Chemical Composition and In Vitro Antioxidant and Antimicrobial Activities of the Marine Cyanolichen Lichina pygmaea Volatile Compounds
Volatile compounds from the marine cyanolichen , collected from the Moroccan Atlantic coast, were extracted by hydrodistillation and their putative chemical composition was investigated by gas chromatography coupled to mass spectrometry (GC/MS). Based on the obtained results, volatile compounds (LPV...
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| Published in | Marine drugs Vol. 20; no. 3; p. 169 |
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| Main Authors | , , , , , , , , |
| Format | Journal Article |
| Language | English |
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| Abstract | Volatile compounds from the marine cyanolichen
, collected from the Moroccan Atlantic coast, were extracted by hydrodistillation and their putative chemical composition was investigated by gas chromatography coupled to mass spectrometry (GC/MS). Based on the obtained results,
volatile compounds (LPVCs) were mainly dominated by sesquiterpenes compounds, where
-himachalene,
-himachalene, (
)-2,4 decadienal and
-himachalene were assumed to be the most abundant constituents, with percentage of 37.51%, 11.71%, 8.59% and 7.62%, respectively. LPVCs depicted significant antimicrobial activity against all tested strains (
CCMM B3,
DSM 50090,
ATCC 8739 and
CCMM-L4) with minimum inhibitory concentration (MIC) values within the range of 1.69-13.5 mg/mL. Moreover, this LPVC showed interesting scavenging effects on the 2,2-diphenyl-1-picrylhydrazyl radical with an IC
of 0.21 mg/mL. LPVCs could be an approving resource with moderate antimicrobial potential and interesting antioxidant activity for cosmetics and pharmaceutical applications. |
|---|---|
| AbstractList | Volatile compounds from the marine cyanolichen
, collected from the Moroccan Atlantic coast, were extracted by hydrodistillation and their putative chemical composition was investigated by gas chromatography coupled to mass spectrometry (GC/MS). Based on the obtained results,
volatile compounds (LPVCs) were mainly dominated by sesquiterpenes compounds, where
-himachalene,
-himachalene, (
)-2,4 decadienal and
-himachalene were assumed to be the most abundant constituents, with percentage of 37.51%, 11.71%, 8.59% and 7.62%, respectively. LPVCs depicted significant antimicrobial activity against all tested strains (
CCMM B3,
DSM 50090,
ATCC 8739 and
CCMM-L4) with minimum inhibitory concentration (MIC) values within the range of 1.69-13.5 mg/mL. Moreover, this LPVC showed interesting scavenging effects on the 2,2-diphenyl-1-picrylhydrazyl radical with an IC
of 0.21 mg/mL. LPVCs could be an approving resource with moderate antimicrobial potential and interesting antioxidant activity for cosmetics and pharmaceutical applications. Volatile compounds from the marine cyanolichen Lichina pygmaea, collected from the Moroccan Atlantic coast, were extracted by hydrodistillation and their putative chemical composition was investigated by gas chromatography coupled to mass spectrometry (GC/MS). Based on the obtained results, Lichina pygmaea volatile compounds (LPVCs) were mainly dominated by sesquiterpenes compounds, where γ-himachalene, β-himachalene, (2E,4E)-2,4 decadienal and α-himachalene were assumed to be the most abundant constituents, with percentage of 37.51%, 11.71%, 8.59% and 7.62%, respectively. LPVCs depicted significant antimicrobial activity against all tested strains (Staphylococcus aureus CCMM B3, Pseudomonas aeruginosa DSM 50090, Escherichia coli ATCC 8739 and Candida albicans CCMM-L4) with minimum inhibitory concentration (MIC) values within the range of 1.69–13.5 mg/mL. Moreover, this LPVC showed interesting scavenging effects on the 2,2-diphenyl-1-picrylhydrazyl radical with an IC50 of 0.21 mg/mL. LPVCs could be an approving resource with moderate antimicrobial potential and interesting antioxidant activity for