Wick Lukas M, Egli Thomas
Department of Environmental Microbiology and Molecular Ecotoxicology, Swiss Federal Institute for Environmental Science and Technology, PO Box 611, 8600 Dübendorf, Switzerland.
Adv Biochem Eng Biotechnol. 2004;89:1-45. doi: 10.1007/b93957.
In order to survive under and adapt to different conditions Escherichia coli has evolved elaborate systems that are able to sense and respond to environmental stimuli. Very often, different stresses act on a bacterium simultaneously and a variety of stresses have similar effects on cellular molecules and processes. Therefore, the various stress response systems have to interact (cross talk) with each other. A complex network of global regulatory systems with a multitude of molecular components ensures a coordinated and effective answer. Such regulatory components include DNA, mRNAs, sRNAs, proteins, such as DNA-and RNA binding proteins, alternative sigma factors and two-component systems, as well as small molecular weight molecules, as for example (p)ppGpp. These regulatory systems govern the expression of a plethora of further effectors that aim at maintaining stability of the cellular equilibrium under the various conditions. Using five of the most important stress response systems, we will discuss the roles and mechanisms of such regulatory and effector molecules in more detail. The heat shock response, controlled by the sigma factor sigma32, and the envelope stress response, controlled by the sigma factor sigmaE and the Cpx two-component system, both result in an increased expression of chaperones and proteases in response to misfolded proteins. The cold shock response governs expression of RNA chaperones and ribosomal factors, ensuring accurate translation at low temperatures. The general stress response depends on the sigma factor sigmaS, which controls the expression of more than 50 genes conferring resistance to many different stresses. The (p)ppGpp-dependent stringent response reduces the cellular protein synthesis capacity and controls further global responses upon nutritional downshift. A lot has been learned in recent years about the mechanisms of action of single components. However, the main challenge for the future is to achieve an understanding of the interactions of these components under different physiological conditions.
为了在不同条件下生存并适应环境,大肠杆菌进化出了复杂的系统,能够感知并响应环境刺激。通常,不同的压力会同时作用于细菌,多种压力对细胞分子和过程具有相似的影响。因此,各种应激反应系统必须相互作用(相互影响)。由众多分子成分组成的复杂全局调控系统网络确保了协调有效的反应。这些调控成分包括DNA、mRNA、sRNA、蛋白质,如DNA和RNA结合蛋白、替代西格玛因子和双组分系统,以及小分子重量分子,例如(p)ppGpp。这些调控系统控制着大量其他效应物的表达,旨在在各种条件下维持细胞平衡的稳定性。我们将使用五个最重要的应激反应系统,更详细地讨论此类调控和效应分子的作用及机制。由西格玛因子sigma32控制的热休克反应,以及由西格玛因子sigmaE和Cpx双组分系统控制的包膜应激反应,都会因错误折叠的蛋白质而导致伴侣蛋白和蛋白酶的表达增加。冷休克反应控制RNA伴侣蛋白和核糖体因子的表达,确保在低温下准确翻译。一般应激反应取决于西格玛因子sigmaS,它控制着50多个赋予对多种不同压力抗性的基因的表达。依赖(p)ppGpp的严格反应会降低细胞蛋白质合成能力,并在营养水平下降时控制进一步的全局反应。近年来,人们对单个成分的作用机制有了很多了解。然而,未来的主要挑战是了解这些成分在不同生理条件下的相互作用。