The influence of the size and nature of basic activators on Clostridium perfringens polynucleotide phosphorylase-catalysed polyadenylic acid synthesis
- 1 May 1969
- journal article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 112 (4) , 497-503
- https://doi.org/10.1042/bj1120497
Abstract
1. Basic oligo- and poly-(amino acids) stimulate polyadenylic acid synthesis by purified Clostridium perfringens polynucleotide phosphorylase (nucleoside diphosphate–polyribonucleotide nucleotidyltransferase, EC 2.7.7.8). 2. The effectiveness of the activators increases with chain length up to approx. 20–30 residues. 3. Polymers of the l and dl series are equally effective on a weight-for-weight basis. 4. l-Lysine, d-lysine, diethylamine and triethylamine, as hydrochlorides or hydrobromides, all stimulate the reaction markedly if their concentration is high enough. Their effect is similar to that of sodium chloride. 5. The size of the product depends primarily on the Mg2+ concentration and basic polymers have a relatively limited effect on it. 6. Polyadenylic acid itself undergoes an Mg2+-catalysed non-enzymic hydrolysis.Keywords
This publication has 6 references indexed in Scilit:
- The preferential loss of the polylysine- or polyornithine-stimulated activity of Clostridium perfringens polynucleotide phosphorylase during proteolysisBiochemical Journal, 1969
- A study by polyacrylamide-gel electrophoresis of the effect of proteolysis on Micrococcus lysodeikticus polynucleotide phosphorylaseBiochemical Journal, 1968
- Irreversible Heat Inactivation of Transfer Ribonucleic AcidsJournal of Biological Chemistry, 1967
- Protein-Nucleic Acid Interaction. I. Nuclease-Resistant Polylysine-Ribonucleic Acid Complexes*Biochemistry, 1966
- *VERHALTEN UND SPEZIFITAT VON CER, LANTHAN, EISEN UND ALUMINIUM ALS PHOSPHATASEMODELLE GEGENUBER PHYSIOLOGISCH WICHTIGEN PHOSPHORSAUREVERBINDUNGEN WIE ZUCKERPHOSPHORSAUREN, ADENYLSAUREN, ADENOSINTRIPHOSPHORSAURE UND ANDEREN1954
- *VERHALTEN UND SPEZIFITAT VON CER UND LANTHAN ALS PHOSPHATASE-MODELLE GEGENUBER NUCLEINSAUREN UND MONONUCLEOTIDEN1954