A liquid handling platform for standardised quantification of cell-free enzymatic activity encoded by antimicrobial resistance genes

ABSTRACT Antimicrobial resistance (AMR) is a growing global threat to human health, and rapid methods for characterising emerging antimicrobial resistance genes (ARGs) are needed. Here, we develop a semi-automated workflow using cell-free gene expression (CFE) systems to measure the activity of two ARGs encoded on plasmid DNA that produce rifampicin-inactivating and gentamicin-inactivating enzymes. We validated the use of a small benchtop Myra liquid handling system compared to manual pipetting, with no statistical differences observed. After optimising the pre-incubation time of ARGs and dispensing protocol, expression of aac(3)-IIa increased the half-maximal inhibition concentration (IC50) of gentamicin by over 150-fold, while arr-3 increased the IC50 of rifampicin by approximately 20-fold compared to controls. This methodology for rapid, semi-automated ARG characterisation offers a strategy to combat AMR by assessing novel ARGs identified through genomic surveillance or profiling activity of new or derivative antibiotics.

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Publication Details

Journal
Synthetic Biology
Published
2026-08-27
DOI
https://doi.org/10.1093/synbio/ysag010
Primary Topic
Pharmaceutical and Antibiotic Environmental Impacts
Type
article
Field-Weighted Citation Impact
0.00

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article

A liquid handling platform for standardised quantification of cell-free enzymatic activity encoded by antimicrobial resistance genes

Molly Bergum, Simon J. Moore, J. Mark Sutton, Sahana Suthakaran et al.
Synthetic Biology
Pharmaceutical and Antibiotic Environmental Impacts
article

A liquid handling platform for standardised quantification of cell-free enzymatic activity encoded by antimicrobial resistance genes

Molly Bergum, Simon J. Moore, J. Mark Sutton, Sahana Suthakaran, Bethany Martin
article en

Abstract

ABSTRACT Antimicrobial resistance (AMR) is a growing global threat to human health, and rapid methods for characterising emerging antimicrobial resistance genes (ARGs) are needed. Here, we develop a semi-automated workflow using cell-free gene expression (CFE) systems to measure the activity of two ARGs encoded on plasmid DNA that produce rifampicin-inactivating and gentamicin-inactivating enzymes. We validated the use of a small benchtop Myra liquid handling system compared to manual pipetting, with no statistical differences observed. After optimising the pre-incubation time of ARGs and dispensing protocol, expression of aac(3)-IIa increased the half-maximal inhibition concentration (IC50) of gentamicin by over 150-fold, while arr-3 increased the IC50 of rifampicin by approximately 20-fold compared to controls. This methodology for rapid, semi-automated ARG characterisation offers a strategy to combat AMR by assessing novel ARGs identified through genomic surveillance or profiling activity of new or derivative antibiotics.

Synthetic Biology
Defence Science and Technology Laboratory (GB), King's College London (GB), Imperial College London (GB)
Biotechnology and Biological Sciences Research Council
Openalex Percentile: Top 71%
Pharmaceutical and Antibiotic Environmental Impacts
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A liquid handling platform for standardised quantification of cell-free enzymatic activity encoded by antimicrobial resistance genes — Molly Bergum, Simon J. Moore, et al. · Synthetic Biology (2026) | TGRS Research Map | TGRS