Reprogramming bacteria to seek and destroy an herbicide

Journal name:
Nature Chemical Biology
Volume:
6,
Pages:
464–470
Year published:
DOI:
doi:10.1038/nchembio.369
Received
Accepted
Published online

Abstract

A major goal of synthetic biology is to reprogram cells to perform complex tasks. Here we show how a combination of in vitro and in vivo selection rapidly identifies a synthetic riboswitch that activates protein translation in response to the herbicide atrazine. We further demonstrate that this riboswitch can reprogram bacteria to migrate in the presence of atrazine. Finally, we show that incorporating a gene from an atrazine catabolic pathway allows these cells to seek and destroy atrazine.

At a glance

Figures

  1. Chemical structures and synthetic scheme.
    Figure 1: Chemical structures and synthetic scheme.

    Left, the structure of atrazine (1); right, scheme for the synthesis of an atrazine derivative bound to solid support.

  2. Progress of the SELEX experiment.
    Figure 2: Progress of the SELEX experiment.

    The fraction of the RNA pool bound to the atrazine-derivatized column after each round of SELEX. Counterselection against hydroxyatrazine (1 mM) was performed after round 9.

  3. Motility selection for riboswitches.
    Figure 3: Motility selection for riboswitches.

    (a) To select riboswitches, a library of atrazine-binding aptamers is cloned upstream of a randomized sequence in the 5′ UTR of the cheZ gene that controls E. coli motility. The randomized sequence can become an expression platform that couples ligand binding and gene expression. (b) Schematic of selection scheme. The library of sequences is introduced in to a cheZ-deficient strain of E. coli, and cells are plated at the center of a Petri dish containing semisolid medium without atrazine. Cells that do not move are selected, and the process is repeated. Finally, cells are plated in the presence of atrazine (500 μM) and the cells that migrate are chosen.

  4. In vivo characterization of atrazine-dependent riboswitches.
    Figure 4: In vivo characterization of atrazine-dependent riboswitches.

    (a) Dose-response relationship for β-galactosidase activity (measured in Miller units) versus atrazine and hydroxyatrazine concentration. Dashed lines indicate that the compounds began to precipitate from the solution. (b) Motility of riboswitch-containing cells grown for 16 h at 30 °C on semisolid agar in the absence and presence of atrazine (500 μM). The diameter of the plates is 85 mm. (c) Migration radii of reprogrammed cells as a function of time. The cells were inoculated on swarm agar plates either in the presence (filled circles, 500 μM) or absence (open circles) of atrazine. Migration radius was measured using a ruler from images generated at intervals of 2 h, beginning 6 h after inoculation. The uncertainties in measurement are smaller than the symbols.

  5. Characterization of atrazine-dependent riboswitches.
    Figure 5: Characterization of atrazine-dependent riboswitches.

    (a) Polyacrylamide gel electrophoresis of RNA products generated by in-line probing of 5′-32P labeled RNA. The full-length RNA contained the entire 5′ UTR and the first 56 nucleotides of the coding region. NR, T1 and OH represent no reaction, partial digest with RNase T1 (G-specific cleavage) and partial digest with alkali, respectively. RNA was incubated in the absence (−) or presence (+) of 1 mM atrazine. Product bands corresponding to cleavage after G residues are numbered and marked with filled arrowheads. Red arrowheads mark the nucleotides that react less in the presence of atrazine; green arrowheads mark the positions that react more. The insert corresponds to the N10 region. (b) Proposed mechanism of atrazine-dependent activation. Secondary structures are from Mfold48, 49 and the structure-probing data in a. In the absence of atrazine ('off' state), the N10 region forms a pseudoknot with part of the N40 region, sequestering the ribosome-binding site. In the presence of atrazine ('on' state), the conformation on the right is favored. Nucleotides from the pseudoknot structure are boxed, the N10 region is in bold italics, less reactive nucleotides are red and more reactive ones are green. The numbers correspond to the sites as marked in a. (c) Sequence, structure and in vivo β-galactosidase activity of the mutated riboswitch. The mutated nucleotides are shown in red. The in vivo β-galactosidase assay (measured in Miller units) was conducted in E. coli in the absence (white bar) and presence of atrazine (750 μM, black bar).

  6. Motility of reprogrammed E. coli cells expressing GFP.
    Figure 6: Motility of reprogrammed E. coli cells expressing GFP.

    The images on the left were taken under white light whereas images on the right were taken under epi-UV light at 365-nm wavelength using a bandpass filter. (a) Cells containing cheZ under the control of the synthetic riboswitch, but lacking atzA. No atrazine catabolism is observed. (b) Cells containing both cheZ under the control of the synthetic riboswitch and atzA. These cells show concentric circles due to cell motility and atrazine catabolism, which is indicated by the dark circles. White circles are cells fluorescing under UV light.

Compounds

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Author information

Affiliations

  1. Department of Chemistry and Center for Fundamental and Applied Molecular Evolution, Emory University, Atlanta, Georgia, USA.

    • Joy Sinha,
    • Samuel J Reyes &
    • Justin P Gallivan

Contributions

J.P.G. conceived the research. J.S. performed the molecular and microbiology experiments; S.J.R. carried out the synthetic chemistry. J.S. and J.P.G. analyzed data and wrote the paper.

Competing financial interests

The authors declare no competing financial interests.

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