TY - JOUR A1 - Roden, E. A1 - Kappler, A. A1 - Bauer, I. A1 - Jiang, J. A1 - Paul, Andrea A1 - Stoesser, R. A1 - Konishi, H. A1 - Xu, H. T1 - Extracellular electron transfer through microbial reduction of solid-phase humic substances KW - Natural organic-matter KW - Electron-acceptors KW - Reducing bacteria KW - Ferric iron KW - Reduction KW - Acid KW - Groundwater KW - Release KW - Kinetics KW - PH PY - 2010 DO - https://doi.org/10.1038/NGEO870 SN - 1752-0894 SN - 1752-0908 VL - 3 SP - 417 EP - 421 PB - Nature Publishing Group CY - London AN - OPUS4-22345 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Sieksmeyer, T. A1 - He, S. A1 - Esparza-Mora, M. A. A1 - Jiang, S. A1 - Petrasiunaite, V. A1 - Kuropka, B. A1 - Banasiak, Robert A1 - Julseth, M. J. A1 - Weise, C. A1 - Johnston, P. R. A1 - Rodriguez-Rojas, A. A1 - McMahon, Dino Peter T1 - Eating in a losing cause: Limited benefit of modifed macronutrient consumption following infection in the oriental cockroach Blatta orientalis N2 - Background: Host–pathogen interactions can lead to dramatic changes in host feeding behaviour. One aspect of this includes self-medication, where infected individuals consume substances such as toxins or alter their macronutrient consumption to enhance immune competence. Another widely adopted animal response to infection is illness-induced anorexia, which is thought to assist host immunity directly or by limiting the nutritional resources available to pathogens. Here, we recorded macronutrient preferences of the global pest cockroach, Blatta orientalis to investigate how shifts in host macronutrient dietary preference and quantity of carbohydrate (C) and protein (P) interact with immunity following bacterial infection. Results: We fnd that B. orientalis avoids diets enriched for P under normal conditions, and that high P diets reduce cockroach survival in the long term. However, following bacterial challenge, cockroaches signifcantly reduced their overall nutrient intake, particularly of carbohydrates, and increased the relative ratio of protein (P:C) consumed. Surprisingly, these behavioural shifts had a limited efect on cockroach immunity and survival, with minor changes to immune protein abundance and antimicrobial activity between individuals placed on diferent diets, regardless of infection status. Conclusions: We show that cockroach feeding behaviour can be modulated by a pathogen, resulting in an illness-induced anorexia-like feeding response and a shift from a C-enriched to a more P:C equal diet. However, our results also indicate that such responses do not provide signifcant immune protection in B. orientalis, suggesting that the host’s dietary shift might also result from random rather than directed behaviour. The lack of an apparent beneft of the shift in feeding behaviour highlights a possible reduced importance of diet in immune regulation in these invasive animals, although further investigations employing pathogens with alternative infection strategies are warranted. KW - Animal immune system KW - A key interface KW - Host and symbiont ecology KW - Behavioural mechanisms KW - Biotic environment PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-550022 DO - https://doi.org/10.1186/s12862-022-02007-8 SN - 2730-7182 VL - 22 IS - 1 SP - 1 EP - 14 PB - Springer Nature CY - London, UK AN - OPUS4-55002 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Jiang, Shan A1 - Wang, T. A1 - Behren, S. A1 - Westerlind, U. A1 - Gawlitza, Kornelia A1 - Persson, J. L. A1 - Rurack, Knut T1 - Sialyl-Tn Antigen-Imprinted Dual Fluorescent Core–Shell Nanoparticles for Ratiometric Sialyl-Tn Antigen Detection and Dual-Color Labeling of Cancer Cells N2 - Sialyl-Tn (STn or sialyl-Thomsen-nouveau) is a carbohydrate antigen expressed by more than 80% of human carcinomas. We here report a strategy for ratiometric STn detection and dual-color cancer cell labeling, particularly, by molecularly imprinted polymers (MIPs). Imprinting was based on spectroscopic studies of a