• 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

玉米根中促进植物生长细菌巴西固氮螺菌SmR1菌株的实时荧光定量PCR定量分析

Real-time PCR quantification of the plant growth promoting bacteria Herbaspirillum seropedicae strain SmR1 in maize roots.

作者信息

Pereira Tomás Pellizzaro, do Amaral Fernanda Plucani, Dall'Asta Pamela, Brod Fábio Cristiano Angonesi, Arisi Ana Carolina Maisonnave

机构信息

Departamento de Ciência e Tecnologia de Alimentos, Centro de Ciências Agrárias, Universidade Federal de Santa Catarina, Rod. Admar Gonzaga, 1346, Florianópolis, SC, 88034-001, Brazil.

出版信息

Mol Biotechnol. 2014 Jul;56(7):660-70. doi: 10.1007/s12033-014-9742-4.

DOI:10.1007/s12033-014-9742-4
PMID:24563376
Abstract

The plant growth promoting bacteria Herbaspirillum seropedicae SmR1 is an endophytic diazotroph found in several economically important crops. Considering that methods to monitor the plant-bacteria interaction are required, our objective was to develop a real-time PCR method for quantification of PGPB H. seropedicae in the rhizosphere of maize seedlings. Primer pairs were designed, and their specificity was verified using DNA from 12 different bacterial species. Ten standard curves of qPCR assay using HERBAS1 primers and tenfold serial dilutions of H. seropedicae SmR1 DNA were performed, and PCR efficiency of 91 % and correlation coefficient of 0.99 were obtained. H. seropedicae SmR1 limit of detection was 10(1) copies (corresponding to 60.3 fg of bacterial DNA). qPCR assay using HERBAS1 was used to detect and quantify H. seropedicae strain SmR1 in inoculated maize roots, cultivated in vitro and in pots, harvested 1, 4, 7, and 10 days after inoculation. The estimated bacterial DNA copy number per gram of root was in the range 10(7)-10(9) for plants grown in vitro and it was around 10(6) for plants grown in pots. Primer pair HERBAS1 was able to quantify H. seropedicae SmR1, and this assay can be useful for monitoring plant-bacteria interaction.

摘要

促进植物生长的细菌巴西固氮螺菌SmR1是一种内生固氮菌,存在于几种具有重要经济价值的作物中。鉴于需要监测植物与细菌相互作用的方法,我们的目标是开发一种实时PCR方法,用于定量玉米幼苗根际中的促生细菌巴西固氮螺菌。设计了引物对,并使用来自12种不同细菌物种的DNA验证了其特异性。使用HERBAS1引物进行了qPCR分析的10条标准曲线以及巴西固氮螺菌SmR1 DNA的十倍系列稀释,获得了91%的PCR效率和0.99的相关系数。巴西固氮螺菌SmR1的检测限为10(1)个拷贝(相当于60.3 fg的细菌DNA)。使用HERBAS1的qPCR分析用于检测和定量接种后1、4、7和10天收获的、在体外和盆栽中培养的接种玉米根中的巴西固氮螺菌菌株SmR1。对于体外生长的植物,每克根中估计的细菌DNA拷贝数在10(7)-10(9)范围内,对于盆栽植物,该数字约为10(6)。引物对HERBAS1能够定量巴西固氮螺菌SmR1,该分析可用于监测植物与细菌的相互作用。

相似文献

1
Real-time PCR quantification of the plant growth promoting bacteria Herbaspirillum seropedicae strain SmR1 in maize roots.玉米根中促进植物生长细菌巴西固氮螺菌SmR1菌株的实时荧光定量PCR定量分析
Mol Biotechnol. 2014 Jul;56(7):660-70. doi: 10.1007/s12033-014-9742-4.
2
Inoculation of Herbaspirillum seropedicae strain SmR1 increases biomass in maize roots DKB 390 variety in the early stages of plant development.施氏假单胞菌菌株 SmR1 的接种可增加玉米根系 DKB 390 品种在植物发育早期的生物量。
Arch Microbiol. 2022 Jun 8;204(7):373. doi: 10.1007/s00203-022-02986-8.
3
Importance of Poly-3-Hydroxybutyrate Metabolism to the Ability of Herbaspirillum seropedicae To Promote Plant Growth.聚 3-羟基丁酸代谢对促进植物生长的希瓦氏菌属能力的重要性。
Appl Environ Microbiol. 2019 Mar 6;85(6). doi: 10.1128/AEM.02586-18. Print 2019 Mar 15.
4
Evidence for the endophytic colonization of Phaseolus vulgaris (common bean) roots by the diazotroph Herbaspirillum seropedicae.证据表明,固氮菌 Herbaspirillum seropedicae 能够定殖在普通菜豆(Phaseolus vulgaris)的根部。
Braz J Med Biol Res. 2011 Mar;44(3):182-5. doi: 10.1590/s0100-879x2011007500004. Epub 2011 Jan 14.
5
Expressed proteins of Herbaspirillum seropedicae in maize (DKB240) roots-bacteria interaction revealed using proteomics.利用蛋白质组学揭示了巴西固氮螺菌在玉米(DKB240)根-细菌相互作用中的表达蛋白。
Appl Biochem Biotechnol. 2014 Nov;174(6):2267-77. doi: 10.1007/s12010-014-1197-3. Epub 2014 Aug 31.
6
Maize root lectins mediate the interaction with Herbaspirillum seropedicae via N-acetyl glucosamine residues of lipopolysaccharides.玉米根凝集素通过脂多糖的N-乙酰葡糖胺残基介导与血清巴西固氮螺菌的相互作用。
PLoS One. 2013 Oct 9;8(10):e77001. doi: 10.1371/journal.pone.0077001. eCollection 2013.
7
Genomic comparison of the endophyte Herbaspirillum seropedicae SmR1 and the phytopathogen Herbaspirillum rubrisubalbicans M1 by suppressive subtractive hybridization and partial genome sequencing.通过抑制差减杂交和部分基因组测序对内生菌 Herbaspirillum seropedicae SmR1 和植物病原菌 Herbaspirillum rubrisubalbicans M1 进行基因组比较。
FEMS Microbiol Ecol. 2012 May;80(2):441-51. doi: 10.1111/j.1574-6941.2012.01309.x. Epub 2012 Feb 13.
8
Essential Genes for In Vitro Growth of the Endophyte Herbaspirillum seropedicae SmR1 as Revealed by Transposon Insertion Site Sequencing.转座子插入位点测序揭示的内生固氮菌巴西固氮螺菌SmR1体外生长必需基因
Appl Environ Microbiol. 2016 Oct 27;82(22):6664-6671. doi: 10.1128/AEM.02281-16. Print 2016 Nov 15.
9
Molecular adaptations of Herbaspirillum seropedicae during colonization of the maize rhizosphere.巴西固氮螺菌在玉米根际定殖过程中的分子适应性
Environ Microbiol. 2016 Sep;18(8):2343-56. doi: 10.1111/1462-2920.12887. Epub 2015 Jun 11.
10
RNA-seq transcriptional profiling of Herbaspirillum seropedicae colonizing wheat (Triticum aestivum) roots.定殖于小麦(普通小麦)根际的固氮螺菌的RNA测序转录谱分析
Plant Mol Biol. 2016 Apr;90(6):589-603. doi: 10.1007/s11103-016-0430-6. Epub 2016 Jan 22.

引用本文的文献

1
Designing and validation of specific primers for the quantitative detection of bacteria in sugarcane inoculant.设计和验证用于定量检测甘蔗接种剂中细菌的特异性引物。
Braz J Microbiol. 2023 Dec;54(4):2627-2640. doi: 10.1007/s42770-023-01144-6. Epub 2023 Oct 16.
2
Optimization of Molecular Methods for Detecting Duckweed-Associated Bacteria.检测浮萍相关细菌的分子方法优化
Plants (Basel). 2023 Feb 15;12(4):872. doi: 10.3390/plants12040872.
3
Multiomic Approaches Reveal Hormonal Modulation and Nitrogen Uptake and Assimilation in the Initial Growth of Maize Inoculated with .

本文引用的文献

1
Quantification of rice blast disease progressions through Taqman real-time PCR.利用 Taqman 实时 PCR 对稻瘟病进展进行定量分析。
Mol Biotechnol. 2013 Sep;55(1):43-8. doi: 10.1007/s12033-012-9632-6.
2
Rapid identification of bacterial isolates from wheat roots by high resolution whole cell MALDI-TOF MS analysis.利用高分辨率全细胞 MALDI-TOF MS 分析快速鉴定小麦根部分离菌。
J Biotechnol. 2013 Jun 10;165(3-4):167-74. doi: 10.1016/j.jbiotec.2013.04.001. Epub 2013 Apr 13.
3
Single-tube nested real-time PCR as a new highly sensitive approach to trace hazelnut.
多组学方法揭示了接种……的玉米初始生长过程中的激素调节以及氮素吸收与同化
Plants (Basel). 2022 Dec 22;12(1):48. doi: 10.3390/plants12010048.
4
Inoculation of Herbaspirillum seropedicae strain SmR1 increases biomass in maize roots DKB 390 variety in the early stages of plant development.施氏假单胞菌菌株 SmR1 的接种可增加玉米根系 DKB 390 品种在植物发育早期的生物量。
Arch Microbiol. 2022 Jun 8;204(7):373. doi: 10.1007/s00203-022-02986-8.
5
Sorghum Growth Promotion by and : Putative Mechanisms Revealed by Genomics and Metagenomics.固氮螺菌和伯克氏菌促进高粱生长:基因组学和宏基因组学揭示的潜在机制
Microorganisms. 2020 May 13;8(5):725. doi: 10.3390/microorganisms8050725.
6
promotes maize growth but fails to control the maize leaf anthracnose.促进玉米生长,但无法防治玉米叶炭疽病。
Physiol Mol Biol Plants. 2019 Jan;25(1):167-176. doi: 10.1007/s12298-018-0616-2. Epub 2018 Oct 27.
7
The Endophytic Bacterial Microbiota Associated with Sweet Sorghum () Is Modulated by the Application of Chemical N Fertilizer to the Field.与甜高粱()相关的内生细菌微生物群受到田间施用化学氮肥的调节。
Int J Genomics. 2018 Sep 30;2018:7403670. doi: 10.1155/2018/7403670. eCollection 2018.
8
Effect of and strains on sorghum growth is plant genotype dependent.[具体菌株名称]和[具体菌株名称]菌株对高粱生长的影响取决于植物基因型。 (你提供的原文中“Effect of and strains”部分内容缺失,请补充完整准确信息以便更精准翻译)
PeerJ. 2018 Jul 24;6:e5346. doi: 10.7717/peerj.5346. eCollection 2018.
9
Strain-specific quantification of root colonization by plant growth promoting rhizobacteria Bacillus firmus I-1582 and Bacillus amyloliquefaciens QST713 in non-sterile soil and field conditions.在非无菌土壤和田间条件下,植物促生根际细菌解淀粉芽孢杆菌 I-1582 和枯草芽孢杆菌 QST713 对根定植的种特异性定量。
PLoS One. 2018 Feb 15;13(2):e0193119. doi: 10.1371/journal.pone.0193119. eCollection 2018.
10
Differential growth responses of Brachypodium distachyon genotypes to inoculation with plant growth promoting rhizobacteria.短柄草基因型对接种促进植物生长的根际细菌的差异生长反应
Plant Mol Biol. 2016 Apr;90(6):689-97. doi: 10.1007/s11103-016-0449-8. Epub 2016 Feb 13.
单管嵌套实时 PCR 作为一种新的高灵敏度方法来追踪榛子。
J Agric Food Chem. 2012 Aug 22;60(33):8103-10. doi: 10.1021/jf302898z. Epub 2012 Aug 13.
4
Plant growth-promoting rhizobacteria affect the growth and nutrient uptake of Fraxinus americana container seedlings.植物促生根际细菌影响美国白蜡容器苗的生长和养分吸收。
Appl Microbiol Biotechnol. 2013 May;97(10):4617-25. doi: 10.1007/s00253-012-4255-1. Epub 2012 Jul 10.
5
Polymerase chain reaction assay for rapid, sensitive detection, and identification of Colletotrichum gloeosporioides causing greater yam anthracnose.聚合酶链反应检测法用于快速、灵敏地检测和鉴定引起大薯炭疽病的胶孢炭疽菌。
Mol Biotechnol. 2012 Nov;52(3):277-84. doi: 10.1007/s12033-012-9496-9.
6
Genomic comparison of the endophyte Herbaspirillum seropedicae SmR1 and the phytopathogen Herbaspirillum rubrisubalbicans M1 by suppressive subtractive hybridization and partial genome sequencing.通过抑制差减杂交和部分基因组测序对内生菌 Herbaspirillum seropedicae SmR1 和植物病原菌 Herbaspirillum rubrisubalbicans M1 进行基因组比较。
FEMS Microbiol Ecol. 2012 May;80(2):441-51. doi: 10.1111/j.1574-6941.2012.01309.x. Epub 2012 Feb 13.
7
Herbaspirillum seropedicae rfbB and rfbC genes are required for maize colonization.土壤杆菌 Herbaspirillum seropedicae 的 rfbB 和 rfbC 基因对于玉米的定殖是必需的。
Environ Microbiol. 2010 Aug;12(8):2233-44. doi: 10.1111/j.1462-2920.2010.02187.x. Epub 2010 Mar 7.
8
A rapid and simple PCR method for identifying isolates of the genus Azospirillum within populations of rhizosphere bacteria.一种快速简单的 PCR 方法,可用于鉴定根际细菌群体中属名 Azospirillum 的分离株。
J Appl Microbiol. 2011 Oct;111(4):915-24. doi: 10.1111/j.1365-2672.2011.05115.x. Epub 2011 Sep 8.
9
Genome of Herbaspirillum seropedicae strain SmR1, a specialized diazotrophic endophyte of tropical grasses.巴西固氮螺菌 SmR1 菌株基因组,一种热带禾本科植物专性共生固氮内生菌。
PLoS Genet. 2011 May;7(5):e1002064. doi: 10.1371/journal.pgen.1002064. Epub 2011 May 12.
10
Development and validation of real-time PCR screening methods for detection of cry1A.105 and cry2Ab2 genes in genetically modified organisms.开发和验证实时 PCR 筛选方法,用于检测转基因生物中的 cry1A.105 和 cry2Ab2 基因。
Anal Bioanal Chem. 2011 May;400(5):1433-42. doi: 10.1007/s00216-011-4875-9. Epub 2011 Mar 29.