Top quark pair production via e+e−e^{+}e^{-} collision in the littlest Higgs model with T-parity at the ILC

In the littlest Higgs model with T-parity, we studied the contributions of the new particles to the top-quark pair production via $e^{+}e^{-}$ collision at the International Linear Collider. We calculated the top-quark pair production cross section and found this process can generate significantly relative correction. The result may be a sensitive probe of the littlest Higgs model with T-parity

Top quark rare three-body decays in the littlest Higgs model with T-parity

In the littlest Higgs model with T-parity (LHT), the mirror quarks have flavor structures and will contribute to the top quark flavor changing neutral current. In this work, we perform an extensive investigation of the top quark rare three-body decays $t\to cVV (V=\gamma,Z,g)$ and $t\to cf\bar{f} (f=b,\tau,\mu,e)$ at one-loop level. Our results show that the branching ratios of $t\to cgg$ and $t\to cb\bar{b}$ could reach $\mathcal {O}(10^{-3})$ in the favorite parameter space of the littlest Higgs model with T-parity, which implies that these decays may be detectable at the LHC or ILC, while for the other decays, their rates are too small to be observable at the present or future colliders.Comment: 12 pages, 10 figure

A new and efficient method for purification of poly-γ- glutamic acid from high-viscosity fermentation broth

Purpose: To devise an efficient strategy for the separation and recovery of high-quality γ-PGA by investigation of the physical properties, pigment properties and microfiltration mode of high-viscosity fermentation broth.Methods: The bacterial strain, Bacillus subtilis 115, was used in this study. The viscosity of the fermentation broth was determined by digital viscometer with spindle SP-2 at 25 oC. The concentrations of glucose and L-glutamate were analyzed with a biosensor equipped with both glucose oxidase and Lglutamate oxidase electrodes. The pigment in the fermentation liquid was scanned with a UV spectrophotometer at wavelength range of 200 - 500 nm and was removed using activated carbon. Measurement of IR spectrum was performed using an IR spectrophotometer with KBr pellet. Results: The results showed that the γ-PGA yield was 35 g/L. The viscosity of the fermentation broth was 1600 mPa.s at the end of the batch fermentation. After 3-fold dilution, the viscosity was reduced to one-fortieth of the original value at 65 °C for 30 min., which allowed effective removal of Bacillus subtilis 115 from the broth. Maximum UV absorption of the pigment was occurred at 260 nm. The pigment was removed by shaking with 0.6 % activated carbon powder at 50 rpm for 20 min, resulting in 88 % decolorization. Concentration with hollow-fiber membrane (MWCO 500,000) resulted in complete removal of residual glucose and glutamic acid from the aqueous solution of γ-PGA. The molecular weight of the γ-PGA was 1095 kDa, and its UV scanning spectrum showed an absorption peak at 216 nm. The decomposition temperature (Td) of the γ-PGA was 312.92 oC. Its IR spectrum was consistent with the presence of carboxyl, hydroxyl, carbonyl and amide groups.Conclusion: An efficient method for the extraction and purification of high-quality γ-PGA from highviscosity fermentation broth.Keywords: Bacillus subtilis 115, γ-Polyglutamic acid, De-pigmentation, Activated carbon, Ultra-filtration, High-viscosity fermentation brot

Schmeissneria: A missing link to angiosperms?

BACKGROUND: The origin of angiosperms has been under debate since the time of Darwin. While there has been much speculation in past decades about pre-Cretaceous angiosperms, including Archaefructus, these reports are controversial. The earliest reliable fossil record of angiosperms remains restricted to the Cretaceous, even though recent molecular phylogenetic studies suggest an origin for angiosperms much earlier than the current fossil record. RESULTS: In this paper, after careful SEM and light microscopic work, we report fossils with angiospermous traits of the Jurassic age. The fossils were collected from the Haifanggou Formation (middle Jurassic) in western Liaoning, northeast China. They include two female structures and an associated leaf on the same slab. One of the female structures is physically connected to the apex of a short shoot. The female organs are borne in pairs on short peduncles that are arranged along the axis of the female structure. Each of the female organs has a central unit that is surrounded by an envelope with characteristic longitudinal ribs. Each central unit has two locules completely separated by a vertical septum. The apex of the central unit is completely closed. The general morphology places these fossils into the scope of Schmeissneria, an early Jurassic genus that was previously attributed to Ginkgoales. CONCLUSION: Because the closed carpel is a character only found in angiosperms, the closed apex of the central unit suggests the presence of angiospermy in Schmeissneria. This angiospermous trait implies either a Jurassic angiosperm or a new seed plant group parallel to angiosperms and other known seed plants. As an angiosperm, the Liassic age (earliest Jurassic) of Schmeissneria microstachys would suggest an origin of angiosperms during the Triassic. Although still uncertain, this could have a great impact on our perspective of the history, diversity and systematics of seed plants and angiosperms

Lysine residues of interferon regulatory factor 7 affect the replication and transcription activatormediated lytic replication of Kaposi’s sarcomaassociated herpesvirus/human herpesvirus 8

Kaposi’s sarcoma-associated herpesvirus (KSHV) infection goes through latent and lytic phases, which are controlled by the viral replication and transcription activator (RTA). Upon KSHV infection, the host responds by suppressing RTA-activated lytic gene expression through interferon regulatory factor 7 (IRF-7), a key regulator of host innate immune response. Lysine residues are potential sites for post-translational modification of IRF-7, and were suggested to be critical for its activity. In this study, we analysed the 15 lysine residues for their effects on IRF-7 function by site-directed mutagenesis. We found that some mutations affect the ability of IRF-7 to activate interferon (IFN)-a1 and IFN-b promoters, to suppress RTA-mediated lytic gene expression and to repress KSHV reactivation and lytic replication. However, other mutations affect only a subset of these four functions. These findings demonstrate that the lysine residues of IRF-7 play important roles in mediating IFN synthesis and modulating viral lytic replication