@article{Krasenbrink2025,

title = {Sulfoquinovose is exclusively metabolized by the gut microbiota and degraded differently in mice and humans},

author = {Julia Krasenbrink and Buck T. Hanson and Anna S. Weiss and Sabrina Borusak and Tomohisa Sebastian Tanabe and Michaela Lang and Georg Aichinger and Bela Hausmann and David Berry and Andreas Richter and Doris Marko and Marc Mussmann and David Schleheck and Bärbel Stecher and Alexander Loy},

doi = {10.1186/s40168-025-02175-x},

issn = {2049-2618},

year  = {2025},

date = {2025-12-00},

journal = {Microbiome},

volume = {13},

number = {1},

publisher = {Springer Science and Business Media LLC},

abstract = {Abstract

          

            Background

            Sulfoquinovose (SQ) is a green-diet-derived sulfonated glucose and a selective substrate for a limited number of human gut bacteria. Complete anaerobic SQ degradation via interspecies metabolite transfer to sulfonate-respiring bacteria produces hydrogen sulfide, which has dose- and context-dependent health effects. Here, we studied potential SQ degradation by the mammalian host and the impact of SQ supplementation on human and murine gut microbiota diversity and metabolism.

          

          

            Results

            

              13CO2 breath tests with germ-free C57BL/6 mice gavaged with 13C-SQ were negative. Also, SQ was not degraded by human intestinal cells in vitro, indicating that SQ is not directly metabolized by mice and humans. Addition of increasing SQ concentrations to human fecal microcosms revealed dose-dependent responses of the microbiota and corroborated the relevance of Agathobacter rectalis and Bilophila wadsworthia in cooperative degradation of SQ to hydrogen sulfide via interspecies transfer of 2,3-dihydroxy-1-propanesulfonate (DHPS). Similar to the human gut microbiome, the genetic capacity for SQ or DHPS degradation is sparsely distributed among bacterial species in the gut of conventional laboratory mice. Escherichia coli and Enterocloster clostridioformis were identified as primary SQ degraders in the mouse gut. SQ and DHPS supplementation experiments with conventional laboratory mice and their intestinal contents showed that SQ was incompletely catabolized to DHPS. Although some E. clostridioformis genomes encode an extended sulfoglycolytic pathway for both SQ and DHPS fermentation, SQ was only degraded to DHPS by a mouse-derived E. clostridioformis strain.

          

          

            Conclusions

            Our findings suggest that SQ is solely a nutrient for the gut microbiota and not for mice and humans, emphasizing its potential as a prebiotic. SQ degradation by the microbiota of conventional laboratory mice differs from the human gut microbiota by absence of DHPS degradation activity. Hence, the microbiota of conventional laboratory mice does not fully represent the SQ metabolism in humans, indicating the need for alternative model systems to assess the impact of SQ on human health. This study advances our understanding of how individual dietary compounds shape the microbial community structure and metabolism in the gut and thereby potentially influence host health.

          },

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Tomin2025,

title = {Increased antioxidative defense and reduced advanced glycation end-product formation by metabolic adaptation in non-small-cell-lung-cancer patients},

author = {Tamara Tomin and Sophie Elisabeth Honeder and Laura Liesinger and Daniela Gremel and Bernhard Retzl and Joerg Lindenmann and Luka Brcic and Matthias Schittmayer and Ruth Birner-Gruenberger},

doi = {10.1038/s41467-025-60326-y},

issn = {2041-1723},

year  = {2025},

date = {2025-12-00},

journal = {Nat Commun},

volume = {16},

number = {1},

publisher = {Springer Science and Business Media LLC},

abstract = {Abstract

          Reactive oxygen species can oxidatively modify enzymes to reroute metabolism according to tumor needs, rendering identification of oxidized proteins important for understanding neoplastic survival mechanisms. Thiol groups are most susceptible to oxidative modifications but challenging to analyze in clinical settings. We here describe the protein and small-molecular thiol oxidation landscape of 70 human lung tumors (and their paired healthy counter parts) and demonstrate that cancer adapts metabolism to increase glutathione synthesis to counteract oxidative stress. Glyoxalases, the key enzymes in the detoxification of methylglyoxal, a byproduct of glycolysis and precursor of advanced glycation end-products, are compromised by oxidation and downregulation. Despite decreased methylglyoxal detoxification capacity, cancers do not accumulate advanced glycation end-products. Since in vitro downregulation or inhibition of GAPDH upregulates glyoxalases, we propose that tumors reduce methylglyoxal by activating GAPDH.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Weinberger2025b,

title = {Proteomic and metabolomic profiling of extracellular vesicles produced by human gut archaea},

author = {Viktoria Weinberger and Barbara Darnhofer and Himadri B. Thapa and Polona Mertelj and Régis Stentz and Emily Jones and Gerlinde Grabmann and Rokhsareh Mohammadzadeh and Tejus Shinde and Christina Karner and Jennifer Ober and Rokas Juodeikis and Dominique Pernitsch and Kerstin Hingerl and Tamara Zurabishvili and Christina Kumpitsch and Torben Kuehnast and Beate Rinner and Heimo Strohmaier and Dagmar Kolb and Kathryn Gotts and Thomas Weichhart and Thomas Köcher and Harald Köfeler and Simon R. Carding and Stefan Schild and Christine Moissl-Eichinger},

doi = {10.1038/s41467-025-60271-w},

issn = {2041-1723},

year  = {2025},

date = {2025-12-00},

journal = {Nat Commun},

volume = {16},

number = {1},

publisher = {Springer Science and Business Media LLC},

abstract = {Abstract

          Gastrointestinal bacteria interact with the host and each other through various mechanisms, including the production of extracellular vesicles (EVs). However, the composition and potential roles of EVs released by gut archaea are poorly understood. Here, we study EVs produced by four strains of human gut-derived methanogenic archaea: Methanobrevibacter smithii ALI, M. smithii GRAZ-2, M. intestini, and Methanosphaera stadtmanae. The size (~130 nm) and morphology of these EVs are comparable to those of bacterial EVs. Proteomic and metabolomic analyses reveal that the archaeal EVs are enriched in putative adhesins or adhesin-like proteins, free glutamic and aspartic acid, and choline glycerophosphate. The archaeal EVs are taken up by macrophages in vitro and elicit species-specific responses in immune and epithelial cell lines, including production of chemokines such as CXCL9, CXCL11, and CX3CL1. The EVs produced by M. intestini strongly induce pro-inflammatory cytokine IL-8 in epithelial cells. Future work should examine whether archaeal EVs play roles in the interactions of archaea with other gut microbes and with the host.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Ódor2025,

