Pleiotropic effects of a relC mutation in Streptomyces antibioticus

J Bacteriol. 1991 Apr;173(7):2297-300. doi: 10.1128/jb.173.7.2297-2300.1991.

Abstract

Ochi (Agric. Biol. Chem. 51:829-835, 1987) has isolated a relaxed mutant of Streptomyces antibioticus, designated relC49, relC49 accumulates significantly lower levels of ppGpp than the parent stain, IMRU3720. At its maximum, the ppGpp level in relC49 was only one-fourth that observed in strain IMRU3720. Interestingly, a burst of ppGpp synthesis between 18 and 22 h of growth in IMRU3720 coincided with the onset of actinomycin production in that strain. As shown previously, the activity in protein synthesis of ribosomes from strain IMRU3720 decreases with the age of the culture. The decrease in activity was less pronounced in cultures of relC49. relC49 mycelium contains reduced levels of phenoxazinone synthase, a key enzyme involved in actinomycin biosynthesis. The rel mutation prevents the normal increase in the activity of one of the other enzymes required for production of the antibiotic, 3-hydroxyanthanilate-4-methyltransferase, and a third enzyme, actinomycin synthetase I, appears to be completely absent from relC49 mycelium. Levels of phenoxazinone synthease mRNA were examined by RNA dot blotting with the cloned phenoxazinone synthase gene as a probe. mRNA levels for phenoxazinone synthase were dramatically reduced in relC49 compared with strain IMRU3720. These results are discussed in terms of the possible regulation of the onset of actinomycin production by ppGpp.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Dactinomycin / biosynthesis
  • Gene Expression Regulation, Bacterial
  • Guanosine Tetraphosphate / metabolism
  • Mutation
  • Oxidoreductases / genetics
  • RNA, Bacterial / metabolism
  • RNA, Messenger / metabolism
  • Ribosomes / metabolism
  • Streptomyces antibioticus / genetics*

Substances

  • RNA, Bacterial
  • RNA, Messenger
  • Dactinomycin
  • Guanosine Tetraphosphate
  • Oxidoreductases
  • 2-aminophenol oxidase