Glutamic acid is a carrier for hydrazine during the biosyntheses of fosfazinomycin and kinamycin
The natural products fosfazinomycin A and kinamycin D are structurally distinct except for a nitrogen-nitrogen (N-N) bond. Here, the authors show that fosfazinomycin and kinamycin share a common pathway for N-N bond formation that is different from pathways found for other natural products.
Guardado en:
Autores principales: | Kwo-Kwang A. Wang, Tai L. Ng, Peng Wang, Zedu Huang, Emily P. Balskus, Wilfred A. van der Donk |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2018
|
Materias: | |
Acceso en línea: | https://doaj.org/article/0bfcbb1345f341b6b1521cc37c83a8a0 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Atmospheric reaction of hydrazine plus hydroxyl radical
por: Hamed Douroudgari, et al.
Publicado: (2021) -
Antioxidant and toxicity studies of biosynthesized cerium oxide nanoparticles in rats
por: Khorrami MB, et al.
Publicado: (2019) -
Self-powered H2 production with bifunctional hydrazine as sole consumable
por: Xijun Liu, et al.
Publicado: (2018) -
Renal targeting potential of a polymeric drug carrier, poly-L-glutamic acid, in normal and diabetic rats
por: Chai HJ, et al.
Publicado: (2017) -
On the function of biosynthesized cellulose as barrier against bacterial colonization of VAD drivelines
por: Julius Kaemmel, et al.
Publicado: (2021)