Relevant bibliographies by topics / UDP-glucose dehydrogenase

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  1. Dissertations / Theses

Academic literature on the topic 'UDP-glucose dehydrogenase'

Author: Grafiati
Published: 4 June 2021
Last updated: 18 February 2022

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Dissertations / Theses on the topic "UDP-glucose dehydrogenase"

1

Ge, Xue. "Covalent catalysis in the UDP-glucose dehydrogenase reaction." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape3/PQDD_0019/NQ48638.pdf.

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2

Campbell, Robert E. "The structure and mechanism of UDP-glucose dehydrogenase." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape2/PQDD_0019/NQ56519.pdf.

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3

Van, der Merwe Jennie. "Isolation and evaluation of the sugarcane UDP-glucose dehydrogenase gene and promoter." Thesis, Link to the online version, 2006. http://hdl.handle.net/10019/1254.

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4

Roman, Elisabet. "Studies on the Role of UDP-Glucose Dehydrogenase in Polysaccharide Biosynthesis." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Univ.-bibl. [distributör], 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-4657.

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5

Johansson, Henrik. "Gene regulation of UDP-glucose synthesis and metabolism in plants." Doctoral thesis, Umeå University, Plant Physiology, 2003. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-93.

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<p>Photosynthesis captures light from the sun and converts it into carbohydrates, which are utilised by almost all living organisms. The conversion between the different forms of carbohydrates is the basis to form almost all biological molecules.</p><p>The main intention of this thesis has been to study the role of UDP-glucose in carbohydrate synthesis and metabolism, and in particular the genes that encode UDP-glucose pyrophosphorylase (UGPase) and UDP-glucose dehydrogenase (UGDH) in plants and their regulation. UGPase converts glucose-1-phosphate to UDP-glucose, which can be utilised for suc
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6

Ramoutar, Rakeshnie. "The development of an in situ hybridisation technique to determine the gene expression patterns of UDP-Glucose dehydrogenase, pyrophosphate-dependent phosphofructokinase and UDP-Glucose pyrophosphorylase in sugarcane internodal tissues." Thesis, Stellenbosch : Stellenbosch University, 2003. http://hdl.handle.net/10019.1/49795.

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Thesis (MSc)--University of Stellenbosch, 2003.<br>ENGLISH ABSTRACT: The cellular expression of the enzymes implicated in regulating sucrose metabolism and accumulation in sugarcane is poorly understood. The present study was therefore aimed at the development of an in situ hybridisation (ISH) technique to study differential gene expression among the various cell types of the sugarcane culm. This technique in conjunction with northern and western blotting was then used to determine the sites of cellular and tissue specific expression of the cytosolic enzymes, UDP-Glc dehydrogenase, pyrop
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7

Brinck, Jonas. "The expression and regulation of hyaluronan synthases and their role in glycosaminoglycan synthesis." Doctoral thesis, Uppsala University, Department of Medical Biochemistry and Microbiology, 2000. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-505.

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<p>The glycosaminoglycan hyaluronan is an essential component of the extracellular matrix in all higher organisms, affecting cellular processes such as migration, proliferation and differentiation. Hyaluronan is synthesized by a plasma membrane bound hyaluronan synthase (HAS) which exists in three genetic isoforms. This thesis focuses on the understanding of the hyaluronan biosynthesis by studies on the expression and regulation of the HAS proteins.</p><p>In order to characterize the structural and functional properties of the HAS isoforms we developed a method to solubilize HAS protein(s) whi
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8

Rocha, Joana Raquel M. "Structure to function studies in UDP-glucose dehydrogenases and nitroreductases." Doctoral thesis, Universidade Nova de Lisboa. Instituto de Tecnologia Química e Biológica, 2010. http://hdl.handle.net/10362/4077.

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The thesis is divided into two parts corresponding to structural studies on two different proteins. The first part concerns the study of two UDP-glucose dehydrogenases (UGDs) from Sphingomonas elodea ATCC 31461 and Burkholderia cepacia IST 408, both involved in exopolysaccharide production. Their relevance arises because some of these bacterial exopolysaccharides are valuable as established biotechnological products, the former case, whilst others are highly problematic, when used by pathogens in biofilm formation over biological surfaces, as the latter case, namely in the human lungs.
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9

Ya-Ting and 周雅婷. "Cloning of the Human UDP-Glucose Dehydrogenase." Thesis, 2007. http://ndltd.ncl.edu.tw/handle/18434607712380211459.

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碩士<br>中山醫學大學<br>營養學研究所<br>95<br>In this study, the search tool BLAST (Basic Local Alignment Search Tool), based on NCBI (National Center for Biotechnology Information) was used against nucleotide and protein database. The analysis found a UDP-glucose dehydrogenase (UGDH) of zebrafish (NCBI accession number NM_131852/ NP_571927) and human (NCBI accession number NM_131852/ NP_571927). The UGDH cDNA of zebrafish and human were successfully amplified with a continuous open reading frame of 1482 and 1485 bps encoding a protein of 493 and 494 amino acids with a calculated molecular mass of 54.480 an
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10

Ge, Xue. "Covalent catalyst in the UDP-glucose dehydrogenase." Thesis, 2000. http://hdl.handle.net/2429/11419.

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UDP-glucose dehydrogenase from Streptococcus pyogenes (EC 1.1.1.22) is a NAD ⁺- dependent enzyme that catalyzes the 4-electron oxidation of UDP-glucose to UDPglucuronic acid without the release of an aldehyde intermediate. This enzyme is interesting because its single active site carries out two sequential oxidations, converting an alcohol to a carboxylic acid, whereas most NAD+-dependent dehydrogenases catalyze only a single step of oxidation. The recombinant dehydrogenase was purified to homogeneity and determined to have a k[sub cal] of 1.8 ± 0.1 s⁻¹ and an apparent K[sub m] of 20 ±
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