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Jeong Hee Kim

Publications and source records attributed to Jeong Hee Kim.

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Non-perturbative Bacterial Identification Directly from Solid Agar Plates Using Raman

Raman spectroscopy is a promising tool for microbial identification, yet its implementation in microbiology and clinical workflow is still restricted due to the accompanying additional preparation required to focus on microbial signals. Here, we demonstrate Raman-based bacterial identification directly from unopened, inverted agar plates, the same conditions used during incubation. Our approach enabled identification with single gene-level sensitivity using two Escherichia coli variants, differing only in green fluorescent protein (GFP) expression, across diverse media and substrate material conditions, despite the interrogation path traversing 3-4 mm thick background material. We integrated traditional density functional theory (DFT)-based material computation with machine learning analysis, achieving over 97.7% classification accuracy, surpassing the performance of standard measurements from opened plates by 10.8% higher mean accuracy and 0.76% less variance. We further demonstrated Raman mapping-based colony identification via Raman peaks characteristic to GFPmut3 chromophore structure generated by DFT. Our approach is robust to changes in algorithms or substrate materials and promises real-time, non-perturbative monitoring of bacterial growth, biofilm formation, and antimicrobial resistance development.

q-bio.QM

Interplay of Electrostatic Interaction and Steric Repulsion between Bacteria and Gold Surface Influences Raman Enhancement

Plasmonic nanostructures have wide applications in photonics including pathogen detection and diagnosis via Surface-Enhanced Raman Spectroscopy (SERS). Despite major role plasmonics play in signal enhancement, electrostatics in SERS is yet to be fully understood and harnessed. Here, we perform a systematic study of electrostatic interactions between 785 nm resonant gold nanorods designed to harbor zeta potentials of +29, +16, 0 and -9 mV spanning positive neutral and negative domains. SERS activity is tested on representative Gram-negative Escherichia coli and Gram-positive Staphylococcus epidermidis bacteria with zeta potentials of -30 and -23 mV respectively in water. Raman spectroscopy and Cryo-Electron microscopy reveal that +29, +16, 0 and -9 mV nanorods give SERS enhancement of 7.2X, 3.6X, 4.2X, 1.3X to Staphylococcus epidermidis and 3.9X, 2.8X, 2.9X, 1.1X to Escherichia coli. Theoretical results show that electrostatics play the major role among all interaction forces in determining cell-nanorod proximity and signal enhancement. We identify steric repulsion due to cell protrusions to be the critical opposing force. Finally, a design principle is proposed to estimate the electrostatic strength in SERS. Our work provides new insights into the principle of bacteria-nanorod interactions, enabling reproducible and precise biomolecular readouts, critical for next-generation point-of-care diagnostics and smart healthcare applications.

q-bio.CB