The integration of GC–MS and LC–MS to assay the metabolomics profiling in Panax ginseng and Panax quinquefolius reveals a tissue- and species-specific connectivity of primary metabolites and ginsenosides accumulation

[Display omitted] •Tissue-specific profiling of primary and secondary metabolites in two different species of ginseng by using GC- and LC-MS.•Revealed a complex consecutive coordination of primary and secondary metabolism and corresponding pathways.•149 primary metabolites and 10 ginsenosides were i...

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Published inJournal of pharmaceutical and biomedical analysis Vol. 135; pp. 176 - 185
Main Authors Liu, Jia, Liu, Yang, Wang, Yu, Abozeid, Ann, Zu, Yuan-Gang, Tang, Zhong-Hua
Format Journal Article
LanguageEnglish
Published England Elsevier B.V 20.02.2017
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Abstract [Display omitted] •Tissue-specific profiling of primary and secondary metabolites in two different species of ginseng by using GC- and LC-MS.•Revealed a complex consecutive coordination of primary and secondary metabolism and corresponding pathways.•149 primary metabolites and 10 ginsenosides were identified from tissues-specific in P. ginseng and P. quinquefolius.•To investigate the contribution of tissue-specific C and N metabolism to the biosynthesis of ginsenosides.•Ginsenosides was dependent on main and lateral root energy metabolism and independent of leaf and petiole photosynthesis. The traditional medicine Ginseng mainly including Panax ginseng and Panax quinquefolius is the most widely consumed herbal product in the world. Despite the extensive investigation of biosynthetic pathway of the active compounds ginsenosides, our current understanding of the metabolic interlink between ginsenosides synthesis and primary metabolism at the whole-plant level. In this study, the tissue-specific profiling of primary and the secondary metabolites in two different species of ginseng were investigated by gas chromatography- and liquid chromatography coupled to mass spectrometry. A complex continuous coordination of primary- and secondary-metabolic network was modulated by tissues and species factors during growth. The results showed that altogether 149 primary compounds and 10 ginsenosides were identified from main roots, lateral roots, stems, petioles and leaves in P. ginseng and P. quinquefolius. The partial least squares-discriminate analysis (PLS-DA) revealed obvious compounds distinction among tissue-specific districts relative to species. To survey the dedication of carbon and nitrogen metabolism in different tissues to the accumulation of ginsenosides, we inspected the tissue-specific metabolic changes. Our study testified that the ginsenosides content was dependent on main roots and lateral roots energy metabolism, whereas independent of leaves and petiole photosynthesis during ginsenosides accumulation. When tow species were compared, the results indicated that high rates of C assimilation to C accumulation are closely associated with ginsenosides accumulation in P. ginseng main roots and P. quinquefolius lateral roots, respectively. Taken together, our results suggest that tissue-specific metabolites profiling dynamically changed in process of ginsenosides biosynthesis, which may offer a new train of thoughts to the mechanisms of the ginsenosides biosynthesis at the metabolite level.
AbstractList [Display omitted] •Tissue-specific profiling of primary and secondary metabolites in two different species of ginseng by using GC- and LC-MS.•Revealed a complex consecutive coordination of primary and secondary metabolism and corresponding pathways.•149 primary metabolites and 10 ginsenosides were identified from tissues-specific in P. ginseng and P. quinquefolius.•To investigate the contribution of tissue-specific C and N metabolism to the biosynthesis of ginsenosides.•Ginsenosides was dependent on main and lateral root energy metabolism and independent of leaf and petiole photosynthesis. The traditional medicine Ginseng mainly including Panax ginseng and Panax quinquefolius is the most widely consumed herbal product in the world. Despite the extensive investigation of biosynthetic pathway of the active compounds ginsenosides, our current understanding of the metabolic interlink between ginsenosides synthesis and primary metabolism at the whole-plant level. In this study, the tissue-specific profiling of primary and the secondary metabolites in two different species of ginseng were investigated by gas chromatography- and liquid chromatography coupled to mass spectrometry. A complex continuous coordination of primary- and secondary-metabolic network was modulated by tissues and species factors during growth. The results showed that altogether 149 primary compounds and 10 ginsenosides were identified from main roots, lateral roots, stems, petioles and leaves in P. ginseng and P. quinquefolius. The partial least squares-discriminate analysis (PLS-DA) revealed obvious compounds distinction among tissue-specific districts relative to species. To survey the dedication of carbon and nitrogen metabolism in different tissues to the accumulation of ginsenosides, we inspected the tissue-specific metabolic changes. Our study testified that the ginsenosides content was dependent on main roots and lateral roots energy metabolism, whereas independent of leaves and petiole photosynthesis during ginsenosides accumulation. When tow species were compared, the results indicated that high rates of C assimilation to C accumulation are closely associated with ginsenosides accumulation in P. ginseng main roots and P. quinquefolius lateral roots, respectively. Taken together, our results suggest that tissue-specific metabolites profiling dynamically changed in process of ginsenosides biosynthesis, which may offer a new train of thoughts to the mechanisms of the ginsenosides biosynthesis at the metabolite level.
The traditional medicine Ginseng mainly including Panax ginseng and Panax quinquefolius is the most widely consumed herbal product in the world. Despite the extensive investigation of biosynthetic pathway of the active compounds ginsenosides, our current understanding of the metabolic interlink between ginsenosides synthesis and primary metabolism at the whole-plant level. In this study, the tissue-specific profiling of primary and the secondary metabolites in two different species of ginseng were investigated by gas chromatography- and liquid chromatography coupled to mass spectrometry. A complex continuous coordination of primary- and secondary-metabolic network was modulated by tissues and species factors during growth. The results showed that altogether 149 primary compounds and 10 ginsenosides were identified from main roots, lateral roots, stems, petioles and leaves in P. ginseng and P. quinquefolius. The partial least squares-discriminate analysis (PLS-DA) revealed obvious compounds distinction among tissue-specific districts relative to species. To survey the dedication of carbon and nitrogen metabolism in different tissues to the accumulation of ginsenosides, we inspected the tissue-specific metabolic changes. Our study testified that the ginsenosides content was dependent on main roots and lateral roots energy metabolism, whereas independent of leaves and petiole photosynthesis during ginsenosides accumulation. When tow species were compared, the results indicated that high rates of C assimilation to C accumulation are closely associated with ginsenosides accumulation in P. ginseng main roots and P. quinquefolius lateral roots, respectively. Taken together, our results suggest that tissue-specific metabolites profiling dynamically changed in process of ginsenosides biosynthesis, which may offer a new train of thoughts to the mechanisms of the ginsenosides biosynthesis at the metabolite level.
Author Abozeid, Ann
Tang, Zhong-Hua
Liu, Yang
Wang, Yu
Liu, Jia
Zu, Yuan-Gang
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  organization: Key Laboratory of Plant Ecology, Northeast Forestry University, Harbin 150040, China
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  organization: Key Laboratory of Plant Ecology, Northeast Forestry University, Harbin 150040, China
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  organization: Key Laboratory of Plant Ecology, Northeast Forestry University, Harbin 150040, China
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  surname: Abozeid
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/28038384$$D View this record in MEDLINE/PubMed
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Keywords Carbon and nitrogen metabolism
Tissue specific
P. ginseng and P. quinquefolius
Ginsenosides
Language English
License This is an open access article under the CC BY-NC-ND license.
Copyright © 2016 The Author(s). Published by Elsevier B.V. All rights reserved.
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  article-title: GC–MS metabolic profiling of Cabernet Sauvignon and Merlot cultivars during grapevine berry development and network analysis reveals a stage- and cultivar-dependent connectivity of primary metabolites
  publication-title: Metabolomics
  doi: 10.1007/s11306-015-0927-z
– volume: 31
  start-page: 1015
  year: 2008
  ident: 10.1016/j.jpba.2016.12.026_bib0030
  article-title: Ultra-performance LC/TOF MS analysis of medicinal Panax herbs for metabolomic research
  publication-title: J. Sep. Sci.
  doi: 10.1002/jssc.200700650
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Snippet [Display omitted] •Tissue-specific profiling of primary and secondary metabolites in two different species of ginseng by using GC- and LC-MS.•Revealed a...
The traditional medicine Ginseng mainly including Panax ginseng and Panax quinquefolius is the most widely consumed herbal product in the world. Despite the...
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SubjectTerms Carbon and nitrogen metabolism
Chromatography, Liquid - methods
Gas Chromatography-Mass Spectrometry - methods
Ginsenosides
Ginsenosides - analysis
Ginsenosides - metabolism
Metabolomics - methods
P. ginseng and P. quinquefolius
Panax - chemistry
Panax - metabolism
Plant Leaves - chemistry
Plant Leaves - metabolism
Plant Roots - chemistry
Plant Roots - metabolism
Saponins - analysis
Saponins - metabolism
Species Specificity
Tissue Distribution - physiology
Tissue specific
Title The integration of GC–MS and LC–MS to assay the metabolomics profiling in Panax ginseng and Panax quinquefolius reveals a tissue- and species-specific connectivity of primary metabolites and ginsenosides accumulation
URI https://dx.doi.org/10.1016/j.jpba.2016.12.026
https://www.ncbi.nlm.nih.gov/pubmed/28038384
Volume 135
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