• From left: Prof. S. Sano, Dr. M. Nakao (Tokushima University, Japan)

      zoom

Synthesis of the Siderophore Erythrochelin

Shigeki Sano reports the synthesis of the hydroxamate-type siderophore erythrochelin.

Synthesis of Erythrochelin: A Hydroxamate-Type Siderophore from Saccharopolyspora erythraea: M. Nakao, S. Tsuji, S. Kitaike, S. Sano

Synthesis 2016, DOI: 10.1055/s-0035-1560564


Erythrochelin is a natural tetrapeptide whose synthesis and specific optical rotation have been recently described for the first time by the group of Professor Shigeki Sano from Tokushima University (Japan). Key step in the synthesis is a cyclization of the dipeptide precursor to provide the core 2,5-diketopiperazine ring.

 

  • Synthesis of erythrochelin

      zoom

Professor Sano commented:

“The first synthesis of erythrochelin, a hydroxamate-type siderophore from Saccharopolyspora erythraea, is described and its metal-chelating ability with not only Fe(III) but also Mg(II) is confirmed based on ESI-MS analysis.” 

Get Trial Access to the chemistry journals
Download SYNFORM or read it online