Please use this identifier to cite or link to this item:
https://doi.org/10.1038/msb.2011.55
DC Field | Value | |
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dc.title | Engineering microbes to sense and eradicate Pseudomonas aeruginosa, a human pathogen | |
dc.contributor.author | Saeidi, N | |
dc.contributor.author | Wong, C.K | |
dc.contributor.author | Lo, T.-M | |
dc.contributor.author | Nguyen, H.X | |
dc.contributor.author | Ling, H | |
dc.contributor.author | Leong, S.S.J | |
dc.contributor.author | Poh, C.L | |
dc.contributor.author | Chang, M.W | |
dc.date.accessioned | 2020-10-20T08:11:56Z | |
dc.date.available | 2020-10-20T08:11:56Z | |
dc.date.issued | 2011 | |
dc.identifier.citation | Saeidi, N, Wong, C.K, Lo, T.-M, Nguyen, H.X, Ling, H, Leong, S.S.J, Poh, C.L, Chang, M.W (2011). Engineering microbes to sense and eradicate Pseudomonas aeruginosa, a human pathogen. Molecular Systems Biology 7 : 521. ScholarBank@NUS Repository. https://doi.org/10.1038/msb.2011.55 | |
dc.identifier.issn | 1744-4292 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/178171 | |
dc.description.abstract | Synthetic biology aims to systematically design and construct novel biological systems that address energy, environment, and health issues. Herein, we describe the development of a synthetic genetic system, which comprises quorum sensing, killing, and lysing devices, that enables Escherichia coli to sense and kill a pathogenic Pseudomonas aeruginosa strain through the production and release of pyocin. The sensing, killing, and lysing devices were characterized to elucidate their detection, antimicrobial and pyocin release functionalities, which subsequently aided in the construction of the final system and the verification of its designed behavior. We demonstrated that our engineered E. coli sensed and killed planktonic P. aeruginosa, evidenced by 99% reduction in the viable cells. Moreover, we showed that our engineered E. coli inhibited the formation of P. aeruginosa biofilm by close to 90%, leading to much sparser and thinner biofilm matrices. These results suggest that E. coli carrying our synthetic genetic system may provide a novel synthetic biology-driven antimicrobial strategy that could potentially be applied to fighting P. aeruginosa and other infectious pathogens. © 2011 EMBO and Macmillan Publishers Limited. | |
dc.publisher | EMBO Press | |
dc.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20201031 | |
dc.subject | pyocin | |
dc.subject | antiinfective agent | |
dc.subject | bacterial protein | |
dc.subject | drug derivative | |
dc.subject | gamma butyrolactone | |
dc.subject | green fluorescent protein | |
dc.subject | homoserine | |
dc.subject | hybrid protein | |
dc.subject | n (3 oxododecanoyl)homoserine lactone | |
dc.subject | N-(3-oxododecanoyl)homoserine lactone | |
dc.subject | pyocin | |
dc.subject | article | |
dc.subject | bacterial strain | |
dc.subject | cell viability | |
dc.subject | controlled study | |
dc.subject | Escherichia coli | |
dc.subject | genetic engineering and gene technology | |
dc.subject | nonhuman | |
dc.subject | priority journal | |
dc.subject | protein secretion | |
dc.subject | Pseudomonas aeruginosa | |
dc.subject | quorum sensing | |
dc.subject | antibiosis | |
dc.subject | biofilm | |
dc.subject | biosynthesis | |
dc.subject | chemistry | |
dc.subject | drug effect | |
dc.subject | Escherichia coli | |
dc.subject | gene expression regulation | |
dc.subject | genetic procedures | |
dc.subject | genetics | |
dc.subject | growth, development and aging | |
dc.subject | human | |
dc.subject | metabolism | |
dc.subject | methodology | |
dc.subject | microbiology | |
dc.subject | pathogenicity | |
dc.subject | plasmid | |
dc.subject | Pseudomonas infection | |
dc.subject | quorum sensing | |
dc.subject | reporter gene | |
dc.subject | synthetic biology | |
dc.subject | transgenic organism | |
dc.subject | Escherichia coli | |
dc.subject | Pseudomonas aeruginosa | |
dc.subject | Escherichia coli | |
dc.subject | Pseudomonas aeruginosa | |
dc.subject | 4-Butyrolactone | |
dc.subject | Anti-Bacterial Agents | |
dc.subject | Antibiosis | |
dc.subject | Bacterial Proteins | |
dc.subject | Biofilms | |
dc.subject | Biosensing Techniques | |
dc.subject | Escherichia coli | |
dc.subject | Gene Expression Regulation, Bacterial | |
dc.subject | Genes, Reporter | |
dc.subject | Green Fluorescent Proteins | |
dc.subject | Homoserine | |
dc.subject | Humans | |
dc.subject | Organisms, Genetically Modified | |
dc.subject | Plasmids | |
dc.subject | Pseudomonas aeruginosa | |
dc.subject | Pseudomonas Infections | |
dc.subject | Pyocins | |
dc.subject | Quorum Sensing | |
dc.subject | Recombinant Fusion Proteins | |
dc.subject | Synthetic Biology | |
dc.type | Article | |
dc.contributor.department | CIVIL AND ENVIRONMENTAL ENGINEERING | |
dc.contributor.department | BIOCHEMISTRY | |
dc.contributor.department | BIOMEDICAL ENGINEERING | |
dc.description.doi | 10.1038/msb.2011.55 | |
dc.description.sourcetitle | Molecular Systems Biology | |
dc.description.volume | 7 | |
dc.description.page | 521 | |
dc.published.state | published | |
Appears in Collections: | Staff Publications Elements |
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