Importance of benzoyltransferase GcnE and lysine benzoylation of alcohol dehydrogenase AdhB in pathogenesis and aflatoxin production in Aspergillus flavus.

IF 5.1 1区 生物学 Q1 MICROBIOLOGY mBio Pub Date : 2024-11-27 DOI:10.1128/mbio.02665-24
Xuan Chen, Lihan Wu, Yuqi Zhang, Sen Wang, Shihua Wang
{"title":"Importance of benzoyltransferase GcnE and lysine benzoylation of alcohol dehydrogenase AdhB in pathogenesis and aflatoxin production in <i>Aspergillus flavus</i>.","authors":"Xuan Chen, Lihan Wu, Yuqi Zhang, Sen Wang, Shihua Wang","doi":"10.1128/mbio.02665-24","DOIUrl":null,"url":null,"abstract":"<p><p>Lysine benzoylation (Kbz) is a newly identified post-translational modification associated with active transcription and metabolism in eukaryotes. However, whether Kbz exists in pathogenic fungi and its function remains unknown. Here, we demonstrated for the first time that Kbz is present in <i>Aspergillus flavus</i> and identified 60 benzoylated sites on 46 benzoylated proteins by global benzoylome analysis. Our data demonstrated that alcohol dehydrogenase B (AdhB) is regulated by benzoylation on lysine 321 (K321), and mutations of Kbz site in AdhB significantly reduced the alcohol dehydrogenase activity <i>in vivo</i> and <i>in vitro</i>. Both <i>adhB</i> deletion mutant and benzoylated site mutants (K321R and K321A) exhibited similar phenotype, including decreased conidiation and seed colonization, increased sclerotia formation and aflatoxin production, and more sensitive to cell wall damage stress. We also found that GcnE has benzoyltransferase activity <i>in vitro</i> and <i>in vivo</i>, and its repression leads to decreased Kbz level and enzymatic activity of AdhB. The catalytic site E139 is important for the benzoyltransferase function of GcnE. Our study uncovers a previously unknown mechanism by which benzoylation regulates AdhB activity to affect the development, secondary metabolism, pathogenicity, and stress response of <i>A. flavus</i>. Meanwhile, it points out the important role of Kbz in the pathogenicity of pathogenic fungi.IMPORTANCE<i>Aspergillus flavus</i> is a ubiquitous opportunistic pathogen of plants and animals, which produces carcinogenic and toxic secondary metabolite aflatoxin. <i>A. flavus</i> and aflatoxin contamination have emerged as a global food safety concern. Currently, post-translational modification plays crucial modulatory roles in the fungal development and virulence, but the role of benzoylation in fungal pathogenicity remains undetermined, which limits the development of prevention and control technique. Here, we first identified 46 benzoylated proteins in <i>A. flavus</i>, and found that benzoyltransferase GcnE exerted effects on pathogenicity and aflatoxin production by regulating the benzoylation of AdhB. This finding not only provided valuable information for prevention and control of <i>A. flavus</i> contamination, but also offered basic knowledge for investigation of the regulation mechanism of secondary metabolism in other fungi.</p>","PeriodicalId":18315,"journal":{"name":"mBio","volume":" ","pages":"e0266524"},"PeriodicalIF":5.1000,"publicationDate":"2024-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"mBio","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/mbio.02665-24","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Lysine benzoylation (Kbz) is a newly identified post-translational modification associated with active transcription and metabolism in eukaryotes. However, whether Kbz exists in pathogenic fungi and its function remains unknown. Here, we demonstrated for the first time that Kbz is present in Aspergillus flavus and identified 60 benzoylated sites on 46 benzoylated proteins by global benzoylome analysis. Our data demonstrated that alcohol dehydrogenase B (AdhB) is regulated by benzoylation on lysine 321 (K321), and mutations of Kbz site in AdhB significantly reduced the alcohol dehydrogenase activity in vivo and in vitro. Both adhB deletion mutant and benzoylated site mutants (K321R and K321A) exhibited similar phenotype, including decreased conidiation and seed colonization, increased sclerotia formation and aflatoxin production, and more sensitive to cell wall damage stress. We also found that GcnE has benzoyltransferase activity in vitro and in vivo, and its repression leads to decreased Kbz level and enzymatic activity of AdhB. The catalytic site E139 is important for the benzoyltransferase function of GcnE. Our study uncovers a previously unknown mechanism by which benzoylation regulates AdhB activity to affect the development, secondary metabolism, pathogenicity, and stress response of A. flavus. Meanwhile, it points out the important role of Kbz in the pathogenicity of pathogenic fungi.IMPORTANCEAspergillus flavus is a ubiquitous opportunistic pathogen of plants and animals, which produces carcinogenic and toxic secondary metabolite aflatoxin. A. flavus and aflatoxin contamination have emerged as a global food safety concern. Currently, post-translational modification plays crucial modulatory roles in the fungal development and virulence, but the role of benzoylation in fungal pathogenicity remains undetermined, which limits the development of prevention and control technique. Here, we first identified 46 benzoylated proteins in A. flavus, and found that benzoyltransferase GcnE exerted effects on pathogenicity and aflatoxin production by regulating the benzoylation of AdhB. This finding not only provided valuable information for prevention and control of A. flavus contamination, but also offered basic knowledge for investigation of the regulation mechanism of secondary metabolism in other fungi.

