Sandoval-Calderón Mario, Guan Ziqiang, Sohlenkamp Christian
Centro de Ciencias Genómicas, Universidad Nacional Autónoma de México, Cuernavaca, Mexico.
Department of Biochemistry, Duke University Medical Center, Durham, NC, USA.
Biochimie. 2017 Oct;141:21-29. doi: 10.1016/j.biochi.2017.05.008. Epub 2017 May 15.
Bacteria belonging to the genus Streptomyces are among the most prolific producers of antibiotics. Research on cellular membrane biosynthesis and turnover is lagging behind in Streptomyces compared to related organisms like Mycobacterium tuberculosis. While natural products discovery in Streptomyces is evidently a priority in order to discover new antibiotics to combat the increase in antibiotic resistant pathogens, a better understanding of this cellular compartment should provide insights into the interplay between core and secondary metabolism. However, some of the pathways for membrane lipid biosynthesis are still incomplete. In addition, while it has become clear that remodelling of the membrane is necessary for coping with environmental stress and for morphological differentiation, the detailed mechanisms of these adaptations remain elusive. Here, we aim to provide a summary of what is known about the polar lipid composition in Streptomyces, the biosynthetic pathways of polar lipids, and to highlight current gaps in understanding function, dynamics and biosynthesis of these essential molecules.
链霉菌属细菌是抗生素的最多产生产者之一。与结核分枝杆菌等相关生物相比,链霉菌中细胞膜生物合成和周转的研究相对滞后。虽然显然优先在链霉菌中发现天然产物以发现新的抗生素来对抗抗生素耐药病原体的增加,但更好地了解这个细胞区室应该能深入了解核心代谢和次级代谢之间的相互作用。然而,一些膜脂生物合成途径仍然不完整。此外,虽然已经清楚膜重塑对于应对环境压力和形态分化是必要的,但这些适应的详细机制仍然难以捉摸。在这里,我们旨在总结关于链霉菌中极性脂质组成、极性脂质生物合成途径的已知信息,并突出当前在理解这些必需分子的功能、动态和生物合成方面的差距。