title = {Epidemic-induced local awareness behavior inferred from surveys and genetic sequence data},

author = {Gergely Ódor and Márton Karsai},

doi = {10.1038/s41467-025-59508-5},

issn = {2041-1723},

year  = {2025},

date = {2025-12-00},

journal = {Nat Commun},

volume = {16},

number = {1},

publisher = {Springer Science and Business Media LLC},

abstract = {Abstract

          Behavior-disease models suggest that pandemics can be contained cost-effectively if individuals take preventive actions when disease prevalence rises among their close contacts. However, assessing local awareness behavior in real-world datasets remains a challenge. Through the analysis of mutation patterns in clinical genetic sequence data, we propose an efficient approach to quantify the impact of local awareness by identifying superspreading events and assigning containment scores to them. We validate the proposed containment score as a proxy for local awareness in simulation experiments, and find that it was correlated positively with policy stringency during the COVID-19 pandemic. Finally, we observe a temporary drop in the containment score during the Omicron wave in the United Kingdom, matching a survey experiment we carried out in Hungary during the corresponding period of the pandemic. Our findings bring important insight into the field of awareness modeling through the analysis of large-scale genetic sequence data, one of the most promising data sources in epidemics research.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Mohammadzadeh2025,

title = {Age-related dynamics of predominant methanogenic archaea in the human gut microbiome},

author = {Rokhsareh Mohammadzadeh and Alexander Mahnert and Tejus Shinde and Christina Kumpitsch and Viktoria Weinberger and Helena Schmidt and Christine Moissl-Eichinger},

doi = {10.1186/s12866-025-03921-9},

issn = {1471-2180},

year  = {2025},

date = {2025-12-00},

journal = {BMC Microbiol},

volume = {25},

number = {1},

publisher = {Springer Science and Business Media LLC},

abstract = {Abstract

          

            Background

            The reciprocal relationship between aging and alterations in the gut microbiota is a subject of ongoing research. While the role of bacteria in the gut microbiome is well-documented, specific changes in the composition of methanogens during extreme aging and the impact of high methane production in general on health remain unclear. This study was designed to explore the association of predominant methanogenic archaea within the human gut and aging.

          

          

            Methods

            Shotgun metagenomic data from the stool samples of young adults (n = 127, Age: 19–59 y), older adults (n = 86, Age: 60–99 y), and centenarians (n = 34, age: 100–109 years) were analyzed.

          

          

            Results

            Our findings reveal a compelling link between age and the prevalence of high methanogen phenotype, while overall archaeal diversity diminishes. Surprisingly, the archaeal composition of methanogens in the microbiome of centenarians appears more akin to that of younger adults, showing an increase in Methanobrevibacter smithii, rather than Candidatus Methanobrevibacter intestini. Remarkably, Ca. M. intestini emerged as a central player in the stability of the archaea-bacteria network in adults, paving the way for M. smithii in older adults and centenarians. Notably, centenarians exhibit a highly complex and stable network of these two methanogens with other bacteria. The mutual exclusion between Lachnospiraceae and these methanogens throughout all age groups suggests that these archaeal communities may compensate for the age-related drop in Lachnospiraceae by co-occurring with Oscillospiraceae.

          

          

            Conclusions

            This study underscores the dynamics of archaeal microbiome in human physiology and aging. It highlights age-related shifts in methanogen composition, emphasizing the significance of both M. smithii and Ca. M. intestini and their partnership with butyrate-producing bacteria for potential enhanced health.

          },

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Burger2025,

title = {Discovery of the antifungal compound ilicicolin K through genetic activation of the ilicicolin biosynthetic pathway in Trichoderma reesei},

author = {Isabella Burger and Matthias Schmal and Kathrin Peikert and Lukas Fourtis and Christoph Suster and Christian Stanetty and Dominik Schnalzer and Barbara Hufnagel and Thomas Böttcher and Ruth Birner-Gruenberger and Robert L. Mach and Astrid R. Mach-Aigner and Matthias Schittmayer and Christian Zimmermann},

doi = {10.1186/s13068-025-02628-3},

issn = {2731-3654},

year  = {2025},

date = {2025-12-00},

journal = {Biotechnol. Biofuels Bioprod.},

volume = {18},

number = {1},

publisher = {Springer Science and Business Media LLC},

abstract = {Abstract

          

            Background

            Given the global rise in antimicrobial resistance, the discovery of novel antimicrobial agents and production processes thereof are of utmost importance. To this end we have activated the gene cluster encoding for the biosynthesis of the potent antifungal compound ilicicolin H in the fungus Trichoderma reesei. While the biosynthetic gene cluster (BGC) is silent under standard cultivation conditions, we achieved BGC activation by genetically overexpressing the transcription factor TriliR.

          

          

            Results

            Successful activation was confirmed by RT-qPCR, proteomic and metabolomic analyses. Metabolomic profiling upon BGC expression revealed high-yield production of ilicicolin H. To elucidate the enzymatically highly diverse functionality of this BGC, we employed a combination of overexpression and deletions of individual genes in the BGC. While we hardly observed any of the previously reported side- or shunt products associated with heterologous ilicicolin H expression, we discovered that Trichoderma reesei produces a novel member of the ilicicolin family using a metabolomic molecular networking approach. This new compound, ilicicolin K, is expressed in substantial amounts in the genetically engineered Trichoderma reesei. Ilicicolin K differs from ilicicolin H in its structure by a second hydroxylation of the tyrosine derived phenol and an additional ring formed by an intramolecular ether bridge of the hydroxyl group at the pyridone towards the tyrosine moiety of the molecule. Bioactivity tests of ilicicolin K revealed a strong antifungal activity against Saccharomyces cerevisiae and a moderate activity against the human pathogen Candida auris, an emerging multi-drug resistant fungus.

