journal article·2024-11-13Open access

Facile Mechanochemical Functionalization of Hydrophobic Substrates for Single-Walled Carbon Nanotube Based Optical Reporters of Hydrolase Activity

Abbas Elhambakhsh, Mohaddeseh Abbasi, Cole R. Dutter, Marshall D. McDaniel, Brett VanVeller, Andrew C. Hillier, Nigel F. Reuel

ACS Applied Materials & Interfaces· Volume 16· Issue 45

Abstract

Single walled carbon nanotubes (SWCNT) have recently been demonstrated as modular, near-infrared (nIR) probes for reporting hydrolase activity; however, these have been limited to naturally amphipathic substrate targets used to noncovalently functionalize the hydrophobic nanoparticles. Many relevant substrate targets are hydrophobic (such as recalcitrant biomass) and pose a challenge for modular functionalization. In this work, a facile mechanochemistry approach was used to couple insoluble substrates, such as lignin, to SWCNT using l-lysine amino acid as a linker and tip sonication as the mechanochemical energy source. The proposed coupling mechanism is ion pairing between the lysine amines and lignin carboxylic acids, as evidenced by FTIR, NMR, SEM, and elemental analyses. The limits of detection for the lignin-lysine-SWCNT (LLS) probe were established using commercial enzymes and found to be 0.25 ppm (volume basis) of the formulated product. Real-world use of the LLS probes was shown by evaluating soil hydrolase activities of soil samples gathered from different corn root proximal locations and soil types. Additionally, the probes were used to determine the effect of storage temperature on the measured enzyme response. The modularity of this mechanochemical functionalization approach is demonstrated with other substrates such as zein and 9-anthracenecarboxylic acid, which further corroborate the mechanochemical mechanism.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Photoreceptor and optogenetics research · Carbon Nanotubes in Composites · Supramolecular Self-Assembly in Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemical and Biological Engineering, Iowa State University, 618 Bissell Rd., Ames, Iowa 50011, United States

Department of Chemistry, Iowa State University, Ames, Iowa 50011, United States

Department of Agronomy, Iowa State University, Ames, Iowa 50011, United States

Funding

National Institute of Food and Agriculture · National Institute of General Medical Sciences · National Science Foundation · Iowa State VPR Seed Grant Fund

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