Contribution of gentamicin 2'-N-acetyltransferase to the O acetylation of peptidoglycan in Providencia stuartii
Open Access
- 1 August 1995
- journal article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 177 (15) , 4303-4310
- https://doi.org/10.1128/jb.177.15.4303-4310.1995
Abstract
A collection of Providencia stuartii mutants which either underexpress or overexpress aac(2')-Ia, the chromosomal gene coding for gentamicin 2'-N-acetyltransferase (EC 2.3.1.59), have been characterized phenotypically as possessing either lower or higher levels of peptidoglycan O acetylation, respectively, than the wild type. These mutants were subjected to both negative-staining and thin-section electron microscopy. P. stuartii PR100, with 42% O acetylation of peptidoglycan compared with 52% O acetylation in the wild type, appeared as irregular rods. In direct contrast, P. stuartii strains PR50.LM3 and PR51, with increased levels of peptidoglycan O acetylation (65 and 63%, respectively), appeared as coccobacilli and chain formers, respectively. Membrane blebbing was also observed with the chain-forming strain PR51. Thin sectioning of this mutant indicated that it was capable of proper constriction and separation. P. stuartii PM1, when grown to mid-exponential phase, did not have altered peptidoglycan O-acetylation levels, and cellular morphology remained similar to that of wild-type strains. However, continued growth into stationary phase resulted in a 15% increase in peptidoglycan O acetylation concomitant with a change of some cells from a rod-shaped to a coccobacillus-shaped morphology. The fact that these apparent morphological changes were directly related to levels of O acetylation support the view that this modification plays a role in the maintenance of peptidoglycan structure, presumably through the control of autolytic activity.Keywords
This publication has 42 references indexed in Scilit:
- A wide-host-range suicide vector for improving reverse genetics in Gram-negative bacteria: inactivation of the blaA gene of Yersinia enterocoliticaGene, 1991
- Dependence of lysozyme‐catalysed solubilization of Proteus mirabilis peptidoglycan on the extent of O‐acetylationEuropean Journal of Biochemistry, 1991
- Cross-linking and O-Acetylation of Newly Synthesized Peptidoglycan in Staphylococcus aureus HMicrobiology, 1989
- Progress of O-Acetylation and Cross-linking of Peptidoglycan in Neisseria gonorrhoeae Grown in the Presence of PenicillinMicrobiology, 1987
- Murein biosynthesis in synchronized cells of Proteus mirabilisEuropean Journal of Biochemistry, 1987
- O-Acetylation of Peptidoglycan in Neisseria gonorrhoeae. Investigation of Lipid-linked Intermediates and Glycan Chains Newly Incorporated into the Cell WallMicrobiology, 1986
- Searching for autolysin functions. Characterization of a pneumococcal mutant deleted in the lytA geneEuropean Journal of Biochemistry, 1986
- Penicillin-binding Proteins and the Future of -Lactam Antibiotics: The Seventh Fleming LectureMicrobiology, 1983
- Synthesis and modification of the peptidoglycan inNeisseria gonorrhoeaeFEMS Microbiology Letters, 1983
- Development of Lysozyme-Resistance in Micrococcus Lysodiekticus and its Association With an Increased O-Acetyl Content of the Cell WallNature, 1958