Topics in Microbial PhysiologyP. Tauro International Bioscience Publishers, 1974 - 275 pagine |
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Risultati 1-3 di 48
Pagina 157
... presence of low molecular weight compounds which are formed either inside the cell or enter the cell from the outside enviro- ment . 3 ENZYME INDUCTION . It has been know for long that in bacteria certain enzymes are synthesised only in ...
... presence of low molecular weight compounds which are formed either inside the cell or enter the cell from the outside enviro- ment . 3 ENZYME INDUCTION . It has been know for long that in bacteria certain enzymes are synthesised only in ...
Pagina 161
... presence of arginine , contain only traces of ornithine transcarbamylase . However , as soon as arginine is wihdrawn from the growth medium the differential rate of enzyme synthesis increases by about 1000 folds and remains constant ...
... presence of arginine , contain only traces of ornithine transcarbamylase . However , as soon as arginine is wihdrawn from the growth medium the differential rate of enzyme synthesis increases by about 1000 folds and remains constant ...
Pagina 244
... presence of nitrate sea water , corroding concrete strict aerobe with properties very similar to those of T. thio- structures canal and river water , salt water , peat , composts , mud parus 56 optimum growth pH near neutrality ...
... presence of nitrate sea water , corroding concrete strict aerobe with properties very similar to those of T. thio- structures canal and river water , salt water , peat , composts , mud parus 56 optimum growth pH near neutrality ...
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