.; Mhatre, N. S. Advances in Applied Microbiology, In: Wayne, W. U. Ed., 1965.
  • Fogarty, W. M.; Kelly, C. T. In Topics in Enzyme and Fermentation Biotechnology; Wiseman, A., Ed., 1979.
  • Vihinen, M.; Mantsala, P. Crit Rev. Biochem. Mol. Biol. 1989, 24, 329–418.
  • Lonsane, B. K.; Ramesh, M. V. Adv. Appl. Microbiol. 1990, 35, 1–56.
  • Nikolov, Z. L.; Reily, P. J. In Biocatalysts for Industry; Dordick, J. S., Ed. Plenum Press, New York, 1991.
  • Liu, Y.; Jia, S.; Ran, J.; Wu, S. Catal. Commun. 2010, 11, 364–367.
  • Yamamoto, T. In Handbook of Amylases and Related Enzymes: Their Source, Isolation Methods, Properties and Applications; Amylase Research Society of Japan, Ed., Pergamon Press, Oxford, 1988.
  • Bahar, T.; Celebi, S. S. Enzyme Microb. Technol. 2000, 26, 28–33.
  • Roig, M. G.; Kennedy, J. F.; Garaita, M. G. J. Biomater. Sci. Polym. Ed. 1994, 6, 661–673.
  • Ida, J.; Matsuyama, T.; Yamamoto, H. Biochem. Eng. J. 2000, 5, 179–184.
  • Yang, Y.; Chase, H. A. Biotechnol. Appl. Biochem. 1998, 28, 145–154.
  • Chen, J. P.; Sun, Y. M.; Chu, D. H. Biotechnol. Prog. 1998, 14, 473–478.
  • Bryjak, J. Bioprocess Eng. 1995, 13, 177–181.
  • Mateo, C.; Palomo, J. M.; Fernandez-Lorente, G.; Guisan, J. M.; Fernandez-Lafuente, R. Enzyme Microb. Technol. 2007, 40, 1451–1463.
  • Akgol, S.; Ozturk, N.; Denizli, A. J. Appl. Polym. Sci. 2010, 115, 1608–1615.
  • Cong, L.; Kaul, R.; Dissing, U.; Mattiasson, B. J. Biotechnol. 1995, 42, 75–84.
  • Tischer, W.; Kashe, V. Biotechnology 1999, 17, 326–335.
  • Ye, P.; Xu, Z. K.; Che, A. F.; Wu, J.; Seta, F. Biomaterials 2005, 26, 6394–6403.
  • Rebros, V.; Rosenberg, M.; Mlichova, Z.; Kristofıkova, L. Food Chem. 2007, 102, 784–787.
  • Sankalia, V.; Mashru, V.; Sankalia, J. M.; Sutariya, V. B. Eur. J. Pharm. Biopharm. 2007, 65, 215–232.
  • Peng, K.; Hidajat, K.; Udin, M. S. J. Colloid Interface Sci. 2004, 271, 277–283.
  • Choi, S. W.; Kwon, H. Y.; Kim, W. S.; Kim, J. H. Colloids Surf. A 2002, 201, 283–289.
  • Ozturk, N.; Akgol, S.; Arisoy, M.; Denizli, A. Sep. Purif. Technol. 2007, 58, 83–90.
  • Kim, J.; Grate, J. W.; Wang, P. Chem. Eng. Sci. 2006, 61, 1017–1026.
  • Tuzmen, N.; Kalburcu T.; Denizli A. Process Biochem. 2012, 47, 26–33.
  • Porath, J.; Carlson, J.; Olsson, I.; Belfrage, G. Nature 1975, 258, 598–599.
  • Gaberc-Porekar, V.; Menart, V. J. Biochem. Biophys. Methods 2001, 49, 335–360.
  • Arnold, F. H. Bio. Technology 1991, 9, 150–155.
  • Gutierrez, R. E.; Martin del Vale, M.; Galan, M. A. Sep. Purif. Rev. 2007, 36, 71–111.
  • Kubota, N.; Nakagawa, Y.; Eguchi, Y. J. Appl. Polym. Sci. 1996, 62, 1153–1160.
  • Lawal, O. S. Food Chem. 2006, 95, 101–107.
  • Ueda, E. K. M.; Gout, P. W.; Morganti, L. J. Chromatogr. A 2003, 988, 1–23. Mosbach, K. Sci. Am. 1971, 224, 26–33.
  • He, D.; Cai, Y.; Wei, W.; Nie, L.; Yao, S. Biochem. Engineer. J. 2000, 6, 7–11.
  • Tanyolac, D.; Yuruksoy, B. I.; Ozdural, A. R. Biochem. Eng. J. 1998, 2, 179–186.
  • O’Neill, S. P.; Dunnill, P.; Lilly, M. D. Biotechnol. Bioeng. 1971, 13, 337–352.
  • Lopez, G. P.; Ratner, B. D.; Rapoza, R. J.; Horbett, T. A. Macromol. Symp. 1993, 26, 3247–3253.
  • Arica, M. Y.; Senel, S.; Alaeddinoglu, N. G.; Patir, S.; Denizli, A. J. Appl. Polym. Sci. 2000, 75, 1685–1692.
  • Aksoy, S.; Tumturk, H.; Hasirci, N. J. Biotechnol. 1998, 60, 37–46.
  • Turunc, O.; Kahraman, M. V.; Akdemir, Z. S.; Kayaman-Apohan, N.; Gungor, A. Food Chem. 2009, 112, 992–997.
  • Kara, A.; Osman, B.; Yavuz, H.; Be ̧sirli N., Denizli A. React. Funct. Polym. 2005, 62, 61–68.
  • Chang, M. Y.; Juang, R. S. Process Biochem. 2004, 39, 1087–1090.
  • Reddy, K. R. C.; Kayastha, A. M. J. Mol. Catal. B: Enzym. 1994, 38, 104–112.
Turkish Journal of Chemistry-Cover
  • ISSN: 1300-0527
  • Yayın Aralığı: 6
  • Yayıncı: TÜBİTAK
Sayıdaki Diğer Makaleler

