| Title | Limited hydrolysis of tRNA by phosphodiesterase. |
| Publication Type | Journal Article |
| Year of Publication | 1975 |
| Authors | Philipps GR, Chiemprasert T |
| Journal | Hoppe Seylers Z Physiol Chem |
| Volume | 356 |
| Issue | 7 |
| Pagination | 1097-104 |
| Date Published | 1975 Jul |
| ISSN | 0018-4888 |
| Keywords | Adenosine Monophosphate, Base Sequence, Cytidine Monophosphate, Escherichia coli, Hydrogen-Ion Concentration, Hydrolysis, Magnesium, Nucleotidyltransferases, Phosphoric Diester Hydrolases, RNA, Transfer |
| Abstract | Digestion of tRNA by electrophoretically pure phosphodiesterase is limited to a short sequence of nucleotides at the 3'-terminus. On the average, four percent of all nucleotides can be released from tRNA. The optimum Mg2 concentration is 10mM and the optimum pH 9.2. The mode of action is a random attack by the enzyme on the substrate. The terminal AMP is completely removed at 15 degrees C after short incubation; about 400 mol of AMP were removed per min by 1 mol of enzyme. The following CMP residues are released much more slowly; at 15 degrees C incompletely, and at 37 degrees C more or less completely in 1 h. In about 50% of the tRNA molecules, the fourth nucleotide could be removed in very long incubations or with very high enzyme concentrations. |
| DOI | 10.1515/bchm2.1975.356.2.1097 |
| Alternate Journal | Hoppe Seylers Z Physiol Chem |
| PubMed ID | 296 |
