SUMMARY: The uptake of aliphatic amides by Pseudomonas aeruginosa 8602 was studied by using 1-14C-acetamide and 1-14C-N-acetylacetamide (a non-metabolizable analogue). 1-14C-acetamide was accumulated by the wild-type strains and by an amidase-negative mutant. The maximum ratio of internal to external concentration measured was 100:1. 1-14C-N-acetylacetamide was concentrated by the wild-type strain and the maximum ratio of internal to external concentration measured was 80:1. No difference was detected in amide uptake as between induced and non-induced cultures of the wild-type or mutant strains. It is concluded that the organism possesses a constitutative permease for these amides. Cyano-acetamide had no significant effect on N-acetylacetamide accumulation by the wild-type strain at concentrations which repressed amidase synthesis. Repression of amidase synthesis by amide analogue repressors is therefore not due to inhibition of amide uptake by the bacteria.
No takes yet. Share an insight, caveat, or question.
Brammar et al. (1966) studied this question.
Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context: