With increasing interest in the role of taste related fatty acids in food, pharmacology, health and diseases, objective study of this chemosensory parameter has assumed importance. The potential of NMR metabolomics to fingerprint chemosensory properties has been explored in the context of non-polar phytocompounds in this study. Non-polar fractions obtained by dual phase (chloroform-methanol/water) extraction of select dietary plants (n=24) were studied using proton NMR spectroscopy. Partial Least Squares Discriminant Analysis of the spectral data showed distinct chemosensory based clustering. NMR based chemosensory studies of non-polar phytocompounds could open new applications in sensorial sciences related to lipids and fatty acids.
The chemosensory property of taste is no more restricted to only taste buds since taste receptors are now known to be present in tissues outside the oral cavity, for example in digestive and respiratory systems1. Their roles in regulating various physiological processes are currently a matter of indepth study1. At the same time, recent studies have provided compelling evidence of fat as a sixth taste2. The chemoreception of lipids and fatty acids, their physiological consequences, their impact on health and implications for diseases such as obesity are also gaining much attention2. All these have renewed interest and widened the scope of chemosensory properties of dietary ingredients and their role in diseases. Applications of NMR in sensory sciences have long been an area of research interest. The present work explores the role of NMR metabolomics of non-polar phytocompounds of dietary and nutraceutical plants from different chemosensory groups.
Extraction of non-polar phytocompounds: Twenty four plants from four chemosensory categories (sweet, astringent, bitter and pungent) were studied. Some of the plants examined were Phoenix sylvestris, Vitis vinifera, Cocos nucifera, Ficus racemosa, Momordica charantia, Piper nigrum and Piper longum. The plant parts were subjected to dual phase (chloroform-methanol/water) extraction to separate the polar from the non-polar compounds. The extracts were dried using rotary vacuum concentrator to remove the solvent.
NMR studies: The non-polar compounds were dissolved in CDCl3 containing 0.1% TMS, which served as the reference. 1D Proton NMR spectra were acquired at 700 MHz (Agilent, USA) using the following parameters: relaxation delay - 14 sec, no. of scans - 64, spectral width - 12 ppm, data points - 32 K. Peak assignments were carried out using NMRShift database library.
Data analysis: The NMR data were binned and bucketed at intervals of 0.04 ppm for Partial Least Squares Discriminant Analysis (PLS-DA) (Metaboanalyst 3.0). Spectral data post-processing, binning and bucketing were carried out using MestReC.
1. L Feng. Taste perception: from the tongue to the testis. Mol Human Reprodn, 19, 349-360, 2013
2. Besnard P, Passilly-Degrace P, Khan NA. Taste of Fat: A Sixth Taste Modality? Physiol Rev, 96, 151-176, 2016.