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http://dx.doi.org/10.1016/0014-4894(72)90026-4 | DOI Listing |
Glycobiology
January 2025
Wellcome Centre for Anti-Infectives Research, Biological Chemistry and Drug Discovery, School of Life Sciences, Dow Street, University of Dundee, Dundee DD1 5HN, United Kingdom.
For studies involving glycosyltransferases and nucleotide sugar transporters, radioactive nucleotide sugars are critical reagents. Of these, GDP-L-[3H]Fucose is currently commercially unavailable. Here, we present a facile approach for the preparation of GDP-[3H]-L-Fucose, using the enzymatic machinery present in the cytosol of the non-infectious and easily cultivated protozoan, Crithidia fasciculata, and its purification by solid phase extraction ion exchange chromatography.
View Article and Find Full Text PDFmSphere
October 2024
Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Trypanosomatids are single-celled parasites responsible for human and animal disease. Typically, colonization of an insect host is required for transmission. Stable attachment of parasites to insect tissues their single flagellum coincides with differentiation and morphological changes.
View Article and Find Full Text PDFJ Biol Chem
August 2024
Wellcome Centre for Anti-Infectives Research, Division of Biological Chemistry and Drug Discovery, School of Life Sciences, University of Dundee, Dundee, Scotland, UK. Electronic address:
Exp Parasitol
July 2024
Department of Biology, Villanova University, Villanova, PA, 19085, USA. Electronic address:
Crithidia bombi is a trypanosomatid parasite that infects several species of bumble bees (Bombus spp.), by adhering to their intestinal tract. Crithidia bombi infection impairs learning and reduces survival of workers and the fitness of overwintering queens.
View Article and Find Full Text PDFPLoS Pathog
February 2024
Institute for Immunology and Infection Research, School of Biological Sciences, University of Edinburgh, Ashworth laboratories, Charlotte Auerbach Road, Edinburgh, United Kingdom.
Trypanosomatid parasites undergo developmental regulation to adapt to the different environments encountered during their life cycle. In Trypanosoma brucei, a genome wide selectional screen previously identified a regulator of the protein family ESAG9, which is highly expressed in stumpy forms, a morphologically distinct bloodstream stage adapted for tsetse transmission. This regulator, TbREG9.
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