100645-45-2Relevant academic research and scientific papers
Chemo-enzymatic synthesis of p-nitrophenyl β-D-galactofuranosyl disaccharides from Aspergillus sp. fungal-type galactomannan
Ota, Ryo,Okamoto, Yumi,Vavricka, Christopher J.,Oka, Takuji,Matsunaga, Emiko,Takegawa, Kaoru,Kiyota, Hiromasa,Izumi, Minoru
, p. 99 - 103 (2019/01/16)
β-D-Galactofuranose (Galf) is a component of polysaccharides and glycoconjugates. There are few reports about the involvement of galactofuranosyltransferases and galactofuranosidases (Galf-ases) in the synthesis and degradation of galactofuranose-containing glycans. The cell walls of filamentous fungi in the genus Aspergillus include galactofuranose-containing polysaccharides and glycoconjugates, such as O-glycans, N-glycans, and fungal-type galactomannan, which are important for cell wall integrity. In this study, we investigated the synthesis of p-nitrophenyl β-D-galactofuranoside and its disaccharides by chemo-enzymatic methods including use of galactosidase. The key step was selective removal of the concomitant pyranoside by enzymatic hydrolysis to purify p-nitrophenyl β-D-galactofuranoside, a promising substrate for β-D-galactofuranosidase from Streptomyces species.
Identification and characterization of a novel galactofuranose-specific β-D-galactofuranosidase from Streptomyces species
Matsunaga, Emiko,Higuchi, Yujiro,Mori, Kazuki,Yairo, Nao,Oka, Takuji,Shinozuka, Saki,Tashiro, Kosuke,Izumi, Minoru,Kuhara, Satoru,Takegawa, Kaoru
, (2015/10/28)
β-D-galactofuranose (Galf) is a component of polysaccharides and glycoconjugates and its transferase has been well analyzed. However, no β-D-galactofuranosidase (Galf-ase) gene has been identified in any organism. To search for a Galf-ase gene we screened
Facile synthesis of per-O-tort-butyldimethylsilyl-β-D-galactofuranose and efficient glyeosylation via the galactofuranosyl iodide
Baldoni, Luciana,Marino, Carla
supporting information; experimental part, p. 1994 - 2003 (2009/08/07)
The synthesis of crystalline per-0-TBS-β-D-galactofuranose (Aβ) as a new precursor of D-Galf units is described. Anomeric iodination by reaction with TMSI followed by in situ coupling with simple alcohols and a wide variety of glycosyl acceptors, in the absence of a promoter, was employed as a new efficient glycosylation method for the assembly of D-galactofuranosyl moieties with high β-stereoselectivity. Under the mild conditions of this reaction labile protective groups, like acetals, and furanosyl linkages are preserved.
An original chemoenzymatic route for the synthesis of β-D- galactofuranosides using an α-l-arabinofuranosidase
Remond, Caroline,Plantier-Royon, Richard,Aubry, Nathalie,O'Donohue, Michael J.
, p. 637 - 644 (2007/10/03)
Galactofuranose is a widespread component of cell wall polysaccharides in bacteria, protozoa and fungi, but is totally absent in mammals. Importantly, galactofuranose is a key constituent of major cell envelope polysaccharides in pathogenic mycobacteria.
Non-natural aldofuranosides as substrates of a β-glucosidase
Tauss, Andreas,Greimel, Peter,Rupitz, Karen,Steiner, Andreas J.,Stuetz, Arnold E.,Withers, Stephen G.,Wrodnigg, Tanja M.
, p. 159 - 165 (2007/10/03)
Based on glycosidase inhibitory activities of some known 1,4-iminoalditols, four aldofuranosides, (4-nitro)phenyl β-d-glucofuranoside, -β-d-galactofuranoside, -α-l-idofuranoside and -α-l- altrofuranoside, were identified as possible substrates of glucosid
