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Secretion systems in Gram-negative bacteria

Khoi Nguyen Hoang Le 1 ORCID logo
Thanh Tan Nguyen 2
Hieu Tran Van 3, * ORCID logo
  1. Department of Molecular and Enviromental Biotechnology, Faculty of Biology - Biotechnology, University of Science, Ho Chi Minh City
  2. Laboratory of Biosensor, Faculty of Biology - Biotechnology, University of Science, Ho Chi Minh City
  3. Faculty of Biology - Biotechnology, University of Science, VNU-HCM Vietnam
Correspondence to: Hieu Tran Van, Faculty of Biology - Biotechnology, University of Science, VNU-HCM Vietnam. ORCID: https://orcid.org/0000-0003-2782-5232. Email: tvhieu@hcmus.edu.vn.
Volume & Issue: Vol. 9 No. 1 (2025) | Page No.: 3296-3306 | DOI: 10.32508/stdjns.v9i1.1311
Published: 2025-03-31

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This article is published with open access by Viet Nam National University Ho Chi Minh City, Viet Nam. This article is distributed under the terms of the Creative Commons Attribution License (CC-BY 4.0) which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.

Abstract

Biotechnology’s fast development in expressing novel proteins has been substantially facilitated, particularly in the context of recombinant protein expression in bacteria. Currently, intracellular, secretory, and surface-displayed modes of protein expression are utilized in bacteria. However, the surface display of proteins in Gram-negative bacterial species is still limited by several factors. The challenges in protein expression on the surface of Gram-negative bacteria stem from the complex structure of their cell wall, which is composed of two membrane layers. Therefore, a suitable transport system is required for recombinant protein surface expression. Previous research has indicated that bacterial secretion systems are vital to their survival. In Gram-negative bacteria, secretion systems are classified into those that translocate across a single membrane and those that translocate across both membranes. While Sec and Tat are single-membrane translocation systems, the Type I secretion system (T1SS), Type II secretion system (T2SS), Type III secretion system (T3SS), Type IV secretion system (T4SS), Type V secretion system (T5SS), and Type VI secretion system (T6SS) are double-membrane translocation systems that facilitate the export of polypeptide chains synthesized within the cell to the external environment. In this overview, the distinctive features of each secretion system will be discussed, along with their potential applications for directing recombinant proteins onto the membranes using these systems.

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