Abstract
Enzyme recognition element-based biosensors are very attractive for biosensor application due to a variety of measurable reaction products arising from a catalytic process. In this study, biosensor recognition elements have been developed via engineer bacterial enzymes (carboxylesterases (CEs)) which will used for narcotic detection because of their role in narcotics metabolism. The modification (insertion of cys-tag) allows the enzyme to bind into a transducer surface of a biosensor which will translate the reaction product into the detection system. The results demonstrate the successful isolation, cloning, expression, and purification of recombinant (pnbA1 and pnbA2), and engineered (pnbA1-cys and pnbA2-cys) bacterial carboxylesterases. Enzyme capability to hydrolyse cocaine into benzoylecgonine and methanol was quantified using HPLC. Both enzymes showed broad maximal activity between pH (8.0, 8.5, and 9.0), PnbA1 temperature stability ranging between (25 and 45 °C); however, PnbA2 stability range was (25–40 °C). Insertion of cys-tag at the N-terminal of the enzyme did not limit entrance to the active site which is located at the base of a cavity with dimensions 20 by 13 by 18 Å, and did not prevent substrate hydrolysis. Bacterial carboxylesterases pnbA1 and pnbA2 mimic hCE1 and not hCE2 in its reaction pathways hydrolysing cocaine into benzoylecgonine and methanol rather than ecgonine methyl ester and benzoic acid. These results are the first experimental evidence confirming the capability of bacterial carboxylesterase to hydrolyse cocaine into its main metabolites, therefore opening up the possibility to use these enzymes in numerous biotechnological applications in addition to a cocaine biosensor.





Similar content being viewed by others
References
Bencharit, S., Morton, C. L., Howard-Williams, E. L., Danks, M. K., Potter, P. M., & Redinbo, M. R. (2002). Structural insights into CPT-11 activation by mammalian carboxylesterases. Natural Structural Biology, 9, 337–342.
Meghji, K., Ward, O. P., & Araujo, A. (1990). Production, purification, and properties of extracellular carboxyl esterases from Bacillus subtilis NRRL 365. American Society for Microbiology, 56, 3735–3740.
Ileperuma, N. R., Marshall, S. D. G., Squire, C. J., Baker, H. M., Oakeshott, J. G., Russell, R. J., Plummer, K. M., Newcomb, R. D., & Baker, E. N. (2007) High-resolution crystal structure of plant carboxylesterases AeCXE1, from Actinidia eriantha, and its complex with a high-affinity inhibitor paraxon. Biochemistry 46, 1851–1859.
Sayali, K., Patil, S., & Surekha, S. (2013). Microbial esterases: An overview. International Journal of Current Microbiology and Applied Sciences, 2, 135–146.
Xie, G., Liu, M., Zhu, H., & Lei, B. (2008). Esterase SeE of Streptococcus equi ssp. equi is a novel nonspecific carboxylic ester hydrolase. FEMS Microbiology Letters, 289, 181–186.
Lopes, D. B., Fraga, L. P., Fleuri, L. F., & Macedo, G. A. (2011). Lipases and Esterases—to what extent this classification be applied accurately. Food Science and Technology, 31, 608–613.
Montella, I. R., Schama, R., & Valle, D. (2012). The classification of esterases: An important gene family involved in insecticide resistance—a review. Memórias do Instituto Oswaldo Cruz, 107, 437–449.
Ollis, D. L., Cheah, E., Cygler, M., Dijkstra, B., Frolow, F., Franken, S. M., et al. (1992). The alpha/beta hydrolase fold. Protein Engineering, 5, 197–211.
Nardini, M., & Dijkstra, B. W. (1999). a/ß hydrolase fold enzymes: The family keeps growing. Current Opinion in Structural Biology, 9, 732–737.
Pindel, E. V., Kedishvili, N. Y., Abraham, T. L., Brzezinski, M. R., Zhang, A., Dean, R. A., et al. (1997). Purification and cloning of a broad substrate specificity human liver carboxylesterase that catalyzes the hydrolysis of cocaine and heroin. Journal of Biological Chemistry, 272, 14769–14775.
Weirdl, M., Morton, C. L., Nguyen, N. K., Redinbo, M. R., & Potter, P. M. (2004). Molecular modeling of CPT-11 metabolism by carboxylesterases (CEs) use of pnb CE as a model. Biochemistry, 43, 1874–1882.
Wheelock, C. E., Phillips, B. M., Anderson, B. S., Miller, J. L., Miller, M. J., et al. (2008). Application of carboxylesterase activity in environmental monitoring and toxicity identification protocol (TIEs). Reviews of Environmental Contamination and Toxicology, 195, 117–178.
