{"type": "FeatureCollection", "features": [{"id": "10.3389/fmicb.2022.813480", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:20:49Z", "type": "Journal Article", "created": "2022-03-01", "title": "Metatranscriptomic analyses unravel dynamic changes in the microbial and metabolic transcriptional profiles in artisanal Austrian hard-cheeses during ripening", "description": "<p>Vorarlberger Bergk\uffc3\uffa4se (VB) is an artisanal Austrian washed-rind hard cheese produced from alpine cows\uffe2\uff80\uff99 raw milk without the addition of ripening cultures. Ripening time is a key factor in VB, as it strongly influences the microbial communities present in the cheeses and the organoleptic properties of the product. In this study, the microbial and metabolic transcriptional profiles in VB rinds at different ripening times were investigated. VB products before (30\uffe2\uff80\uff89days of ripening) and after (90\uffe2\uff80\uff89days of ripening) selling were selected, RNA was extracted and subjected to shotgun metatranscriptomic sequencing. The analysis revealed some of the previously described abundant bacterial taxa of Brevibacterium, Corynebacterium, Halomonas, Psychrobacter, and Staphylococcus to be highly active in VB rinds. Additionally, the investigation of most important metabolic pathways in cheese ripening clearly showed differences in the gene transcription profiles and the active microbiota between the two ripening points investigated. At 30\uffe2\uff80\uff89days of ripening, metabolic events related with the degradation of residual lactose, lactate, citrate, proteolysis, and lipolysis were significantly more transcribed and mainly associated with Staphylococcus. On the other hand, genes involved in the degradation of smaller compounds derived from previous metabolism (i.e., metabolism of free amino acids and fatty acids) were significantly more expressed in VB rinds with 90 of ripening, and mainly associated with Brevibacterium and Corynebacterium. These latter metabolic activities are responsible of the generation of compounds, such as methanethiol and 2,3-butanediol, that are very important for the flavor and aroma characteristics of cheeses. This study shows the dynamic changes in the gene transcriptional profiles associated with energy substrates metabolism and the generation of organoleptic compounds during VB ripening and uncovers bacterial taxa as key drivers of the ripening process. These taxa might be the target for future studies toward an accelerated cheese ripening and the enhancement of its organoleptic properties.</p>", "keywords": ["2. Zero hunger", "0301 basic medicine", "0303 health sciences", "791", "metatranscriptomics", "organoleptic compounds", "cheese ripening", "DegreeDisciplines::Life Sciences::Animal Sciences", "microbial dynamics", "Microbiology", "QR1-502", "differential gene transcription", "03 medical and health sciences", "metabolic pathways", "Bacteria; Identification; Quality; Communities; Microflora; Alignment; Pathways; Products; Genes; Acid", "DegreeDisciplines::Life Sciences::Food Science::Food Microbiology"]}, "links": [{"href": "https://doi.org/10.3389/fmicb.2022.813480"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/Frontiers%20in%20Microbiology", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "10.3389/fmicb.2022.813480", "name": "item", "description": "10.3389/fmicb.2022.813480", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/10.3389/fmicb.2022.813480"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2022-03-01T00:00:00Z"}}, {"id": "10.1093/femsle/fnab100", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:18:25Z", "type": "Journal Article", "created": "2021-07-30", "title": "Transcriptomic markers of fungal growth, respiration and carbon-use efficiency", "description": "ABSTRACT                <p>Fungal metabolic carbon acquisition and its subsequent partitioning between biomass production and respiration, i.e. the carbon-use efficiency (CUE), are central parameters in biogeochemical modeling. However, current available techniques for estimating these parameters are all associated with practical and theoretical shortcomings, making assessments unreliable. Gene expression analyses hold the prospect of phenotype prediction by indirect means, providing new opportunities to obtain information about metabolic priorities. We cultured four different fungal isolates (Chalara longipes, Laccaria bicolor, Serpula lacrymans and Trichoderma harzianum) in liquid media with contrasting nitrogen availability and measured growth rates and respiration to calculate CUE. By relating gene expression markers to measured carbon fluxes, we identified genes coding for 1,3-\uffce\uffb2-glucan synthase and 2-oxoglutarate dehydrogenase as suitable markers for growth and respiration, respectively, capturing both intraspecific variation as well as within-strain variation dependent on growth medium. A transcript index based on these markers correlated significantly with differences in CUE between the fungal isolates. Our study paves the way for the use of these markers to assess differences in growth, respiration and CUE in natural fungal communities, using metatranscriptomic or the RT-qPCR approach.</p", "keywords": ["0301 basic medicine", "growth", "Fungal Proteins", "Laccaria", "03 medical and health sciences", "Ascomycota", "Research Letter", "Biologiska vetenskaper", "Trichoderma", "0303 health sciences", "metatranscriptomics", "Ecology", "Basidiomycota", "Biochemistry and Molecular Biology", "Fungi", "Biological Sciences", "Carbon", "Microbiology (Microbiology in the medical area to be 30109)", "Hypocreales", "carbon-use efficiency", "gene markers", "fungi", "Transcriptome", "respiration", "Biomarkers"]}, "links": [{"href": "https://pub.epsilon.slu.se/26755/1/hasby_f_a_et_al_220119.pdf"}, {"href": "http://academic.oup.com/femsle/article-pdf/368/15/fnab100/39805403/fnab100.pdf"}, {"href": "https://doi.org/10.1093/femsle/fnab100"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/FEMS%20Microbiology%20Letters", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "10.1093/femsle/fnab100", "name": "item", "description": "10.1093/femsle/fnab100", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/10.1093/femsle/fnab100"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2021-08-01T00:00:00Z"}}, {"id": "10.1080/1040841x.2022.2132850", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:18:19Z", "type": "Journal Article", "created": "2022-10-26", "title": "Bioinformatic approaches for studying the microbiome of fermented food", "description": "High-throughput DNA sequencing-based approaches continue to revolutionise our understanding of microbial ecosystems, including those associated with fermented foods. Metagenomic and metatranscriptomic approaches are state-of-the-art biological profiling methods and are employed to investigate a wide variety of characteristics of microbial communities, such as taxonomic membership, gene content and the range and level at which these genes are expressed. Individual groups and consortia of researchers are utilising these approaches to produce increasingly large and complex datasets, representing vast populations of microorganisms. There is a corresponding requirement for the development and application of appropriate bioinformatic tools and pipelines to interpret this data. This review critically analyses the tools and pipelines that have been used or that could be applied to the analysis of metagenomic and metatranscriptomic data from fermented foods. In addition, we critically analyse a number of studies of fermented foods in which these tools have previously been applied, to highlight the insights that these approaches can provide.", "keywords": ["2. Zero hunger", "0301 basic medicine", "metatranscriptomics", "Microbiota", "0206 medical engineering", "high-throughput sequencing", "Computational Biology", "High-Throughput Nucleotide Sequencing", "bioinformatics", "02 engineering and technology", "fermented foods", "03 medical and health sciences", "Metagenome", "Metagenomics", "Fermented