课题基金 / 基金详情

Molecular mechanism of cell curvature in the spiral-shaped bacterium Rhodospirillum rubrum

Molecular mechanism of cell curvature in the spiral-shaped bacterium Rhodospirillum rubrum
螺旋状细菌红色红螺菌细胞曲率的分子机制
批准号:
450420164
负责人:
Professor Dr. Martin Rudolf Thanbichler
金额:
$0.0万
依托单位国家:
德国
项目类别:
Research Grants
财政年份:
--
资助国家:
德国
项目状态:
未结题
起止时间:

项目摘要

项目成果

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
Bacteria show a high diversity of cell shapes, which in most cases are determined by the peptidoglycan cell wall. Previous work has revealed that the prototypical rod-shaped morphologies of standard model organisms are generated by two major peptidoglycan biosynthetic complexes, the elongasome and the divisome. In these complexes, synthetic, lytic and regulatory proteins are combined to coordinately remodel the peptidoglycan layer in order to generate the cylindrical and spherical elements of the cell, respectively. However, the mechanisms underlying the establishment of more complex morphologies are still poorly understood. Widespread variations of the common rod shape are curved or spiral morphologies, which arise by differential growth of the rod-shaped peptidoglyan layer at the inner and outer curvature. Curved shapes are commonly found among bacteria, and it appears that the underlying shape-generating mechanisms differ fundamentally between different lineages. However, even for well-investigated systems, the precise modes of action of the shape determinants identified are still unclear. Here, we propose to study the establishment of cell curvature in the spiral-shaped bacterium Rhodospirillum rubrum. In preliminary work, we have identified a novel peptidoglycan-binding outer-membrane lipoprotein, PapS, which forms a filament-like structure at the outer curvature of the R. rubrum cell and is essential for its spiral morphology. PapS is highly conserved among the members of the Rhodospirillaceae, a family comprising a large number of curved and spiral-shaped species, suggesting that it represents a key cell shape determinant in this lineage. We propose to unravel the function of PapS using a combination of cell biological, genetic, biochemical and biophysical approaches. These studies will provide insight into a novel and widespread pathway of shape determination in bacteria and thus significantly further our understanding of bacterial cell wall biosynthesis and morphogenesis.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
国内基金
海外基金
配子生成素GGN不同位点突变损伤分子伴侣BIP及HSP90B1功能导致精子形成障碍的发病机理
  • 批准号:
    82371616
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    姚晨成
  • 依托单位:
糖尿病ED中成纤维细胞衰老调控内皮细胞线粒体稳态失衡的机制研究
  • 批准号:
    82371634
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    赵福军
  • 依托单位:
骨髓ISG+NAMPT+中性粒细胞介导抗磷脂综合征B细胞异常活化的机制研究
  • 批准号:
    82371799
  • 项目类别:
    面上项目
  • 资助金额:
    47.00万元
  • 批准年份:
    2023
  • 负责人:
    杨程德
  • 依托单位:
IL-4协同精氨酸优化种植初期巨噬细胞胞葬作用和成骨微环境的作用及机制研究
  • 批准号:
    82370923
  • 项目类别:
    面上项目
  • 资助金额:
    48.00万元
  • 批准年份:
    2023
  • 负责人:
    张文杰
  • 依托单位: