Total Synthesis of the Conjugation-Ready Tetrasaccharide Repeating Unit of <i>Acinetobacter baumannii</i> MAR13-1452 (K125) Capsular Polysaccharide for Vaccine Development

<i>Acinetobacter baumannii</i> is a highly drug-resistant pathogen that causes severe hospital infections and urgently requires new treatment strategies. Surface-exposed glycans of these bacteria have emerged as promising vaccine targets due to their immunogenic potential. Here, we report the first total synthesis of the tetrasaccharide repeating unit of <i>Acinetobacter baumannii</i> MAR13-1452 (K125). The presence of rare deoxy amino sugars and the exclusive 1,2-<i>cis</i> glycosidic linkages within the tetrasaccharide make its synthesis more challenging. A one-pot oligosaccharide assembly enabled efficient and facile synthesis of the target molecule.

Authors

Institutions

Publication Details

Journal
Organic Letters
Published
2025-06-17
DOI
https://doi.org/10.1021/acs.orglett.5c02016
Citations
2
Primary Topic
Carbohydrate Chemistry and Synthesis
Type
article
Field-Weighted Citation Impact
1.87

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Total Synthesis of the Conjugation-Ready Tetrasaccharide Repeating Unit of Acinetobacter baumannii MAR13-1452 (K125) Capsular Polysaccharide for Vaccine Development

Yongmei Yin, Zhen-Hua Dang, Xingxing Kang, Haoyu Xue et al.
2 citations
Organic Letters
Carbohydrate Chemistry and Synthesis
1.87
article

Total Synthesis of the Conjugation-Ready Tetrasaccharide Repeating Unit of Acinetobacter baumannii MAR13-1452 (K125) Capsular Polysaccharide for Vaccine Development

Yongmei Yin, Zhen-Hua Dang, Xingxing Kang, Haoyu Xue, Yu Zhou, Xianwei Ding, Hongzhen Jin, Ke Feng, Jia Tian, Wei Guang Zhao
article en
2 citations

Abstract

<i>Acinetobacter baumannii</i> is a highly drug-resistant pathogen that causes severe hospital infections and urgently requires new treatment strategies. Surface-exposed glycans of these bacteria have emerged as promising vaccine targets due to their immunogenic potential. Here, we report the first total synthesis of the tetrasaccharide repeating unit of <i>Acinetobacter baumannii</i> MAR13-1452 (K125). The presence of rare deoxy amino sugars and the exclusive 1,2-<i>cis</i> glycosidic linkages within the tetrasaccharide make its synthesis more challenging. A one-pot oligosaccharide assembly enabled efficient and facile synthesis of the target molecule.

Organic LettersVol. 27(25)
Qingdao University (CN), Nankai University (CN), Affiliated Hospital of Qingdao University (CN), Qingdao Municipal Hospital (CN), State Key Laboratory of Chemical Engineering (CN), State Key Laboratory of Medicinal Chemical Biology
National Natural Science Foundation of China, Fundamental Research Funds for the Central Universities, Tianjin Science and Technology Program
Zero hunger
Openalex Percentile: Top 15%
Carbohydrate Chemistry and Synthesis
1.87
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.