Relevant bibliographies by topics / Cholerae sialidase

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  1. Journal articles
  2. Dissertations / Theses
  3. Conference papers

Academic literature on the topic 'Cholerae sialidase'

Author: Grafiati
Published: 4 June 2021
Last updated: 20 February 2023

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Journal articles on the topic "Cholerae sialidase"

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Jung, K., M. Pergande, and S. Klotzek. "Sialidase from different sources compared for electrophoretically separating serum alkaline phosphatase fractions from liver and bone." Clinical Chemistry 35, no. 9 (September 1, 1989): 1955–57. http://dx.doi.org/10.1093/clinchem/35.9.1955.

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Abstract We compared sialidase (neuraminidase; EC 3.2.1.18) from Vibrio cholerae, Clostridium perfringens, and Arthrobacter ureafaciens, seeking to improve the electrophoretic separation of the liver and bone isoenzymes of alkaline phosphatase (EC 3.1.3.1) on cellulose acetate membranes. Resolution is decisively determined by the type and activity of sialidase used in the preincubation of serum sample. Sialidase from Arthrobacter ureafaciens is not suited for this method. For optimal separation of the two isoenzymes we recommend the use of sialidase from Vibrio cholerae, determination of its a
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Khedri, Zahra, Yanhong Li, Hongzhi Cao, Jingyao Qu, Hai Yu, Musleh M. Muthana, and Xi Chen. "Synthesis of selective inhibitors against V. cholerae sialidase and human cytosolic sialidase NEU2." Organic & Biomolecular Chemistry 10, no. 30 (2012): 6112. http://dx.doi.org/10.1039/c2ob25335f.

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Dhanushkodi, Anandh, and Michael P. McDonald. "Intracranial V. cholerae Sialidase Protects against Excitotoxic Neurodegeneration." PLoS ONE 6, no. 12 (December 15, 2011): e29285. http://dx.doi.org/10.1371/journal.pone.0029285.

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Watson, Jacqueline N., Tara L. Knoll, Johnny H. Chen, Doug T. H. Chou, Thor J. Borgford та Andrew J. Bennet. "Use of conformationally restricted pyridinium α-D-N-acetylneuraminides to probe specificity in bacterial and viral sialidases". Biochemistry and Cell Biology 83, № 2 (1 квітня 2005): 115–22. http://dx.doi.org/10.1139/o04-126.

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Investigations into subtle changes in the catalytic activity of sialidases have been performed using enzymes from several different origins, and their results have been compared. This work highlights the potential pitfalls encountered when extending conclusions derived from mechanistic studies on a single enzyme even to those with high-sequence homology. Specifically, a panel of 5 pyridinium N-acetylneuraminides were used as substrates in a study that revealed subtle differences in the catalytic mechanisms used by 4 different sialidase enzymes. The lowest reactivity towards the artificial (pyr
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5

Chuenkova, M., and M. E. Pereira. "Trypanosoma cruzi trans-sialidase: enhancement of virulence in a murine model of Chagas' disease." Journal of Experimental Medicine 181, no. 5 (May 1, 1995): 1693–703. http://dx.doi.org/10.1084/jem.181.5.1693.

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Trypanosoma cruzi, the etiological agent of Chagas' disease, expresses a trans-sialidase at highest levels in infective trypomastigotes, where it attaches to the plasma membrane by a glycophosphoinositol linkage. Bound enzyme sheds into the extracellular milieu in a soluble form. Experiments performed in vitro suggest that the trans-sialidase participates in several parameters of T. cruzi-host interactions, like cell adhesion and complement resistance. However, the role that membrane-bound and soluble trans-sialidase plays in the infection of mammals is not understood. To begin to study the ro
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Slack, Teri J., Wanqing Li, Dashuang Shi, John B. McArthur, Gengxiang Zhao, Yanhong Li, An Xiao, et al. "Triazole-linked transition state analogs as selective inhibitors against V. cholerae sialidase." Bioorganic & Medicinal Chemistry 26, no. 21 (November 2018): 5751–57. http://dx.doi.org/10.1016/j.bmc.2018.10.028.

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7

Powell, L. D., S. W. Whiteheart, and G. W. Hart. "Cell surface sialic acid influences tumor cell recognition in the mixed lymphocyte reaction." Journal of Immunology 139, no. 1 (July 1, 1987): 262–70. http://dx.doi.org/10.4049/jimmunol.139.1.262.

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Abstract The Ia+ B cell lymphoma, AKTB-1b, fails to stimulate thymic lymphocytes in a one-way mixed lymphocyte reaction unless pretreated with sialidase or inhibitors of N-linked oligosaccharide processing. A comparison of different sialidases and sialyltransferases suggests that the removal of only a subset of total surface sialic acid, rather than net desialylation of the cell surface, is required. Three sialidases were compared, including Vibrio cholerae (VC) and Clostridium perfringens (CP), which will cleave alpha 2-3, alpha 2-6, and alpha 2-8, sialic acid linkages, and Newcastle Disease
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Mann, Maretta C., Robin J. Thomson, Jeffrey C. Dyason, Sarah McAtamney, and Mark von Itzstein. "Modelling, synthesis and biological evaluation of novel glucuronide-based probes of Vibrio cholerae sialidase." Bioorganic & Medicinal Chemistry 14, no. 5 (March 2006): 1518–37. http://dx.doi.org/10.1016/j.bmc.2005.10.004.

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Wilson, Jennifer C., Robin J. Thomson, Jeffrey C. Dyason, Pas Florio, Kaylene J. Quelch, Samia Abo, and Mark von Itzstein. "The design, synthesis and biological evaluation of neuraminic acid-based probes of Vibrio cholerae sialidase." Tetrahedron: Asymmetry 11, no. 1 (January 2000): 53–73. http://dx.doi.org/10.1016/s0957-4166(99)00552-2.

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Wallimann, Kurt, and Andrea Vasella. "Phosphonic-Acid Analogues of the N-Acetyl-2-deoxyneiiraniinic Acids: Synthesis and Inhibition ofVibrio cholerae Sialidase." Helvetica Chimica Acta 73, no. 5 (August 8, 1990): 1359–72. http://dx.doi.org/10.1002/hlca.19900730523.

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Dissertations / Theses on the topic "Cholerae sialidase"

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Mann, Maretta Clare, and n/a. "Sialylmimetics as Potential Inhibitors fo Vibrio Cholerae Sialidase." Griffith University. Institute for Glycomics, 2004. http://www4.gu.edu.au:8080/adt-root/public/adt-QGU20061006.083947.

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Cholera is an epidemic infectious diarrhoeal disease that for centuries has proven its frightening ability to cause rapid and widespread loss of human life. All symptoms associated with cholera are a result of rapid dehydration due to infection by pathogenic strains of the bacterium Vibrio cholerae. The damaging effects associated with cholera are mainly attributed to the toxin, which is secreted by the bacterium and infects cells lining the gastrointestinal tract. A sialidase, also secreted by the bacterium, is believed to facilitate toxin uptake by the gastrointestinal epithelium. V. cholera
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Mann, Maretta Clare. "Sialylmimetics as Potential Inhibitors fo Vibrio Cholerae Sialidase." Thesis, Griffith University, 2004. http://hdl.handle.net/10072/367187.

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Cholera is an epidemic infectious diarrhoeal disease that for centuries has proven its frightening ability to cause rapid and widespread loss of human life. All symptoms associated with cholera are a result of rapid dehydration due to infection by pathogenic strains of the bacterium Vibrio cholerae. The damaging effects associated with cholera are mainly attributed to the toxin, which is secreted by the bacterium and infects cells lining the gastrointestinal tract. A sialidase, also secreted by the bacterium, is believed to facilitate toxin uptake by the gastrointestinal epithelium. V. cholera
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Conference papers on the topic "Cholerae sialidase"

1

Haselhorst, Thomas, Carolyn Trower, Jennifer Wilson, Ross Coppel, and Mark von Itzstein. "EPITOPE MAPPING BY SATURATION TRANSFER DIFFERENCE NMR OF SIALIC ACID MIMETICS WITH VIBRIO CHOLERAE SIALIDASE." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.514.

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Journal articles
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