Random mntagenesis of the gene for bacteriophage T7 RNA polymerase
β Scribed by Rechinsky, Vladimir O. ;Kostyuk, Dmitry A. ;Lyakhov, Dmitry L. ;Chernov, Boris K. ;Kochetkov, Sergei N.
- Publisher
- Springer
- Year
- 1993
- Tongue
- English
- Weight
- 421 KB
- Volume
- 238
- Category
- Article
- ISSN
- 0026-8925
No coin nor oath required. For personal study only.
β¦ Synopsis
Random mutagenesis of the gene for bacteriophage T7 RNA polymerase was used to identify functionally essential amino acid residues of the enzyme. A two-plasmid system was developed that permits the straightforward isolation of T7 RNA polymerase mutants that had lost almost all catalytic activity. It was shown that substitutions of Thr and Ala for Pro at the position 563, Ser for Tyr571, Pro for Thr636, Asp for Tyr639 and of Cys for Phe646 resulted in inactivation of the enzyme. It is noteworthy that all these mutations are limited to two short regions that are highly conservative in sequences of monomeric RNA polymerases.
π SIMILAR VOLUMES
We determined the nucleotide sequence of gene 1 of Klebsiella phage K11, which is a member of the T7 group of phages. The largest open reading frame corresponds to a polypeptide with 906 amino acids and a molecular weight of 100,383 daltons. The deduced amino acid sequence of this polypeptide shows
## Abstract Bacteriophage T3βinduced RNA polymerase is rapidly inactivated at 42Β°C. Addition of T3 DNA delays this process for 30 s and reduces the rate with which the enzyme activity is lsot indicating that a labile binary complex between T3 DNA and polymerase must have been formed. The ternary co