cosmetics and pharmaceutical applications. Volatile compounds from the marine cyanolichen Lichina pygmaea , collected from the Moroccan Atlantic coast, were extracted by hydrodistillation and their putative chemical composition was investigated by gas chromatography coupled to mass spectrometry (GC/MS). Based on the obtained results, Lichina pygmaea volatile compounds (LPVCs) were mainly dominated by sesquiterpenes compounds, where γ -himachalene, β -himachalene, ( 2E,4E )-2,4 decadienal and α -himachalene were assumed to be the most abundant constituents, with percentage of 37.51%, 11.71%, 8.59% and 7.62%, respectively. LPVCs depicted significant antimicrobial activity against all tested strains ( Staphylococcus aureus CCMM B3, Pseudomonas aeruginosa DSM 50090, Escherichia coli ATCC 8739 and Candida albicans CCMM-L4) with minimum inhibitory concentration (MIC) values within the range of 1.69–13.5 mg/mL. Moreover, this LPVC showed interesting scavenging effects on the 2,2-diphenyl-1-picrylhydrazyl radical with an IC 50 of 0.21 mg/mL. LPVCs could be an approving resource with moderate antimicrobial potential and interesting antioxidant activity for cosmetics and pharmaceutical applications. |
| Author | Nafis, Ahmed Vasconcelos, Vitor Hassouani, Meryem Hassani, Lahcen Mazoir, Noureddine Sabour, Brahim Reani, Abdeltif Sanad, Hiba Belattmania, Zahira |
| AuthorAffiliation | 2 Department of Biology, Faculty of Sciences El Jadida, University Chouaib Doukkali, P.O. Box 20, El Jadida 24000, Morocco; ahmed.nafis@edu.uca.ac.ma 5 Department of Biology, Faculty of Sciences, University of Porto, Rua do Campo Alegre, 4169-007 Porto, Portugal 4 Laboratory of Microbial Biotechnologies, Agrosciences and Environment, Faculty of Sciences Semlalia, University Cadi Ayyad, P.O. Box 2390, Marrakech 40001, Morocco; lhassani@uca.ac.ma 3 CIIMAR, Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Terminal de Cruzeiros do Porto de Leixões, Av. General Norton de Matos, s/n, 4450-208 Matosinhos, Portugal 1 Laboratory of Plant Biotechnology, Ecology and Ecosystem Valorization—URL CNRST N°10, Faculty of Sciences El Jadida, University Chouaib Doukkali, P.O. Box 20, El Jadida 24000, Morocco; hiba.sanad.ucd@gmail.com (H.S.); belattmania.z@ucd.ac.ma (Z.B.); m.hassouani@gmail.com (M.H.); mazoirn@gmail.com (N.M.); abreani@yahoo.fr (A.R.); sabour.b@ucd.ac.ma (B |
| AuthorAffiliation_xml | – name: 2 Department of Biology, Faculty of Sciences El Jadida, University Chouaib Doukkali, P.O. Box 20, El Jadida 24000, Morocco; ahmed.nafis@edu.uca.ac.ma – name: 5 Department of Biology, Faculty of Sciences, University of Porto, Rua do Campo Alegre, 4169-007 Porto, Portugal – name: 1 Laboratory of Plant Biotechnology, Ecology and Ecosystem Valorization—URL CNRST N°10, Faculty of Sciences El Jadida, University Chouaib Doukkali, P.O. Box 20, El Jadida 24000, Morocco; hiba.sanad.ucd@gmail.com (H.S.); belattmania.z@ucd.ac.ma (Z.B.); m.hassouani@gmail.com (M.H.); mazoirn@gmail.com (N.M.); abreani@yahoo.fr (A.R.); sabour.b@ucd.ac.ma (B.S.) – name: 3 CIIMAR, Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Terminal de Cruzeiros do Porto de Leixões, Av. General Norton de Matos, s/n, 4450-208 Matosinhos, Portugal – name: 4 Laboratory of Microbial Biotechnologies, Agrosciences and Environment, Faculty of Sciences Semlalia, University Cadi Ayyad, P.O. Box 2390, Marrakech 40001, Morocco; lhassani@uca.ac.ma |
