Emmanuel Tope Oluwabusola, Stephen A Jackson, Cristina Brunati, Stefanie Gackstatter, Hannah Vedder, Marianna Iorio, Gargee Chawande, Lekha Menon Margassery, Giang-Son Nguyen, David J Clarke, Rainer Ebel, Marcel Jaspars, Alan D W Dobson
{"title":"深海链霉菌B188M101生物活性卤化代谢物的集成组学发现","authors":"Emmanuel Tope Oluwabusola, Stephen A Jackson, Cristina Brunati, Stefanie Gackstatter, Hannah Vedder, Marianna Iorio, Gargee Chawande, Lekha Menon Margassery, Giang-Son Nguyen, David J Clarke, Rainer Ebel, Marcel Jaspars, Alan D W Dobson","doi":"10.3390/md23090362","DOIUrl":null,"url":null,"abstract":"<p><p>Using the one-strain-many-compounds (OSMAC) culturing approach, metabolomic studies, and bioassay-guided purification, we have isolated and characterised three new chlorinated natural products, agelolines B-D (<b>1</b>-<b>3</b>), together with two known compounds, ageloline A (<b>4</b>) and gausemycin A (<b>5</b>), which have been identified by high-resolution mass spectrometry and 1D and 2D NMR analyses. The preliminary evaluation of three small-scale extracts (M400, R358 and SGG) against the fish pathogen, <i>Aeromonas salmonicida</i> subsp. <i>achromogenes</i> KELDUR265-87, showed that the R358 extract displayed significant activity. Furthermore, the natural products (<b>1</b>-<b>5</b>) were evaluated against the fish pathogen <i>Aeromonas salmonicida</i> and human pathogens (<i>Stenotrophomonas maltophilia</i> L2125, <i>Staphylococcus aureus</i> ATCC6538P, and <i>S. pneumoniae</i> L44) using a serial dilution assay. Compound <b>3</b> displayed activity against <i>Staphylococcus aureus</i> ATCC6538P, <i>S. maltophilia</i> L2125, and <i>S. pneumoniae</i> L44 with MIC values of 6, 32, and 64 µg/mL, respectively. Interestingly, only gausemycin A (<b>5</b>) exhibited considerable inhibition against <i>A. salmonicida</i> with an MIC value of 32 µg/mL, and the activity increased by two-fold when supplemented with 0.45 mM calcium salt, while <b>2</b> and <b>4</b> showed moderate inhibition against <i>S. maltophilia</i> L2125. The biosynthetic pathways of compounds <b>1</b>-<b>4</b> were proposed. This is the first report of specific inhibition of <i>A. salmonicida</i> by <b>5</b>.</p>","PeriodicalId":18222,"journal":{"name":"Marine Drugs","volume":"23 9","pages":""},"PeriodicalIF":5.4000,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12471526/pdf/","citationCount":"0","resultStr":"{\"title\":\"Integrated Omics-Based Discovery of Bioactive Halogenated Metabolites from the Deep-Sea <i>Streptomyces</i> sp. B188M101.\",\"authors\":\"Emmanuel Tope Oluwabusola, Stephen A Jackson, Cristina Brunati, Stefanie Gackstatter, Hannah Vedder, Marianna Iorio, Gargee Chawande, Lekha Menon Margassery, Giang-Son Nguyen, David J Clarke, Rainer Ebel, Marcel Jaspars, Alan D W Dobson\",\"doi\":\"10.3390/md23090362\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Using the one-strain-many-compounds (OSMAC) culturing approach, metabolomic studies, and bioassay-guided purification, we have isolated and characterised three new chlorinated natural products, agelolines B-D (<b>1</b>-<b>3</b>), together with two known compounds, ageloline A (<b>4</b>) and gausemycin A (<b>5</b>), which have been identified by high-resolution mass spectrometry and 1D and 2D NMR analyses. The preliminary evaluation of three small-scale extracts (M400, R358 and SGG) against the fish pathogen, <i>Aeromonas salmonicida</i> subsp. <i>achromogenes</i> KELDUR265-87, showed that the R358 extract displayed significant activity. Furthermore, the natural products (<b>1</b>-<b>5</b>) were evaluated against the fish pathogen <i>Aeromonas salmonicida</i> and human pathogens (<i>Stenotrophomonas maltophilia</i> L2125, <i>Staphylococcus aureus</i> ATCC6538P, and <i>S. pneumoniae</i> L44) using a serial dilution assay. Compound <b>3</b> displayed activity against <i>Staphylococcus aureus</i> ATCC6538P, <i>S. maltophilia</i> L2125, and <i>S. pneumoniae</i> L44 with MIC values of 6, 32, and 64 µg/mL, respectively. Interestingly, only gausemycin A (<b>5</b>) exhibited considerable inhibition against <i>A. salmonicida</i> with an MIC value of 32 µg/mL, and the activity increased by two-fold when supplemented with 0.45 mM calcium salt, while <b>2</b> and <b>4</b> showed moderate inhibition against <i>S. maltophilia</i> L2125. The biosynthetic pathways of compounds <b>1</b>-<b>4</b> were proposed. 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Integrated Omics-Based Discovery of Bioactive Halogenated Metabolites from the Deep-Sea Streptomyces sp. B188M101.
Using the one-strain-many-compounds (OSMAC) culturing approach, metabolomic studies, and bioassay-guided purification, we have isolated and characterised three new chlorinated natural products, agelolines B-D (1-3), together with two known compounds, ageloline A (4) and gausemycin A (5), which have been identified by high-resolution mass spectrometry and 1D and 2D NMR analyses. The preliminary evaluation of three small-scale extracts (M400, R358 and SGG) against the fish pathogen, Aeromonas salmonicida subsp. achromogenes KELDUR265-87, showed that the R358 extract displayed significant activity. Furthermore, the natural products (1-5) were evaluated against the fish pathogen Aeromonas salmonicida and human pathogens (Stenotrophomonas maltophilia L2125, Staphylococcus aureus ATCC6538P, and S. pneumoniae L44) using a serial dilution assay. Compound 3 displayed activity against Staphylococcus aureus ATCC6538P, S. maltophilia L2125, and S. pneumoniae L44 with MIC values of 6, 32, and 64 µg/mL, respectively. Interestingly, only gausemycin A (5) exhibited considerable inhibition against A. salmonicida with an MIC value of 32 µg/mL, and the activity increased by two-fold when supplemented with 0.45 mM calcium salt, while 2 and 4 showed moderate inhibition against S. maltophilia L2125. The biosynthetic pathways of compounds 1-4 were proposed. This is the first report of specific inhibition of A. salmonicida by 5.
期刊介绍:
Marine Drugs (ISSN 1660-3397) publishes reviews, regular research papers and short notes on the research, development and production of drugs from the sea. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible, particularly synthetic procedures and characterization information for bioactive compounds. There is no restriction on the length of the experimental section.