TY - CONF A1 - Exner, T. T1 - Evaluation anthropogener Marker als Normalisierungsfaktoren für die SARS-CoV-2 Abwassersurveillance zur epidemiologischen Lagebewertung N2 - Im Rahmen der weltweiten Corona-Pandemie fordert die EU-Kommission seit März 2021 die systematische Erfassung und Überwachung von SARS-CoV-2 über das Abwasser, welche der Entscheidungsfindung bezüglich bevölkerungsbezogener Maßnahmen dienen soll. Hierbei können Trendanalysen für die epidemiologische Lagebewertung abgeleitet werden, sofern ein großer Anteil des kommunalen Abwassers der Bevölkerung durch das Monitoring abdeckt wird. Die Datenerhebung erfolgt somit unabhängig vom individuellen Test- und Meldeverhalten der Bevölkerung. Eine bedeutende Herausforderung bei der Bestimmung der Gensequenzen mittels polymerase chain reaction (PCR) stellen standortabhängige Faktoren des Einzugsgebietes sowie Schwankungen der Durchflussrate und der Abwasserzusammensetzung dar. Zu den möglichen Ursachen zählen Verdünnungseffekte durch Regen- und Schmelzwasser, Größenunterschiede des kommunalen Entwässerungssystems, Veränderungen der Demografie und Zuflüsse von Indirekteinleitern. Um eine verbesserte Korrelation quantitativ ermittelter Genkopien des SARS-CoV-2 aus der jeweiligen Abwasserprobe mit dem Anteil der infizierten Bevölkerung zu erzeugen, ist eine Normalisierung der PCR Daten vorzunehmen. Neben relativ einfach zu ermittelnden physikalischen Größen, wie der mittleren Durchflussrate oder der Leitfähigkeit, die Aufschlüsse über den Anteil von Fremd- und Regenwasser ermöglichen, können auch anthropogene Marker, wie Spurenstoffe und Surrogatviren im Abwasser, als direkte Indikatoren für menschliche Fäkalien aus dem häuslichen Abwasser dienen. Im Folgenden soll eine vergleichende Untersuchung von vier Spurenstoffen ‒ Koffein (CAF), Carbamazepin (CBZ), Diclofenac (DCF), Isolithocholsäure (ILA) ‒ sowie einem Surrogatvirus (SV) (Pepper mild mottle virus (PMMoV) oder CrAssphage), die Eignung der jeweiligen Paramater als Normalisierungsfaktoren analysieren. Die Untersuchung fand an 19 Standorten über drei Monate im Rahmen einer Studie aus dem Projekt ESI-CorA statt. T2 - Wasser 2024 (Jahrestagung der Wasserchemischen Gesellschaft der GDCh) CY - Limburg an der Lahn, Germany DA - 06.05.2024 KW - ELISA KW - Immunoassay PY - 2024 AN - OPUS4-60992 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schneider, Rudolf T1 - Spurenstoffe im Rohabwasser: Möglichkeiten und Perspektiven für den One-Health-Ansatz N2 - Der One-Health-Ansatz hat die Gesundheit von Mensch, Tier und Umwelt im Fokus. Dazu ist eine interdisziplinäre Zusammenarbeit von Akteuren aus Human- und Veterinärmedizin sowie den Umweltwissenschaften notwendig. Ein Ineinandergreifen von methodischen Ansätzen und der Analytik wird angestrebt. Im Zuge der anstehenden Novellierung (2924) der EU-Kommunalabwasserrichtlinie (91/271/EWG) wird die Umsetzung eines One-Health-Ansatzes bereits adressiert. Dazu gehört zum einen der Ausbau und die Prozessüberwachung einer vierten Reinigungsstufe in Klärwerken. Zum anderen ist europaweit die Infrastruktur einer Abwassersurveillance zur Überwachung von Krankheitserregern zu gewährleisten. Dies wird aktuell in Deutschland mit dem Projekt AMELAG ("Abwassermonitoring zur epidemiologischen Lagebewertung") mit zwei Probennahmen pro Woche auf ca. 170 Kläranlagen umgesetzt. T2 - 6. Mülheimer Wasseranalytisches Seminar (MWAS 2024) CY - Mülheim an der Ruhr, Germany DA - 10.09.2024 KW - ELISA KW - Spurenstoffe KW - Koffein KW - Carbamazepin KW - Diclofenac KW - Immunoassay PY - 2024 AN - OPUS4-60993 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Ecke, Alexander A1 - Bell, Jérémy A1 - Schneider, Rudolf T1 - From Laboratory Immunoassays to Immunosensors with an Integrated Microfluidic Flow System N2 - This research summary describe efforts to the development of a three-dimensional microfluidic flow cell for improved electrochemical substrate detection in HRP/TMB-based immunoassays. This work provides a valuable advancement in the sensitivity and integration of immunoassay technologies, aiding in the refinement of diagnostic tools. KW - Antikörper KW - Immunoassay KW - Microfluidics KW - Electrochemical detection KW - Biosensor PY - 2025 UR - https://www.elveflow.com/microfluidics-research-summaries/from-laboratory-immunoassays-to-immunosensors-with-an-integrated-microfluidic-flow-system/ SP - 1 EP - 4 CY - Paris AN - OPUS4-62674 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schneider, Rudolf T1 - Monitoring trace substances in wastewater and surface water by immunoanalytical assays and sensors N2 - Monitoring the elimination of trace substances in wastewater treatment plants, as required in the recast of the EU Urban Wastewater Treatment Directive and the new Kommunalabwasserrichtlinie (KARL), creates a need for on-site analyses in wastewater treatment plants. Immunoanalytical methods can be carried out on site, e.g. in the form of rapid tests, but continuously