Thermosensitive mutants of Escherichia coli K-12 altered in the catalytic Subunit and in a Regulatory factor of the glutamy-transfer ribonucleic acid synthetase
- PMID: 1092645
- PMCID: PMC246064
- DOI: 10.1128/jb.122.2.352-358.1975
Thermosensitive mutants of Escherichia coli K-12 altered in the catalytic Subunit and in a Regulatory factor of the glutamy-transfer ribonucleic acid synthetase
Abstract
The glutamyl-transfer ribonucleic acid synthetase (GluRS) of a partial revertants (ts plus or minus) of the thermosensitive (ts) mutant strain JP1449 (LOcus gltx) and of a ts mutant strain EM111-ts1 with a lesion in or near the locus gltx have been studied to find the relation between these two genetic loci known to influence the GluRS activity in vitro and the presence of a catalytic subunit and of a regulatory subunit in the GluRS purified from Escherichia coli K-12. The ts character of strain JP1449-18ts plus or minus is co-transduced with the marker dsdA at the same frequency as is the ts character of strain JP1449. Its purified GluRS is very thermolabile and its Km for glutamate is higher than that of a wild-type GluRS. These results indicate that the locus gltX is in the structural gene for the catalytic subunit of this enzyme. The location of the mutation causing the partial ts reversion in strain JP1449-18ts plus or minus is discussed. The GluRS purified from the ts mutant strain EM111-ts1 has the same stability as the wild-type enzyme, but its Km forglutamate increases with the temperature, suggesting that the locus gltE codes for a regulatory factor, possibly for the polypeptide chain that is co-purified with the catalytic subunit.
Similar articles
-
Derepressed levels of glutamate synthase and glutamine synthetase in Escherichia coli mutants altered in glutamyl-transfer ribonucleic acid synthetase.J Bacteriol. 1975 Sep;123(3):843-50. doi: 10.1128/jb.123.3.843-850.1975. J Bacteriol. 1975. PMID: 239924 Free PMC article.
-
Isolation and partial characterization of a temperature-sensitive Escherichia coli mutant with altered glutaminyl-transfer ribonucleic acid synthetase.J Bacteriol. 1974 Oct;120(1):154-8. doi: 10.1128/jb.120.1.154-158.1974. J Bacteriol. 1974. PMID: 4153616 Free PMC article.
-
Isolation and characterization of a regulatory mutant of an aminoacyl-transfer ribonucleic acid synthetase in Escherichia coli K-12.J Bacteriol. 1973 Mar;113(3):1096-103. doi: 10.1128/jb.113.3.1096-1103.1973. J Bacteriol. 1973. PMID: 4570769 Free PMC article.
-
Regulation of the biosynthesis of aminoacyl-transfer ribonucleic acid synthetases and of transfer ribonucleic acid in Escherichia coli. V. Mutants with increased levels of valyl-transfer ribonucleic acid synthetase.J Bacteriol. 1979 Jul;139(1):165-75. doi: 10.1128/jb.139.1.165-175.1979. J Bacteriol. 1979. PMID: 378953 Free PMC article.
-
Glutamyl-tRNA sythetase.Biol Chem. 1997 Nov;378(11):1313-29. Biol Chem. 1997. PMID: 9426192 Review.
Cited by
-
Functions of the gene products of Escherichia coli.Microbiol Rev. 1993 Dec;57(4):862-952. doi: 10.1128/mr.57.4.862-952.1993. Microbiol Rev. 1993. PMID: 7508076 Free PMC article. Review.
-
Growth rate modulation of four aminoacyl-transfer ribonucleic acid synthetases in enteric bacteria.J Bacteriol. 1976 May;126(2):634-45. doi: 10.1128/jb.126.2.634-645.1976. J Bacteriol. 1976. PMID: 177401 Free PMC article.
-
Two modes of metabolic regulation of lysyl-transfer ribonucleic acid synthetase in Escherichia coli K-12.J Bacteriol. 1977 Aug;131(2):589-97. doi: 10.1128/jb.131.2.589-597.1977. J Bacteriol. 1977. PMID: 328487 Free PMC article.
-
Direct glutaminyl-tRNA biosynthesis and indirect asparaginyl-tRNA biosynthesis in Pseudomonas aeruginosa PAO1.J Bacteriol. 2004 Feb;186(3):767-76. doi: 10.1128/JB.186.3.767-776.2004. J Bacteriol. 2004. PMID: 14729703 Free PMC article.
-
Isolation of temperature-sensitive aminoacyl-tRNA synthetase mutants from an Escherichia coli strain harboring the pemK plasmid.Mol Gen Genet. 1993 Apr;238(1-2):169-76. doi: 10.1007/BF00279544. Mol Gen Genet. 1993. PMID: 8479423
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources