The transpeptidation reaction performed by the membranes of Streptomyces strain R61 fits the general rate equation for an enzyme-catalysed bimolecular reaction. The same membranes (E) interact with beta-lactams (I) to form inactive penicillin-enzyme-membrane complexes (EI) of rather high stability, which subsequently break down (E + I leads to EI leads to E + degradation products). The enzyme is regenerated and the antibiotic is released in the form of an inactive metabolite. With benzylpenicillin, the degradation product is benzylpenicilloic acid. The reaction is heat-labile. The first step of the reaction (E + I leads to EI) is characterized by a second-order rate constant (kformation in M-1 s-1) and the second step (EI leads to E + degra...
The specificity of the Streptomyces R61 penicillin-sensitive D-Ala-D-Ala peptidase has been re-exami...
The values ofthe kinetic parameters that govern the interactions between the Streptomyces K15 DD-pep...
Streptomyces R61 and S. rimosus have an atypical penicillin-binding protein (PBP) pattern characteri...
The Km, app. values of the membrane-bound transpeptidase of Streptomyces R61 for the donor Ac2-L-Lys...
On the basis of steady-state kinetics, inhibition of the exocellular dd-carboxypeptidase-trans-pepti...
The simplest model for the interaction between the exocellular DD-carboxypeptidase-transpeptidase fr...
High-affinity penicillin binding sites from which the antibiotic could not be removed by washings at...
Kinetics and optical studies of Streptomyces DD-carboxypeptidases-transpeptidases led to the conclus...
The values of the kinetic parameters that govern the interactions between the Streptomyces K15 DD-pe...
The interaction between the exocellular DD-carboxypeptidase-transpeptidase of Streptomyces R61 and b...
The exocellular DD-carboxypeptidase-transpeptidase of Streptomyces R39 is inhibited by beta-lactam a...
Benzylpenicillin and cephaloridine reacted with the exocellular dd-carboxypeptidase–transpeptidase f...
The DD-carboxypeptidase-exchange membrane-bound enzyme in Streptococcus faecalis ATCC 9790 reacts wi...
The circular dichroism of the dd-carboxypeptidase-transpeptidase from Streptomyces R61 shows in the ...
Additional evidence is given that in Streptomyces strains R39, R61, and K11 the same enzyme performs...
The specificity of the Streptomyces R61 penicillin-sensitive D-Ala-D-Ala peptidase has been re-exami...
The values ofthe kinetic parameters that govern the interactions between the Streptomyces K15 DD-pep...
Streptomyces R61 and S. rimosus have an atypical penicillin-binding protein (PBP) pattern characteri...
The Km, app. values of the membrane-bound transpeptidase of Streptomyces R61 for the donor Ac2-L-Lys...
On the basis of steady-state kinetics, inhibition of the exocellular dd-carboxypeptidase-trans-pepti...
The simplest model for the interaction between the exocellular DD-carboxypeptidase-transpeptidase fr...
High-affinity penicillin binding sites from which the antibiotic could not be removed by washings at...
Kinetics and optical studies of Streptomyces DD-carboxypeptidases-transpeptidases led to the conclus...
The values of the kinetic parameters that govern the interactions between the Streptomyces K15 DD-pe...
The interaction between the exocellular DD-carboxypeptidase-transpeptidase of Streptomyces R61 and b...
The exocellular DD-carboxypeptidase-transpeptidase of Streptomyces R39 is inhibited by beta-lactam a...
Benzylpenicillin and cephaloridine reacted with the exocellular dd-carboxypeptidase–transpeptidase f...
The DD-carboxypeptidase-exchange membrane-bound enzyme in Streptococcus faecalis ATCC 9790 reacts wi...
The circular dichroism of the dd-carboxypeptidase-transpeptidase from Streptomyces R61 shows in the ...
Additional evidence is given that in Streptomyces strains R39, R61, and K11 the same enzyme performs...
The specificity of the Streptomyces R61 penicillin-sensitive D-Ala-D-Ala peptidase has been re-exami...
The values ofthe kinetic parameters that govern the interactions between the Streptomyces K15 DD-pep...
Streptomyces R61 and S. rimosus have an atypical penicillin-binding protein (PBP) pattern characteri...