Topics in Microbial PhysiologyP. Tauro International Bioscience Publishers, 1974 - 275 pagine |
Dall'interno del libro
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Pagina 43
... molecular weight of the purified enzyme from E. coli is 109,000 ( 77 ) . Equilibirum density centrifugation in systems containing guanidine - HCI and mercaptoethanol which are known to cause dissociation of protein molecules , does not ...
... molecular weight of the purified enzyme from E. coli is 109,000 ( 77 ) . Equilibirum density centrifugation in systems containing guanidine - HCI and mercaptoethanol which are known to cause dissociation of protein molecules , does not ...
Pagina 93
... molecular weight of about 3 × 106 , and a sedimentation coefficient of 70S . They can be dissociated into two subunits with Sedimentation coefficients of 50S and 30S respectively . Yeasts contain two classes of ribosomes , cytoplasmic ...
... molecular weight of about 3 × 106 , and a sedimentation coefficient of 70S . They can be dissociated into two subunits with Sedimentation coefficients of 50S and 30S respectively . Yeasts contain two classes of ribosomes , cytoplasmic ...
Pagina 123
... structure of the enzyme system involved ( 74 ) . In yeast , the different enzyme compo- nents form a very stable aggregate which may be isolated as a single protein of a molecular weight of 2.3 millions . It appears free of ...
... structure of the enzyme system involved ( 74 ) . In yeast , the different enzyme compo- nents form a very stable aggregate which may be isolated as a single protein of a molecular weight of 2.3 millions . It appears free of ...
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