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Comparative Analyses of the Transcriptome and Proteome of Escherichia coli C321.△A and Further Improving Its Noncanonical Amino Acids Containing Protein Expression Ability by Integration of T7 RNA Polymerase

Incorporation of noncanonical amino acids (ncAAs) into proteins has been proven to be a powerful tool to manipulate protein structure and function, and to investigate many biological processes. Improving the yields of ncAA-containing proteins is of great significance in industrial-scale applications...

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Autores principales: Yi, Huawei, Zhang, Jing, Ke, Famin, Guo, Xiurong, Yang, Jian, Xie, Peijuan, Liu, Li, Wang, Qin, Gao, Xiaowei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8511705/
https://www.ncbi.nlm.nih.gov/pubmed/34659179
http://dx.doi.org/10.3389/fmicb.2021.744284
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author Yi, Huawei
Zhang, Jing
Ke, Famin
Guo, Xiurong
Yang, Jian
Xie, Peijuan
Liu, Li
Wang, Qin
Gao, Xiaowei
author_facet Yi, Huawei
Zhang, Jing
Ke, Famin
Guo, Xiurong
Yang, Jian
Xie, Peijuan
Liu, Li
Wang, Qin
Gao, Xiaowei
author_sort Yi, Huawei
collection PubMed
description Incorporation of noncanonical amino acids (ncAAs) into proteins has been proven to be a powerful tool to manipulate protein structure and function, and to investigate many biological processes. Improving the yields of ncAA-containing proteins is of great significance in industrial-scale applications. Escherichia coli C321.ΔA was generated by the replacement of all known amber codons and the deletion of RF1 in the genome and has been proven to be an ideal host for ncAA-containing protein expression using genetic code expansion. In this study, we investigated the transcriptome and proteome profiles of this first codon reassignment strain and found that some functions and metabolic pathways were differentially expressed when compared with those of its parent strain. Genes involved in carbohydrate and energy metabolism were remarkably downregulated. Our results may provide important clues about the growth defects in E. coli C321.ΔA. Furthermore, we improved the yields of ncAA-containing proteins in E. coli C321.ΔA by integrating the T7 RNA polymerase system.
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spelling pubmed-85117052021-10-14 Comparative Analyses of the Transcriptome and Proteome of Escherichia coli C321.△A and Further Improving Its Noncanonical Amino Acids Containing Protein Expression Ability by Integration of T7 RNA Polymerase Yi, Huawei Zhang, Jing Ke, Famin Guo, Xiurong Yang, Jian Xie, Peijuan Liu, Li Wang, Qin Gao, Xiaowei Front Microbiol Microbiology Incorporation of noncanonical amino acids (ncAAs) into proteins has been proven to be a powerful tool to manipulate protein structure and function, and to investigate many biological processes. Improving the yields of ncAA-containing proteins is of great significance in industrial-scale applications. Escherichia coli C321.ΔA was generated by the replacement of all known amber codons and the deletion of RF1 in the genome and has been proven to be an ideal host for ncAA-containing protein expression using genetic code expansion. In this study, we investigated the transcriptome and proteome profiles of this first codon reassignment strain and found that some functions and metabolic pathways were differentially expressed when compared with those of its parent strain. Genes involved in carbohydrate and energy metabolism were remarkably downregulated. Our results may provide important clues about the growth defects in E. coli C321.ΔA. Furthermore, we improved the yields of ncAA-containing proteins in E. coli C321.ΔA by integrating the T7 RNA polymerase system. Frontiers Media S.A. 2021-09-29 /pmc/articles/PMC8511705/ /pubmed/34659179 http://dx.doi.org/10.3389/fmicb.2021.744284 Text en Copyright © 2021 Yi, Zhang, Ke, Guo, Yang, Xie, Liu, Wang and Gao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Yi, Huawei
Zhang, Jing
Ke, Famin
Guo, Xiurong
Yang, Jian
Xie, Peijuan
Liu, Li
Wang, Qin
Gao, Xiaowei
Comparative Analyses of the Transcriptome and Proteome of Escherichia coli C321.△A and Further Improving Its Noncanonical Amino Acids Containing Protein Expression Ability by Integration of T7 RNA Polymerase
title Comparative Analyses of the Transcriptome and Proteome of Escherichia coli C321.△A and Further Improving Its Noncanonical Amino Acids Containing Protein Expression Ability by Integration of T7 RNA Polymerase
title_full Comparative Analyses of the Transcriptome and Proteome of Escherichia coli C321.△A and Further Improving Its Noncanonical Amino Acids Containing Protein Expression Ability by Integration of T7 RNA Polymerase
title_fullStr Comparative Analyses of the Transcriptome and Proteome of Escherichia coli C321.△A and Further Improving Its Noncanonical Amino Acids Containing Protein Expression Ability by Integration of T7 RNA Polymerase
title_full_unstemmed Comparative Analyses of the Transcriptome and Proteome of Escherichia coli C321.△A and Further Improving Its Noncanonical Amino Acids Containing Protein Expression Ability by Integration of T7 RNA Polymerase
title_short Comparative Analyses of the Transcriptome and Proteome of Escherichia coli C321.△A and Further Improving Its Noncanonical Amino Acids Containing Protein Expression Ability by Integration of T7 RNA Polymerase
title_sort comparative analyses of the transcriptome and proteome of escherichia coli c321.△a and further improving its noncanonical amino acids containing protein expression ability by integration of t7 rna polymerase
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8511705/
https://www.ncbi.nlm.nih.gov/pubmed/34659179
http://dx.doi.org/10.3389/fmicb.2021.744284
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