TY - CONF A1 - Gorbushina, Anna T1 - A genetic toolbox for exploring the life style of the rock-inhabiting black fungus Knufia petricola N2 - After their discovery on rock surfaces in cold and hot deserts, a polyphyletic group of ascomycetous black fungi was found to dominate a range of hostile environments – natural and man-made, from salterns to dishwashers, roofs and solar panels. Together with bacteria and algae they may establish subaerial biofilms and cause weathering of the surfaces they grow on. Their impressive survival abilities as well as their constitutive protective pigmentation and cluster-like microcolony organisation are similar in environmental isolates as well as in heat-tolerant opportunistic pathogens of animals and humans. The exact genetic properties that ensure their survival in extreme environments can be studied if some black fungi were amenable to genetic manipulations. We selected the rock-inhabiting fungus Knufia petricola (class Eurotiomycetes, order Chaetothyriales) that grows moderately in axenic culture and exhibits all the characteristics of microcolonial black fungi such as yeast-like cell growth, absence of reproductive structures and constitutive dihydroxynaphthalene (DHN) melanogenesis (Nai et al. 2013, Fungal Genet Biol). We developed protocols to efficiently generate and transform protoplasts resulting in stable homokaryotic transformants by targeting genes involved in pigment synthesis and expressing fluorescent reporter genes. Hence, endogenous and foreign genes can be expressed from episomal AMA1-containing plasmids and genome-integrated DNA constructs. Moderate rates of homologous recombination allow for both ectopic and targeted integrations. CRISPR-Cas9 was further validated as a strategy for obtaining selection marker-free mutants and silencing via RNA interference as an approach to study essential genes. Availability of this genetic toolbox and an annotated genome sequence of the strain A95 is paving the way for studying interactions of K. petricola with environmental stressors, material surfaces, soil matrices and phototrophic symbionts. T2 - European Conference on Fungal Genetics (ECFG15) CY - Rome, Italy DA - 17.02.2020 KW - black fungi KW - genomics KW - genetics PY - 2020 AN - OPUS4-50593 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Wen, Keqing A1 - Gorbushina, Anna A1 - Schwibbert, Karin A1 - Bell, Jérémy T1 - A microfluidic platform for monitoring biofilm formation in flow under defined hydrodynamic conditions N2 - Bacterial adhesion on surfaces of medical, water and food applications may lead to infections, water or food spoilage and human illness. In comparison to traditional static and macro flow chamber assays for biofilm formation studies, microfluidic chips allow in situ monitoring of biofilm formation under various flow regimes, have better environment control and smaller sample requirements. In this work, a novel microfluidic platform is developed to investigate biofilm adhesion under precisely controlled bacteria concentration, temperature, and flow conditions. This platform central unit is a single-inlet microfluidic flow cell with a 5 mm wide chamber designed and tested to achieve ultra-homogenous flow in the central area of chamber. Within this area, defined microstructures are integrated that will disturb the homogeneity of the flow, thus changing bacterial adhesion pattern. Here we present the monitoring of bacterial biofilm formation in a microfluidic chip equipped with a microstructure known as micro-trap. This feature is based on a 3D bacteria trap designed by Di Giacomo et al. and successfully used to sequester motile bacteria. At first, fluorescent particles similar in size to Escherichia coli (E. coli) are used to simulate bacteria flow inside the flow cell and at the micro-trap. The turbulences induced by the trap are analyzed by imaging and particle tracking velocimetry (PTV). Secondly, the model strain E. coli TG1, ideal and well described for biofilm studies, is used to analyze biofilm formation in the micro-trap. Therefore, a stable fluorescent strain E. coli TG1-MRE-Tn7-141 is constructed by using Tn7 transposon mutagenesis according to the method described by Schlechter et al. Sequestering of E. coli cells within the micro-trap was followed using epifluorescence microscopy. The novel microfluidic platform shows great potential for assessment of bacterial adhesion under various flow regimes. The performance of structural feature with respect to the generation of turbulences that promote or reduce bacterial adhesion can be systematically examined. The combination of flow analysis and fluorescent strain injection into the microfluidic chip shows that the micro-trap is useful for capturing bacteria at defined positions and to study how flow conditions, especially micro-turbulences, can affect biofilm formation. It represents a powerful and versatile tool for studying the relation between topography and bacteria adhesion. T2 - International Conference on Miniaturized Systems for Chemistry and Life Sciences CY - Katowice, Poland DA - 15.10.2023 KW - Biofilm KW - E. coli KW - Microfluidics KW - Velocimetry KW - Fluorescence PY - 2023 AN - OPUS4-59593 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Erdmann, Eileen T1 - A random mutagenesis approach to elucidate the biology of extremotolerant black fungi N2 - Microcolonial black fungi ubiquitously inhabit sun-exposed natural and man-made surfaces of our planet. To promote genetic studies, which are hindered by slow growth, lack of sexual cycles and transformation difficulties, CRISPR/Cas9-based genetic tools were implemented (Erdmann et al. 2022, Front Fungal Biol). Now efficient targeted mutagenesis of the rock inhabitant Knufia petricola (Eurotiomycetes/Chaetothyriales) - as a representative of the polyphyletic group of black fungi - enables the elucidation of extremotolerance, oligotrophism, unusual types of cell division, mineral weathering and symbiotic interactions. Still more progress on assigning functions to yet unknown genes can be expected if a forward genetics approach is available. We chose the two-component Activator/ Dissociation (Ac/Ds) transposon system from maize for generating a collection of insertional mutants by in-vivo mutagenesis of K. petricola. For the optimal use of this genetic tool, an inducible promoter for the expression of the Ac transposase (AcTPase) and by this the regulatable transposition of the resistance cassette-containing Ds transposon is desired. However, endogenous promoters for nitrate assimilation and galactose catabolism - often used in fungi for regulatable gene expression - are not inducible by their substrates in K. petricola suggesting that the regulatory networks for nutrient acquisition differ significantly in oligotrophic fungi. Therefore, the metabolism-independent Tet-on system was combined with the AcTPase coding sequence and subsequently transformed into Ds-carrying K. petricola strains. In total, four auxotrophic Ac|Ds starter strains containing the Ds transposon at different position of ade2 or ura3 were generated. The cultivation of these strains with doxycycline for induction of TET::Ac and subsequent selection of cells on ADE/URA-lacking media resulted in prototrophic colonies (revertants) for some but not all Ac|Ds strains. Currently, the transposition events in the obtained revertants are studied to validate the procedure. First amplicon sequencing of excision sites revealed footprint patterns, proving the transposon jumped. T2 - 16th European Conference on Fungal Genetics CY - Innsbruck, Austria DA - 05.03.2023 KW - Rock-inhabiting fungi KW - Foward genetics KW - In-vivo mutagenesis PY - 2023 AN - OPUS4-57144 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Cook, Jake Thomas T1 - Assessment of concrete bioreceptivity in algal biofilm green façade systems N2 - Algal biofilm façades are an alternative to traditional green façades which can help to improve biodiversity and air quality within cities. They present a low maintenance approach in which subaerial algae are grown directly on concrete substrates. The intrinsic bioreceptivity of the substrate is a critical factor in successful facade colonisation. Existing research has identified several environmental and material properties which influence concrete bioreceptivity, however a consensus has yet to be made on which properties are most influential and how the interaction between properties may promote algal biofilm growth under specific conditions. T2 - International Conference on Bio-Based Building Materials CY - Vienna, Austria DA - 21.06.2023 KW - Concrete KW - Façade KW - Bio-receptive KW - Extracellular polymeric substances KW - Fractional factorial PY - 2023 UR - https://www.rilem.net/agenda/5th-international-conference-on-bio-based-building-materials-1501 AN - OPUS4-58976 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Strzelczyk, Rebecca T1 - Constant emitting reference material for emissions test procedures N2 - Since nowadays people spend most of their time indoors, a healthy environment is essential. Volatile organic compounds (VOCs) emitted from furniture and building materials are reported to cause health complaints. Therefore, the usage of low emitting materials will improve the indoor air quality. Quantitative VOC emission testing is usually conducted in emission test chambers under specified controlled conditions as described in DIN 16000-9 and DIN EN 16516. For reasons of quality control/quality assurance (QC/QA) and for a better comparability of test results from different laboratories, suitable emission reference materials (ERM) are needed. Here, it is important to have a homogenous material with known emission rates over a specific time. Different approaches can be found in literature, inter alia polymer films loaded with the target compound to be released again, or a lacquer material to which a VOC mixture is added. After curing of the lacquer, the material can be loaded into a test chamber. Drawback of those approaches are their relatively fast decreasing emission profiles. For QC/QA purposes according to the test standards, VOC sources with constant emission profiles are desirable. The EU-funded research project MetrIAQ “Metrology for the determination of emissions of dangerous substances from building materials into indoor air” is working on a multi-component ERM with an envisaged instability of ≤ 10 % in the emission rate over at least 14 days. Within a doctoral thesis porous materials are impregnated with VOCs. Supercritical CO2 is used as solvent. Thus, the impregnated material does not contain any solvent that may show a measurable amount of emission in the emission test chamber. Furthermore, CO2 has the benefits to have a good availability and low costs. For the selection of porous materials several properties like the pore size, the surface, and the interaction with the components in the atmosphere need to be considered. The impregnation method is optimised while the different porous materials are tested. For the selection of porous materials the pores need to be large enough for the VOC molecules, further influence of the pore size is tested. T2 - Healthy Buildings CY - Aachen, Germany DA - 11.06.2023 KW - VOC KW - Emission KW - Quality assurance KW - Reference material PY - 2023 AN - OPUS4-59842 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schumacher, Julia T1 - DHN melanin synthesis in the rock inhabitant Knufia petricola N2 - DHN (1,8-dihydroxynaphthalene) melanin is produced by different Ascomycetes via slightly differing biosynthetic routes. The polyketide synthases (PKS) release the heptaketide YWA1, the hexaketide AT4HN or the pentaketide T4HN. The first two products are deacetylated by ‘yellowish-green’ hydrolases to T4HN, and T4HN is further converted by a core set of enzymes to DHN. Final polymerization steps are accomplished by multicopper oxidases (MCOs). The involved genes are tightly clustered, partially clustered or widely distributed in the genomes of DHN melanin-producing fungi. DHN melanogenesis is often regulated in a spatial and temporal fashion resulting e.g. in melanized reproduction, survival and/or infection structures. In contrast, a polyphyletic group of Ascomycetes (microcolonial fungi/ black yeast) dwelling in hostile habitats such as bare rock surfaces in hot and cold deserts, exhibits constitutive melanogenesis. Here, we report on the identification and functional characterization of the DHN melanogenic genes of Knufia petricola as a representative of the Chaetothyriales, the sister order of the Eurotiales. Orthologs for all melanogenic genes were identified in the genome of K. petricola A95, including one gene encoding the polyketide synthase (KpPKS1), two genes encoding ‘yellowish-green’ hydrolases (KpYGH1,2), two genes encoding THN reductases (KpTHR1,2) and one gene encoding a scytalone dehydratase (KpSDH1). Ten genes encoding MCOs were identified, all MCOs are predicted to be secreted. The genes are not clustered in the genome but are highly expressed. Gene functions are studied by generation of single, double, and multiple deletion mutants in K. petricola and by heterologous expression in Saccharomyces cerevisiae for reconstruction of the synthesis pathway. T2 - VAAM Fachgruppentagung "Molecular Biology of Fungi" CY - Kaiserslautern, Germany DA - 07.09.2022 KW - DHN melanin KW - Genetics KW - Biodegradation PY - 2022 AN - OPUS4-55676 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schumacher, Julia T1 - DHN melanin synthesis in the rock inhabitant Knufia petricola N2 - DHN (1,8-dihydroxynaphthalene) melanin is produced by Ascomycetes via slightly differing synthetic routes. Polyketide synthases release YWA1, AT4HN or T4HN. YWA1 and AT4HN are deacetylated by ‘yellowish-green’ hydrolases, and T4HN is converted by a core set of enzymes to DHN. Final polymerization steps are accomplished by multicopper oxidases. The melanogenic genes are tightly, partially or not clustered in the genomes, and are often regulated in a spatial and/or temporal fashion. By contrast, microcolonial fungi/black yeasts – a polyphyletic group of Ascomycetes dwelling in hostile habitats such as bare rock surfaces – feature constitutive DHN melanogenesis. Here, we report on the DHN melanogenic genes of Knufia petricola (Eurotiomycetes/Chaetothyriales). T2 - 16th European Conference on Fungal Genetics CY - Innsbruck, Austria DA - 05.03.2023 KW - DHN melanin KW - Fungus KW - Biosynthesis PY - 2023 AN - OPUS4-57143 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schumacher, Julia T1 - DHN melanin – synthesis, regulation, and functions in Knufia petricola N2 - Dihydroxynaphthalene (DHN) melanin is produced by diverse Ascomycetes via slightly differing biosynthetic routes. The polyketide synthases (PKS) release the heptaketide YWA1, the hexaketide AT4HN or the pentaketide T4HN. The first two products are deacetylated by ‘yellowish-green’ hydrolases to T4HN, and T4HN is further converted by a core set of enzymes to DHN. Final polymerization steps are accomplished by multicopper oxidases. DHN melanogenesis is often regulated in a spatial and temporal fashion resulting e.g., in melanized reproduction and survival structures of the foliar plant pathogen Botrytis cinerea (Schumacher 2016, Mol Microbiol). In contrast, microcolonial black fungi exhibit constitutive melanogenesis. Here, DHN melanin builds a protective layer around all vegetative cells thus contributing to the survival of diverse environmental stresses even without specialized reproduction structures. For studying the regulation and relevance of DHN melanogenesis for tolerance of abiotic and biotic stresses, adhesion to substrates and subsequent damage of colonized surfaces, the rock-inhabiting fungus Knufia petricola was chosen as gene functions in this fungus can be studied by CRISPR/Cas9-based genome editing. The putative melanogenic genes were identified in the genome of K. petricola, deleted to confirm their involvement in DHN melanogenesis and co-expressed in Saccharomyces cerevisiae for reconstruction of the synthesis pathway. Phenotypes of deletion mutants are studied for specifying the functions of DHN melanin in K. petricola. T2 - IUBMB Focused Meeting on Extremophilic Fungi (FUN-EX) CY - Ljubliana, Slovenia DA - 19.09.2023 KW - Pigment KW - Fungus KW - Heterologous expression PY - 2023 AN - OPUS4-58430 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dehkohneh, Abolfazl T1 - Effect of Carbon and Nitrogen on Growth of the Oligotrophic and Extremotolerant Fungus Knufia petricola N2 - Introduction: Rock-inhabiting black fungi are renowned for their constitutive melanin production, extremotolerance and ubiquitous colonization of oligotrophic, natural or anthropogenic subaerial