Frenkiel-Krispin Daphna, Minsky Abraham
Department of Organic Chemistry, The Weizmann Institute of Science, Rehovot 76100, Israel.
J Struct Biol. 2006 Nov;156(2):311-9. doi: 10.1016/j.jsb.2006.05.014. Epub 2006 Jul 8.
For enzymatic activities to be effectively carried out, basic prerequisites must be met. Many enzymatic tasks require continuous consumption and dissipation of energy, sometimes in massive amounts. Some activities, such as DNA replication, transcription, and repair through homologous recombination rely upon templates that provide the information required for these transactions. Yet, circumstances where intracellular energy pools are severely depleted, or where intact templates are not available, frequently occur. Moreover, the fact that in order to reach their targets, enzymes must cope with an extremely crowded and viscous cellular milieu that drastically slows down their diffusion is often neglected. These impediments are particularly evident under stress conditions such as prolonged starvation or continuous exposure to DNA-damaging agents. Here we survey recent studies, which imply that when enzymatically-mediated DNA repair pathways are hindered, alternative strategies are deployed, whose common denominator is the reorganization of bacterial nucleoids into morphologies that promote DNA repair and protection.
为了使酶活性能够有效发挥,必须满足一些基本前提条件。许多酶促任务需要持续消耗和散能,有时消耗量巨大。一些活动,如DNA复制、转录以及通过同源重组进行的修复,依赖于提供这些过程所需信息的模板。然而,细胞内能量储备严重耗尽或完整模板不可用的情况经常发生。此外,酶为了到达其作用靶点,必须应对极其拥挤且黏稠的细胞环境,这会极大地减缓它们的扩散,而这一事实常常被忽视。在诸如长期饥饿或持续暴露于DNA损伤剂等应激条件下,这些障碍尤为明显。在此,我们综述了近期的研究,这些研究表明,当酶介导的DNA修复途径受阻时,会采用替代策略,其共同特点是将细菌类核重组成促进DNA修复和保护的形态。