An extracellular factor regulating expression of the chromosomal aminoglycoside 2'-N-acetyltransferase of Providencia stuartii

PN Rather, MM Parojcic… - Antimicrobial agents and …, 1997 - Am Soc Microbiol
PN Rather, MM Parojcic, MR Paradise
Antimicrobial agents and chemotherapy, 1997Am Soc Microbiol
The chromosomal aac (2')-Ia gene in Providencia stuartii encodes a housekeeping 2'-N-
acetyltransferase [AAC (2')-Ia] involved in the acetylation of peptidoglycan. In addition, the
AAC (2')-Ia enzyme also acetylates and confers resistance to the clinically important
aminoglycoside antibiotics gentamicin, tobramycin, and netilmicin. Expression of the aac (2')-
Ia gene was found to be strongly influenced by cell density, with a sharp decrease in aac (2')-
Ia mRNA accumulation as cells approached stationary phase. This decrease was mediated …
The chromosomal aac(2')-Ia gene in Providencia stuartii encodes a housekeeping 2'-N-acetyltransferase [AAC(2')-Ia] involved in the acetylation of peptidoglycan. In addition, the AAC(2')-Ia enzyme also acetylates and confers resistance to the clinically important aminoglycoside antibiotics gentamicin, tobramycin, and netilmicin. Expression of the aac(2')-Ia gene was found to be strongly influenced by cell density, with a sharp decrease in aac(2')-Ia mRNA accumulation as cells approached stationary phase. This decrease was mediated by the accumulation of an extracellular factor, designated AR (for acetyltransferase repressing)-factor. AR-factor was produced in both minimal and rich media and acted in a manner that was strongly dose dependent. The activity of AR-factor was also pH dependent, with optimal activity at pH 8.0 and above. Biochemical characterization of conditioned media from P. stuartii has shown that AR-factor is between 500 and 1,000 Da in molecular size and is heat stable. In addition, AR-factor was inactivated by a variety of proteases, suggesting that it may be a small peptide.
American Society for Microbiology