Metabolomics of endemic six Astragalus species by combined NMR and GC‐MS analysis

Introduction Astragalus anthylloides, A. dipsaceus, A. karamasicus, A. lycius, A. sigmoideus and A. xylobasis var. angustus are an endemic and generally grow in the Irano‐Turanian phytogeographic region of Turkey. Astragalus species contain saponins, polysaccharides, and phenolics, while the toxic c...

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Veröffentlicht in:Phytochemical analysis 2020-05, Vol.31 (3), p.306-313
Hauptverfasser: Sahin Yaglioglu, Ayse, Temirturk, Murat, Ugur, Emic, Dolarslan, Melda, Demirtas, Ibrahim
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container_start_page 306
container_title Phytochemical analysis
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creator Sahin Yaglioglu, Ayse
Temirturk, Murat
Ugur, Emic
Dolarslan, Melda
Demirtas, Ibrahim
description Introduction Astragalus anthylloides, A. dipsaceus, A. karamasicus, A. lycius, A. sigmoideus and A. xylobasis var. angustus are an endemic and generally grow in the Irano‐Turanian phytogeographic region of Turkey. Astragalus species contain saponins, polysaccharides, and phenolics, while the toxic compounds include imidazoline alkaloids, nitro toxins, and selenium derivatives. Objectives To apply a combined metabolomic fingerprinting approach by nuclear magnetic resonance (NMR) and gas chromatography‐mass spectrometry (GC‐MS) of endemic six Astragalus species extract. Methodology The whole plant collected in Turkey of six endemic Astragalus subsp. were dried and then extracted with hexane, chloroform, ethylacetate, n‐butanol and methanol solvents, respectively. The hexane extracts were analyzed by GC‐MS. Carbon‐13 (13C)‐NMR analyzes of all extracts were performed. In both analyses, a biomarker was obtained. Results The hexane extracts were determined as palmitic acid, arachidic acid, behenic acid, and linolenic acid as the main components. As a result of 13C‐NMR analyzes, in hexane, chloroform, and ethylacetate the extracts detected were palmitic acid, arachidic acid, behenic acid, and linolenic acid. d‐Pinitol was obtained using 13C‐NMR analyzes with n‐butanol and methanol extracts. Conclusion This study demonstrated that d‐pinitol is a biomarker for the endemic six Astragalus subsp. Introduction: The six Astragalus species are an endemic to Turkey. Objectives: to apply a combined metabolomic fingerprinting approach by NMR and GC‐MS of six Astragalus species extract. Methodology: The six Astragalus were exracted with solvent at different polarity. Then, the extracts were analyzed by GC‐MS and 13CNMR analyzes to determined the biomarkers. Results: D‐Pinitol was obtained at 13C NMR analyzes of the n‐BuOH and MeOH extracts. Conclusion:D‐pinitol is a biomarker for the species.
