{"title":"Signal Peptide-Guided Delivery of a Mucin-Like Collagen Analogue for Periplasmic Barrier Reinforcement: A Platform for Enhancing Microbial Survival","authors":"Zilong Zhao, Weigang Yuwen, Wensha Zhu, Linlin Qu and Daidi Fan*, ","doi":"10.1021/acssynbio.5c00607","DOIUrl":null,"url":null,"abstract":"<p >The environmental resistance exhibited by microorganisms is concerned with their ability to withstand and adapt to an array of detrimental environmental conditions, with their survival and reproductive success being threatened. Within the realm of biotechnology, which emphasizes stress resistance, a critical role in bacterial adaptive strategies to environmental fluctuations is assumed to be in the periplasmic space. An innovative methodology to augment bacterial tolerance to stress by employing a mucin-mimetic collagen analogue, designated as S1552 (which is secreted into the periplasmic compartment), is introduced by this investigation. Exceptional protective barrier attributes are highly regarded in S1552. An appropriate signal peptide for the periplasmic expression of S1552 in <i>Escherichia coli</i> was identified by employing computational analysis (<i>in silico</i>). The fusion protein of S1552 and the DsbA signal peptide (DS1552) is efficiently translocated into the periplasmic space of <i>E. coli</i>. This approach not only fortifies the cellular barrier but also significantly enhances the bacterium’s resistance to a variety of stressors, including elevated salinity, high osmotic stress, extreme pH values, antibiotics, toxicants, and heavy metal ions. Meanwhile, this pioneering application has the potential to be extended to other bacteria with a periplasmic space, enhancing their viability and proliferation in harsh environments.</p>","PeriodicalId":26,"journal":{"name":"ACS Synthetic Biology","volume":"14 9","pages":"3767–3783"},"PeriodicalIF":3.9000,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Synthetic Biology","FirstCategoryId":"99","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acssynbio.5c00607","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
The environmental resistance exhibited by microorganisms is concerned with their ability to withstand and adapt to an array of detrimental environmental conditions, with their survival and reproductive success being threatened. Within the realm of biotechnology, which emphasizes stress resistance, a critical role in bacterial adaptive strategies to environmental fluctuations is assumed to be in the periplasmic space. An innovative methodology to augment bacterial tolerance to stress by employing a mucin-mimetic collagen analogue, designated as S1552 (which is secreted into the periplasmic compartment), is introduced by this investigation. Exceptional protective barrier attributes are highly regarded in S1552. An appropriate signal peptide for the periplasmic expression of S1552 in Escherichia coli was identified by employing computational analysis (in silico). The fusion protein of S1552 and the DsbA signal peptide (DS1552) is efficiently translocated into the periplasmic space of E. coli. This approach not only fortifies the cellular barrier but also significantly enhances the bacterium’s resistance to a variety of stressors, including elevated salinity, high osmotic stress, extreme pH values, antibiotics, toxicants, and heavy metal ions. Meanwhile, this pioneering application has the potential to be extended to other bacteria with a periplasmic space, enhancing their viability and proliferation in harsh environments.
期刊介绍:
The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism.
Topics may include, but are not limited to:
Design and optimization of genetic systems
Genetic circuit design and their principles for their organization into programs
Computational methods to aid the design of genetic systems
Experimental methods to quantify genetic parts, circuits, and metabolic fluxes
Genetic parts libraries: their creation, analysis, and ontological representation
Protein engineering including computational design
Metabolic engineering and cellular manufacturing, including biomass conversion
Natural product access, engineering, and production
Creative and innovative applications of cellular programming
Medical applications, tissue engineering, and the programming of therapeutic cells
Minimal cell design and construction
Genomics and genome replacement strategies
Viral engineering
Automated and robotic assembly platforms for synthetic biology
DNA synthesis methodologies
Metagenomics and synthetic metagenomic analysis
Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction
Gene optimization
Methods for genome-scale measurements of transcription and metabolomics
Systems biology and methods to integrate multiple data sources
in vitro and cell-free synthetic biology and molecular programming
Nucleic acid engineering.