• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

丁香假单胞菌丁香致病变种中编码脂环肽植物毒素的基因表达受植物信号分子调控。

The expression of genes encoding lipodepsipeptide phytotoxins by Pseudomonas syringae pv. syringae is coordinated in response to plant signal molecules.

作者信息

Wang Nian, Lu Shi-En, Wang Jianlin, Chen Z Jeffrey, Gross Dennis C

机构信息

Department of Plant Pathology and Microbiology and 2Department of Soil and Crop Sciences, Texas A&M University, College Station 77843, USA.

出版信息

Mol Plant Microbe Interact. 2006 Mar;19(3):257-69. doi: 10.1094/MPMI-19-0257.

DOI:10.1094/MPMI-19-0257
PMID:16570656
Abstract

Specific plant signal molecules are known to induce syringomycin production and expression of syrB1, a syringomycin synthetase gene, in Pseudomonas syringae pv. syringae. This report demonstrates that syringopeptin production likewise is activated by plant signal molecules and that the GacS, SalA, and SyrF regulatory pathway mediates transmission of plant signal molecules to the syr-syp biosynthesis apparatus. Syringopeptin production by BR132 was increased two-fold by addition of arbutin (100 microM) and D-fructose (0.1%) to syringomycin minimal medium (SRM). Among 10 plant phenolic compounds tested, only the phenolic glucosides arbutin, salicin, and phenyl-beta-D-glucopyranoside induced substantially the beta-glucuronidase (GUS) activity of a sypA::uidA reporter from 242 U per 10(8) CFU without plant signal molecules up to 419 U per 10(8) CFU with plant signal molecules. Syringopeptin production was found to be controlled by the SalA/SyrF regulon because no toxin was detected from cultures of B301DSL7 (i.e., salA mutant) and B301DSL1 (i.e., syrF mutant), and the expression of sypA::uidA was decreased approximately 99 and 94% in salA (B301DSL30) and syrF (B301DNW31) mutant backgrounds, respectively. Subgenomic analysis of transcriptional expression with a 70-mer oligonucleotide microarray demonstrated that the syr-syp genes are induced 2.5- to 10.5-fold by addition of arbutin and D-fructose to SRM. This study establishes that plant signal molecules are transmitted through the GacS, SalA/SyrF pathway to activate the coordinated transcriptional expression of the syr-syp genes.

摘要

已知特定的植物信号分子可诱导丁香假单胞菌丁香致病变种产生丁香霉素并表达syrB1(一种丁香霉素合成酶基因)。本报告表明,丁香肽的产生同样受到植物信号分子的激活,并且GacS、SalA和SyrF调控途径介导植物信号分子向syr - syp生物合成装置的传递。通过向丁香霉素基本培养基(SRM)中添加熊果苷(100微摩尔)和D - 果糖(0.1%),BR132产生的丁香肽增加了两倍。在所测试的10种植物酚类化合物中,只有酚糖苷熊果苷、水杨苷和苯基 - β - D - 葡萄糖苷能显著诱导sypA::uidA报告基因的β - 葡萄糖醛酸酶(GUS)活性,在没有植物信号分子的情况下,每10⁸CFU的活性为242 U,而在有植物信号分子时,每10⁸CFU的活性高达419 U。发现丁香肽的产生受SalA/SyrF调节子控制,因为在B301DSL7(即salA突变体)和B301DSL1(即syrF突变体)的培养物中未检测到毒素,并且在salA(B301DSL30)和syrF(B301DNW31)突变体背景下,sypA::uidA的表达分别降低了约99%和94%。用70聚体寡核苷酸微阵列对转录表达进行亚基因组分析表明,向SRM中添加熊果苷和D - 果糖可使syr - syp基因的表达诱导2.5至10.5倍。本研究证实植物信号分子通过GacS、SalA/SyrF途径传递,以激活syr - syp基因的协同转录表达。