operating (immuno-bio)sensors would be ideal. And antibody-based methods have the inherent disadvantage that one antibody must be used per analyte and therefore only a small number of substances can be analysed. A set of indicators has been integrated in the directives in accordance with the list of the Kompetenzzentrum Spurenstoffe BW (KomS) and offer points of reference here. Yet, in order to be able to use immunoanalytical methods for their monitoring, (DIN/ISO) standards are required that define the necessary quality requirements and quality management measures for the sensors. In addition, for the larger part of the indicators, the required antibodies have yet to be developed and made commercially available in the long term. The talk will highlight our previous work on high-throughput methods, such as ELISA, regarding the presence of anthropogenic markers and some indicators as well as research approaches for sensor technology that could be used on-site, and will provide an overview of deficits and future efforts. T2 - Kolloquium der Abteilung Technische Umweltchemie und Sensortechnik CY - Stuttgart, Germany DA - 21.05.2025 KW - Antibodies KW - Immunoassay KW - Microfluidics KW - Biosensor KW - Trace substances PY - 2025 AN - OPUS4-63501 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Schneider, Rudolf T1 - Wasserdiagnose durch die Verwendung von Markern N2 - Die Überwachung des gesamten Wasserkreislaufs auf Mikroverunreinigungen ist aus gesundheitlicher und ökologischer Hinsicht wünschenswert und gewinnt durch den Klimawandel und das zunehmende Erfordernis der Wiederverwendung des Brauchwassers weiter an Bedeutung. Die schnellen und kostengünstigen antikörperbasierten Methoden („Immunoassays“) können helfen, Informationslücken zu schließen und kürzere Reaktionszeiten zu ermöglichen. Von Labormethoden über tragbare Analysengeräte bis hin zu Online-Sensoren sind viele Formate möglich (u. a. ELISA, Abb. 1). Es muss zudem die Bereitstellung der notwendigen, hochqualitativen Antikörper gewährleistet werden. Da aber gilt „1 Analyt – 1 Antikörper“, ist die Herstellung eines Konsenses bezüglich der vordringlich zu bestimmenden Indikatoren/Marker notwendig. Auch die Normung der Verfahren ist parallel in Angriff zu nehmen. KW - Antikörper KW - Immunoassay KW - Abwasser KW - ELISA PY - 2025 UR - https://analyticalscience.wiley.com/content/article-do/wasserdiagnose-durch-die-verwendung-von-markern VL - 2025 IS - 1 SP - 1 EP - 4 PB - WILEY CY - Hoboken, NJ, USA AN - OPUS4-63508 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Russo, Francesco Friedrich T1 - Low energy-electron ionisation mass spectrometry in non-targeted analysis N2 - The high throughput and sensitivity of mass spectrometry has resulted in a broad application in non-targeted screenings (NTS). Gas chromatography electron ionisation mass spectrometry (GC-EI-MS) methods show high reproducibility of fragmentation patterns, good separation, and vast spectral libraries. A significant disadvantage of standard 70 eV EI is the high degree of fragmentation with a possible loss of the molecular ion signal. The loss of molecular ion signal results in an increased difficulty in identifying compounds absent from spectral libraries as it precludes a straightforward molecular formula assignment. The high degree of fragmentation, and the resulting depletion of high m/z signals, also results in a reduced discriminatory power. The disadvantages of EI-MS are approached by soft ionisation techniques and, more recently, low energy (LE) EI-MS. LE-EI is a softer version of EI, which keeps high similarity with the standard 70 eV EI spectra and the good chromatographic properties of GC, while reducing the depletion of higher m/z ion signals. LE-EI-MS has been applied doping analytics[1], metabolomics[2], and fingerprinting of foods[3]. Our objective is the comparison of LE-EI-MS to alternative soft ionisation methods, e.g. APCI-MS, and the development of a NTS workflow for LE-EI-MS, including a highly automated data processing and annotation pipeline. In a first phase 13 compound libraries (705 compounds) will be measured at 14, 18, and 70 eV. Molecular ion abundance and similarity to standard 70 eV spectra are going to be evaluated. Furthermore, common neutral losses and fragments will be identified and included into an annotation tool. If the tool shows satisfying performance, it will be published (either as a standalone package or as an expansion to the InterpretMSSpectrum[4, 5] R package). T2 - ANAKON 2025 CY - Leipzig, Germany DA - 10.03.2025 KW - Mass Spectrometry (MS) KW - Low Energy Electron Ionisation Mass Spectrometry (LE-EI-MS) KW - Non-tagreted analysis PY - 2025 AN - OPUS4-62781 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Piechotta, Christian T1 - Development, Validation and Application of an Accelerated Weathering Protocol for Assessing Bisphenol A Release from Polycarbonate Materials into the environment N2 - Bisphenol A (BPA) is under continuous regulatory scrutiny and listed as substance of very high concern (SVHC). Particular concern is related to its frequent detection in surface waters, despite being readily biodegradable. Several studies have been conducted to investigate sources and pathways of BPA in the environment, concluding that its main use as monomer in polycarbonate (PC) contributes only marginally to environmental BPA releases over its life cycle. To better understand the actual releases of BPA from PC under environmental conditions, a newly developed methodology (Federal Institute for Materials Research and Testing, BAM) was applied, which comprises a novel accelerated weathering protocol for polycarbonate (PC) materials, combined with an advanced analytical setup allowing for improved detection of BPA at trace level concentrations. The weathering protocol achieves a 13.6-fold acceleration compared to Central European outdoor conditions and simulates environmental stressors (global radiation, rain, temperature variations) in a laboratory weathering chamber, with simultaneous BPA release measurements using an organic isotope dilution calibration LC-MS/MS approach. Validation was performed in parallel outdoor exposure tests, by using haze and yellowness index measurements as reference parameters. PC sample types representative of major polycarbonate applications were examined: Samples with different levels of UV-protection as used in transparent sheets used outdoor in construction or housings in Electro- and Electronic applications as well as samples with a protective coating as used in automotive applications (headlamps, glazing and construction). Results demonstrated consistently low total BPA releases of around 0.3 mg m⁻² for samples with exposed PC surfaces, while releases from coated samples were significantly reduced by around two orders of magnitude. In all cases examined, the BPA release ceased to zero after a period of four to six weeks, equivalent to approximately 1 to 1.5 years of outdoor exposure. This suggests that potential BPA releases diminish to virtually zero after that timespan. While the newly developed test method is not suitable for routine laboratory implementation, it provides crucial quantitative data on BPA release from PC materials during accelerated environmental weathering. T2 - Umwelt 2025 CY - Dessau, Germany DA - 22.09.2025 KW - Bisphenol A KW - Polycarbonate KW - Weathering PY - 2025 AN - OPUS4-64664 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Piechotta, Christian T1 - The European Metrology Network for Pollution Monitoring – EMN POLMO N2 - The EU’s Green Deal acknowledges that « the EU needs to better monitoring, report, prevent and remedy pollution from air, water, soil and consumer products and to look more systematically at all policies and regulations ». In order to address these challenges, the Commission launched a new Strategy for Sustainability in October 2020, and adopted a Zero-pollution Action Plan for air, water and soil, in 2021. The comparability and trueness of measurements are often compromised by the lack of intact traceability chains and appropriate quality controls, for example attained by the use of matrix-matched certified reference materials, participation in interlaboratory comparisons and other validation schemes . Noticeable improvements are apprehended after practical demonstrations and scientific discussions on the importance of traceability to the SI with stakeholders and end-users . The European Metrology Network for Pollution Monitoring (EMN POLMO) was created in 2022 to provide metrology support to the environmental community and industry involved in the monitoring of variety of pollutants, including chemical pollutants, radionuclides, biological & microbiological, and nano and micro particles, in the three environmental compartments (air, water and soil). Recently, light pollution and noise pollution have been included in the scope of the network. One of the main goals of POLMO is to bridge the interests of the different stakeholder and end-user, and to contribute to environmental sustainability through the provision of tools and resources, required to perform accurate, comparable measurements. The POLMO Strategic Research Agenda identifies the key measurement challenges and opportunities in pollution monitoring and sets out a roadmap for future research and development. T2 - BIPM - 150 years of meter convention CY - Versailles, France DA - 20.05.2025 KW - POLMO KW - EMN PY - 2025 AN - OPUS4-64662 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Piechotta, Christian T1 - Development, Validation and Application of an Accelerated Weathering Protocol for Assessing Bisphenol A Release from Polycarbonate Materials into the environment N2 - Bisphenol A (BPA) is under continuous regulatory scrutiny and listed as substance of very high concern (SVHC). Particular concern is related to its frequent detection in surface waters, despite being