Septum Asymmetry as a Cell Fate Determinant
隔膜不对称作为细胞命运的决定因素
基本信息
- 批准号:6626191
- 负责人:
- 金额:$ 4.16万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2002
- 资助国家:美国
- 起止时间:2002-06-01 至 2005-05-31
- 项目状态:已结题
- 来源:
- 关键词:Bacillus subtilis antiseptic sterilization bacterial genetics bacterial proteins cell differentiation cellular polarity chromosome movement developmental genetics fluorescence resonance energy transfer food sanitation gene environment interaction gene mutation intermolecular interaction membrane proteins microorganism reproduction microscopy polymerase chain reaction postdoctoral investigator protein localization protein structure function reporter genes spores transcription factor
项目摘要
DESCRIPTION (provided by applicant): The overall objective of the proposed
research is to characterize the molecular events that establish cell
differentiation during spore formation in Bacillus subtilis. Bacterial spores
are highly resistant to many common sterilization techniques and often are
implicated in food-borne illness. Understanding the process of sporulation
should allow for the development of new, more effective sterilization
techniques. The proposed experiments are conceptually based on a model where
the developmental pathway leading to spore formation is established, in part,
by the asymmetric distribution of integral membrane proteins across the
sporulation septum. This model will be tested by methods designed to determine
both the distribution of proteins across the septum, and the mechanisms by
which these proteins are restricted to one or the other cell following
division. These methods are broadly applicable to the study of other
disciplines and therefore, should contribute generally to science and
ultimately to human health.
简介(由申请人提供):建议的整体目标
研究是描述建立细胞的分子事件的特征
枯草芽孢杆菌芽胞形成过程中的分化。细菌孢子
对许多常见的消毒技术具有高度的抵抗力,而且通常是
与食源性疾病有关。了解产孢子的过程
应允许开发新的、更有效的绝育方法
技巧。拟议的实验在概念上基于一个模型,在该模型中
部分地建立了导致孢子形成的发育途径,
由于整膜蛋白在整个细胞膜上的不对称分布
孢子形成隔膜。该模型将通过设计用于确定
无论是蛋白质在隔膜上的分布,还是通过
这些蛋白质被限制在下面的一个或另一个细胞上
组织。这些方法广泛适用于研究其他
因此,应该普遍地为科学和
最终影响到人类健康。
项目成果
期刊论文数量(0)
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会议论文数量(0)
专利数量(0)
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