# Luminescence-Based Strategies for Detecting β-Lactamase Activity: A Review of the Last Decade

**Authors:** Michał Jakub Korytkowski, Anna Baraniak, Alicja Boryło, Paweł Rudnicki-Velasquez

PMC · DOI: 10.3390/life16020250 · 2026-02-02

## TL;DR

This paper reviews recent advances in luminescence-based methods for detecting β-lactamase activity, which could improve rapid diagnostics for antibiotic resistance.

## Contribution

The paper provides a comprehensive review of luminescence-based strategies for β-lactamase detection developed between 2015 and 2025.

## Key findings

- Luminescent assays offer rapid, sensitive detection of β-lactamase activity within minutes.
- Recent trends include self-immobilizing fluorogenic probes and AI-assisted mobile platforms for diagnostics.
- These methods can distinguish between different types of β-lactamases like AmpC, ESBL, and carbapenemases.

## Abstract

Rapid detection of β-lactamase activity is becoming increasingly important as β-lactam resistance spreads at an alarming rate and conventional diagnostics often require several hours to deliver actionable results. Over the past decade, methods based on luminescence, bioluminescence, chemiluminescence, and fluorescence have become powerful tools for the functional assessment of resistance resulting from β-lactamase activity. These approaches provide highly sensitive, activity-based readouts, often within minutes, and frequently rely on simple optical instrumentation. In this review, we summarize recent developments in luminescent probe design between 2015 and 2025, with emphasis on reaction mechanisms, analytical performance, and the ability of these systems to discriminate between different β-lactamases, including narrow-spectrum enzymes, AmpC, ESBL, and carbapenemases. We also discuss their applications in bacterial cultures, clinical isolates, complex biological matrices and, in some cases, in vivo models. While luminescent assays are not yet positioned to replace standard susceptibility testing, they offer a practical and increasingly robust complement to culture-based and molecular methods. The emerging trends highlighted here, such as self-immobilizing fluorogenic probes, chemiluminescent relay systems, nanomaterial-based sensors and AI-assisted mobile platforms, suggest that luminescent β-lactamase detection could play a meaningful role in future rapid diagnostics and resistance surveillance.