readily biodegradable. Several studies have been conducted to investigate sources and pathways of BPA in the environment, concluding that its main use as monomer in polycarbonate (PC) contributes only marginally to environmental BPA releases over its life cycle. To better understand the actual releases of BPA from PC under environmental conditions, a newly developed methodology (Federal Institute for Materials Research and Testing, BAM) was applied, which comprises a novel accelerated weathering protocol for polycarbonate (PC) materials, combined with an advanced analytical setup allowing for improved detection of BPA at trace level concentrations. The weathering protocol achieves a 13.6-fold acceleration compared to Central European outdoor conditions and simulates environmental stressors (global radiation, rain, temperature variations) in a laboratory weathering chamber, with simultaneous BPA release measurements using an organic isotope dilution calibration LC-MS/MS approach. Validation was performed in parallel outdoor exposure tests, by using haze and yellowness index measurements as reference parameters. PC sample types representative of major polycarbonate applications were examined: Samples with different levels of UV-protection as used in transparent sheets used outdoor in construction or housings in Electro- and Electronic applications as well as samples with a protective coating as used in automotive applications (headlamps, glazing and construction). Results demonstrated consistently low total BPA releases of around 0.3 mg m⁻² for samples with exposed PC surfaces, while releases from coated samples were significantly reduced by around two orders of magnitude. In all cases examined, the BPA release ceased to zero after a period of four to six weeks, equivalent to approximately 1 to 1.5 years of outdoor exposure. This suggests that potential BPA releases diminish to virtually zero after that timespan. While the newly developed test method is not suitable for routine laboratory implementation, it provides crucial quantitative data on BPA release from PC materials during accelerated environmental weathering. T2 - Umwelt 2025 CY - Dessau, Germany DA - 22.09.2025 KW - Bisphenol A KW - Polycarbonate KW - Weathering PY - 2025 AN - OPUS4-64665 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogel, Christian T1 - Per- and Polyfluoroalkyl Substances (PFAS) in Sewage Sludge and Wastewater-based Fertilizers N2 - Per- and polyfluoroalkyl substances (PFAS) are chemicals which were developed to improve humanity’s quality of life. Due to their high chemical stability and resistance to degradation by heat or acids, PFAS were used in a variety of consumer products. The continuous use of PFAS in household products and the discharge of PFAS from industrial plants into the sewer system resulted in the contamination of effluents and sewage sludge from wastewater treatment plants (WWTPs) (Roesch et al. 2022). Since sewage sludge is often used as fertilizer, its application on agricultural soils has been observed as a significant entry path for PFAS into the environment, specifically in our food chain. In Germany the sewage sludge/biosolid application on agricultural land was banned with the amendment of the German Sewage Sludge Ordinance and by 2029 sewage sludge application will be totally prohibited. However, phosphorus (P) from sewage sludge should still be recycled in WWTPs of cities with a population larger than 50,000 residents. To produce high-quality P-fertilizers for a circular economy, PFAS and other pollutants (e.g. pesticides and pharmaceuticals) must be separated from sewage sludge. Due to the strong diversity of industrial PFAS usage it is not clear if a safe application of novel recycled P-fertilizers from WWTPs can be guaranteed. Therefore, we analyzed various sewage sludges and wastewater-based fertilizers. Sewage sludge (SL) samples from various WWTPs in Germany and Switzerland, six sewage sludge ashes (SSA) from Germany, six thermally treated SL and SSA samples with different additives (temperatures: 700-1050 °C), two pyrolyzed SL samples (temperature: 400 °C) and two struvite samples from Germany and Canada were analyzed. The goal was to quantify PFAS in sewage sludges and wastewater-based P-fertilizers with the sum parameter extractable organic fluorine (EOF) by combustion ion chromatography (CIC). The results were compared with data from classical LC-MS/MS target analysis as well as selected samples by HR-MS suspect screening. The EOF values of the SLs mainly range between 154 and 538 µg/kg except for one SL which showed an elevated EOF value of 7209 µg/kg due to high organofluorine contamination. For the SSA samples the EOF values were lower and values between LOQ (approx. 