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抗生素致死性与膜生物能量学。

Antibiotic Lethality and Membrane Bioenergetics.

机构信息

Department of Immunology and Microbiology, University of Colorado, Aurora, CO, United States.

Department of Immunology and Microbiology, University of Colorado, Aurora, CO, United States.

出版信息

Adv Microb Physiol. 2018;73:77-122. doi: 10.1016/bs.ampbs.2018.06.002. Epub 2018 Jul 20.

Abstract

A growing body of research suggests bacterial metabolism and membrane bioenergetics affect the lethality of a broad spectrum of antibiotics. Electrochemical gradients spanning energy-transducing membranes are the foundation of the chemiosmotic hypothesis and are essential for life; accordingly, their dysfunction appears to be a critical factor in bacterial death. Proton flux across energy-transducing membranes is central for cellular homeostasis as vectorial proton translocation generates a proton motive force used for ATP synthesis, pH homeostasis, and maintenance of solute gradients. Our recent investigations indicate that maintenance of pH homeostasis is a critical factor in antibiotic killing and suggest an imbalance in proton flux initiates disruptions in chemiosmotic gradients that lead to cell death. The complex and interconnected relationships between electron transport systems, central carbon metabolism, oxidative stress generation, pH homeostasis, and electrochemical gradients provide challenging obstacles to deciphering the roles for each of these processes in antibiotic lethality. In this chapter, we will present evidence for the pH homeostasis hypothesis of antibiotic lethality that bactericidal activity flows from disruption of cellular energetics and loss of chemiosmotic homeostasis. A holistic understanding of the interconnection of energetic processes and antibiotic activity may direct future research toward the development of more effective therapeutic interventions.

摘要

越来越多的研究表明,细菌代谢和膜生物能影响广谱抗生素的致死率。跨能量转换膜的电化学梯度是化学渗透假说的基础,是生命所必需的;因此,它们的功能障碍似乎是细菌死亡的一个关键因素。质子穿过能量转换膜的流动对于细胞内稳态至关重要,因为向量质子转移产生质子动力用于 ATP 合成、pH 内稳态和溶质梯度的维持。我们最近的研究表明,维持 pH 内稳态是抗生素杀伤的关键因素,并表明质子流动的不平衡会引发化学渗透梯度的破坏,从而导致细胞死亡。电子传递系统、中心碳代谢、氧化应激产生、pH 内稳态和电化学梯度之间复杂而相互关联的关系,为破译这些过程在抗生素致死性中的作用带来了挑战。在本章中,我们将提出 pH 内稳态假说,即抗生素致死性是由于细胞能量的破坏和化学渗透平衡的丧失导致的。对能量过程和抗生素活性之间的相互联系的全面理解,可能会指导未来的研究朝着开发更有效的治疗干预措施的方向发展。

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