Efficient determination and pesticide control by means of immobilization of acetylcholinesterase

Authors

  • Elvan Hasanoğlu Özkan Department of Chemistry, Faculty of Science, Gazi University, 06500 Teknikkullar, Ankara, TURKEY
  • Nurdan Kurnaz Yetim Kırklareli University, Faculty of Arts and Science, Department of Chemistry, Kırklareli, Turkey
  • Murat Gümüş
  • Nurşen Sarı Department of Chemistry, Faculty of Science, Gazi University, 06500 Teknikkullar, Ankara, TURKEY
  • Ali Dişli Department of Chemistry, Faculty of Science, Gazi University, 06500 Teknikkullar, Ankara, TURKEY

DOI:

https://doi.org/10.20450/mjcce.2017.1178

Keywords:

Schiff bases, spectroscopy, pesticides,

Abstract

Supports involving tetrazole (o/m/p-F-Tet-1H) were prepared to detect pesticides. This novel te-trazole including fluorine in different positions was attached to nanoparticles (2AEPS-(o/m/p-F-Tet-1H)) by a condensation method. Primarily, the tetrazole derivatives were characterized by 1H-NMR,13C-NMR and LC-MS. Then, nanoparticles were prepared by a condensation method in non-aqueous medium and characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, gel permeation chromatography. The enzymatic properties of immobilized acetylcholinesterase (AChE) were investigated for the determination of phosmet. This research is the first example.

References

F. Abrishami, M. Ebrahimikia, F. Rafiee, Synthesis of 5-substituted 1H-tetrazoles using a recyclable hetero-geneous nanonickel ferrite catalyst, Appl. Organomet. Chem., 29, 730–735 (2015).

B. Sreedhar, A. Suresh Kumar, D. Yada, CuFe2O4 nanoparticles: a magnetically recoverable and reusable catalyst for the synthesis of 5-substituted 1H-tetrazoles, Tetrahedron Lett., 52, 3565–3569 (2011).

V. Rama, K. Kanagaraj, K. Pitchumani, Syntheses of 5-substituted 1H-tetrazoles catalyzed by reusable CoY zeolite, J. Org. Chem., 76, 9090–9095 (2011).

D. Kundu, A. Majee, A. Hajra, Indium triflate-catalyzed one-pot synthesis of 1-substituted-1H-1, 2, 3, 4-tetrazoles under solvent-free conditions, Tetrahedron Lett., 50, 2668–2670 (2009).

Y. Bhalla, E. Puri, P. Monga, S. Sapra, Medicinal and chemical aspects of tetrazoles: an overview, iP-Planet, 1, 20–30 (2013).

F. Dehghani, A. R. Sardarian, M. Esmaeilpour, Salen complex of Cu(II) supported on superparamagnetic Fe3O4•SiO2 nanoparticles: An efficient and recyclable catalyst for synthesis of 1- and 5-substituted 1H-tetrazoles, J. Org. Chem.,743, 87–96 (2013).

M. L. Kantam, K. B. Shiva Kumar, C. H. Sridhar, Nanocrystalline ZnO as an efficient heterogeneous catalyst for the synthesis of 5-Substituted 1H-Tetrazoles, Adv. Synth. Catal., 347, 1212–1214 (2005).

Q. Q Ren, L. Y. Bai, X. S. Zhang, Z. Y. Ma, B. Liu, Y. D. Zhao, Y. C. Cao, Preparation, modification and application of hollow gold nanospheres, J. Nanomater. DOİ:10.1155/2015/534070 (2015).

N. Kurnaz Yetim, E. Hasanoğlu Özkan, B. Danış, H. Tümtürk, N. Sarı, Research on the repeated use of novel ferrocene tagged nanomaterial for determination of glucose, Int. J. Polym. Mater. Polym. Biomater., 64, 888–893 (2015).

M. B. Brena, F. Batista-Viera, Methods in Biotechno¬logy: Immobilization of Enzymes and Cells, Second Edition Edited by: J. M. Guisan Humana Press Inc., Totowa, NJ.