60 µg/kg) and 121 µg/kg could be detected. For the pyrolyzed SLs no EOF values above the LOQ were detected. Moreover, the two wastewater-based struvite fertilizers contain 96 and 112 µg/kg EOF, respectively. In contrast to the EOF values, the sum of PFAS target values were relatively low for all SLs. Additional applied PFAS HR-MS suspect screening aimed to tentatively identify PFAS that could contribute to the hitherto unknown part of the EOF value. The majority of the detected fluorinated compounds are legacy PFAS such as short- and long-chain perfluorocarboxylic acids (PFCA), perfluorosulfonic acids (PFSA), polyfluoroalkyl phosphate esters (PAPs) and perfluorophosphonic acids (PFPA). Moreover, fluorinated pesticides, pharmaceutical as well as aromatic compounds were also identified, which are all included in the EOF parameter. Our research revealed that the current PFAS limit of 100 µg/kg for the sum of PFOS + PFOA in the German Fertilizer Ordinance is no longer up to date. Since the number of known PFAS already exceeds 10,000, the ordinance limit should be updated accordingly. Recent regulations and restrictions on using long-chain PFAS (≥C8) have resulted in a significant shift in the industry towards (ultra-)short-chain alternatives, and other, partly unknown, emerging PFAS. Ultimately, also fluorinated pesticides and pharmaceuticals, which end up as ultrashort PFAS in the WWTPs, have to be considered as possible pollutants in fertilizers from wastewater, too. T2 - Dioxin Konferenz CY - Maastricht, Netherlands DA - 10.09.2023 KW - Combustion Ion Chromatography KW - Per- and Polyfluoroalkyl substances (PFAS) KW - Sewage sludge KW - Fertilizer PY - 2023 AN - OPUS4-58345 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Geburtig, Anja T1 - Umfassende Analyse von Leachabels aus rezyklierten HDPE-Kanistern N2 - Es wurde untersucht, welche Substanzen aus rHDPE-Post-Consumer-Rezyklat herausgelöst und nachgewiesen werden können (Non-Target-Analytik). Die Substanzen wurden sowohl chemisch als auch anwendungsbezogen systematisiert. Diskutiert wurde die Nutzung der Ergebnisse zur Festlegung von Qualitätskriterien von rHDPE sowie zur Verbesserung des mechanischen Recycling-Prozesses. T2 - 20. Gefahrgut-Technik-Tage CY - Berlin, Germany DA - 13.11.2025 KW - rHDPE KW - Rezyklat KW - Leachables PY - 2025 AN - OPUS4-64852 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Braymer, Joseph T1 - Methanobacterium IM1 as a model organism to study MIC N2 - Microbiologically influenced corrosion (MIC), also known as biocorrosion, is a process where microbes corrode metal surfaces causing detrimental damage to manmade infrastructure. Several studies, mainly under anaerobic conditions, have identified sulfate-reducing bacteria and methanogens as key players in biocorrosion. However, an important issue is that most MIC-related microbes at the moment are non-culturable. In addition, improved technologies (i.e., omics, biochemical, and microscopy methods) are needed to study, detect, simulate, and modulate MIC-related cases. Therefore, the selection of strains that can cause MIC, are culturable, and are genetically accessible, are of high importance for establishing new methods to study MIC on the molecular level. For example, the archaeal strain Methanobacterium IM1 has caught great attention due to its involvement in biocorrosion processes. Genes encoding for a novel enzyme (MIC NiFe-hydrogenase) have been proposed in this methanogen to be directly related to the e T2 - International Biodeterioration and Biodegradation Symposium 19 CY - Berlin, Germany DA - 11.09.2024 KW - Biocorrosion KW - Methanogen KW - Iron KW - Hydrogenase KW - Mechanism PY - 2024 AN - OPUS4-61508 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Braymer, Joseph T1 - Yeast [FeFe]-hydrogenase-like protein Nar1 binds a [2Fe-2S] cluster N2 - Iron-sulfur (Fe/S) clusters are essential cofactors in many cellular processes and their synthesis as well as insertion into proteins must be tightly orchestrated. Nar1 is an essential eukaryotic protein proposed to function as an Fe/S cluster trafficking factor in the cytosolic iron-sulfur assembly (CIA) pathway. However, such a role has remained unclear due to difficulties in purifying adequate amounts of cofactor-bound protein. The [FeFe]-hydrogenase-like protein has two conserved binding sites for [4Fe-4S] clusters but does not show hydrogenase activity in vivo due to the lack of an active site [2Fe]H cofactor. In the presentation, I will discuss a new preparation procedure for Nar1 that facilitated studies by UV-Vis, EPR, and Mössbauer spectroscopies, along with native mass spectrometry (1). Nar1 recombinantly produced in E. coli contained a [4Fe-4S] cluster, bound presumably at site 1, along with an unexpected [2Fe-2S] cluster bound at an unknown site. Fe/S reconstitution reactions installed a second [4Fe-4S] cluster at site 2, leading to protein with up to three Fe/S cofactors. It is proposed that the [2Fe-2S] cluster occupies a cavity in Nar1 that is filled by the [2Fe]H cofactor in [FeFe]-hydrogenases. Strikingly, two of the Fe/S clusters were rapidly destroyed by molecular oxygen, linking Nar1 oxygen