VRK2 is a novel Ser-Thr kinase whose VRK2A isoform is located in the endoplasmic reticulum and mitochondrial membranes. We have studied the potential role that VRK2A has in the regulation of mitochondrial-mediated apoptosis. VRK2A can regulate the intrinsic apoptotic pathway in two different ways. The VRK2A protein directly interacts with Bcl-xL, but not with Bcl-2, Bax, Bad, PUMA or Binp-3L. VRK2A does not compete with Bax for interaction with Bcl-xL, and these proteins can form a complex that reduces apoptosis. Thus, high VRK2 levels confer protection against apoptosis. In addition, VRK2 knockdown results in an increased expression of BAX gene expression that is mediated by its proximal promoter, thus VRK2A behaves as a negative regulator of BAX. Low levels of VRK2A causes an increase in mitochondrial Bax protein level, leading to an increase in the release of cytochrome C and caspase activation, detected by PARP processing. VRK2A loss results in an increase in cell death that can be detected by an increase in annexinV+ cells. Low levels of VRK2A increase cell sensitivity to induction of apoptosis by chemotherapeutic drugs like camptothecin or doxorubicin. We conclude that VRK2A protein is a novel modulator of apoptosis.

The present investigation is centered on the study of the growth curves of E. coli and C. xerosis bacteria in the presence of nanosize particles of Zinc Oxide. Previous works demonstrated the sensitivity of the bacteria, when these were reproduced in media that contain nanoparticles of luminescent silicon and Cobalt Ferrite. Doped ZnO nanocrystals were synthesized by conventional precipitation in ethanol solutions as reported by Spanhel and Anderson for bare ZnO. In our case, the syntheses were carried out under room-temperature conditions.The experimental results of E. coli bacteria in contact with a stable suspension of nanoparticles of Zinc Oxide, shows a growth curve without adaptation period. Moreover a short and slowly logarithmic stage has been observed, reaching the stationary stage after approximately four hours compared with one in absence of the nanoparticles (standard curve). During the observations, a change in the lifetime of the bacteria (metabolism) with particulate was noticed,as well as the beginning of the mortality stage. However, different results were recorded for silicon and ferrite. For the case of the bacteria C. xerosis, the curve with particles is above its standard curve, for all times with none of the oscillations which occured in the nanometer silicon. For these bacteria the beginning of the mortality stage is observed when they have particles. For both bacteria with Zinc Oxide nanoparticles this occurs approximately after nine hours.

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