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Antifungal and Antibacterial Activities of Mexican Tarragon (Tagetes lucida)

Mexican tarragon (Tagetes lucida Cv. Asteraceae:  Campanulatae) is an important, nutritious plant and an effective herbal medicine. Seven coumarins, 7,8-dihydroxycoumarin (4), umbelliferone (7-hydroxycoumarin) (5), scoparone (6,7-dimethoxycoumarin) (7), esculetin (6,7-dihydroxycoumarin) (11), 6-hydr...

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Published in:Journal of agricultural and food chemistry 2006-05, Vol.54 (10), p.3521-3527
Main Authors: Céspedes, Carlos L, Avila, J. Guillermo, Martínez, Andrés, Serrato, Blanca, Calderón-Mugica, José C, Salgado-Garciglia, Rafael
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cited_by cdi_FETCH-LOGICAL-a436t-930d94d3fb91c5bd0197df3f6a7900a7617efcca776e66a0bd3f68bf7e9d91233
cites cdi_FETCH-LOGICAL-a436t-930d94d3fb91c5bd0197df3f6a7900a7617efcca776e66a0bd3f68bf7e9d91233
container_end_page 3527
container_issue 10
container_start_page 3521
container_title Journal of agricultural and food chemistry
container_volume 54
creator Céspedes, Carlos L
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Salgado-Garciglia, Rafael
description Mexican tarragon (Tagetes lucida Cv. Asteraceae:  Campanulatae) is an important, nutritious plant and an effective herbal medicine. Seven coumarins, 7,8-dihydroxycoumarin (4), umbelliferone (7-hydroxycoumarin) (5), scoparone (6,7-dimethoxycoumarin) (7), esculetin (6,7-dihydroxycoumarin) (11), 6-hydroxy-7-methoxycoumarin (12), herniarin (7-methoxycoumarin) (13), and scopoletin (6-methoxy-7-hydroxycoumarin) (14), and three flavonoids, patuletin (18), quercetin (19), and quercetagetin (20), were isolated from CH2Cl2 and MeOH extracts from aerial parts of T. lucida. In addition, 6,7-diacetoxy coumarin (15), 6-methoxy-7-acetylcoumarin (16), and 6-acetoxy-7-methoxycoumarin (17) derivatives were synthesized. 8-Methoxypsoralen (1), 8-acetyl-7-hydroxycoumarin (2), 7,8-dihydroxy-6-methoxycoumarin (3), 6,7-dimethoxy-4-methylcoumarin (6), 5,7-dihydroxy-4-methylcoumarin (8), 4-hydroxycoumarin (9), 4-hydroxy-6,7-dimethylcoumarin (10), naringenin (21), glycoside-7-rhamnonaringin (22), and rutin (23) were commercially obtained (Sigma-Aldrich). All of these compounds and extracts (M1 and M2) were assayed against bacteria and fungi. The antibacterial activity was determined on Bacillus subtilis, Escherichia coli, Proteus mirabilis, Klebsiella pneumoniae, Salmonella typhi, Salmonella sp., Shigella boydii, Shigella sp., Enterobacter aerogenes, Enterobacter agglomerans, Sarcina lutea, Staphylococcus epidermidis, Staphylococcus aureus, Yersinia enterolitica, Vibrio cholerae (three El Tor strains, CDC-V12, clinic case, and INDRE-206, were obtained from contaminated water), and V. cholerae (NO-O1). The evaluated fungi were Aspergillus niger, Penicillium notatum, Fusarium moniliforme, Fusarium sporotrichum, Rhizoctonia solani, and Trichophyton mentagrophytes. The most active compounds against Gram-positive and -negative bacteria were the dihydroxylated coumarins 3 and 4. In addition, 2−4, 6, 7, and 11 showed an interesting activity against V. cholerae, a key bacterium in the contaminated water; 2−4 were the most active. Coumarins were the most effective compounds against Gram-negative bacteria. The extract MeOH/CH2Cl2 (1:4) M2 at 0.4 μg/disk inhibited the growth of E. coli and P. mirabilis (40%), K. pneumoniae (31.1%), Salmonella sp. (35.5%), and Shigella sp. (0%) at 72 h of culture. The dimethoxy compounds 6 and 7 showed a strong activity against fungal strains, especially T. mentagrophytes and R. solani (100% of inhibition at 125.0 and 250.0 μg/mL, respectively). Keywords: Taget
doi_str_mv 10.1021/jf053071w