          

          

            Conclusions

            By activating a silent BGC in T. reesei, we obtained a high-yielding strain for the production of the antifungal compounds ilicicolin H and the novel ilicicolin K. These two compounds share some structural properties and are thus highly likely to act on the fungal cytochrome bc1 complex, a component of the mitochondrial repository chain. However, they possess different bioactive properties, which might suggest that ilicicolin K may overcome certain limitations of ilicicolin H.

          

          

            Graphical Abstract

          },

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Bale2025,

title = {Unusual Plastoquinones in Non‐Phototrophic Nitrifying Bacteria},

author = {Nicole J. Bale and Hayato Fujimura and Petra Pjevac and Michel Koenen and Hikaru Ikeda and Satohiro Itagaki and Yojiro Yamamoto and Johanna Palmetzhofer and Christopher J. Sedlacek and Hayk Palabikyan and Jaap S. Sinninghe Damsté and Michael Wagner and Hiroshi Shiigi and Holger Daims},

doi = {10.1111/1758-2229.70174},

issn = {1758-2229},

year  = {2025},

date = {2025-08-00},

journal = {Environ Microbiol Rep},

volume = {17},

number = {4},

publisher = {Wiley},

abstract = {ABSTRACTIsoprenoid quinones are important compounds in most organisms. They are essential in electron and proton transport in respiratory and photosynthetic electron transport chains, and additional functions include oxidative stress defence. The biologically most relevant quinones are naphthoquinones including menaquinone and benzoquinones including ubiquinone and plastoquinone. They differ in their polar headgroup structures, physicochemical properties, and distribution among organisms. Menaquinone is the most widespread quinone in prokaryotes, ubiquinone occurs only in bacteria of the phylum Pseudomonadota and eukaryotes, and plastoquinone exists in phototrophic Cyanobacteria and plants. We found that chemolithoautotrophic nitrifying bacteria of the genus Nitrospira (phylum Nitrospirota) exclusively possess unusual methyl‐plastoquinones with a standard redox potential below that of canonical plastoquinone and ubiquinone but above menaquinone, suggesting functional roles in reverse electron transport, ammonia oxidation, alternative energy metabolisms, and oxidative stress mitigation. This extends the known diversity of quinones and suggests that plastoquinone derivatives are essential in ecologically important, non‐phototrophic bacteria.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{FMKop2025,

title = {Comparative genome analysis reveals broad phylogenetic and functional diversity within the order \textit{Nitrospirales}},

author = {Linnea F M Kop and Hanna Koch and Daan Speth and Claudia Lüke and Eva Spieck and Mike S M Jetten and Holger Daims and Sebastian Lücker},

doi = {10.1093/ismejo/wraf151},

issn = {1751-7370},

year  = {2025},

date = {2025-07-22},

urldate = {2025-07-22},

journal = {The ISME Journal},

volume = {19},

issue = {1},

pages = {wraf151},

publisher = {Oxford University Press (OUP)},

abstract = {<jats:title>Abstract</jats:title>

               <jats:p>Nitrification, a key process in the nitrogen cycle, involves the oxidation of ammonia to nitrite and nitrate by a diverse group of chemolithoautotrophic microorganisms. The order Nitrospirales (referred to in literature as the genus Nitrospira), which includes both nitrite-oxidizing and complete ammonia-oxidizing bacteria, plays a central role in this process. We sequenced the genomes of nine Nitrospirales members, incorporating genomes from previously unsequenced taxonomic Nitrospirales lineages. A comprehensive genomic analysis of these new Nitrospirales was conducted, which included an examination of their habitat distribution, phylogenetic diversity, and functional capabilities. This was complemented by the construction of and comparison to a database of 446 non-redundant, high-quality Nitrospirales genomes. Our phylogenomic analysis uncovered the presence of additional unclassified lineages and provided a comparison between genome-based and 16S rRNA gene-based taxonomies. Whereas some Nitrospirales lineages seem to exhibit habitat preferences, others are found across a wide variety of ecosystems, suggesting a broad niche spectrum. This capacity to adapt to different environmental conditions is also reflected in the high variability and modularity of the respiratory chain and nitrogen assimilation mechanisms. Additionally, we found evidence of quorum sensing systems in species beyond lineage II, implying a broader ecological role for this communication mechanism within the Nitrospirales. Finally, we identified a set of conserved genes unique to nitrite oxidoreductase-containing Nitrospirales, providing insights into the emergence of this functional group. In conclusion, our study emphasizes the adaptability of the various nitrifying classes of the order Nitrospirales to diverse environments and reveals the presence of new taxonomic lineages.</jats:p>},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Breyer2025,

title = {The contribution of pelagic fungi to ocean biomass},

author = {Eva Breyer and Constanze Stix and Sophie Kilker and Benjamin R.K. Roller and Fragkiski Panagou and Charlotte Doebke and Chie Amano and Daniel E.M. Saavedra and Guillem Coll-García and Barbara Steger-Mähnert and Jordi Dachs and Naiara Berrojalbiz and Maria Vila-Costa and Cristina Sobrino and Antonio Fuentes-Lema and Franz Berthiller and Martin F. Polz and Federico Baltar},

doi = {10.1016/j.cell.2025.05.004},

issn = {0092-8674},

year  = {2025},

date = {2025-07-00},

journal = {Cell},

volume = {188},

number = {15},

pages = {3992--4002.e13},

publisher = {Elsevier BV},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Gruseck2025,

title = {Flavonoid Stability and Biotransformation in Agricultural Soils: Effects of Hydroxylation, Methoxylation, and Glycosylation},

author = {Richard Gruseck and Thilo Hofmann and Michael Zumstein},

doi = {10.1021/acs.jafc.5c02814},

issn = {1520-5118},

year  = {2025},

date = {2025-06-11},

journal = {J. Agric. Food Chem.},

volume = {73},

number = {23},

pages = {14245--14252},

publisher = {American Chemical Society (ACS)},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Quinn-Bohmann2025,

