Induced production of defensive secondary metabolites from Aspergillus fumigatiaffinis by co-culture with Aspergillus alabamensis

IF 3.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Zhibo Hu , Haishan Cui , Qiang Wang , Cheng Li , Senhua Chen , Zhizeng Gao , Lan Liu , Bo Peng , Jing Li
{"title":"Induced production of defensive secondary metabolites from Aspergillus fumigatiaffinis by co-culture with Aspergillus alabamensis","authors":"Zhibo Hu ,&nbsp;Haishan Cui ,&nbsp;Qiang Wang ,&nbsp;Cheng Li ,&nbsp;Senhua Chen ,&nbsp;Zhizeng Gao ,&nbsp;Lan Liu ,&nbsp;Bo Peng ,&nbsp;Jing Li","doi":"10.1016/j.phytochem.2024.114187","DOIUrl":null,"url":null,"abstract":"<div><p>Seven previously undescribed compounds, including four diketomorpholine alkaloids (<strong>1</strong>‒<strong>4</strong>), one indole diketopiperazine alkaloid (<strong>9</strong>), one chromone (<strong>10</strong>), and one benzoic acid derivative (<strong>13</strong>), and nine known compounds (<strong>5</strong>–<strong>8</strong>, <strong>11</strong>, <strong>12</strong>, and <strong>14</strong>–<strong>16</strong>) were isolated from two different fungal sources. Nine of these metabolites (<strong>1</strong>–<strong>9</strong>) were obtained from a seagrass-derived <em>Aspergillus alabamensis</em> SYSU-6778, while the others were obtained from a mixed culture of <em>A. alabamensis</em> SYSU-6778 and a co-isolated fungus <em>A</em>. <em>fumigatiaffinis</em> SYSU-6786. The chemical structures of the compounds were deduced via spectroscopic techniques (including HRESIMS, 1D and 2D NMR), chemical reactions, and ECD calculations. It is worth noting that compound <strong>10</strong> was identified as a defensive secondary metabolite of strain SYSU-6786, produced through the induction of compound <strong>8</strong> under co-culture conditions. Compounds <strong>3</strong> and <strong>4</strong> possessed a naturally rare isotryptophan core. Moreover, compounds <strong>1</strong> and <strong>2</strong> exhibited potent inhibitory activities against fish pathogenic bacterium <em>Edwardsiella ictalurid,</em> with minimum inhibitory concentration values of 10.0 μg/mL for both compounds.</p></div>","PeriodicalId":20170,"journal":{"name":"Phytochemistry","volume":null,"pages":null},"PeriodicalIF":3.2000,"publicationDate":"2024-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0031942224002243","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Seven previously undescribed compounds, including four diketomorpholine alkaloids (14), one indole diketopiperazine alkaloid (9), one chromone (10), and one benzoic acid derivative (13), and nine known compounds (58, 11, 12, and 1416) were isolated from two different fungal sources. Nine of these metabolites (19) were obtained from a seagrass-derived Aspergillus alabamensis SYSU-6778, while the others were obtained from a mixed culture of A. alabamensis SYSU-6778 and a co-isolated fungus A. fumigatiaffinis SYSU-6786. The chemical structures of the compounds were deduced via spectroscopic techniques (including HRESIMS, 1D and 2D NMR), chemical reactions, and ECD calculations. It is worth noting that compound 10 was identified as a defensive secondary metabolite of strain SYSU-6786, produced through the induction of compound 8 under co-culture conditions. Compounds 3 and 4 possessed a naturally rare isotryptophan core. Moreover, compounds 1 and 2 exhibited potent inhibitory activities against fish pathogenic bacterium Edwardsiella ictalurid, with minimum inhibitory concentration values of 10.0 μg/mL for both compounds.

Abstract Image

通过与 alabamensis 曲霉共培养诱导烟曲霉产生防御性次生代谢物。
从两种不同的真菌来源中分离出了七种以前未曾描述过的化合物,包括四种二酮吗啉生物碱(1-4)、一种吲哚二酮哌嗪生物碱(9)、一种色酮(10)和一种苯甲酸衍生物(13),以及九种已知化合物(5-8、11、12 和 14-16)。其中九种代谢物(1-9)是从海草衍生的 alabamensis 黑曲霉 SYSU-6778 中获得的,而其他代谢物则是从 alabamensis 黑曲霉 SYSU-6778 和共分离真菌 A. fumigatiaffinis SYSU-6786 的混合培养物中获得的。化合物的化学结构是通过光谱技术(包括 HRESIMS、一维和二维核磁共振)、化学反应和 ECD 计算推导出来的。值得注意的是,化合物 10 被鉴定为 SYSU-6786 菌株的一种防御性次级代谢产物,是在共培养条件下通过诱导化合物 8 而产生的。化合物 3 和 4 具有天然稀有的异色氨酸核心。此外,化合物 1 和 2 对鱼类病原菌 Edwardsiella ictalurid 具有很强的抑制活性,两种化合物的最低抑制浓度值均为 10.0 μg/mL。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Phytochemistry
Phytochemistry 生物-植物科学
CiteScore
6.40
自引率
7.90%
发文量
443
审稿时长
39 days
期刊介绍: Phytochemistry is a leading international journal publishing studies of plant chemistry, biochemistry, molecular biology and genetics, structure and bioactivities of phytochemicals, including ''-omics'' and bioinformatics/computational biology approaches. Phytochemistry is a primary source for papers dealing with phytochemicals, especially reports concerning their biosynthesis, regulation, and biological properties both in planta and as bioactive principles. Articles are published online as soon as possible as Articles-in-Press and in 12 volumes per year. Occasional topic-focussed special issues are published composed of papers from invited authors.
文献相关原料
公司名称 产品信息 采购帮参考价格
阿拉丁 Florfenicol
¥20.00~¥217704.00
上海源叶 kanamycin
¥180.00~¥15015.00
阿拉丁 Triadimefon
¥89.00~¥11920.00
×
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:481959085
Book学术官方微信