Related Experiment Video
Updated: Dec 1, 2025

Site-Directed Mutagenesis for In Vitro and In Vivo Experiments Exemplified with RNA Interactions in Escherichia Coli
Published on: February 5, 2019
Metabolic Perturbations Caused by the Over-Expression of mcr-1 in Escherichia coli
Yi-Yun Liu1,2,3, Yan Zhu2, Hasini Wickremasinghe2
1National Risk Assessment Laboratory for Antimicrobial Resistance of Animal Original Bacteria, Guangdong Provincial Key Laboratory of Veterinary Pharmaceutics Development and Safety Evaluation, Key Laboratory of Zoonosis of Ministry of Agricultural and Rural Affairs, College of Veterinary Medicine, South China Agricultural University, Guangzhou, China.
Abstract:
Rapid dissemination of the plasmid-born polymyxin resistance gene mcr-1 poses a critical medical challenge. MCR-1 expression is tightly controlled and imposes a fitness cost on the bacteria. We used growth studies and metabolomics to examine growth and metabolic changes within E. coli TOP10 at 8 and 24 h in response to different levels of expression of mcr-1. Induction of mcr-1 greatly increased expression at 8 h and markedly reduced bacterial growth; membrane disruption and cell lysis were evident at this time. At 24 h, the expression of mcr-1 dramatically declined with restored growth and membrane integrity, indicating regulation of mcr-1 expression in bacteria to maintain membrane homeostasis. Intermediates of peptide and lipid biosynthesis were the most commonly affected metabolites when mcr-1 was overexpressed in E. coli. Cell wall biosynthesis was dramatically affected with the accumulation of lipids including fatty acids, glycerophospholipids and lysophosphatidylethanolamines, especially at 8 h. In contrast, levels of intermediate metabolites of peptides, amino sugars, carbohydrates and nucleotide metabolism and secondary metabolites significantly decreased. Moreover, the over-expression of mcr-1 resulted in a prolonged reduction in intermediates associated with pentose phosphate pathway and pantothenate and CoA biosynthesis. These findings indicate that over-expression of mcr-1 results in global metabolic perturbations that mainly involve disruption to the bacterial membrane, pentose phosphate pathway as well as pantothenate and CoA biosynthesis.
Insights
The polymyxin resistance gene mcr-1 causes severe metabolic disruption in E. coli, impacting bacterial membranes and essential biosynthesis pathways. Bacterial growth and membrane integrity are restored as mcr-1 expression is regulated.
Area of Science:
- Microbiology
- Molecular Biology
- Biochemistry
Background:
- The plasmid-borne polymyxin resistance gene, mcr-1, is rapidly spreading globally.
- MCR-1 expression is tightly regulated and incurs a fitness cost on bacteria.
Purpose of the Study:
- To investigate the growth and metabolic consequences of mcr-1 gene expression in E. coli.
- To understand the regulatory mechanisms of mcr-1 expression and its impact on bacterial homeostasis.
Main Methods:
- Growth studies were performed on E. coli TOP10.
- Metabolomic analysis was conducted at 8 and 24 hours post-induction of mcr-1.
- Bacterial growth, membrane integrity, and metabolite levels were assessed.
Main Results:
- mcr-1 overexpression initially reduced bacterial growth and caused membrane disruption.
- At later time points, mcr-1 expression declined, restoring growth and membrane integrity.
- Metabolomic analysis revealed significant alterations in lipid, peptide, carbohydrate, and nucleotide metabolism, particularly affecting the pentose phosphate pathway and pantothenate and CoA biosynthesis.
Conclusions:
- mcr-1 expression leads to significant metabolic perturbations, including membrane damage and disruption of key biosynthetic pathways.
- E. coli regulates mcr-1 expression to maintain membrane homeostasis and bacterial survival.
- Understanding these metabolic impacts is crucial for combating the spread of antibiotic resistance.
Related Concept Videos
Stringent Response in E. coli
Inducible Operons: lac Operon