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Guillermo ; Martínez, Andrés ; Serrato, Blanca ; Calderón-Mugica, José C ; Salgado-Garciglia, Rafael</creator><creatorcontrib>Céspedes, Carlos L ; Avila, J. Guillermo ; Martínez, Andrés ; Serrato, Blanca ; Calderón-Mugica, José C ; Salgado-Garciglia, Rafael</creatorcontrib><description>Mexican tarragon (Tagetes lucida Cv. Asteraceae:  Campanulatae) is an important, nutritious plant and an effective herbal medicine. Seven coumarins, 7,8-dihydroxycoumarin (4), umbelliferone (7-hydroxycoumarin) (5), scoparone (6,7-dimethoxycoumarin) (7), esculetin (6,7-dihydroxycoumarin) (11), 6-hydroxy-7-methoxycoumarin (12), herniarin (7-methoxycoumarin) (13), and scopoletin (6-methoxy-7-hydroxycoumarin) (14), and three flavonoids, patuletin (18), quercetin (19), and quercetagetin (20), were isolated from CH2Cl2 and MeOH extracts from aerial parts of T. lucida. In addition, 6,7-diacetoxy coumarin (15), 6-methoxy-7-acetylcoumarin (16), and 6-acetoxy-7-methoxycoumarin (17) derivatives were synthesized. 8-Methoxypsoralen (1), 8-acetyl-7-hydroxycoumarin (2), 7,8-dihydroxy-6-methoxycoumarin (3), 6,7-dimethoxy-4-methylcoumarin (6), 5,7-dihydroxy-4-methylcoumarin (8), 4-hydroxycoumarin (9), 4-hydroxy-6,7-dimethylcoumarin (10), naringenin (21), glycoside-7-rhamnonaringin (22), and rutin (23) were commercially obtained (Sigma-Aldrich). All of these compounds and extracts (M1 and M2) were assayed against bacteria and fungi. The antibacterial activity was determined on Bacillus subtilis, Escherichia coli, Proteus mirabilis, Klebsiella pneumoniae, Salmonella typhi, Salmonella sp., Shigella boydii, Shigella sp., Enterobacter aerogenes, Enterobacter agglomerans, Sarcina lutea, Staphylococcus epidermidis, Staphylococcus aureus, Yersinia enterolitica, Vibrio cholerae (three El Tor strains, CDC-V12, clinic case, and INDRE-206, were obtained from contaminated water), and V. cholerae (NO-O1). The evaluated fungi were Aspergillus niger, Penicillium notatum, Fusarium moniliforme, Fusarium sporotrichum, Rhizoctonia solani, and Trichophyton mentagrophytes. The most active compounds against Gram-positive and -negative bacteria were the dihydroxylated coumarins 3 and 4. In addition, 2−4, 6, 7, and 11 showed an interesting activity against V. cholerae, a key bacterium in the contaminated water; 2−4 were the most active. Coumarins were the most effective compounds against Gram-negative bacteria. The extract MeOH/CH2Cl2 (1:4) M2 at 0.4 μg/disk inhibited the growth of E. coli and P. mirabilis (40%), K. pneumoniae (31.1%), Salmonella sp. (35.5%), and Shigella sp. (0%) at 72 h of culture. The dimethoxy compounds 6 and 7 showed a strong activity against fungal strains, especially T. mentagrophytes and R. solani (100% of inhibition at 125.0 and 250.0 μg/mL, respectively). 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Psychology ; fungi ; Fungi - drug effects ; Fusarium moniliforme ; Klebsiella pneumoniae ; medicinal plants ; Molecular Structure ; natural additives ; Penicillium notatum ; Plant Components, Aerial - chemistry ; plant extracts ; Plant Extracts - isolation &amp; purification ; Plant Extracts - pharmacology ; plant pathogenic fungi ; Proteus mirabilis ; Rhizoctonia solani ; Salmonella typhi ; Sarcina ; Shigella ; Shigella boydii ; Sporotrichum ; Staphylococcus aureus ; Staphylococcus epidermidis ; Tagetes ; Tagetes - chemistry ; Tagetes lucida ; Trichophyton mentagrophytes ; Vibrio cholerae ; Yersinia</subject><ispartof>Journal of agricultural and food chemistry, 2006-05, Vol.54 (10), p.3521-3527</ispartof><rights>Copyright © 2006 American Chemical Society</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a436t-930d94d3fb91c5bd0197df3f6a7900a7617efcca776e66a0bd3f68bf7e9d91233</citedby><cites>FETCH-LOGICAL-a436t-930d94d3fb91c5bd0197df3f6a7900a7617efcca776e66a0bd3f68bf7e9d91233</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=17782149$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19127719$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Céspedes, Carlos L</creatorcontrib><creatorcontrib>Avila, J. Guillermo</creatorcontrib><creatorcontrib>Martínez, Andrés</creatorcontrib><creatorcontrib>Serrato, Blanca</creatorcontrib><creatorcontrib>Calderón-Mugica, José C</creatorcontrib><creatorcontrib>Salgado-Garciglia, Rafael</creatorcontrib><title>Antifungal and Antibacterial