Topics in Microbial PhysiologyP. Tauro International Bioscience Publishers, 1974 - 275 pagine |
Dall'interno del libro
Risultati 1-3 di 20
Pagina 14
... residues of N - acetylmuramic acid and N - acetylglucosamine linked in 1,4 linkages . Muramic acid is an amino sugar ... residues . The tetrapeptides are linked by a peptide bond between the N - terminal amino group of the peptides and ...
... residues of N - acetylmuramic acid and N - acetylglucosamine linked in 1,4 linkages . Muramic acid is an amino sugar ... residues . The tetrapeptides are linked by a peptide bond between the N - terminal amino group of the peptides and ...
Pagina 15
... residue would represent a group of soluble molecules , rather than an insoluble macromolecular network . The ... residues form the bridge between the alanine of one tetrapeptide and the lysine of another . Other cross - bridges ...
... residue would represent a group of soluble molecules , rather than an insoluble macromolecular network . The ... residues form the bridge between the alanine of one tetrapeptide and the lysine of another . Other cross - bridges ...
Pagina 131
... residues . These results suggest that the tyrosine and arginine residues are not essential for ACP activity but that the lysine residues may have a modifying effect on the plant ACP . Both bacterial ACPs had higher specific activities ...
... residues . These results suggest that the tyrosine and arginine residues are not essential for ACP activity but that the lysine residues may have a modifying effect on the plant ACP . Both bacterial ACPs had higher specific activities ...
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