Foods"]}, "links": [{"href": "https://www.tandfonline.com/doi/pdf/10.1080/1040841X.2022.2132850"}, {"href": "https://doi.org/10.1080/1040841x.2022.2132850"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/Critical%20Reviews%20in%20Microbiology", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "10.1080/1040841x.2022.2132850", "name": "item", "description": "10.1080/1040841x.2022.2132850", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/10.1080/1040841x.2022.2132850"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2022-10-26T00:00:00Z"}}, {"id": "10.1186/s13568-024-01764-7", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:19:22Z", "type": "Journal Article", "created": "2024-09-28", "title": "Metagenomic analyses of a consortium for the bioremediation of hydrocarbons polluted soils", "description": "Abstract<p>A bacterial consortium was isolated from a soil in Noblejas (Toledo, Spain) with a long history of mixed hydrocarbons pollution, by enrichment cultivation. Serial cultures of hydrocarbons polluted soil samples were grown in a minimal medium using diesel (1\uffc2\uffa0mL/L) as the sole carbon and energy source. The bacterial composition of the Noblejas Consortium (NC) was determined by sequencing 16S rRNA gene amplicon libraries. The consortium contained around 50 amplicon sequence variants (ASVs) and the major populations belonged to the genera Pseudomonas, Enterobacter, Delftia, Stenotrophomonas, Achromobacter, Acinetobacter, Novosphingobium, Allorhizobium-Neorhizobium-Rhizobium, Ochrobactrum and Luteibacter. All other genera were below 1%. Metagenomic analysis of NC has shown a high abundance of genes encoding enzymes implicated in aliphatic and (poly) aromatic hydrocarbons degradation, and almost all pathways for hydrocarbon degradation are represented. Metagenomic analysis has also allowed the construction of metagenome assembled genomes (MAGs) for the major players of NC. Metatranscriptomic analysis has shown that several of the ASVs are implicated in hydrocarbon degradation, being Pseudomonas, Acinetobacter and Delftia the most active populations.</p", "keywords": ["metagenomics", "Bacterial consortium; Bioremediation; Metagenomics; Metatranscriptomics; Total petroleum hydrocarbons", "metatranscriptomics", "Bacterial consortium", "Biolog\u00eda y Biomedicina / Biolog\u00eda", "Microbiology", "QR1-502", "Total petroleum hydrocarbons", "total petroleum hydrocarbons", "bioremediation", "Original Article", "Metagenomics", "Bioremediation", "TP248.13-248.65", "Metatranscriptomics", "Biotechnology"]}, "links": [{"href": "https://doi.org/10.1186/s13568-024-01764-7"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/AMB%20Express", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "10.1186/s13568-024-01764-7", "name": "item", "description": "10.1186/s13568-024-01764-7", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/10.1186/s13568-024-01764-7"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2024-09-28T00:00:00Z"}}, {"id": "10.21769/bioprotoc.3799", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:20:31Z", "type": "Journal Article", "created": "2020-10-19", "title": "Low-cost and High-throughput RNA-seq Library Preparation for Illumina Sequencing from Plant Tissue", "description": "Transcriptome analysis can provide clues to biological processes affected in different genetic backgrounds or/and under various conditions. The price of RNA sequencing (RNA-seq) has decreased enough so that medium- to large-scale transcriptome analyses in a range of conditions are feasible. However, the price and variety of options for library preparation of RNA-seq can still be daunting to those who would like to use RNA-seq for their first time or for a single experiment. Among the criteria for selecting a library preparation protocol are the method of RNA isolation, nucleotide fragmentation to obtain desired size range, and library indexing to pool sequencing samples for multiplexing. Here, we present a high-quality and a high-throughput option for preparing libraries from polyadenylated mRNA for transcriptome analysis. Both high-quality and high-throughput protocol options include steps of mRNA enrichment through magnetic bead-enabled precipitation of the poly-A tail, cDNA synthesis, and then fragmentation and adapter addition simultaneously through Tn5-mediated 'tagmentation'. All steps of the protocols have been validated with Arabidopsis thaliana leaf and seedling tissues and streamlined to work together, with minimal cost in money and time, thus intended to provide a beginner-friendly start-to-finish RNA-seq library preparation for transcriptome analysis.", "keywords": ["0301 basic medicine", "570", "0303 health sciences", "Arabidopsis thaliana", "QH301-705.5", "Plant", "580 Plants (Botany)", "Multiplexing", "Tagmentation", "03 medical and health sciences", "10126 Department of Plant and Microbial Biology", "10211 Zurich-Basel Plant Science Center", "RNA-seq", "Biology (General)", "Transcriptomics"]}, "links": [{"href": "https://escholarship.org/content/qt44f1027m/qt44f1027m.pdf"}, {"href": "https://doi.org/10.21769/bioprotoc.3799"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/BIO-PROTOCOL", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "10.21769/bioprotoc.3799", "name": "item", "description": "10.21769/bioprotoc.3799", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/10.21769/bioprotoc.3799"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2020-01-01T00:00:00Z"}}, {"id": "10.25491/nvg8-j585", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:20:40Z", "type": "Dataset", "title": "GTEX-V955-0926-SM-4JBJ8", "description": "Sample ID: GTEX-V955-0926-SM-4JBJ8", "keywords": ["transcriptomics", "annotation", "phenotype", "gtex", "gene regulation"], "contacts": [{"organization": "Consortium, The GTEx", "roles": ["creator"]}]}, "links": [{"href": "https://doi.org/10.25491/nvg8-j585"}, {"rel": "self", "type": "application/geo+json", "title": "10.25491/nvg8-j585", "name": "item", "description": "10.25491/nvg8-j585", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/10.25491/nvg8-j585"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2017-01-01T00:00:00Z"}}, {"id": "10.25491/xydj-cr77", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:20:40Z", "type": "Dataset", "title": "GTEX-13OW7-1626-SM-5IJDH", "description": "Sample ID: GTEX-13OW7-1626-SM-5IJDH", "keywords": ["transcriptomics", "annotation", "phenotype", "gtex", "gene regulation"], "contacts": [{"organization": "Consortium, The GTEx", "roles": ["creator"]}]}, "links": [{"href": "https://doi.org/10.25491/xydj-cr77"}, {"rel": "self", "type": "application/geo+json", "title": "10.25491/xydj-cr77", "name": "item", "description": "10.25491/xydj-cr77", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/10.25491/xydj-cr77"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2017-01-01T00:00:00Z"}}, {"id": "10.3390/genes10080601", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:20:59Z", "type": "Journal Article", "created": "2019-08-09", "title": "Genetic Potential of the Biocontrol Agent Pseudomonas brassicacearum (Formerly P. trivialis) 3Re2-7 Unraveled by Genome Sequencing and Mining, Comparative Genomics and Transcriptomics", "description": "<p>The genus Pseudomonas comprises many known plant-associated microbes with plant growth promotion and disease suppression properties. Genome-based studies allow the prediction of the underlying mechanisms using genome mining tools and the analysis of the genes unique for a strain by implementing comparative genomics. Here, we provide the genome sequence of the strain Pseudomonas brassicacearum 3Re2-7, formerly known as P. trivialis and P. reactans, elucidate its revised taxonomic classification, experimentally verify the gene predictions by transcriptome sequencing, describe its genetic biocontrol potential and contextualize it to other known Pseudomonas biocontrol agents. The P. brassicacearum 3Re2-7 genome comprises a circular chromosome with a size of 6,738,544 bp and a GC-content of 60.83%. 