A study toward development of an automated microbial metabolism laboratory Monthly progress report

Life detection systems based on phosphate and sulfur uptake for automated microbial metabolism laborator

Life Detection Subsystem Progress Report No. 1

Radioisotopic biochemical probe for extraterrestrial life detection based on cell uptake of phosphate and sulfu

Review of the West Indian species of Efferia Coquillett (Diptera: Asilidae): Part 1. Bahamas, Cayman Islands, Cuba, and Jamaica

The genus Efferia Coquillett from the Bahamas, Cayman Islands, Cuba, and Jamaica is reviewed. The fauna now totals 16 species with 6 new species described (Ef. bellardii n. sp., Ef. bromleyi n. sp., Ef. hinei n. sp., Ef. insula n. sp., Ef. pina n. sp., and Ef. vinalensis n. sp.). Cuba has the greatest diversity with 10 species, Jamaica 3, the Bahamas 2, and the Cayman Islands 1. Efferia stylata (Fabricius) is removed from the species list of these West Indian islands. The wings of Ef. caymanensis Scarbrough and Ef. bromleyi, spermathecae of Ef. bromleyi, Ef. cubensis (Bromley), Ef. insula, Ef. nigritarsis (Hine), and terminalia of all species are illustrated. Keys for the identification of the species are provided. Specimens of two additional species from Cuba are in too poor a condition to be described but their terminalia are illustrated and the species are included in the key to the males

Mode stability in delta Scuti stars: linear analysis versus observations in open clusters

A comparison between linear stability analysis and observations of pulsation modes in five delta Scuti stars, belonging to the same cluster, is presented. The study is based on the work by Michel et al. (1999), in which such a comparison was performed for a representative set of model solutions obtained independently for each individual star considered. In this paper we revisit the work by Michel et al. (1999) following, however, a new approach which consists in the search for a single, complete, and coherent solution for all the selected stars, in order to constrain and test the assumed physics describing these objects. To do so, refined descriptions for the effects of rotation on the determination of the global stellar parameters and on the adiabatic oscillation frequency computations are used. In addition, a crude attempt is made to study the role of rotation on the prediction of mode instabilities.The present results are found to be comparable with those reported by Michel et al. (1999). Within the temperature range log T_eff = 3.87-3.88 agreement between observations and model computations of unstable modes is restricted to values for the mixing-length parameter alpha_nl less or equal to 1.50. This indicates that for these stars a smaller value for alpha_nl is required than suggested from a calibrated solar model. We stress the point that the linear stability analysis used in this work still assumes stellar models without rotation and that further developments are required for a proper description of the interaction between rotation and pulsation dynamics.Comment: 8 pages, 4 figures, 3 tables. (MNRAS, in press

Role of Membrane GM1 on Early Neuronal Membrane Actions of Aβ During Onset of Alzheimer\u27s Disease

The ability of beta-amyloid peptide (Aβ) to disrupt the plasma membrane through formation of pores and membrane breakage has been previously described. However, the molecular determinants for these effects are largely unknown. In this study, we examined if the association and subsequent membrane perforation induced by Aβ was dependent on GM1levels. Pretreatment of hippocampal neurons with D-PDMP decreased GM1 and Aβ clustering at the membrane (Aβ fluorescent-punctas/20 μm, control = 16.2 ± 1.1 vs. D-PDMP = 6.4 ± 0.4, p \u3c 0.001). Interestingly, membrane perforation with Aβ occurred with a slower time course when the GM1 content was diminished (time to establish perforated configuration (TEPC) (min): control = 7.8 ± 2 vs. low GM1 = 12.1 ± 0.5, p \u3c 0.01), suggesting that the presence of GM1 in the membrane can modulate the distribution and the membrane perforation by Aβ. On the other hand, increasing GM1 facilitated the membrane perforation (TEPC: control = 7.8 ± 2 vs. GM1 = 6.2 ± 1 min, p \u3c 0.05). Additionally, using Cholera Toxin Subunit-B (CTB) to block the interaction of Aβ with GM1 attenuated membrane perforation significantly. Furthermore, pretreatment with CTB decreased the membrane association of Aβ (fluorescent-punctas/20 μm, Aβ: control = 14.8 ± 2.5 vs. CTB = 8 ± 1.4, p \u3c 0.05), suggesting that GM1 also plays a role in both association of Aβ with the membrane and in perforation. In addition, blockade of the Aβ association with CTB inhibited synaptotoxicity. Taken together, our results strongly suggest that membrane lipid composition can affect the ability of Aβ to associate and subsequently perforate the plasma membrane thereby modulating its neurotoxicity in hippocampal neurons

On the ongoing multiple blowout in NGC 604

Several facts regarding the structure of NGC 604 are examined here. The three main cavities, produced by the mechanical energy from massive stars which in NGC 604 are spread over a volume of 10$^6$ pc$^3$, are shown here to be undergoing blowout into the halo of M33. High resolution long slit spectroscopy is used to track the impact from massive stars while HST archive data is used to display the asymmetry of the nebula. NGC 604 is found to be a collection of photoionized filaments and sections of shells in direct contact with the thermalized matter ejected by massive stars. The multiple blowout events presently drain the energy injected by massive stars and thus the densest photoionized gas is found almost at rest and is expected to suffer a slow evolution.Comment: 15 pages (11 text), 4 figures. To be published in Ap

The nucleotidohydrolases DCTPP1 and dUTPase are involved in the cellular response to decitabine

Decitabine (5-aza-2acute;-deoxycytidine, aza-dCyd) is an anticancer drug used clinically for the treatment of myelodysplastic syndromes and acute myeloid leukemia that can act as a DNA-demethylating or genotoxic agent in a dose-dependent manner. On the other hand, DCTPP1 and dUTPase are two "house-cleaning" nucleotidohydrolases involved in the elimination of non-canonical nucleotides. Here we show that exposure of HeLa cells to decitabine up-regulates the expression of several pyrimidine metabolic enzymes including DCTPP1, dUTPase, dCMP deaminase and thymidylate synthase thus suggesting their contribution to the cellular response to this anticancer nucleoside. We present several lines of evidence supporting that, in addition to the formation of aza-dCTP, an alternative cytotoxic mechanism for decitabine may involve the formation of aza-dUMP, a potential thymidylate synthase inhibitor. Indeed, dUTPase or DCTPP1 down-regulation enhanced the cytotoxic effect of aza-dCyd producing an accumulation of nucleoside triphosphates containing uracil as well as uracil misincorporation and double-strand breaks in genomic DNA. Moreover, DCTPP1 hydrolyzes the triphosphate form of decitabine with similar kinetic efficiency than its natural substrate dCTP and prevents decitabine-induced global DNA demethylation. The data suggest that the nucleotidohydrolases DCTPP1 and dUTPase are factors involved in the mode of action of decitabine with potential value as enzymatic targets to improve decitabine-based chemotherapy