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 - TY - THES A1 - Ecke, Alexander T1 - Integrated Diagnostics of Pharmaceutical Contaminants in Water Supply and Management Systems N2 - The contamination of drinking water with pharmaceuticals represents a severe health risk. In order to monitor the drinking water quality continuously and enable quick countermeasures in case of contamination, novel sensors are required. Here, immunoanalytical methods based on the binding of the analyte to highly selective antibodies can be helpful. In this work, magnetic bead-based immunoassays (MBBAs) have been developed for the detection of two relevant contaminants of drinking water: diclofenac (DCF) and amoxicillin (AMX). In case of the latter, not only the parent drug is of interest in the risk assessment but also its hydrolysis products (HPs). In a comprehensive study, the influence of external factors and intrinsic properties of the water on the rate of hydrolysis was investigated. As the hydrolysis of AMX further impacts the recognition by the antibody, a strategy to analyze samples with unknown hydrolysis degree of AMX was established employing the enzyme β-lactamase in sample preparation. For both analytes, the MBBAs enable the fast quantification with results obtained in less than one hour which represents a major improvement over conventional immunoassays like the enzyme-linked immunosorbent assay (ELISA). Compared to the respective ELISAs with the same antibodies, the MBBAs further exhibit improved analytical parameters such as a broader measurement range and lower limits of detection. Due to the magnetic properties of the beads that serve as a platform for the assays, they are suitable for the mobile and automated detection at the point-of-care. An integrated diagnostic system was designed in which electrochemical detection with chronoamperometry on a microfluidic chip allows for further miniaturization of the system to enable monitoring of the drinking water quality online in water supply pipes at waterworks. N2 - Die Kontamination von Trinkwasser mit Arzneimitteln stellt eine ernste Gesundheitsgefahr dar. Um die Trinkwasserqualität kontinuierlich überwachen und im Falle einer Verunreinigung zeitnah reagieren zu können, sind neuartige Sensoren erforderlich. Hier können immunanalytische Methoden, die auf der Bindung des Analyten an hochselektive Antikörper beruhen, hilfreich sein. In dieser Arbeit wurden magnetpartikelbasierte Immunoassays (MBBAs) für zwei relevante Kontaminanten des Trinkwassers entwickelt: Diclofenac (DCF) und Amoxicillin (AMX). Bei letzterem erwiesen sich neben der Ausgangsverbindung auch dessen Hydrolyseprodukte (HPs) als relevant für die Gefährdungsbeurteilung. In einer umfassenden Studie wurde der Einfluss von externen Faktoren und intrinsischen Eigenschaften des Wassers auf die Hydrolysegeschwindigkeit untersucht. Da die Hydrolyse von AMX auch die Erkennung durch den Antikörper beeinflusst, wurde eine Strategie zur Analyse von Proben mit unbekanntem Hydrolysegrad von AMX unter Verwendung des Enzyms β-Lactamase in der Probenvorbereitung entwickelt. Für beide Analyten ermöglichen die MBBAs eine schnelle Quantifizierung mit Ergebnissen in weniger als einer Stunde, was eine wesentliche Verbesserung gegenüber herkömmlichen Immunoassays wie dem Enzyme-linked Immunosorbent Assay (ELISA) darstellt. Im Vergleich zu den entsprechenden ELISAs mit denselben Antikörpern weisen die MBBAs zudem verbesserte analytische Parameter auf, wie einen breiteren Messbereich und niedrigere Nachweisgrenzen. Aufgrund der magnetischen Eigenschaften der Partikel, die als Plattform für die Assays dienen, eignen sie sich für den mobilen und automatisierten Einsatz vor Ort. Ein integriertes Diagnosesystem, bei dem die elektrochemische Detektion mittels Chronoamperometrie auf einem mikrofluidischen Chip eine weitere Miniaturisierung des Systems ermöglicht, wurde entworfen, um die Überwachung der Trinkwasserqualität online in Wasserwerken zu ermöglichen. KW - Antibiotics KW - Immunoassay KW - Amoxicillin KW - Diclofenac KW - Biosensor KW - Antibodies PY - 2023 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-591901 DO - https://doi.org/10.18452/25853 SP - 1 EP - 129 CY - Berlin AN - OPUS4-59190 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -