Molecular cloning and primary structure of the Escherichia coli methionyl-tRNA synthetase gene.
The intact metG gene was cloned in plasmid pBR322 from an F32 episomal gene library by complementation of a structural mutant, metG83. The Escherichia coli strain transformed with this plasmid (pX1) overproduced methionyl-tRNA synthetase 40-fold. Maxicell analysis showed that three major polypeptide...
שמור ב:
| הוצא לאור ב: | J Bacteriol |
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| Principais autores: | , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
American Society for Microbiology (ASM)
1984
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC215828/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6094501/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jb.160.3.1115-1122.1984 |
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