bioRxivBiochemistry
Deuterium-depletion has no significant impact on the mutation rate of Escherichia coli, invalidating the Double D-Bridge Hypothesis
Abstract
Deuterium (D), the second most abundant isotope of hydrogen is present in natural waters at an approximate concentration of 145-155 ppm (cca. 1.5E-4 atom/atom). D is known to influence various biological processes due to its physical and chemical properties, which significantly differ from those of hydrogen. For example, increasing D-concentration to >1000-fold above its natural abundance has been shown to increase the frequency of genetic mutations in several species. The Double D-Bridge Hypothesis, formulated with the intent of explaining the mechanism of D-mutagenicity is based on the calculation that the theoretical frequency of A:T base pairs that comprise two D-bridges instead of H-bridges is 2E-8, which is equal to the mutation rate of certain species. To experimentally challenge this hypothesis, and to infer the mutagenicity of D present at natural concentrations, we investigated the effect of a nearly 100-fold reduction of D concentration on the bacterial mutation rate. Using fluctuation tests, we measured the mutation rate of three Escherichia coli genes (cycA, ackA and galK) in media containing D at either <2 ppm or 150 ppm concentrations. Out of 15 pair-wise fluctuation analyses, nine indicated a significant decrease, while three marked the significant increase of the mutation/culture value upon D-depletion. Overall, growth in D-depleted minimal medium led to a geometric mean of 0.663-fold (95% confidence interval: 0.483-0.911) change in the mutation rate. This falls nowhere near the expected 10,000-fold reduction, indicating that the Double D-Bridge Hypothesis does not hold. In addition, the combined results did not display a statistically significant change in the mutation/culture value, the mutation rate or the mutant frequency upon D-depletion. The potential mutagenic effect of D present at natural concentrations on E. coli is therefore below the limit of detection using the indicated methods.
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Working together to control mutation: how collective peroxide detoxification determines microbial mutation rate plasticity
R. Green, H. Wang, … C. G. Knight·bioRxiv·Sep 27, 2023
- Opposing effects of population density and stress on Escherichia coli mutation rate
R. Krasovec, H. Richards, … C. G. Knight·bioRxiv·Jan 30, 2018
- The Distribution of Bacterial Doubling Times in the Wild
B. Gibson, D. Wilson, … A. Eyre-Walker·bioRxiv·Nov 6, 2017
- Environmental and genetic influence on rate and spectrum of spontaneous mutations in Escherichia coli
D. R. Gifford, A. Bhattacharyya, … C. G. Knight·bioRxiv·Apr 6, 2023
- Fitness effects of new mutations are small and heavily confounded with non-genetic sources of variation in Escherichia coli
Julie Michelle Grosse-Sommer, Dhobasheni Newman, Jarrod D. Hadfield·bioRxiv·Aug 25, 2026
- Detection of DNA replication errors and 8-oxo-dGTP-mediated mutations in E. coli by Duplex DNA Sequencing
Niketa Bhawsinghka, Adam Burkholder, Roel M. Schaaper·bioRxiv·Oct 21, 2022