surfaces, including marble monuments and solar panels. Knufia petricola is a model for these fungi as it is genetically amenable and has their typical characteristics. It is capable of colonizing and deteriorating minerals and produces extracellular polymeric substances that facilitate attachment. Objectives: The objective of this study is to understand how such an organism is able to grow in environments depleted of C and/or N. Method: K. petricola growth parameters (colony extension and thickness, biomass, CO2 respiration and carbon-use efficiency (CUE)) were analysed for different C to N ratios (C:N), changing both the C and N concentrations and sources. The study utilized a dual-scale approach, examining biofilm formation on agar (macroscale) and growth of a single cell into a microcolony in a microfluidic device (microscale). This methodology provided insights into the nutritional requirements and growth behaviours of K. petricola across different spatial scales. Findings: Our macroscale analysis indicated optimal growth at the C:N ratio of 60. The morphological analysis demonstrated that when nitrate is utilized as the N source, colonies tend to exhibit filamentous growth at their edges, especially when glucose is available as C source. In contrast, when ammonium is the N source, the colony surface appears smooth (Fig. 1A). Moreover, C or N depletion led to higher substrate penetration, mostly through filaments at the edge of the biofilm. Notably, the lowest carbon concentration yielded reduced biomass C:N ratio and the peak biomass C:N ratio was observed at the medium C:N ratio of 60, suggesting a potential correlation between C:N ratio and optimal growth (Fig. 1B). The CUE was however quite low, ca. 0.4-0.6, being lowest when C and N were limiting. Concurrently, microscale analyses of single cells revealed that increasing the C:N ratio from 0.6 to 60 caused (1) shorter cell cycles and (2) more branching, no branching formed without C and N (Fig. 1C). This led to a denser colony at optimal conditions and a rather extended morphology under C or N limitations. Conclusion: The findings demonstrate that the depletion of either carbon or nitrogen results in enhanced substrate penetration, predominantly through edge filaments. Notably, the optimal growth and peak biomass C:N ratio of 60 suggest both a correlation with and importance of the medium C:N ratio. Specifically, the lowest carbon input led to a reduced biomass C:N ratio, while the peak biomass C:N ratio was achieved at the medium C:N ratio of 60. T2 - FEMS MICRO conference CY - Milano, Italy DA - 14.07.2025 KW - Black fungi KW - Carbon-use efficiency KW - Polyextremotolerant KW - Oligotrophs KW - Rock-inhabiting fungi PY - 2025 AN - OPUS4-65038 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dehkohneh, Abolfazl T1 - From microscale to macroscale: environmental conditions and growth patterns of the black fungus Knufia petricola N2 - Environmental, black fungi are known for their oligotrophic lifestyle and melanin production and ubiquitous colonisers of natural and anthropogenic subaerial surfaces like marble monuments, washing machine soap dispensers and solar panels. Even though their growth is generally unappreciated, prevention or inhibition thereof is still to be accomplished. We have chosen the black fungus Knufia petricola as a model species to study these organisms as it is genetically amenable, able to colonise and deteriorate minerals and produces extracellular polymeric substances allowing attachment. Our goal is simple: the quantitative description of its growth on various environmental conditions to create a mathematical model which could allow the development of a mitigation strategy. The conditions to be tested are the quantity and type of carbon and nitrogen sources, the pH and the presence of neighbouring colonies. The mathematical model is in development using the iDynoMiCS 2.0 platform. Our first results showed that the growth rate is negatively correlated to the colony forming units (i.e. the presence of a neighbouring colony). Although interesting with respect to mitigation, we therefore have chosen to track the growth of single colonies. On a macro-scale, the highest extension rates of colonies were at pH 5, 0.01M NO3, 0.01M NH4, 0.1M glucose, and 0.1M sucrose. Interesting are the similar rates in the range of 0.01M to 0.1M for carbon, and that CO2 production on similar conditions correlates well with these results. On a microscale, we have followed the growth of single cells using a custom-made microfluidic flow cell. Overall, first results show that medium containing more carbon not necessarily affected the growth rate but rather the quantity of branches produced by a single cell. This rapidly results in a more compact microcolony versus the more extended colonies on C-deficient media. This more profound knowledge on the growth of black fungi will allow to dissect their role in material deterioration and colonisation. T2 - CurvoBio 2024 CY - Warsaw, Poland DA - 28.08.2024 KW - Black fungi KW - Rock-inhabiting fungi KW - Fungal biofilm KW - Individual-based modelling KW - Biocorrosion PY - 2024 AN - OPUS4-62270 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dehkohneh, Abolfazl T1 - From microscale to macroscale: how environmental conditions impact the growth of the black fungus Knufia petricola N2 - Environmental, black fungi are known for their oligotrophic lifestyle and melanin production and ubiquitous colonisers of natural and anthropogenic subaerial surfaces like marble monuments, washing machine soap dispensers and solar