Abstract
This paper reports the partial characterization of two temperature-sensitive mutants of Escherichia coli with alterations in ribosomal ribonucleic acid (rRNA) metabolism at the restrictive temperature. Both mutants continue to synthesize deoxyribonucleic acid and protein at 42 C but showed little or no accumulation of RNA. Both strains are inducible for beta-galactosidase at the restrictive temperature, showing that messenger RNA synthesis continues and that the messenger RNA is translated into functional protein. One of the strains, 2S474, shows a rather severe depression (sevenfold) in the synthesis of all classes of RNA at 42 C. In addition, the synthesis of rRNA is selectively depressed, with the percentage of rRNA synthesis. However, there appears to be a selective depression in the rate of rRNA synthesis and, possibly, in the conversion of p16S rRNA to m16S rRNA.
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Selected References
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- 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]
- Chaney S. G., Schlessinger D. Escherichia coli mutants deficient in RNA accumulation at high temperature. Biochim Biophys Acta. 1975 Jan 6;378(1):80–91. doi: 10.1016/0005-2787(75)90139-2. [DOI] [PubMed] [Google Scholar]
- Corte G., Schlessinger D., Longo D., Venkov P. Transformation of 17 s to 16 s ribosomal RNA using ribonuclease II of Escherichia coli. J Mol Biol. 1971 Sep 14;60(2):325–338. doi: 10.1016/0022-2836(71)90297-x. [DOI] [PubMed] [Google Scholar]
- Craig E., Cremer K., Schlessinger D. Metabolism of T4 messenger RNA, host messenger RNA and ribosomal RNA in T4-infected Escherichia coli B. J Mol Biol. 1972 Nov 28;71(3):701–715. doi: 10.1016/s0022-2836(72)80033-0. [DOI] [PubMed] [Google Scholar]
- Fiil N., Friesen J. D. Isolation of "relaxed" mutants of Escherichia coli. J Bacteriol. 1968 Feb;95(2):729–731. doi: 10.1128/jb.95.2.729-731.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gallant J., Margason G., Finch B. On the turnover of ppGpp in Escherichia coli. J Biol Chem. 1972 Oct 10;247(19):6055–6058. [PubMed] [Google Scholar]
- Gesteland R. F. Isolation and characterization of ribonuclease I mutants of Escherichia coli. J Mol Biol. 1966 Mar;16(1):67–84. doi: 10.1016/s0022-2836(66)80263-2. [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]
- Haseltine W. A., Block R. Synthesis of guanosine tetra- and pentaphosphate requires the presence of a codon-specific, uncharged transfer ribonucleic acid in the acceptor site of ribosomes. Proc Natl Acad Sci U S A. 1973 May;70(5):1564–1568. doi: 10.1073/pnas.70.5.1564. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Khan S. R., Yamazaki H. Correlation between guanosine tetraphosphate accumulation and degree of amino acid control of ribonucleic acid accumulation during nutritionally slowed growth in Escherichia coli. Biochemistry. 1974 Jun 18;13(13):2785–2788. doi: 10.1021/bi00710a019. [DOI] [PubMed] [Google Scholar]
- Khesin R. B., Mindlin S. Z., Gorlenko Z. M., Ilyina T. S. Temperature sensitive mutations affecting RNA synthesis in Escherichia coli. Mol Gen Genet. 1968;103(2):194–208. doi: 10.1007/BF00427146. [DOI] [PubMed] [Google Scholar]
- Khesin R. B., Shemyakin M. F., Gorlenko A. M., Mindlin S. Z., Ilyina T. S. Studies on the RNA polymerase in Escherichia coli K12 using the mutation affecting its activity. J Mol Biol. 1969 Jun 28;42(3):401–411. doi: 10.1016/0022-2836(69)90232-0. [DOI] [PubMed] [Google Scholar]
- LEIVE L. ACTINOMYCIN SENSITIVITY IN ESCHERICHIA COLI PRODUCED BY EDTA. Biochem Biophys Res Commun. 1965 Jan 4;18:13–17. doi: 10.1016/0006-291x(65)90874-0. [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]
- MUNKRES K. D., RICHARDS F. M. THE PURIFICATION AND PROPERTIES OF NEUROSPORA MALATE DEHYDROGENASE. Arch Biochem Biophys. 1965 Mar;109:466–479. doi: 10.1016/0003-9861(65)90391-7. [DOI] [PubMed] [Google Scholar]
- Moses R. E., Richardson C. C. Replication and repair of DNA in cells of Escherichia coli treated with toluene. Proc Natl Acad Sci U S A. 1970 Oct;67(2):674–681. doi: 10.1073/pnas.67.2.674. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Patterson D., Weinstein M., Marshall S., Gillespie D. A new RNA synthesis mutant of E. coli. Biochem Genet. 1971 Dec;5(6):563–578. doi: 10.1007/BF00485674. [DOI] [PubMed] [Google Scholar]
- Rose J. K., Mosteller R. D., Yanofsky C. Tryptophan messenger ribonucleic acid elongation rates and steady-state levels of tryptophan operon enzymes under various growth conditions. J Mol Biol. 1970 Aug;51(3):541–550. doi: 10.1016/0022-2836(70)90007-0. [DOI] [PubMed] [Google Scholar]
- Ryan A. M., Borek E. The relaxed control phenomenon. Prog Nucleic Acid Res Mol Biol. 1971;11:193–228. doi: 10.1016/s0079-6603(08)60328-1. [DOI] [PubMed] [Google Scholar]
- Schlessinger D., Apirion D. Escherichia coli ribosomes: recent developments. Annu Rev Microbiol. 1969;23:387–426. doi: 10.1146/annurev.mi.23.100169.002131. [DOI] [PubMed] [Google Scholar]
- Yuan D., Shen V. Stability of ribosomal and transfer ribonucleic acid in Escherichia coli B/r after treatment with ethylenedinitrilotetraacetic acid and rifampicin. J Bacteriol. 1975 May;122(2):425–432. doi: 10.1128/jb.122.2.425-432.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