E. Hasanoğlu Özkan, N. Kurnaz Yetim, H. Tümtürk, N. Sarı, Immobilization of acetylcholinesterase on Pt(II) and Pt(IV) attached nanoparticles for the determination of pesticides , Dalton. Trans., 44, 16865–16872 (2015).

A. P. Periasamy, Y. Umasankar, S. M. Chen, Nanomaterials-acetylcholinesterase enzyme matrices for organophosphorus pesticides electrochemical sensors: A Review, Sensors, 9, 4034–4055 (2009).

N. A. Buckley, D. Roberts, M. Eddleston, Overcoming apathy in research on organophosphate poisoning, The B M J, 329, 1231–1233 (2004).

J. Warner, S. Andreescu, An acetylcholinesterase (AChE) biosensor with enhanced solvent resistance based on chitosan for the detection of pesticides, Talanta, 146, 279–284 (2016).

J. C. Kauer, W. A. Sheppard, 1-Aryltetrazoles synthesis and properties, The J. Org. Chem., 32, 3580–3592 (1967).

E. Lieber, T. Enkoji, Synthesis and properties of 5-(Substituted) mercaptotetrazoles, J. Org. Chem., 26, 4472–4479 (1961).

A. Dişli, M. Salman, Synthesis of some new 5-substituted 1H-tetrazoles, Russ. J. Org. Chem., 45,151–153 (2009).

A. Dişli, S. Mercan, S. Yavuz, Synthesis and antimicrobial activity of new pyrimidine derivatives incorporating 1H-tetrazol-5-ylthio moiety, J. Heterocycl. Chem, 50, 1446–1450 (2013).

G. D. Çelik, A. Dişli, Y. Öner, L. Açık, Synthesis of some novel amino and thiotetrazole purine derivatives and investigation of their antimicrobial activity and DNA interactions, Med. Chem. Res., 22, 1470–1479 (2013).

S. Muralikrishna, P. Raveendrareddy, L. K. Ravindranath, S. Harikrishna, P. R Jagadeeswara, Syn-thesis characterization and antitumor activity of thiazole derivatives containing indole moiety bearing-tetrazole, Der Pharma Chem., 5, 87–93 (2013).

E. Bozkır, N. Sarı, H. Öğütçü, Polystyrene containing carbinolamine/azomethine potentially useful as anti-microbial agent: synthesis and biological evaluation, J. Inorg. Organomet. Polym. Mater., 22, 1146–1155 (2012).

N. Özdem, E. Hasanoğlu Özkan, N. Sarı, F. Arslan, H. Tümtürk, Immobilization of Glucose Oxidase attached to new nanospheres including azomethine, Macromol. Res., 22, 1282–1287 (2014).

M. C. Moscatelli, A. Lagomarsino, A. M. V. Garzillo, A. Pignataro, S. Grego, β-Glucosidase kinetic parameters as indicators of soil quality under conventional and organic cropping systems applying two analytical approaches, Ecol. Indıc., 13, 322–327 (2012).

E. Hasanoğlu Özkan, N. Kurnaz Yetim, D. Nartop, N. Sarı, J. Ind. and Eng. Chem., 25, 180–185 (2015).

Downloads

Published

2017-06-23

How to Cite

Hasanoğlu Özkan, E., Kurnaz Yetim, N., Gümüş, M., Sarı, N., & Dişli, A. (2017). Efficient determination and pesticide control by means of immobilization of acetylcholinesterase. Macedonian Journal of Chemistry and Chemical Engineering, 36(1), 119–128. https://doi.org/10.20450/mjcce.2017.1178

Issue

Vol. 36 No. 1 (2017)

Section

Materials Chemistry

License

The authors agree to the following licence: Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)

  • Adapt — remix, transform, and build upon the material
  • for any purpose, even commercially.
The licensor cannot revoke these freedoms as long as you follow the license terms.

 Under the following terms:

  • Attribution — You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use.

  • NonCommercial — You may not use the material for commercial purposes.