Anita Barta, Agostina Salusso, Norbert Kúsz, Róbert Berkecz, Jan Schlauer, Dragica Purger, Judit Hohmann, Maria Cecilia Carpinella, Andrea Vasas
{"title":"具有抗菌和抑制生物膜形成活性的蔺草中的菲族化合物","authors":"Anita Barta, Agostina Salusso, Norbert Kúsz, Róbert Berkecz, Jan Schlauer, Dragica Purger, Judit Hohmann, Maria Cecilia Carpinella, Andrea Vasas","doi":"10.1021/acs.jnatprod.4c00577","DOIUrl":null,"url":null,"abstract":"<p><p>Continuing our search for bioactive compounds in species from the Juncaceae family, <i>Juncus articulatus</i> was investigated. Ten previously undescribed phenanthrenes─articulins A-J (<b>1</b>-<b>10</b>)─and ten known compounds─juncuenin B, dehydrojuncuenin B, juncatrin B, ensifolins E, F, H, I, K, juncuenin D, and luzulin A (<b>11</b>-<b>20</b>)─along with other compounds, have been isolated and identified. The isolated compounds were evaluated for antibacterial activity against <i>Escherichia coli</i>, <i>Pseudomonas aeruginosa</i>, methicillin-susceptible <i>Staphylococcus aureus</i> (MSSA), and methicillin-resistant <i>Staphylococcus aureus</i> (MRSA). Compounds <b>12</b> and <b>14</b> exhibited the most potent activity against planktonic and sessile MSSA and MRSA with minimum inhibitory concentration (MIC) values of 15.1 μM (<b>12</b> for both bacterial strains) and 15.3 μM (<b>14</b> for both bacterial strains). Compounds <b>15</b>, <b>17</b>, and <b>18</b> also exhibited activity against both strains, although to a lower extent, with MIC values ranging from 30.0 to 56.8 μM. The inhibition of biofilm formation of these compounds was observed at 15.1-114.3 μM. This study elucidates the phenanthrene composition of <i>J. articulatus</i> and the antibacterial effect of these compounds.</p>","PeriodicalId":47,"journal":{"name":"Journal of Natural Products ","volume":" ","pages":"2068-2080"},"PeriodicalIF":3.3000,"publicationDate":"2024-08-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11348428/pdf/","citationCount":"0","resultStr":"{\"title\":\"Phenanthrenes from <i>Juncus articulatus</i> with Antibacterial and Biofilm Formation Inhibitory Activity.\",\"authors\":\"Anita Barta, Agostina Salusso, Norbert Kúsz, Róbert Berkecz, Jan Schlauer, Dragica Purger, Judit Hohmann, Maria Cecilia Carpinella, Andrea Vasas\",\"doi\":\"10.1021/acs.jnatprod.4c00577\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Continuing our search for bioactive compounds in species from the Juncaceae family, <i>Juncus articulatus</i> was investigated. Ten previously undescribed phenanthrenes─articulins A-J (<b>1</b>-<b>10</b>)─and ten known compounds─juncuenin B, dehydrojuncuenin B, juncatrin B, ensifolins E, F, H, I, K, juncuenin D, and luzulin A (<b>11</b>-<b>20</b>)─along with other compounds, have been isolated and identified. The isolated compounds were evaluated for antibacterial activity against <i>Escherichia coli</i>, <i>Pseudomonas aeruginosa</i>, methicillin-susceptible <i>Staphylococcus aureus</i> (MSSA), and methicillin-resistant <i>Staphylococcus aureus</i> (MRSA). Compounds <b>12</b> and <b>14</b> exhibited the most potent activity against planktonic and sessile MSSA and MRSA with minimum inhibitory concentration (MIC) values of 15.1 μM (<b>12</b> for both bacterial strains) and 15.3 μM (<b>14</b> for both bacterial strains). Compounds <b>15</b>, <b>17</b>, and <b>18</b> also exhibited activity against both strains, although to a lower extent, with MIC values ranging from 30.0 to 56.8 μM. The inhibition of biofilm formation of these compounds was observed at 15.1-114.3 μM. This study elucidates the phenanthrene composition of <i>J. articulatus</i> and the antibacterial effect of these compounds.</p>\",\"PeriodicalId\":47,\"journal\":{\"name\":\"Journal of Natural Products \",\"volume\":\" \",\"pages\":\"2068-2080\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2024-08-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11348428/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Natural Products \",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.jnatprod.4c00577\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/8/9 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Natural Products ","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1021/acs.jnatprod.4c00577","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/9 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Phenanthrenes from Juncus articulatus with Antibacterial and Biofilm Formation Inhibitory Activity.
Continuing our search for bioactive compounds in species from the Juncaceae family, Juncus articulatus was investigated. Ten previously undescribed phenanthrenes─articulins A-J (1-10)─and ten known compounds─juncuenin B, dehydrojuncuenin B, juncatrin B, ensifolins E, F, H, I, K, juncuenin D, and luzulin A (11-20)─along with other compounds, have been isolated and identified. The isolated compounds were evaluated for antibacterial activity against Escherichia coli, Pseudomonas aeruginosa, methicillin-susceptible Staphylococcus aureus (MSSA), and methicillin-resistant Staphylococcus aureus (MRSA). Compounds 12 and 14 exhibited the most potent activity against planktonic and sessile MSSA and MRSA with minimum inhibitory concentration (MIC) values of 15.1 μM (12 for both bacterial strains) and 15.3 μM (14 for both bacterial strains). Compounds 15, 17, and 18 also exhibited activity against both strains, although to a lower extent, with MIC values ranging from 30.0 to 56.8 μM. The inhibition of biofilm formation of these compounds was observed at 15.1-114.3 μM. This study elucidates the phenanthrene composition of J. articulatus and the antibacterial effect of these compounds.
期刊介绍:
The Journal of Natural Products invites and publishes papers that make substantial and scholarly contributions to the area of natural products research. Contributions may relate to the chemistry and/or biochemistry of naturally occurring compounds or the biology of living systems from which they are obtained.
Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.
When new compounds are reported, manuscripts describing their biological activity are much preferred.
Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.