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利用[具体对象]中的荚膜多糖合成途径作为基因糖工程平台。

Leveraging the Capsular Polysaccharide Synthesis Pathway in as a Genetic Glycoengineering Platform.

作者信息

Wong Cheryl Kang-Rou, Chun Ye-Yu, Su Tong, Sham Lok-To

机构信息

Infectious Diseases Translational Research Programme and Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117545, Singapore.

出版信息

ACS Bio Med Chem Au. 2025 May 8;5(3):342-349. doi: 10.1021/acsbiomedchemau.5c00010. eCollection 2025 Jun 18.

Abstract

Engineering carbohydrates in living cells is one of the overarching goals of biology. In this Perspective, we discuss recent work in response to this challenge. Compared with eukaryotic cells, bacteria are fast-growing and genetically tractable. At the species level, glycans in prokaryotes are highly variable, contrasting with the homogeneity of surface glycans, such as capsular polysaccharides (CPSs), at the strain level. We exploited the conditional essentiality of the CPS synthesis pathway in to overcome the challenges of biochemically monitoring the engineered glycan products. While this strategy seems feasible, this glycoengineering platform is limited by the specificity of the capsule transporters and the glycosyltransferase inventories that can be introduced into the pneumococcus. Mutants that relax transporter specificity have been isolated, enabling us to inactivate otherwise essential glycosyltransferases. Ongoing work aims to harness this technology to synthesize medically relevant glycans, including Lewis antigens and tumor markers.

摘要

在活细胞中构建碳水化合物是生物学的首要目标之一。在这篇观点文章中,我们讨论了应对这一挑战的近期工作。与真核细胞相比,细菌生长迅速且易于进行基因操作。在物种水平上,原核生物中的聚糖高度可变,这与菌株水平上表面聚糖(如荚膜多糖,CPSs)的同质性形成对比。我们利用CPS合成途径的条件必要性来克服对工程化聚糖产物进行生化监测的挑战。虽然这一策略似乎可行,但这个糖工程平台受到荚膜转运蛋白的特异性以及可引入肺炎链球菌的糖基转移酶库的限制。已经分离出了使转运蛋白特异性降低的突变体,这使我们能够使原本必需的糖基转移酶失活。正在进行的工作旨在利用这项技术合成与医学相关的聚糖,包括Lewis抗原和肿瘤标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a2f/12186847/136e28ce63f8/bg5c00010_0001.jpg

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