## Full-text entities

- **Genes:** OXA-2 [NCBI Gene 13906543], CTX-M-1 [NCBI Gene 13909205], KPC-2 [NCBI Gene 18983503], OXA-1 [NCBI Gene 8319151], Carbapenemase [NCBI Gene 13906542], F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}, TEM-1 [NCBI Gene 2716540], ESBL [NCBI Gene 13906541], AmpC [NCBI Gene 7872529]
- **Diseases:** antibiotic (MESH:D004761), BLRB (MESH:C000719206), Gram (MESH:D016908), injury to (MESH:D014947), AMR (MESH:D060467), CPO (MESH:D046349), deaths (MESH:D003643), toxicity (MESH:D064420), urinary tract infection (MESH:D014552), skin wound infection (MESH:D014946), peritonitis (MESH:D010538), infection (MESH:D007239), PKU (MESH:D010661), negative (MESH:D064726), CPOs (MESH:D000092124), bacterial (MESH:D001424), infectious diseases (MESH:D003141), MRSA (MESH:D013203)
- **Chemicals:** thioether (MESH:D013440), zinc (MESH:D015032), oxygen (MESH:D010100), Na2S (MESH:C033479), quinone methide (MESH:C068040), acids (MESH:D000143), gold (MESH:D006046), saline (MESH:D012965), MMT (MESH:C009907), PA (MESH:D011478), singlet-oxygen (MESH:D026082), metal (MESH:D008670), carbon (MESH:D002244), monobactams (MESH:D008997), D-luciferin (MESH:C532924), ester (MESH:D004952), FMNH2 (MESH:C540087), N (MESH:D009584), azide (MESH:D001386), 7-hydroxycoumarin-4-acetic acid (MESH:C102522), EDTA (MESH:D004492), merocyanine (MESH:C548873), IMP (MESH:D007291), ceftiofur sodium (MESH:C053503), relebactam (MESH:C568736), thiophenol (MESH:C042983), meropenem (MESH:D000077731), ebselen (MESH:C042986), CHAPS (MESH:C028213), coumarin (MESH:C030123), benzene sulfonate (MESH:C032365), vancomycin (MESH:D014640), TPE (MESH:C000617116), Carbapenem (MESH:D015780), PenG (MESH:D010400), avibactam (MESH:C543519), Amplex Red (MESH:C470430), water (MESH:D014867), Pd (MESH:D010165), cephamycins (MESH:D002513), aldehyde (MESH:D000447), benzyl ether (MESH:C076624), hydroxybenzyl alcohol (MESH:C018966), methicillin (MESH:D008712), cefamandole nafate sodium (MESH:C012810), ethanol (MESH:D000431), HS-CL (MESH:D006851), 4-(4-dimethylaminophenylazo)benzoic acid (MESH:C063127), GES (MESH:D005857), tazobactam (MESH:D000078142), copper (MESH:D003300), vitamin C (MESH:D001205), acetic acid (MESH:D019342), faropenem (MESH:C107057), SYTO 9 (MESH:C103389), sulbactam (MESH:D013407), benzoate (MESH:D001565), disulfide (MESH:D004220), cefalexin (MESH:D002506), penicillin (MESH:D010406)
- **Species:** Bacillus subtilis (species) [taxon 1423], Escherichia coli (E. coli, species) [taxon 562], Acinetobacter baumannii ATCC 19606 = CIP 70.34 = JCM 6841 (strain) [taxon 575584], Klebsiella pneumoniae (species) [taxon 573], Pseudomonas aeruginosa (species) [taxon 287], Mus musculus (house mouse, species) [taxon 10090], Aliivibrio fischeri (species) [taxon 668], Enterococcus faecalis (species) [taxon 1351], Enterobacterales (order) [taxon 91347], Pseudomonas aeruginosa PAO1 (strain) [taxon 208964], Streptococcus pyogenes (species) [taxon 1314], Homo sapiens (human, species) [taxon 9606], Enterobacter cloacae (species) [taxon 550], Escherichia coli DH5[alpha] (strain) [taxon 668369], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Mycobacterium tuberculosis (species) [taxon 1773], Staphylococcus aureus (species) [taxon 1280], Acinetobacter baumannii (species) [taxon 470], Serratia marcescens (species) [taxon 615], Citrobacter freundii (species) [taxon 546], Escherichia coli NDM-1 (strain) [taxon 1411081], Klebsiella aerogenes (species) [taxon 548], Enterococcus faecium (species) [taxon 1352]
- **Cell lines:** 15692 — Homo sapiens (Human), Transformed cell line (CVCL_6A69), ATCC 13883 — Homo sapiens (Human), Ataxia telangiectasia syndrome, Transformed cell line (CVCL_1M10), BIN-3 — Homo sapiens (Human), Ovarian carcinoma, Cancer cell line (CVCL_QX91), ATCC — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023), ZJU — Homo sapiens (Human), Invasive breast carcinoma of no special type, Cancer cell line (CVCL_XC11), LMG194 — Homo sapiens (Human), Finite cell line (CVCL_H961), BL-21 — Homo sapiens (Human), EBV-related Burkitt lymphoma, Cancer cell line (CVCL_M639), NCTC 13440 — Homo sapiens (Human), Glycine encephalopathy, Finite cell line (CVCL_CX13), P. putida OUS82 — Homo sapiens (Human), Finite cell line (CVCL_3108), CMY-2 — Homo sapiens (Human), Down syndrome, Cancer cell line (CVCL_A602)

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12941553/full.md

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Source: https://tomesphere.com/paper/PMC12941553