Source abstract
Abstract
The emerging field of biofabrication capitalizes on nature's ability to create materials with a wide range of well-defined physical and electronic properties. Particularly, there is a current push to utilize programmed, self-organization of living cells for material fabrication. However, much research is still necessary at the interface of synthetic biology and materials engineering to make biofabrication a viable technique to develop functional devices. Here, the authors exploit the ability of Escherichia coli to contribute to material fabrication by designing and optimizing growth platforms to direct inorganic nanoparticle (NP) synthesis, specifically cadmium sulfide (CdS) NPs, onto porous polycarbonate membranes. Additionally, current, nonbiological, chemical synthesis methods for CdS NPs are typically energy intensive and use high concentrations of hazardous cadmium precursors. Using biosynthesis methods through microorganisms could potentially alleviate these issues by precipitating NPs with less energy and lower concentrations of toxic precursors. The authors adopted extracellular precipitation strategies to form CdS NPs on the membranes as bacterial/membrane composites and characterized them by spectroscopic and imaging methods, including energy dispersive spectroscopy, and scanning and transmission electron microscopy. This method allowed us to control the localization of NP precipitation throughout the layered bacterial/membrane composite, by varying the timing of the cadmium precursor addition. Additionally, the authors demonstrated the photodegradation of methyl orange using the CdS functionalized porous membranes, thus confirming the photocatalytic properties of these composites for eventual translation to device development. If combined with the genetically programmed self-organization of cells, this approach promises to directly pattern CdS nanostructures on solid supports.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Department of Mechanical Engineering and Materials Science, Duke University, 144 Hudson Hall Box 90300, Durham, North Carolina 27708
Department of Biomedical Engineering, Duke University, 101 Science Drive, Durham, North Carolina 27708
Department of Biomedical Engineering, Duke University, 101 Science Drive, Durham, North Carolina 27708; Center for Genomic and Computational Biology, Duke University, 101 Science Drive, Durham, North Carolina 27708; and Department of Molecular Genetics and Microbiology, Duke University School of Medicine, DUMC 3710, Durham, North Carolina 27710
Department of Mechanical Engineering and Materials Science, Duke University, 144 Hudson Hall Box 90300, Durham, North Carolina 27708 and Department of Biomedical Engineering, Duke University, 101 Science Drive, Durham, North Carolina 27708
Funding
HHS | NIH | National Institute of Biomedical Imaging and Bioengineering · DOD | United States Navy | Office of Naval Research