Blum S, Fielder H P, Groth I, Kempter C, Stephan H, Nicholson G, Metzger J W, Jung G
Biologisches Institut, Universität Tübingen, Germany.
J Antibiot (Tokyo). 1995 Jul;48(7):619-25. doi: 10.7164/antibiotics.48.619.
A new member of the quinoxaline group antibiotics has been detected by HPLC-diode-array screening. The main compound produced by Streptomyces tendae strain Tü 4031 showed a high degree of similarity in the UV-visible spectral region with echinomycin and their structural similarity was confirmed by structure elucidation using electron tandem mass spectrometry and 2D nuclear magnetic resonance. The new compound, named echinoserine, is a non-cyclic form of echinomycin, but it is not a biosynthetic precursor. Echinoserine is less antibiotically active than echinomycin.