Design of a large dynamic range readout unit for the PSD detector of DAMPE

A large dynamic range is required by the Plastic Scintillator Detector (PSD) of DArk Matter Paricle Explorer (DAMPE), and a double-dynode readout has been developed. To verify this design, a prototype detector module has been constructed and tested with cosmic rays and heavy ion beams. The results match with the estimation and the readout unit could easily cover the required dynamic range

Effects of Symmetry Energy in the Reaction 40Ca+124Sn at 140 MeV/nucleon

The density-dependent symmetry energy is a hot topic in nuclear physics. Many laboratories over the world are planning to perform related experiments to probe the symmetry energy. Based on the semiclassical Boltzmann-Uehling-Uhlenbeck (BUU) transport model, we study the effects of nuclear symmetry energy in the central reaction 40Ca+124Sn at 140MeV/nucleon in the laboratory system. It is found that the rapidity distribution of free nucleon's neutron-to-proton ratio is sensitive to the symmetry energy, especially at large rapidities. The free neutron-to-proton ratios at small or large rapidities may reflect high or low density behavior of nuclear symmetry energy. To probe the density dependence of nuclear symmetry energy, it is better to give the kinetic distribution and the rapidity distribution of emitted nucleons at the same time.Comment: 4 pages, 6 figures. arXiv admin note: text overlap with arXiv:1204.085

Ispitivanje antioksidativne aktivnosti in vitro polipeptida meduze (Rhopilema esculentum)

Jellyfish gelatin was hydrolyzed by different proteases to obtain antioxidative polypeptides. The gelatin hydrolysate obtained by progressive hydrolysis using trypsin and Properase E exhibited the highest hydrolysis degree and antioxidant activity. Three series of gelatin polypeptides (SCP1, SCP2 and SCP3) were obtained by ultrafiltrating the gelatin hydrolysate through molecular mass cut-off membranes of 10, 6 and 2 kDa, respectively. Amino acid composition analysis showed that SCP3 had the highest total hydrophobic amino acid content. The in vitro antioxidant tests demonstrated that SCP2 had the strongest hydroxyl radical and hydrogen peroxide scavenging activities and metal chelating ability, while SCP3 showed the highest reducing power, antioxidant activity in linoleic acid emulsion system and superoxide anion radical scavenging activity. The results support the feasibility of jellyfish gelatin as a natural antioxidant polypeptide provider, and enzymatic hydrolysis and ultrafiltration could be potent future processing technologies to utilize the abundant jellyfish resource.Hidrolizom želatine iz meduze pomoću različitih proteaza dobiveni su polipeptidi antioksidativnih svojstava. Najveći stupanj hidrolize i najbolja antioksidativna svojstva imao je hidrolizat dobiven progresivnom hidrolizom pomoću tripsina i Properase E. Ultrafiltracijom hidrolizata kroz membrane (10, 6 i 2 kDa) dobivene su tri serije polipeptida želatine: SCP1, SCP2 i SCP3. Analizom aminokiselinskoga sastava ustanovljeno je da SCP3 ima najveći ukupni udio hidrofobnih aminokiselina. Antioksidativni testovi in vitro pokazali su da SCP2 ima najveću sposobnost uklanjanja hidroksilnih radikala i vodikova peroksida te keliranja metala, a SCP3 najveću redukcijsku moć, najbolju antioksidativnu aktivnost u emulzijskom sustavu linoleinske kiseline te sposobnost uklanjanja superoksidnih aniona. Rezultati potvrđuju da se želatina iz meduze može upotrijebiti kao izvor prirodnih antioksidativnih polipeptida, a enzimska hidroliza i ultrafiltracija kao postupci prerade za njezino iskorištavanje

Ispitivanje antioksidativne aktivnosti in vitro polipeptida meduze (Rhopilema esculentum)

Jellyfish gelatin was hydrolyzed by different proteases to obtain antioxidative polypeptides. The gelatin hydrolysate obtained by progressive hydrolysis using trypsin and Properase E exhibited the highest hydrolysis degree and antioxidant activity. Three series of gelatin polypeptides (SCP1, SCP2 and SCP3) were obtained by ultrafiltrating the gelatin hydrolysate through molecular mass cut-off membranes of 10, 6 and 2 kDa, respectively. Amino acid composition analysis showed that SCP3 had the highest total hydrophobic amino acid content. The in vitro antioxidant tests demonstrated that SCP2 had the strongest hydroxyl radical and hydrogen peroxide scavenging activities and metal chelating ability, while SCP3 showed the highest reducing power, antioxidant activity in linoleic acid emulsion system and superoxide anion radical scavenging activity. The results support the feasibility of jellyfish gelatin as a natural antioxidant polypeptide provider, and enzymatic hydrolysis and ultrafiltration could be potent future processing technologies to utilize the abundant jellyfish resource.Hidrolizom želatine iz meduze pomoću različitih proteaza dobiveni su polipeptidi antioksidativnih svojstava. Najveći stupanj hidrolize i najbolja antioksidativna svojstva imao je hidrolizat dobiven progresivnom hidrolizom pomoću tripsina i Properase E. Ultrafiltracijom hidrolizata kroz membrane (10, 6 i 2 kDa) dobivene su tri serije polipeptida želatine: SCP1, SCP2 i SCP3. Analizom aminokiselinskoga sastava ustanovljeno je da SCP3 ima najveći ukupni udio hidrofobnih aminokiselina. Antioksidativni testovi in vitro pokazali su da SCP2 ima najveću sposobnost uklanjanja hidroksilnih radikala i vodikova peroksida te keliranja metala, a SCP3 najveću redukcijsku moć, najbolju antioksidativnu aktivnost u emulzijskom sustavu linoleinske kiseline te sposobnost uklanjanja superoksidnih aniona. Rezultati potvrđuju da se želatina iz meduze može upotrijebiti kao izvor prirodnih antioksidativnih polipeptida, a enzimska hidroliza i ultrafiltracija kao postupci prerade za njezino iskorištavanje

Pseudogap, Superconducting Energy Scale, and Fermi Arcs in Underdoped Cuprate Superconductors

Through the measurements of magnetic field dependence of specific heat in $La_{2-x}Sr_xCuO_4$ in zero temperature limit, we determined the nodal slope $v_\Delta$ of the quasiparticle gap. It is found that $v_\Delta$ has a very similar doping dependence of the pseudogap temperature $T^*$ or value $\Delta_p$. Meanwhile the virtual maximum gap at ($\pi,0$) derived from $v_\Delta$ is found to follow the simple relation $\Delta_q=0.46k_BT^*$ upon changing the doping concentration. This strongly suggests a close relationship between the pseudogap and superconductivity. It is further found that the superconducting transition temperature is determined by both the residual density of states of the pseudogap phase and the nodal gap slope in the zero temperature limit, namely, $T_c \approx \beta v_\Delta \gamma_n(0)$, where $\gamma_n(0)$ is the extracted zero temperature value of the normal state specific heat coefficient which is proportional to the size of the residual Fermi arc $k_{arc}$. This manifests that the superconductivity may be formed by forming a new gap on the Fermi arcs near nodes below $T_c$. These observations mimic the key predictions of the SU(2) slave boson theory based on the general resonating-valence-bond (RVB) picture.Comment: 6 pages, 6 figures, to be published in Phys. Rev.

HutZ is required for biofilm formation and contributes to the pathogenicity of Edwardsiella piscicida

International audienceAbstractEdwardsiella piscicida is a severe fish pathogen. Haem utilization systems play an important role in bacterial adversity adaptation and pathogenicity. In this study, a speculative haem utilization protein, HutZEp, was characterized in E. piscicida. hutZEp is encoded with two other genes, hutW and hutX, in an operon that is similar to the haem utilization operon hutWXZ identified in V. cholerae. However, protein activity analysis showed that HutZEp is probably not related to hemin utilization. To explore the biological role of HutZEp, a markerless hutZEp in-frame mutant strain, TX01ΔhutZ, was constructed. Deletion of hutZEp did not significantly affect bacterial growth in normal medium, in iron-deficient conditions, or in the presence of haem but significantly retarded bacterial biofilm growth. The expression of known genes related to biofilm growth was not affected by hutZEp deletion, which indicated that HutZEp was probably a novel factor promoting biofilm formation in E. piscicida. Compared to the wild-type TX01, TX01ΔhutZ exhibited markedly compromised tolerance to acid stress and host serum stress. Pathogenicity analysis showed that inactivation of hutZEp significantly impaired the ability of E. piscicida to invade and reproduce in host cells and to infect host tissue. In contrast to TX01, TX01ΔhutZ was defective in blocking host macrophage activation. The expression of hutZEp was directly regulated by the ferric uptake regulator Fur. This study is the first functional characterization of HutZ in a fish pathogen, and these findings suggested that HutZEp is essential for E. piscicida biofilm formation and contributes to host infection