Topics in Microbial PhysiologyP. Tauro International Bioscience Publishers, 1974 - 275 pagine |
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Pagina 98
... factors were designated as F1 F2 and F3 . The initiation factors have now been prepared in a very highly purified form and their function in the initi- ation process is being clarified ( 36 , 37 , 38 ) . The binding of the mRNA to the ...
... factors were designated as F1 F2 and F3 . The initiation factors have now been prepared in a very highly purified form and their function in the initi- ation process is being clarified ( 36 , 37 , 38 ) . The binding of the mRNA to the ...
Pagina 99
... factors , now called elongation factors , were designated as T and G. Further work led to the dissociation of factor T into factors Ts and Tu ( 41 ) . All these factors were necessary for the polymerization of amino acids from aminoacyl ...
... factors , now called elongation factors , were designated as T and G. Further work led to the dissociation of factor T into factors Ts and Tu ( 41 ) . All these factors were necessary for the polymerization of amino acids from aminoacyl ...
Pagina 104
... factors ( 54 ) . Using this system it was possible to dissociate the release factor from E. coli into two components ( 55 ) which respond to different sets of terminator codons . One of these components , R1 , is active with UAA and UAG ...
... factors ( 54 ) . Using this system it was possible to dissociate the release factor from E. coli into two components ( 55 ) which respond to different sets of terminator codons . One of these components , R1 , is active with UAA and UAG ...
Sommario
3 | 28 |
In Vitro Synthesis of | 41 |
In vivo Replication of Bacterial | 49 |
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Acad Acta activity addition amino acid amount appears bacteria bacteriophages bases binding Biochem Biol Biophys biosynthesis bond bound catalyzed cell chain Chem chromosome coli complex components compounds contain cytoplasmic dependant direction DNA polymerase DNA synthesis double electron enzyme evidence example experiments extracts factors fatty acid fixation formation function gene genetic glucose growing growth incorporated inducer inhibited initiation involved isolated labelled lipid mechanism membrane molecule mutants Natl Nature nitrogen nitrogenase nucleotides observed occurs operator operon organisms oxidation peptide phosphate poly polypeptide presence Proc protein purified reaction reduction region regulation replication repression repressor residues ribosomes role sequence shown similar single specific step strand structure studies substrates subunits suggested sulphur synthesis synthetase Table template transcription transfer tRNA various vitro vivo wall