ENTRY OF ESCHERICHIA-COLI INTO STATIONARY-PHASE IS INDICATED BY ENDOGENOUS AND EXOGENOUS ACCUMULATION OF NUCLEOBASES

Citation
U. Rinas et al., ENTRY OF ESCHERICHIA-COLI INTO STATIONARY-PHASE IS INDICATED BY ENDOGENOUS AND EXOGENOUS ACCUMULATION OF NUCLEOBASES, Applied and environmental microbiology, 61(12), 1995, pp. 4147-4151
Citations number
45
Categorie Soggetti
Microbiology,"Biothechnology & Applied Migrobiology
ISSN journal
00992240
Volume
61
Issue
12
Year of publication
1995
Pages
4147 - 4151
Database
ISI
SICI code
0099-2240(1995)61:12<4147:EOEISI>2.0.ZU;2-V
Abstract
Endogenous and exogenous accumulation of nucleobases was observed when Escherichia coli entered the stationary phase. The onset of the stati onary phase was accompanied by excretion of uracil and xanthine, Excep t for uracil and xanthine, other nucleobases (except for minor amounts of hypoxanthine), nucleosides, and nucleotides (except for cyclic AMP ) were not detected in significant amounts in the culture medium. In a ddition to exogenous accumulation of nucleobases, stationary-phase cel ls increased the endogenous concentrations of free nucleobases. In con trast to extracellular nucleobases, hypoxanthine was the dominating in tracellular nucleobase and xanthine was present only in minor concentr ations inside the cells. Excretion of nucleobases was always connected to declining growth rates. It was observed in response to entry into the stationary phase independent of the initial cause of the cessation of cell growth (e.g., starvation for essential nutrients), In additio n, transient accumulation of exogenous nucleobases was observed during perturbations of balanced growth conditions such as energy source dow nshifts. The nucleobases uracil and xanthine are the final breakdown p roducts of pyrimidine (uracil and cytosine) and purine (adenine and gu anine) bases, respectively, Hypoxanthine is the primary degradation pr oduct of adenine, which is further oxidized to xanthine. The endogenou s and exogenous accumulation of these nucleobases in response to entry into the stationary phase is attributed to degradation of rRNA.