1,971 research outputs found

    The Nullity of Bicyclic Signed Graphs

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    Let \Gamma be a signed graph and let A(\Gamma) be the adjacency matrix of \Gamma. The nullity of \Gamma is the multiplicity of eigenvalue zero in the spectrum of A(\Gamma). In this paper we characterize the signed graphs of order n with nullity n-2 or n-3, and introduce a graph transformation which preserves the nullity. As an application we determine the unbalanced bicyclic signed graphs of order n with nullity n-3 or n-4, and signed bicyclic signed graphs (including simple bicyclic graphs) of order n with nullity n-5

    A novel strategy for rapid identification of the fruits of Illicium verum and Illicium anisatum using electronic nose and tongue technology

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    Purpose: To develop an effective and rapid strategy for the identification of fruits of I. verum and I. anisatum based on their odor and taste.Methods: Electronic nose (E-nose) and electronic tongue (E-tongue) technology was used to identify the fruits of I. verum (FIV) and I. anisatum (FIA). Samples of FIA, FIV, and FIA : FIV mixtures in different proportions (1 : 3, 1 : 1, and 3 : 1) were prepared to evaluate the identification abilities of E-nose and Etongue methods. Samples were powdered and sifted through a standard sieve (aperture size 355 ± 13 μm) for E-nose analysis. Each sample was refluxed with water for 1 h before E-tongue analysis. The acquired data were analyzed by principal component analysis (PCA) and discriminant factor analysis (DFA).Results: Based on the signals acquired by E-nose and E-tongue analyses, a total of 90 data points each were used for PCA. The three principal component values for E-nose analysis were PC1 = 93.89 %, PC2 = 6.08 %, and PC3 = 0.03 %, and those for E-tongue analysis were PC1 = 98.72 %, PC2 = 0.68 %, and PC3 = 0.57 %. The sample data were significantly divided into two groups representing FIV and FIA. Furthermore, E-nose and E-tongue assessments combined with PCA and DFA analyses effectively identified FIV, FIA and their mixtures.Conclusion: The use of E-nose and E-tongue technology is an effective and rapid strategy to identify the fruits of I. verum and I. anisatum and their mixtures. This strategy may also offer an effective method for detection of adulterants.Keywords: Illicium verum, Illicium anisatum, Discrimination, Electronic nose, Electronic tongue, Safety, Principal component analysis, Discriminant factor analysi

    An Intelligent and Secure Health Monitoring Scheme Using IoT Sensor Based on Cloud Computing

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    Internet of Things (IoT) is the network of physical objects where information and communication technology connect multiple embedded devices to the Internet for collecting and exchanging data. An important advancement is the ability to connect such devices to large resource pools such as cloud. The integration of embedded devices and cloud servers offers wide applicability of IoT to many areas of our life. With the aging population increasing every day, embedded devices with cloud server can provide the elderly with more flexible service without the need to visit hospitals. Despite the advantages of the sensor-cloud model, it still has various security threats. Therefore, the design and integration of security issues, like authentication and data confidentiality for ensuring the elderly’s privacy, need to be taken into consideration. In this paper, an intelligent and secure health monitoring scheme using IoT sensor based on cloud computing and cryptography is proposed. The proposed scheme achieves authentication and provides essential security requirements

    High-level expression and molecular characterization of a recombinant prolidase from Escherichia coli NovaBlue

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    Long-term use of organophosphorus (OP) compounds has become an increasing global problem and a major threat to sustainability and human health. Prolidase is a proline-specific metallopeptidase that can offer an efficient option for the degradation of OP compounds. In this study, a full-length gene from Escherichia coli NovaBlue encoding a prolidase (EcPepQ) was amplified and cloned into the commercially-available vector pQE-30 to yield pQE-EcPepQ. The overexpressed enzyme was purified from the cell-free extract of isopropyl thio-β-D-galactoside IPTG-induced E. coli M15 (pQE-EcPepQ) cells by nickel-chelate chromatography. The molecular mass of EcPepQ was determined to be about 57 kDa by 12% sodium dodecyl sulfate–polyacrylamide gel electrophoresis and the result of size-exclusion chromatography demonstrated that the enzyme was mainly present in 25 mM Tris–HCl buffer (pH 8.0) as a dimeric form. The optimal conditions for EcPepQ activity were 60 °C, pH 8.0, and 0.1 mM Mn2+ ion. Kinetic analysis with Ala-Pro as the substrate showed that the Km and kcat values of EcPepQ were 8.8 mM and 926.5 ± 2.0 s−1, respectively. The thermal unfolding of EcPepQ followed a two-state process with one well-defined unfolding transition of 64.2 °C. Analysis of guanidine hydrochloride (GdnHCl)-induced denaturation by tryptophan emission fluorescence spectroscopy revealed that the enzyme had a [GdnHCl]0.5,N-U value of 1.98 M. The purified enzyme also exhibited some degree of tolerance to various water/organic co-solvents. Isopropanol and tetrahydrofuran were very detrimental to the enzymatic activity of EcPepQ; however, other more hydrophilic co-solvents, such as formamide, methanol, and ethylene glycol, were better tolerated. Eventually, the non-negative influence of some co-solvents on both catalytic activity and structural stability of EcPepQ allows to adjust the reaction conditions more suitable for EcPepQ-catalyzed bioprocess
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