Topics in Microbial PhysiologyP. Tauro International Bioscience Publishers, 1974 - 275 pagine |
Dall'interno del libro
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Pagina 7
... membrane " shrinks " away from the wall The membrane can also be differentiated from the cell wall in gram - positive organisms by preparation of protoplasts . Enzymes are used to digest the cell wall , pro- ducing osmotically fragile ...
... membrane " shrinks " away from the wall The membrane can also be differentiated from the cell wall in gram - positive organisms by preparation of protoplasts . Enzymes are used to digest the cell wall , pro- ducing osmotically fragile ...
Pagina 8
... membrane fatty acids are elaidate ( 4 ) . Similarly , a mutant of Escherichia coli which requires unsaturated fatty ... membrane proteins . Phenotypically these mutants show unusual sensitivity to antibiotics and detergents ( 6 ) ...
... membrane fatty acids are elaidate ( 4 ) . Similarly , a mutant of Escherichia coli which requires unsaturated fatty ... membrane proteins . Phenotypically these mutants show unusual sensitivity to antibiotics and detergents ( 6 ) ...
Pagina 12
... membrane structures which vary characteristically in appearance with the species ( 35 ) . There have also been reports of membrane bodies associated with nitrogen fixation in Azotobacter ( 36 ) . E. Inhibitors with a site of action at ...
... membrane structures which vary characteristically in appearance with the species ( 35 ) . There have also been reports of membrane bodies associated with nitrogen fixation in Azotobacter ( 36 ) . E. Inhibitors with a site of action at ...
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