Topics in Microbial PhysiologyP. Tauro International Bioscience Publishers, 1974 - 275 pagine |
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Pagina 21
... transfer reactions had been characterized and purified lipopolysaccharide acceptor preparations were made , it was found that some lipids had to be added back to the preparations in order for the transfer reactions to occur ( 60 ) . In ...
... transfer reactions had been characterized and purified lipopolysaccharide acceptor preparations were made , it was found that some lipids had to be added back to the preparations in order for the transfer reactions to occur ( 60 ) . In ...
Pagina 126
... Transfer CH3 - ICH2 - CH2n.1 - COSC . Terminal reaction Palmityl - Transfer ( FMN ) Enzyme NADPH . HSp CH3 ( CH2 - CH2in.1 - COSC . HS Enzyme Enzyme HSP CH3 - CH2 - CH2-1 Cosp Enzym NADP HSP HS CH - ICHT CH2in . 205 , Enzyme . HSCOA ...
... Transfer CH3 - ICH2 - CH2n.1 - COSC . Terminal reaction Palmityl - Transfer ( FMN ) Enzyme NADPH . HSp CH3 ( CH2 - CH2in.1 - COSC . HS Enzyme Enzyme HSP CH3 - CH2 - CH2-1 Cosp Enzym NADP HSP HS CH - ICHT CH2in . 205 , Enzyme . HSCOA ...
Pagina 224
... transfer agents for Nitrogenases of fac- ultative aerobic , photosynthetic and symbiotic systems . In addi- tion , how the transfer agents are coupled to the Nitrogenase needs to be worked out . The number of electrons transferred at ...
... transfer agents for Nitrogenases of fac- ultative aerobic , photosynthetic and symbiotic systems . In addi- tion , how the transfer agents are coupled to the Nitrogenase needs to be worked out . The number of electrons transferred 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