Topics in Microbial PhysiologyP. Tauro International Bioscience Publishers, 1974 - 275 pagine |
Dall'interno del libro
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Pagina 202
... azoferredoxin or Fe protein , contains iron and acid labile sulfide . Azoferre- doxin purified from some organisms is cold labile . Neither molybdoferredoxin nor azoferredoxin have been shown to have any enzymatic activity by themselves ...
... azoferredoxin or Fe protein , contains iron and acid labile sulfide . Azoferre- doxin purified from some organisms is cold labile . Neither molybdoferredoxin nor azoferredoxin have been shown to have any enzymatic activity by themselves ...
Pagina 204
... Azoferredoxin precipitates down as a complex with protamine sulfate , while molybdoferredoxin remains in the supernatant solution . Azoferredoxin is released into solution by phos- phocellulose treatment which has a higher affinity for ...
... Azoferredoxin precipitates down as a complex with protamine sulfate , while molybdoferredoxin remains in the supernatant solution . Azoferredoxin is released into solution by phos- phocellulose treatment which has a higher affinity for ...
Pagina 211
... azoferredoxin from azotobacter , although it is similar to the clostridial protein in its oxygen and cold inactivation . The properties of azoferredoxin from C. pasteurianum and K. pneumoniae are presented in Table 3 . Table 3 ...
... azoferredoxin from azotobacter , although it is similar to the clostridial protein in its oxygen and cold inactivation . The properties of azoferredoxin from C. pasteurianum and K. pneumoniae are presented in Table 3 . Table 3 ...
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