Activities of Mexican Tarragon (Tagetes lucida)</title><title>Journal of agricultural and food chemistry</title><addtitle>J. Agric. Food Chem</addtitle><description>Mexican tarragon (Tagetes lucida Cv. Asteraceae:  Campanulatae) is an important, nutritious plant and an effective herbal medicine. Seven coumarins, 7,8-dihydroxycoumarin (4), umbelliferone (7-hydroxycoumarin) (5), scoparone (6,7-dimethoxycoumarin) (7), esculetin (6,7-dihydroxycoumarin) (11), 6-hydroxy-7-methoxycoumarin (12), herniarin (7-methoxycoumarin) (13), and scopoletin (6-methoxy-7-hydroxycoumarin) (14), and three flavonoids, patuletin (18), quercetin (19), and quercetagetin (20), were isolated from CH2Cl2 and MeOH extracts from aerial parts of T. lucida. In addition, 6,7-diacetoxy coumarin (15), 6-methoxy-7-acetylcoumarin (16), and 6-acetoxy-7-methoxycoumarin (17) derivatives were synthesized. 8-Methoxypsoralen (1), 8-acetyl-7-hydroxycoumarin (2), 7,8-dihydroxy-6-methoxycoumarin (3), 6,7-dimethoxy-4-methylcoumarin (6), 5,7-dihydroxy-4-methylcoumarin (8), 4-hydroxycoumarin (9), 4-hydroxy-6,7-dimethylcoumarin (10), naringenin (21), glycoside-7-rhamnonaringin (22), and rutin (23) were commercially obtained (Sigma-Aldrich). All of these compounds and extracts (M1 and M2) were assayed against bacteria and fungi. The antibacterial activity was determined on Bacillus subtilis, Escherichia coli, Proteus mirabilis, Klebsiella pneumoniae, Salmonella typhi, Salmonella sp., Shigella boydii, Shigella sp., Enterobacter aerogenes, Enterobacter agglomerans, Sarcina lutea, Staphylococcus epidermidis, Staphylococcus aureus, Yersinia enterolitica, Vibrio cholerae (three El Tor strains, CDC-V12, clinic case, and INDRE-206, were obtained from contaminated water), and V. cholerae (NO-O1). The evaluated fungi were Aspergillus niger, Penicillium notatum, Fusarium moniliforme, Fusarium sporotrichum, Rhizoctonia solani, and Trichophyton mentagrophytes. The most active compounds against Gram-positive and -negative bacteria were the dihydroxylated coumarins 3 and 4. In addition, 2−4, 6, 7, and 11 showed an interesting activity against V. cholerae, a key bacterium in the contaminated water; 2−4 were the most active. Coumarins were the most effective compounds against Gram-negative bacteria. The extract MeOH/CH2Cl2 (1:4) M2 at 0.4 μg/disk inhibited the growth of E. coli and P. mirabilis (40%), K. pneumoniae (31.1%), Salmonella sp. (35.5%), and Shigella sp. (0%) at 72 h of culture. The dimethoxy compounds 6 and 7 showed a strong activity against fungal strains, especially T. mentagrophytes and R. solani (100% of inhibition at 125.0 and 250.0 μg/mL, respectively). Keywords: Tagetes lucida; Mexican tarragon; antibacterial; antifungal; simple coumarins; spice</description><subject>animal pathogenic bacteria</subject><subject>animal pathogenic fungi</subject><subject>Anti-Bacterial Agents - chemistry</subject><subject>Anti-Bacterial Agents - isolation &amp; purification</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>antibacterial properties</subject><subject>Antifungal Agents - chemistry</subject><subject>Antifungal Agents - isolation &amp; purification</subject><subject>Antifungal Agents - pharmacology</subject><subject>antifungal properties</subject><subject>Aroma and flavouring agent industries</subject><subject>Aspergillus niger</subject><subject>Asteraceae</subject><subject>Bacillus subtilis</subject><subject>Bacteria - drug effects</subject><subject>Biological and medical sciences</subject><subject>chemical structure</subject><subject>coumarins</subject><subject>Coumarins - chemistry</subject><subject>Coumarins - isolation &amp; purification</subject><subject>Coumarins - pharmacology</subject><subject>Dietary Supplements</subject><subject>Enterobacter aerogenes</subject><subject>Enterobacter agglomerans</subject><subject>Escherichia coli</subject><subject>Flavonoids - chemistry</subject><subject>Flavonoids - isolation &amp; purification</subject><subject>Flavonoids - pharmacology</subject><subject>Food industries</subject><subject>Food microbiology</subject><subject>food preservatives</subject><subject>Fundamental and applied biological sciences. 