doi_str_mv 10.1002/pca.2896
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Astragalus species contain saponins, polysaccharides, and phenolics, while the toxic compounds include imidazoline alkaloids, nitro toxins, and selenium derivatives. Objectives To apply a combined metabolomic fingerprinting approach by nuclear magnetic resonance (NMR) and gas chromatography‐mass spectrometry (GC‐MS) of endemic six Astragalus species extract. Methodology The whole plant collected in Turkey of six endemic Astragalus subsp. were dried and then extracted with hexane, chloroform, ethylacetate, n‐butanol and methanol solvents, respectively. The hexane extracts were analyzed by GC‐MS. Carbon‐13 (13C)‐NMR analyzes of all extracts were performed. In both analyses, a biomarker was obtained. Results The hexane extracts were determined as palmitic acid, arachidic acid, behenic acid, and linolenic acid as the main components. As a result of 13C‐NMR analyzes, in hexane, chloroform, and ethylacetate the extracts detected were palmitic acid, arachidic acid, behenic acid, and linolenic acid. d‐Pinitol was obtained using 13C‐NMR analyzes with n‐butanol and methanol extracts. Conclusion This study demonstrated that d‐pinitol is a biomarker for the endemic six Astragalus subsp. Introduction: The six Astragalus species are an endemic to Turkey. Objectives: to apply a combined metabolomic fingerprinting approach by NMR and GC‐MS of six Astragalus species extract. Methodology: The six Astragalus were exracted with solvent at different polarity. Then, the extracts were analyzed by GC‐MS and 13CNMR analyzes to determined the biomarkers. Results: D‐Pinitol was obtained at 13C NMR analyzes of the n‐BuOH and MeOH extracts. Conclusion:D‐pinitol is a biomarker for the species.</description><identifier>ISSN: 0958-0344</identifier><identifier>EISSN: 1099-1565</identifier><identifier>DOI: 10.1002/pca.2896</identifier><identifier>PMID: 31943462</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Acids ; Alkaloids ; Astragalus anthylloides ; Astragalus dipsaceus ; Astragalus karamasicus ; Astragalus lycius ; Astragalus sigmoideus ; Astragalus subsp ; Astragalus xylobasis angustus ; biomarker ; Biomarkers ; Butanol ; Carbon 13 ; Chloroform ; d‐pinitol ; endemic ; Endemic species ; Fingerprinting ; Gas chromatography ; Gas Chromatography-Mass Spectrometry ; Imidazoline ; Linolenic acid ; Magnetic Resonance Spectroscopy ; Mass spectrometry ; Mass spectroscopy ; Metabolomics ; Methanol ; NMR ; Nuclear magnetic resonance ; Palmitic acid ; Phenols ; Plant Extracts ; Polysaccharides ; Saccharides ; Saponins ; Selenium ; Toxins ; Turkey</subject><ispartof>Phytochemical analysis, 2020-05, Vol.31 (3), p.306-313</ispartof><rights>2020 John Wiley &amp; Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3496-d13099ba2ba7a477159783280aec8fb4a27b29dcb0bac341df20230196b5a7f23</citedby><cites>FETCH-LOGICAL-c3496-d13099ba2ba7a477159783280aec8fb4a27b29dcb0bac341df20230196b5a7f23</cites><orcidid>0000-0002-7668-6286</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpca.2896$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpca.2896$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27915,27916,45565,45566</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31943462$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sahin Yaglioglu, Ayse</creatorcontrib><creatorcontrib>Temirturk, Murat</creatorcontrib><creatorcontrib>Ugur, Emic</creatorcontrib><creatorcontrib>Dolarslan, Melda</creatorcontrib><creatorcontrib>Demirtas, Ibrahim</creatorcontrib><title>Metabolomics of endemic six Astragalus species by combined NMR and GC‐MS analysis</title><title>Phytochemical analysis</title><addtitle>Phytochem Anal</addtitle><description>Introduction Astragalus anthylloides, A. dipsaceus, A. karamasicus, A. lycius, A. sigmoideus and A. xylobasis var. angustus are an endemic and generally grow in the Irano‐Turanian phytogeographic region of Turkey. Astragalus species contain saponins, polysaccharides, and phenolics, while the toxic compounds include imidazoline alkaloids, nitro toxins, and selenium derivatives. Objectives To apply a combined metabolomic fingerprinting approach by nuclear magnetic resonance (NMR) and gas chromatography‐mass spectrometry (GC‐MS) of endemic six Astragalus species extract. Methodology The whole plant collected in Turkey of six endemic Astragalus subsp. were dried and then extracted with hexane, chloroform, ethylacetate, n‐butanol and methanol solvents, respectively. The hexane extracts were analyzed by GC‐MS. Carbon‐13 (13C)‐NMR analyzes of all extracts were performed. In both analyses, a biomarker was obtained. Results The hexane extracts were determined as palmitic acid, arachidic acid, behenic acid, and linolenic acid as the main components. As a result of 13C‐NMR analyzes, in hexane, chloroform, and ethylacetate the extracts detected were palmitic acid, arachidic acid, behenic acid, and linolenic acid. d‐Pinitol was obtained using 13C‐NMR analyzes with n‐butanol and methanol extracts. Conclusion This study demonstrated that d‐pinitol is a biomarker for the endemic six Astragalus subsp. Introduction: The six Astragalus species are an endemic to Turkey. Objectives: to apply a combined metabolomic fingerprinting approach by NMR and GC‐MS of six Astragalus species extract. Methodology: The six Astragalus were exracted with solvent at different polarity. Then, the extracts were analyzed by GC‐MS and 13CNMR analyzes to determined the biomarkers. Results: D‐Pinitol was obtained at 13C NMR analyzes of the n‐BuOH and MeOH extracts. 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Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Phytochemical analysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sahin Yaglioglu, Ayse</au><au>Temirturk, Murat</au><au>Ugur, Emic</au><au>Dolarslan, Melda</au><au>Demirtas, Ibrahim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolomics of endemic six Astragalus species by combined NMR and GC‐MS analysis</atitle><jtitle>Phytochemical analysis</jtitle><addtitle>Phytochem Anal</addtitle><date>2020-05</date><risdate>2020</risdate><volume>31</volume><issue>3</issue><spage>306</spage><epage>313</epage><pages>306-313</pages><issn>0958-0344</issn><eissn>1099-1565</eissn><abstract>Introduction Astragalus anthylloides, A. dipsaceus, A. karamasicus, A. lycius, A. sigmoideus and A. xylobasis var. angustus are an endemic and generally grow in the Irano‐Turanian phytogeographic region of Turkey. Astragalus species contain saponins, polysaccharides, and phenolics, while the toxic compounds include imidazoline alkaloids, nitro toxins, and selenium derivatives. Objectives To apply a combined metabolomic fingerprinting approach by nuclear magnetic resonance (NMR) and gas chromatography‐mass spectrometry (GC‐MS) of endemic six Astragalus species extract. Methodology The whole plant collected in Turkey of six endemic Astragalus subsp. were dried and then extracted with hexane, chloroform, ethylacetate, n‐butanol and methanol solvents, respectively. The hexane extracts were analyzed by GC‐MS. Carbon‐13 (13C)‐NMR analyzes of all extracts were performed. In both analyses, a biomarker was obtained. Results The hexane extracts were determined as palmitic acid, arachidic acid, behenic acid, and linolenic acid as the main components. As a result of 13C‐NMR analyzes, in hexane, chloroform, and ethylacetate the extracts detected were palmitic acid, arachidic acid, behenic acid, and linolenic acid. d‐Pinitol was obtained using 13C‐NMR analyzes with n‐butanol and methanol extracts. Conclusion This study demonstrated that d‐pinitol is a biomarker for the endemic six Astragalus subsp. Introduction: The six Astragalus species are an endemic to Turkey. Objectives: to apply a combined metabolomic fingerprinting approach by NMR and GC‐MS of six Astragalus species extract. Methodology: The six Astragalus were exracted with solvent at different polarity. Then, the extracts were analyzed by GC‐MS and 13CNMR analyzes to determined the biomarkers. Results: D‐Pinitol was obtained at 13C NMR analyzes of the n‐BuOH and MeOH extracts. Conclusion:D‐pinitol is a biomarker for the species.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31943462</pmid><doi>10.1002/pca.2896</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-7668-6286</orcidid></addata></record>
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subjects Acids
Alkaloids
Astragalus anthylloides
Astragalus dipsaceus
Astragalus karamasicus
Astragalus lycius
Astragalus sigmoideus
Astragalus subsp
Astragalus xylobasis angustus
biomarker
Biomarkers
Butanol
Carbon 13
Chloroform
d‐pinitol
endemic
Endemic species
Fingerprinting
Gas chromatography
Gas Chromatography-Mass Spectrometry
Imidazoline
Linolenic acid
Magnetic Resonance Spectroscopy
Mass spectrometry
Mass spectroscopy
Metabolomics
Methanol
NMR
Nuclear magnetic resonance
Palmitic acid
Phenols
Plant Extracts
Polysaccharides
Saccharides
Saponins
Selenium
Toxins
Turkey
title Metabolomics of endemic six Astragalus species by combined NMR and GC‐MS analysis
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