Chaitrali Shevkar, Ramani Weerasinghe, Gurudutt Dubey, Renuka N Attanayake, Gothamie Weerakoon, Kiran Kalia, Priyani Paranagama, Abhijeet S Kate
{"title":"红树伴生地衣多核小孢子内生真菌黄孢Phanerochaete chrysosporium抗癌铅的生物勘探。","authors":"Chaitrali Shevkar, Ramani Weerasinghe, Gurudutt Dubey, Renuka N Attanayake, Gothamie Weerakoon, Kiran Kalia, Priyani Paranagama, Abhijeet S Kate","doi":"10.1007/s12088-024-01424-1","DOIUrl":null,"url":null,"abstract":"<p><p>Endolichenic fungi (ELF) are gaining attention as a promising source for novel cytotoxic compounds. In this study, lichens <i>Bactrospora</i> <i>myriadea</i> and <i>Arthonia</i> <i>antillarum</i>, collected from the mangroves of Negombo Lagoon in Sri Lanka, were examined to identify their associated ELFs. <i>Phanerochaete</i> <i>chrysosporium</i>, <i>Lasiodiplodia</i> <i>theobromae</i>, and <i>Xylaria</i> <i>feejeensis</i> were isolated from <i>B</i>. <i>myriadea</i>, while <i>Xylaria</i> <i>psidii</i>, <i>Daldinia</i> <i>eschscholtzii</i>, and <i>Nodulisporium</i> sp. were obtained from <i>A</i>. <i>antillarum</i>. The ethyl acetate extracts of these ELFs were screened for cytotoxic activity against the MCF-7 cell line, with <i>P</i>. <i>chrysosporium</i> extract showing potent cytotoxicity. The purified compounds from this extract were identified as spirolaxine (<b>1</b>), phanerosporic acid (<b>2</b>), and 5-(14-hydroxypentadecyl)-resorcinol (<b>3</b>). Their structures were determined using Fourier Transform Infrared, Nuclear Magnetic Resonance spectroscopy and Liquid Chromatography-High Resolution mass spectrometry, while their absolute configurations were established through circular dichroism and time-dependent density functional theory calculations. The compounds demonstrated moderate cytotoxic activity against human breast (MCF-7), oral (CAL-27), and lung (A549) cancer cell lines. Compound <b>1</b> exhibited the strongest cytotoxicity against oral cancer, with an IC<sub>50</sub> value of 10.62 ± 0.02 µM. Compound <b>2</b> was effective against both MCF-7 and A549 cell lines, with IC<sub>50</sub> values of 9.86 ± 0.02 µM and 6.66 ± 0.04 µM, respectively. This is the first report of compound <b>3</b> from a natural source, as it was previously documented only as a semi-synthetic derivative of compound <b>2</b>. The study highlights the potential of the ELF <i>P</i>. <i>chrysosporium</i> to produce cytotoxic secondary metabolites.</p><p><strong>Graphical abstract: </strong></p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s12088-024-01424-1.</p>","PeriodicalId":13316,"journal":{"name":"Indian Journal of Microbiology","volume":"65 2","pages":"1037-1046"},"PeriodicalIF":2.1000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12246278/pdf/","citationCount":"0","resultStr":"{\"title\":\"Bioprospecting of Endolichenic Fungus <i>Phanerochaete</i> <i>chrysosporium</i> from Mangrove Associated Lichen <i>Bactrospora</i> <i>myriadea</i> for Anticancer Leads.\",\"authors\":\"Chaitrali Shevkar, Ramani Weerasinghe, Gurudutt Dubey, Renuka N Attanayake, Gothamie Weerakoon, Kiran Kalia, Priyani Paranagama, Abhijeet S Kate\",\"doi\":\"10.1007/s12088-024-01424-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Endolichenic fungi (ELF) are gaining attention as a promising source for novel cytotoxic compounds. In this study, lichens <i>Bactrospora</i> <i>myriadea</i> and <i>Arthonia</i> <i>antillarum</i>, collected from the mangroves of Negombo Lagoon in Sri Lanka, were examined to identify their associated ELFs. <i>Phanerochaete</i> <i>chrysosporium</i>, <i>Lasiodiplodia</i> <i>theobromae</i>, and <i>Xylaria</i> <i>feejeensis</i> were isolated from <i>B</i>. <i>myriadea</i>, while <i>Xylaria</i> <i>psidii</i>, <i>Daldinia</i> <i>eschscholtzii</i>, and <i>Nodulisporium</i> sp. were obtained from <i>A</i>. <i>antillarum</i>. The ethyl acetate extracts of these ELFs were screened for cytotoxic activity against the MCF-7 cell line, with <i>P</i>. <i>chrysosporium</i> extract showing potent cytotoxicity. The purified compounds from this extract were identified as spirolaxine (<b>1</b>), phanerosporic acid (<b>2</b>), and 5-(14-hydroxypentadecyl)-resorcinol (<b>3</b>). Their structures were determined using Fourier Transform