Plant Physiol. Drug Metab Dispos
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First published online June 11, 2008; 10.1104/pp.108.120493

Plant Physiology 147:1805-1821 (2008)
© 2008 American Society of Plant Biologists

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BIOCHEMICAL PROCESSES AND MACROMOLECULAR STRUCTURES

Quantitative 1H Nuclear Magnetic Resonance Metabolite Profiling as a Functional Genomics Platform to Investigate Alkaloid Biosynthesis in Opium Poppy1,[W]

Jillian M. Hagel, Aalim M. Weljie, Hans J. Vogel and Peter J. Facchini*

Department of Biological Sciences, University of Calgary, Calgary, Alberta, Canada T2N 1N4

Opium poppy (Papaver somniferum) produces a diverse array of bioactive benzylisoquinoline alkaloids and has emerged as a versatile model system to study plant alkaloid metabolism. The plant is widely cultivated as the only commercial source of the narcotic analgesics morphine and codeine. Variations in plant secondary metabolism as a result of genetic diversity are often associated with perturbations in other metabolic pathways. As part of a functional genomics platform, we used 1H nuclear magnetic resonance (NMR) metabolite profiling for the analysis of primary and secondary metabolism in opium poppy. Aqueous and chloroform extracts of six different opium poppy cultivars were subjected to chemometric analysis. Principle component analysis of the 1H NMR spectra for latex extracts clearly distinguished two varieties, including a low-alkaloid variety and a high-thebaine, low-morphine cultivar. Distinction was also made between pharmaceutical-grade opium poppy cultivars and a condiment variety. Such phenotypic differences were not observed in root extracts. Loading plots confirmed that morphinan alkaloids contributed predominantly to the variance in latex extracts. Quantification of 34 root and 21 latex metabolites, performed using Chenomx NMR Suite version 4.6, showed major differences in the accumulation of specific alkaloids in the latex of the low-alkaloid and high-thebaine, low-morphine varieties. Relatively few differences were found in the levels of other metabolites, indicating that the variation was specific for alkaloid metabolism. Exceptions in the low-alkaloid cultivar included an increased accumulation of the alkaloid precursor tyramine and reduced levels of sucrose, some amino acids, and malate. Real-time polymerase chain reaction analysis of 42 genes involved in primary and secondary metabolism showed differential gene expression mainly associated with alkaloid biosynthesis. Reduced alkaloid levels in the condiment variety were associated with the reduced abundance of transcripts encoding several alkaloid biosynthetic enzymes.


1 This work was supported by a Natural Sciences and Engineering Research Council of Canada Discovery Grant (to P.J.F.). J.M.H. is the recipient of an Alberta Ingenuity Graduate Student Scholarship. A.M.W. is the recipient of an Alberta Ingenuity Industrial Fellowship. The Bio-NMR Center is supported by grants from the Canadian Institutes of Health Research and the University of Calgary. P.J.F. holds the Canada Research Chair in Plant Metabolic Processes Biotechnology.

The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Peter J. Facchini (pfacchin{at}ucalgary.ca).

[W] The online version of this article contains Web-only data.

www.plantphysiol.org/cgi/doi/10.1104/pp.108.120493

* Corresponding author; e-mail pfacchin{at}ucalgary.ca.

Received April 3, 2008; accepted June 5, 2008; published June 11, 2008.


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