6267 genes were annotated, of which 6113 were shown to be transcribed in rich medium and/or in the presence of Rhizoctonia solani. Genome mining identified genes related to biocontrol traits such as secondary metabolite and siderophore biosynthesis, plant growth promotion, inorganic phosphate solubilization, biosynthesis of lipo- and exopolysaccharides, exoproteases, volatiles and detoxification. Core genome analysis revealed, that the 3Re2-7 genome exhibits a high collinearity with the representative genome for the species, P. brassicacearum subsp. brassicacearum NFM421. Comparative genomics allowed the identification of 105 specific genes and revealed gene clusters that might encode specialized biocontrol mechanisms of strain 3Re2-7. Moreover, we captured the transcriptome of P. brassicacearum 3Re2-7, confirming the transcription of the predicted biocontrol-related genes. The gene clusters coding for 2,4-diacetylphloroglucinol (phlABCDEFGH) and hydrogen cyanide (hcnABC) were shown to be highly transcribed. Further genes predicted to encode putative alginate production enzymes, a pyrroloquinoline quinone precursor peptide PqqA and a matrixin family metalloprotease were also found to be highly transcribed. With this study, we provide a basis to further characterize the mechanisms for biocontrol in Pseudomonas species, towards a sustainable and safe application of P. brassicacearum biocontrol agents.</p>", "keywords": ["COMPARATIVE GENOMICS", "0301 basic medicine", "570", "Antifungal Agents", "Plant-growth promotion", "Biolog\u00eda", "comparative genomics", "Phloroglucinol", "PLANT-GROWTH PROMOTION", "Article", "Rhizoctonia", "transcriptomics", "03 medical and health sciences", "https://purl.org/becyt/ford/1.6", "Genome mining", "Hydrogen Cyanide", "Pseudomonas", "genome mining", "RNA SEQUENCING", "TRANSCRIPTOMICS", "biocontrol", "GENOME MINING", "PSEUDOMONASBRASSICACEARUM", "https://purl.org/becyt/ford/1", "Transcriptomics", "0303 health sciences", "Comparative genomics", "Biocontrol", "RNA sequencing", "<i>Pseudomonas brassicacearum</i>", "BIOCONTROL", "Pseudomonas brassicacearum", "Biological Control Agents", "Genes", " Bacterial", "Transcriptome", "plant-growth promotion"]}, "links": [{"href": "http://www.mdpi.com/2073-4425/10/8/601/pdf"}, {"href": "https://www.mdpi.com/2073-4425/10/8/601/pdf"}, {"href": "https://doi.org/10.3390/genes10080601"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/Genes", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "10.3390/genes10080601", "name": "item", "description": "10.3390/genes10080601", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/10.3390/genes10080601"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2019-08-09T00:00:00Z"}}, {"id": "10.3390/ijms26020673", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:21:00Z", "type": "Journal Article", "created": "2025-01-15", "title": "Biofilm Formation, Modulation, and Transcriptomic Regulation Under Stress Conditions in Halomicronema sp.", "description": "<?xml version='1.0' encoding='UTF-8'?><article><p>In nature, bacteria often form heterogeneous communities enclosed in a complex matrix known as biofilms. This extracellular matrix, produced by the microorganisms themselves, serves as the first barrier between the cells and the environment. It is composed mainly of water, extracellular polymeric substances (EPS), lipids, proteins, and DNA. Cyanobacteria form biofilms and have unique characteristics such as oxygenic photosynthesis, nitrogen fixation, excellent adaptability to various abiotic stress conditions, and the ability to secrete a variety of metabolites and hormones. This work focused on the characterization of the cyanobacterium Halomicronema sp. strain isolated from a brackish environment. This study included microscopic imaging, determination of phenolic content and antioxidant capacity, identification of chemicals interfering with biofilm formation, and transcriptomic analysis by RNA sequencing and real-time PCR. Gene expression analysis was centered on genes related to the production of EPS and biofilm-related transcription factors. This study led to the identification of wza1 and wzt as EPS biomarkers and luxR-05665, along with genes belonging to the TetR/AcrR and LysR families, as potential biomarkers useful for studying and monitoring biofilm formation under different environmental conditions. Moreover, this work revealed that Halomicronema sp. can grow even in the presence of strong abiotic stresses, such as high salt, and has good antioxidant properties.</p></article>", "keywords": ["570", "Extracellular Polymeric Substance Matrix", "Gene Expression Profiling", "Gene Expression Regulation", " Bacterial", "stress resilience", "Cyanobacteria", "cyanobacteria", "Article", "transcriptomics", "Bacterial Proteins", "Halomicronema sp", "Stress", " Physiological", "Biofilms", "biofilm formation", "EPS", "Transcriptome"], "contacts": [{"organization": "Marina Caldara, Henk Bolhuis, Marta Marmiroli, Nelson Marmiroli,", "roles": ["creator"]}]}, "links": [{"href": "https://doi.org/10.3390/ijms26020673"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/International%20Journal%20of%20Molecular%20Sciences", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "10.3390/ijms26020673", "name": "item", "description": "10.3390/ijms26020673", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/10.3390/ijms26020673"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2025-01-15T00:00:00Z"}}, {"id": "10.3390/microorganisms8010013", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:21:03Z", "type": "Journal Article", "created": "2019-12-20", "title": "Genome Analyses and Genome-Centered Metatranscriptomics of Methanothermobacter wolfeii Strain SIV6, Isolated from a Thermophilic Production-Scale Biogas Fermenter", "description": "<?xml version='1.0' encoding='UTF-8'?><article><p>In the thermophilic biogas-producing microbial community, the genus Methanothermobacter was previously described to be frequently abundant. The aim of this study was to establish and analyze the genome sequence of the archaeal strain Methanothermobacter wolfeii SIV6 originating from a thermophilic industrial-scale biogas fermenter and compare it to related reference genomes. The circular chromosome has a size of 1,686,891 bases, featuring a GC content of 48.89%. Comparative analyses considering three completely sequenced Methanothermobacter strains revealed a core genome of 1494 coding sequences and 16 strain specific genes for M. wolfeii SIV6, which include glycosyltransferases and CRISPR/cas associated genes. Moreover, M. wolfeii SIV6 harbors all genes for the hydrogenotrophic methanogenesis pathway and genome-centered metatranscriptomics indicates the high metabolic activity of this strain, with 25.18% of all transcripts per million (TPM) belong to the hydrogenotrophic methanogenesis pathway and 18.02% of these TPM exclusively belonging to the mcr operon. This operon encodes the different subunits of the enzyme methyl-coenzyme M reductase (EC: 2.8.4.1), which catalyzes the final and rate-limiting step during methanogenesis. Finally, fragment recruitment of metagenomic reads from the thermophilic biogas fermenter on the SIV6 genome showed that the strain is abundant (1.2%) within the indigenous microbial community. Detailed analysis of the archaeal isolate M. wolfeii SIV6 indicates its role and function within the microbial community of the thermophilic biogas fermenter, towards a better understanding of the biogas production process and a microbial-based management of this complex process.</p></article>", "keywords": ["2. Zero hunger", "0301 basic medicine", "570", "Methanothermobacter wolfeii", "metagenomics", "0303 health sciences", "metatranscriptomics", "thermophilic biogas fermenter", "comparative analyses", "Methanothermobacter wolfeii; thermophilic biogas fermenter; genome mining; comparative analyses; CRISPR/cas; metabolic pathway reconstruction; metagenomics; fragment recruitment; metatranscriptomics", "CRISPR/<i>cas</i>", "metabolic pathway reconstruction", "7. Clean energy", "Article", "03 medical and health sciences", "CRISPR/cas", "genome mining", "8. Economic growth", "<i>Methanothermobacter wolfeii</i>", "fragment recruitment"]}, "links": [{"href": "http://www.mdpi.com/2076-2607/8/1/13/pdf"}, {"href": "https://www.mdpi.com/2076-2607/8/1/13/pdf"}, {"href": "https://doi.org/10.3390/microorganisms8010013"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/Microorganisms", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "10.3390/microorganisms8010013", "name": "item", "description": "10.3390/microorganisms8010013", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/10.3390/microorganisms8010013"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2019-12-20T00:00:00Z"}}, {"id": "11381/3018373", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:25:02Z", "type": "Journal Article", "created": "2025-01-15", "title": "Biofilm Formation, Modulation, and Transcriptomic Regulation Under Stress Conditions in Halomicronema sp.", "description": "<?xml version='1.0' encoding='UTF-8'?