Role of the counterions on the adsorption of ionic surfactants.

A theory accounting for the effect of the counterions on the adsorption constant, K, is proposed. The experimental values of K were determined by using surface and interfacial tension isotherms measured by us or available in the literature. By accounting for the adsorption energy u 0 of the counterion, a generalization of Gouy equation and a modified expression for the adsorption constant, K, are derived. The adsorption energy is calculated from the London equation, which involves the polarizabilities alpha 0i and the ionization potentials Ii of the respective components and the radius Rh of the hydrated ion. By careful analysis of the available experimental data for alpha 0i, Ii and Rh, coupled with some reasonable hypothesis, we succeeded to obtain linear dependences between the calculated values of u 0 and the experimental data for lnK with slopes rather close to the theoretical ones. The obtained results for u 0 were used to calculate the disjoining pressure isotherms of foam films stabilized by DTAF, DTACl and DTABr. It turned out that the type of the counterion has significant effect on the disjoining pressure.

Brc1-mediated DNA repair and damage tolerance.

The structural maintenance of chromosome (SMC) proteins are key elements in controlling chromosome dynamics. In eukaryotic cells, three essential SMC complexes have been defined: cohesin, condensin, and the Smc5/6 complex. The latter is essential for DNA damage responses; in its absence both repair and checkpoint responses fail. In fission yeast, the UV-C and ionizing radiation (IR) sensitivity of a specific hypomorphic allele encoding the Smc6 subunit, rad18-74 (renamed smc6-74), is suppressed by mild overexpression of a six-BRCT-domain protein, Brc1. Deletion of brc1 does not result in a hypersensitivity to UV-C or IR, and thus the function of Brc1 relative to the Smc5/6 complex has remained unclear. Here we show that brc1Delta cells are hypersensitive to a range of radiomimetic drugs that share the feature of creating lesions that are an impediment to the completion of DNA replication. Through a genetic analysis of brc1Delta epistasis and by defining genes required for Brc1 to suppress smc6-74, we find that Brc1 functions to promote recombination through a novel postreplication repair pathway and the structure-specific nucleases Slx1 and Mus81. Activation of this pathway through overproduction of Brc1 bypasses a repair defect in smc6-74, reestablishing resolution of lesions by recombination.