panels. Even though their growth is generally unappreciated, prevention or inhibition thereof is still to be accomplished. We have chosen the black fungus Knufia petricola as a model species to study these organisms as it is genetically amenable, able to colonise and deteriorate minerals and produces extracellular polymeric substances allowing attachment. Our goal is simple: the quantitative description of its growth on various environmental conditions to create a mathematical model which could allow the development of a mitigation strategy. The conditions to be tested are the quantity and type of carbon and nitrogen sources, the pH and the presence of neighbouring colonies. The mathematical model is in development using the iDynoMiCS 2.0 platform. Our first results showed that the growth rate is negatively correlated to the colony forming units (i.e. the presence of a neighbouring colony). Although interesting with respect to mitigation, we therefore have chosen to track the growth of single colonies. On a macro-scale, the highest extension rates of colonies were at pH 5, 0.01M NO3, 0.01M NH4, 0.1M glucose, and 0.1M sucrose. Interesting are the similar rates in the range of 0.01M to 0.1M for carbon, and that CO2 production on similar conditions correlates well with these results. On a microscale, we have followed the growth of single cells using a custom-made microfluidic flow cell. Overall, first results show that medium containing more carbon not necessarily affected the growth rate but rather the quantity of branches produced by a single cell. This rapidly results in a more compact microcolony versus the more extended colonies on C-deficient media. This more profound knowledge on the growth of black fungi will allow to dissect their role in material deterioration and colonisation. T2 - International Biodeterioration & Biodegradation Society (IBBS) CY - Berlin, Germany DA - 09.09.2024 KW - Black fungi KW - Rock-inhabiting fungi KW - Fungal biofilm KW - Individual-based modelling PY - 2024 AN - OPUS4-62141 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gorbushina, Anna T1 - From rocks to riches: Knufia petricola as model and expression platform N2 - Black fungi belong to different classes of Ascomycota but evolved similar morpho-physiological adaptations such as yeast-like growth and constitutive melanin formation to colonize extreme competition-free environments. They are ubiquitously found on air-exposed surfaces, from ancient marble monuments to modern solar panels. The rock inhabitant Knufia petricola was chosen to become a model for these extremotolerant black fungi. Plasmid-based and ribonucleoprotein-based CRISPR/Cas9 techniques were introduced to precisely introduce one to multiple double strand breaks into the DNA to modify, replace or add sequences to the genome either using the available selection marker systems (hygR, natR, genR, baR, suR) or by marker-free approaches. Multiplexing is very efficient, allowing for four or more simultaneous genome editing events. The newly generated cloning vectors containing the Tet on construct for doxycycline-controlled gene expression, and the validated sites in the K. petricola genome for color-selectable (pks1, phs1, ade2) or neutral insertion (igr1 to 5) of expression constructs complete the reverse genetics toolbox. One or multiple endogenous or heterologous genes can be expressed on demand from different genomic loci or from a single construct by using 2A self-cleaving peptides. We thus can express genes from synthetic clusters in a non-pigmented background (Δpks1/Δphs1). The fact that K. petricola only produces few secondary metabolites (DHN melanin, carotenoids, mycosporines and a siderophore) and plant cell-wall degrading enzymes but is capable to take the burden of acetyl-CoA-consuming metabolism and protein secretion renders K. petricola a promising host for the expression of heterologous genes encoding high-end secondary metabolites and enzymes. T2 - 12th International Mycological Congress (IMC12) CY - Maastricht, Netherlands DA - 11.08.2024 KW - Fungus KW - Genetic engineering KW - Heterologous gene expression KW - Cell factory PY - 2024 AN - OPUS4-60838 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dehkohneh, Abolfazl T1 - Fungal biofilms on materials: describing and modelling growth of the black fungus Knufia petricola N2 - Fungi that grow as biofilms are associated with clinical settings as well as various cases of material fouling and material damage. Black fungi as biofilm formers have been rarely studied so far. Their conspicuous dark pigmentation, EPS production, adhesion capabilities and adaptations to stresses allow black fungi to develop biofilms on materials under harsh conditions. For example, rock-inhabiting black fungi withstand sun irradiation and dehydration and are therefore ubiquitous on arid surfaces like solar panels and marble monuments. To understand and control their ability to colonise and deteriorate materials, one should assess and model black fungi’s growth patterns. But so far, no mathematical model has been developed to describe their growth. Knufia petricola A95, representing rock-inhabiting fungi from Chaetothyriales, is genetically amenable and can serve as a model for biofilm studies in black fungi. The primary objective of this project is to develop a growth model for K. petricola A95 which will enable to define and predict material colonisation of black fungi. Dedicated experimental work with K. petricola will allow the quantitative assessment of the impact of environmental conditions (e.g. pH, nutrients, etc.) on