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Engineered bacterial biofilms immobilizing nanoparticles enable diverse catalytic applications

Science China Press


IMAGE: Diverse catalytic applications of tunable functional E. coli biofilms with anchored nano-objects. (a) The biofilm-anchored Au NPs enable the recyclable catalytic reduction of the toxic p-nitrophenol (PNP) into the harmless... view more 

Credit: ©Science China Press

Nano-scale objects (1 - 100 nm) are desirable nano-catalysts featured with more catalytic active sites due to higher surface-area-to-volume ratios. The nano-scale nature brings several attendant challenges such as leakage of nano-catalysts to ambient environment and difficulties in reusing nanocatalysts over repeated reaction cycles. A major strategy for addressing these challenges has been the immobilization of nano-objects on various substrates via a variety of technological approaches. However, inorganic and bio-derived or bio-inspired substrates obviously lack "biology-only" attributes like self-regeneration, cellular-growth-based scalability, and the ability of cells to biosynthesize complex enzymes, substrates, co-enzymes, or other required reagents or reaction components in situ. Moreover, studies that have immobilized nano-objects directly on cell surfaces have reported damage to cells.

The Zhong group from the Materials and Physical Biology Division, at ShanghaiTech University has made a major conceptual advance in developing a new abiotic/biotic interface towards the integration and immobilization of nanoscale objects with living cells for catalysis. Very briefly, they successfully showed how engineered amyloid monomers expressed, secreted and assembled in the extracellular matrix of living Escherichia coli (E. coli) biofilms can be harnessed to anchor functional nano-scale catalysts to make highly efficient, scalable, tunable, and reusable living catalyst systems. In their proof-of-concept studies, they have demonstrated three simple catalytic systems, including biofilm-anchored gold nanoparticles to degrade the pollutant p-nitrophenol, biofilm-anchored hybrid Cd0.9Zn0.1S quantum dots (QDs) and gold nanoparticles to efficiently degrade organic dyes, and biofilm-anchored CdSeS@ZnS QDs in a dual bacterial strain semi-artificial photosynthesis system for hydrogen production. As revealed in their studies, the extracellular matrix in biofilms indeed provides an ideal milieu for interfacing and anchoring nano-objects for direct catalysis and for their integration with the metabolism of living cells: even after multiple rounds of reactions, nano-catalysts were still robustly anchored to biofilms and the E. coli cells were still alive for easy regeneration. Importantly, such an approach would open up the extremely powerful and unique attributes of living systems.

There is a large diversity of bacterial biofilms with different functionalities in nature, and their study thus lays the conceptual foundation for coupling the uniquely dynamic properties and capacities of these living materials with the highly reactive nanoparticles to innovatively solve challenges in bioremediation, bioconversion, and energy. Their research will spur further research for creating more efficient and industrially important reaction systems by building and integrating more intricate biofilms/inorganic hybrid catalytic systems.


See the article:

Xinyu Wang†, Jiahua Pu†, Yi Liu, Fang Ba, Mengkui Cui, Ke Li, Yu Xie, Yan Nie, Qixi Mi, Tao Li, Lingli Liu, Manzhou Zhu, Chao Zhong

Immobilization of functional nano-objects in living engineered bacterial biofilms for catalytic applications

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