1H NMR based metabolite profiling for optimizing the ethanol extraction of Wolfiporia cocos.
Journal: 2018/November - Saudi Journal of Biological Sciences
ISSN: 1319-562X
Abstract:
Metabolite profiling of Wolfiporia cocos (family: Polyporaceae) had been much advancement in recent days, and its analysis by nuclear magnetic resonance (NMR) spectroscopy has become well established. However, the highly important trait of W. cocos still needs advanced protocols despite some standardization. Partial least squares discriminant analysis (PLS-DA) was used as the multivariate statistical analysis of the 1H NMR data set. The PLS-DA model was validated, and the key metabolites contributing to the separation in the score plots of different ethanol W. cocos extract. 1H NMR spectroscopy of W. cocos identified 33 chemically diverse metabolites in D2O, consisting of 13 amino acids, 11 organic acids 2 sugars, 3 sugar alcohols, 1 nucleoside, and 3 others. Among these metabolites, the levels of tyrosine, proline, methionine, sarcosine, choline, acetoacetate, citrate, 4-aminobutyrate, aspartate, maltose, malate, lysine, xylitol, lactate threonine, leucine, valine, isoleucine, uridine, guanidoacetate, arabitol, mannitol, glucose, and betaine were increased in the 95% ethanol extraction sample compared with the levels in other samples, whereas level of acetate, phenylalanine, alanine, succinate, and fumarate were significantly increased in the 0% ethanol extraction sample. A biological triterpenoid, namely pachymic acid, was detected from different ethanol P. cocos extract using 1H-NMR spectra were found in CDCl3. This is the first report to perform the metabolomics profiling of different ethanol W. cocos extract. These researches suggest that W. cocos can be used to obtain substantial amounts of bioactive ingredients for use as potential pharmacological and nutraceuticals agents.
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Saudi J Biol Sci 25(6): 1128-1134

<sup>1</sup>H NMR based metabolite profiling for optimizing the ethanol extraction of <em>Wolfiporia cocos</em>

Institute for Healthcare and Life Science, International St. Mary’s Hospital and College of Medicine, Catholic Kwandong University, Incheon 22711, Republic of Korea
College of Pharmacy, Chung-Ang University, Republic of Korea
Mushroom Research Division, National Institute of Horticultural and Herbal Science, Rural Development Administration, Republic of Korea
Department of Microbiology, College of Medicine, Catholic Kwandong University, Republic of Korea
Hyung-Kyoon Choi: rk.ca.uac@iohcykyh; Gi-Ho Sung: rk.ca.ukc@03379gnus
Corresponding authors at: Institute for Healthcare and Life Science, International St. Mary’s Hospital and College of Medicine, Catholic Kwandong University, Incheon 22711, Republic of Korea (G.-H. Sung); College of Pharmacy, Chung-Ang University, Republic of Korea (H.-K. Choi) rk.ca.uac@iohcykyh, rk.ca.ukc@03379gnus
Hyung-Kyoon Choi: rk.ca.uac@iohcykyh; Gi-Ho Sung: rk.ca.ukc@03379gnus
Received 2018 Feb 22; Revised 2018 Apr 2; Accepted 2018 Apr 4.
This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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Peer review under responsibility of King Saud University.

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