urea-containing green-fluorescent monomer 1 and STn-Thr-Na (sodium salt of Neu5Acα2-6GalNAcα-O-Thr). A few-nanometer-thin green-fluorescent polymer shell, in which STn-Thr-Na was imprinted with 1, other comonomers, and a cross-linker, was synthesized from the surface of red-emissive carbon nanodot (R-CND)-doped silica nanoparticles, resulting in dual fluorescent STn-MIPs. Dual-color labeling of cancer cells was achieved since both red and green emissions were detected in two separate channels of the microscope and an improved accuracy was obtained in comparison with single-signal MIPs. The flow cytometric cell analysis showed that the binding of STn-MIPs was significantly higher (p < 0.001) than that of non-imprinted polymer (NIP) control particles within the same cell line, allowing to distinguish populations. Based on the modularity of the luminescent core–fluorescent MIP shell architecture, the concept can be transferred in a straightforward manner to other target analytes. KW - Cancer KW - Core−shell particles KW - Dual-color labeling glycan KW - Molecular imprinting PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-563106 DO - https://doi.org/10.1021/acsanm.2c03252 SP - 1 EP - 14 PB - ACS Publications AN - OPUS4-56310 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Yao, J. A1 - Jiang, T. A1 - Ji, Y. A1 - An-Stepec, Biwen Annie A1 - Koerdt, Andrea A1 - Cai, Z. A1 - Dong, C. A1 - Ge, Y. A1 - Qi, Z. T1 - Water-Fueled Autocatalytic Bactericidal Pathway based on e-Fenton-Like Reactions Triggered by Galvanic Corrosion and Extracellular Electron Transfer N2 - Water is generally considered to be an undesirable substance in fuel system, which may lead to microbial contamination. The antibacterial strategies that can turn water into things of value with high disinfection efficacy have been urgently needed for fuel system. Here, we reveal a water-fueled autocatalytic bactericidal pathway comprised by bi-metal micro-electrode system, which can spontaneously produce reactive oxygen species (mainly H2O2 and O2•–) by the electron Fenton-like reaction in water medium without external energy., The respiratory chain component of bacteria and the galvanic corrosion on the coated metals were two electron sources in the system. The specific model of Ag-Ru water-fueled autocatalytic (WFA) microelectrode particles presents extremely high disinfection efficiency (>99.9999%) in less than one hour for three aerobic bacteria (Escherichia coli, Pseudomonas aeruginosa and Bacillus subtilis) in LB media and high disinfection efficiency for the anaerobic bacteria (Desulfovibrio alaskensis) in Postgate E media without natural light irradiation. Overall, the novel WFA Ag-Ru antibacterial material explored in this study has a high potential for sterilizing applications in fuel system and this work provides the potential for the development of non-chemical and water-based antibacterial materials, such as WFA Ag-Ru antibacterial coating on stainless steel. KW - Fenton-like reaction KW - Reactive oxygen species KW - Disinfection Fuel KW - Silver KW - Ruthenium KW - MIC PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-555186 DO - https://doi.org/10.1016/j.jhazmat.2022.129730 SN - 0304-3894 VL - 440 SP - 1 EP - 11 PB - Elsevier CY - Amsterdam AN - OPUS4-55518 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Jiang, J. A1 - Bauer, I. A1 - Paul, Andrea A1 - Kappler, A. T1 - Arsenic redox changes by microbially and chemically formed semiquinone radicals and hydroquinones in a humic substance model quinone N2 - Arsenic is a redox-active metalloid whose toxicity and mobility strongly depends on its oxidation state, with arsenite (As(III)) being more toxic and mobile than arsenate (As(V)). Humic substances (HS) are also redox-active and can potentially react with arsenic and change its redox state. In this study we show that semiquinone radicals produced during microbial or chemical reduction of a HS model quinone (AQDS, 9,10-anthraquinone-2,6-disulfonic acid) are strong oxidants. They