Yu-Ping Wu, Hua-Yin Liu, Heng Yao, Gao-Kun Zhao, Yu-Long Su, Xue-Ru Song, Wei Li, Wei-Guang Wang, Qiu-Fen Hu, Ling-Duo Bu, Guang-Hui Kong
{"title":"从烟曲霉内生真菌中提取的两种新型抗菌苯并氮卓类药物","authors":"Yu-Ping Wu, Hua-Yin Liu, Heng Yao, Gao-Kun Zhao, Yu-Long Su, Xue-Ru Song, Wei Li, Wei-Guang Wang, Qiu-Fen Hu, Ling-Duo Bu, Guang-Hui Kong","doi":"10.1007/s10600-025-04746-8","DOIUrl":null,"url":null,"abstract":"<p>In this study, two new benzoazepines (<b>1</b> and <b>2</b>), together with five known analogs (<b>3–7</b>) were isolated from the cigar-tobacco-derived endophytic Aspergillus fumigatus. Their structures were determined by means of HR-ESI-MS and extensive 1D and 2D NMR spectroscopic studies. All compounds were evaluated for their antibacterial activities against five nitrosobacteria strains <i>Nitrosomonas communis</i>, <i>Nitrosomonas nitrosa</i>, <i>Nitrosospira multiformis</i>, <i>Nitrobacter winogradskyi</i>, and <i>Nitrospira inopinata</i>. Interestingly, compounds <b>1–7</b> exhibited notable antibacterial activity with bacteriostatic diameters within the range 13.8 ± 1.9–26.3 ± 2.5 mm against five nitrosobacteria strains, and most of the bacteriostatic diameters are higher than that of positive controls. Owing to the nitrosobacteria having the ability to convert nitrogen components into nitrite in tobacco, and then converting to tobacco-specific nitrosamines (TSNAs), the above compounds have the potential to reduce TSNAs in tobacco by inhibiting nitrosobacteria during the fermentation process of tobacco leaves.</p>","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"61 4","pages":"737 - 741"},"PeriodicalIF":0.9000,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Two New Antibacterial Benzoazepines from a Cigar-Tobacco-Derived Endophytic Aspergillus fumigatus\",\"authors\":\"Yu-Ping Wu, Hua-Yin Liu, Heng Yao, Gao-Kun Zhao, Yu-Long Su, Xue-Ru Song, Wei Li, Wei-Guang Wang, Qiu-Fen Hu, Ling-Duo Bu, Guang-Hui Kong\",\"doi\":\"10.1007/s10600-025-04746-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>In this study, two new benzoazepines (<b>1</b> and <b>2</b>), together with five known analogs (<b>3–7</b>) were isolated from the cigar-tobacco-derived endophytic Aspergillus fumigatus. Their structures were determined by means of HR-ESI-MS and extensive 1D and 2D NMR spectroscopic studies. All compounds were evaluated for their antibacterial activities against five nitrosobacteria strains <i>Nitrosomonas communis</i>, <i>Nitrosomonas nitrosa</i>, <i>Nitrosospira multiformis</i>, <i>Nitrobacter winogradskyi</i>, and <i>Nitrospira inopinata</i>. Interestingly, compounds <b>1–7</b> exhibited notable antibacterial activity with bacteriostatic diameters within the range 13.8 ± 1.9–26.3 ± 2.5 mm against five nitrosobacteria strains, and most of the bacteriostatic diameters are higher than that of positive controls. Owing to the nitrosobacteria having the ability to convert nitrogen components into nitrite in tobacco, and then converting to tobacco-specific nitrosamines (TSNAs), the above compounds have the potential to reduce TSNAs in tobacco by inhibiting nitrosobacteria during the fermentation process of tobacco leaves.</p>\",\"PeriodicalId\":514,\"journal\":{\"name\":\"Chemistry of Natural Compounds\",\"volume\":\"61 4\",\"pages\":\"737 - 741\"},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2025-07-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemistry of Natural Compounds\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s10600-025-04746-8\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry of Natural Compounds","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s10600-025-04746-8","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Two New Antibacterial Benzoazepines from a Cigar-Tobacco-Derived Endophytic Aspergillus fumigatus
In this study, two new benzoazepines (1 and 2), together with five known analogs (3–7) were isolated from the cigar-tobacco-derived endophytic Aspergillus fumigatus. Their structures were determined by means of HR-ESI-MS and extensive 1D and 2D NMR spectroscopic studies. All compounds were evaluated for their antibacterial activities against five nitrosobacteria strains Nitrosomonas communis, Nitrosomonas nitrosa, Nitrosospira multiformis, Nitrobacter winogradskyi, and Nitrospira inopinata. Interestingly, compounds 1–7 exhibited notable antibacterial activity with bacteriostatic diameters within the range 13.8 ± 1.9–26.3 ± 2.5 mm against five nitrosobacteria strains, and most of the bacteriostatic diameters are higher than that of positive controls. Owing to the nitrosobacteria having the ability to convert nitrogen components into nitrite in tobacco, and then converting to tobacco-specific nitrosamines (TSNAs), the above compounds have the potential to reduce TSNAs in tobacco by inhibiting nitrosobacteria during the fermentation process of tobacco leaves.
期刊介绍:
Chemistry of Natural Compounds publishes reviews and general articles about the structure of different classes of natural compounds, the chemical characteristics of botanical families, genus, and species, to establish the comparative laws and connection between physiological activity and the structure of substances.