Infrared, Nuclear Magnetic Resonance spectroscopy and Liquid Chromatography-High Resolution mass spectrometry, while their absolute configurations were established through circular dichroism and time-dependent density functional theory calculations. The compounds demonstrated moderate cytotoxic activity against human breast (MCF-7), oral (CAL-27), and lung (A549) cancer cell lines. Compound <b>1</b> exhibited the strongest cytotoxicity against oral cancer, with an IC<sub>50</sub> value of 10.62 ± 0.02 µM. Compound <b>2</b> was effective against both MCF-7 and A549 cell lines, with IC<sub>50</sub> values of 9.86 ± 0.02 µM and 6.66 ± 0.04 µM, respectively. This is the first report of compound <b>3</b> from a natural source, as it was previously documented only as a semi-synthetic derivative of compound <b>2</b>. The study highlights the potential of the ELF <i>P</i>. <i>chrysosporium</i> to produce cytotoxic secondary metabolites.</p><p><strong>Graphical abstract: </strong></p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s12088-024-01424-1.</p>\",\"PeriodicalId\":13316,\"journal\":{\"name\":\"Indian Journal of Microbiology\",\"volume\":\"65 2\",\"pages\":\"1037-1046\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2025-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12246278/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Indian Journal of Microbiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1007/s12088-024-01424-1\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/12/11 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian Journal of Microbiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s12088-024-01424-1","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/12/11 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
Bioprospecting of Endolichenic Fungus Phanerochaetechrysosporium from Mangrove Associated Lichen Bactrosporamyriadea for Anticancer Leads.
Endolichenic fungi (ELF) are gaining attention as a promising source for novel cytotoxic compounds. In this study, lichens Bactrosporamyriadea and Arthoniaantillarum, collected from the mangroves of Negombo Lagoon in Sri Lanka, were examined to identify their associated ELFs. Phanerochaetechrysosporium, Lasiodiplodiatheobromae, and Xylariafeejeensis were isolated from B. myriadea, while Xylariapsidii, Daldiniaeschscholtzii, and Nodulisporium sp. were obtained from A. antillarum. The ethyl acetate extracts of these ELFs were screened for cytotoxic activity against the MCF-7 cell line, with P. chrysosporium extract showing potent cytotoxicity. The purified compounds from this extract were identified as spirolaxine (1), phanerosporic acid (2), and 5-(14-hydroxypentadecyl)-resorcinol (3). Their structures were determined using Fourier Transform Infrared, Nuclear Magnetic Resonance spectroscopy and Liquid Chromatography-High Resolution mass spectrometry, while their absolute configurations were established through circular dichroism and time-dependent density functional theory calculations. The compounds demonstrated moderate cytotoxic activity against human breast (MCF-7), oral (CAL-27), and lung (A549) cancer cell lines. Compound 1 exhibited the strongest cytotoxicity against oral cancer, with an IC50 value of 10.62 ± 0.02 µM. Compound 2 was effective against both MCF-7 and A549 cell lines, with IC50 values of 9.86 ± 0.02 µM and 6.66 ± 0.04 µM, respectively. This is the first report of compound 3 from a natural source, as it was previously documented only as a semi-synthetic derivative of compound 2. The study highlights the potential of the ELF P. chrysosporium to produce cytotoxic secondary metabolites.
Graphical abstract:
Supplementary information: The online version contains supplementary material available at 10.1007/s12088-024-01424-1.
期刊介绍:
Indian Journal of Microbiology is the official organ of the Association of Microbiologists of India (AMI). It publishes full-length papers, short communication reviews and mini reviews on all aspects of microbiological research, published quarterly (March, June, September and December). Areas of special interest include agricultural, food, environmental, industrial, medical, pharmaceutical, veterinary and molecular microbiology.