oxidize arsenite to arsenate, thus decreasing As toxicity and mobility. This reaction depends strongly on pH with more arsenite (up to 67.3%) being oxidized at pH 11 compared to pH 7 (12.6% oxidation) and pH 3 (0.5% oxidation). In addition to As(III) oxidation by semiquinone radicals, hydroquinones that were also produced during quinone reduction reduced As(V) to As(III) at neutral and acidic pH values (less than 12%) but not at alkaline pH. In order to understand redox reactions between arsenite/arsenate and reduced/oxidized HS, we quantified the radical content in reduced quinone solutions and constructed Eh-pH diagrams that explain the observed redox reactions. The results from this study can be used to better predict the fate of arsenic in the environment and potentially explain the occurrence of oxidized As(V) in anoxic environments. KW - Natural organic-matter KW - Electron-acceptors KW - Reducing bacteria KW - Ferric iron KW - Reduction KW - Acid KW - Groundwater KW - Release KW - Kinetics KW - pH PY - 2009 DO - https://doi.org/10.1021/es803112a SN - 0013-936X SN - 1520-5851 VL - 43 IS - 10 SP - 3639 EP - 3645 PB - ACS Publ. CY - Washington, DC AN - OPUS4-19982 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Yao, Dongxu A1 - Wirth, Cynthia A1 - Zeng, Y.-P. A1 - Jiang, D. A1 - Günster, Jens A1 - Heinrich, J. T1 - Near zero shrinkage porous Al2O3 prepared via 3D-printing and reaction bonding N2 - Porous Al2O3 with high porosity (~45%), remarkable flexural strength (~70 MPa), and low dimensional change (~1–2%), was produced by indirect 3D printing and reaction bonding. Coarse Al with good flowability was carried out printing green body. The green body was heat treated to get fully oxidized, volume expansion during oxidation simultaneously formed strong neck bonding, not only brought good strength, but also restricted shrinkage. Porous Al2O3 with architecture of macro pores designed by 3D printing and micro pores in the strut formed by packing of particles was obtained. The near zero shrinkage can facilitate precise design of product with complex shape. KW - Al2O3 reaction bonding PY - 2015 DO - https://doi.org/10.1016/j.matlet.2015.02.037 SN - 0167-577x SN - 1873-4979 VL - 147 SP - 116 EP - 118 PB - North-Holland Publ. Co. CY - Amsterdam AN - OPUS4-34960 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Liu, J.-Y. A1 - Hou, X.-N. A1 - Tian, Y. A1 - Jiang, L. A1 - Deng, S. A1 - Röder, B. A1 - Ermilov, Eugeny T1 - Photoinduced energy and charge transfer in a bis(triphenylamine)-BODIPY-C60 artificial photosynthetic system N2 - Triphenylamines (TPAs), boron dipyrromethenes (BODIPYs) and fullerenes C60 are excellent building blocks for the design of artificial photosynthetic systems. In the present work, we report the synthesis, characterization and detailed photophysical studies of a novel (TPA)2–BODIPY–C60 tetrad in polar and nonpolar solvents. The absorption spectrum of this compound covered virtually the entire visible Region (350–700 nm) and could be interpreted as a superposition of the spectra of individual components. Upon TPA-part excitation, a fast and very efficient excitation energy transfer (EET) delivers the excitation to the BODIPY moiety resulting in complete quenching of the TPA first excited singlet state as well as the appearance of the BODIPY fluorescence. The efficiency of EET process was estimated to be 1. Direct or indirect (via EET) excitation of the BODIPY-part of the tetrad is followed by photoinduced charge transfer to the charge-separated state BODIPY+–C60- irrespective of the solvent used. In polar N,N-dimethylformamide (DMF)charge recombination occurs directly to the ground state with the Charge recombination rate, kCR, slower than 108 s-1, whereas in nonpolar toluene (TOL) a small energy gap between the charge-separated state and first excited singlet state of the BODIPY moiety facilitates the back charge transfer process. The latter results in the appearance of thermally activated delayed fluorescence. The rate of charge separation was found to be ca. 2 times faster in TOL than in DMF. KW - Charge transfer KW - Energy transfer KW - Artificial photosynthesis KW - BODIPY KW - TPA KW - Fullerene C60 PY - 2016 DO - https://doi.org/10.1039/c6ra06841c SN - 2046-2069 VL - 6 IS - 62 SP - 57293 EP - 57305 AN - OPUS4-37080 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Yao, Dongxu A1 - Xia, Y. A1 - Zuo, K.