dc.citation.endPage |
196 |
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dc.citation.startPage |
185 |
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dc.citation.title |
ACS SYMPOSIUM SERIES |
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dc.citation.volume |
762 |
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dc.contributor.author |
Gu, M.B. |
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dc.contributor.author |
Mitchell, Robert J. |
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dc.contributor.author |
Kim, J.H. |
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dc.date.accessioned |
2023-12-22T12:09:06Z |
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dc.date.available |
2023-12-22T12:09:06Z |
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dc.date.created |
2014-09-18 |
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dc.date.issued |
2000 |
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dc.description.abstract |
Through the use of the recombinant bacterium TV 1061, containing a grpE-luxCDABE fusion, and a previously developed continuous toxicity monitoring system we were able to detect protein damaging toxicity in aqueous systems. This bacterial strain is responsive to the toxicity of protein-damaging agents and produces a bioluminescent response in their presence. The system uses the two-stage mini-bioreactors previously developed in our lab which allows stability even under the conditions that the toxicity greatly exceeded the sub-lethal level. The response of the strain under these conditions shows a unique signature when compared to previously tested strains. |
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dc.identifier.bibliographicCitation |
ACS SYMPOSIUM SERIES, v.762, pp.185 - 196 |
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dc.identifier.issn |
0097-6156 |
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dc.identifier.scopusid |
2-s2.0-0039845514 |
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dc.identifier.uri |
https://scholarworks.unist.ac.kr/handle/201301/6305 |
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dc.language |
영어 |
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dc.publisher |
American Chemical Society |
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dc.title |
Continuous monitoring of protein damaging toxicity using a recombinant bioluminescent Escherichia coli |
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dc.type |
Article |
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dc.description.journalRegisteredClass |
scopus |
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