><article><p>In nature, bacteria often form heterogeneous communities enclosed in a complex matrix known as biofilms. This extracellular matrix, produced by the microorganisms themselves, serves as the first barrier between the cells and the environment. It is composed mainly of water, extracellular polymeric substances (EPS), lipids, proteins, and DNA. Cyanobacteria form biofilms and have unique characteristics such as oxygenic photosynthesis, nitrogen fixation, excellent adaptability to various abiotic stress conditions, and the ability to secrete a variety of metabolites and hormones. This work focused on the characterization of the cyanobacterium Halomicronema sp. strain isolated from a brackish environment. This study included microscopic imaging, determination of phenolic content and antioxidant capacity, identification of chemicals interfering with biofilm formation, and transcriptomic analysis by RNA sequencing and real-time PCR. Gene expression analysis was centered on genes related to the production of EPS and biofilm-related transcription factors. This study led to the identification of wza1 and wzt as EPS biomarkers and luxR-05665, along with genes belonging to the TetR/AcrR and LysR families, as potential biomarkers useful for studying and monitoring biofilm formation under different environmental conditions. Moreover, this work revealed that Halomicronema sp. can grow even in the presence of strong abiotic stresses, such as high salt, and has good antioxidant properties.</p></article>", "keywords": ["570", "Extracellular Polymeric Substance Matrix", "Gene Expression Profiling", "Gene Expression Regulation", " Bacterial", "stress resilience", "Cyanobacteria", "cyanobacteria", "Article", "transcriptomics", "Bacterial Proteins", "Halomicronema sp", "Stress", " Physiological", "Biofilms", "biofilm formation", "EPS", "Transcriptome"]}, "links": [{"href": "https://doi.org/11381/3018373"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/International%20Journal%20of%20Molecular%20Sciences", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "11381/3018373", "name": "item", "description": "11381/3018373", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/11381/3018373"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2025-01-15T00:00:00Z"}}, {"id": "2977681695", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:26:06Z", "type": "Journal Article", "created": "2019-10-04", "title": "Different expression pattern of flowering pathway genes contribute to male or female organ development during floral transition in the monoecious weedAmbrosia artemisiifoliaL. (Asteraceae)", "description": "<p>The highly allergenic and invasive weedAmbrosia artemisiifoliaL. is a monoecius plant with separated male and female flowers. The genetic regulation of floral morphogenesis is a less understood field in the reproduction biology of this species. Therefore the objective of this work was to investigate the genetic control of sex determination during floral organogenesis. To this end, we performed a genome-wide transcriptional profiling of vegetative and generative tissues during the plant development comparing wild-growing and in vitro cultivated plants. RNA-seq on Illumina NextSeq 500 platform with an integrative bioinformatics analysis indicated differences in 80 floral gene expressions depending on photoperiodic and endogenous initial signals. Sex specificity of genes was validated based on RT-qPCR experiments. We found 11 and 16 uniquely expressed genes in female and male transcriptomes that were responsible particularly to maintain fertility and against abiotic stress. High gene expression of homologous such as FD, FT, TFL1 and CAL, SOC1, AP1 were characteristic to male and female floral meristems during organogenesis. Homologues transcripts of LFY and FLC were not found in the investigated generative and vegetative tissues. The repression of AP1 by TFL1 homolog was demonstrated in male flowers resulting exclusive expression of AP2 and PI that controlled stamen and carpel formation in the generative phase. Alterations of male and female floral meristem differentiation were demonstrated under photoperiodic and hormonal condition changes by applying in vitro treatments.</p", "keywords": ["0301 basic medicine", "0303 health sciences", "QH301-705.5", "Bioinformatics", "R", "03 medical and health sciences", "Organ development", "Medicine", "Flowering pathway", "14. Life underwater", "Biology (General)", "Transcriptomics", "Ambrosia artemisiifolia", "Monoecious"]}, "links": [{"href": "https://doi.org/2977681695"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/PeerJ", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "2977681695", "name": "item", "description": "2977681695", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/2977681695"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2019-10-04T00:00:00Z"}}, {"id": "2995045825", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:26:07Z", "type": "Journal Article", "created": "2019-12-20", "title": "Genome Analyses and Genome-Centered Metatranscriptomics of Methanothermobacter wolfeii Strain SIV6, Isolated from a Thermophilic Production-Scale Biogas Fermenter", "description": "<?xml version='1.0' encoding='UTF-8'?><article><p>In the thermophilic biogas-producing microbial community, the genus Methanothermobacter was previously described to be frequently abundant. The aim of this study was to establish and analyze the genome sequence of the archaeal strain Methanothermobacter wolfeii SIV6 originating from a thermophilic industrial-scale biogas fermenter and compare it to related reference genomes. The circular chromosome has a size of 1,686,891 bases, featuring a GC content of 48.89%. Comparative analyses considering three completely sequenced Methanothermobacter strains revealed a core genome of 1494 coding sequences and 16 strain specific genes for M. wolfeii SIV6, which include glycosyltransferases and CRISPR/cas associated genes. Moreover, M. wolfeii SIV6 harbors all genes for the hydrogenotrophic methanogenesis pathway and genome-centered metatranscriptomics indicates the high metabolic activity of this strain, with 25.18% of all transcripts per million (TPM) belong to the hydrogenotrophic methanogenesis pathway and 18.02% of these TPM exclusively belonging to the mcr operon. This operon encodes the different subunits of the enzyme methyl-coenzyme M reductase (EC: 2.8.4.1), which catalyzes the final and rate-limiting step during methanogenesis. Finally, fragment recruitment of metagenomic reads from the thermophilic biogas fermenter on the SIV6 genome showed that the strain is abundant (1.2%) within the indigenous microbial community. Detailed analysis of the archaeal isolate M. wolfeii SIV6 indicates its role and function within the microbial community of the thermophilic biogas fermenter, towards a better understanding of the biogas production process and a microbial-based management of this complex process.</p></article>", "keywords": ["0301 basic medicine", "2. Zero hunger", "570", "Methanothermobacter wolfeii", "metagenomics", "0303 health sciences", "metatranscriptomics", "thermophilic biogas fermenter", "comparative analyses", "Methanothermobacter wolfeii; thermophilic biogas fermenter; genome mining; comparative analyses; CRISPR/cas; metabolic pathway reconstruction; metagenomics; fragment recruitment; metatranscriptomics", "CRISPR/<i>cas</i>", "metabolic pathway reconstruction", "7. Clean energy", "Article", "03 medical and health sciences", "CRISPR/cas", "genome mining", "8. Economic growth", "<i>Methanothermobacter wolfeii</i>", "fragment recruitment"]}, "links": [{"href": "http://www.mdpi.com/2076-2607/8/1/13/pdf"}, {"href": "https://www.mdpi.com/2076-2607/8/1/13/pdf"}, {"href": "https://doi.org/2995045825"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/Microorganisms", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "2995045825", "name": "item", "description": "2995045825", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/2995045825"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2019-12-20T00:00:00Z"}}, {"id": "10.7717/peerj.7421", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:24:30Z", "type": "Journal Article", "created": "2019-10-04", "title": "Different expression pattern of flowering pathway genes contribute to male or female organ development during floral transition in the monoecious weedAmbrosia artemisiifoliaL. (Asteraceae)", "description": "<p>The highly allergenic and invasive weedAmbrosia artemisiifoliaL. is a monoecius plant with separated male and female flowers. The genetic regulation of floral morphogenesis is a less understood field in the reproduction biology of this species. Therefore the objective of this work was to investigate the genetic control of sex determination during floral organogenesis. To this end, we performed a genome-wide transcriptional profiling of vegetative and generative tissues during the plant development comparing wild-growing and in vitro cultivated plants. RNA-seq on Illumina NextSeq 500 platform with an integrative bioinformatics analysis indicated differences in 80 floral gene expressions depending on photoperiodic and endogenous initial signals. Sex specificity of genes was validated based on RT-qPCR experiments. We found 11 and 16 uniquely expressed genes in female and male transcriptomes that were responsible particularly to maintain fertility and against abiotic stress. High gene expression of homologous such as FD, FT, TFL1 and CAL, SOC1, AP1 were characteristic to male and female floral meristems during organogenesis. Homologues transcripts of LFY and FLC were not found in the investigated generative and vegetative tissues. The repression of AP1 by TFL1 homolog was demonstrated in male flowers resulting exclusive expression of AP2 and PI that controlled stamen and carpel formation in the generative phase. Alterations of male and female floral meristem differentiation were demonstrated under photoperiodic and hormonal condition changes by applying in vitro treatments.</p", "keywords": ["0301 basic medicine", "0303 health sciences", "QH301-705.5", "Bioinformatics", "R", "03 medical and health sciences", "Organ development", "Medicine", "Flowering pathway", "14. Life underwater", "Biology (General)", "Transcriptomics", "Ambrosia artemisiifolia", "Monoecious"]}, "links": [{"href": "https://doi.org/10.7717/peerj.7421"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/PeerJ", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "10.7717/peerj.7421", "name": "item", "description": "10.7717/peerj.7421", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/10.7717/peerj.7421"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2019-10-04T00:00:00Z"}}, {"id": "10486/717838", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:24:51Z", "type": "Journal Article", "created": "2024-09-28", "title": "Metagenomic analyses of a consortium for the bioremediation of hydrocarbons polluted soils", "description": "Abstract<p>A bacterial consortium was isolated from a soil in Noblejas (Toledo, Spain) with a long history of mixed hydrocarbons pollution, by enrichment cultivation. Serial cultures of hydrocarbons polluted soil samples were grown in a minimal medium using diesel (1\uffc2\uffa0mL/L) as the sole carbon and energy source. The bacterial composition of the Noblejas Consortium (NC) was determined by sequencing 16S rRNA gene amplicon libraries. The consortium contained around 50 amplicon sequence variants (ASVs) and the major populations belonged to the genera Pseudomonas, Enterobacter, Delftia, Stenotrophomonas, Achromobacter, Acinetobacter, Novosphingobium, Allorhizobium-Neorhizobium-Rhizobium, Ochrobactrum and Luteibacter. All other genera were below 1%. Metagenomic analysis of NC has shown a high abundance of genes encoding enzymes implicated in aliphatic and (poly) aromatic hydrocarbons degradation, and almost all pathways for hydrocarbon degradation are represented. Metagenomic analysis has also allowed the construction of metagenome assembled genomes (MAGs) for the major players of NC. Metatranscriptomic analysis has shown that several of the ASVs are implicated in hydrocarbon degradation, being Pseudomonas, Acinetobacter and Delftia the most active populations.</p", "keywords": ["metagenomics", "Bacterial consortium; Bioremediation; Metagenomics; Metatranscriptomics; Total petroleum hydrocarbons", "metatranscriptomics", "Bacterial consortium", "Biolog\u00eda y Biomedicina / Biolog\u00eda", "Microbiology", "QR1-502", "Total petroleum hydrocarbons", "total petroleum hydrocarbons", "bioremediation", "Original Article", "Metagenomics", "Bioremediation", "TP248.13-248.65", "Metatranscriptomics", "Biotechnology"]}, "links": [{"href": "https://doi.org/10486/717838"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/AMB%20Express", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "10486/717838", "name": "item", "description": "10486/717838", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/10486/717838"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2024-09-28T00:00:00Z"}}, {"id": "11336/151981", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:25:00Z", "type": "Journal Article", "created": "2019-08-09", "title": "Genetic Potential of the Biocontrol Agent Pseudomonas brassicacearum (Formerly P. trivialis) 3Re2-7 Unraveled by Genome Sequencing and Mining, Comparative Genomics and Transcriptomics", "description": "<?xml version='1.0' encoding='UTF-8'?><article><p>The genus Pseudomonas comprises many known plant-associated microbes with plant growth promotion and disease suppression properties. Genome-based studies allow the prediction of the underlying mechanisms using genome mining tools and the analysis of the genes unique for a strain by implementing comparative genomics. Here, we provide the genome sequence of the strain Pseudomonas brassicacearum 3Re2-7, formerly known as P. trivialis and P. reactans, elucidate its revised taxonomic classification, experimentally verify the gene predictions by transcriptome sequencing, describe its genetic biocontrol potential and contextualize it to other known Pseudomonas biocontrol agents. The P. brassicacearum 3Re2-7 genome comprises a circular chromosome with a size of 6,738,544 bp and a GC-content of 60.83%. 6267 genes were annotated, of which 6113 were shown to be transcribed in rich medium and/or in the presence of Rhizoctonia solani. Genome mining identified genes related to biocontrol traits such as secondary metabolite and siderophore biosynthesis, plant growth promotion, inorganic phosphate solubilization, biosynthesis of lipo- and exopolysaccharides, exoproteases, volatiles and detoxification. Core genome analysis revealed, that the 3Re2-7 genome exhibits a high collinearity with the representative genome for the species, P. brassicacearum subsp. brassicacearum NFM421. Comparative genomics allowed the identification of 105 specific genes and revealed gene clusters that might encode specialized biocontrol mechanisms of strain 3Re2-7. Moreover, we captured the transcriptome of P. brassicacearum 3Re2-7, confirming the transcription of the predicted biocontrol-related genes. The gene clusters coding for 2,4-diacetylphloroglucinol (phlABCDEFGH) and hydrogen cyanide (hcnABC) were shown to be highly transcribed. Further genes predicted to encode putative alginate production enzymes, a pyrroloquinoline quinone precursor peptide PqqA and a matrixin family metalloprotease were also found to be highly transcribed. With this study, we provide a basis to further characterize the mechanisms for biocontrol in Pseudomonas species, towards a sustainable and safe application of P. brassicacearum biocontrol agents.