| Author_xml | – sequence: 1 givenname: Hiba surname: Sanad fullname: Sanad, Hiba organization: Laboratory of Plant Biotechnology, Ecology and Ecosystem Valorization-URL CNRST N°10, Faculty of Sciences El Jadida, University Chouaib Doukkali, P.O. Box 20, El Jadida 24000, Morocco – sequence: 2 givenname: Zahira orcidid: 0000-0003-1415-3625 surname: Belattmania fullname: Belattmania, Zahira organization: Laboratory of Plant Biotechnology, Ecology and Ecosystem Valorization-URL CNRST N°10, Faculty of Sciences El Jadida, University Chouaib Doukkali, P.O. Box 20, El Jadida 24000, Morocco – sequence: 3 givenname: Ahmed surname: Nafis fullname: Nafis, Ahmed organization: Department of Biology, Faculty of Sciences El Jadida, University Chouaib Doukkali, P.O. Box 20, El Jadida 24000, Morocco – sequence: 4 givenname: Meryem surname: Hassouani fullname: Hassouani, Meryem organization: CIIMAR, Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Terminal de Cruzeiros do Porto de Leixões, Av. General Norton de Matos, s/n, 4450-208 Matosinhos, Portugal – sequence: 5 givenname: Noureddine orcidid: 0000-0002-6359-1739 surname: Mazoir fullname: Mazoir, Noureddine organization: Laboratory of Plant Biotechnology, Ecology and Ecosystem Valorization-URL CNRST N°10, Faculty of Sciences El Jadida, University Chouaib Doukkali, P.O. Box 20, El Jadida 24000, Morocco – sequence: 6 givenname: Abdeltif surname: Reani fullname: Reani, Abdeltif organization: Laboratory of Plant Biotechnology, Ecology and Ecosystem Valorization-URL CNRST N°10, Faculty of Sciences El Jadida, University Chouaib Doukkali, P.O. Box 20, El Jadida 24000, Morocco – sequence: 7 givenname: Lahcen surname: Hassani fullname: Hassani, Lahcen organization: Laboratory of Microbial Biotechnologies, Agrosciences and Environment, Faculty of Sciences Semlalia, University Cadi Ayyad, P.O. Box 2390, Marrakech 40001, Morocco – sequence: 8 givenname: Vitor orcidid: 0000-0003-3585-2417 surname: Vasconcelos fullname: Vasconcelos, Vitor organization: Department of Biology, Faculty of Sciences, University of Porto, Rua do Campo Alegre, 4169-007 Porto, Portugal – sequence: 9 givenname: Brahim orcidid: 0000-0002-5569-0980 surname: Sabour fullname: Sabour, Brahim organization: Laboratory of Plant Biotechnology, Ecology and Ecosystem Valorization-URL CNRST N°10, Faculty of Sciences El Jadida, University Chouaib Doukkali, P.O. Box 20, El Jadida 24000, Morocco |
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, collected from the Moroccan Atlantic coast, were extracted by hydrodistillation and their putative chemical... Volatile compounds from the marine cyanolichen Lichina pygmaea, collected from the Moroccan Atlantic coast, were extracted by hydrodistillation and their... Volatile compounds from the marine cyanolichen Lichina pygmaea , collected from the Moroccan Atlantic coast, were extracted by hydrodistillation and their... |
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| SubjectTerms | Algae Anti-Infective Agents - chemistry Anti-Infective Agents - isolation & purification Anti-Infective Agents - pharmacology Antiinfectives and antibacterials Antimicrobial activity Antimicrobial agents antioxidant and antimicrobial activities Antioxidants Antioxidants - chemistry Antioxidants - isolation & purification Antioxidants - pharmacology Aquatic plants Ascomycota - chemistry Biofilms Biphenyl Compounds - chemistry Candida albicans - drug effects Candida albicans - growth & development Chemical composition Cosmetics Cyanobacteria Disease resistance E coli Escherichia coli - drug effects Escherichia coli - growth & development Gas chromatography Gram-negative bacteria Lichens Lichina pygmaea Mass spectrometry Mass spectroscopy Metabolites Minimum inhibitory concentration Phenols Picrates - chemistry Pseudomonas aeruginosa Pseudomonas aeruginosa - drug effects Pseudomonas aeruginosa - growth & development Scavenging Sesquiterpenes Sesquiterpenes - analysis Sesquiterpenes - isolation & purification Sesquiterpenes - pharmacology Staphylococcus aureus - drug effects Staphylococcus aureus - growth & development VOCs Volatile compounds Volatile organic compounds Volatile Organic Compounds - chemistry Volatile Organic Compounds - isolation & purification Volatile Organic Compounds - pharmacology |
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| Title | Chemical Composition and In Vitro Antioxidant and Antimicrobial Activities of the Marine Cyanolichen Lichina pygmaea Volatile Compounds |
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