Abstract
DNA sequencing data showed that five clinical isolates of Escherichia coli with reduced susceptibility to ceftazidime, ceftriaxone, and cefotaxime contain an ampC gene that is preceded by a strong promoter. Transcription from the strong promoter was 8- to 18-fold higher than that from the promoter from a susceptible isolate. RNA studies showed that mRNA stability does not play a role in the control of AmpC synthesis.
Cite
CITATION STYLE
Nelson, E. C., & Gay Elisha, B. (1999). Molecular basis of ampC hyperproduction in clinical isolates of Escherichia coli. Antimicrobial Agents and Chemotherapy, 43(4), 957–959. https://doi.org/10.1128/aac.43.4.957
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