Dynamics of enzyme aggregates of carbon core metabolism in growing and starved cells / a. Interactome studies

生长和饥饿细胞中碳核心代谢酶聚集体的动力学/a。

• 批准号: BB/F003412/1
• 负责人: Colin Harwood
• 金额: $ 46.07万
• 依托单位: Newcastle University
• 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
• 起止时间: 2007 至 无数据
• 项目状态: 已结题
• 来源: https://gtr.ukri.org/projects?ref=BB%2FF003412%2F1
• 关键词: Dynamics; enzyme; aggregates; carbon; core

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.

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。除了作为模型系统之外，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。