From the Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas 75390
J Biol Chem. 2018 Nov 30;293(48):18693-18701. doi: 10.1074/jbc.TM118.005670. Epub 2018 Sep 25.
Most of the phylogenetic diversity of life is found in bacteria and archaea, and is reflected in the diverse metabolism and functions of bacterial and archaeal polyamines. The polyamine spermidine was probably present in the last universal common ancestor, and polyamines are known to be necessary for critical physiological functions in bacteria, such as growth, biofilm formation, and other surface behaviors, and production of natural products, such as siderophores. There is also phylogenetic diversity of function, indicated by the role of polyamines in planktonic growth of different species, ranging from absolutely essential to entirely dispensable. However, the cellular molecular mechanisms responsible for polyamine function in bacterial growth are almost entirely unknown. In contrast, the molecular mechanisms of essential polyamine functions in archaea are better understood: covalent modification by polyamines of translation factor aIF5A and the agmatine modification of tRNA As with bacterial hyperthermophiles, archaeal thermophiles require long-chain and branched polyamines for growth at high temperatures. For bacterial species in which polyamines are essential for growth, it is still unknown whether the molecular mechanisms underpinning polyamine function involve covalent or noncovalent interactions. Understanding the cellular molecular mechanisms of polyamine function in bacterial growth and physiology remains one of the great challenges for future polyamine research.
生命的大部分系统发育多样性存在于细菌和古菌中,这反映在细菌和古菌多胺的多样代谢和功能上。多胺亚精胺可能存在于最后一个共同的祖先中,并且多胺被认为是细菌中关键生理功能所必需的,例如生长、生物膜形成和其他表面行为,以及天然产物如铁载体的产生。多胺的功能也存在系统发育多样性,这表明多胺在不同物种的浮游生长中的作用范围从绝对必需到完全可有可无。然而,负责细菌生长中多胺功能的细胞分子机制几乎完全未知。相比之下,多胺在古菌中必需的功能的分子机制理解得更好:多胺对翻译因子 aIF5A 的共价修饰和细菌高温生物中 tRNA 的胍基精氨酸修饰。古菌嗜热菌需要长链和支链多胺才能在高温下生长。对于多胺对生长至关重要的细菌物种,仍然不知道支持多胺功能的分子机制是否涉及共价或非共价相互作用。理解多胺在细菌生长和生理中的细胞分子机制仍然是未来多胺研究的重大挑战之一。