ASSEMBLY OF THE SPORE COAT OF B SUBTILIS
枯草芽孢杆菌孢子衣的组装
基本信息
- 批准号:6624175
- 负责人:
- 金额:$ 25.83万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1996
- 资助国家:美国
- 起止时间:1996-05-01 至 2006-05-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION (provided by applicant): Bacterial spores are among the most
extraordinary cell types found in nature. These specialized dormant cells are
resistant to virtually all forms of environmental assault but retain the
capacity to metamorphose into a growing cell as soon as conditions are
favorable. These abilities depend on the outermost protective shell that
surrounds the spore, a multilayered protein armor called the coat, which gives
the spore structural integrity and excludes all large molecules. In spite of
the amazing capabilities bestowed on spores by the coat, we know relatively
little about how it is built and how it provides protection. In this proposal,
we seek to identify the contacts between known coat proteins in Bacillus
subtilis spores as well as to discover novel coat proteins and the contacts
they make within the coat. In particular, we will determine which coat proteins
interact with two key proteins, called CotE and SpoIVA, that play important
roles in coat assembly. These studies will help us understand the formation of
this highly resistant cell type and the basis for its durability. Ultimately,
we intend to define the biochemical interactions that direct spore coat
assembly. This will provide a broader understanding of the molecular basis of
complex assembly events, a question of general relevance to cell biology. The
interest of this project is not confined to basic research, however, as
bacterial spores from a variety of organisms, particularly clostridia, are
major food pathogens and the spores produced by a relative of B. subtilis, B.
anthracis, can be used as a highly effective bioweapon. Much of the potency of
these pathogens is due to the coat, which permits rapid spore dispersal and
makes decontamination very difficult with current technology. Studies of coat
assembly may reveal novel approaches to combat these disease-causing agents.
描述(申请人提供):细菌孢子是最多的
自然界中发现的特殊细胞类型。这些特殊的休眠细胞是
抵抗几乎所有形式的环境攻击,但保留
一旦条件成熟,就有能力蜕变为生长细胞
有利的。这些能力依赖于最外层的保护壳
孢子周围有一层名为外套的多层蛋白质盔甲,它提供了
孢子结构完整,不包括所有大分子。尽管
被毛赋予孢子的惊人能力,我们知道相对
几乎没有关于它是如何建造的,以及它是如何提供保护的。在这份提案中,
我们试图确定芽孢杆菌中已知外壳蛋白之间的联系。
枯草杆菌孢子以及发现新的外壳蛋白和接触
他们在大衣里做的。特别是,我们将确定哪些外壳蛋白
与两种关键蛋白质相互作用,称为Cote和SpoIVA,这两种蛋白质发挥重要作用
在涂层装配中的角色。这些研究将有助于我们了解
这种高度耐受的细胞类型是其耐用性的基础。最终,
我们打算定义直接影响孢子被的生化相互作用。
集合。这将提供对分子基础的更广泛的理解。
复杂的组装事件,这是一个与细胞生物学普遍相关的问题。这个
然而,这个项目的兴趣并不局限于基础研究,因为
来自各种生物体,特别是梭状芽胞杆菌的细菌孢子是
主要食物病原菌和枯草芽孢杆菌、枯草芽孢杆菌、枯草杆菌亲缘菌株产生的孢子。
炭疽菌可作为一种高效的生物武器。它的大部分效力
这些病原体是由被毛引起的,它允许孢子快速扩散和
用目前的技术使去污变得非常困难。关于涂层的研究
组装可能会揭示对抗这些致病因子的新方法。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Adam Driks其他文献
Adam Driks的其他文献
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{{ truncateString('Adam Driks', 18)}}的其他基金
Localization and characterization of the Clostridium difficile biofilm
艰难梭菌生物膜的定位和表征
- 批准号:
8418693 - 财政年份:2012
- 资助金额:
$ 25.83万 - 项目类别:
Localization and characterization of the Clostridium difficile biofilm
艰难梭菌生物膜的定位和表征
- 批准号:
8228571 - 财政年份:2012
- 资助金额:
$ 25.83万 - 项目类别:
A novel anti-spore nasal vaccine for protection from anthrax
一种新型抗孢子鼻疫苗,可预防炭疽病
- 批准号:
8699135 - 财政年份:2011
- 资助金额:
$ 25.83万 - 项目类别:
A novel anti-spore nasal vaccine for protection from anthrax
一种新型抗孢子鼻疫苗,可预防炭疽病
- 批准号:
8077052 - 财政年份:2011
- 资助金额:
$ 25.83万 - 项目类别:
A novel anti-spore nasal vaccine for protection from anthrax
一种新型抗孢子鼻疫苗,可预防炭疽病
- 批准号:
8502611 - 财政年份:2011
- 资助金额:
$ 25.83万 - 项目类别:
A novel anti-spore nasal vaccine for protection from anthrax
一种新型抗孢子鼻疫苗,可预防炭疽病
- 批准号:
8892970 - 财政年份:2011
- 资助金额:
$ 25.83万 - 项目类别:
A novel anti-spore nasal vaccine for protection from anthrax
一种新型抗孢子鼻疫苗,可预防炭疽病
- 批准号:
8322006 - 财政年份:2011
- 资助金额:
$ 25.83万 - 项目类别:
IDENTIFICATION OF B. ANTRACIS SPORE-SURFACE PROTEINS
B.ANTRACIS 孢子表面蛋白的鉴定
- 批准号:
6562224 - 财政年份:2002
- 资助金额:
$ 25.83万 - 项目类别:
IDENTIFICATION OF B. ANTRACIS SPORE-SURFACE PROTEINS
B.ANTRACIS 孢子表面蛋白的鉴定
- 批准号:
6665140 - 财政年份:2002
- 资助金额:
$ 25.83万 - 项目类别:
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