49
Views
10
CrossRef citations to date
0
Altmetric
Original Articles

Optimized Biosensors Based on Purified Enzymes and Engineered Yeasts: Detection of Inhibitors of Cholinesterases on Grapes

, , , , &
Pages 1683-1699 | Received 15 Dec 2003, Accepted 15 Feb 2004, Published online: 22 Aug 2007
 

Abstract

Purified acetyl cholinesterase (AChE) from electric eel or engineered yeasts (Kluyveromyces lactis) expressing cholinesterase activity from rat, were immobilised on a nylon membrane for the measurement of residual cholinesterase activity after inhibition by the organophosphorous insecticide Paraoxon (diethyl p‐nitrophenyl phosphate). Measurement was separately operated after the incubation (inhibition) step. The measurement of the residual enzyme activity was therefore performed in a standardised solution with a choline electrochemical biosensor, without any interference, avoiding the use of protecting selective membranes. Both commercial amperometric sensor and screen‐printed electrodes, produced and optimized in the laboratory, were used. The time consuming incubation step was simultaneously performed on several samples, thus lowering the analysis time per sample. Good limit of detection (LOD) (0.1 µg/L) and reproducibility were obtained for the analysis of paraoxon. A simple procedure for the detection of cholinesterase inhibitors on grapes was then developed. The procedure itself could be further extended to several fruits and vegetables, giving a simple but effective tool to verify the absence of residues of anticholinesterasic insecticides.

Acknowledgments

This work was partly supported by COSMIC Project (ENEA “Target Project on Biosensors and Bioelectronics”) and RoseProMilk (the 5th FW UE‐QLK1‐CT2001‐01617). We would like to acknowledge Prof. C. Palleschi of the University of Rome “La Sapienza” for his valuable suggestions and for providing us with engineered K. lactis yeast.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.