the growth behaviour at the biofilm and single cells level. Data which will be used to validate and develop an individual-based model (based on the iDynoMICS modelling platform) that explains how fungal biofilms form, colonise materials, and cause deterioration. Thus far, research has been conducted on the impact of different concentrations and sources of major elements (e.g. C, N, …), as well as trace elements (e.g. Cu, Mg, …), on the colony shape and biomass of Knufia petricola A95 biofilms. To study the behaviour of single cells, the length of the cell cycle in different growth media has been determined via the combined use of microfluidic devices and confocal microscopy. T2 - IUBMB Focused Meeting on Extremophilic Fungi (FUN-EX) CY - Ljubljana, Slovenia DA - 19.09.2023 KW - Biofilm KW - Rock-inhabiting fungus KW - Mathematical modelling PY - 2023 AN - OPUS4-58438 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gerrits, Ruben T1 - Genetic engineering of a black rock-inhabiting fungus shows its strengths and weaknesses  N2 - Environmental black fungi are known to inhabit anthropogenic habitats like marble monuments, solar panels, indoor walls and even washing machines. These pests are generally assumed to persist and grow in these environments due to their melanin production and oligotrophic lifestyle, respectively. We aimed to confirm these assumptions and to find methods to mitigate their substrate colonisation and deterioration by looking at their ability to produce melanin and take up iron, the latter being a general weakness of aerobes. This was done by means of selecting one species, Knufia petricola, and applying CRISPR/Cas9-mediated genome editing techniques. This showed that K. petricola produces one siderophore; deletion of its encoding gene showing no strong phenotypic effects. Deletion of the other iron uptake mechanism – reductive iron assimilation (RIA) – did however cause a strong growth deficiency at iron depleted conditions. Both together reveal that K. petricola has a weak siderophore and relies on RIA to acquire iron, reflecting a natural habitat free of competition for iron. This comes at a price: K. petricola but also other black fungi isolated from solar panels are extremely sensitive to mediocre iron chelators, offering us a mitigation strategy. Melanin, although adsorbing and reducing iron, did not have an observable effect on iron uptake. The pigment did however affect the fungal ability to withstand desiccation: pigment-deficient mutants were not able to withstand a prolonged incubation in a desiccator. This is a clear advantage in the colonisation of dry subaerial surfaces. T2 - 12th International Mycological Congress (IMC12) CY - Maastricht, Netherlands DA - 12.08.2024 KW - Iron uptake KW - Black fungi KW - Melanin PY - 2024 AN - OPUS4-62269 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gerrits, Ruben T1 - Iron uptake by the rock-inhabiting fungus Knufia petricola N2 - Iron is arguably the most essential metal in living organisms. For rock-inhabiting fungi its acquisition might be unconventional as they (1) tend to inhabit iron-deficient, oxygen-rich surfaces like marble monuments and solar panels and (2) produce the black, iron-adsorbing pigment melanin. We used a range of analytical methods, ongoing mineral dissolution experiments and gene deletion mutants of the model rock-inhabiting fungus Knufia petricola to figure out the mechanisms and substrate deteriorating effects of iron uptake by these organisms. To study both siderophore-mediated and reductive iron assimilation (RIA), genes like sidC, encoding a putative siderophore synthetase and ftr1 and fet3 encoding the subunits of an iron permease-oxidase were deleted. At iron deficient conditions, growth of the wild type (WT) and ΔsidC mutant was similar, whereas growth of the Δftr1-fet3 mutant and the double mutant ΔsidC/Δftr1-fet3 was diminished and absent, respectively. We were not able to detect the siderophore of K. petricola and the WT and mutants were not able to grow at low concentrations of strong iron chelators. However, in a cross-feeding experiment, an overexpression strain of sidC allowed more growth of ΔsidC/Δftr1-fet3 on iron deficient medium than the WT, whereas the ΔsidC mutant could not do so at all. Compared to the WT, the sidC overexpression strain also withstood oxidative stress better and had a shorter lag time and higher growth rate. Combined, these results indicate that K. petricola relies more on RIA than siderophore-mediated uptake as it likely excretes low quantities of a primarily intracellular siderophore. Interestingly, Δftr1-fet3 had a higher iron content than the WT at iron deficient conditions. This difference disappeared upon deletion of melanin synthesis (Δpks1 vs. Δpks1/Δftr1-fet3): melanin-bound iron can likely not be used without RIA. K. petricola’s chelation incapacity implies a habitat free of competition for iron while offering us a mitigation strategy. T2 - ECFG16 CY - Innsbruck, Austria DA - 05.03.2023 KW - Siderophore KW - Melanin KW - Reductive iron assimilation PY - 2023 AN - OPUS4-57148 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Frelih, Milena T1 - Material-Microbiome Interactions N2 - Estimations show that the anthropogenic mass, the technosphere, already exceeds the biomass on Earth. Understanding the technosphere-environment interactions and their impacts is key to safe and healthy ecosystems and human societies. At BAM, we aim at promoting awareness for microorganisms living and evolving in contact with human-made materials and technical systems. We are creating