</p></article>", "keywords": ["COMPARATIVE GENOMICS", "0301 basic medicine", "570", "Antifungal Agents", "Plant-growth promotion", "Biolog\u00eda", "comparative genomics", "Phloroglucinol", "PLANT-GROWTH PROMOTION", "Article", "Rhizoctonia", "12. Responsible consumption", "transcriptomics", "03 medical and health sciences", "https://purl.org/becyt/ford/1.6", "Genome mining", "Hydrogen Cyanide", "Pseudomonas", "genome mining", "RNA SEQUENCING", "TRANSCRIPTOMICS", "biocontrol", "GENOME MINING", "PSEUDOMONASBRASSICACEARUM", "https://purl.org/becyt/ford/1", "Transcriptomics", "2. Zero hunger", "0303 health sciences", "Comparative genomics", "Biocontrol", "RNA sequencing", "<i>Pseudomonas brassicacearum</i>", "3. Good health", "BIOCONTROL", "Pseudomonas brassicacearum", "Biological Control Agents", "Genes", " Bacterial", "Transcriptome", "plant-growth promotion"]}, "links": [{"href": "http://www.mdpi.com/2073-4425/10/8/601/pdf"}, {"href": "https://www.mdpi.com/2073-4425/10/8/601/pdf"}, {"href": "https://doi.org/11336/151981"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/Genes", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "11336/151981", "name": "item", "description": "11336/151981", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/11336/151981"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2019-08-09T00:00:00Z"}}, {"id": "3093542655", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:26:16Z", "type": "Journal Article", "created": "2020-10-19", "title": "Low-cost and High-throughput RNA-seq Library Preparation for Illumina Sequencing from Plant Tissue", "description": "Transcriptome analysis can provide clues to biological processes affected in different genetic backgrounds or/and under various conditions. The price of RNA sequencing (RNA-seq) has decreased enough so that medium- to large-scale transcriptome analyses in a range of conditions are feasible. However, the price and variety of options for library preparation of RNA-seq can still be daunting to those who would like to use RNA-seq for their first time or for a single experiment. Among the criteria for selecting a library preparation protocol are the method of RNA isolation, nucleotide fragmentation to obtain desired size range, and library indexing to pool sequencing samples for multiplexing. Here, we present a high-quality and a high-throughput option for preparing libraries from polyadenylated mRNA for transcriptome analysis. Both high-quality and high-throughput protocol options include steps of mRNA enrichment through magnetic bead-enabled precipitation of the poly-A tail, cDNA synthesis, and then fragmentation and adapter addition simultaneously through Tn5-mediated 'tagmentation'. All steps of the protocols have been validated with Arabidopsis thaliana leaf and seedling tissues and streamlined to work together, with minimal cost in money and time, thus intended to provide a beginner-friendly start-to-finish RNA-seq library preparation for transcriptome analysis.", "keywords": ["0301 basic medicine", "570", "0303 health sciences", "Arabidopsis thaliana", "QH301-705.5", "Plant", "580 Plants (Botany)", "Multiplexing", "Tagmentation", "03 medical and health sciences", "10126 Department of Plant and Microbial Biology", "10211 Zurich-Basel Plant Science Center", "RNA-seq", "Biology (General)", "Transcriptomics"]}, "links": [{"href": "https://escholarship.org/content/qt44f1027m/qt44f1027m.pdf"}, {"href": "https://doi.org/3093542655"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/BIO-PROTOCOL", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "3093542655", "name": "item", "description": "3093542655", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/3093542655"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2020-01-01T00:00:00Z"}}, {"id": "3191592786", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:26:23Z", "type": "Journal Article", "created": "2021-07-30", "title": "Transcriptomic markers of fungal growth, respiration and carbon-use efficiency", "description": "ABSTRACT                <p>Fungal metabolic carbon acquisition and its subsequent partitioning between biomass production and respiration, i.e. the carbon-use efficiency (CUE), are central parameters in biogeochemical modeling. However, current available techniques for estimating these parameters are all associated with practical and theoretical shortcomings, making assessments unreliable. Gene expression analyses hold the prospect of phenotype prediction by indirect means, providing new opportunities to obtain information about metabolic priorities. We cultured four different fungal isolates (Chalara longipes, Laccaria bicolor, Serpula lacrymans and Trichoderma harzianum) in liquid media with contrasting nitrogen availability and measured growth rates and respiration to calculate CUE. By relating gene expression markers to measured carbon fluxes, we identified genes coding for 1,3-\uffce\uffb2-glucan synthase and 2-oxoglutarate dehydrogenase as suitable markers for growth and respiration, respectively, capturing both intraspecific variation as well as within-strain variation dependent on growth medium. A transcript index based on these markers correlated significantly with differences in CUE between the fungal isolates. Our study paves the way for the use of these markers to assess differences in growth, respiration and CUE in natural fungal communities, using metatranscriptomic or the RT-qPCR approach.</p", "keywords": ["0301 basic medicine", "growth", "Fungal Proteins", "Laccaria", "03 medical and health sciences", "Ascomycota", "Research Letter", "Biologiska vetenskaper", "Trichoderma", "0303 health sciences", "metatranscriptomics", "Ecology", "Basidiomycota", "Biochemistry and Molecular Biology", "Fungi", "Biological Sciences", "Carbon", "Microbiology (Microbiology in the medical area to be 30109)", "Hypocreales", "carbon-use efficiency", "gene markers", "fungi", "Transcriptome", "respiration", "Biomarkers"]}, "links": [{"href": "https://pub.epsilon.slu.se/26755/1/hasby_f_a_et_al_220119.pdf"}, {"href": "http://academic.oup.com/femsle/article-pdf/368/15/fnab100/39805403/fnab100.pdf"}, {"href": "https://doi.org/3191592786"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/FEMS%20Microbiology%20Letters", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "3191592786", "name": "item", "description": "3191592786", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/3191592786"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2021-08-01T00:00:00Z"}}, {"id": "50|_____OmicsDI::acbfc5fca5fef3bf7778b7ffa0d20ee8", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:26:49Z", "type": "Dataset", "title": "Sulforaphane protects from T cell mediated autoimmune disease by inhibition of interleukin 23 and 12 in dendritic cells", "description": "Sulforaphane (SFN), an isothiocyanate, is part of an important group of naturally occurring small molecules with antiinflammatory properties. Even though the published reports are vague, most are best conceivable with an inhibition of T cell functions. We therefore analyzed the effect of SFN on T cell-mediated autoimmune disease. Feeding mice with SFN protected from severe experimental autoimmune encephalomyelitis (EAE). Disease amelioration was associated with reduced interleukin (IL)-17 and IFN-gamma expression in draining lymph nodes. In vitro, SFN treatment of T cells did not directly alter T cell cytokine secretion. In contrast, SFN treatment of dendritic cells (DC) inhibited TLR4-induced IL-12 and IL-23 production and the cytokine profile of T cells stimulated by SFN-treated DC. SFN suppressed TLR4-induced nuclear factor kappa B (NF\u03baB) activity, without affecting the degradation of its inhibitor (I\u03baB). Instead, SFN treatment of DC resulted in strong expression of the stress response protein heme oxygenase-1 (HO-1), which interacts with NF\u03baB p65 and inhibits its activity. Consistent with these findings, HO-1 bound to p65 and subsequently inhibited the p65 promoter activity within the IL23a and IL12b promoter region. Importantly, SFN suppressed Il23a and Il12b expression in vivo and silenced Th17/Th1 responses within the CNS . Our data show that SFN improves Th17/Th1-mediated autoimmune disease by inducing HO-1 and inhibiting p65-regulated IL-23 and IL-12 expression. Treatment-control experiment with two replicates per condition", "keywords": ["Transcriptomics", "3. Good health"]}, "links": [{"href": "https://doi.org/50|_____OmicsDI::acbfc5fca5fef3bf7778b7ffa0d20ee8"}, {"rel": "self", "type": "application/geo+json", "title": "50|_____OmicsDI::acbfc5fca5fef3bf7778b7ffa0d20ee8", "name": "item", "description": "50|_____OmicsDI::acbfc5fca5fef3bf7778b7ffa0d20ee8", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/50|_____OmicsDI::acbfc5fca5fef3bf7778b7ffa0d20ee8"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2014-02-13T00:00:00Z"}}, {"id": "50|_____OmicsDI::b3fcd5a36942334160f9f62c5f537589", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:26:49Z", "type": "Dataset", "title": "The