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        <datestamp>2026-10-01T16:18:46Z</datestamp>
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          <dc:title>Investigating the importance of queuosine (Q) as a novel micronutrient in human ageing and brain health</dc:title>
          <dc:creator>Swathine Chandrasekaran (24292004)</dc:creator>
          <dc:subject>PUREID: 660115194</dc:subject>
          <dc:subject>micronutrients</dc:subject>
          <dc:subject>tRNA Modifications</dc:subject>
          <dc:subject>queuosine</dc:subject>
          <dc:subject>LC-MS/MS Assay</dc:subject>
          <dc:subject>gut microbiome</dc:subject>
          <dc:subject>human and animal nutrition</dc:subject>
          <dc:subject>dietary intervention</dc:subject>
          <dc:description>Queuosine (Q),a micronutrient derived primarily from the gut microbiome and dietary intake, plays a crucial role in RNA modification and cellular function. This thesis explores the human requirement for Q by quantifying its presence in commonly consumed foods, assessing its levels inhuman biological samples, and evaluating the influence of the gut microbiome on its availability. A dual extraction method and an advanced LC-MS/MS analytical technique were developed and validated to accurately detect both free and tRNA-bound Q metabolites across various sample types. Analysis of a wide range of UK-based dietary items revealed that Q is unevenly distributed, with dairy products, particularly fermented varieties like probiotic yoghurt, emerging as the richest sources. High levels of various Q metabolites were also identified in edible mushrooms and certain animal-derived foods. Data from the NIDAS cohort showed a wide range in daily Q intake among UK adults, influenced by dietary diversity, with a higher intake associated with consumption of multiple Q-rich food sources. A novel SPE and LC-MS/MS method enabled robust extraction and quantification of queuine (q) and Q in human blood. Analysis of blood revealed that q is the predominant circulating form, while Q is present only in trace amounts. Baseline serum q levels correlated with dietary intake, implying the role of diet in q acquisition. Finally, the contribution of the gut microbiota to Q availability was explored through a piglet study, demonstrating that microbial composition, dietary transitions, and zinc supplementation influenced Q metabolite levels. These findings underscore the complex interplay between diet, host metabolism, and the microbiome in regulating Q bioavailability. This research establishes the foundation and advances our understanding of the human requirement for dietary micronutrient Q and its derivatives.&lt;br&gt;&lt;br&gt;&lt;i&gt;Thesis embargoed until 31st December 2030&lt;/i&gt;&lt;br&gt;</dc:description>
          <dc:date>2026-10-01T16:18:46Z</dc:date>
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          <dc:identifier>10.17034/32805056.v1</dc:identifier>
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          <dc:rights>All Rights Reserved</dc:rights>
          <dc:rights>Open Access after 2030-12-31</dc:rights>
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