Sirvi Märksõna "acetogen" järgi
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listelement.badge.dso-type Kirje , listelement.badge.access-status Embargo , CRISPRi knockdown of acetate and 2,3-butanediol production-related genes in a gas-fermenting acetogen(Tartu Ülikool, 2023) Kõrgnurm, Koit; Tartu Ülikool. Loodus- ja täppisteaduste valdkond; Tartu Ülikool. Molekulaar- ja rakubioloogia instituutGas fermentation allows to convert carbon oxide emissions into value-added products using acetogen bacteria. This thesis aimed at creating a CRISPR/Cas9-based gene knockdown (KD) system to reduce expression of two genes in the model-acetogen C. autoethanogenum: 1) alpha-acetolactate decarboxylase (budA) in the 2,3-butanediol (2,3-BDO) and 2) phosphotransacetylase (pta) in the acetate synthesis pathway. Six KD plasmids were designed where single guide RNAs (sgRNAs) targeted three unique positions per gene, plus one plasmid as a non-targeting control. Notably, KD of budA expression abolished 2,3-BDO production but showed varied effects on autotrophic growth. pta KD strains showed strong repression of ptaexpression, slower growth for two sgRNAs, and, surprisingly, higher acetate-to-ethanol ratios than the control strain. This work contributes towards engineering and understanding of acetogen metabolism by establishing a gene KD system for a model-acetogenlistelement.badge.dso-type Kirje , listelement.badge.access-status Embargo , CRISPRi knockdown of acetate and 2,3-butanediol production-related genes in a gas-fermenting acetogen(Tartu Ülikool, 2023) Kõrgnurm, Koit; Tartu Ülikool. Loodus- ja täppisteaduste valdkond; Tartu Ülikool. Molekulaar- ja rakubioloogia instituutGas fermentation allows to convert carbon oxide emissions into value-added products using acetogen bacteria. This thesis aimed at creating a CRISPR/Cas9-based gene knockdown (KD) system to reduce expression of two genes in the model-acetogen C. autoethanogenum: 1) alpha-acetolactate decarboxylase (budA) in the 2,3-butanediol (2,3-BDO) and 2) phosphotransacetylase (pta) in the acetate synthesis pathway. Six KD plasmids were designed where single guide RNAs (sgRNAs) targeted three unique positions per gene, plus one plasmid as a non-targeting control. Notably, KD of budA expression abolished 2,3-BDO production but showed varied effects on autotrophic growth. pta KD strains showed strong repression of pta expression, slower growth for two sgRNAs, and, surprisingly, higher acetate-to-ethanol ratios than the control strain. This work contributes towards engineering and understanding of acetogen metabolism by establishing a gene KD system for a model-acetogen.listelement.badge.dso-type Kirje , listelement.badge.access-status Embargo , Effects of Disruption of Genes With Unknown Function in the C1-Fixing Gene Cluster on a Gas-Fermenting Acetogen(Tartu Ülikool, 2025) Vorontsova, Mariia; Valgepea, Kaspar, juhendaja; Nwaokorie, Ugochi Jennifer, juhendaja; Tartu Ülikool. Loodus- ja täppisteaduste valdkond; Tartu Ülikool. Bioinseneeria instituutGas fermentation is a promising technology for producing chemicals, fuels, and feed proteins from greenhouse gases and solid waste using gas-fermenting microbes. Acetogens are the most attractive biocatalysts for gas fermentation as they can use C1 gases carbon monoxide (CO) and carbon dioxide (CO2) as their sole carbon source using the Wood-Ljungdahl pathway (WLP). Genes encoding WLP enzymes are located in a C1-fixing gene cluster that also contains several genes with unclear function. In this work, the role of two such genes were investigated through gene disruption in the model-acetogen Clostridium autoethanogenum. For this, CRISPR/Cas9n plasmids were constructed and used for knock-out (KO) of the glycine cleavage system H protein (gcvH) and double knock-out (dKO) of gcvH and the first 80 bp of the adjacent acsV gene. Phenotypic characterisation of ∆gcvH in autotrophic batch cultures revealed significant growth defects and altered yields of acetate and 2,3-butanediol (2,3-BDO) compared to the parental LAbrini strain. Additionally, ∆gcvH showed a very long lag phase during growth without yeast extract. Supplementing cultures with glycine shortened the lag phase but did not restore normal growth, suggesting gcvH involvement in glycine synthesis. Notably, the dKO ∆gcvH∆acsV strain failed to grow autotrophically and phenotypic characterisation of heterotrophic batch cultures revealed significant growth defects and higher 2,3-BDO and ethanol product yields compared to LAbrini. Our findings shed light on the potential links between the glycine cleavage system and WLP and contribute towards a better understanding of carbon fixation in acetogens.listelement.badge.dso-type Kirje , listelement.badge.access-status Embargo , Growth and phenotype characterization of laboratory evolved gas-fermenting acetogen strains(Tartu Ülikool, 2022) Yar Saqib, Asfand; Tartu Ülikool. Loodus- ja täppisteaduste valdkond; Tartu Ülikool. Tehnoloogiainstituut