kinase TNIK is an essential activator of Wnt target genes", "description": "Wnt signalling maintains the undifferentiated state of intestinal crypt/progenitor cells through the TCF4/\u00df-catenin activating transcriptional complex. In colorectal cancer, activating mutations in Wnt pathway components lead to inappropriate activation of the TCF4/\u00df-catenin transcriptional program and tumourigenesis in the gut epithelium. The mechanisms by which TCF4/\u00df-catenin activate key target genes are not well understood. Using a proteomics approach, we identified Tnik, a member of the Germinal centre kinase family, as a Tcf4 interactor in the proliferative crypts of mouse small intestine. Tnik is recruited to promoters of Wnt target genes in mouse crypts and in Ls174T colorectal cancer cells in a \u00df-catenin dependent manner. Depletion of TNIK and expression of TNIK kinase mutants abrogated TCF-LEF transcription, highlighting the essential role of the kinase activity in Wnt target gene activation. siRNA depletion of TNIK followed by expression array analysis demonstrated that TNIK is an essential and exclusive activator of Wnt induced transcriptional program. As an essential component in the TCF4/\u00df-catenin activator complex, the kinase TNIK may present an attractive candidate for drug targeting in colorectal cancer. HEK293T cells: Wnt3A vs control medium (CM) induction for 4, 7 and 9 hours; si-TNIK vs si-control after Wnt3A induction at 4 and 7 hours (2 biological replicates for 7 hour time point); dyeswap for each experiment (i.e. 12 arrays in total).", "keywords": ["Transcriptomics", "3. Good health"]}, "links": [{"href": "https://doi.org/50|_____OmicsDI::b3fcd5a36942334160f9f62c5f537589"}, {"rel": "self", "type": "application/geo+json", "title": "50|_____OmicsDI::b3fcd5a36942334160f9f62c5f537589", "name": "item", "description": "50|_____OmicsDI::b3fcd5a36942334160f9f62c5f537589", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/50|_____OmicsDI::b3fcd5a36942334160f9f62c5f537589"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2010-08-18T00:00:00Z"}}, {"id": "E-GEOD-45252", "type": "Feature", "geometry": null, "properties": {"license": "unspecified", "updated": "2026-07-25T16:27:57Z", "type": "Dataset", "title": "Diel growth of Thalassiosira pseudonana", "description": "Transcript levels of all T. pseudonana genes was measured every twelve hours throughout the batch (non-chemostatic) growth of axenic cells grown in large glass bioreactors on a 12hr:12hr dark:light cycle for five days. The data were analyzed to reveal the physiological and regulatory changes that recurred in this diatom when transitioning between dark and light conditions, as well as from exponential phase to stationary, nutrient limited conditions. The longitudinal experiment was performed with two replicates, at 400 and 800ppm CO2. Two growth experiments were conducted, with 10 and 9 longitudinal samples collected from each experiment, respectively. Two-color arrays were used with dye flips for labeling. A common internal reference sample was used for one channel on each array. Expression changes for longitudinal analysis were calculated as the difference from the mean log2 expression ratio for each to the common reference sample, for each gene, over all samples within an experiment. For the analysis of diel states in T. pseudonana, samples from the two series were matched according to the time from innoculation, and divided into four classes: dawn samples (taken at the end of each dark phase), dusk samples (taken at the end of each light phase), exponential samples (the first five samples in each series prior to a drop in growth rate on Day 3), and stationary samples (all samples including following the drop in growth rate on Day 3).", "keywords": ["Transcriptomics"]}, "links": [{"href": "https://doi.org/E-GEOD-45252"}, {"rel": "self", "type": "application/geo+json", "title": "E-GEOD-45252", "name": "item", "description": "E-GEOD-45252", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/E-GEOD-45252"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2013-04-18T00:00:00Z"}}, {"id": "PMC6779118", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:28:10Z", "type": "Journal Article", "created": "2019-10-04", "title": "Different expression pattern of flowering pathway genes contribute to male or female organ development during floral transition in the monoecious weedAmbrosia artemisiifoliaL. (Asteraceae)", "description": "<p>                     The highly allergenic and invasive weed                     Ambrosia artemisiifolia                     L. is a monoecius plant with separated male and female flowers. The genetic regulation of floral morphogenesis is a less understood field in the reproduction biology of this species. Therefore the objective of this work was to investigate the genetic control of sex determination during floral organogenesis. To this end, we performed a genome-wide transcriptional profiling of vegetative and generative tissues during the plant development comparing wild-growing and in vitro cultivated plants. RNA-seq on Illumina NextSeq 500 platform with an integrative bioinformatics analysis indicated differences in 80 floral gene expressions depending on photoperiodic and endogenous initial signals. Sex specificity of genes was validated based on RT-qPCR experiments. We found 11 and 16 uniquely expressed genes in female and male transcriptomes that were responsible particularly to maintain fertility and against abiotic stress. High gene expression of homologous such as FD, FT, TFL1 and CAL, SOC1, AP1 were characteristic to male and female floral meristems during organogenesis. Homologues transcripts of LFY and FLC were not found in the investigated generative and vegetative tissues. The repression of AP1 by TFL1 homolog was demonstrated in male flowers resulting exclusive expression of AP2 and PI that controlled stamen and carpel formation in the generative phase. Alterations of male and female floral meristem differentiation were demonstrated under photoperiodic and hormonal condition changes by applying in vitro treatments.                   </p", "keywords": ["0301 basic medicine", "0303 health sciences", "QH301-705.5", "Bioinformatics", "R", "03 medical and health sciences", "Organ development", "Medicine", "Flowering pathway", "14. Life underwater", "Biology (General)", "Transcriptomics", "Ambrosia artemisiifolia", "Monoecious"]}, "links": [{"href": "https://doi.org/PMC6779118"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/PeerJ", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "PMC6779118", "name": "item", "description": "PMC6779118", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/PMC6779118"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2019-10-04T00:00:00Z"}}, {"id": "PMC7022856", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:28:11Z", "type": "Journal Article", "created": "2019-12-20", "title": "Genome Analyses and Genome-Centered Metatranscriptomics of Methanothermobacter wolfeii Strain SIV6, Isolated from a Thermophilic Production-Scale Biogas Fermenter", "description": "<?xml version='1.0' encoding='UTF-8'?><article><p>In the thermophilic biogas-producing microbial community, the genus Methanothermobacter was previously described to be frequently abundant. The aim of this study was to establish and analyze the genome sequence of the archaeal strain Methanothermobacter wolfeii SIV6 originating from a thermophilic industrial-scale biogas fermenter and compare it to related reference genomes. The circular chromosome has a size of 1,686,891 bases, featuring a GC content of 48.89%. Comparative analyses considering three completely sequenced Methanothermobacter strains revealed a core genome of 1494 coding sequences and 16 strain specific genes for M. wolfeii SIV6, which include glycosyltransferases and CRISPR/cas associated genes. Moreover, M. wolfeii SIV6 harbors all genes for the hydrogenotrophic methanogenesis pathway and genome-centered metatranscriptomics indicates the high metabolic activity of this strain, with 25.18% of all transcripts per million (TPM) belong to the hydrogenotrophic methanogenesis pathway and 18.02% of these TPM exclusively belonging to the mcr operon. This operon encodes the different subunits of the enzyme methyl-coenzyme M reductase (EC: 2.8.4.1), which catalyzes the final and rate-limiting step during methanogenesis. Finally, fragment recruitment of metagenomic reads from the thermophilic biogas fermenter on the SIV6 genome showed that the strain is abundant (1.2%) within the indigenous microbial community. Detailed analysis of the archaeal isolate M. wolfeii SIV6 indicates its role and function within the microbial community of the thermophilic biogas fermenter, towards a better understanding of the biogas production process and a microbial-based management of this complex process.