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Microbiology (Reading) ; 166(11): 1019-1024, 2020 11.
Article in English | MEDLINE | ID: mdl-33108264

ABSTRACT

A formylglycine-generating enzyme (FGE)-sulfatase-based whole-cell biosensor was genetically improved into a single-copy system by integrating the Sinorhizobium meliloti transcriptional activator ChpR and the chpA promoter-FGE-sulfatase fusion into the Escherichia coli chromosome. The sensitivity was further enhanced through a random mutagenesis of the chpR. The new integrated biosensor offered both a lower detection limit [5 nM chlorpyrifos (CPF)] and fluorescence background. The ready-to-use kit was developed using silica gel for on-field detection. The biosensor kit was stable for 20 days when stored at 4 °C. Moreover, a 1-(1-naphthylmethyl)-piperazine (NMP) efflux pump inhibitor can improve the sensitivity by 57 %.


Subject(s)
Biosensing Techniques/methods , Chlorpyrifos/isolation & purification , Pesticides/isolation & purification , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Directed Molecular Evolution , Escherichia coli/drug effects , Escherichia coli/genetics , Escherichia coli/metabolism , Glycine/analogs & derivatives , Glycine/metabolism , Limit of Detection , Piperazines/pharmacology , Promoter Regions, Genetic , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Sinorhizobium meliloti/genetics , Sulfatases/genetics , Sulfatases/metabolism , Transcription Factors/genetics , Transcription Factors/metabolism
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