Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Enzymes penicillin acyl transferase

When H2O deacetylates the acyl-enzyme, phenylacetic acid is formed. When nucleophiles other than H2O deacylate the acyl-enzyme, a new condensation product, in this case phenylacetyl-O-R or phenylacetyl-NH-R is formed. By definition the hydrolysis of these condensation products can be catalyzed by the same enzyme that catalyzes their formation in equation 10.1. Thus, when the acyl-enzyme is formed from phenylacetyl-glycine or phenylacetyl-O-Me, this gives rise to an alternative process to produce Penicillin G, in addition to the thermodynamically controlled (= equilibrium controlled) condensation of phenylacetic acid and 6-aminopenicillanic acid (6-APA). This reaction that involves an activated side chain is a kinetically controlled (= rate controlled) process where the hydrolase acts as a transferase (Kasche, 1986 1989). [Pg.367]


See other pages where Enzymes penicillin acyl transferase is mentioned: [Pg.679]    [Pg.680]    [Pg.681]    [Pg.679]    [Pg.680]    [Pg.681]    [Pg.363]    [Pg.363]    [Pg.363]    [Pg.199]    [Pg.91]   
See also in sourсe #XX -- [ Pg.848 ]

See also in sourсe #XX -- [ Pg.801 ]




SEARCH



Acyl-transferase

Acylation enzymic

Enzyme acylation

Transferases enzymes

© 2024 chempedia.info