• 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

姜隔孢叶点霉中与姜炭疽菌合成和致病性改变相关的突变体。

Mutants of Cercospora kikuchii Altered in Cercosporin Synthesis and Pathogenicity.

机构信息

Agricultural Research Service, U.S. Department of Agriculture, and Department of Plant Pathology, North Carolina State University, Raleigh, North Carolina 27695-7616.

出版信息

Appl Environ Microbiol. 1991 Oct;57(10):2940-5. doi: 10.1128/aem.57.10.2940-2945.1991.

DOI:10.1128/aem.57.10.2940-2945.1991
PMID:16348567
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC183901/
Abstract

We have obtained spontaneous and UV-induced stable mutants, altered in the synthesis of cercosporin, of the fungal soybean pathogen Cercospora kikuchii. The mutants were isolated on the basis of colony color on minimal medium. The UV-induced mutants accumulated, at most, 2% of wild-type cercosporin levels on all media tested. In contrast, cercosporin accumulation by the spontaneous mutants was strongly medium regulated, occurring only on potato dextrose medium but at concentrations comparable to those produced by the wild-type strain. UV-induced mutants unable to synthesize cercosporin on any medium were unable to incite lesions when inoculated onto the soybean host. Cercosporin was reproducibly isolated from all inoculated leaves showing lesions. Although cercosporin involvement in disease has been indirectly suggested by many previous studies, this is the first report in which mutants blocked in cercosporin synthesis have been used to demonstrate that cercosporin is a crucial pathogenicity factor for this fungal genus.

摘要

我们已经获得了在大豆叶斑病菌(Cercospora kikuchii)的几丁素合成中发生自发和 UV 诱导稳定突变的突变体。这些突变体是基于最小培养基上的菌落颜色分离得到的。在所有测试的培养基上,UV 诱导的突变体最多积累了野生型几丁素水平的 2%。相比之下,自发突变体的几丁素积累受到培养基的强烈调控,仅在土豆葡萄糖培养基上发生,但浓度与野生型菌株产生的浓度相当。在任何培养基上都不能合成几丁素的 UV 诱导突变体在接种到大豆宿主上时无法引发病变。从所有显示病变的接种叶片中可重复性地分离出几丁素。尽管几丁素在疾病中的作用已被许多先前的研究间接表明,但这是首次使用无法合成几丁素的突变体来证明几丁素是该真菌属的关键致病性因素的报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd74/183901/61065ba1c041/aem00063-0171-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd74/183901/cbf08b61ee89/aem00063-0170-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd74/183901/66f1969f0fab/aem00063-0170-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd74/183901/a7201d600d6e/aem00063-0171-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd74/183901/61065ba1c041/aem00063-0171-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd74/183901/cbf08b61ee89/aem00063-0170-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd74/183901/66f1969f0fab/aem00063-0170-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd74/183901/a7201d600d6e/aem00063-0171-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd74/183901/61065ba1c041/aem00063-0171-b.jpg

相似文献

1
Mutants of Cercospora kikuchii Altered in Cercosporin Synthesis and Pathogenicity.姜隔孢叶点霉中与姜炭疽菌合成和致病性改变相关的突变体。
Appl Environ Microbiol. 1991 Oct;57(10):2940-5. doi: 10.1128/aem.57.10.2940-2945.1991.
2
Isolation of Light-Enhanced cDNAs of Cercospora kikuchii.分离增强光照条件下的梨叶点霉菌 cDNA。
Appl Environ Microbiol. 1991 Sep;57(9):2671-6. doi: 10.1128/aem.57.9.2671-2676.1991.
3
The AVR4 effector is involved in cercosporin biosynthesis and likely affects the virulence of Cercospora cf. flagellaris on soybean.AVR4 效应子参与了尾孢菌素生物合成,并可能影响 Cercospora cf. flagellaris 对大豆的毒力。
Mol Plant Pathol. 2020 Jan;21(1):53-65. doi: 10.1111/mpp.12879. Epub 2019 Oct 23.
4
Vegetative Compatibility Groups in Cercospora kikuchii, the Causal Agent of Cercospora Leaf Blight and Purple Seed Stain in Soybean.大豆叶枯病和紫斑病病原菌姜隔尾孢菌的营养体亲和群
Phytopathology. 2005 Mar;95(3):257-61. doi: 10.1094/PHYTO-95-0257.
5
Over-expression of the cercosporin facilitator protein, CFP, in Cercospora kikuchii up-regulates production and secretion of cercosporin.在菊池尾孢菌中,尾孢菌素转运蛋白CFP的过表达上调了尾孢菌素的产生和分泌。
FEMS Microbiol Lett. 2001 Oct 16;204(1):89-93. doi: 10.1111/j.1574-6968.2001.tb10868.x.
6
CFP, the putative cercosporin transporter of Cercospora kikuchii, is required for wild type cercosporin production, resistance, and virulence on soybean.CFP是菊池尾孢菌假定的尾孢菌素转运蛋白,是野生型尾孢菌素产生、对大豆的抗性和毒力所必需的。
Mol Plant Microbe Interact. 1999 Oct;12(10):901-10. doi: 10.1094/MPMI.1999.12.10.901.
7
[Cercospora kikuchii isolated from Province of Santa Fe (Argentina): genetic variability and cercosporin production].[从圣菲省(阿根廷)分离得到的菊池尾孢菌:遗传变异性与尾孢菌素的产生]
Rev Iberoam Micol. 2008 Dec 31;25(4):237-41. doi: 10.1016/s1130-1406(08)70056-1.
8
The CTB1 gene encoding a fungal polyketide synthase is required for cercosporin biosynthesis and fungal virulence of Cercospora nicotianae.编码真菌聚酮合酶的CTB1基因是烟草尾孢菌中尾孢菌素生物合成和真菌毒力所必需的。
Mol Plant Microbe Interact. 2005 May;18(5):468-76. doi: 10.1094/MPMI-18-0468.
9
Distribution and Sequestration of Cercosporin by cf. .叶点霉 cf. 对尾孢菌素的分布和固定
Phytopathology. 2024 Aug;114(8):1822-1831. doi: 10.1094/PHYTO-09-23-0310-R. Epub 2024 Aug 1.
10
In Vitro Screening of Various Bacterially Produced Double-Stranded RNAs for Silencing cf. Target Genes and Suppressing Cercosporin Production.体外筛选各种细菌产生的双链 RNA 以沉默 cf. 靶基因并抑制尾孢菌素的产生。
Phytopathology. 2021 Jul;111(7):1228-1237. doi: 10.1094/PHYTO-09-20-0409-R. Epub 2021 Sep 7.

引用本文的文献

1
What are the 100 most cited fungal genera?被引用次数最多的100个真菌属有哪些?
Stud Mycol. 2024 Jul;108:1-411. doi: 10.3114/sim.2024.108.01. Epub 2024 Jul 15.
2
Does Abiotic Host Stress Favour Dothideomycete-Induced Disease Development?非生物宿主胁迫是否有利于座囊菌纲真菌引发的疾病发展?
Plants (Basel). 2022 Jun 20;11(12):1615. doi: 10.3390/plants11121615.
3
White Leaf Spot Caused by : A Re-emerging Disease of Brassicaceae.白菜白斑病:芸薹属作物再现性病害。

本文引用的文献

1
Light-induced production of singlet oxygen and superoxide by the fungal toxin, cercosporin.光诱导真菌毒素藤黄绿菌素产生单线态氧和超氧自由基。
Plant Physiol. 1983 Nov;73(3):855-7. doi: 10.1104/pp.73.3.855.
2
Changes in tobacco cell membrane composition and structure caused by cercosporin.麦角甾醇生物合成抑制剂对烟草细胞膜组成和结构的影响。
Plant Physiol. 1983 Apr;71(4):763-6. doi: 10.1104/pp.71.4.763.
3
Peroxidation of tobacco membrane lipids by the photosensitizing toxin, cercosporin.通过光敏毒素,串珠镰孢菌素,对烟草细胞膜脂质的过氧化作用。
Front Cell Infect Microbiol. 2020 Oct 28;10:588090. doi: 10.3389/fcimb.2020.588090. eCollection 2020.
4
The AVR4 effector is involved in cercosporin biosynthesis and likely affects the virulence of Cercospora cf. flagellaris on soybean.AVR4 效应子参与了尾孢菌素生物合成,并可能影响 Cercospora cf. flagellaris 对大豆的毒力。
Mol Plant Pathol. 2020 Jan;21(1):53-65. doi: 10.1111/mpp.12879. Epub 2019 Oct 23.
5
Evaluation of soybean genotypes for reaction to natural field infection by Cercospora species causing purple seed stain.评价大豆基因型对由尾孢菌引起的自然田间感染的反应,导致紫色种子斑点。
PLoS One. 2019 Oct 10;14(10):e0222673. doi: 10.1371/journal.pone.0222673. eCollection 2019.
6
Non-invasive Presymptomatic Detection of Infection and Identification of Early Metabolic Responses in Sugar Beet.甜菜感染的非侵入性症状前检测及早期代谢反应的鉴定
Front Plant Sci. 2016 Sep 22;7:1377. doi: 10.3389/fpls.2016.01377. eCollection 2016.
7
The genome of the emerging barley pathogen Ramularia collo-cygni.新出现的大麦病原菌柱隔孢菌的基因组。
BMC Genomics. 2016 Aug 9;17:584. doi: 10.1186/s12864-016-2928-3.
8
The past, present and future of secondary metabolite research in the Dothideomycetes.座囊菌纲次生代谢产物研究的过去、现在与未来
Mol Plant Pathol. 2015 Jan;16(1):92-107. doi: 10.1111/mpp.12162. Epub 2014 Jul 7.
9
Species concepts in Cercospora: spotting the weeds among the roses.Cercospora 物种概念:在玫瑰丛中发现杂草。
Stud Mycol. 2013 Jun 30;75(1):115-70. doi: 10.3114/sim0012.
10
Molecular mechanism of quinone signaling mediated through S-quinonization of a YodB family repressor QsrR.通过 YodB 家族阻遏物 QsrR 的 S-醌基化介导的醌信号分子的分子机制。
Proc Natl Acad Sci U S A. 2013 Mar 26;110(13):5010-5. doi: 10.1073/pnas.1219446110. Epub 2013 Mar 11.
Plant Physiol. 1982 Jun;69(6):1361-4. doi: 10.1104/pp.69.6.1361.
4
Isolation and characterization of mutants blocked in T-2 toxin biosynthesis.T-2毒素生物合成受阻突变体的分离与鉴定
Appl Environ Microbiol. 1987 Aug;53(8):1855-9. doi: 10.1128/aem.53.8.1855-1859.1987.