1. A continuous reaction network that produces RNA precursors.
- Author
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Yi R, Tran QP, Ali S, Yoda I, Adam ZR, Cleaves HJ 2nd, and Fahrenbach AC
- Subjects
- Acetaldehyde analogs & derivatives, Acetaldehyde chemical synthesis, Acetaldehyde chemistry, Cyanamide chemical synthesis, Cyanamide chemistry, Gamma Rays, Imidazoles chemical synthesis, Imidazoles chemistry, Origin of Life, Oxazoles chemical synthesis, Oxazoles chemistry, Photochemistry, Water chemistry, Evolution, Chemical, Models, Chemical, RNA chemical synthesis, RNA chemistry
- Abstract
Continuous reaction networks, which do not rely on purification or timely additions of reagents, serve as models for chemical evolution and have been demonstrated for compounds thought to have played important roles for the origins of life such as amino acids, hydroxy acids, and sugars. Step-by-step chemical protocols for ribonucleotide synthesis are known, but demonstrating their synthesis in the context of continuous reaction networks remains a major challenge. Herein, compounds proposed to be important for prebiotic RNA synthesis, including glycolaldehyde, cyanamide, 2-aminooxazole, and 2-aminoimidazole, are generated from a continuous reaction network, starting from an aqueous mixture of NaCl, NH
4 Cl, phosphate, and HCN as the only carbon source. No well-timed addition of any other reagents is required. The reaction network is driven by a combination of γ radiolysis and dry-down. γ Radiolysis results in a complex mixture of organics, including the glycolaldehyde-derived glyceronitrile and cyanamide. This mixture is then dried down, generating free glycolaldehyde that then reacts with cyanamide/NH3 to furnish a combination of 2-aminooxazole and 2-aminoimidazole. This continuous reaction network models how precursors for generating RNA and other classes of compounds may arise spontaneously from a complex mixture that originates from simple reagents., Competing Interests: The authors declare no competing interest.- Published
- 2020
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