title = {Moving from genome-scale to community-scale metabolic models for the human gut microbiome},

author = {Nick Quinn-Bohmann and Alex V. Carr and Christian Diener and Sean M. Gibbons},

doi = {10.1038/s41564-025-01972-2},

issn = {2058-5276},

year  = {2025},

date = {2025-05-00},

journal = {Nat Microbiol},

volume = {10},

number = {5},

pages = {1055--1066},

publisher = {Springer Science and Business Media LLC},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Becher2025,

title = {A cost-effective vessel-on-a-chip for high shear stress applications in vascular biology},

author = {Clarissa Becher and Martin Frauenlob and Florian Selinger and Peter Ertl and Marie-José Goumans and Gonzalo Sanchez-Duffhues},

doi = {10.1016/j.mvr.2025.104814},

issn = {0026-2862},

year  = {2025},

date = {2025-05-00},

urldate = {2025-05-00},

journal = {Microvascular Research},

volume = {160},

pages = {104814},

publisher = {Elsevier BV},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Sherman2025,

title = {The Invisible Footprint of Climbing Shoes: High Exposure to Rubber Additives in Indoor Facilities},

author = {Anya Sherman and Thibault Masset and Lukas Wimmer and Leah K. Maruschka and Lea Ann Dailey and Thorsten Hüffer and Florian Breider and Thilo Hofmann},

doi = {10.1021/acsestair.5c00017},

issn = {2837-1402},

year  = {2025},

date = {2025-04-24},

journal = {ACS EST Air},

publisher = {American Chemical Society (ACS)},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Weinberger2025,

title = {Expanding the cultivable human archaeome: Methanobrevibacter intestini sp. nov. and strain Methanobrevibacter smithii ‘GRAZ-2’ from human faeces},

author = {Viktoria Weinberger and Rokhsareh Mohammadzadeh and Marcus Blohs and Kerstin Kalt and Alexander Mahnert and Sarah Moser and Marina Cecovini and Polona Mertelj and Tamara Zurabishvili and Bhawna Arora and Jacqueline Wolf and Tejus Shinde and Tobias Madl and Hansjörg Habisch and Dagmar Kolb and Dominique Pernitsch and Kerstin Hingerl and William Metcalf and Christine Moissl-Eichinger},

doi = {10.1099/ijsem.0.006751},

issn = {1466-5034},

year  = {2025},

date = {2025-04-16},

urldate = {2025-04-16},

journal = {International Journal of Systematic and Evolutionary Microbiology},

volume = {75},

number = {4},

publisher = {Microbiology Society},

abstract = {<jats:p>Two mesophilic, hydrogenotrophic methanogens, WWM1085 and <jats:italic>M. smithii</jats:italic> GRAZ-2, were isolated from human faecal samples. WWM1085 was isolated from an individual in the United States and represents a novel species within the genus <jats:italic>Methanobrevibacter. M. smithii</jats:italic> GRAZ-2 (=DSM 116045) was retrieved from a faecal sample of a European, healthy woman and represents a novel strain within this species. Both <jats:italic>Methanobrevibacter</jats:italic> representatives form non-flagellated, short rods with variable morphologies and the capacity to form filaments. Both isolates showed the typical fluorescence of F<jats:sub>420</jats:sub> and methane production. Compared to <jats:italic>M. smithii</jats:italic> GRAZ-2, WWM1085 did not accumulate formate when grown with H<jats:sub>2</jats:sub> and CO<jats:sub>2</jats:sub>. The optimal growth conditions were at 35–39 °C and pH 6.5–7.5. Full genome sequencing revealed a genomic difference of WWM1085 to the type strain of <jats:italic>M. smithii</jats:italic> DSM 861 (=PS<jats:sup>T</jats:sup>), with 93.55% average nucleotide identity (ANI) and major differences in the sequence of its <jats:italic>mcrA</jats:italic> gene (3.3% difference in nucleotide sequence). Differences in the 16S rRNA gene sequence were very minor, and thus distinction based on this gene marker might not be possible. <jats:italic>M. smithii</jats:italic> GRAZ-2 was identified as a novel strain within the species <jats:italic>Methanobrevibacter smithii</jats:italic> (ANI 99.04% to <jats:italic>M. smithii</jats:italic> DSM 861 [=PS<jats:sup>T</jats:sup>]). Due to the major differences between WWM1085 and <jats:italic>M. smithii</jats:italic> type strain <jats:italic>M. smithii</jats:italic> DSM 861 (=PS<jats:sup>T</jats:sup>) in phenotypic, genomic and metabolic features, we propose <jats:italic>Methanobrevibacter intestini</jats:italic> sp. nov. as a novel species with WWM1085 as the type strain (DSM 116060<jats:sup>T</jats:sup> = CECT 30992<jats:sup>T</jats:sup>).</jats:p>},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Wichmann2025,

title = {Conserved specificity of extracellular wastewater peptidases revealed by multiplex substrate profiling by mass spectrometry},

author = {Natalie Wichmann and Josephine Meibom and Tamar Kohn and Michael Zumstein},

doi = {10.1007/s10311-025-01834-7},

issn = {1610-3661},

year  = {2025},

date = {2025-04-12},

journal = {Environ Chem Lett},

publisher = {Springer Science and Business Media LLC},

abstract = {Abstract

           Peptide-based chemicals are promising for numerous applications including home and personal care and medical treatments. To better understand and control the environmental fate of peptide-based chemicals, in-depth knowledge on the specificity of wastewater peptidases is needed. Here, we employed multiplex substrate profiling by mass spectrometry to obtain specificity profiles of extracellular peptidases derived from influent and aeration tanks of three full-scale wastewater treatment plants. Specificities were confirmed by fluorogenic peptidase substrates. Our results revealed highly similar specificity profiles across wastewater treatment plants. We found that hydrolysis by extracellular wastewater peptidases is favored when positively charged amino acid residues surround the cleavage site and disfavored when negatively charged amino acid residues surround the cleavage site.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Kwon2025,

title = {Vertical DNA Nanostructure Arrays: Facilitating Functionalization on Macro-Scale Surfaces},