-h. A1 - Jiang, D. A1 - Günster, Jens A1 - Zeng, Y.-P. A1 - Heinrich, J.G. T1 - Porous Si3N4 ceramics prepared via partial nitridation and SHS N2 - Porous Si3N4 ceramics were prepared via partial nitridation and self-propagating high temperature synthesis (SHS) process. Raw Si and additive Y2O3 were mixed and molded under 10 MPa into a compact, the compact was partial nitridation at 1300 °C to form a porous Si/Si3N4, and then it was buried in a Si/Si3N4 bed for SHS to obtain porous Si3N4 with rod-like β-Si3N4 morphology. The processing combined the advantages of the nitridation of Si and SHS with low cost, low shrinkage and time saving. Porous Si3N4 with a porosity of 47%, a strength of 143 MPa were obtained by this method. KW - Si3N4 KW - Strength KW - Porosity PY - 2013 DO - https://doi.org/10.1016/j.jeurceramsoc.2012.08.033 SN - 0955-2219 SN - 1873-619X VL - 33 IS - 2 SP - 371 EP - 374 PB - Elsevier CY - Oxford AN - OPUS4-31282 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Yao, Dongxu A1 - Xia, Y. A1 - Zuo, K.-h. A1 - Jiang, D. A1 - Günster, Jens A1 - Zeng, Y.-P. A1 - Heinrich, J.G. T1 - The effect of fabrication parameters on the mechanical properties of sintered reaction bonded porous Si3N4 ceramics N2 - Porous silicon nitride ceramics were prepared via sintered reaction bonded silicon nitride at 1680 °C. The grain size of nitrided Si3N4 and diameter of post-sintered ß-Si3N4 are controlled by size of raw Si. Porosity of 42.14–46.54% and flexural strength from 141 MPa to 165 MPa were obtained. During post-sintering with nano Y2O3 as sintering additive, nano Y2O3 can promote the formation of small ß-Si3N4 nuclei, but the large amount of ß-Si3N4 (>20%) after nitridation also works as nuclei site for precipitation, in consequence the growth of fine ß-Si3N4 grains is restrained, the length is shortened, and the improvement on flexural strength is minimized. The effect of nano SiC on the refinement of the ß-Si3N4 grains is notable because of the pinning effect, while the effect of nano C on the refinement of the ß-Si3N4 grains is not remarkable due to the carbothermal reaction and increase in viscosity of the liquid phase. KW - Porous ceramics KW - Silicon nitride KW - Reaction bonding KW - Anisotropic grain growth KW - Ceramic PY - 2014 DO - https://doi.org/10.1016/j.jeurceramsoc.2014.06.018 SN - 0955-2219 SN - 1873-619X VL - 34 IS - 15 SP - 3461 EP - 3467 PB - Elsevier CY - Oxford AN - OPUS4-32542 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Yao, Dongxu A1 - Xia, Y. A1 - Zuo, K.-h. A1 - Zeng, Y.-P. A1 - Jiang, D. A1 - Günster, Jens A1 - Heinrich, J.G. T1 - Gradient porous silicon nitride prepared via vacuum foaming and freeze drying N2 - Gradient porous silicon nitride (Si3N4) was fabricated by a novel vacuum foaming and freeze drying process. Aqueous Si3N4 slurries were foamed at vacuum pressure of 50–90 kPa, the green body was obtained by the freeze drying process, a gradient pore structure with porosities of 72–90% was achieved after pressureless sintering at 1680 °C. The porosity was increased with decreasing vacuum pressure. The pore structure consists of large pores (~100 μm) on top, medium pores (~45 μm) on the wall of the large pores, and small pores (~0.7 μm) in the matrix. Such gradient porous Si3N4 with macro- and micro-pores has potential application as high temperature filters. KW - Silicon nitride KW - Graded PY - 2015 DO - https://doi.org/10.1016/j.matlet.2014.11.067 SN - 0167-577x SN - 1873-4979 VL - 141 SP - 138 EP - 140 PB - Elsevier B.V. CY - Amsterdam AN - OPUS4-35177 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -