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本文引用的文献

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Redox Characterization of Electrode-Immobilized Bacterial Microcompartment Shell Proteins Engineered To Bind Metal Centers.工程化结合金属中心的电极固定化细菌微区室外壳蛋白的氧化还原特性分析
ACS Appl Bio Mater. 2020 Jan 21;3(1):685-692. doi: 10.1021/acsabm.9b01023. Epub 2020 Jan 8.
2
Using Genetic Code Expansion for Protein Biochemical Studies.利用遗传密码扩展进行蛋白质生化研究。
Front Bioeng Biotechnol. 2020 Oct 19;8:598577. doi: 10.3389/fbioe.2020.598577. eCollection 2020.
3
Prokaryotic Organelles: Bacterial Microcompartments in and .原核细胞器: 和 中的细菌微隔间。
EcoSal Plus. 2020 Oct;9(1). doi: 10.1128/ecosalplus.ESP-0025-2019.
4
Site-Specific Incorporation of Two ncAAs for Two-Color Bioorthogonal Labeling and Crosslinking of Proteins on Live Mammalian Cells.在活哺乳动物细胞上对蛋白质进行双色生物正交标记和交联的两种 ncAA 的位点特异性掺入。
Cell Rep. 2020 Jun 23;31(12):107811. doi: 10.1016/j.celrep.2020.107811.
5
Engineered bacterial microcompartments: apps for programming metabolism.工程化细菌微室:用于代谢编程的应用。
Curr Opin Biotechnol. 2020 Oct;65:225-232. doi: 10.1016/j.copbio.2020.05.001. Epub 2020 Jun 15.
6
Life cycle of a cyanobacterial carboxysome.蓝藻羧化体的生命周期。
Sci Adv. 2020 May 6;6(19):eaba1269. doi: 10.1126/sciadv.aba1269. eCollection 2020 May.
7
Decoding the stoichiometric composition and organisation of bacterial metabolosomes.解析细菌代谢体的化学计量组成和结构。
Nat Commun. 2020 Apr 24;11(1):1976. doi: 10.1038/s41467-020-15888-4.
8
Apparent size and morphology of bacterial microcompartments varies with technique.细菌微室的表观大小和形态随技术而变化。
PLoS One. 2020 Mar 9;15(3):e0226395. doi: 10.1371/journal.pone.0226395. eCollection 2020.
9
Genetic Characterization of a Glycyl Radical Microcompartment Used for 1,2-Propanediol Fermentation by Uropathogenic Escherichia coli CFT073.用于 1,2-丙二醇发酵的尿路致病性大肠杆菌 CFT073 甘氨酰基自由基微区室的遗传特征。
J Bacteriol. 2020 Apr 9;202(9). doi: 10.1128/JB.00017-20.
10
Effect of metabolosome encapsulation peptides on enzyme activity, coaggregation, incorporation, and bacterial microcompartment formation.代谢体包封肽对酶活性、共聚集、掺入和细菌微隔间形成的影响。
Microbiologyopen. 2020 May;9(5):e1010. doi: 10.1002/mbo3.1010. Epub 2020 Feb 13.

引入非天然氨基酸用于研究和工程化细菌微隔间。

Introducing noncanonical amino acids for studying and engineering bacterial microcompartments.

机构信息

Cell and Molecular Biology Program, University of Arkansas, Fayetteville, AR, USA.

Department of Chemistry and Biochemistry, University of Arkansas, Fayetteville, AR, USA.

出版信息

Curr Opin Microbiol. 2021 Jun;61:67-72. doi: 10.1016/j.mib.2021.03.004. Epub 2021 Apr 1.

DOI:10.1016/j.mib.2021.03.004
PMID:33813159
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8169543/
Abstract

Bacterial microcompartments (BMCs) with selectively permeable shells and encapsulated enzyme cores are well-suited candidates for nano-bioreactors because of their advantages of enhancing pathway flux and protection against toxic products. To better study and engineer protein-based BMCs, a series of protein chemistry approaches are adopted. As one of the most advanced techniques, genetic code expansion can introduce various noncanonical amino acids (ncAAs) with diverse functional groups into target proteins, thus providing powerful tools for protein studies and engineering. This review summarizes and proposes useful tools based on current development of the genetic code expansion technique towards challenges in BMC studies and engineering.

摘要

细菌微隔间(BMCs)具有选择性渗透的外壳和包裹的酶核心,是纳米生物反应器的理想候选物,因为它们具有增强途径通量和防止有毒产物的优势。为了更好地研究和设计基于蛋白质的 BMCs,采用了一系列蛋白质化学方法。作为最先进的技术之一,遗传密码扩展可以将各种具有不同功能基团的非标准氨基酸(ncAAs)引入目标蛋白质中,从而为蛋白质研究和工程提供了强大的工具。本综述总结并提出了基于遗传密码扩展技术当前发展的有用工具,以应对 BMC 研究和工程中的挑战。