sensitivity in vitro to phenotypes observed previously in vivo. Our biochemical results, therefore, validate a direct link between cellular oxygen concentrations and the functioning of the CIA pathway via Nar1. How these results impact our understanding of the biogenesis of Fe/S proteins will be discussed. T2 - Advances in Structural Analysis of Biomolecules CY - Berlin, Germany DA - 23.10.2025 KW - Biocorrosion KW - Hydrogenases KW - Metalloprotein KW - Microbes PY - 2025 AN - OPUS4-64491 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CHAP A1 - Braymer, Joseph A1 - Pierik, Antonio ED - Leimkühler, Silke ED - Schwarz, Günter ED - Lenz, Oliver ED - Einsle, Oliver T1 - Chapter 4: Iron–Sulfur Protein Maturation in the Cytosol of Eukaryotes N2 - Cytosolic and nuclear proteins that bind iron–sulfur (Fe/S) clusters play essential roles in various eukaryotic cellular processes. Studies in yeast and human models have detailed the biogenesis requirements for [2Fe–2S] and [4Fe–4S] cytosolic proteins. Both types of Fe/S clusters require the mitochondrial Fe/S cluster pathway (ISC), the mitochondrial transporterAtm1, and the presence of glutathione, whereas [4Fe–4S] clusters are further strictly dependent on the conserved cytosolic Fe/S cluster assembly (CIA) pathway. Here, we outline the general requirements for cytosolic Fe/S protein biogenesis and the challenges in assigning cytosolic Fe/S proteins and briefly discuss the relevance to disease and for biotechnology. KW - Biocorrosion KW - Hydrogenases KW - Metalloprotein KW - Iron-sulfur clusters KW - Microbes PY - 2025 UR - https://www.wiley-vch.de/de?option=com_eshop&view=product&isbn=9783527352555 SN - 978-3-527-35255-5 SP - 1 EP - 49 PB - Wiley VHC-Verlag ET - 1 AN - OPUS4-64497 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schneider, Rudolf J. T1 - Evaluating the Normalization Potential of Anthropogenic Markers in Wastewater: Monitoring Influents of German Treatment Plants by ELISA N2 - Wastewater-based epidemiology (WBE) has emerged as a vital tool for pandemic preparedness, offering early warning capabilities and supporting public health interventions. In Germany, combined sewer systems are prevalent, leading to fluctuations in wastewater volume and com-position due to rainwater inflow, especially through street drains. This variability complicates the quantitative measurement of pathogens and pollutants in wastewater. While human excretion provides constant inputs, these parameters are often non-specific, lost, or degraded during transport. Pharmaceuticals—such as carbamazepine, diclofenac, and clarithromycin—as well as commonly consumed substances like caffeine, exhibit sufficiently high concentrations and good chemical stability in wastewater and are not subject to seasonal fluctuations. Antibody-based methods, particularly Enzyme-Linked Immunosorbent Assays (ELISA), offer a cost-effective alternative to complex chromatographic techniques for monitoring anthropogenic markers. They demonstrate superior normalization quality compared to the frequently used quantitative PCR-based marker Pepper mild mottle virus (PMMoV). T2 - 6th International Conference on Risk Assessment of Pharmaceuticals in the Environment - ICRAPHE CY - Aveiro, Portugal DA - 20.10.2025 KW - Carbamazepin KW - Koffein KW - Spurenstoffe KW - Anthropogener Marker Immunoassay PY - 2025 AN - OPUS4-64432 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Russo, Francesco Friedrich T1 - Gas chromatography low energy-electron ionisation mass spectrometry (GC LE EI MS) as a softer ionisation method for non-targeted analysis N2 - Mass spectrometry (MS)-based non-targeted screening (NTS) methods are important tools due to their high throughput and sensitivity. The high throughput and sensitivity have contributed to the method’s increased adoption in forensic, health, and environmental sciences. Gas chromatography electron ionisation mass spectrometry (GC-EI-MS) methods in particular show high reproducibility of fragmentation patterns and have the advantage of vast spectral libraries. Nevertheless, the high energy imparted to molecules by standard 70 eV EI sources frequently results in a loss of the molecular ion signal. The depleted molecular ion signal renders the identification of compounds not included in spectral libraries more difficult, as straightforward molecular formula assignment is not achieved. Furthermore, the high degree of fragmentation and the resulting depletion of signals with high m/z, leads to reduced discriminatory power. Soft ionisation techniques alleviate the inherent disadvantages of EI-MS in molecular formula determination but do not harness the knowledge stored in EI spectral libraries. Low energy (LE)-EI-MS, being a softer version of EI, has recently seen increased interest. LE-EI-MS keeps high spectral similarity with the standard 70 eV EI while reducing the depletion of signals of molecular ions and of higher m/z ions. The hyphenation of LE-EI-MS to GC