Abstract | AIMS: The aims of this study were to identify analogues of L-proline which inhibit the growth of Escherichia coli in both laboratory culture media and normal human urine and to study their mechanisms of uptake. METHODS AND RESULTS: The susceptibility of E. coli to L-proline analogues was studied by radial streak assays on agar plates and by minimal inhibitory concentration determinations in liquid media. Only L- selenaproline (SCA) inhibited growth in Mueller-Hinton medium and human urine as well as in glucose minimal medium. L-Proline did not prevent the inhibition of growth by SCA and strains defective in L-proline transport were as susceptible to SCA as wild-type strains. However, E. coli was resistant to SCA in the presence of L-cysteine and L-cystine. Spontaneous mutants selected for resistance to SCA or L- selenocystine were resistant to the other compound and had reduced growth in minimal medium containing L-cysteine or L-cystine as the sole sulfur source. CONCLUSIONS: L- selenaproline inhibited the growth of E. coli under conditions that may occur in the urinary tract and appeared to be taken up by the L-cystine transport system. SIGNIFICANCE AND IMPACT OF THE STUDY:
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Authors | C E Deutch, M E Arballo, L N Cooks, J M Gomes, T M Williams, T Aboul-Fadl, J C Roberts |
Journal | Letters in applied microbiology
(Lett Appl Microbiol)
Vol. 43
Issue 4
Pg. 392-8
(Oct 2006)
ISSN: 0266-8254 [Print] England |
PMID | 16965369
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
- Culture Media
- Organoselenium Compounds
- selenaproline
- Proline
- Cysteine
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Topics |
- Bacteriological Techniques
(methods)
- Culture Media
(metabolism, pharmacology)
- Cysteine
(metabolism)
- Escherichia coli
(drug effects, genetics, growth & development)
- Humans
- Microbial Sensitivity Tests
- Organoselenium Compounds
(chemistry, pharmacology, urine)
- Proline
(analogs & derivatives, chemistry, pharmacology, urine)
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