The multifarious short-term regulation of ammonium assimilation of Escherichia coli:: dissection using an in silico replica

被引:42
作者
Bruggeman, FJ
Boogerd, FC
Westerhoff, HV
机构
[1] Vrije Univ Amsterdam, CRBCS, Inst Mol Cell Biol, NL-1081 HV Amsterdam, Netherlands
[2] Univ Amsterdam, SILS, NL-1012 WX Amsterdam, Netherlands
[3] Stellenbosch Inst Adv Studies, Stellenbosch, South Africa
基金
英国生物技术与生命科学研究理事会;
关键词
ammonium assimilation; systems biology; glutamine synthetase; robustness; silicon cell;
D O I
10.1111/j.1742-4658.2005.04626.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ammonium assimilation in Escherichia coli is regulated through multiple mechanisms (metabolic, signal transduction leading to covalent modification, transcription, and translation), which (in-)directly affect the activities of its two ammonium-assimilating enzymes, i.e. glutamine synthetase (GS) and glutamate dehydrogenase (GDH). Much is known about the kinetic properties of the components of the regulatory network that these enzymes are part of, but the ways in which, and the extents to which the network leads to subtle and quasi-intelligent regulation are unappreciated. To determine whether our present knowledge of the interactions between and the kinetic properties of the components of this network is complete - to the extent that when integrated in a kinetic model it suffices to calculate observed physiological behaviour - we now construct a kinetic model of this network, based on all of the kinetic data on the components that is available in the literature. We use this model to analyse regulation of ammonium assimilation at various carbon statuses for cells that have adapted to low and high ammonium concentrations. We show how a sudden increase in ammonium availability brings about a rapid redirection of the ammonium assimilation flux from GS/glutamate synthase (GOGAT) to GDH. The extent of redistribution depends on the nitrogen and carbon status of the cell. We develop a method to quantify the relative importance of the various regulators in the network. We find the importance is shared among regulators. We confirm that the adenylylation state of GS is the major regulator but that a total of 40% of the regulation is mediated by ADP (22%), glutamate (10%), glutamine (7%) and ATP (1%). The total steady-state ammonium assimilation flux is remarkably robust against changes in the ammonium concentration, but the fluxes through GS and GDH are completely nonrobust. Gene expression of GOGAT above a threshold value makes expression of GS under ammonium-limited conditions, and of GDH under glucose-limited conditions, sufficient for ammonium assimilation.
引用
收藏
页码:1965 / 1985
页数:21
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