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MINORITY PREDOCTORAL FELLOWSHIP PROGRAM

少数族裔博士前奖学金计划

基本信息

批准号：
7257808
负责人：
CARLOS C GOLLER
金额：
$ 2.83万
依托单位：
EMORY UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2005
资助国家：
美国
起止时间：
2005-07-01 至 2008-06-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7257808
关键词：
Accounting Address Affect Affinity Chromatography Bacteria Bacterial Adhesins Bacterial Adhesion Binding Binding Sites Biological Assay Cations Cells Complement DNA DNA Binding DNA-Binding Proteins Data Defect Development Disruption Drug Metabolic Detoxication Elements Enterobacteriaceae Escherichia coli Eubacterium Exhibits Family Fellowship Program Genes Genetic Screening Genetic Transcription Glucosamine Goals Gram-Negative Bacteria Green Fluorescent Proteins Growth Hydrogen Peroxide In Vitro Infection Kinetics Knowledge Laboratories LacZ Genes Laser Scanning Confocal Microscopy Maps Measures Mediating Microbial Biofilms Minority Molecular Monovalent Cations Mutagenesis Na(+)-K(+)-Exchanging ATPase Operon Padan Parents Pattern Personal Satisfaction Phenotype Physiological Physiology Plasmids Play Polymerase Chain Reaction Polymers Polysaccharides Primer Extension Process Production Promoter Regions Prostaglandins A Proteobacteria Pseudomonas fluorescens Range Regulation Regulatory Pathway Reporter Reporting Research Reverse Transcription Role Sequence Analysis Signal Transduction Sodium Specificity Staging Staphylococcus epidermidis Stimulus Technology Time Transcript Yersinia pestis antiporter clinically significant in vivo insight microbial mutant pre-doctoral promoter research study response

项目摘要

DESCRIPTION (provided by applicant): Bacterial biofilms are medically important and continue to account for a major percentage of microbial infections in the body. Although vast amounts of knowledge have been obtained in the field of biofilm research, the regulatory mechanisms that determine the development and triggering of biofilm formation are only starting to be elucidated. It has been hypothesized that bacteria might exploit cation concentrations to activate mechanisms required for biofilm formation; however, mechanistic information concerning this process has not been obtained. A genetic screen for mutants in E. coli with altered biofiolm phenotypes indicated that NhaR, a sodium pump regulator, plays an important role in biofilm formation. Moreover, data suggest that NhaR may be involved in the activation of the pgaABCD operon, required for synthesis of a biofilm polysaccharide adhesin. Specific aims include the molecular characterization of the interaction of NhaR with the pgaABCD operon with the long-term goal of beginning to elucidate the physiological significance of NhaR and cation concentration in biofilm formation.

描述（由申请人提供）：细菌生物膜在医学上很重要，并且继续占体内微生物感染的主要百分比。虽然在生物膜研究领域已经获得了大量的知识，但决定生物膜形成的发展和触发的调节机制才刚刚开始阐明。据推测，细菌可能会利用阳离子浓度来激活生物膜形成所需的机制;然而，尚未获得有关该过程的机制信息。对E.结果表明，NhaR是一种钠泵调节剂，在生物膜形成中起重要作用。此外，数据表明，NhaR可能参与激活的pgaABCD操纵子，所需的生物膜多糖粘附素的合成。具体目标包括NhaR与pgaABCD操纵子相互作用的分子表征，其长期目标是开始阐明NhaR和阳离子浓度在生物膜形成中的生理意义。