Inside Back Cover: Synthesis of a Pentasaccharide Repeating Unit of Lipopolysaccharide Derived from Virulent E. coli O1 and Identification of a Glycotope Candidate of Avian Pathogenic E. coli O1 (Angew. Chem. Int. Ed. 4/2021)

Identification of the glycotope of avian pathogenic E. coli (APEC) O1 is important for the design of a new generation of improved and safer vaccines. In their Research Article on page 1789, Daisuke Takahashi, Kazunobu Toshima, and co‐workers synthesize the unique pentasaccharide derived from virulen...

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Veröffentlicht in:	Angewandte Chemie International Edition 2021-01, Vol.60 (4), p.2167-2167
Hauptverfasser:	Nishi, Nobuya, Seki, Katsunori, Takahashi, Daisuke, Toshima, Kazunobu
Format:	Artikel
Sprache:	eng
Schlagworte:	avian pathogenic Escherichia coli boron-mediated aglycon delivery glycoconjugate glycotope β-rhamnoside
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description	Identification of the glycotope of avian pathogenic E. coli (APEC) O1 is important for the design of a new generation of improved and safer vaccines. In their Research Article on page 1789, Daisuke Takahashi, Kazunobu Toshima, and co‐workers synthesize the unique pentasaccharide derived from virulent E. coli O1 and reveal that the pentasaccharide is a glycotope candidate of APEC O1, with great potential as an antigen for vaccine development.
doi_str_mv	10.1002/anie.202015610
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subjects	avian pathogenic Escherichia coli boron-mediated aglycon delivery glycoconjugate glycotope β-rhamnoside
title	Inside Back Cover: Synthesis of a Pentasaccharide Repeating Unit of Lipopolysaccharide Derived from Virulent E. coli O1 and Identification of a Glycotope Candidate of Avian Pathogenic E. coli O1 (Angew. Chem. Int. Ed. 4/2021)
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