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N-glycolyl chondroitin synthesis using metabolically engineered E. coli

N-glycolyl chondroitin (Gc-CN) is a metabolite of N-glycolylneuraminic acid (Neu5Gc), a sialic acid that is commonly found in mammals, but not humans. Humans can incorporate exogenous Neu5Gc into their tissues from eating red meat. Neu5Gc cannot be biosynthesized by humans due to an evolutionary mut...

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Autores principales: Awofiranye, Adeola E., Baytas, Sultan N., Xia, Ke, Badri, Abinaya, He, Wenqin, Varki, Ajit, Koffas, Mattheos, Linhardt, Robert J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7429809/
https://www.ncbi.nlm.nih.gov/pubmed/32803432
http://dx.doi.org/10.1186/s13568-020-01084-6
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author Awofiranye, Adeola E.
Baytas, Sultan N.
Xia, Ke
Badri, Abinaya
He, Wenqin
Varki, Ajit
Koffas, Mattheos
Linhardt, Robert J.
author_facet Awofiranye, Adeola E.
Baytas, Sultan N.
Xia, Ke
Badri, Abinaya
He, Wenqin
Varki, Ajit
Koffas, Mattheos
Linhardt, Robert J.
author_sort Awofiranye, Adeola E.
collection PubMed
description N-glycolyl chondroitin (Gc-CN) is a metabolite of N-glycolylneuraminic acid (Neu5Gc), a sialic acid that is commonly found in mammals, but not humans. Humans can incorporate exogenous Neu5Gc into their tissues from eating red meat. Neu5Gc cannot be biosynthesized by humans due to an evolutionary mutation and has been implicated in causing inflammation causing human diseases, such as cancer. The study Neu5Gc is important in evolutionary biology and the development of potential cancer biomarkers. Unfortunately, there are several limitations to detecting Neu5Gc. The elimination of Neu5Gc involves a degradative pathway leading to the incorporation of N-glycolyl groups into glycosaminoglycans (GAGs), such as Gc-CN. Gc-CN has been found in humans and in animals including mice, lamb and chimpanzees. Here, we present the biosynthesis of Gc-CN in bacteria by feeding chemically synthesized N-glycolylglucosamine to Escherichia coli. A metabolically engineered strain of E. coli K4, fed with glucose supplemented with GlcNGc, converted it to N-glycolylgalactosamine (GalNGc) that could then be utilized as a substrate in the chondroitin biosynthetic pathway. The final product, Gc-CN was converted to disaccharides using chondroitin lyase ABC and analyzed by liquid chromatography–tandem mass spectrometry with multiple reaction monitoring detection. This analysis showed the incorporation of GalNGc into the backbone of the chondroitin oligosaccharide.
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spelling pubmed-74298092020-08-20 N-glycolyl chondroitin synthesis using metabolically engineered E. coli Awofiranye, Adeola E. Baytas, Sultan N. Xia, Ke Badri, Abinaya He, Wenqin Varki, Ajit Koffas, Mattheos Linhardt, Robert J. AMB Express Original Article N-glycolyl chondroitin (Gc-CN) is a metabolite of N-glycolylneuraminic acid (Neu5Gc), a sialic acid that is commonly found in mammals, but not humans. Humans can incorporate exogenous Neu5Gc into their tissues from eating red meat. Neu5Gc cannot be biosynthesized by humans due to an evolutionary mutation and has been implicated in causing inflammation causing human diseases, such as cancer. The study Neu5Gc is important in evolutionary biology and the development of potential cancer biomarkers. Unfortunately, there are several limitations to detecting Neu5Gc. The elimination of Neu5Gc involves a degradative pathway leading to the incorporation of N-glycolyl groups into glycosaminoglycans (GAGs), such as Gc-CN. Gc-CN has been found in humans and in animals including mice, lamb and chimpanzees. Here, we present the biosynthesis of Gc-CN in bacteria by feeding chemically synthesized N-glycolylglucosamine to Escherichia coli. A metabolically engineered strain of E. coli K4, fed with glucose supplemented with GlcNGc, converted it to N-glycolylgalactosamine (GalNGc) that could then be utilized as a substrate in the chondroitin biosynthetic pathway. The final product, Gc-CN was converted to disaccharides using chondroitin lyase ABC and analyzed by liquid chromatography–tandem mass spectrometry with multiple reaction monitoring detection. This analysis showed the incorporation of GalNGc into the backbone of the chondroitin oligosaccharide. Springer Berlin Heidelberg 2020-08-17 /pmc/articles/PMC7429809/ /pubmed/32803432 http://dx.doi.org/10.1186/s13568-020-01084-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Awofiranye, Adeola E.
Baytas, Sultan N.
Xia, Ke
Badri, Abinaya
He, Wenqin
Varki, Ajit
Koffas, Mattheos
Linhardt, Robert J.
N-glycolyl chondroitin synthesis using metabolically engineered E. coli
title N-glycolyl chondroitin synthesis using metabolically engineered E. coli
title_full N-glycolyl chondroitin synthesis using metabolically engineered E. coli
title_fullStr N-glycolyl chondroitin synthesis using metabolically engineered E. coli
title_full_unstemmed N-glycolyl chondroitin synthesis using metabolically engineered E. coli
title_short N-glycolyl chondroitin synthesis using metabolically engineered E. coli
title_sort n-glycolyl chondroitin synthesis using metabolically engineered e. coli
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7429809/
https://www.ncbi.nlm.nih.gov/pubmed/32803432
http://dx.doi.org/10.1186/s13568-020-01084-6
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