巴西青霉和诺米曲霉菌的真菌决斗导致米托司罗胺A和Kitrinomycin A的双重诱导

IF 3.3 2区 生物学 Q2 CHEMISTRY, MEDICINAL Journal of Natural Products Pub Date : 2023-09-22 DOI:10.1021/acs.jnatprod.3c00593
Michael S. Cowled, John A. Kalaitzis, Andrew Crombie, Rachel Chen, Nicolau Sbaraini, Ernest Lacey and Andrew M. Piggott*, 
{"title":"巴西青霉和诺米曲霉菌的真菌决斗导致米托司罗胺A和Kitrinomycin A的双重诱导","authors":"Michael S. Cowled,&nbsp;John A. Kalaitzis,&nbsp;Andrew Crombie,&nbsp;Rachel Chen,&nbsp;Nicolau Sbaraini,&nbsp;Ernest Lacey and Andrew M. Piggott*,&nbsp;","doi":"10.1021/acs.jnatprod.3c00593","DOIUrl":null,"url":null,"abstract":"<p >Cocultivation of the fungi <i>Penicillium brasilianum</i> MST-FP1927 and <i>Aspergillus nomius</i> MST-FP2004 resulted in the reciprocal induction of two new compounds, miktospiromide A (<b>1</b>) from <i>A</i>. <i>nomius</i> and kitrinomycin A (<b>2</b>) from <i>P</i>. <i>brasilianum</i>. A third new compound, kitrinomycin B (<b>3</b>), was also identified from an axenic culture of <i>P</i>. <i>brasilianum</i>, along with the previously reported compounds austalide K (<b>4</b>), 17<i>S</i>-dihydroaustalide K (<b>5</b>), verruculogen (<b>6</b>), and fumitremorgin B (<b>7</b>). The structures of <b>1</b>–<b>3</b> were elucidated by detailed spectroscopic analysis and DFT calculations, while <b>4</b>–<b>7</b> were identified by comparison to authentic standards. The genome of <i>A</i>. <i>nomius</i> MST-FP2004 was sequenced, and a putative biosynthetic gene cluster for <b>1</b> was identified. Compound <b>2</b> showed activity against murine melanoma NS-1 cells (LD<sub>99</sub> 7.8 μM) and the bovine parasite <i>Tritrichomonas foetus</i> (LD<sub>99</sub> 4.8 μM).</p>","PeriodicalId":47,"journal":{"name":"Journal of Natural Products ","volume":"86 10","pages":"2398–2406"},"PeriodicalIF":3.3000,"publicationDate":"2023-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Fungal Duel between Penicillium brasilianum and Aspergillus nomius Results in Dual Induction of Miktospiromide A and Kitrinomycin A\",\"authors\":\"Michael S. Cowled,&nbsp;John A. Kalaitzis,&nbsp;Andrew Crombie,&nbsp;Rachel Chen,&nbsp;Nicolau Sbaraini,&nbsp;Ernest Lacey and Andrew M. Piggott*,&nbsp;\",\"doi\":\"10.1021/acs.jnatprod.3c00593\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Cocultivation of the fungi <i>Penicillium brasilianum</i> MST-FP1927 and <i>Aspergillus nomius</i> MST-FP2004 resulted in the reciprocal induction of two new compounds, miktospiromide A (<b>1</b>) from <i>A</i>. <i>nomius</i> and kitrinomycin A (<b>2</b>) from <i>P</i>. <i>brasilianum</i>. A third new compound, kitrinomycin B (<b>3</b>), was also identified from an axenic culture of <i>P</i>. <i>brasilianum</i>, along with the previously reported compounds austalide K (<b>4</b>), 17<i>S</i>-dihydroaustalide K (<b>5</b>), verruculogen (<b>6</b>), and fumitremorgin B (<b>7</b>). The structures of <b>1</b>–<b>3</b> were elucidated by detailed spectroscopic analysis and DFT calculations, while <b>4</b>–<b>7</b> were identified by comparison to authentic standards. The genome of <i>A</i>. <i>nomius</i> MST-FP2004 was sequenced, and a putative biosynthetic gene cluster for <b>1</b> was identified. Compound <b>2</b> showed activity against murine melanoma NS-1 cells (LD<sub>99</sub> 7.8 μM) and the bovine parasite <i>Tritrichomonas foetus</i> (LD<sub>99</sub> 4.8 μM).</p>\",\"PeriodicalId\":47,\"journal\":{\"name\":\"Journal of Natural Products \",\"volume\":\"86 10\",\"pages\":\"2398–2406\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2023-09-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Natural Products \",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.jnatprod.3c00593\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Natural Products ","FirstCategoryId":"99","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jnatprod.3c00593","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

摘要

巴西青霉MST-FP1927和挪威曲霉菌MST-FP2004的共培养导致两种新化合物的相互诱导,即来自挪威曲霉菌的米克螺旋酰胺A(1)和来自巴西曲霉菌的基特里霉素A(2)。第三种新化合物,基特里霉素B(3),也从巴西乳杆菌的无菌培养物中鉴定出来,以及先前报道的化合物austalide K(4)、17S二氢austalid K(5)、疣原(6)和烟精B(7)。1-3的结构通过详细的光谱分析和DFT计算得到了阐明,而4-7的结构通过与真实标准的比较得到了鉴定。对A.nomius MST-FP2004的基因组进行了测序,并鉴定了1的生物合成基因簇。化合物2显示出对小鼠黑色素瘤NS-1细胞(LD99 7.8μM)和牛寄生虫Tritrichomonas胎儿(LD99 4.8μM)的活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Fungal Duel between Penicillium brasilianum and Aspergillus nomius Results in Dual Induction of Miktospiromide A and Kitrinomycin A

Cocultivation of the fungi Penicillium brasilianum MST-FP1927 and Aspergillus nomius MST-FP2004 resulted in the reciprocal induction of two new compounds, miktospiromide A (1) from A. nomius and kitrinomycin A (2) from P. brasilianum. A third new compound, kitrinomycin B (3), was also identified from an axenic culture of P. brasilianum, along with the previously reported compounds austalide K (4), 17S-dihydroaustalide K (5), verruculogen (6), and fumitremorgin B (7). The structures of 13 were elucidated by detailed spectroscopic analysis and DFT calculations, while 47 were identified by comparison to authentic standards. The genome of A. nomius MST-FP2004 was sequenced, and a putative biosynthetic gene cluster for 1 was identified. Compound 2 showed activity against murine melanoma NS-1 cells (LD99 7.8 μM) and the bovine parasite Tritrichomonas foetus (LD99 4.8 μM).

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
9.10
自引率
5.90%
发文量
294
审稿时长
2.3 months
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.
期刊最新文献
Discovery of Sporachelins by Genome Mining of a Micromonospora Strain. In Vitro Biological Target Screening and Colloidal Aggregation of Minor Cannabinoids. Tyrosinase Inhibitory Properties of Compounds Isolated from Artocarpus integer Roots. Discovery, Biosynthesis, Total Synthesis, and Biological Activities of Solanapyrones: [4 + 2] Cycloaddition-Derived Polyketides of Fungal Origin. Discovery of Chalcone Derivatives as Bifunctional Molecules with Anti-SARS-CoV-2 and Anti-inflammatory Activities.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1