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Guillermo ; Martínez, Andrés ; Serrato, Blanca ; Calderón-Mugica, José C ; Salgado-Garciglia, Rafael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a436t-930d94d3fb91c5bd0197df3f6a7900a7617efcca776e66a0bd3f68bf7e9d91233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>animal pathogenic bacteria</topic><topic>animal pathogenic fungi</topic><topic>Anti-Bacterial Agents - chemistry</topic><topic>Anti-Bacterial Agents - isolation &amp; purification</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>antibacterial properties</topic><topic>Antifungal Agents - chemistry</topic><topic>Antifungal Agents - isolation &amp; purification</topic><topic>Antifungal Agents - pharmacology</topic><topic>antifungal properties</topic><topic>Aroma and flavouring agent industries</topic><topic>Aspergillus niger</topic><topic>Asteraceae</topic><topic>Bacillus subtilis</topic><topic>Bacteria - drug effects</topic><topic>Biological and medical sciences</topic><topic>chemical structure</topic><topic>coumarins</topic><topic>Coumarins - chemistry</topic><topic>Coumarins - isolation &amp; purification</topic><topic>Coumarins - pharmacology</topic><topic>Dietary Supplements</topic><topic>Enterobacter aerogenes</topic><topic>Enterobacter agglomerans</topic><topic>Escherichia coli</topic><topic>Flavonoids - chemistry</topic><topic>Flavonoids - isolation &amp; purification</topic><topic>Flavonoids - pharmacology</topic><topic>Food industries</topic><topic>Food microbiology</topic><topic>food preservatives</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>fungi</topic><topic>Fungi - drug effects</topic><topic>Fusarium moniliforme</topic><topic>Klebsiella pneumoniae</topic><topic>medicinal plants</topic><topic>Molecular Structure</topic><topic>natural additives</topic><topic>Penicillium notatum</topic><topic>Plant Components, Aerial - chemistry</topic><topic>plant extracts</topic><topic>Plant Extracts - isolation &amp; purification</topic><topic>Plant Extracts - pharmacology</topic><topic>plant pathogenic fungi</topic><topic>Proteus mirabilis</topic><topic>Rhizoctonia solani</topic><topic>Salmonella typhi</topic><topic>Sarcina</topic><topic>Shigella</topic><topic>Shigella boydii</topic><topic>Sporotrichum</topic><topic>Staphylococcus aureus</topic><topic>Staphylococcus epidermidis</topic><topic>Tagetes</topic><topic>Tagetes - chemistry</topic><topic>Tagetes lucida</topic><topic>Trichophyton mentagrophytes</topic><topic>Vibrio cholerae</topic><topic>Yersinia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Céspedes, Carlos L</creatorcontrib><creatorcontrib>Avila, J. Guillermo</creatorcontrib><creatorcontrib>Martínez, Andrés</creatorcontrib><creatorcontrib>Serrato, Blanca</creatorcontrib><creatorcontrib>Calderón-Mugica, José C</creatorcontrib><creatorcontrib>Salgado-Garciglia, Rafael</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Céspedes, Carlos L</au><au>Avila, J. Guillermo</au><au>Martínez, Andrés</au><au>Serrato, Blanca</au><au>Calderón-Mugica, José C</au><au>Salgado-Garciglia, Rafael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antifungal and Antibacterial Activities of Mexican Tarragon (Tagetes lucida)</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2006-05-17</date><risdate>2006</risdate><volume>54</volume><issue>10</issue><spage>3521</spage><epage>3527</epage><pages>3521-3527</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><coden>JAFCAU</coden><abstract>Mexican tarragon (Tagetes lucida Cv. Asteraceae:  Campanulatae) is an important, nutritious plant and an effective herbal medicine. Seven coumarins, 7,8-dihydroxycoumarin (4), umbelliferone (7-hydroxycoumarin) (5), scoparone (6,7-dimethoxycoumarin) (7), esculetin (6,7-dihydroxycoumarin) (11), 6-hydroxy-7-methoxycoumarin (12), herniarin (7-methoxycoumarin) (13), and scopoletin (6-methoxy-7-hydroxycoumarin) (14), and three flavonoids, patuletin (18), quercetin (19), and quercetagetin (20), were isolated from CH2Cl2 and MeOH extracts from aerial parts of T. lucida. In addition, 6,7-diacetoxy coumarin (15), 6-methoxy-7-acetylcoumarin (16), and 6-acetoxy-7-methoxycoumarin (17) derivatives were synthesized. 