{"title":"壳青霉与费青霉共培养的线性聚酮。","authors":"Guihong Yu, Peng Sun, Reyilamu Aierken, Chunxiao Sun, Zhenzhen Zhang, Qian Che, Guojian Zhang, Tianjiao Zhu, Qianqun Gu, Mingyu Li, Dehai Li","doi":"10.1007/s42995-021-00125-8","DOIUrl":null,"url":null,"abstract":"<p><p>Two new polyketides, penifellutins A (<b>1</b>) and B (<b>2</b>), possessing a 22 carbon linear skeleton, were isolated from a co-culture of the deep-sea-derived fungi <i>Penicillium crustosum</i> PRB-2 and <i>Penicillium fellutanum</i> HDN14-323. Meanwhile, two esterification products of <b>1</b>, penifellutins C (<b>3</b>) and D (<b>4</b>), were obtained because compound <b>1</b> could be esterified spontaneously when stored in methanol. Their configurations were difficult to determine because of chiral central crowdedness, structural flexibility and instability. As such, we solved this issue by comprehensively using Mo<sub>2</sub>(OAc)<sub>4</sub>-based CD experiments, density functional theory calculation of <sup>13</sup>C NMR, DP4 + probability analysis and many chemical reactions, including making acetonide derivative, Mosher's method, PGME method, etc. Compounds <b>1</b> and <b>2</b> show obvious inhibitory activity on the liver hyperplasia of zebrafish larvae at a concentration of 10 μmol/L, while <b>3</b> and <b>4</b> show no activity, indicating that two carboxyls in the structure are important active sites.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s42995-021-00125-8.</p>","PeriodicalId":53218,"journal":{"name":"Marine Life Science & Technology","volume":"4 2","pages":"237-244"},"PeriodicalIF":5.8000,"publicationDate":"2022-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10077197/pdf/42995_2021_Article_125.pdf","citationCount":"5","resultStr":"{\"title\":\"Linear polyketides produced by co-culture of <i>Penicillium crustosum</i> and <i>Penicillium fellutanum</i>.\",\"authors\":\"Guihong Yu, Peng Sun, Reyilamu Aierken, Chunxiao Sun, Zhenzhen Zhang, Qian Che, Guojian Zhang, Tianjiao Zhu, Qianqun Gu, Mingyu Li, Dehai Li\",\"doi\":\"10.1007/s42995-021-00125-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Two new polyketides, penifellutins A (<b>1</b>) and B (<b>2</b>), possessing a 22 carbon linear skeleton, were isolated from a co-culture of the deep-sea-derived fungi <i>Penicillium crustosum</i> PRB-2 and <i>Penicillium fellutanum</i> HDN14-323. Meanwhile, two esterification products of <b>1</b>, penifellutins C (<b>3</b>) and D (<b>4</b>), were obtained because compound <b>1</b> could be esterified spontaneously when stored in methanol. Their configurations were difficult to determine because of chiral central crowdedness, structural flexibility and instability. As such, we solved this issue by comprehensively using Mo<sub>2</sub>(OAc)<sub>4</sub>-based CD experiments, density functional theory calculation of <sup>13</sup>C NMR, DP4 + probability analysis and many chemical reactions, including making acetonide derivative, Mosher's method, PGME method, etc. Compounds <b>1</b> and <b>2</b> show obvious inhibitory activity on the liver hyperplasia of zebrafish larvae at a concentration of 10 μmol/L, while <b>3</b> and <b>4</b> show no activity, indicating that two carboxyls in the structure are important active sites.</p><p><strong>Supplementary information: </strong>The online version contains supplementary material available at 10.1007/s42995-021-00125-8.</p>\",\"PeriodicalId\":53218,\"journal\":{\"name\":\"Marine Life Science & Technology\",\"volume\":\"4 2\",\"pages\":\"237-244\"},\"PeriodicalIF\":5.8000,\"publicationDate\":\"2022-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10077197/pdf/42995_2021_Article_125.pdf\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Marine Life Science & Technology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s42995-021-00125-8\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MARINE & FRESHWATER BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Marine Life Science & Technology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s42995-021-00125-8","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MARINE & FRESHWATER BIOLOGY","Score":null,"Total":0}
Linear polyketides produced by co-culture of Penicillium crustosum and Penicillium fellutanum.
Two new polyketides, penifellutins A (1) and B (2), possessing a 22 carbon linear skeleton, were isolated from a co-culture of the deep-sea-derived fungi Penicillium crustosum PRB-2 and Penicillium fellutanum HDN14-323. Meanwhile, two esterification products of 1, penifellutins C (3) and D (4), were obtained because compound 1 could be esterified spontaneously when stored in methanol. Their configurations were difficult to determine because of chiral central crowdedness, structural flexibility and instability. As such, we solved this issue by comprehensively using Mo2(OAc)4-based CD experiments, density functional theory calculation of 13C NMR, DP4 + probability analysis and many chemical reactions, including making acetonide derivative, Mosher's method, PGME method, etc. Compounds 1 and 2 show obvious inhibitory activity on the liver hyperplasia of zebrafish larvae at a concentration of 10 μmol/L, while 3 and 4 show no activity, indicating that two carboxyls in the structure are important active sites.
Supplementary information: The online version contains supplementary material available at 10.1007/s42995-021-00125-8.
期刊介绍:
Marine Life Science & Technology (MLST), established in 2019, is dedicated to publishing original research papers that unveil new discoveries and theories spanning a wide spectrum of life sciences and technologies. This includes fundamental biology, fisheries science and technology, medicinal bioresources, food science, biotechnology, ecology, and environmental biology, with a particular focus on marine habitats.
The journal is committed to nurturing synergistic interactions among these diverse disciplines, striving to advance multidisciplinary approaches within the scientific field. It caters to a readership comprising biological scientists, aquaculture researchers, marine technologists, biological oceanographers, and ecologists.