Literature DB >> 31815459

Total Syntheses of Conjugation-Ready Trisaccharide Repeating Units of Pseudomonas aeruginosa O11 and Staphylococcus aureus Type 5 Capsular Polysaccharide for Vaccine Development.

Archanamayee Behera1, Diksha Rai1, Suvarn S Kulkarni1.   

Abstract

Pseudomonas aeruginosa belongs to the group of three "critical priority" multi-drug-resistant pathogens listed by WHO and is responsible for severe and often deadly infections such as bloodstream infections and pneumonia. Staphylococcus aureus is also a "high priority" pathogen which is a major cause of serious nosocomial infections such as bacteremia, sepsis, and endocarditis. Owing to their ability to adapt resistance to almost any antibiotics, vaccines against these pathogens are urgently required. These pathogens express structurally unique and densely functionalized glycans on their surfaces which are absent on the host cells. Such carbohydrate antigens are valuable targets for the development of glycoconjugate vaccines and diagnostics. Here, we report the first total synthesis of the conjugation-ready trisaccharide repeating unit of Pseudomonas aeruginosa O11 via a highly stereoselective and efficient assembly of a rare l-fucosamine- and d-fucosamine-containing 1,2-cis-linked disaccharide motif and its regioselective glycosylation at O3. A systematic study was conducted for the notoriously difficult glycosylation with the most unreactive axial 4-OH of the rare disaccharide, and the successful outcome was utilized to accomplish the total synthesis of an aminopropyl linker-attached trisaccharide repeating unit of Staphylococcus aureus capsular polysaccharide type 5, which is also a potential antigen for immunotherapy and vaccine development. The judicious selection of protecting groups and reaction conditions allowed the stereoselective assembly and selective functional group interconversions to access the structurally complex linker-attached trisaccharide repeating units, which are valuable tools for immunological evaluation and vaccine development. The strategy is useful for the synthesis of other structurally related complex glycans.

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Year:  2019        PMID: 31815459     DOI: 10.1021/jacs.9b11309

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  9 in total

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Review 2.  Recent progress in chemical synthesis of bacterial surface glycans.

Authors:  Riyao Li; Hai Yu; Xi Chen
Journal:  Curr Opin Chem Biol       Date:  2020-09-11       Impact factor: 8.822

Review 3.  Polysaccharide-based nanomedicines for cancer immunotherapy: A review.

Authors:  Yujun Zeng; Yufan Xiang; Ruilong Sheng; Helena Tomás; João Rodrigues; Zhongwei Gu; Hu Zhang; Qiyong Gong; Kui Luo
Journal:  Bioact Mater       Date:  2021-03-18

4.  Total Syntheses of Conjugation-Ready Repeating Units of Acinetobacter baumannii AB5075 for Glycoconjugate Vaccine Development.

Authors:  Shuo Zhang; Peter H Seeberger
Journal:  Chemistry       Date:  2021-11-05       Impact factor: 5.020

5.  Total Synthesis of the Tetrasaccharide Haptens of Vibrio vulnificus MO6-24 and BO62316 and Immunological Evaluation of Their Protein Conjugates.

Authors:  Han Zhang; Xiaohan Wang; Youhui Meng; Xiaoyu Yang; Qingpeng Zhao; Jian Gao
Journal:  JACS Au       Date:  2021-11-09

6.  Synthesis of Oligosaccharides Resembling the Streptococcus suis Serotype 18 Capsular Polysaccharide as a Basis for Glycoconjugate Vaccine Development.

Authors:  Rajat Kumar Singh; Julinton Sianturi; Peter H Seeberger
Journal:  Org Lett       Date:  2022-03-21       Impact factor: 6.005

7.  Total Synthesis of Tri-, Hexa- and Heptasaccharidic Substructures of the O-Polysaccharide of Providencia rustigianii O34.

Authors:  Somayeh Ahadi; Shahid I Awan; Daniel B Werz
Journal:  Chemistry       Date:  2020-04-28       Impact factor: 5.236

8.  Conjugation of Synthetic Trisaccharide of Staphylococcus aureus Type 8 Capsular Polysaccharide Elicits Antibodies Recognizing Intact Bacterium.

Authors:  Ming Zhao; Chunjun Qin; Lingxin Li; Haotian Xie; Beining Ma; Ziru Zhou; Jian Yin; Jing Hu
Journal:  Front Chem       Date:  2020-04-28       Impact factor: 5.221

9.  Total synthesis of the O-antigen repeating unit of Providencia stuartii O49 serotype through linear and one-pot assemblies.

Authors:  Tanmoy Halder; Somnath Yadav
Journal:  Beilstein J Org Chem       Date:  2021-12-13       Impact factor: 2.883

  9 in total

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