8-Methoxypsoralen (1), 8-acetyl-7-hydroxycoumarin (2), 7,8-dihydroxy-6-methoxycoumarin (3), 6,7-dimethoxy-4-methylcoumarin (6), 5,7-dihydroxy-4-methylcoumarin (8), 4-hydroxycoumarin (9), 4-hydroxy-6,7-dimethylcoumarin (10), naringenin (21), glycoside-7-rhamnonaringin (22), and rutin (23) were commercially obtained (Sigma-Aldrich). All of these compounds and extracts (M1 and M2) were assayed against bacteria and fungi. The antibacterial activity was determined on Bacillus subtilis, Escherichia coli, Proteus mirabilis, Klebsiella pneumoniae, Salmonella typhi, Salmonella sp., Shigella boydii, Shigella sp., Enterobacter aerogenes, Enterobacter agglomerans, Sarcina lutea, Staphylococcus epidermidis, Staphylococcus aureus, Yersinia enterolitica, Vibrio cholerae (three El Tor strains, CDC-V12, clinic case, and INDRE-206, were obtained from contaminated water), and V. cholerae (NO-O1). The evaluated fungi were Aspergillus niger, Penicillium notatum, Fusarium moniliforme, Fusarium sporotrichum, Rhizoctonia solani, and Trichophyton mentagrophytes. The most active compounds against Gram-positive and -negative bacteria were the dihydroxylated coumarins 3 and 4. In addition, 2−4, 6, 7, and 11 showed an interesting activity against V. cholerae, a key bacterium in the contaminated water; 2−4 were the most active. Coumarins were the most effective compounds against Gram-negative bacteria. The extract MeOH/CH2Cl2 (1:4) M2 at 0.4 μg/disk inhibited the growth of E. coli and P. mirabilis (40%), K. pneumoniae (31.1%), Salmonella sp. (35.5%), and Shigella sp. (0%) at 72 h of culture. The dimethoxy compounds 6 and 7 showed a strong activity against fungal strains, especially T. mentagrophytes and R. solani (100% of inhibition at 125.0 and 250.0 μg/mL, respectively). Keywords: Tagetes lucida; Mexican tarragon; antibacterial; antifungal; simple coumarins; spice</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>19127719</pmid><doi>10.1021/jf053071w</doi><tpages>7</tpages></addata></record>
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identifier ISSN: 0021-8561
ispartof Journal of agricultural and food chemistry, 2006-05, Vol.54 (10), p.3521-3527
issn 0021-8561
1520-5118
language eng
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source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
subjects animal pathogenic bacteria
animal pathogenic fungi
Anti-Bacterial Agents - chemistry
Anti-Bacterial Agents - isolation & purification
Anti-Bacterial Agents - pharmacology
antibacterial properties
Antifungal Agents - chemistry
Antifungal Agents - isolation & purification
Antifungal Agents - pharmacology
antifungal properties
Aroma and flavouring agent industries
Aspergillus niger
Asteraceae
Bacillus subtilis
Bacteria - drug effects
Biological and medical sciences
chemical structure
coumarins
Coumarins - chemistry
Coumarins - isolation & purification
Coumarins - pharmacology
Dietary Supplements
Enterobacter aerogenes
Enterobacter agglomerans
Escherichia coli
Flavonoids - chemistry
Flavonoids - isolation & purification
Flavonoids - pharmacology
Food industries
Food microbiology
food preservatives
Fundamental and applied biological sciences. Psychology
fungi
Fungi - drug effects
Fusarium moniliforme
Klebsiella pneumoniae
medicinal plants
Molecular Structure
natural additives
Penicillium notatum
Plant Components, Aerial - chemistry
plant extracts
Plant Extracts - isolation & purification
Plant Extracts - pharmacology
plant pathogenic fungi
Proteus mirabilis
Rhizoctonia solani
Salmonella typhi
Sarcina
Shigella
Shigella boydii
Sporotrichum
Staphylococcus aureus
Staphylococcus epidermidis
Tagetes
Tagetes - chemistry
Tagetes lucida
Trichophyton mentagrophytes
Vibrio cholerae
Yersinia
title Antifungal and Antibacterial Activities of Mexican Tarragon (Tagetes lucida)
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