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Current Selection
Status : Active
Research Topic : Cell Reprogramming
Field of Research : Cell Metabolism
Australian State/Territory : SA
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Biochemistry and Cell Biology (3)
Cell Metabolism (3)
Analytical Biochemistry (1)
Cell Development, Proliferation and Death (1)
Cell and Nuclear Division (1)
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  • Active Funded Activity

    Discovery Projects - Grant ID: DP210103065

    Funder
    Australian Research Council
    Funding Amount
    $472,496.00
    Summary
    Signaling in the crypt: a novel metabolic pathway in intestinal stem cells. The gut is the most rapidly renewing tissue in the body, driven by a highly active stem cell niche. Bile acids are emerging as critical regulators of this stem cell niche and disruption of bile acid homeostasis has profoundly adverse effects on intestinal renewal and hence gut health. We are addressing a critical gap in our understanding of how bile acids are controlled within stem cell niche. The aim of the project is .... Signaling in the crypt: a novel metabolic pathway in intestinal stem cells. The gut is the most rapidly renewing tissue in the body, driven by a highly active stem cell niche. Bile acids are emerging as critical regulators of this stem cell niche and disruption of bile acid homeostasis has profoundly adverse effects on intestinal renewal and hence gut health. We are addressing a critical gap in our understanding of how bile acids are controlled within stem cell niche. The aim of the project is to define the critical role of a novel enzyme called UGT8 in controlling intestinal stem cell response to bile acids; this is achieved by modulating UGT8 activity in intestinal stem cell models and determining the effects on stem cell function and the key signalling pathways that control intestinal homeostasis and renewal.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP220103531

    Funder
    Australian Research Council
    Funding Amount
    $480,564.00
    Summary
    How do cells survive nutrient stress? Insight into mechanisms. This project studies cell survival under nutrient stress in eukaryotes. Building on extensive preliminary data that identifies novel TOR (Target of Rapamycin) Complex 2 (TORC2) control points it expects to generate new knowledge of critical and conserved features of stress control of macroautophagy that ensures cell survival. It uses interdisciplinary and innovative approaches to validate and characterize nutrient-stress dependent si .... How do cells survive nutrient stress? Insight into mechanisms. This project studies cell survival under nutrient stress in eukaryotes. Building on extensive preliminary data that identifies novel TOR (Target of Rapamycin) Complex 2 (TORC2) control points it expects to generate new knowledge of critical and conserved features of stress control of macroautophagy that ensures cell survival. It uses interdisciplinary and innovative approaches to validate and characterize nutrient-stress dependent signaling. Expected outcomes include novel insights into environmental control of cell proliferation and forging cross institutional collaborations. This knowledge benefits basic and applied biology and is relevant to industries/projects utilizing living cells as nutrient supports cell survival and proliferation.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP220103934

    Funder
    Australian Research Council
    Funding Amount
    $621,200.00
    Summary
    Structure and metabolism of bioactive carbohydrates from brown algae. Brown algae produce a diversity of species-specific carbohydrates in their cell walls that exhibit a variety of biological activities that can be exploited for the development of functional food and biopharmaceutical formulations. However, the metabolic pathways responsible for the biosynthesis of these carbohydrates are poorly characterised. This multidisciplinary project aims to understand the molecular events that control t .... Structure and metabolism of bioactive carbohydrates from brown algae. Brown algae produce a diversity of species-specific carbohydrates in their cell walls that exhibit a variety of biological activities that can be exploited for the development of functional food and biopharmaceutical formulations. However, the metabolic pathways responsible for the biosynthesis of these carbohydrates are poorly characterised. This multidisciplinary project aims to understand the molecular events that control the structure and metabolism of bioactive carbohydrates in the prominent Australian brown alga Ecklonia radiata, with particular focus on alginates and fucoidans. This knowledge will be used to produce in yeast bioactive oligosaccharides that are of high commercial interest to the biopharmaceutical industry.
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