Kavaratamides:利用比较化学地理分析法从海洋蓝藻 Moorena bouillonii 中发现线性脂十二肽。

IF 3.6 2区 生物学 Q2 CHEMISTRY, MEDICINAL
Byeol Ryu, Evgenia Glukhov, Thaiz R. Teixeira, Conor R. Caffrey, Saranya Madiyan, Valsamma Joseph, Nicole E. Avalon, Christopher A. Leber, C. Benjamin Naman and William H. Gerwick*, 
{"title":"Kavaratamides:利用比较化学地理分析法从海洋蓝藻 Moorena bouillonii 中发现线性脂十二肽。","authors":"Byeol Ryu,&nbsp;Evgenia Glukhov,&nbsp;Thaiz R. Teixeira,&nbsp;Conor R. Caffrey,&nbsp;Saranya Madiyan,&nbsp;Valsamma Joseph,&nbsp;Nicole E. Avalon,&nbsp;Christopher A. Leber,&nbsp;C. Benjamin Naman and William H. Gerwick*,&nbsp;","doi":"10.1021/acs.jnatprod.4c00242","DOIUrl":null,"url":null,"abstract":"<p >Kavaratamide A (<b>1</b>), a new linear lipodepsipeptide possessing an unusual isopropyl-<i>O</i>-methylpyrrolinone moiety, was discovered from the tropical marine filamentous cyanobacterium <i>Moorena bouillonii</i> collected from Kavaratti, India. A comparative chemogeographic analysis of <i>M</i>. <i>bouillonii</i> collected from six different geographical regions led to the prioritized isolation of this metabolite from India as distinctive among our data sets. AI-based structure annotation tools, including SMART 2.1 and DeepSAT, accelerated the structure elucidation by providing useful structural clues, and the full planar structure was elucidated based on comprehensive HRMS, MS/MS fragmentation, and NMR data interpretation. Subsequently, the absolute configuration of <b>1</b> was determined using advanced Marfey’s analysis, modified Mosher’s ester derivatization, and chiral-phase HPLC. The structures of kavaratamides B (<b>2</b>) and C (<b>3</b>) are proposed based on a detailed analysis of their MS/MS fragmentations. The biological activity of kavaratamide A was also investigated and found to show moderate cytotoxicity to the D283-medullablastoma cell line.</p>","PeriodicalId":47,"journal":{"name":"Journal of Natural Products ","volume":"87 6","pages":"1601–1610"},"PeriodicalIF":3.6000,"publicationDate":"2024-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/epdf/10.1021/acs.jnatprod.4c00242","citationCount":"0","resultStr":"{\"title\":\"The Kavaratamides: Discovery of Linear Lipodepsipeptides from the Marine Cyanobacterium Moorena bouillonii Using a Comparative Chemogeographic Analysis\",\"authors\":\"Byeol Ryu,&nbsp;Evgenia Glukhov,&nbsp;Thaiz R. Teixeira,&nbsp;Conor R. Caffrey,&nbsp;Saranya Madiyan,&nbsp;Valsamma Joseph,&nbsp;Nicole E. Avalon,&nbsp;Christopher A. Leber,&nbsp;C. Benjamin Naman and William H. Gerwick*,&nbsp;\",\"doi\":\"10.1021/acs.jnatprod.4c00242\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Kavaratamide A (<b>1</b>), a new linear lipodepsipeptide possessing an unusual isopropyl-<i>O</i>-methylpyrrolinone moiety, was discovered from the tropical marine filamentous cyanobacterium <i>Moorena bouillonii</i> collected from Kavaratti, India. A comparative chemogeographic analysis of <i>M</i>. <i>bouillonii</i> collected from six different geographical regions led to the prioritized isolation of this metabolite from India as distinctive among our data sets. AI-based structure annotation tools, including SMART 2.1 and DeepSAT, accelerated the structure elucidation by providing useful structural clues, and the full planar structure was elucidated based on comprehensive HRMS, MS/MS fragmentation, and NMR data interpretation. Subsequently, the absolute configuration of <b>1</b> was determined using advanced Marfey’s analysis, modified Mosher’s ester derivatization, and chiral-phase HPLC. The structures of kavaratamides B (<b>2</b>) and C (<b>3</b>) are proposed based on a detailed analysis of their MS/MS fragmentations. The biological activity of kavaratamide A was also investigated and found to show moderate cytotoxicity to the D283-medullablastoma cell line.</p>\",\"PeriodicalId\":47,\"journal\":{\"name\":\"Journal of Natural Products \",\"volume\":\"87 6\",\"pages\":\"1601–1610\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2024-06-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.acs.org/doi/epdf/10.1021/acs.jnatprod.4c00242\",\"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.4c00242\",\"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.4c00242","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

Kavaratamide A (1)是一种新的线性脂二肽,具有一个不寻常的异丙基-O-甲基吡咯烷酮分子,是从印度卡瓦拉蒂采集的热带海洋丝状蓝藻 Moorena bouillonii 中发现的。通过对从六个不同地理区域收集的 M. bouillonii 进行化学地理学比较分析,在我们的数据集中优先从印度分离出了这种独特的代谢物。基于人工智能的结构注释工具,包括 SMART 2.1 和 DeepSAT,通过提供有用的结构线索加速了结构的阐明,并根据全面的 HRMS、MS/MS 片段和 NMR 数据解释阐明了完整的平面结构。随后,利用先进的马菲分析法、改进的莫舍酯衍生法和手性相高效液相色谱法确定了 1 的绝对构型。根据对其 MS/MS 片段的详细分析,提出了卡伐他胺 B (2) 和 C (3) 的结构。此外,还对卡伐他胺 A 的生物活性进行了研究,发现它对 D283 髓母细胞瘤细胞系具有适度的细胞毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Kavaratamides: Discovery of Linear Lipodepsipeptides from the Marine Cyanobacterium Moorena bouillonii Using a Comparative Chemogeographic Analysis

The Kavaratamides: Discovery of Linear Lipodepsipeptides from the Marine Cyanobacterium Moorena bouillonii Using a Comparative Chemogeographic Analysis

Kavaratamide A (1), a new linear lipodepsipeptide possessing an unusual isopropyl-O-methylpyrrolinone moiety, was discovered from the tropical marine filamentous cyanobacterium Moorena bouillonii collected from Kavaratti, India. A comparative chemogeographic analysis of M. bouillonii collected from six different geographical regions led to the prioritized isolation of this metabolite from India as distinctive among our data sets. AI-based structure annotation tools, including SMART 2.1 and DeepSAT, accelerated the structure elucidation by providing useful structural clues, and the full planar structure was elucidated based on comprehensive HRMS, MS/MS fragmentation, and NMR data interpretation. Subsequently, the absolute configuration of 1 was determined using advanced Marfey’s analysis, modified Mosher’s ester derivatization, and chiral-phase HPLC. The structures of kavaratamides B (2) and C (3) are proposed based on a detailed analysis of their MS/MS fragmentations. The biological activity of kavaratamide A was also investigated and found to show moderate cytotoxicity to the D283-medullablastoma cell line.

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.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信