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- W2000579217 abstract "A membrane fraction from Pseudomonas aeruginosa KM 338 was shown to catalyze in vitro peptidoglycan synthesis from uridine 5′-diphosphate- N -acetylmuramyl- l -alanyl- d - glutamyl-meso-diaminopimelyl- d -alanyl- d -alanine and uridine 5′-diphosphate- N -acetylglucosamine. Synthesized peptidoglycan was partially cross-linked by transpeptidation, which was accompanied by the release of d -alanine. This reaction was strongly inhibited by 25 and 50 μg of penicillin G and carbenicillin per ml respectively, whereas the intact cells were relatively resistant to penicillins (minimal inhibitory concentration of penicillin G and carbenicillin, 30 and 0.125 mg/ml, respectively). Soluble d -alanine carboxypeptidase present in P. aeruginosa KM 338 was studied as well, which was found almost completely inhibited by penicillin G and carbenicillin (10 μg/ml)." @default.
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- W2000579217 date "1974-12-01" @default.
- W2000579217 modified "2023-09-25" @default.
- W2000579217 title "Penicillin-Resistant Mechanisms in Pseudomonas aeruginosa : Effects of Penicillin G and Carbenicillin on Transpeptidase and d -Alanine Carboxypeptidase Activities" @default.
- W2000579217 doi "https://doi.org/10.1128/aac.6.6.672" @default.
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