author = {Hyeonjun Kwon and Jihoon Shin and Siqi Sun and Rong Zhu and Sarah Stainer and Peter Hinterdorfer and Sang-Joon Cho and Dong-Hwan Kim and Yoo Jin Oh},

doi = {10.1021/acsnano.5c03100},

issn = {1936-086X},

year  = {2025},

date = {2025-04-09},

journal = {ACS Nano},

publisher = {American Chemical Society (ACS)},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Krammer2025,

title = {A general approach for activity-based protein profiling of oxidoreductases with redox-differentiated diarylhalonium warheads},

author = {Leo Krammer and Barbara Darnhofer and Marko Kljajic and Laura Liesinger and Matthias Schittmayer and Dmytro Neshchadin and Georg Gescheidt and Alexander Kollau and Bernd Mayer and Roland C. Fischer and Silvia Wallner and Peter Macheroux and Ruth Birner-Gruenberger and Rolf Breinbauer},

doi = {10.1039/d4sc08454c},

issn = {2041-6539},

year  = {2025},

date = {2025-04-09},

journal = {Chem. Sci.},

volume = {16},

number = {15},

pages = {6240--6256},

publisher = {Royal Society of Chemistry (RSC)},

abstract = {A general chemoproteomic profiling approach for oxidoreductases with conceptually novel probes based on diarylhalonium salts is reported.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Saeidi2025,

title = {Towards a better understanding of sorption of persistent and mobile contaminants to activated carbon: Applying data analysis techniques with experimental datasets of limited size},

author = {Navid Saeidi and Laura Lotteraner and Gabriel Sigmund and Thilo Hofmann and Martin Krauss and Katrin Mackenzie and Anett Georgi},

url = {https://doi.org/10.1016/j.watres.2024.123032},

doi = {10.1016/j.watres.2024.123032},

issn = {0043-1354},

year  = {2025},

date = {2025-04-00},

urldate = {2025-04-00},

journal = {Water Research},

volume = {274},

publisher = {Elsevier BV},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Savchenko2025,

title = {Chitinivorax: The New Kid on the Block of Bacterial 2-Alkyl-4(1\textit{H})-quinolone Producers},

author = {Viktoriia Savchenko and Xiaoqian Annie Yu and Martin F. Polz and Thomas Böttcher},

doi = {10.1021/acschembio.5c00046},

issn = {1554-8937},

year  = {2025},

date = {2025-03-27},

journal = {ACS Chem. Biol.},

publisher = {American Chemical Society (ACS)},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Lintner2025,

title = {Tire-derived compounds, phthalates, and trace metals in the Kiel Fjord (Germany)},

author = {Michael Lintner and Charlotte Henkel and Ruoting Peng and Petra Heinz and Martin Stockhausen and Thilo Hofmann and Thorsten Hüffer and Nina Keul},

url = {https://www.sciencedirect.com/science/article/pii/S0025326X25000566#ab0015},

doi = {10.1016/j.marpolbul.2025.117581},

issn = {0025-326X},

year  = {2025},

date = {2025-03-00},

urldate = {2025-03-00},

journal = {Marine Pollution Bulletin},

volume = {212},

publisher = {Elsevier BV},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Woh2025,

title = {Reevaluation of the gastrointestinal methanogenic archaeome in multiple sclerosis and its association with treatment},

author = {Pei Yee Woh and Yehao Chen and Christina Kumpitsch and Rokhsareh Mohammadzadeh and Laura Schmidt and Christine Moissl-Eichinger},

editor = {Henning Seedorf},

doi = {10.1128/spectrum.02183-24},

issn = {2165-0497},

year  = {2025},

date = {2025-02-25},

journal = {Microbiol Spectr},

publisher = {American Society for Microbiology},

abstract = {ABSTRACT

          

            

            

              The role of the gut archaeal microbiome (archaeome) in health and disease remains poorly understood. Methanogenic archaea have been linked to multiple sclerosis (MS), but prior studies were limited by small cohorts and inconsistent methodologies. To address this, we re-evaluated the association between methanogenic archaea and MS using metagenomic data from the International Multiple Sclerosis Microbiome Study. We analyzed gut microbiome profiles from 115 MS patients and 115 healthy household controls across Buenos Aires (27.8%), Edinburgh (33.9%), New York (10.4%), and San Francisco (27.8%). Metagenomic sequences were taxonomically classified using kraken2/bracken and a curated profiling database to detect archaea, specifically

              Methanobrevibacter

              species. Most MS patients were female (80/115), aged 25–72 years (median: 44.5), and 70% were undergoing treatment, including dimethyl fumarate (

              n

              = 21), fingolimod (

              n

              = 20), glatiramer acetate (

              n

              = 14), interferon (

              n

              = 18), natalizumab (

              n

              = 6), or ocrelizumab/rituximab (

              n

              = 1). We found no significant differences in overall archaeome profiles between MS patients and controls. However, treated MS patients exhibited higher abundances of

              Methanobrevibacter smithii

              and

              M.

              sp900766745 compared to untreated patients. Notably,

              M.

              sp900766745 abundance correlated with lower disease severity scores in treated patients. Our results suggest that gut methanogens are not directly associated with MS onset or progression but may reflect microbiome health during treatment. These findings highlight potential roles for

              M. smithii

              and

              M.

              sp900766745 in modulating treatment outcomes, warranting further investigation into their relevance to gut microbiome function and MS management.

            

            

              IMPORTANCE

              Multiple sclerosis (MS) is a chronic neuroinflammatory disease affecting the central nervous system, with approximately 2.8 million people diagnosed worldwide, mainly young adults aged 20–30 years. While recent studies have focused on bacterial changes in the MS microbiome, the role of gut archaea has been less explored. Previous research suggested a potential link between methanogenic archaea and MS disease status, but these findings remained inconclusive. Our study addresses this gap by investigating the gut archaeal composition in MS patients and examining how it changes in response to treatment. By focusing on methanogens, we aim to uncover novel insights into their role in MS, potentially revealing new biomarkers or therapeutic targets. This research is crucial for enhancing our understanding of the gut microbiome’s impact on MS and improving patient management.

