Topics in Microbial PhysiologyP. Tauro International Bioscience Publishers, 1974 - 275 pagine |
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Pagina 45
... coli DNA polymerase differs from normal E. coli polymerase in chromatographic properties and heat tolerance ( 1 ) . Partially purified E. coli polymerase can be eluted from a phosphocellulose column by 0.15 to 0.2 M potassium phosphate ...
... coli DNA polymerase differs from normal E. coli polymerase in chromatographic properties and heat tolerance ( 1 ) . Partially purified E. coli polymerase can be eluted from a phosphocellulose column by 0.15 to 0.2 M potassium phosphate ...
Pagina 48
... coli and the dna E locus of E. coli is the structural gene for DNA polymerase III . One reason as to why the cell could have two different enzymes for catalysing DNA synthesis is perhaps that when one is used under normal conditions for ...
... coli and the dna E locus of E. coli is the structural gene for DNA polymerase III . One reason as to why the cell could have two different enzymes for catalysing DNA synthesis is perhaps that when one is used under normal conditions for ...
Pagina 131
... coli system , the condensing enzyme , the enoyl - ACP - hydrase and the NADPH - enoyl - reductase are absolutely specific for ACP derivatives ( 136-138 ) . No flavine component could be detec- ted in highly purified preparations of E. coli ...
... coli system , the condensing enzyme , the enoyl - ACP - hydrase and the NADPH - enoyl - reductase are absolutely specific for ACP derivatives ( 136-138 ) . No flavine component could be detec- ted in highly purified preparations of E. coli ...
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