Free spermidine evokes superoxide radicals that manifest toxicity

Author:

Kumar Vineet1,Mishra Rajesh Kumar1,Ghose Debarghya1,Kalita Arunima1,Dhiman Pulkit12,Prakash Anand1,Thakur Nirja1,Mitra Gopa3,Chaudhari Vinod D12,Arora Amit1ORCID,Dutta Dipak1ORCID

Affiliation:

1. Division of Molecular Biochemistry and Microbiology, CSIR Institute of Microbial Technology

2. Division of Medicinal Chemistry, CSIR Institute of Microbial Technology

3. Clinical Proteomics Unit, Division of Molecular Medicine, St. John's Research Institute, St John's Medical College

Abstract

Spermidine and other polyamines alleviate oxidative stress, yet excess spermidine seems toxic to Escherichia coli unless it is neutralized by SpeG, an enzyme for the spermidine N-acetyl transferase function. Thus, wild-type E. coli can tolerate applied exogenous spermidine stress, but ΔspeG strain of E. coli fails to do that. Here, using different reactive oxygen species (ROS) probes and performing electron paramagnetic resonance spectroscopy, we provide evidence that although spermidine mitigates oxidative stress by lowering overall ROS levels, excess of it simultaneously triggers the production of superoxide radicals, thereby causing toxicity in the ΔspeG strain. Furthermore, performing microarray experiment and other biochemical assays, we show that the spermidine-induced superoxide anions affected redox balance and iron homeostasis. Finally, we demonstrate that while RNA-bound spermidine inhibits iron oxidation, free spermidine interacts and oxidizes the iron to evoke superoxide radicals directly. Therefore, we propose that the spermidine-induced superoxide generation is one of the major causes of spermidine toxicity in E. coli.

Funder

Council of Scientific and Industrial Research (CSIR), India

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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