Synthesis of C6-modified mannose 1-phosphates and evaluation of derived sugar nucleotides against GDP-mannose dehydrogenase

Sufferers of cystic fibrosis are at significant risk of contracting chronic bacterial lung infections. The dominant pathogen in these cases is mucoid Such infections are characterised by overproduction of the exopolysaccharide alginate. We present herein the design and chemoenzymatic synthesis of su...

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Veröffentlicht in:Beilstein journal of organic chemistry 2022, Vol.18 (1), p.1379-1384
Hauptverfasser: Ahmadipour, Sanaz, Wahart, Alice J C, Dolan, Jonathan P, Beswick, Laura, Hawes, Chris S, Field, Robert A, Miller, Gavin J
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Sprache:eng
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Zusammenfassung:Sufferers of cystic fibrosis are at significant risk of contracting chronic bacterial lung infections. The dominant pathogen in these cases is mucoid Such infections are characterised by overproduction of the exopolysaccharide alginate. We present herein the design and chemoenzymatic synthesis of sugar nucleotide tools to probe a critical enzyme within alginate biosynthesis, GDP-mannose dehydrogenase (GMD). We first synthesise C6-modified glycosyl 1-phosphates, incorporating 6-amino, 6-chloro and 6-sulfhydryl groups, followed by their evaluation as substrates for enzymatic pyrophosphorylative coupling. The development of this methodology enables access to GDP 6-chloro-6-deoxy-ᴅ-mannose and its evaluation against GMD.
ISSN:1860-5397
2195-951X
1860-5397
DOI:10.3762/bjoc.18.142