Abstract
A temperature-sensitive mutant of Escherichia coli HAK88 which has been shown to have a lesion in elongation factor Ts (EFTs) was studied with repsect to its metabolism of guanosine 5'-diphosphate, 2'(3')-diphosphate (ppGpp) and the associated failure of ribosomal ribonucleic acid (rRNA) accumulation at the nonpermissive temperature. Results reported here show that (i) when EFTs is nonfunctional, a full complement of charged transfer RNA (tRNA) cannot prevent accumulation of ppGpp (magic spot) and the stringent failure of rRNA accumulation; (ii) chloramphenicol prevents magic spot (MS) formation and the stringent response not by increasing the percentage of charged tRNA, but possibly by somehow interfering directly with the synthesis of MS; and (iii) tetracycline can lead to MS disappearance without resumption of RNA synthesis. Thus, the absence of MS and the presence of a functional RNA polymerase and charged tRNA are not sufficient to support rRNA accumulation in vivo. An additional element in the regulatory system is suggested.
MeSH Terms
Adenosine Triphosphate/metabolism
Amino Acids/metabolism
Carbon Radioisotopes
Chloramphenicol/pharmacology
Escherichia coli/metabolism
Guanine Nucleotides/metabolism
Guanosine Triphosphate/metabolism
Mutation
Peptide Elongation Factors/biosynthesis
Phosphorus Radioisotopes
RNA, Bacterial/biosynthesis
RNA, Ribosomal/biosynthesis
RNA, Transfer/metabolism
Temperature
Tetracycline/pharmacology
Tritium
Uracil/metabolism
Chemicals
Amino Acids
Carbon Radioisotopes
Guanine Nucleotides
Peptide Elongation Factors
Phosphorus Radioisotopes
RNA, Bacterial
RNA, Ribosomal
Tritium
Uracil
Chloramphenicol
Guanosine Triphosphate
Adenosine Triphosphate
RNA, Transfer
Tetracycline
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Glazier K
Schlessinger D
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19 references, click to expand
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