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Updated: Feb 21, 2026

Colorimetric Detection of Bacteria Using Litmus Test
Published on: September 17, 2016
Harnessing soft DNA nanospheres as a superior alternative to hard nanoparticles for boosting DNAzyme-based
Hengxin Yu1, Guohai Lin2, Jing Jiang2
1Fujian Provincial Engineering Research Center of Rural Waste Recycling Technology, College of Environmental and Safety Engineering, Fuzhou University, Fuzhou, 350108, PR China; Fujian Key Laboratory of Functional Marine Sensing Materials, College of Materials and Chemical Engineering, Minjiang University, Fuzhou, Fujian, 350108, PR China.
Abstract:
Lead ions (Pb2+), as a persistent and bioaccumulative environmental toxin, pose a significant threat to public health, demanding ultrasensitive and field-deployable detection methods. Conventional sensors often struggle with a trade-off between sensitivity and stability, especially when employing hard nanomaterial enhancers like gold nanoparticles. However, the practical utility of these inorganic nanoprobes is often compromised by their susceptibility to surface passivation (biofouling) and aggregation in salt-rich or protein-rich environments. Herein, we introduce a novel concept of a soft-matter DNA nanoreactor for engineering a high-performance colorimetric biosensor. This nanoreactor is self-assembled from a single palindromic DNA strand into a DNA nanosphere (DS), creating a spatially confined microenvironment. By anchoring a Pb2+-specific DNAzyme system onto this platform, we developed the DS-S-Dz probe. The nanoreactor architecture dramatically enhances the catalytic efficiency of the DNAzyme through a profound spatial confinement effect, which accelerates the Pb2+-triggered cleavage of a substrate strand and subsequent release of a G-rich sequence. This liberated sequence then folds into a G-quadruplex/hemin DNAzyme, catalyzing a robust colorimetric reaction. This strategy effectively suppresses background noise while amplifying the target signal, achieving a remarkable limit of detection of 0.96 nM, a 50-fold improvement over the non-amplified system (48 nM) and well below the EPA safety limit (72 nM). The sensor demonstrated exceptional selectivity against a panel of interfering metal ions and proved its robustness and accuracy in complex real-world samples like tap water and milk. This work presents a paradigm shift from simple nanoparticle enhancement to the rational design of programmable DNA nanoreactors, offering a powerful and elegant platform for sensitive and reliable environmental monitoring.

