4.4 Article

Genetic engineering biofilms in situ using ultrasound-mediated DNA delivery

Journal

MICROBIAL BIOTECHNOLOGY
Volume 14, Issue 4, Pages 1580-1593

Publisher

WILEY
DOI: 10.1111/1751-7915.13823

Keywords

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Funding

  1. EPSRC [EP/M002403/1, EP/N009746/1]
  2. Commonwealth Scholarship Commission in the form of Commonwealth Rutherford Fellowship [SGRF-2017-471]
  3. Jardine Foundation
  4. EPSRC [EP/N009746/1, EP/M002403/1] Funding Source: UKRI

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The study demonstrated the successful introduction of plasmids into established non-competent bacterial biofilms using ultrasound-mediated DNA delivery technique. This method allowed for expression of exogenous genes and functional effects in biofilms, enhancing their potential applications in environments, industries, and medical fields.
The ability to directly modify native and established biofilms has enormous potential in understanding microbial ecology and application of biofilm in 'real-world' systems. However, efficient genetic transformation of established biofilms at any scale remains challenging. In this study, we applied an ultrasound-mediated DNA delivery (UDD) technique to introduce plasmid to established non-competent biofilms in situ. Two different plasmids containing genes coding for superfolder green fluorescent protein (sfGFP) and the flavin synthesis pathway were introduced into established bacterial biofilms in microfluidic flow (transformation efficiency of 3.9 +/- 0.3 x 10(-7) cells in biofilm) and microbial fuel cells (MFCs), respectively, both employing UDD. Gene expression and functional effects of genetically modified bacterial biofilms were observed, where some cells in UDD-treated Pseudomonas putida UWC1 biofilms expressed sfGFP in flow cells and UDD-treated Shewanella oneidensis MR-1 biofilms generated significantly (P < 0.05) greater (61%) bioelectricity production (21.9 +/- 1.2 mu A cm(-2)) in MFC than a wild-type control group (similar to 13.6 +/- 1.6 mu A cm(-2)). The effects of UDD were amplified in subsequent growth under selection pressure due to antibiotic resistance and metabolism enhancement. UDD-induced gene transfer on biofilms grown in both microbial flow cells and MFC systems was successfully demonstrated, with working volumes of 0.16 cm(3) and 300 cm(3), respectively, demonstrating a significant scale-up in operating volume. This is the first study to report on a potentially scalable direct genetic engineering method for established non-competent biofilms, which can be exploited in enhancing their capability towards environmental, industrial and medical applications.

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