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
苯甲酰转移酶 GcnE 和醇脱氢酶 AdhB 的赖氨酸苯甲酰化在黄曲霉的致病和黄曲霉毒素生产中的重要性。
赖氨酸苯甲酰化(Kbz)是一种新发现的翻译后修饰,与真核生物中的活性转录和新陈代谢有关。然而,病原真菌中是否存在 Kbz 及其功能仍然未知。在这里,我们首次证明了黄曲霉中存在 Kbz,并通过全局苯甲酰化组分析在 46 个苯甲酰化蛋白上鉴定出了 60 个苯甲酰化位点。我们的数据表明,醇脱氢酶 B(AdhB)受赖氨酸 321(K321)上苯甲酰化的调控,而 AdhB 中 Kbz 位点的突变会显著降低醇脱氢酶在体内和体外的活性。adhB缺失突变体和苯甲酰化位点突变体(K321R和K321A)都表现出相似的表型,包括分生和种子定殖能力下降、硬菌丝形成和黄曲霉毒素产生增加,以及对细胞壁损伤胁迫更敏感。我们还发现 GcnE 在体外和体内都具有苯甲酰转移酶活性,它的抑制会导致 Kbz 水平和 AdhB 酶活性的降低。催化位点E139对GcnE的苯甲酰转移酶功能非常重要。我们的研究揭示了苯甲酰化调控 AdhB 活性以影响黄曲霉发育、次生代谢、致病性和应激反应的未知机制。重要意义黄曲霉菌是一种无处不在的动植物机会致病菌,可产生致癌和有毒的次级代谢产物黄曲霉毒素。黄曲霉菌和黄曲霉毒素污染已成为全球关注的食品安全问题。目前,翻译后修饰在真菌的生长发育和毒力中起着重要的调节作用,但苯甲酰化在真菌致病性中的作用仍未确定,这限制了防控技术的发展。在此,我们首次鉴定了黄曲霉中的46种苯甲酰化蛋白,发现苯甲酰转移酶GcnE通过调节AdhB的苯甲酰化对致病性和黄曲霉毒素的产生产生影响。这一发现不仅为防治黄曲霉污染提供了有价值的信息,也为研究其他真菌次生代谢的调控机制提供了基础知识。
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 去求助
来源期刊
mBio
mBio MICROBIOLOGY-
CiteScore
10.50
自引率
3.10%
发文量
762
审稿时长
1 months
期刊介绍: mBio® is ASM''s first broad-scope, online-only, open access journal. mBio offers streamlined review and publication of the best research in microbiology and allied fields.
期刊最新文献
Competence induction of homologous recombination genes protects pneumococcal cells from genotoxic stress. Development and utilization of Treponema pallidum expressing green fluorescent protein to study spirochete-host interactions and antibody-mediated clearance: expanding the toolbox for syphilis research. m6A demethylase CpALKBH regulates CpZap1 mRNA stability to modulate the development and virulence of chestnut blight fungus. Naturally occurring influenza reassortment in pigs facilitates the emergence of intrahost virus subpopulations with distinct genotypes and replicative fitness. RNA stability is regulated by both RNA polyadenylation and ATP levels, linking RNA and energy metabolisms in Escherichia coli.
×
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