相似文献

1
The expression of genes encoding lipodepsipeptide phytotoxins by Pseudomonas syringae pv. syringae is coordinated in response to plant signal molecules.丁香假单胞菌丁香致病变种中编码脂环肽植物毒素的基因表达受植物信号分子调控。
Mol Plant Microbe Interact. 2006 Mar;19(3):257-69. doi: 10.1094/MPMI-19-0257.
2
Oligonucleotide microarray analysis of the salA regulon controlling phytotoxin production by Pseudomonas syringae pv. syringae.丁香假单胞菌丁香致病变种中控制植物毒素产生的salA调控子的寡核苷酸微阵列分析。
Mol Plant Microbe Interact. 2005 Apr;18(4):324-33. doi: 10.1094/MPMI-18-0324.
3
Characterization of the transcriptional activators SalA and SyrF, Which are required for syringomycin and syringopeptin production by Pseudomonas syringae pv. syringae.丁香假单胞菌丁香致病变种产生丁香霉素和丁香肽所需的转录激活因子SalA和SyrF的特性分析
J Bacteriol. 2006 May;188(9):3290-8. doi: 10.1128/JB.188.9.3290-3298.2006.
4
Identification of the syr-syp box in the promoter regions of genes dedicated to syringomycin and syringopeptin production by Pseudomonas syringae pv. syringae B301D.丁香假单胞菌丁香致病变种B301D中负责丁香霉素和丁香肽素合成的基因启动子区域中syr - syp框的鉴定。
J Bacteriol. 2006 Jan;188(1):160-8. doi: 10.1128/JB.188.1.160-168.2006.
5
Characterization of the salA, syrF, and syrG regulatory genes located at the right border of the syringomycin gene cluster of Pseudomonas syringae pv. syringae.丁香假单胞菌丁香致病变种丁香霉素基因簇右边界处的salA、syrF和syrG调控基因的特性分析
Mol Plant Microbe Interact. 2002 Jan;15(1):43-53. doi: 10.1094/MPMI.2002.15.1.43.
6
A physical map of the syringomycin and syringopeptin gene clusters localized to an approximately 145-kb DNA region of Pseudomonas syringae pv. syringae strain B301D.丁香霉素和丁香杆菌素基因簇的物理图谱定位于丁香假单胞菌丁香致病变种B301D菌株约145 kb的DNA区域。
Mol Plant Microbe Interact. 2001 Dec;14(12):1426-35. doi: 10.1094/MPMI.2001.14.12.1426.
7
Plant signal molecules activate the syrB gene, which is required for syringomycin production by Pseudomonas syringae pv. syringae.植物信号分子激活丁香假单胞菌丁香致病变种产生丁香霉素所需的syrB基因。
J Bacteriol. 1991 Sep;173(18):5784-92. doi: 10.1128/jb.173.18.5784-5792.1991.
8
The contribution of syringopeptin and syringomycin to virulence of Pseudomonas syringae pv. syringae strain B301D on the basis of sypA and syrB1 biosynthesis mutant analysis.基于sypA和syrB1生物合成突变体分析,研究丁香假单胞菌丁香致病变种B301D中丁香肽素和丁香霉素对其毒力的贡献。
Mol Plant Microbe Interact. 2001 Mar;14(3):336-48. doi: 10.1094/MPMI.2001.14.3.336.
9
Characterization of salA, syrF, and syrG Genes and Attendant Regulatory Networks Involved in Plant Pathogenesis by Pseudomonas syringae pv. syringae B728a.丁香假单胞菌丁香致病变种B728a中参与植物致病过程的salA、syrF和syrG基因及其相关调控网络的表征
PLoS One. 2016 Mar 8;11(3):e0150234. doi: 10.1371/journal.pone.0150234. eCollection 2016.
10
The PseEF efflux system is a virulence factor of Pseudomonas syringae pv. syringae.PseEF 外排系统是丁香假单胞菌 pv. 丁香致病变种的毒力因子。
J Microbiol. 2012 Feb;50(1):79-90. doi: 10.1007/s12275-012-1353-9. Epub 2012 Feb 27.

引用本文的文献

1
Does regulation hold the key to optimizing lipopeptide production in for biotechnology?监管是实现生物技术中脂肽生产优化的关键吗?
Front Bioeng Biotechnol. 2024 Feb 27;12:1363183. doi: 10.3389/fbioe.2024.1363183. eCollection 2024.
2
Identification and Characterization of Pseudomonas syringae pv. syringae, a Causative Bacterium of Apple Canker in Korea.韩国苹果溃疡病致病菌丁香假单胞菌丁香致病变种的鉴定与特性分析
Plant Pathol J. 2023 Feb;39(1):88-107. doi: 10.5423/PPJ.OA.08.2022.0121. Epub 2023 Feb 1.
3
The Evanescent GacS Signal.
短暂的GacS信号
Microorganisms. 2020 Nov 6;8(11):1746. doi: 10.3390/microorganisms8111746.
4
Fungal-Associated Molecules Induce Key Genes Involved in the Biosynthesis of the Antifungal Secondary Metabolites Nunamycin and Nunapeptin in the Biocontrol Strain Pseudomonas fluorescens In5.真菌相关分子诱导生物防治菌株荧光假单胞菌 In5 中参与抗真菌次生代谢物 nunamycin 和 nunapeptin 生物合成的关键基因。
Appl Environ Microbiol. 2020 Oct 15;86(21). doi: 10.1128/AEM.01284-20.
5
Cherry picking by pseudomonads: After a century of research on canker, genomics provides insights into the evolution of pathogenicity towards stone fruits.假单胞菌的择优行为:在对溃疡病进行了一个世纪的研究之后,基因组学为核果致病力的进化提供了见解。
Plant Pathol. 2020 Aug;69(6):962-978. doi: 10.1111/ppa.13189. Epub 2020 May 6.
6
Bioorganic chemistry of signaling molecules in microbial communication.微生物通讯中信号分子的生物有机化学
J Pestic Sci. 2019 Aug 20;44(3):200-207. doi: 10.1584/jpestics.J19-02.
7
Regulation of bacterial virulence by Csr (Rsm) systems.Csr(Rsm)系统对细菌毒力的调控
Microbiol Mol Biol Rev. 2015 Jun;79(2):193-224. doi: 10.1128/MMBR.00052-14.
8
Mangotoxin production of Pseudomonas syringae pv. syringae is regulated by MgoA.丁香假单胞菌 pv. 丁香致病变种的芒果毒素产生受 MgoA 调控。
BMC Microbiol. 2014 Feb 21;14:46. doi: 10.1186/1471-2180-14-46.
9
Characterization of five ECF sigma factors in the genome of Pseudomonas syringae pv. syringae B728a.丁香假单胞菌 pv. 丁香致病变种 B728a 基因组中五个 ECF sigma 因子的特性。
PLoS One. 2013;8(3):e58846. doi: 10.1371/journal.pone.0058846. Epub 2013 Mar 14.
10
Genetic and functional characterization of cyclic lipopeptide white-line-inducing principle (WLIP) production by rice rhizosphere isolate Pseudomonas putida RW10S2.水稻根际分离菌 Pseudomonas putida RW10S2 产生的环状脂肽类白纹诱导原(WLIP)的遗传和功能特征。
Appl Environ Microbiol. 2012 Jul;78(14):4826-34. doi: 10.1128/AEM.00335-12. Epub 2012 Apr 27.