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Overproduction of Tyrosyl-tRNA Synthetase is Toxic to Escherichia Coli: a Genetic Analysis

Overview
Journal J Bacteriol
Specialty Microbiology
Date 1990 Jul 1
PMID 2113914
Citations 13
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Abstract

The tyrS genes from Escherichia coli and Bacillus stearothermophilus were toxic to E. coli when they were carried by plasmids with very high copy numbers (pEMBL8 and pEMBL9). We quantified this effect by comparing the efficiencies of plating of E. coli derivatives harboring recombinant plasmids in various experimental conditions. The toxicity was apparent at both 30 and 37 degrees C. It increased with the growth temperature, the strength of the tyrS promoter, and the copy number of the plasmidic vector. Two- to threefold enhancement of tyrS expression raised the toxicity 300-fold. Point mutations in tyrS that prevent interaction between its product, tyrosyl-tRNA synthetase, and tRNA(Tyr) but do not alter the rate of formation of tyrosyl-adenylate abolished the toxicity. Thus, the toxic effect was due to high cellular levels of synthetase activity. At 30 degrees C, the cellular concentration of tyrosyl-tRNA synthetase reached 55% of that of soluble proteins and led to decreased beta-galactosidase stability. We discuss possible causes of this toxic effect and describe its applications to the study of the recognition and interaction between the synthetase and tRNA(Tyr).

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References
1.
DE BOER H, Comstock L, Vasser M . The tac promoter: a functional hybrid derived from the trp and lac promoters. Proc Natl Acad Sci U S A. 1983; 80(1):21-5. PMC: 393301. DOI: 10.1073/pnas.80.1.21. View

2.
Barker D, Bruton C, Winter G . The tyrosyl-tRNA synthetase from Escherichia coli. Complete nucleotide sequence of the structural gene. FEBS Lett. 1982; 150(2):419-23. DOI: 10.1016/0014-5793(82)80781-3. View

3.
Winter G, Koch G, Hartley B, Barker D . The amino acid sequence of the tyrosyl-tRNA synthetase from Bacillus stearothermophilus. Eur J Biochem. 1983; 132(2):383-7. DOI: 10.1111/j.1432-1033.1983.tb07374.x. View

4.
Wilkinson A, Fersht A, Blow D, Winter G . Site-directed mutagenesis as a probe of enzyme structure and catalysis: tyrosyl-tRNA synthetase cysteine-35 to glycine-35 mutation. Biochemistry. 1983; 22(15):3581-6. DOI: 10.1021/bi00284a007. View

5.
Waye M, Winter G, Wilkinson A, Fersht A . Deletion mutagenesis using an 'M13 splint': the N-terminal structural domain of tyrosyl-tRNA synthetase (B. stearothermophilus) catalyses the formation of tyrosyl adenylate. EMBO J. 1983; 2(10):1827-9. PMC: 555366. DOI: 10.1002/j.1460-2075.1983.tb01665.x. View