Ginsenosides and Polysaccharides from Ginseng Co-Fermented with Multi-Enzyme-Coupling Probiotics Improve In Vivo Immunomodulatory Effects.

The active components of ginseng, such as ginsenosides and polysaccharides, have high therapeutic value in treating cancer, decreasing obesity, and enhancing immunity. However, simple primary ginseng treatment cannot maximize this medicinal potential. Therefore, in this study, Panax ginseng was co-fermented with multi-enzyme-coupling probiotics to obtain a fermentation broth with higher levels of ginsenosides, polysaccharides, and probiotics. When compared to other treatment methods for cyclophosphamide-induced immunosuppression in mice, the results reveal that the P. ginseng fermentation broth treated with multi-enzyme-coupling probiotics could significantly improve the immune function of immunosuppressive mice and restore intestinal flora stability. Overall, this processing method will provide a novel strategy for promoting the application of ginseng and the relief of immunosuppression.

Cellobiose phosphorylase from Caldicellulosiruptor bescii catalyzes reversible phosphorolysis via different kinetic mechanisms.

In the process of yielding biofuels from cellulose degradation, traditional enzymatic hydrolysis, such as ß-glucosidase catalyzing cellobiose, can barely resolve the contradiction between cellulose degradation and bioenergy conservation. However, it has been shown that cellobiose phosphorylase provides energetic advantages for cellobiose degradation through a phosphorolytic pathway, which has attracted wide attention. Here, the cellobiose phosphorylase gene from Caldicellulosiruptor bescii (CbCBP) was cloned, expressed, and purified. Analysis of the enzymatic properties and kinetic mechanisms indicated that CbCBP catalyzed reversible phosphorolysis and had good thermal stability and broad substrate selectivity. In addition, the phosphorolytic reaction of cellobiose by CbCBP proceeded via an ordered Bi Bi mechanism, while the synthetic reaction proceeded via a ping pong Bi Bi mechanism. The present study lays the foundation for optimizing the degradation of cellulose and the synthesis of functional oligosaccharides.

Dynamic Reference Selection-Based Self-Localization Algorithm for Drifted Underwater Acoustic Networks.

Self-localization has become one of the major areas of research in drifted underwater acoustic networks (DUANs) since many applications are based on the knowledge of nodes' positions. However, self-localization for DUANs faces two main challenges: the insufficient anchors and the varying network topology. Both affect the localization performance seriously. In this paper, we focus on these two challenges and propose a dynamic reference selection-based self-localization algorithm for DUANs (DRSL) to improve the localization performance. First, an optimal reference selection scheme is presented to solve the insufficient anchors' problem. The selected optimal reference node can not only assist the insufficient anchors in accomplishing the localization procedure, but also obviously increase the localization accuracy. Based on the proposed optimal reference selection scheme, a dynamic reference selection-based self-localization algorithm is proposed to solve the topology changing problem. The proposed algorithm can improve the localization performance for DUANs significantly by selecting the reference node dynamically according to the predicted network topology, which is more suitable for DUANs with mobile sensor nodes. Simulation results show that the proposed DRSL algorithm can increase the localization accuracy greatly with insufficient anchor nodes and varying network topology. In addition, DRSL algorithm also has a lower communication cost than other anchor-free approaches, which distinctly demonstrates the advantages of the proposed DRSL algorithm.

A Double Rate Localization Algorithm with One Anchor for Multi-Hop Underwater Acoustic Networks.

Localization is a basic issue for underwater acoustic networks (UANs). Currently, most localization algorithms only perform well in one-hop networks or need more anchors which are not suitable for the underwater environment. In this paper, we proposed a double rate localization algorithm with one anchor for multi-hop underwater acoustic networks (DRL). The algorithm firstly presents a double rate scheme which separates the localization procedure into two modes to increase the ranging accuracy in multi-hop UANs while maintaining the transmission rate. Then an optimal selection scheme of reference nodes was proposed to reduce the influence of references' topology on localization performance. The proposed DRL algorithm can be used in the multi-hop UANs to increase the localization accuracy and reduce the usage of anchor nodes. The simulation and experimental results demonstrated that the proposed DRL algorithm has a better localization performance than the previous algorithms in many aspects such as accuracy and communication cost, and is more suitable to the underwater environment.

Incorporation of polyamidoamine sweeping and electrokinetic supercharging for in-line DNA fragment preconcentration.

We report an approach for in-line preconcentration of DNA fragments using dendritic polyamidoamine generation 2.0 (PAMAM G 2.0) as sweeping agent. During the experiment, a plug of PAMAM G 2.0 was hydrodynamically injected first, followed by field-amplified sample injection (FASI) of DNA fragments, which were concurrently swept by PAMAMs via DNA-PAMAM complexation. Then, a segment of releasing agent, sodium dodecyl sulfate (SDS), was hydrodynamically introduced and subsequently electrophoretically driven to interact with the DNA-PAMAM complexes, forming more stable supramolecular SDS-PAMAM complexes and releasing the initially bound DNA fragments. The excess dodecyl sulfate anion also acted as terminating electrolyte in the separation, thereby the DNA fragments were enriched by the joint effects of FASI, sweeping and transient isotachophoresis. We term the approach PAMAM sweeping-electrokinetic supercharging (EKS). Because the mobility of the DNA-PAMAM complex was very low, the proposed method allowed long-time sample injection without notable loss in separation efficiency. Under the optimum conditions, the PAMAM sweeping-EKS strategy improved the detection sensitivity of DNA fragments by more than 30 folds relative to the conventional FASI. Moreover, due to the sweeping process incorporated, the approach can be applied to enrichment of DNA fragments in highly saline matrix.

Polyamidoamine-grafted silica nanoparticles as pseudostationary phases for capillary electrochromatographic separation of proteins.

Polyamidoamine-grafted silica nanoparticles were synthesized, characterized and investigated for the feasibility as pseudostationary phases in alkaline buffer for separation of cationic and anionic proteins, viz., lysozyme, cytochrome C, gamma globulin, and myoglobin. Neither bare silica nanoparticles nor polyamidoamines nor their mixtures as pseudostationary phases could lead to simultaneous separation of the four proteins. However, polyamidoamine-grafted silica nanoparticles not only suppressed the irreversible wall adsorption of the cationic lysozyme and cytochrome C, but also provided selectivity toward all the proteins. We found that polyamidoamine generation two-modified silica nanoparticles were the optimum pseudostationary phases with respect to detection sensitivity and separation efficiency; presence of the nanoparticles at 0.01% in the running buffer of 12.5 mM tetraborate/phosphate at pH 9.1 resulted in baseline resolution of the four proteins.

Sensitive and selective capillary electrophoretic analysis of proteins by zirconia nanoparticle-enhanced copper (II)-catalyzed luminol-hydrogen peroxide chemiluminescence.

We report herein a sensitive, selective, convenient CE determination of heme proteins in complex matrices by a sodium-dodecyl-sulfate-assisted, zirconia nanoparticle-enhanced copper (II)-catalyzed luminol-hydrogen peroxide chemiluminescence (CCLHPCL). Introducing a segment of sodium dodecyl sulfate to the capillary after sample injection not only rendered selective detection by quenching the luminescence signals from the non-heme proteins but also owning to the suppressed protein adsorption, led to significant improvement in separation efficiency and detection sensitivity. The signals were further improved by addition of ZrO(2) nanoparticles to the chemiluminescence solution. Compared with the conventional CCLHPCL, the detection limits (S/N=3) were improved by 10.2-22.0 folds, with 7.8×10(-9), 3.3×10(-9) and 1.5×10(-9) M for three model proteins, viz, myoglobin, hemoglobin and cytochrome C, respectively. Because the method did not require sophisticated pretreatment, it was convenient to analyze heme proteins in complex matrices, as demonstrated, hemoglobin in human blood and spiked human urine samples.

Efficient one-pot synthesis of polyfunctionalized thiophenes via an amine-mediated ring opening of EWG-activated 2-methylene-1,3-dithioles.

An amine-mediated ring-opening reaction of EWG-activated 2-methylene-1,3-dithioles (EWG = electron-withdrawing group) was disclosed, and a new route to highly substituted thiophenes was developed via the ring opening of 1,3-dithioles and subsequent intramolecular annulation and amine substitution. This one-pot reaction could proceed efficiently under mild conditions.