Topics in Microbial PhysiologyP. Tauro International Bioscience Publishers, 1974 - 275 pagine |
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Pagina 73
... activity requires all four deoxy - ribonucleoside triphosphates and a divalent cation Mg ++ or Mn ++ ( 56 ) . Omission of one of the four deoxy - ribonucleoside triphos- phates results in cessation of enzyme activity . The pH optimum ...
... activity requires all four deoxy - ribonucleoside triphosphates and a divalent cation Mg ++ or Mn ++ ( 56 ) . Omission of one of the four deoxy - ribonucleoside triphos- phates results in cessation of enzyme activity . The pH optimum ...
Pagina 227
... activity . Therefore , ammonia and its chemical analogs affect only the synthesis of the enzyme and not its activity . Research is in progress to study as to what happens during the lag when the ammonia supply is exhausted and the ...
... activity . Therefore , ammonia and its chemical analogs affect only the synthesis of the enzyme and not its activity . Research is in progress to study as to what happens during the lag when the ammonia supply is exhausted and the ...
Pagina 228
... activity of the enzyme . These inhibitors are discussed in some detail in an earlier section . The only physiological control known so far on the activity is exerted by the ratio of ATP / ADP . In the presence of substrate level ATP ...
... activity of the enzyme . These inhibitors are discussed in some detail in an earlier section . The only physiological control known so far on the activity is exerted by the ratio of ATP / ADP . In the presence of substrate level ATP ...
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