Difference between revisions of "Team:Edinburgh/HeroinBiosensor"
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There are two key enzymes for a heroin biosensor which allow the quantity to be visualised, heroin esterase and morphine dehydrogenase. Heroin esterase, a serine esterase<sup>1</sup>, de-acetylates the acetylester group of heroin to produce 6-acetylmorphine. This process occurs a second time on the C-6 group producing morphine. The morphine produced is then oxidised to produce morphinone by the second enzyme morphine dehydrogenase. The NADP+ to NADPH reduction allows a coupled assay which has included FMN oxidoreductase and luciferase in a previous heroin biosensor<sup>2</sup>. To make the biosensor produce colour to the visible eye, and not light, we incorporated Nitrotetrazolium Blue (NBT) instead of the FMN oxidoreductase and luciferase. NBT, when coupled with phenozine methosulfate (PMS), reacts with the NADPH produced to create an insoluble purple-blue formazan<sup>3</sup>. The intensity of the formazan indicates the heroin purity. | There are two key enzymes for a heroin biosensor which allow the quantity to be visualised, heroin esterase and morphine dehydrogenase. Heroin esterase, a serine esterase<sup>1</sup>, de-acetylates the acetylester group of heroin to produce 6-acetylmorphine. This process occurs a second time on the C-6 group producing morphine. The morphine produced is then oxidised to produce morphinone by the second enzyme morphine dehydrogenase. The NADP+ to NADPH reduction allows a coupled assay which has included FMN oxidoreductase and luciferase in a previous heroin biosensor<sup>2</sup>. To make the biosensor produce colour to the visible eye, and not light, we incorporated Nitrotetrazolium Blue (NBT) instead of the FMN oxidoreductase and luciferase. NBT, when coupled with phenozine methosulfate (PMS), reacts with the NADPH produced to create an insoluble purple-blue formazan<sup>3</sup>. The intensity of the formazan indicates the heroin purity. | ||
Revision as of 16:57, 18 September 2015
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There are two key enzymes for a heroin biosensor which allow the quantity to be visualised, heroin esterase and morphine dehydrogenase. Heroin esterase, a serine esterase1, de-acetylates the acetylester group of heroin to produce 6-acetylmorphine. This process occurs a second time on the C-6 group producing morphine. The morphine produced is then oxidised to produce morphinone by the second enzyme morphine dehydrogenase. The NADP+ to NADPH reduction allows a coupled assay which has included FMN oxidoreductase and luciferase in a previous heroin biosensor2. To make the biosensor produce colour to the visible eye, and not light, we incorporated Nitrotetrazolium Blue (NBT) instead of the FMN oxidoreductase and luciferase. NBT, when coupled with phenozine methosulfate (PMS), reacts with the NADPH produced to create an insoluble purple-blue formazan3. The intensity of the formazan indicates the heroin purity.
Heroin esterase was isolated from Rhodococcus erythropolis strain H1 in 1994 from the garden soil at Cambridge and is able to use heroin as its sole carbon source4. The gene her encodes this enzyme and has the ability to be expressed in the chassis Escherichia coli1. The sequence for our enzyme used the original sequence from Rathbone, et al., and was then codon optimised for E. coli. The RFC25 prefix and suffix were added along which required all illegal sites (EcoRI, SpeI, AgeI, NotI, NgoMIV and XbaI) to be removed. As this was a difficult sequence to make as a gBlock, it was ordered as a gene in an ampicillin backbone where it was then digested and ligated into the pSB1C3 backbone.
Morphine dehydrogenase, the second enzyme required for this biosensor, was isolated from Pseudomonas putida M10 in 1993. This enzyme is capable of oxidising morphine and codeine to morphinone and codeinone but not thebaine allowing high specificity5. The sequence was obtained from Willey, et al., for the structural gene morA6. After codon optimizing the sequence for E. coli, adding the RFC25 prefix and suffix and getting rid of illegal restriction sites we were able to order the gBlock from IDT.
The idea for the heroin biosensor is to put crude cell extract of the two enzymes fused to CBDs to allow the enzymes to be immobilised on the paper. The mixture of the two lysates with NBT and PMS freeze dried on the paper allows the production of a blue colour in the presence of heroin in a solution. The intensity of the blue colour depends on the concentration of heroin as it shows how much NADPH is being reduced. Morphine and codeine are two major contaminants of heroin7 which will yield false positives on the biosensor as the morphine dehydrogenase can oxidise them thereby making the NADPH produced not derived from heroin. This means that there will actually be two biosensors for heroin purity. One will have heroin esterase and morphine dehydrogenase while the other will have just morphine dehydrogenase. This will only produce a blue colour if morphine and codeine are present on their own. The difference in colour intensity between these two should represent the heroin purity, this can be read and calculated by an app.
References
1Rathbone, D. A., Holt, P. J., Lowe, C. R., & Bruce, N. C. (1997). Molecular analysis of the Rhodococcus sp. strain H1 her gene and characterization of its product, a heroin esterase, expressed in Escherichia coli. Applied and environmental microbiology, 63(5), 2062-2066.
2Rathbone, D. A., HOLT, P. J., Lowe, C. R., & Bruce, N. C. (1996). The Use of a Novel Recombinant Heroin Esterase in the Development of an Illicit Drugs Biosensora. Annals of the New York Academy of Sciences, 799(1), 90-96.
3Mayer, K. M., & Arnold, F. H. (2002). A colorimetric assay to quantify dehydrogenase activity in crude cell lysates. Journal of biomolecular screening, 7(2), 135-140.
4Cameron, G. W., Jordan, K. N., Holt, P. J., Baker, P. B., Lowe, C. R., & Bruce, N. C. (1994). Identification of a heroin esterase in Rhodococcus sp. strain H1. Applied and environmental microbiology, 60(10), 3881-3883.
5Bruce, N. C., Wilmot, C. J., Jordan, K. N., Trebilcock, A. E., Stephens, L. D. G., & Lowe, C. R. (1990). Microbial degradation of the morphine alkaloids: identification of morphinone as an intermediate in the metabolism of morphine by Pseudomonas putida M10. Archives of microbiology, 154(5), 465-470.
6Willey, D. L., Caswell, D. A., Lowe, C. R., & Bruce, N. C. (1993). Nucleotide sequence and over-expression of morphine dehydrogenase, a plasmid-encoded gene from Pseudomonas putida M10. Biochem. J, 290, 539-544.
7Balayssac, S., Retailleau, E., Bertrand, G., Escot, M. P., Martino, R., Malet-Martino, M., & Gilard, V. (2014). Characterization of heroin samples by 1 H NMR and 2D DOSY 1 H NMR. Forensic science international, 234, 29-38.