Document Detail


Preparation of cells permeable to macromolecules by treatment with toluene: studies of transfer ribonucleic acid nucleotidyltransferase.
MedLine Citation:
PMID:  4597454     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Transfer ribonucleic acid (tRNA) nucleotidyltransferase was studied after making cells permeable to macromolecules by treatment with toluene. The conditions of toluene treatment necessary for obtaining maximal activity were defined. Toluene treatment was most efficient when carried out for 5 min at 37 C at pH 9.0 on log-phase cells. No activity could be detected if cells were treated at 0 C, or in the presence of MgCl(2), or if the cells were in the stationary phase of growth. However, inclusion of lysozyme and ethylenediaminetetraacetic acid during the toluene treatment did render stationary phase cells permeable. The properties of tRNA nucleotidyltransferase from toluene-treated cells were essentially identical to those of purified enzyme with regard to pH optimum, specificity for nucleoside triphosphates and tRNA, and apparent K(m) values for substrates. In addition to tRNA nucleotidyltransferase, a variety of other enzymes which incorporate adenosine 5'-triphosphate into acid-precipitable material could also be detected in toluene-treated cells. Centrifugation of cells treated with toluene revealed that tRNA nucleotidyltransferase leaked out of cells, whereas other activities remained associated with the cell pellets. Chromatography of the material extracted from toluene-treated cells on Sephadex G-100 indicated that toluene treatment selectively extracts lower molecular weight proteins. The usefulness of such a procedure as an initial step in purification of such enzymes, and its application to tRNA nucleotidyltransferase, is discussed.
Authors:
M P Deutscher
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Journal of bacteriology     Volume:  118     ISSN:  0021-9193     ISO Abbreviation:  J. Bacteriol.     Publication Date:  1974 May 
Date Detail:
Created Date:  1974-07-16     Completed Date:  1974-07-16     Revised Date:  2010-09-10    
Medline Journal Info:
Nlm Unique ID:  2985120R     Medline TA:  J Bacteriol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  633-9     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Adenosine / analysis
Adenosine Monophosphate / analysis
Adenosine Triphosphate / metabolism
Carbon Radioisotopes
Cell Membrane Permeability
Chromatography
Escherichia coli / analysis,  drug effects,  enzymology*,  metabolism
Hydrogen-Ion Concentration
Mutation
Phosphorus Radioisotopes
RNA Nucleotidyltransferases / isolation & purification,  metabolism*
RNA, Bacterial / analysis,  biosynthesis
RNA, Transfer / analysis,  biosynthesis
Temperature
Time Factors
Toluene / pharmacology*
Chemical
Reg. No./Substance:
0/Carbon Radioisotopes; 0/Phosphorus Radioisotopes; 0/RNA, Bacterial; 108-88-3/Toluene; 56-65-5/Adenosine Triphosphate; 58-61-7/Adenosine; 61-19-8/Adenosine Monophosphate; 9014-25-9/RNA, Transfer; EC 2.7.7.-/RNA Nucleotidyltransferases
Comments/Corrections

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