Protocols for Test

E.coli Top10 was used for all the experiments and grown in Luria–Bertani (LB) medium or M9 minimal medium using glycerol as the carbon source. Kanamycin (10 μg/mL), ampicillin (50 μg/mL) and chloramphenicol (170 μg/mL) were added as appropriate.

Protocol 1
E.coli was grown overnight in LB medium at 37 °C and then diluted 100-fold in fresh LB medium in 96-well plates (Corning Incorporated, 3599). Then each culture (200 μL) was induced for 12 hours at 30°C with inducers of different concentrations. Then the fluorescence intensity of cultures was measured by microplate reader (Thermo) or LSRFortessa flow cytometer (BD Biosciences).

Protocol 2
E.coli was grown overnight in LB medium at 37 °C and then diluted 100-fold in fresh LB medium in 96-well plates (Corning Incorporated, 3599). After 3 hours’ culture at 30 °C, each culture (200 μL) was induced for 7 hours with inducers of different concentrations. Then the fluorescence intensity of cultures was measured by microplate reader (Thermo) or LSRFortessa flow cytometer (BD Biosciences).

Protocol 3
E.coli was grown overnight in LB medium at 37 °C and then diluted 100-fold in fresh LB medium in 96-well plates (Corning Incorporated, 3599). After 6 hours’ culture at 30 °C, each culture (200 μL) was centrifuged at 4000 r.p.m. for 10 minutes and was suspended in 200 μL of fresh LB medium containing inducers of different concentrations for 4 hours. Then the fluorescence intensity of cultures was measured by microplate reader (Thermo) or LSRFortessa flow cytometer (BD Biosciences).

Protocol 4
E.coli was grown overnight in LB medium at 37 °C and then diluted 100-fold in fresh LB medium in 96-well plates (Corning Incorporated, 3599). Then each culture (200 μL) was induced for 12 hours at 37°C with inducers of different concentrations. Then the fluorescence intensity of cultures was measured by microplate reader (Thermo) or LSRFortessa flow cytometer (BD Biosciences).

Protocol 5
E.coli was grown overnight in LB medium at 37 °C and then diluted 100-fold in fresh M9 minimal medium in 96-well plates (Corning Incorporated, 3599). Then each culture (200 μL) was induced for 12 hours at 30°C with inducers of different concentrations. Then the fluorescence intensity of cultures was measured by microplate reader (Thermo) or LSRFortessa flow cytometer (BD Biosciences).

Protocol 6
E.coli was grown overnight in LB medium at 37 °C and then diluted 100-fold in fresh M9 minimal medium in microcentrifuge tubes (1.5 mL, Axygen). Then each culture (200 μL) was induced for 12 hours at 30°C with inducers of different concentrations. Then the fluorescence intensity of cultures was measured by microplate reader (Thermo) or LSRFortessa flow cytometer (BD Biosciences).

Primary Test
Primary Test aims to investigate whether a particular biosensor could be induced by the aromatic compounds mentioned in previous studies.
Inducers (summarized from previous studies) were added into the LB medium at 1000 μM (for the non-cytotoxic compounds) or 100 μM (for the cytotoxic compounds).

ON-OFF Test
ON-OFF Test functions to determine aromatic compounds that can induce a certain biosensor.
78 aromatic compounds were individually added into the LB medium at 1000 μM (for the non-cytotoxic compounds), 100 μM (for the cytotoxic compounds) or 10μM (for benzene). (For detail of all the compounds, Click Here).

Dose-response Curve Test
Dose-response Curve Test is to deeply characterize the relationship between fluorescence intensity (or induction ratio) and the concentration of inducers.
Inducers summarized from ON-OFF Test were individually added into the LB medium at concentration ranging from micro-molar to mili-molar.

Orthogonality Test
Orthogonality Test aims to prove that a compound which is not an inducer will not influence the detection of inducers.
Two kinds of aromatic compounds (one is an inducer while the other isn’t for a particular biosensor) were added together into the LB medium at concentration ranging from micro-molar to mili-molar.

Microplate Reader
E.coli were harvested by centrifugation at 4000 r.p.m. for 10 minutes and then resuspended in 200 μl of PBS (phosphate-buffered saline). OD600 and GFPuv fluorescence (excitation 485 nm and emission 515 nm) was measured using microplate reader (Thermo).
As for the data analysis, OD600 and fluorescence intensity of PBS measured in the same way was subtracted as blank. Fluorescence intensity of each well was normalized by OD600 of the same well. The average of fluorescence intensity was obtained from three replicates performed on different 96-well plates.

Flow cytometry analysis
Flow cytometer data were obtained using an LSRFortessa flow cytometer (BD Biosciences). All the data were gated by forward and side scatter, and each data consists of at least 10,000 cells. The geometry mean fluorescence was calculated with FlowJo. The average of means was obtained from three replicates performed on different 96-well plates.