On the basis of embedded cluster calculations, we propose a new model for the structure of paramagnetic color centers at the MgO surface usually denoted as F(S)(H)(+) (an electron trapped near an adsorbed proton). These centers are produced by exposing the surface of polycrystalline MgO to H(2) followed by UV irradiation. We demonstrate that properties of H atom absorbed at surface sites such as step edges (MgO(step)) and reverse corner sites (MgO(RC)), formed at the intersection of two step edges, are compatible with a number of features observed for F(S)(H)(+). Our calculations suggest that (i) H(2) dissociates at the reverse corner site heterolytically and that there is no barrier for this exothermic reaction; (ii) the calculated vibrations of the resulting MgO(RC)(H(+))(H(-)) complex are fully consistent with the measured ones; (iii) desorption of a neutral H atom from the diamagnetic precursor requires UV light and leads to the formation of stable neutral paramagnetic centers at the surface, MgO(step)(H(+))(e(-))(trapped) and MgO(RC)(H(+))(e(-))(trapped). The computed isotropic hyperfine coupling constants and optical transitions of these centers are in broad agreement with the existing experimental data. We argue that these centers, which do not belong to the class of "oxygen vacancies", are two of the many possible forms of the F(S)(H)(+) defect center.

Journal Article↗

PubMed2002

Differences in the susceptibility of Streptococcus pyogenes to rokitamycin and erythromycin A revealed by morphostructural atomic force microscopy.

The aim of this study was to use atomic force microscopy (AFM), an innovative type of microscopy, to investigate the different behaviours of erythromycin A (a 14-membered ring) and rokitamycin (a 16-membered ring) in disrupting the morphology of Streptococcus pyogenes with the M phenotype. AFM scanning and sensing of the topography of a sample makes it possible to obtain simultaneous high-resolution digital measurements of the x, y and z coordinates at any point on the bacteria surface. The images obtained before and 2, 4 and 6 h after incubation with erythromycin A (32 mg/L) and rokitamycin (2 mg/L) clearly show that not even high concentrations of erythromycin A interfere with the M phenotype of S. pyogenes, whereas rokitamycin has a progressive action that leads to the formation of abnormally large cells, the loosening of chain structure and the formation of clusters.

Drug Resistance, Bacterial↗