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Chemical composition and biological activities of essential oils of seven Cultivated Apiaceae species.

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  • Additional Information
    • Source:
      Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE
    • Publication Information:
      Original Publication: London : Nature Publishing Group, copyright 2011-
    • Subject Terms:
      Oils, Volatile*/pharmacology ; Oils, Volatile*/chemistry ; Antioxidants*/pharmacology ; Antioxidants*/chemistry ; Antioxidants*/analysis ; Apiaceae*/chemistry ; Daucus carota*/chemistry ; Foeniculum*/chemistry; Cuminum/chemistry ; Gas Chromatography-Mass Spectrometry ; Anti-Bacterial Agents/pharmacology ; Anti-Bacterial Agents/chemistry ; Microbial Sensitivity Tests ; Coriandrum/chemistry ; Seeds/chemistry ; Anethum graveolens/chemistry ; Pimpinella/chemistry ; Plant Oils/pharmacology ; Plant Oils/chemistry ; Apium/chemistry
    • Abstract:
      The Apiaceae family contains many species used as food, spice and medicinal purposes. Different parts of plants including seeds could be used to obtain essential (EO) oils from members of the Apiaceae family. In the present study, EOs were components obtained through hydrodistillation from the seeds of anise (Pimpinella anisum), carrot (Daucus carota), celery (Apium graveolens), dill (Anethum graveolens), coriander (Coriandrum sativum), fennel (Foeniculum vulgare), and cumin (Cuminum cyminum). EO constituents were determined with Gas Chromatography/Mass Spectrometry (GC-MS) and Gas Chromatography/Flame Ionization Detector (GC-FID) and their antioxidant capacities were determined with the cupric reducing antioxidant capacity (CUPRAC) and 2,2-diphenyl-1-picryl-hydrazyl-hydrate (DPPH) methods. The antimicrobial activity of EOs were tested against four pathogenic bacteria. Phenylpropanoids in anise (94.87%) and fennel (92.52%), oxygenated monoterpenes in dill (67.59%) and coriander (98.96%), monoterpene hydrocarbons in celery (75.42%), mono- (45.42%) and sesquiterpene- (43.25%) hydrocarbons in carrots, monoterpene hydrocarbon (34.30%) and aromatic hydrocarbons (32.92%) in cumin were the major compounds in the EOs. Anethole in anise and fennel, carotol in carrot, limonene in celery, carvone in dill, linalool in coriander, and cumin aldehyde in cumin were predominant compounds in these EOs. The high hydrocarbon content in cumin EO gave high CUPRAC activity (89.07 µmol Trolox g -1 ), and the moderate monoterpene hydrocarbon and oxygenated monoterpene content in dill EO resulted in higher DPPH activity (9.86 µmol Trolox g -1 ). The in vitro antibacterial activity of EOs against Bacillus cereus, Staphylococcus aureus, Pseudomonas aeruginosa and Escherichia coli was evaluated using the agar diffusion method and the minimum bactericidal concentration was determined. Coriander, cumin and dill EOs showed inhibitory effect against all tested strains except P. aeruginosa. While fennel and celery EOs were effective against E. coli and B. cereus strains, respectively, anise and carrot EOs did not show any antibacterial effect against the tested bacteria. Hierarchical Cluster Analysis (HCA) produced four groups based on EO constituents of seven species. The potential adoption of the cultivated Apiaceae species for EO extraction could be beneficial for the wild species that are endangered by over collection and consumption.
      (© 2024. The Author(s).)
    • References:
      J Pharm Biomed Anal. 2006 Jun 7;41(3):683-93. (PMID: 16520011)
      Int J Mol Sci. 2021 Mar 25;22(7):. (PMID: 33806141)
      Front Microbiol. 2012 Jan 25;3:12. (PMID: 22291693)
      Molecules. 2010 Oct 27;15(11):7532-46. (PMID: 21030907)
      Molecules. 2018 Sep 05;23(9):. (PMID: 30189606)
      Molecules. 2022 Oct 15;27(20):. (PMID: 36296521)
      Plants (Basel). 2021 Jul 26;10(8):. (PMID: 34451574)
      Int J Pharm. 2021 Dec 15;610:121274. (PMID: 34752917)
      Phytochem Anal. 2021 Sep;32(5):820-835. (PMID: 33462938)
      Chem Cent J. 2014 Aug 22;8(1):48. (PMID: 25246942)
      J Agric Food Chem. 2010 Aug 11;58(15):8848-53. (PMID: 20608729)
      Afr J Tradit Complement Altern Med. 2016 Nov 23;14(1):131-137. (PMID: 28480390)
      J Food Sci Technol. 2015 Apr;52(4):2452-7. (PMID: 25829632)
      Nat Prod Res. 2010 Sep;24(14):1287-94. (PMID: 20803372)
      Antioxidants (Basel). 2020 Aug 05;9(8):. (PMID: 32764410)
      Braz J Biol. 2019 Jul-Sep;79(3):432-437. (PMID: 30328892)
      J Poult Sci. 2022 Jan 25;59(1):16-37. (PMID: 35125910)
      J Res Med Sci. 2017 Mar 15;22:37. (PMID: 28465696)
      Molecules. 2020 Nov 14;25(22):. (PMID: 33202694)
      J Agric Food Chem. 2005 Jan 12;53(1):57-61. (PMID: 15631509)
      Chem Biodivers. 2013 Dec;10(12):2278-90. (PMID: 24327447)
      Jundishapur J Nat Pharm Prod. 2012 Spring;7(2):50-5. (PMID: 24624154)
      Nucleic Acids Res. 2015 Jul 1;43(W1):W566-70. (PMID: 25969447)
      Int J Food Sci Nutr. 2006 Aug-Sep;57(5-6):292-304. (PMID: 17135020)
      Food Chem. 2022 Aug 15;385:132633. (PMID: 35279500)
      Molecules. 2022 Oct 19;27(20):. (PMID: 36296660)
      Curr Microbiol. 2016 Feb;72(2):165-172. (PMID: 26553262)
      Anim Biosci. 2021 Mar;34(3):345-353. (PMID: 33705621)
      Foods. 2016 Mar 04;5(1):. (PMID: 28231113)
    • Accession Number:
      0 (Oils, Volatile)
      0 (Antioxidants)
      0 (Anti-Bacterial Agents)
      0 (Plant Oils)
    • Publication Date:
      Date Created: 20240502 Date Completed: 20240502 Latest Revision: 20240509
    • Publication Date:
      20240509
    • Accession Number:
      PMC11066118
    • Accession Number:
      10.1038/s41598-024-60810-3
    • Accession Number:
      38698117