            

          },

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{pmid39966520,

title = {Metagenomic estimation of dietary intake from human stool},

author = {Christian Diener and Hannah D Holscher and Klara Filek and Karen D Corbin and Christine Moissl-Eichinger and Sean M Gibbons},

doi = {10.1038/s42255-025-01220-1},

issn = {2522-5812},

year  = {2025},

date = {2025-02-01},

journal = {Nat Metab},

abstract = {Dietary intake is tightly coupled to gut microbiota composition, human metabolism and the incidence of virtually all major chronic diseases. Dietary and nutrient intake are usually assessed using self-reporting methods, including dietary questionnaires and food records, which suffer from reporting biases and require strong compliance from study participants. Here, we present Metagenomic Estimation of Dietary Intake (MEDI): a method for quantifying food-derived DNA in human faecal metagenomes. We show that DNA-containing food components can be reliably detected in stool-derived metagenomic data, even when present at low abundances (more than ten reads). We show how MEDI dietary intake profiles can be converted into detailed metabolic representations of nutrient intake. MEDI identifies the onset of solid food consumption in infants, shows significant agreement with food frequency questionnaire responses in an adult population and shows agreement with food and nutrient intake in two controlled-feeding studies. Finally, we identify specific dietary features associated with metabolic syndrome in a large clinical cohort without dietary records, providing a proof-of-concept for detailed tracking of individual-specific, health-relevant dietary patterns without the need for questionnaires.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{pmid39707459,

title = {pH-FISH: coupled microscale analysis of microbial identity and acid-base metabolism in complex biofilm samples},

author = {Yumi Chokyu Del Rey and Katharina Kitzinger and Marie Braad Lund and Andreas Schramm and Rikke Louise Meyer and Michael Wagner and Sebastian Schlafer},

doi = {10.1186/s40168-024-01977-9},

issn = {2049-2618},

year  = {2024},

date = {2024-12-01},

journal = {Microbiome},

volume = {12},

number = {1},

pages = {266},

abstract = {BACKGROUND: Correlative structural and chemical imaging of biofilms allows for the combined analysis of microbial identity and metabolism at the microscale. Here, we developed pH-FISH, a method that combines pH ratiometry with fluorescence in situ hybridization (FISH) in structurally intact biofilms for the coupled investigation of microbial acid metabolism and biofilm composition. Careful biofilm handling and modified sample preparation procedures for FISH allowed preservation of the three-dimensional biofilm structure throughout all processing and imaging steps. We then employed pH-FISH to investigate the relationship between local biofilm pH and the distribution of acid-producing (streptococci) and acid-consuming (Veillonella spp.) bacteria in dental biofilms from healthy subjects and caries-active patients.nnRESULTS: The relative abundance of streptococci correlated with low biofilm pH at the field-of-view level, while the opposite trend was observed for Veillonella spp. These results suggest that clusters of streptococci contribute to the formation of acidic pockets inside dental biofilms, whereas Veillonella spp. may have a protective role against biofilm acidification.nnCONCLUSIONS: pH-FISH combines microscale mapping of biofilm pH in real time with structural imaging of the local microbial architecture, and is a powerful method to explore the interplay between biofilm composition and metabolism in complex biological systems. Video Abstract.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{pmid39435044,

title = {Quantification of guanidine in environmental samples using benzoin derivatization and LC-MS analysis},

author = {Richard Gruseck and Marton Palatinszky and Michael Wagner and Thilo Hofmann and Michael Zumstein},

doi = {10.1016/j.mex.2024.102972},

issn = {2215-0161},

year  = {2024},

date = {2024-12-01},

journal = {MethodsX},

volume = {13},

pages = {102972},

abstract = {The recent discovery of guanidine-dependent riboswitches in many microbes raised interest in the biological function and metabolism of this nitrogen-rich compound. However, very little is known about the concentrations of guanidine in the environment. Several methods have been published for quantifying guanidine and guanidino compounds in human urine and blood, often relying on derivatization followed by fluorescence detection. We adapted this analytical approach using benzoin as the derivatization agent to sensitively and selectively quantify guanidine in environmental samples, thereby facilitating future research on the biological and environmental roles of guanidine. This adapted method was applied to human urine, raw wastewater, and biological growth media as relevant matrices. Our liquid chromatography-tandem mass spectrometry analyses of the derivatized solutions identified a different major derivatization product than previously reported. This product was consistently observed across various substrates (guanidine, methylguanidine, and arginine) and derivatization agents (benzoin and anisoin). We observed a constant background signal, restricting our analyses to a lower limit of quantification of 50 nM. Despite this limitation, our method allowed for the quantification of guanidine concentrations significantly lower than those reported in previous derivatization-based studies.•Selective and sensitive detection of guanidine by LC-MS.•Method development and validation for robust detection of guanidine in environmental samples.•Reduction of sample preparation steps and reduced usage of toxic chemicals compared to previous methods.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Canarini2024,

title = {Soil fungi remain active and invest in storage compounds during drought independent of future climate conditions},

author = {Alberto Canarini and Lucia Fuchslueger and Jörg Schnecker and Dennis Metze and Daniel B. Nelson and Ansgar Kahmen and Margarete Watzka and Erich M. Pötsch and Andreas Schaumberger and Michael Bahn and Andreas Richter},

url = {https://pubmed.ncbi.nlm.nih.gov/39613745/},

doi = {10.1038/s41467-024-54537-y},

issn = {2041-1723},

year  = {2024},

date = {2024-12-00},

urldate = {2024-12-00},

journal = {Nat Commun},

volume = {15},

number = {1},

publisher = {Springer Science and Business Media LLC},

abstract = {<jats:title>Abstract</jats:title><jats:p>Microbial growth is central to soil carbon cycling. However, how microbial communities grow under climate change is still largely unexplored. Here we use a unique field experiment simulating future climate conditions (increased atmospheric CO<jats:sub>2</jats:sub> and temperature) and drought concomitantly and investigate impacts on soil microbial activity. We trace <jats:sup>2</jats:sup>H or <jats:sup>18</jats:sup>O applied via water-vapor exchange into membrane (and storage) fatty acids or DNA, respectively, to assess community- and group-level adjustments in soil microbial physiology (replication, storage product synthesis, and carbon use efficiency). We show that, while bacterial growth decreases by half during drought, fungal growth remains stable, demonstrating a remarkable resistance against soil moisture changes. In addition, fungal investment into storage triglycerides increases more than five-fold under drought. Community-level carbon use efficiency (the balance between anabolism and catabolism) is unaffected by drought but decreases in future climate conditions, favoring catabolism. Our results highlight that accounting for different microbial growth strategies can foster our understanding of soil microbial contributions to carbon cycling and feedback on the climate system.</jats:p>},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Fian2024,