</p></article>", "keywords": ["2. Zero hunger", "0301 basic medicine", "570", "Methanothermobacter wolfeii", "metagenomics", "0303 health sciences", "metatranscriptomics", "thermophilic biogas fermenter", "comparative analyses", "CRISPR/<i>cas</i>", "metabolic pathway reconstruction", "7. Clean energy", "Article", "03 medical and health sciences", "CRISPR/cas", "genome mining", "8. Economic growth", "<i>Methanothermobacter wolfeii</i>", "fragment recruitment"]}, "links": [{"href": "http://www.mdpi.com/2076-2607/8/1/13/pdf"}, {"href": "https://www.mdpi.com/2076-2607/8/1/13/pdf"}, {"href": "https://doi.org/PMC7022856"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/Microorganisms", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "PMC7022856", "name": "item", "description": "PMC7022856", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/PMC7022856"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2019-12-20T00:00:00Z"}}, {"id": "PMC7842799", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:28:12Z", "type": "Journal Article", "created": "2020-10-19", "title": "Low-cost and High-throughput RNA-seq Library Preparation for Illumina Sequencing from Plant Tissue", "description": "Transcriptome analysis can provide clues to biological processes affected in different genetic backgrounds or/and under various conditions. The price of RNA sequencing (RNA-seq) has decreased enough so that medium- to large-scale transcriptome analyses in a range of conditions are feasible. However, the price and variety of options for library preparation of RNA-seq can still be daunting to those who would like to use RNA-seq for their first time or for a single experiment. Among the criteria for selecting a library preparation protocol are the method of RNA isolation, nucleotide fragmentation to obtain desired size range, and library indexing to pool sequencing samples for multiplexing. Here, we present a high-quality and a high-throughput option for preparing libraries from polyadenylated mRNA for transcriptome analysis. Both high-quality and high-throughput protocol options include steps of mRNA enrichment through magnetic bead-enabled precipitation of the poly-A tail, cDNA synthesis, and then fragmentation and adapter addition simultaneously through Tn5-mediated 'tagmentation'. All steps of the protocols have been validated with Arabidopsis thaliana leaf and seedling tissues and streamlined to work together, with minimal cost in money and time, thus intended to provide a beginner-friendly start-to-finish RNA-seq library preparation for transcriptome analysis.", "keywords": ["0301 basic medicine", "570", "0303 health sciences", "Arabidopsis thaliana", "QH301-705.5", "Plant", "580 Plants (Botany)", "Multiplexing", "Tagmentation", "03 medical and health sciences", "10126 Department of Plant and Microbial Biology", "10211 Zurich-Basel Plant Science Center", "RNA-seq", "Biology (General)", "Transcriptomics"]}, "links": [{"href": "https://escholarship.org/content/qt44f1027m/qt44f1027m.pdf"}, {"href": "https://doi.org/PMC7842799"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/BIO-PROTOCOL", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "PMC7842799", "name": "item", "description": "PMC7842799", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/PMC7842799"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2020-01-01T00:00:00Z"}}, {"id": "PMC8374604", "type": "Feature", "geometry": null, "properties": {"updated": "2026-07-25T16:28:12Z", "type": "Journal Article", "created": "2021-07-30", "title": "Transcriptomic markers of fungal growth, respiration and carbon-use efficiency", "description": "ABSTRACT                <p>Fungal metabolic carbon acquisition and its subsequent partitioning between biomass production and respiration, i.e. the carbon-use efficiency (CUE), are central parameters in biogeochemical modeling. However, current available techniques for estimating these parameters are all associated with practical and theoretical shortcomings, making assessments unreliable. Gene expression analyses hold the prospect of phenotype prediction by indirect means, providing new opportunities to obtain information about metabolic priorities. We cultured four different fungal isolates (Chalara longipes, Laccaria bicolor, Serpula lacrymans and Trichoderma harzianum) in liquid media with contrasting nitrogen availability and measured growth rates and respiration to calculate CUE. By relating gene expression markers to measured carbon fluxes, we identified genes coding for 1,3-\uffce\uffb2-glucan synthase and 2-oxoglutarate dehydrogenase as suitable markers for growth and respiration, respectively, capturing both intraspecific variation as well as within-strain variation dependent on growth medium. A transcript index based on these markers correlated significantly with differences in CUE between the fungal isolates. Our study paves the way for the use of these markers to assess differences in growth, respiration and CUE in natural fungal communities, using metatranscriptomic or the RT-qPCR approach.</p", "keywords": ["0301 basic medicine", "growth", "Fungal Proteins", "Laccaria", "03 medical and health sciences", "Ascomycota", "Research Letter", "Biologiska vetenskaper", "Trichoderma", "0303 health sciences", "metatranscriptomics", "Ecology", "Basidiomycota", "Biochemistry and Molecular Biology", "Fungi", "Biological Sciences", "Carbon", "Microbiology (Microbiology in the medical area to be 30109)", "Hypocreales", "carbon-use efficiency", "gene markers", "fungi", "Transcriptome", "respiration", "Biomarkers"]}, "links": [{"href": "https://pub.epsilon.slu.se/26755/1/hasby_f_a_et_al_220119.pdf"}, {"href": "http://academic.oup.com/femsle/article-pdf/368/15/fnab100/39805403/fnab100.pdf"}, {"href": "https://doi.org/PMC8374604"}, {"rel": "related", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/FEMS%20Microbiology%20Letters", "name": "related record", "description": "related record", "type": "application/json"}, {"rel": "self", "type": "application/geo+json", "title": "PMC8374604", "name": "item", "description": "PMC8374604", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items/PMC8374604"}, {"rel": "collection", "type": "application/json", "title": "Collection", "name": "collection", "description": "Collection", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main"}], "time": {"date": "2021-08-01T00:00:00Z"}}], "links": [{"rel": "self", "type": "application/geo+json", "title": "This document as GeoJSON", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items?keywords=Transcriptomics&f=json", "hreflang": "en-US"}, {"rel": "alternate", "type": "text/html", "title": "This document as HTML", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items?keywords=Transcriptomics&f=html", "hreflang": "en-US"}, {"rel": "collection", "type": "application/json", "title": "Collection URL", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main", "hreflang": "en-US"}, {"type": "application/geo+json", "rel": "first", "title": "items (first)", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items?keywords=Transcriptomics&", "hreflang": "en-US"}, {"rel": "last", "type": "application/geo+json", "title": "items (last)", "href": "https://repository.soilwise-he.eu/cat/collections/metadata:main/items?keywords=Transcriptomics&offset=25", "hreflang": "en-US"}], "numberMatched": 25, "numberReturned": 25, "distributedFeatures": [], "timeStamp": "2026-07-26T16:04:08.090714Z"}