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Main Authors: Ye, Jinfeng, Zhong, Kan, Hu, Zhi-Fei, Liu, Chang-Cheng, Li, Ming, Wu, Peng, Cao, Hongzhi
Format: Artículo científico
Language:en
Published: Angewandte Chemie (International ed. in English) 2025
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Online Access:https://pubmed.ncbi.nlm.nih.gov/39714328/
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author Ye, Jinfeng
Zhong, Kan
Hu, Zhi-Fei
Liu, Chang-Cheng
Li, Ming
Wu, Peng
Cao, Hongzhi
author_facet Ye, Jinfeng
Zhong, Kan
Hu, Zhi-Fei
Liu, Chang-Cheng
Li, Ming
Wu, Peng
Cao, Hongzhi
Ye, Jinfeng
Zhong, Kan
Hu, Zhi-Fei
Liu, Chang-Cheng
Li, Ming
Wu, Peng
Cao, Hongzhi
collection PubMed - marine biology
contents Sugar Auxiliary Group Assisted Diversity-Oriented Enzymatic Modular Synthesis of 0-Series Ganglioside Glycans. Ye, Jinfeng Zhong, Kan Hu, Zhi-Fei Liu, Chang-Cheng Li, Ming Wu, Peng Cao, Hongzhi Gangliosides Polysaccharides Sialyltransferases Campylobacter jejuni Substrate Specificity Photobacterium N-Acetylgalactosaminyltransferases Sugars Owing to the inaccessibility of β1-4-N-acetylgalactosaminyltransferase for direct glycan chain elongation, the enzymatic synthesis of 0-series gangliosides with extended backbones has not been explored. In this study, sialic acid was enzymatically introduced as an auxiliary group to overcome the limitation of substrate specificity of Campylobacter jejuni β1-4-N-acetylgalactosaminyltransferase (CjCgtA) to achieve the synthesis of desired extended 0-series ganglioside core structures, and the sialic acid auxiliary group could be removed by sialidase at appropriate stages. A bacterial α2-6-sialyltransferase from Photobacterium damselae (Pd2,6ST) exhibited unexpected acceptor substrate specificity for 0-series ganglioside core structures, providing ready access to complex gangliosides bearing the sialyl N-acetylgalactosamine unit. The 0-series ganglioside core structures as the key acceptor substrates were further diversified by sequential enzymatic modular assembly to generate a collection of 31 complex 0-series ganglioside glycans after removal of the sugar auxiliary group of sialic acid at the appropriate stage.
format Artículo científico
id pubmed_39714328
institution PubMed
language en
publishDate 2025
publisher Angewandte Chemie (International ed. in English)
record_format pubmed
spellingShingle Sugar Auxiliary Group Assisted Diversity-Oriented Enzymatic Modular Synthesis of 0-Series Ganglioside Glycans.
Ye, Jinfeng
Zhong, Kan
Hu, Zhi-Fei
Liu, Chang-Cheng
Li, Ming
Wu, Peng
Cao, Hongzhi
Gangliosides
Polysaccharides
Sialyltransferases
Campylobacter jejuni
Substrate Specificity
Photobacterium
N-Acetylgalactosaminyltransferases
Sugars
Sugar Auxiliary Group Assisted Diversity-Oriented Enzymatic Modular Synthesis of 0-Series Ganglioside Glycans. Ye, Jinfeng Zhong, Kan Hu, Zhi-Fei Liu, Chang-Cheng Li, Ming Wu, Peng Cao, Hongzhi Gangliosides Polysaccharides Sialyltransferases Campylobacter jejuni Substrate Specificity Photobacterium N-Acetylgalactosaminyltransferases Sugars Owing to the inaccessibility of β1-4-N-acetylgalactosaminyltransferase for direct glycan chain elongation, the enzymatic synthesis of 0-series gangliosides with extended backbones has not been explored. In this study, sialic acid was enzymatically introduced as an auxiliary group to overcome the limitation of substrate specificity of Campylobacter jejuni β1-4-N-acetylgalactosaminyltransferase (CjCgtA) to achieve the synthesis of desired extended 0-series ganglioside core structures, and the sialic acid auxiliary group could be removed by sialidase at appropriate stages. A bacterial α2-6-sialyltransferase from Photobacterium damselae (Pd2,6ST) exhibited unexpected acceptor substrate specificity for 0-series ganglioside core structures, providing ready access to complex gangliosides bearing the sialyl N-acetylgalactosamine unit. The 0-series ganglioside core structures as the key acceptor substrates were further diversified by sequential enzymatic modular assembly to generate a collection of 31 complex 0-series ganglioside glycans after removal of the sugar auxiliary group of sialic acid at the appropriate stage.
title Sugar Auxiliary Group Assisted Diversity-Oriented Enzymatic Modular Synthesis of 0-Series Ganglioside Glycans.
topic Gangliosides
Polysaccharides
Sialyltransferases
Campylobacter jejuni
Substrate Specificity
Photobacterium
N-Acetylgalactosaminyltransferases
Sugars
url https://pubmed.ncbi.nlm.nih.gov/39714328/