is straightforward, keeping the high chromatographic resolution. LE-EI-MS has shown promise in fluxomics [1], doping analytics [2, 3], metabolomics [4], fingerprinting of foods [5, 6], and the identification of isomers in motor oil mixtures [7]. Our objective is the comparison of LE-EI-MS to alternative soft ionisation methods, e.g. APCI-MS, and the development of a non-targeted LE-EI-MS workflow, including highly automated data processing and annotation pipeline. In a first phase 13 compound libraries are measured at 14, 18, and 70 eV. Molecular ion abundance and similarity to standard 70 eV spectra are evaluated. Furthermore, common neutral losses and fragments are identified and included as an extension of a previously published annotation tool (R package InterpretMSSpectrum [8, 9]). T2 - Adlershofer Forschungforum CY - Berlin, Germany DA - 11.11.2024 KW - Mass Spectrometry (MS) KW - Non-targeted screenings (NTS) KW - Gas Chromatography (GC) KW - Low Energy Electron Ionisation Mass Spectrometry (LE-EI-MS) PY - 2024 AN - OPUS4-61666 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Russo, Francesco F. T1 - Gas chromatograph low energy-electron ionisation mass spectrometry (GC-LE-EI-MS) in non targeted analysis N2 - Non targeted screenings (NTS) are an important tool for forensic, health, and environmental sciences. Mass spectrometry (MS) based NTS methods are characterised by high throughput and high sensitivity. Gas chromatography electron ionisation mass spectrometry (GC EI-MS) methods show high reproducibility of fragmentation patterns, good separation, and vast spectral libraries. Nevertheless, the high energy imparted to molecules by standard 70eV EI sources results in a high degree of fragmentation with a possible loss of the molecular ion signal. The loss of molecular ion signal makes the identification of compounds absent from spectral libraries more difficult by precluding a straightforward molecular formula assignment. Furthermore, the high degree of fragmentation, and the resulting depletion of high m/z signals, results in a reduced discriminatory power. The disadvantages of EI MS are approached by soft ionisation techniques, e.g. electrospray ionisation (ESI). More recently, low energy (LE) EI-MS has awakened interest as a softer version of EI, which still keeps high similarity with the standard 70 eV EI and the good chromatographic properties of GC, while reducing the depletion of higher m/z ion signals and of molecular ions. LE-EI-MS has shown promise in fluxomics[1], doping analytics[2, 3], metabolomics[4], fingerprinting of foods[5, 6], and the identification of isomers in motor oil mixtures[7]. Our objective is the comparison of LE-EI-MS to alternative soft ionisation methods, e.g. APCI-MS, and the development of a non-targeted LE-EI-MS workflow, including a highly automated data processing and annotation pipeline. In a first phase 13 compound libraries (705 compounds) will be measured at 14, 18, and 70 eV. Molecular ion abundance and similarity to standard 70 eV spectra are going to be evaluated. Furthermore, common neutral losses and fragments will be identified and included into an annotation tool. If the tool shows satisfying performance, it will be published (either as a standalone package or as an expansion to the InterpretMSSpectrum[8, 9] R package). T2 - International Symposium on Chromatography (ISC) 2024 CY - Liverpool, UK DA - 06.10.2024 KW - MS KW - Low Energy Electron Ionisation Mass Spectrometry (LE-EI-MS) KW - Mass Spectrometry (MS) KW - Gas Chromatography Mass Spectrometry (GC-MS) KW - Gas Chromatography (GC) PY - 2024 AN - OPUS4-61349 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hantschke, Luisa Lamberta T1 - Determination of background values of PFAS in representative soil samples in Germany N2 - Per- and polyfluoroalkyl substances (PFAS) are a large and ever-growing class of chemicals that are widely used. Due to the strength of the C-F bond, they do not decompose but accumulate in the environment posing a risk for nature and humans alike. While the use of some PFAS, like perfluorooctanoic acid (PFOA) and perfluorooctanoic sulfonic acid (PFOS) is already regulated in the EU, new ‘precursor’ substances are used to replace them. However, these precursors may be equally harmful to the environment. In recent years, many ‘hot spot’ sites with high PFAS contaminations in the soils have been distinguished,but no German-wide background values have been determined yet. Knowing these background values is crucial to understand the degree of PFAS contamination, underpinning future regulatory decisions. 600 soil samples are freshly taken at different sites all over Germany. PFAS are extracted from all samples. The extracts are analysed using LC-MS/MS with 30 PFAS as target compounds. Eluates are produced and analysed using targeted LC-MS/MS. To determine the amount of precursor substances not included in the targeted list, total oxidisable precursor (TOP) assays are performed with different approaches. Additionally, 50 samples taken at the same locations in 2012 are analysed to determine temporal trends of PFAS contamination. The determination of total extractable organically bound fluorine (EOF) is planned for comparison. The aim of the project is to obtain a broad overview of the status and development of the PFAS contamination in soil in Germany. By the preparation and analysis of eluates, the leaching behaviour of the analytes and thereby their mobility in the environment is investigated, helping to understand the transport of PFAS from contaminated soil to water. The use of different TOP assay methods allows to compare their results and usability in routine analysis, thereby giving insights into the amount of PFAS contamination hidden to targeted analysis and helping inspire future analysis strategies. The future comparison of these results to EOF analysis may further underline this point. The large number of samples and the geographic distribution of the sampling is unprecedented in Germany and allows to determine high-risk sites and ‘hot spots’. In the future, the insights from the project may be used as a guide for the political regulation of uses of PFAS. T2 - ANAKON23 CY - Vienna, Austria DA - 11.04.2023 KW - PFAS KW - Soil contamination KW - Background values KW - BBodSChV PY - 2023 AN - OPUS4-57755 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - INPR A1 - Devi, Sarita A1 - Riedel, Soraya A1 - Döring, Sarah A1 - Hiller, Lukas A1 - Flemig, Sabine A1 - Singh, Chandan A1 - Konthur, Zoltán A1 - Hodoroaba, Vasile-Dan A1 - Schneider, Rudolf T1 - Antibodies Functionalized Magnetic Fe-Metal-Organic Framework Based Biosensor for Electrochemical Detection of Tetanus NeuroToxin N2 - This work presents a MOF-integrated microfluidic flow-cell based immunodetection of the tetanus toxoid (TT) using electrochemical technique for the first time. Metal-organic frameworks (MOFs) are coordination polymers, and composed of a metal center and organic linkers. Several synthesis methods have been reported to achieve the desired properties in MOFs. In this work, we report the hydrothermal synthesis of a magnetic and conductive iron-based MOF (Fe-MOF) which was utilized to develop a biosensor in conjugation with the human monoclonal antibody SA13 against TT (anti-TT mAb) for the detection of the tetanus neurotoxin (TeNT). The one-pot synthesis of this magnetic and conductive Fe-MOF was performed in a hydrothermal reactor (108℃) using the Fe3+/Fe2+ precursors as 1.2/1 mmol and dual ligands, i.e., tetrahydroxy-1,4-benzoquinone and 2-aminobenzene-1,4-dicarboxylic acid. The Fe-MOF was characterized using XRD, DLS, FTIR, and electron microscopy. The Fe-MOF was further conjugated with L-phenylalanine (pH 8.6) to increase the electric conductivity of the Fe-MOF (Fe-MOF/Phe) on the screen-printed gold electrode as studied by cyclic voltammetry (CV). The anti-TT mAb was conjugated on the Fe-MOF/Phe surface with the help of ethylenediamine (Fe-MOF/Phe/EDA/anti-TT mAb) delivered good binding affinity for the TT antigen revealing the applicability of this biosensor for TT detection by CV. The limit of detection of the Fe-MOF/Phe/EDA/anti-TT mAb-based biosensor for TT was 9.4 ng/ml in spiked buffer. There is negligible cross-reactivity in the presence of bovine serum albumin. This study shows the applicability of magnetic MOFs in the detection of various other microbial toxins or other biomolecules. KW - Magnetic Metal-Organic Framework KW - Tetanus toxoid KW - L-phenylalanine KW - Antibody KW - Label-free detection KW - Electrochemical immunosensor PY - 2024 DO - https://doi.org/10.2139/ssrn.4935745 SP - 1 EP - 48 PB - Elsevier Inc. AN - OPUS4-62196 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schneider, Rudolf T1 - Antikörperbasierte vor-Ort-Analytik für das Monitoring der Eliminierung von Spurenstoffen in Kläranlagen N2 - Die Überwachung der Eliminierung von Spurenstoffen in Kläranlagen, wie sie die Neufassung der Kommunalabwasserrichtlinie vorschreibt, ruft einen Bedarf an vor-Ort-Analytik in den Kläranlagen hervor. Immunanalytische Methoden können vor Ort, z.B. in Form von Schnelltests, durchgeführt werden, ideal aber wären kontinuierlich arbeitende (Immuno-Bio)Sensoren. Antikörperbasierte Verfahren weisen als Flaschenhals immanent die Einschränkung auf, dass pro Analyt ein Antikörper zum Einsatz kommen muss und dass daher nur eine kleinere Anzahl von Substanzen analysiert werden kann. Die Indikatorenliste der Abwasserrichtlinie liefert hier einen Anhaltspunkt. Der Artikel weist schon bisher existierende Schnell- und Hochdurchsatzverfahren aus, ebenso wie Forschungsansätze für eine Sensorik, die online einsetzbar wäre und gibt einen Überblick über Defizite und Entwicklungen. KW - Antikörper KW - Immunoassay KW - Schnelltests KW - Biosensor PY - 2025 SN - 1618-3258 VL - 31 IS - 1 SP - 12 EP - 14 AN - OPUS4-63510 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -