Role of RNA polymerase in bacterial differentiation

RNA聚合酶在细菌分化中的作用

• 批准号: 8438398
• 负责人: Richard Marc Losick
• 金额: $ 64.91万
• 依托单位: HARVARD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 1976
• 资助国家: 美国
• 起止时间: 1976-02-01 至 2016-02-29
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8438398
• 关键词: Address; Amino Acids; Amyloid fibers; Animal Model; Antibiotic Resistance; Bacillus anthracis; Bacillus subtilis; Back; Bacteria; Bioterrorism; Cells; Communities; Complex; Cytochrome a; DNA-Directed RNA Polymerase; Development; Devices; Electron Transport; Enterococcus; Environment; Event; Exhibits; Feedback; Frequencies; Funding Mechanisms; Gel; Gene Expression; Genes; Genus staphylococcus; Germination; Goals; Gram-Positive Bacteria; Growth; Human; Individual; Laboratory culture; Life; Life Cycle Stages; Lipoproteins; Measures; Mediating; Memory; Microbial Biofilms; Microfluidic Microchips; Molecular Biology; Organism; Peptidoglycan; Phosphotransferases; Plant Roots; Plants; Production; Progress Reports; Property; Pseudomonas; Public Health; Racemases; Relative (related person); Reproduction spores; Research; Role; Sigma Factor; Signal Transduction; Streptococcus; Structure; Surface; Swimming; System; Testing; Time; base; cell type; derepression; free behavior; insight; novel; pathogen; pathogenic bacteria; prevent; programs; research study; sensor histidine kinase; small molecule; success; time use

DESCRIPTION (provided by applicant): The objectives of the project are to uncover the mechanisms of gene control that turn on, and distinguish between, developmental programs of spore formation and matrix production by Bacillus subtilis. Spore formation has been traditionally viewed as a behavior of free-living cells, but we now understand that differentiation also occurs in the context of structured, multicellular communities (biofilms) consisting of chains of matrix-producing cells as well as spore-forming cells. Indeed, the mechanisms that govern entry into sporulation are intimately interwoven with those that govern matrix production. This proposal addresses important gaps in our understanding of sporulation and multicellularity with four specific aims: (1) We will identify the natural environmental signals that trigger spore formation and multicellularity by two sensor histidine kinases. (2) We will visualize cell fate switching between planktonic and matrix-producing states in real time using a newly devised microfluidic device. We will determine how a double-negative feedback loop controls switching and how cells discriminate between alternative fates of spore formation and matrix production. (3) We will determine how D-amino acids are produced late in the life cycle of the biofilm and how they trigger biofilm disassembly. We will determine the regulatory mechanisms that control the expression of the racemase genes that are responsible for D-amino acid production, how D-amino acids are incorporated into the peptidoglycan and how they trigger the release of an amyloid-fiber component of the matrix. (4) We will determine the full cascade of regulatory events that govern the differentiation of a cell into a spore, including the mechanisms that govern switching from one sigma factor to another. Understanding how D-amino acids cause biofilm disassembly will inform strategies for blocking biofilm formation by pathogenic bacteria. Also, research into gene control by B. subtilis, the principal model organism for Gram-positive bacteria, has provided, and will continue to provide, fundamental insights into the molecular biology of related, pathogenic bacteria, such as Staphylococcus, Enterococcus and B. anthracis.

描述(由申请人提供)：该项目的目标是揭示基因控制的启动机制，并区分枯草芽孢杆菌孢子形成和基质产生的发育程序。孢子形成传统上被认为是自由生活的细胞的一种行为，但我们现在了解到，分化也发生在由产生基质的细胞链和形成孢子的细胞链组成的结构化的多细胞群落(生物膜)的背景下。事实上，控制进入产孢子的机制与控制基质产生的机制密切相关。这项建议解决了我们对孢子形成和多细胞特性理解上的重要空白，有四个具体目标：(1)我们将通过两个传感器组氨酸激酶来识别触发孢子形成和多细胞特性的自然环境信号。(2)我们将使用一种新设计的微流控设备实时可视化细胞命运在浮游状态和基质产生状态之间的转换。我们将确定双负反馈回路如何控制开关，以及细胞如何区分孢子形成和基质产生的不同命运。(3)我们将确定D-氨基酸在生物膜生命周期后期是如何产生的，以及它们如何触发生物膜的分解。我们将确定控制外消旋酶基因表达的调控机制，这些外消旋酶基因负责产生D-氨基酸，D-氨基酸如何结合到肽聚糖中，以及它们如何触发基质中淀粉样纤维成分的释放。(4)我们将确定控制细胞分化为孢子的一连串调控事件，包括控制从一个西格玛因子切换到另一个西格玛因子的机制。了解D-氨基酸是如何导致生物膜分解的，将为阻止病原菌形成生物膜的策略提供依据。此外，对革兰氏阳性细菌的主要模式生物枯草杆菌的基因控制的研究已经并将继续提供对相关致病细菌的分子生物学的基本见解，如葡萄球菌、肠球菌和炭疽杆菌。