Abstract
Accumulation of guanosine tetraphosphate (ppGpp) in Escherichia coli strain AS19 valS, carrying a temperature-sensitive valyl-transfer ribonucleic acid synthetase and infected with bacteriophage T7, was studied. Valine starvation was achieved by culturing this strain at 42 C. Addition of rifampin to an uninfected culture at the nonpermissive temperature resulted in loss of accumulated ppGpp; however, cultures infected with phage T7, treated with rifampin, and then shifted to the nonpermissive temperature maintained the ability to accumulate ppGpp. Moreover, treatment of the T7-infected culture with rubidomycin, an antibiotic which inhibits transcription, did not reduce the amount of ppGpp accumulated following shift to the nonpermissive temperature. Measurements of the instantaneous rate of T7 transcription showed that it is not under stringent control of amino acids. ppGpp synthesized in T7-infected E. coli appears to be more stable than its counterpart in an uninfected culture. These results are interpreted to mean that ppGpp production is not directly dependent on transcription and arises instead from inhibition of another reaction, most likely some aspect of translation.
Full text
PDF






Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Cashel M., Gallant J. Two compounds implicated in the function of the RC gene of Escherichia coli. Nature. 1969 Mar 1;221(5183):838–841. doi: 10.1038/221838a0. [DOI] [PubMed] [Google Scholar]
 - Cashel M., Kalbacher B. The control of ribonucleic acid synthesis in Escherichia coli. V. Characterization of a nucleotide associated with the stringent response. J Biol Chem. 1970 May 10;245(9):2309–2318. [PubMed] [Google Scholar]
 - Cashel M., Lazzarini R. A., Kalbacher B. An improved method for thin-layer chromatography of nucleotide mixtures containing 32P-labelled orthophosphate. J Chromatogr. 1969 Mar 11;40(1):103–109. doi: 10.1016/s0021-9673(01)96624-5. [DOI] [PubMed] [Google Scholar]
 - Cashel M. The control of ribonucleic acid synthesis in Escherichia coli. IV. Relevance of unusual phosphorylated compounds from amino acid-starved stringent strains. J Biol Chem. 1969 Jun 25;244(12):3133–3141. [PubMed] [Google Scholar]
 - Erlich H., Laffler T., Gallant J. ppGpp formation in Escherichia coli treated with rifampicin. J Biol Chem. 1971 Oct 10;246(19):6121–6123. [PubMed] [Google Scholar]
 - Gallant J., Irr J., Cashel M. The mechanism of amino acid control of guanylate and adenylate biosynthesis. J Biol Chem. 1971 Sep 25;246(18):5812–5816. [PubMed] [Google Scholar]
 - Goldberg I. H., Friedman P. A. Antibiotics and nucleic acids. Annu Rev Biochem. 1971;40:775–810. doi: 10.1146/annurev.bi.40.070171.004015. [DOI] [PubMed] [Google Scholar]
 - Harshman R. B., Yamazaki H. Formation of ppGpp in a relaxed and stringent strain of Escherichia coli during diauxie lag. Biochemistry. 1971 Oct 12;10(21):3980–3982. doi: 10.1021/bi00797a027. [DOI] [PubMed] [Google Scholar]
 - Harshman R. B., Yamazaki H. MSI accumulation induced by sodium chloride. Biochemistry. 1972 Feb 15;11(4):615–618. doi: 10.1021/bi00754a023. [DOI] [PubMed] [Google Scholar]
 - Lazzarini R. A., Cashel M., Gallant J. On the regulation of guanosine tetraphosphate levels in stringent and relaxed strains of Escherichia coli. J Biol Chem. 1971 Jul 25;246(14):4381–4385. [PubMed] [Google Scholar]
 - Lazzarini R. A., Dahlberg A. E. The control of ribonucleic acid synthesis during amino acid deprivation in Escherichia coli. J Biol Chem. 1971 Jan 25;246(2):420–429. [PubMed] [Google Scholar]
 - Marrs B. L., Yanofsky C. Host and bacteriophage specific messenger RNA degradation in T7-infected Escherichia coli. Nat New Biol. 1971 Dec 8;234(49):168–170. doi: 10.1038/newbio234168a0. [DOI] [PubMed] [Google Scholar]
 - Sekiguchi M., Iida S. Mutants of Escherichia coli permeable to actinomycin. Proc Natl Acad Sci U S A. 1967 Dec;58(6):2315–2320. doi: 10.1073/pnas.58.6.2315. [DOI] [PMC free article] [PubMed] [Google Scholar]
 - Studier F. W. The genetics and physiology of bacteriophage T7. Virology. 1969 Nov;39(3):562–574. doi: 10.1016/0042-6822(69)90104-4. [DOI] [PubMed] [Google Scholar]
 - Summers W. C. The process of infection with coliphage T7. IV. Stability of RNA in bacteriophage-infected cells. J Mol Biol. 1970 Aug;51(3):671–678. doi: 10.1016/0022-2836(70)90015-x. [DOI] [PubMed] [Google Scholar]
 - Tingle M. A., Neidhardt F. C. Mapping of a structural gene for valyl-transfer ribonucleic acid synthetase in Escherichia coli by transduction. J Bacteriol. 1969 May;98(2):837–839. doi: 10.1128/jb.98.2.837-839.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
 - Winslow R. M., Lazzarini R. A. Amino acid regulation of the rates of synthesis and chain elongation of ribonucleic acid in Escherichia coli. J Biol Chem. 1969 Jun 25;244(12):3387–3392. [PubMed] [Google Scholar]
 - Wong J. T., Nazar R. N. Relationship of the MS nucleotides to the regulation of ribonucleic acid synthesis in Escherichia coli. J Biol Chem. 1970 Sep 10;245(17):4591–4593. [PubMed] [Google Scholar]
 
