32 research outputs found

    Ag–ZnO Nanocomposites as a 3D Metal-Enhanced Fluorescence Substrate for the Fluorescence Detection of DNA

    No full text
    Fluorescence enhancement, including metal-enhanced fluorescence (MEF), has been widely explored in the field of biosensor technology. Two- and three-dimensional (2D and 3D) MEF substrate approaches have been developed for biosensors to detect target biomarkers such as genes and proteins. However, several issues remain, not least poor reproducibility caused by limited recognition and diffusion of biomolecules among target molecules, biological probes, and MEF substrates in aqueous environments. Here, an Ag–ZnO nanocomplex as a 3D MEF substrate was developed in two steps: hydrothermal synthesis of ZnO nanowire (NW) as a building block of Ag nanoparticles (NPs), and photochemical deposition of AgNPs on the ZnO NW. Fluorescence enhancement on Ag–ZnO nanocomposites (NCs) compared with the glass substrate was 14.8-, 16.9-, 11.4-, and 14.2-fold in the presence of 10, 20, 40, and 60 base pair (bp) double-stranded (ds) DNA, respectively. The MEF effects on glass, ZnO NW, and Ag–ZnO NCs were analyzed by measuring the fluorescence lifetime of fluorescein (FAM)-labeled dsDNA, and the average lifetimes were 9.76, 9.34, and 7.86 ns, respectively. Ag–ZnO NCs showed a 50-fold higher sensitivity for the detection of dsDNA than Ag nanoisland film (AgNIF) as a 2D MEF substrate. Therefore, Ag–ZnO NCs may have potential as a 3D MEF substrate. The MEF phenomenon might involve broad-range interactions between the surface of the metal nanostructure on Ag–ZnO NCs and fluorophores in various scenarios. Our Ag–ZnO NCs could facilitate the development of sensitive MEF-based biosensors for DNA detection

    Additional file 2: of Nodding behavior couples to vigilance fluctuation in a high-calorie diet model of drowsiness

    No full text
    Figure S2. Analysis of HF effects on drowsy states including nodding behavior. (a) The average length of nodding episode in the no-food and high-fat food groups (unpaired t-test, p = 0.887, no food n = 2 and high-fat n = 4, n.s. indicates ‘not significant’). All error bars represent s.e.m. (b) The mean duration of no food and high-fat food groups during Nd (unpaired t-test, p = 0.886) and Non-Nd states (unpaired t-test p = 0.895, no food n = 2 and high-fat n = 4). All error bars represent s.e.m. (PDF 88 kb

    表紙ほか

    Get PDF
    Additional file 1: Table S1. Intergenic regions of various constitutive promoters in C. amalonaticus Y19

    Enhancing Surface-Enhanced Raman Scattering Intensity through Light Diffuse Reflection on Ag/ZnO Nanowire Arrays

    No full text
    In this study, we present a new strategy to enhance the intensity of surface-enhanced Raman scattering (SERS) signals by using three-dimensional aggregated silver nanoparticles (AgNPs) on the zinc oxide nanowire arrays (Ag/ZnO NWA). The ZnO NWA acts as a light-scattering substrate, providing multidirectional incident light and reflecting a portion of the Raman scattered light, resulting in an improved SERS signal intensity. The composite nanowire structure of the Ag/ZnO NWA was successfully fabricated, and 400 nm ZnO nanowires in the Ag/ZnO NWA exhibit optimal diffuse light reflection, resulting in a significant improvement of the SERS signal intensity. The SERS enhancement factor (EF) for the Ag/ZnO NWA was determined to be EF (ISERS/NSERS)/(IRaman/NRaman) = 3.5 × 106. This substrate generated a ∼7.9-fold increased SERS signal compared to the preaggregated AgNPs in the absence of the ZnO NWA. The detection limit of the Ag/ZnO NWA was estimated by measuring SERS spectra of rhodamine B, enabling discrimination down to 10–15 M. Our approach inducing multidirectional diffuse reflection light to SERS hot spots provides a simple and efficient strategy to enhance SERS signal intensity, with broad implications for other spectroscopic applications

    MOESM1 of Anodic electro-fermentation of 3-hydroxypropionic acid from glycerol by recombinant Klebsiella pneumoniae L17 in a bioelectrochemical system

    Get PDF
    Additional file 1. Additional figures and table. Table S1. Strains and plasmid used in this study. Fig. S1. Cell growth profile of L17W in BES and non-BES (A) and L17K in BES and non-BES (B) and pHprofile of L17W in BES and non-BES (C) and L17K in BES and non-BES (D). Fig. S2. Metabolites profile of L17W (A) and L17K (B) in BES and L17W (C) and L17K (D) in non-BES
    corecore