Direct chemical editing of Gram‐positive bacterial cell walls via an enzyme‐catalyzed oxidative coupling reaction

Abstract Chemically manipulating bacterial surface structures, a cutting‐edge research direction in the biomedical field, predominantly relies on metabolic labeling by now. However, this method may involve daunting precursor synthesis and only labels nascent surface structures. Here, we report a fac...

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Main Authors: Hao‐Ran Jia, Ya‐Xuan Zhu, Yi Liu, Yuxin Guo, Sayed Mir Sayed, Xiao‐Yu Zhu, Xiaotong Cheng, Fu‐Gen Wu
Format: Article
Language:English
Published: Wiley 2022-10-01
Series:Exploration
Subjects:
Online Access:https://doi.org/10.1002/EXP.20220010
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author Hao‐Ran Jia
Ya‐Xuan Zhu
Yi Liu
Yuxin Guo
Sayed Mir Sayed
Xiao‐Yu Zhu
Xiaotong Cheng
Fu‐Gen Wu
author_facet Hao‐Ran Jia
Ya‐Xuan Zhu
Yi Liu
Yuxin Guo
Sayed Mir Sayed
Xiao‐Yu Zhu
Xiaotong Cheng
Fu‐Gen Wu
author_sort Hao‐Ran Jia
collection DOAJ
description Abstract Chemically manipulating bacterial surface structures, a cutting‐edge research direction in the biomedical field, predominantly relies on metabolic labeling by now. However, this method may involve daunting precursor synthesis and only labels nascent surface structures. Here, we report a facile and rapid modification strategy based on a tyrosinase‐catalyzed oxidative coupling reaction (TyOCR) for bacterial surface engineering. This strategy employs phenol‐tagged small molecules and tyrosinase to initiate direct chemical modification of Gram‐positive bacterial cell walls with high labeling efficiency, while Gram‐negative bacteria are inert to this modification due to the hindrance of an outer membrane. By using the biotin‒avidin system, we further present the selective deposition of various materials, including photosensitizer, magnetic nanoparticle, and horseradish peroxidase, on Gram‐positive bacterial surfaces, and realize the purification/isolation/enrichment and naked‐eye detection of bacterial strains. This work demonstrates that TyOCR is a promising strategy for engineering live bacterial cells.
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spelling doaj.art-8e9978369d1a44b8aa755e8eff20066a2022-12-22T03:26:09ZengWileyExploration2766-85092766-20982022-10-0125n/an/a10.1002/EXP.20220010Direct chemical editing of Gram‐positive bacterial cell walls via an enzyme‐catalyzed oxidative coupling reactionHao‐Ran Jia0Ya‐Xuan Zhu1Yi Liu2Yuxin Guo3Sayed Mir Sayed4Xiao‐Yu Zhu5Xiaotong Cheng6Fu‐Gen Wu7State Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering Southeast University Nanjing P. R. ChinaState Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering Southeast University Nanjing P. R. ChinaState Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering Southeast University Nanjing P. R. ChinaState Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering Southeast University Nanjing P. R. ChinaState Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering Southeast University Nanjing P. R. ChinaState Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering Southeast University Nanjing P. R. ChinaState Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering Southeast University Nanjing P. R. ChinaState Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering Southeast University Nanjing P. R. ChinaAbstract Chemically manipulating bacterial surface structures, a cutting‐edge research direction in the biomedical field, predominantly relies on metabolic labeling by now. However, this method may involve daunting precursor synthesis and only labels nascent surface structures. Here, we report a facile and rapid modification strategy based on a tyrosinase‐catalyzed oxidative coupling reaction (TyOCR) for bacterial surface engineering. This strategy employs phenol‐tagged small molecules and tyrosinase to initiate direct chemical modification of Gram‐positive bacterial cell walls with high labeling efficiency, while Gram‐negative bacteria are inert to this modification due to the hindrance of an outer membrane. By using the biotin‒avidin system, we further present the selective deposition of various materials, including photosensitizer, magnetic nanoparticle, and horseradish peroxidase, on Gram‐positive bacterial surfaces, and realize the purification/isolation/enrichment and naked‐eye detection of bacterial strains. This work demonstrates that TyOCR is a promising strategy for engineering live bacterial cells.https://doi.org/10.1002/EXP.20220010biosensingcell surface engineeringlive cellsoxidative couplingtyrosinase
spellingShingle Hao‐Ran Jia
Ya‐Xuan Zhu
Yi Liu
Yuxin Guo
Sayed Mir Sayed
Xiao‐Yu Zhu
Xiaotong Cheng
Fu‐Gen Wu
Direct chemical editing of Gram‐positive bacterial cell walls via an enzyme‐catalyzed oxidative coupling reaction
Exploration
biosensing
cell surface engineering
live cells
oxidative coupling
tyrosinase
title Direct chemical editing of Gram‐positive bacterial cell walls via an enzyme‐catalyzed oxidative coupling reaction
title_full Direct chemical editing of Gram‐positive bacterial cell walls via an enzyme‐catalyzed oxidative coupling reaction
title_fullStr Direct chemical editing of Gram‐positive bacterial cell walls via an enzyme‐catalyzed oxidative coupling reaction
title_full_unstemmed Direct chemical editing of Gram‐positive bacterial cell walls via an enzyme‐catalyzed oxidative coupling reaction
title_short Direct chemical editing of Gram‐positive bacterial cell walls via an enzyme‐catalyzed oxidative coupling reaction
title_sort direct chemical editing of gram positive bacterial cell walls via an enzyme catalyzed oxidative coupling reaction
topic biosensing
cell surface engineering
live cells
oxidative coupling
tyrosinase
url https://doi.org/10.1002/EXP.20220010
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