Chromosomally located gene fusions constructed in Acinetobacter sp. ADP1 for the detection of salicylate

Abstract

Summary Acinetobacter sp. ADP1 is a common soil‐associated bacterium with high natural competency, allowing it to efficiently integrate foreign DNA fragments into its chromosome. This property was exploited to engineer salicylate‐inducible luxCDABE and green fluorescent protein (GFP) variants of Acinetobacter sp. ADP1. Specifically, Acinetobacter sp. ADPWH _lux displayed the higher sensitivity when comparing the two variants (minimum detection c . 0.5–1 µM salicylate) and a faster turnover of the lux marker gene, making it suitable for whole‐cell luminescence assays of salicylate concentration. In contrast, the longer maturation and turnover times of the GFP protein make the Acinetobacter sp. ADPWH _gfp variant more suited to applications involving whole‐cell imaging of the presence of salicylate. The sensitivity of the luxCDABE variant was demonstrated by assaying salicylate production in naphthalene‐degrading cultures. Assays using ADPWH _lux specifically mapped the kinetics of salicylate production from naphthalene and were similar to that observed by high‐performance liquid chromatography (HPLC) data. However, ADPWH _lux exhibited the higher sensitivity, when compared with HPLC, for detecting salicylate production during the first 24 h of naphthalene metabolism. These data demonstrate that the engineered Acinetobacter variants have significant potential for salicylate detection strategies in laboratory and field studies, especially in scenarios where genetic stability of the construct is required for in situ monitoring.

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