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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 %.
- Received:
- Accepted:
- Published Online:
Keyword(s):
aldehyde tag
,
directed evolution
,
error-prone PCR
,
immobilization
,
insecticide
and
pump inhibitor
© 2020 The Authors