Bacterial cell wall synthesis, shape and septation

细菌细胞壁的合成、形状和分隔

• 批准号: 8721967
• 负责人: KEVIN D YOUNG
• 金额: $ 46.79万
• 依托单位: UNIV OF ARKANSAS FOR MED SCIS
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-07-01 至 2017-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8721967
• 关键词: Address; Affect; Antibiotic Therapy; Antibiotics; Bacteria; Bacterial Physiology; Biological Assay; Biological Process; Cell Shape; Cell Wall; Cell division; Cells; Cellular biology; Characteristics; Cosmetics; Cytokinesis; Cytoplasm; Cytoplasmic Protein; Cytoplasmic Structures; Ecology; Effectiveness; Enzymes; Escherichia coli; Exhibits; Fluorescence-Activated Cell Sorting; Generations; Genetic; Geometry; Goals; Grant; Growth; Hand; Immune; Immune system; Infection; Investigation; Knowledge; Light; Link; Maintenance; Medical; Membrane; Metabolism; Methods; Minor; Modeling; Modification; Molds; Morphology; Nature; Nutrient; Nutritional status; Organism; Osmotic Pressure; Pathogenesis; Pathway interactions; Penicillin-Binding Proteins; Peptidoglycan; Play; Predatory Behavior; Process; Property; Proteins; Protocols documentation; Reaction; Recovery; Regulation; Renaissance; Resistance; Resources; Role; Shapes; Signal Transduction; Spheroplasts; Stress; Structure; Surface; System; Techniques; Technology; Time; Virulence; Work; antimicrobial drug; assault; cell motility; coping; in vivo; microorganism; mutant; novel; pathogenic bacteria; periplasm; public health relevance; tool; uptake

DESCRIPTION (provided by applicant): Bacteria exhibit extreme morphological diversity, a fact known since they were first visualized over 300 years ago. Yet only in the last 5-7 years has it become clear that these differences are much more than cosmetic. Instead, cell shape is of fundamental and medical importance, contributing to bacterial survival and virulence by influencing nutrient uptake, cell-to-surface attachment, motility, differentiation, and resistance to predation and host immune assaults. Nor is morphology static: bacteria invest significant resources to manipulate their shapes to cope with changes in growth rate and nutritional status and to respond to antibiotics and other environmental stresses. In short, morphology is not a frivolous or neutral characteristic, but plays crucial roles in bacterial cell biology, ecology and pathogenesis. Despite a recent renaissance in such studies, we understand surprisingly little about how cells create and maintain their shapes. What we do know is that most bacteria are protected by a peptidoglycan cell wall and that the way this wall is synthesized determines cell shape. Our long-term goal is to understand the structure, synthesis, regulation and functional implications of peptidoglycan and the enzymes that create and modify it. To that end, we propose to extend our understanding of bacterial physiology and morphology by pursuing the following Aims. Aim 1] Identify new morphological mechanisms and regulators by applying newly adapted methods for enriching shape mutants via fluorescence- activated cell sorting (FACS). One reason so little is known about these matters is because almost all morphological regulatory agents were discovered accidently. Here, we will use FACS as a genetic tool to enrich, isolate and study morphological mutants in a directed search for new mechanisms that regulate bacterial shape. Aim 2] Identify and characterize the mechanisms required for de novo shape generation by employing a newly devised Spheroplast Recovery assay. Virtually everything known about cell wall synthesis and morphology involves mechanisms that preserve or extend pre-existing walls. Little or nothing is known about how cells re-create their shapes when their walls are damaged severely or removed altogether, as occurs when bacteria encounter host immune systems. We find that survival in these latter circumstances demands new mechanisms to support or supplant the classic maintenance pathways. Aim 3] Characterize critical FtsZ- peptidoglycan reactions, particularly those that will tell us: a) how periplasmic peptidoglycan and penicillin binding proteins control the geometry of the cytoplasmic Z ring during cell division; and b) how cytoplasmic FtsZ triggers the synthesis of peptidoglycan during the critical transition from cell elongation to division. These poorly-understood interactions determine the integrity, shape and propagation of bacterial cells. In summary, these new tools and approaches will enable us to investigate, faster and in greater depth, the numerous mysteries that still obscure our understanding of some of the most basic issues in bacterial physiology. The work will also serve as a model for similar morphological investigations in other organisms.

描述（由申请人提供）： 细菌表现出极端的形态多样性，这是自300多年前第一次被发现以来就知道的事实。然而，只有在过去的5-7年里，人们才清楚地认识到，这些差异不仅仅是表面上的。相反，细胞形状是基本的和医学上的重要性，有助于细菌的生存和毒力，通过影响营养吸收，细胞表面附着，运动，分化和抵抗捕食和宿主免疫攻击。形态学也不是静态的：细菌投入大量资源来操纵它们的形状，以科普生长速率和营养状态的变化，并对抗生素和其他环境压力作出反应。简而言之，形态不是一个轻浮或中性的特征，而是在细菌细胞生物学，生态学和致病机制中起着至关重要的作用。尽管最近这类研究有所复兴，但令人惊讶的是，我们对细胞如何创造和维持其形状的了解甚少。我们所知道的是，大多数细菌都受到肽聚糖细胞壁的保护，而肽聚糖细胞壁的合成方式决定了细胞的形状。我们的长期目标是 了解肽聚糖的结构、合成、调节和功能意义以及产生和修饰肽聚糖的酶。为此，我们建议通过追求以下目标来扩展我们对细菌生理学和形态学的理解。目的1]通过应用新适应的方法通过荧光激活细胞分选（FACS）富集形状突变体来鉴定新的形态学机制和调节剂。对这些问题知之甚少的一个原因是，几乎所有的形态调控因子都是偶然发现的。在这里，我们将使用流式细胞仪作为一种遗传工具，丰富，分离和研究形态突变体的新机制，调节细菌的形状定向搜索。目的2]通过采用新设计的球体恢复测定法来鉴定和表征从头形状产生所需的机制。几乎所有关于细胞壁合成和形态学的已知知识都涉及保留或扩展预先存在的细胞壁的机制。当细胞壁严重受损或完全被移除时，细胞如何重新创建它们的形状，就像细菌遇到宿主免疫系统时发生的那样，人们对此知之甚少或一无所知。我们发现，在后一种情况下生存需要新的机制来支持或取代经典的维持途径。目的3]表征关键的FtsZ-肽聚糖反应，特别是那些将告诉我们：a）周质肽聚糖和青霉素结合蛋白如何在细胞分裂期间控制细胞质Z环的几何形状;和B）细胞质FtsZ如何在从细胞伸长到分裂的关键转变期间触发肽聚糖的合成。这些知之甚少的相互作用决定了细菌细胞的完整性、形状和繁殖。总之，这些新的工具和方法将使我们能够更快、更深入地研究仍然模糊我们对细菌生理学中一些最基本问题的理解的众多谜团。这项工作也将作为其他生物类似形态学研究的模型。