title = {Microplastics in food and drink: perceptions of the risks, challenges, and solutions among individuals in the ‘farm-to-fork’ food chain},

author = {Leonie Fian and Lena M. Schmidlechner and Ulrike Felt and Thilo Hofmann and Mathew P. White and Sabine Pahl},

url = {https://www.tandfonline.com/doi/full/10.1080/13669877.2024.2431900},

doi = {10.1080/13669877.2024.2431900},

issn = {1466-4461},

year  = {2024},

date = {2024-11-26},

urldate = {2024-11-26},

journal = {Journal of Risk Research},

pages = {1--24},

publisher = {Informa UK Limited},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Bauchinger2024,

title = {Characteristics of putative keystones in the healthy adult human gut microbiota as determined by correlation network analysis},

author = {Franziska Bauchinger and David Seki and David Berry},

url = {https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2024.1454634/full},

doi = {10.3389/fmicb.2024.1454634},

issn = {1664-302X},

year  = {2024},

date = {2024-11-20},

urldate = {2024-11-20},

journal = {Front. Microbiol.},

volume = {15},

publisher = {Frontiers Media SA},

abstract = {<jats:p>Keystone species are thought to play a critical role in determining the structure and function of microbial communities. As they are important candidates for microbiome-targeted interventions, the identification and characterization of keystones is a pressing research goal. Both empirical as well as computational approaches to identify keystones have been proposed, and in particular correlation network analysis is frequently utilized to interrogate sequencing-based microbiome data. Here, we apply an established method for identifying putative keystone taxa in correlation networks. We develop a robust workflow for network construction and systematically evaluate the effects of taxonomic resolution on network properties and the identification of keystone taxa. We are able to identify correlation network keystone species and genera, but could not detect taxa with high keystone potential at lower taxonomic resolution. Based on the correlation patterns observed, we hypothesize that the identified putative keystone taxa have a stabilizing effect that is exerted on correlated taxa. Correlation network analysis further revealed subcommunities present in the dataset that are remarkably similar to previously described patterns. The interrogation of available metatranscriptomes also revealed distinct transcriptional states present in all putative keystone taxa. These results suggest that keystone taxa may have stabilizing properties in a subset of community members rather than global effects. The work presented here contributes to the understanding of correlation network keystone taxa and sheds light on their potential ecological significance.</jats:p>},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{pmid39352455,

title = {What determines transfer of carbon from plants to mycorrhizal fungi?},

author = {Rebecca A Bunn and Ana Corrêa and Jaya Joshi and Christina Kaiser and Ylva Lekberg and Cindy E Prescott and Anna Sala and Justine Karst},

doi = {10.1111/nph.20145},

issn = {1469-8137},

year  = {2024},

date = {2024-11-01},

journal = {New Phytol},

volume = {244},

number = {4},

pages = {1199--1215},

abstract = {Biological Market Models are common evolutionary frameworks to understand the maintenance of mutualism in mycorrhizas. 'Surplus C' hypotheses provide an alternative framework where stoichiometry and source-sink dynamics govern mycorrhizal function. A critical difference between these frameworks is whether carbon transfer from plants is regulated by nutrient transfer from fungi or through source-sink dynamics. In this review, we: provide a historical perspective; summarize studies that asked whether plants transfer more carbon to fungi that transfer more nutrients; conduct a meta-analysis to assess whether mycorrhizal plant growth suppressions are related to carbon transfer; and review literature on cellular mechanisms for carbon transfer. In sum, current knowledge does not indicate that carbon transfer from plants is directly regulated by nutrient delivery from fungi. Further, mycorrhizal plant growth responses were linked to nutrient uptake rather than carbon transfer. These findings are more consistent with 'Surplus C' hypotheses than Biological Market Models. However, we also identify research gaps, and future research may uncover a mechanism directly linking carbon and nutrient transfer. Until then, we urge caution when applying economic terminology to describe mycorrhizas. We present a synthesis of ideas, consider knowledge gaps, and suggest experiments to advance the field.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{pmid39572788,

title = {The Parkinson's disease drug entacapone disrupts gut microbiome homoeostasis via iron sequestration},

author = {Fátima C Pereira and Xiaowei Ge and Jannie M Kristensen and Rasmus H Kirkegaard and Klara Maritsch and Dávid Szamosvári and Stefanie Imminger and David Seki and Juwairiyah B Shazzad and Yifan Zhu and Marie Decorte and Bela Hausmann and David Berry and Kenneth Wasmund and Arno Schintlmeister and Thomas Böttcher and Ji-Xin Cheng and Michael Wagner},

doi = {10.1038/s41564-024-01853-0},

issn = {2058-5276},

year  = {2024},

date = {2024-11-01},

journal = {Nat Microbiol},

abstract = {Many human-targeted drugs alter the gut microbiome, leading to implications for host health. However, the mechanisms underlying these effects are not well known. Here we combined quantitative microbiome profiling, long-read metagenomics, stable isotope probing and single-cell chemical imaging to investigate the impact of two widely prescribed drugs on the gut microbiome. Physiologically relevant concentrations of entacapone, a treatment for Parkinson's disease, or loxapine succinate, used to treat schizophrenia, were incubated ex vivo with human faecal samples. Both drugs significantly impact microbial activity, more so than microbial abundance. Mechanistically, entacapone can complex and deplete available iron resulting in gut microbiome composition and function changes. Microbial growth can be rescued by replenishing levels of microbiota-accessible iron. Further, entacapone-induced iron starvation selected for iron-scavenging gut microbiome members encoding antimicrobial resistance and virulence genes. These findings reveal the impact of two under-investigated drugs on whole microbiomes and identify metal sequestration as a mechanism of drug-induced microbiome disturbance.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{pmid39423289,

