Topics in Microbial PhysiologyP. Tauro International Bioscience Publishers, 1974 - 275 pagine |
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Pagina 93
... RIBOSOMES Ribosomes are the sites of protein synthesis in the cell . Ribosomes are made of protein and ribonucleic acid . The relative proportion of these two components varies for different organisms . Microbial ribosomes contain two ...
... RIBOSOMES Ribosomes are the sites of protein synthesis in the cell . Ribosomes are made of protein and ribonucleic acid . The relative proportion of these two components varies for different organisms . Microbial ribosomes contain two ...
Pagina 94
... ribosomes . Therefore , when a new class of protein had to be synthesized , new ribosomes were elaborated by the cellular apparatus . However , experiments essentially with bacterial preparations led to the conclusion that ribosomal RNA ...
... ribosomes . Therefore , when a new class of protein had to be synthesized , new ribosomes were elaborated by the cellular apparatus . However , experiments essentially with bacterial preparations led to the conclusion that ribosomal RNA ...
Pagina 99
... ribosomes ( 39 , 40 ) . These 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 ...
... ribosomes ( 39 , 40 ) . These 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 ...
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