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NMR and GC-MS Based Metabolic Profiling and Free-Radical Scavenging Activities of Cordyceps pruinosa Mycelia Cultivated under Different Media and Light Conditions

Variation of metabolic profiles in Cordyceps pruinosa mycelia cultivated under various media and light conditions was investigated using (1)H nuclear magnetic resonance (NMR) analysis and gas chromatography mass spectrometry (GC-MS) with multivariate statistical analysis. A total of 71 metabolites w...

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Autores principales: Oh, Taek-Joo, Hyun, Sun-Hee, Lee, Seul-Gi, Chun, Young-Jin, Sung, Gi-Ho, Choi, Hyung-Kyoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3946585/
https://www.ncbi.nlm.nih.gov/pubmed/24608751
http://dx.doi.org/10.1371/journal.pone.0090823
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author Oh, Taek-Joo
Hyun, Sun-Hee
Lee, Seul-Gi
Chun, Young-Jin
Sung, Gi-Ho
Choi, Hyung-Kyoon
author_facet Oh, Taek-Joo
Hyun, Sun-Hee
Lee, Seul-Gi
Chun, Young-Jin
Sung, Gi-Ho
Choi, Hyung-Kyoon
author_sort Oh, Taek-Joo
collection PubMed
description Variation of metabolic profiles in Cordyceps pruinosa mycelia cultivated under various media and light conditions was investigated using (1)H nuclear magnetic resonance (NMR) analysis and gas chromatography mass spectrometry (GC-MS) with multivariate statistical analysis. A total of 71 metabolites were identified (5 alcohols, 21 amino acids, 15 organic acids, 4 purines, 3 pyrimidines, 7 sugars, 11 fatty acids, and 5 other metabolites) by NMR and GC-MS analysis. The mycelia grown in nitrogen media and under dark conditions showed the lowest growth and ergosterol levels, essential to a functional fungal cell membrane; these mycelia, however, had the highest levels of putrescine, which is involved in abiotic stress tolerance. In contrast, mycelia cultivated in sabouraud dextrose agar with yeast extract (SDAY) media and under light conditions contained relatively higher levels of fatty acids, including valeric acid, stearic acid, lignoceric acid, myristic acid, oleic acid, palmitoleic acid, hepadecenoic acid, and linoleic acid. These mycelia also had the highest phenolic content and antioxidant activity, and did not exhibit growth retardation due to enhanced asexual development caused by higher levels of linoleic acid. Therefore, we suggested that a light-enriched environment with SDAY media was more optimal than dark condition for cultivation of C. pruinosa mycelia as biopharmaceutical or nutraceutical resources.
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spelling pubmed-39465852014-03-10 NMR and GC-MS Based Metabolic Profiling and Free-Radical Scavenging Activities of Cordyceps pruinosa Mycelia Cultivated under Different Media and Light Conditions Oh, Taek-Joo Hyun, Sun-Hee Lee, Seul-Gi Chun, Young-Jin Sung, Gi-Ho Choi, Hyung-Kyoon PLoS One Research Article Variation of metabolic profiles in Cordyceps pruinosa mycelia cultivated under various media and light conditions was investigated using (1)H nuclear magnetic resonance (NMR) analysis and gas chromatography mass spectrometry (GC-MS) with multivariate statistical analysis. A total of 71 metabolites were identified (5 alcohols, 21 amino acids, 15 organic acids, 4 purines, 3 pyrimidines, 7 sugars, 11 fatty acids, and 5 other metabolites) by NMR and GC-MS analysis. The mycelia grown in nitrogen media and under dark conditions showed the lowest growth and ergosterol levels, essential to a functional fungal cell membrane; these mycelia, however, had the highest levels of putrescine, which is involved in abiotic stress tolerance. In contrast, mycelia cultivated in sabouraud dextrose agar with yeast extract (SDAY) media and under light conditions contained relatively higher levels of fatty acids, including valeric acid, stearic acid, lignoceric acid, myristic acid, oleic acid, palmitoleic acid, hepadecenoic acid, and linoleic acid. These mycelia also had the highest phenolic content and antioxidant activity, and did not exhibit growth retardation due to enhanced asexual development caused by higher levels of linoleic acid. Therefore, we suggested that a light-enriched environment with SDAY media was more optimal than dark condition for cultivation of C. pruinosa mycelia as biopharmaceutical or nutraceutical resources. Public Library of Science 2014-03-07 /pmc/articles/PMC3946585/ /pubmed/24608751 http://dx.doi.org/10.1371/journal.pone.0090823 Text en © 2014 Oh et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Oh, Taek-Joo
Hyun, Sun-Hee
Lee, Seul-Gi
Chun, Young-Jin
Sung, Gi-Ho
Choi, Hyung-Kyoon
NMR and GC-MS Based Metabolic Profiling and Free-Radical Scavenging Activities of Cordyceps pruinosa Mycelia Cultivated under Different Media and Light Conditions
title NMR and GC-MS Based Metabolic Profiling and Free-Radical Scavenging Activities of Cordyceps pruinosa Mycelia Cultivated under Different Media and Light Conditions
title_full NMR and GC-MS Based Metabolic Profiling and Free-Radical Scavenging Activities of Cordyceps pruinosa Mycelia Cultivated under Different Media and Light Conditions
title_fullStr NMR and GC-MS Based Metabolic Profiling and Free-Radical Scavenging Activities of Cordyceps pruinosa Mycelia Cultivated under Different Media and Light Conditions
title_full_unstemmed NMR and GC-MS Based Metabolic Profiling and Free-Radical Scavenging Activities of Cordyceps pruinosa Mycelia Cultivated under Different Media and Light Conditions
title_short NMR and GC-MS Based Metabolic Profiling and Free-Radical Scavenging Activities of Cordyceps pruinosa Mycelia Cultivated under Different Media and Light Conditions
title_sort nmr and gc-ms based metabolic profiling and free-radical scavenging activities of cordyceps pruinosa mycelia cultivated under different media and light conditions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3946585/
https://www.ncbi.nlm.nih.gov/pubmed/24608751
http://dx.doi.org/10.1371/journal.pone.0090823
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