Grob Guillaume, Hemmerle Marine, Yakobov Nathaniel, Mahmoudi Nassira, Fischer Frederic, Senger Bruno, Becker Hubert Dominique
Génétique Moléculaire, Génomique, Microbiologie UMR7156, University of Strasbourg, 4 Allée Konrad Roentgen, Strasbourg, 6700, France.
The Hospital for Sick Children, 555 University Avenue, Toronto, ON M5G 1X8, Canada.
Biochimie. 2022 Dec;203:93-105. doi: 10.1016/j.biochi.2022.09.017. Epub 2022 Sep 30.
The objective of the present review is to provide an insight into modifications of microbial cell walls and membrane constituents by using the aminoacyl-tRNA as amino acid donor. In bacteria, phospholipids are modified by Multiple peptide resistance Factor enzymes and peptidoglycan precursors by so called fem ligases. Although these modifications were thought to be restricted to procaryotes, we discovered enzymes that modify ergosterol (the main component of fungal membrane) with glycine and aspartate. The focus of this review is to present the molecular mechanisms underlying all these processes together with the structure of the enzymes and their substrates. This article also reviews how substrates are recognized and modified and how the products are subsequently exported in various organisms. Finally, the physiological outcome and the discoveries of each family of enzymes is also discussed.
本综述的目的是深入了解利用氨酰-tRNA作为氨基酸供体对微生物细胞壁和膜成分进行的修饰。在细菌中,磷脂由多重肽抗性因子酶修饰,肽聚糖前体由所谓的fem连接酶修饰。尽管这些修饰被认为仅限于原核生物,但我们发现了用甘氨酸和天冬氨酸修饰麦角固醇(真菌膜的主要成分)的酶。本综述的重点是介绍所有这些过程背后的分子机制以及酶及其底物的结构。本文还综述了底物如何被识别和修饰,以及产物随后如何在各种生物体中输出。最后,还讨论了每个酶家族的生理结果和发现。