Singh, B. (2014). Review on microbial carboxylesterase: General properties and role in organophosphate pesticide degradation. Biochemistry and Molecular Biology, 2, 1–6.
Ahmad, S., & Forgash, A. J. (1976). Nonoxidative enzymes in the metabolism of insecticides. Drug Metabolism Reviews, 5, 141–164.
Leinweber, F. J. (1987). Possible physiological roles of carboxyl ester hydrolases. Drug Metabolism Reviews, 18, 379–439.
Diczfalusy, M. A., Bjorkkem, I., Einarsson, C., Hillebrant, C. G., & Alexson, S. E. (2001). Characterization of enzymes involved in formation of ethyl esters of long-chain fatty acids. The Journal of Lipid Research, 42, 1025–1032.
Dolinsky, V. W., Sipione, S., Lehner, R., & Vance, D. E. (2001). The cloning and expression of murine triacylglycerol hydrolase cDNA and the structure of the corresponding gene. Biochimica et Biophysica Acta, 1532, 162–172.
Becker, A., Bottcher, A., Lackner, K. J., Fehringer, P., Notka, F., & Aslandis, C. (1994). Purification, cloning and expression of a human enzyme with acyl coenzyme A: Cholesterol acyltransferase activity, which is identical to liver carboxylesterase. Arteriosclerosis and Thrombosis, 14, 1346–1355.
Jatlow, P. I. (1987). Drug of abuse profile: Cocaine. Clinical Chemistry, 33, 66B–71B.
Bailey, D. N. (1994). Studies of cocaethylene (Ethylcocaine) formation by human tissues in vitro. Journal of Analytical Toxicology, 18, 13–15.
Baingana, F., al’Absi, M., Becker, A. E., & Pringle, B. (2015). Global research challenges and opportunities for mental health and substance-use disorders. Nature, 527, S172–S177.
Holmes, D. (2015). Addition: 4 big questions. Nature, 522, S63.
Jaeger, K. E., & Eggert, T. (2002). Lipases for biotechnology. Current Opinion in Biotechnology, 13, 390–397.
Ewisa, H. E., Abdelalb, A. T., & Lu, C.-D. (2004). Molecular cloning and characterization of two thermostable carboxyl esterases from Geobacillus stearothermophilus. Gene, 329, 187–195.
Bornscheuer, U. T. (2002). Microbial carboxyl esterases: Classification, properties, and application in biocatalysis. FEMS Microbiology Reviews, 26, 73–818.
Zock, J., Cantwell, C., Swartling, J., Hodges, R., Pohl, T., Sutton, K., Rosteck, P. Jr., McGilvray, D., & Queener, S. (1994). The Bacillus subtilis pnbA gene encoding pnitrobenzyl esterase: Cloning, sequence and high-level expression in Escherichia coli. Gene, 151, 37–43.
Quax, W. J., & Broekhuizen, C. P. (1994). Development of a new Bacillus carboxyl esterase for use in the resolution of chiral drugs. Applied Microbiology and Biotechnology, 41, 425–431.
Moore, J. C., & Arnold, F. H. (1996). Directed evolution of a para-nitrobenzyl esterase for aqueous-organic solvents. Nature Biotechnology, 14, 458–467.
Wizard®genomic DNA purification kit. Promega. Technical manual. USA.
PCR master mix, Taq DNA Polymerase. Promega. USA.
Oakeshott, J. G., Claudianos, C., Russell, R. J., & Robin, G. C. (1999). Carboxyl/cholinesterases: A case study of the evolution of a successful multigene family. BioEssays, 21, 1031–1042.
Redinbo, M. R., Bencharit, S., & Potter, P. M. (2003). Human carboxylesterase 1: From drug metabolism to drug discovery. Biochemical Society Transactions, 31, 620–624.
Pindel, E. V., Kedishvili, N. Y., Abraham, T. L., Brzezinski, M. R., Zhang, J., Dean, R. A., et al. (1997). Purification and cloning of a broad substrate specificity human liver carboxylesterase that catalyzes the hydrolysis of cocaine and heroin. Journal of Biological Chemistry, 272, 14769–14775.
Imai, T. (2006). Human carboxylesterase isozymes: Catalytic properties and rational drug design. Drug Metabolism and Pharmacokinetics, 21, 173–185.
Author information
Authors and Affiliations
Corresponding author
Electronic supplementary material
Below is the link to the electronic supplementary material.
Rights and permissions
About this article
Cite this article
Mustafa, S.A. The Development of Bacterial Carboxylesterase Biological Recognition Elements for Cocaine Detection. Mol Biotechnol 60, 601–607 (2018). https://doi.org/10.1007/s12033-018-0098-z
Published:
Issue Date:
DOI: https://doi.org/10.1007/s12033-018-0098-z