Azolylimidazoles: Synthetic strategies and medicinal applications

Bakr Fathy ABDELWAHAB, Rizk Elsayed KHIDRE

On the peculiar reactivity of a C,N-annelated isoindole core

İaroslav BAGLAI, Valérie MARAVAL, Zoia Vsevolodivna VOITENKO

Hard chromium electrodeposition from a trivalent chromium bath containing water-soluble polymer

Vyacheslav PROTSENKO, Viktor GORDIIENKO, Tatiana BUTYRINA, Elena VASIL’EVA, Felix DANILOV

Immobilized metal ion affinity nanospheres for α-amylase immobilization

Adil DENİZLİ, Sinan AKGÖL, Münire Nalan TUZMEN, Tülden KALBURCU

Simulation of impedance spectra of oxalic acid electroreduction to glyoxylic acid: effect of chemical activator, pH, activation energy, and reduction potential

Niyazi Alper TAPAN

Synthesis, structure, and luminescent properties of 2 novel 5-chlorhydroxybenzoate-imidazole metal-organic complexes

Hong CHEN, Siyuan LUO, Xiuling WU, Yongqian WANG, Bo HU

A new and simple DP polarographic method for the determination of uric acid in serum after elimination of the interference of ascorbic acid and dopamine

Ali Cengiz ÇALIŞKAN, Güler SOMER

Experimental investigation of drag reduction effects of polymer additives on turbulent pipe flow using ultrasound Doppler velocimetry

Şerife Zeybek VURAL, Göknur BAYRAM, Yusuf ULUDAĞ

Self-condensation reactions of acyl phosphonates: synthesis of tertiary O-protected a-hydroxyphosphonates

Serkan EYMUR, Mehmet GÖLLÜ, Ayhan Sıtkı DEMİR

Preparation of a novel solid acid catalyst with Lewis and Brønsted acid sites and its application in acetalization

Yijun DU, Linjun SHAO, Lingyan LUO, Si SHI, Chenze QI