TY - THES A1 - Erdmann, Eileen A. T1 - Genetic tools for targeted genome editing and random mutagenesis of the rock-inhabiting black fungus Knufia petricola N2 - Rock-inhabiting black fungi are ubiquitously found on sun-exposed natural and human-made surfaces. These stresstolerant biofilm-formers are known to force the deterioration of the colonized surfaces. Black fungi belong to different classes of Ascomycota (Arthoniomycetes, Eurotiomycetes, and Dothideomycetes) but evolved the same morpho-physiological adaptations such as strong melanized multilayered cell walls and slow yeast-like or meristematic growth to resist extreme environmental conditions. The rock-inhabitant Knufia petricola was chosen as representative of the polyphyletic group of black fungi for studying mineral weathering, biofilm formation, and interaction with phototrophic microbes. For understanding the molecular basis of these traits, the genetic information and its regulation must be explored. Thus, the genome was sequenced, first -omics datasets obtained and protocols for the transformation of protoplasts and CRISPR/Cas9-based genome editing were implemented to enable genetic studies. In scope of this work, the transformation protocol was optimized to improve the regeneration of K. petricola protoplasts. The successful implementation of multiplexed CRISPR/Cas9 and three additional selection marker systems (geneticin/nptII, glufosinate/bar, chlorimuron ethyl/sur) extended the existing strategies for targeted genome editing. While in the first promoter studies only constitutive promoters (PoliC, PgpdA) were identified as appropriate for expression of fluorescent reporter genes in K. petricola, the functionality of an inducible promoter (synthetic TET-on promoter system) could later be demonstrated. The identification and validation of defined genomic insertion sites enabled the neutral or color-based selection (igr1-5 or pks1, phs1, ade2) as well as the detection of correctly integrated expression constructs. Using the color-based transformant screening (black – pink/white/rose) accelerated the selection of transformants, especially for localization and protein-protein interaction studies (e.g., by studying bimolecular fluorescence complementation). Additionally, the fusion of two or three genes via the viral P2A motif was shown to allow the expression of multiple genes from a single expression cassette/integration site. Finally, the established tools enabled the implementation of a forward genetics tool (customized Ac/Ds transposon system) for regulatable in-vivo mutagenesis of K. petricola. The isolation and characterization of revertants/Ds reinsertion mutants demonstrated the functionality of the system which marks an important milestone for assigning functions to yet unknown species- and/or trait-specific genes. In sum, the genetic engineering toolbox is now fully equipped which paves the way for exploring the biology of K. petricola and other black fungi. KW - Microcolonial fungi KW - Genetic engineering KW - CRISPR/Cas9-mediated genome editing KW - DHN melanin KW - Transposon mutagenesis PY - 2024 SP - 1 EP - 231 CY - Berlin AN - OPUS4-62364 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 -