title = {Tailless and filamentous prophages are predominant in marine Vibrio},

author = {Kerrin Steensen and Joana Séneca and Nina Bartlau and Xiaoqian A Yu and Fatima A Hussain and Martin F Polz},

doi = {10.1093/ismejo/wrae202},

issn = {1751-7370},

year  = {2024},

date = {2024-10-01},

urldate = {2024-10-01},

journal = {ISME J},

abstract = {Although tailed bacteriophages (phages) of the class Caudoviricetes are thought to constitute the most abundant and ecologically relevant group of phages that can integrate their genome into the host chromosome, it is becoming increasingly clear that other prophages are widespread. Here, we show that prophages derived from filamentous and tailless phages with genome sizes below 16 kb make up the majority of prophages in marine bacteria of the genus Vibrio. To estimate prophage prevalence unaffected by database biases, we combined comparative genomics and chemical induction of 58 diverse Vibrio cyclitrophicus isolates, resulting in 107 well-curated prophages. Complemented with computationally predicted prophages, we obtained 1,158 prophages from 931 naturally co-existing strains of the family Vibrionaceae. Prophages resembling tailless and filamentous phages predominated, accounting for 80% of all prophages in V. cyclitrophicus and 60% across the Vibrionaceae. In our experimental model, prophages of all three viral realms actively replicated upon induction indicating their ability to transfer to new hosts. Indeed, prophages were rapidly gained and lost, as suggested by variable prophage content between closely related V. cyclitrophicus. Prophages related to filamentous and tailless phages were integrated into only three genomic locations and restored the function of their integration site. Despite their small size, they contained highly diverse accessory genes that may contribute to host fitness, such as phage defense systems. We propose that, like their well-studied tailed equivalent, tailless and filamentous temperate phages are active and highly abundant drivers of host ecology and evolution in marine Vibrio, which have been largely overlooked.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Protsak2024b,

title = {Enhanced selective extraction of indium and gallium using mesoporous sorbents},

author = {Iryna Protsak and Martin Stockhausen and Aaron Brewer and Martin Owton and Thilo Hofmann and Freddy Kleitz},

url = {https://www.sciencedirect.com/science/article/pii/S138589472405959X?via%3Dihub},

doi = {10.1016/j.cej.2024.154468},

issn = {1385-8947},

year  = {2024},

date = {2024-10-00},

urldate = {2024-10-00},

journal = {Chemical Engineering Journal},

volume = {498},

publisher = {Elsevier BV},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{pmid39333700,

title = {Photoaging enhances the leaching of di(2-ethylhexyl) phthalate and transformation products from polyvinyl chloride microplastics into aquatic environments},

author = {Charlotte Henkel and Thorsten Hüffer and Ruoting Peng and Xiaoyu Gao and Subhasis Ghoshal and Thilo Hofmann},

doi = {10.1038/s42004-024-01310-3},

issn = {2399-3669},

year  = {2024},

date = {2024-09-01},

journal = {Commun Chem},

volume = {7},

number = {1},

pages = {218},

abstract = {Increasing chemical pollution is a threat to sustainable water resources worldwide. Plastics and harmful additives released from plastics add to this burden and might pose a risk to aquatic organisms, and human health. Phthalates, which are common plasticizers and endocrine-disrupting chemicals, are released from polyvinyl chloride (PVC) microplastics and are a cause of concern. Therefore, the leaching kinetics of additives, including the influence of environmental weathering, are key to assessing exposure concentrations but remain largely unknown. We show that photoaging strongly enhances the leaching rates of di(2-ethylhexyl) phthalate (DEHP) by a factor of 1.5, and newly-formed harmful transformation products, such as mono(2-ethylhexyl) phthalate (MEHP), phthalic acid, and phthalic anhydride from PVC microplastics into the aquatic environment. Leaching half-lives of DEHP reduced from 449 years for pristine PVC to 121 years for photoaged PVC. Aqueous boundary layer diffusion (ABLD) is the limiting mass transfer process for the release of DEHP from pristine and photoaged PVC microplastics. The leaching of transformation products is limited by intraparticle diffusion (IPD). The calculated mass transfer rates can be used to predict exposure concentrations of harmful additives in the aquatic environment.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Protsak2024,

title = {Advancing Selective Extraction: A Novel Approach for Scandium, Thorium, and Uranium Ion Capture},

author = {Iryna Protsak and Martin Stockhausen and Aaron Brewer and Martin Owton and Thilo Hofmann and Freddy Kleitz},

url = {https://onlinelibrary.wiley.com/doi/10.1002/smsc.202400171},

doi = {10.1002/smsc.202400171},

issn = {2688-4046},

year  = {2024},

date = {2024-08-28},

urldate = {2024-08-28},

journal = {Small Science},

publisher = {Wiley},

abstract = {<jats:p>The potential use of thorium (Th) and uranium (U) as nuclear fuels underscores the importance of developing materials for their sustainable recovery. The production of Th and U requires the separation of these elements from rare‐earth elements (REEs) as they often coexist in various feedstocks. Equally crucial is efficiently isolating scandium (Sc) from REEs, considering its high‐value status and pivotal role in advanced alloy technologies. This study introduces a new selective ligand‐functionalized silica sorbent for extracting Sc, other REEs, Th, and U from solutions with varying pH and elemental compositions. The functionalized sorbent exhibits exceptional selectivity for Sc ions at pH 4 across solutions containing 3–20 elements. It also shows excellent selectivity for Th at pH 2 in 18‐ and 20‐element solutions and substantial selectivity for U in 18‐ and 20‐element solutions at pH 4. Additionally, it efficiently adsorbs neodymium (Nd), dysprosium (Dy), and lanthanum (La) in Sc‐free solutions with a given preference for Nd. The ligand‐functionalized sorbent successfully undergoes ten cycles of reuse which along with its enhanced recovery performance toward targeted elements highlights its industrial application potential.</jats:p>},

keywords = {},

pubstate = {published},

tppubtype = {article}

}