Abstract
Despite growing evidence of the importance of melatonin and serotonin in the plant life, there is still much debate over the stability of melatonin, with extraction and analysis methods varying greatly from lab to lab with respect to time, temperature, light levels, extraction solvents, and mechanical disruption. The variability in methodology has created conflicting results that confound the comparison of studies to determine the role of melatonin in plant physiology. We here describe a fully validated method for the quantification of melatonin, serotonin and their biosynthetic precursors: tryptophan, tryptamine and N-acetylserotonin by liquid chromatography single quadrupole mass spectrometry (LC-MS) in diverse plant species and tissues. This method can be performed on a simple and inexpensive platform, and is both rapid and simple to implement. The method has excellent reproducibility and acceptable sensitivity with percent relative standard deviation (%RSD) in all matrices between 1 and 10% and recovery values of 82–113% for all analytes. Instrument detection limits were 24.4 ng/mL, 6.10 ng/mL, 1.52 ng/mL, 6.10 ng/mL, and 95.3 pg/mL, for serotonin, tryptophan, tryptamine, N-acetylserotonin and melatonin respectively. Method detection limits were 1.62 μg/g, 0.407 μg/g, 0.101 μg/g, 0.407 μg/g, and 6.17 ng/g respectively. The optimized method was then utilized to examine the issue of variable stability of melatonin in plant tissue culture systems. Media composition (Murashige and Skoog, Driver and Kuniyuki walnut or Lloyd and McCown's woody plant medium) and light (16 h photoperiod or dark) were found to have no effect on melatonin or serotonin content. A Youden trial suggested temperature as a major factor leading to degradation of melatonin. Both melatonin and serotonin appeared to be stable across the first 10 days in media, melatonin losses reached a mean minimum degradation at 28 days of approximately 90%; serotonin reached a mean minimum value of approximately 60% at 28 days. These results suggest that melatonin and serotonin show considerable stability in plant systems and these indoleamines and related compounds can be used for investigations that span over 3 weeks.
Highlights
Melatonin (N-acetyl-5-methoxy-tryptamine) is an indoleamine neurohormone, first identified and quantified in plants in 1995 (Dubbels et al, 1995; Hattori et al, 1995)
The method presented in this paper showed good specificity for all compounds due to the use of a single quadrupole system in single ion recording (SIR) mode (Figures 1, 2), with all peaks being completely resolved from surrounding peaks and showing good signal to noise (>3:1) in the linear range
As such there is a rapidly growing body of knowledge examining the roles melatonin plays in plants, many of which employ controlled environment systems and in particular in vitro culture systems, many of which are helping to solidify the role of melatonin in plant processes
Summary
Melatonin (N-acetyl-5-methoxy-tryptamine) is an indoleamine neurohormone, first identified and quantified in plants in 1995 (Dubbels et al, 1995; Hattori et al, 1995). There is controversy in the literature over the stability of melatonin in plants, with both analytical platform, extraction, and analysis methods varying greatly from one report to another with time, temperature, light levels, extraction solvents and mechanical disruption among others all varying widely (Table 1). This has in turn lead to conflicting results between labs, and has contributed to difficulty in confirming and comparing the results across various labs. John’s wort; SPE, solid phase extraction; TLC, thin layer chromatography; ULOQ, upper limit of quantification; UPLC-MS, ultra performance liquid chromatography; UV, ultra violet detection; WPM, Lloyd and McCown’s woody plant medium
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