datasets of biofilms on plastic and other anthropogenic materials and in the context of important technical challenges (e.g. microbially influenced corrosion or biocide-induced antimicrobial resistance). This enables us to identify and examine key organisms in the investigated systems that potentially harbor new, also industrially relevant, species and traits. Further, we explore material effects on aquatic microbial communities, aiming at the development and establishment of innovative and environmentally relevant methodologies. By using bioinformatic and molecular tools and interdisciplinary research, we enhance the understanding of material-microbiome interactions for a safe and sustainable future. T2 - NFDI4Microbiota Annual Conference CY - Cologne, Germany DA - 30.09.2025 KW - Microbiome KW - Microplastics KW - Black fungi KW - Nanoparticles PY - 2025 AN - OPUS4-64637 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Fuentes, Elsa A1 - Prieto, Beatriz A1 - Gorbushina, Anna T1 - Mixed model biofilm: interactions between algae, fungi and cyanobacteria and their effects on granite biodeterioration N2 - Granite, despite being one of the most widely used rocks for building material cultural heritage, is also one of the least studied. Previous works have shown that environmental parameters modulated by climate change will lead to changes in the microbial composition of biofilms grown on stone, but also to changes in the production of EPS, in the composition of pigments and, as a consequence, in the biodeterioration processes that this rock undergoes (Fuentes, 2023). Considering that the colonisation process is highly dynamic, small changes in climatic conditions can lead to the formation of different types of biofilms and diverse interactions between species. Knowing the contribution of the different organisms to the deterioration process is important both to anticipate the consequences that climate change will have on the deterioration of the granite, but also when addressing the processes of recolonization after cleaning, to ensure an improvement of the present situation. So, in order to continue my line of research on granite biodeterioration, the aim of this new project is to study the contribution of each type of organism (green algae, cyanobacteria and fungi) to the process of granite deterioration as well as the specific effect on each mineral, in addition to its role in the resilience and response of biofilms to environmental changes. With this main objective, the effect of the type of substrate on the composition of a model mixed biofilm formed by the fungus Knufia petricola, the algae Jaagichlorella sp. and the cyanobacterium Synechocystis sp. will be studied. The results obtained on granite will be compared with those obtained with other lithic types such as marble or limestone. Furthermore, it will be observed if the different ratios between organisms lead to changes in the capacity of these organisms to generate biodeterioration and to buffer climatic changes. Finally, the susceptibility of each mineral that makes up the granite - quartz, feldspars, micas - to biodeterioration mediated by each type of organism will be analysed. To address these questions, on the one hand, the response of the mixed biofilms as a whole will be evaluated by means of confocal microscopy, PAM, as well as the quantification of pigments and EPS, and on the other hand, the effect of these organisms on the deterioration of the substrates, through the use of SEM and TEM, which will allow the assessment of both the changes in porosity and the appearance of deterioration in the surface layers of the rock. This research will deepen the knowledge of the processes of granite deterioration, which have been limitedly studied in relation to microorganisms; but also aims to provide the scientific community with a model mixed biofilm to increase the reproducibility between experiments, one of the main limitations of this field of study. T2 - 19th International Biodeterioration and Biodegradation Symposium CY - Berlin, Germany DA - 09.09.2024 KW - Biofilm KW - Stone KW - Algae KW - Fungi KW - Cyanobacteria KW - Cultural heritage PY - 2024 AN - OPUS4-62272 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Taghavi Kalajahi, Sara T1 - Pilot Study of a Laboratory- Based Microbiologically Influenced Corrosion (MIC) Test Using Microbiological Consortia Sampled from the Field N2 - Experts widely agree that the verification of microbiologically influenced corrosion (MIC) require the use of multiple lines of evidence (MLOE), including metallurgical, microbiological, operational/historical and environmental/chemical aspects. Existing standards related to MIC, such as NACE TM0106, TMO212 and TM0194, primarily aim to offer guidance on gathering such evidence. Working Group 5 of Euro-MIC COST action 20130 (Achieving standardization) proposed a laboratory-based approach that directly confirms the capability of the sampled consortium of microorganisms, obtained from the specific field location under investigation, to increase and/or alter the corrosion processes. It is necessary to verify this laboratory approach by conducting it in different laboratories, performed by different scientist. In the current study, the experiments based on the laboratory protocol of WG5 were conducted at Endures’s laboratory using environmental samples (sediment and seawater) from the North Sea. Metal coupons (carbon steel C1010) were exposed to sediment and seawater samples with varying microbial inoculums and controls over 150 days. Microbial identification, corrosion product