The sorangicins, novel and powerful inhibitors of eubacterial RNA polymerase isolated from myxobacteria

J Antibiot (Tokyo). 1987 Jan;40(1):7-13. doi: 10.7164/antibiotics.40.7.

Abstract

A new antibiotic, sorangicin, was isolated from the culture supernatant of the myxobacterium, Sorangium (Polyangium) cellulosum strain So cel2. It is a macrocyclic lactone carbonic acid and is produced in two structural variants, sorangicins A and B. In addition small quantities of the respective glycosides, sorangiosids A and B, may be found. The antibiotic acts mainly against Gram-positive bacteria, including myocobacteria, with MIC values between 0.01 and 0.1 microgram/ml, but at higher concentrations (MIC 3 approximately 30 micrograms/ml) Gram-negatives are also inhibited. Yeasts and molds are completely resistant. The new antibiotic is a specific inhibitor of eubacterial RNA polymerase which it blocks, however, only if added before RNA polymerization has started.

Publication types

  • Comparative Study

MeSH terms

  • Aminoglycosides*
  • Anti-Bacterial Agents / pharmacology*
  • DNA-Directed RNA Polymerases / antagonists & inhibitors*
  • Eubacterium / enzymology*
  • Glycosides / isolation & purification
  • Glycosides / pharmacology
  • Gram-Positive Bacteria / drug effects
  • Magnetic Resonance Spectroscopy
  • Microbial Sensitivity Tests
  • Myxococcales / growth & development*
  • Structure-Activity Relationship

Substances

  • Aminoglycosides
  • Anti-Bacterial Agents
  • Glycosides
  • sorangicin A
  • sorangicin B
  • DNA-Directed RNA Polymerases