Galactofuranosyl-containing glycans: Occurrence, synthesis and biochemistry

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Galactofuranosyl units (Galf), mainly in the β-configuration, are constituents of infectious microorganisms, such as the Mycobacteria, trypanosomatids like Trypanosoma cruzi and Leishmania, and fungi like Aspergillus fumigatus. The metabolic pathways involved in the biosynthesis of the microbial gly...

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Autor principal: Marino, C.
Otros Autores: Gallo-Rodriguez, C., de Lederkremer, R.M
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: Nova Science Publishers, Inc. 2012
Acceso en línea:Registro en Scopus
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Biblioteca Central Dr. Luis F. Leloir (FCEN) de Universidad de Buenos Aires
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100 1 |a Marino, C. 
245 1 0 |a Galactofuranosyl-containing glycans: Occurrence, synthesis and biochemistry 
260 |b Nova Science Publishers, Inc.  |c 2012 
270 1 0 |m de Lederkremer, R.M.; CIHIDECAR-CONICET, Departamento de Química Orgánica, Universidad de Buenos Aires, 1428 Buenos Aires, Argentina; email: lederk@qo.fcen.uba.ar 
506 |2 openaire  |e Política editorial 
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520 3 |a Galactofuranosyl units (Galf), mainly in the β-configuration, are constituents of infectious microorganisms, such as the Mycobacteria, trypanosomatids like Trypanosoma cruzi and Leishmania, and fungi like Aspergillus fumigatus. The metabolic pathways involved in the biosynthesis of the microbial glycoconjugates containing Galf are attractive targets for the development of therapeutic agents, because Galf is absent in mammalian cells. The enzymes involved in the biosynthesis of Galf-containing molecules are the UDP-galactopyranosyl mutase, which catalyzes the interconversion of UDP-Galp into UDP-Galf, the donor of Galf units, and the galactofuranosyltransferases, which are responsible for the incorporation of the sugar into the glycoconjugates. In some species, β-D-galactofuranosidases have been identified as responsible for the degradation of the D-Galf containing glycoconjugates. Although the metabolism of β-D-galactofuranosides has been extensively studied, the α-D-Galf biosynthetic and metabolic machinery still remain unclear. The description of the enzymes involved in its metabolism is important, considering that glycoconjugates containing α-D-Galf residues have been also described in several pathogenic microorganisms including bacteria, such as Escherichia coli and Streptococcus pneumoniae, and fungi, such as Paracoccidioides brasiliensis, the causative agent of paracoccidioidomycosis. It is interesting that in the latter Galf is present in both anomeric configurations. Recent methods for the synthesis of galactofuranosides are included in this chapter. © 2012 by Nova Science Publishers, Inc. All rights reserved.  |l eng 
593 |a CIHIDECAR-CONICET, Departamento de Química Orgánica, Universidad de Buenos Aires, 1428 Buenos Aires, Argentina 
700 1 |a Gallo-Rodriguez, C. 
700 1 |a de Lederkremer, R.M. 
773 0 |d Nova Science Publishers, Inc., 2012  |h pp. 207-268  |p Glycans: Biochem., Charact. and Appl.  |z 9781619425415  |t Glycans: Biochemistry, Characterization and Applications 
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856 4 0 |u https://hdl.handle.net/20.500.12110/paper_97816194_v_n_p207_Marino  |y Handle 
856 4 0 |u https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_97816194_v_n_p207_Marino  |y Registro en la Biblioteca Digital 
961 |a paper_97816194_v_n_p207_Marino  |b paper  |c PE 
962 |a info:eu-repo/semantics/bookPart  |a info:ar-repo/semantics/parte de libro  |b info:eu-repo/semantics/publishedVersion 
999 |c 84440 

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