Dynamics of enzyme aggregates of carbon core metabolism in growing and starved cells / a. Interactome studies
Dynamics of enzyme aggregates of carbon core metabolism in growing and starved cells / a. Interactome studies
批准号:
BB/F003412/1
负责人:
Colin Harwood
金额:
$46.07万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2007
资助国家:
英国
项目状态:
已结题
起止时间:
2007 至 --
中文摘要
该项目的目标是开发一个综合的理解代谢和遗传网络,控制从生长到葡萄糖饥饿的模式细菌,枯草芽孢杆菌的过渡。除了充当模型系统之外,B。枯草杆菌是“白色生物技术”的工业主力,因为它是工业酶和其他产品(例如维生素、抗生素、增味剂和生物化学品)的主要生产者。从生长到生长限制的转变是一种基本的生态生理反应,学术研究人员将其作为环境信号处理和整合的模型进行研究。理解这种转变对于主要在营养限制下发生的芽孢杆菌的工业发酵也是至关重要的。我们的方法是将生物数据与调节从生长到饥饿过渡的网络的数学模型相结合。该方法首先在标准化生长条件下定量监测确定的遗传和环境扰动。这些数据用于监管过程的数学建模。随着该计划的发展,我们理解的差距将通过结构性、全基因组网络分析来描述生物数据的失败而暴露出来。我们的概念是在明确定义的(子)项目中不断探索模型和数据的一致性,每个项目都涉及一个实验和一个建模合作伙伴。关键要素是模型驱动的实验设计,通过对关键变量的有针对性的测量来测试基于模型的假设。通过标准化的术语、模型格式和定义的输入/输出信号,模块化的数学模型可以集成到一致的系统表示中。总之,该项目将提供令人信服的证据,证明实验和计算科学家在先进的模式生物上的密切互动可以显着提高我们对微生物高度动态和复杂的调控过程的定量理解,并最终提高我们控制微生物高度动态和复杂调控过程的能力。
英文摘要
The objective of this project is to develop an integrated understanding of the metabolic and genetic network that controls the transition from growth to glucose starvation in the model bacterium, Bacillus subtilis. In addition to serving as a model system, B. subtilis is an industrial workhorse for 'white biotechnology' since it serves is a primary producer of technical enzymes and other products (e.g. vitamins, antibiotics, flavour enhancers and biochemicals). The transition from growth to growth limitation is a fundamental ecophysiological response and is studied by academic researchers as a model for environmental signal processing and integration. Understanding this transition is also pivotal for industrial fermentations of Bacillus that occur predominantly under nutrient limitation. Our approach is to integrate biological data with mathematical models of the networks that regulate the transition from growth to starvation. The approach starts with quantitative monitoring of defined genetic and environmental perturbations under standardized growth conditions. These data are used for mathematical modelling of regulatory processes. As the programme develops, gaps in our understanding will be revealed by the failure of structural, genome-wide network analyses to describe the biological data. Our concept is to continuously probe model and data consistency in clearly defined (sub)projects, each involving an experimental and a modelling partner. The pivotal element is a model-driven experimental design, where model-based hypotheses are tested through targeted measurements of critical variables. Facilitated through standardized nomenclature, model formats, and defined input/output signals, modular mathematical models are then integrated into a consistent systems representation. In summary, the project will provide convincing evidence that close interactions between experimental and computational scientists on a well advanced model organism can significantly advance our quantitative understanding of, and eventually our ability to control, the highly dynamic and complex regulatory processes in microbes.
期刊论文(2)
专著(0)
科研奖励(0)
会议论文
国内基金
海外基金
登录
查看更多内容
酶响应的中性粒细胞外泌体载药体系在眼眶骨缺损修复中的作用及机制研究
-
批准号:82371102
-
项目类别:面上项目
-
资助金额:49.00万元
-
批准年份:2023
-
负责人:苏蕴
-
依托单位:
PCBP1和PCBP2调控cGAS的相变和酶活的机制研究
-
批准号:32370928
-
项目类别:面上项目
-
资助金额:50.00万元
-
批准年份:2023
-
负责人:孙钦秒
-
依托单位:
蛋白精氨酸甲基化转移酶PRMT5调控PPARG促进巨噬细胞M2极化及其在肿瘤中作用的机制研究
-
批准号:82371738
-
项目类别:面上项目
-
资助金额:49.00万元
-
批准年份:2023
-
负责人:郑英霞
-
依托单位:
木质纤维素高效水解多酶混合物(multi-enzyme cocktails)的高通量分析及其理性定制
-
批准号:21176106
-
项目类别:面上项目
-
资助金额:60.0万元
-
批准年份:2011
-
负责人:孙付保
-
依托单位:
Nrf2-ARE通路在脑缺血性卒中的作用及机制研究
-
批准号:30700254
-
项目类别:青年科学基金项目
-
资助金额:15.0万元
-
批准年份:2007
-
负责人:刘晓云
-
依托单位:
非水相微波辐射-酶耦合催化(MIECC)的作用机制
-
批准号:20476038
-
项目类别:面上项目
-
资助金额:22.0万元
-
批准年份:2004
-
负责人:方云
-
依托单位: