A new oxygen modification cyclooctaoxygen binds to nucleic acids as sodium crown complex
Andreas J Kesel1, Craig W Day2, Catherine M Montero3
1Chammünsterstr. 47, D-81827 München, Bayern/Bavaria, Germany.
Biochimica Et Biophysica Acta
|January 31, 2016
Summary
Scientists synthesized cyclooctaoxygen sodium, a novel oxygen allotrope, which binds to nucleic acids and is non-toxic to cells. This discovery offers insights into eukaryotic gene regulation and evolution.
Area of Science:
- Biochemistry
- Molecular Biology
- Genetics
Background:
- Oxygen exhibits multiple allotropic forms, with cyclooctaoxygen predicted in 1990.
- This study focuses on the synthesis and characterization of this predicted oxygen allotrope.
Purpose of the Study:
- To synthesize and characterize cyclooctaoxygen.
- To investigate its interaction with nucleic acids and its potential role in biological systems.
Main Methods:
- In vitro synthesis of cyclooctaoxygen sodium using atmospheric or catalase-generated oxygen, catalyzed by cytosine nucleosides and RNA or ninhydrin.
- Thin-layer chromatography and mobility shift assays to analyze the cyclooctaoxygen sodium complex's interaction with nucleic acids.
Main Results:
- Successful synthesis and isolation of cyclooctaoxygen as a sodium crown complex with cytosine nucleoside hydrochloride.
- The complex binds to RNA and DNA, associates with single-stranded DNA and spermine phosphate.
- Demonstrated low toxicity to cultured mammalian cells at concentrations of 0.1-1.0mM.
Conclusions:
- Cyclooctaoxygen is postulated to form in eukaryotic cells via a catalase reaction involving cytidine and RNA.
- A molecular model suggests cyclooctaoxygen forms an epigenetic shell for eukaryotic DNA, explaining selenium interactions.
- The complex's genome coverage suggests a role in eukaryotic gene regulation and proto-eukaryotic evolution.
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