analysis, and surface morphology assessments were conducted using molecular and microscopy techniques. The results indicate distinct microbial influences, particularly in treatments containing yeast, which fostered heightened anaerobic activity, notably by sulfate-reducing bacteria (SRB). Weight loss measurements and surface analysis revealed elevated corrosion rates and susceptibility to pitting corrosion in microbial inoculum treatments, with yeast presence exacerbating corrosion processes. Elemental analysis confirmed the presence of iron sulfide in corrosion byproducts, affirming SRB activity. The findings emphasize the importance of employing a MLOE approach and investigating pitting corrosion to better understand the impact of microorganisms on metal corrosion in the marine environments. This study contributes to advancing knowledge in the field and developing standardization: the lab-to-field transition for MIC testing. T2 - MIC-STANDS CY - Lisbon, Portugal DA - 24.07.2024 KW - Microbiologically influenced corrosion (MIC), Multiple lines of evidence (MLOE) KW - Marine Corrosion KW - Achieving standardization PY - 2024 AN - OPUS4-61979 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Nitsche, Sarah T1 - The role of the stress-activated MAP kinase SAK1 in Knufia petricola N2 - Mitogen-activated protein (MAP) kinases are highly conserved in animals, plants, and fungi and represent fundamental parts of signaling networks in eukaryotic cells. Black DHN (1,8-dihydroxynaphthalene) melanin and orange carotenoids are produced by many fungi in specific cell types/under certain conditions for protecting cells from abiotic and/or biotic stresses. Microcolonial black fungi constitutively produce DHN melanin, contain the conserved carotenogenic gene cluster, exhibit slow yeast-like growth and survive in extreme environments. Thus, the question arises to which extent pigment formation and responses mediated by the stress-activated MAP kinase module contribute to the observed extremotolerance. We address this question in the rock inhabitant Knufia petricola, the only representative of the extremotolerant black fungi that is genetically amendable. Here, the mutations of pks1, phs1 and both genes result in melanin-free (pink), carotenoid-free (black) and pigment-free (white) strains, respectively (Voigt Knabe et al. 2020, Sci Rep). The gene encoding the stress-activated MAP kinase was deleted in the wild-type and different pigment-deficient backgrounds. In addition, strains were generated that express a GFP-SAK1 fusion protein from the sak1 locus to follow the cytosolic/nuclear shuttling of SAK1 upon stress. Growth of the obtained single, double and triple deletion mutants was tested by dropping cell suspensions on solid media supplemented with different stress-inducing agents. The Δsak1 mutants show slightly reduced growth rates even under non-stress conditions and are hypersensitive to different stress conditions: reduced growth is observed on media inducing, for instance, osmotic, oxidative, membrane, and pH stress, and upon incubation at 30 °C (heat stress). Melanin-free Δsak1 mutants are more sensitive than black Δsak1 mutants to some but not all stress conditions, suggesting that melanin and the SAK1 pathway have complementary roles in protecting K. petricola from stress. T2 - VAAM Fachgruppentragung "Molecular Biology of Fungi" CY - Kaiserslautern, Germany DA - 07.09.2022 KW - Fungus KW - Extremotolerance KW - Signal transduction PY - 2022 AN - OPUS4-55677 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Erdmann, Eileen T1 - Tools for Knufia petricola: new techniques for CRISPR/Cas9-based genome editing N2 - Black microcolonial fungi represent a group of ascomycetes with similar adaptations for existing in natural and anthropogenically created extreme habitats. They exhibit slow yeast-like or meristematic growth, do not form specialized reproduction structures and accumulate the black pigment 1,8-dihydroxynaphthalene (DHN) in the multilayered cell walls. We chose the rock inhabitant Knufia petricola of the Chaetothyriales as a representative for developing methods for genetic manipulation, simulation of mineral weathering and study of symbiotic interactions. Here, we report on the expansion of the genetic toolkit by more efficient multiplex CRISPR/Cas9 using a plasmid-based system for expression of Cas9 and multiple sgRNAs and three additional resistance selection markers. The targeted integration of expression constructs by replacement of essential genes for pigment synthesis allows for an additional color screening of the transformants. The black-pink screening due to the elimination of pks1 (melanin) was applied for promoter studies using GFP fluorescence as reporter, while the black-white screening due to the concurrent elimination of pks1 (melanin) and phs1 (carotenoids) was used to identify transformants that contain the two expression constructs for co-localization or bimolecular fluorescence complementation (BiFC) studies. In addition, two intergenic regions (igr1, igr2) were identified in which expression constructs can be inserted without causing obvious phenotypes. Plasmids of the pNXR-XXX series (Schumacher, 2012) and new compatible entry plasmids were used for fast and easy generation of expression constructs and are suitable for use in other fungal systems as well. T2 - 31st Fungal Genetics Conference CY - USA, CA, Pacific Grove DA - 15.03.2022 KW - Microcolonial fungi KW - Genetic engineering KW - Fluorescent proteins PY - 2022 AN - OPUS4-54586 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -