Proto-metabolism explained

A proto-metabolism is a series of linked chemical reactions in a prebiotic environment that preceded and eventually turned into modern metabolism. Combining ongoing research in astrobiology and prebiotic chemistry, work in this area focuses on reconstructing the connections between potential metabolic processes that may have occurred in early Earth conditions.[1] Proto-metabolism is believed to be simpler than modern metabolism and the Last Universal Common Ancestor (LUCA), as simple organic molecules likely gave rise to more complex metabolic networks. Prebiotic chemists have demonstrated abiotic generation of many simple organic molecules including amino acids,[2] fatty acids,[3] simple sugars,[4] and nucleobases.[5] There are multiple scenarios bridging prebiotic chemistry to early metabolic networks that occurred before the origins of life, also known as abiogenesis. In addition, there are hypotheses made on the evolution of biochemical pathways including the metabolism-first hypothesis, which theorizes how reaction networks dissipate free energy from which genetic molecules and proto-cell membranes later emerge.[6] [7] To determine the composition of key early metabolic networks, scientists have also used top-down approaches to study LUCA and modern metabolism.[8] [9]

Autocatalytic prebiotic chemistries

Autocatalytic reactions are reactions where the reaction product acts as a catalyst for its own formation. Many researchers that study proto-metabolism agree that early metabolic networks likely originated as a set of chemical reactions that form self-sustaining networks.[10] This set of reactions is commonly referred to as an autocatalytic set. Some prebiotic chemistries focus on these autocatalytic reactions including the formose reaction, HCN oligomerization, and formamide chemistry.

Formose reaction

Discovered in 1861 by Aleksandr Butlerov, the formose reaction is a set of two reactions converting formaldehyde (CH2O) to a mixture of simple sugars.[11] [12] Formaldehyde is an intermediate in the oxidation of simple carbon molecules (e.g. methane) and was likely present in early Earth's atmosphere.[13] The first reaction is the slow conversion of formaldehyde (C1 carbon) to glycoaldehyde (C2 carbon) and occurs through an unknown mechanism. The second reaction is the faster and autocatalytic formation of higher weight aldoses and ketoses.[14] The kinetics of the formose reaction are often described as autocatalytic, as the alkaline reaction uses lowest molecular weight sugars as feedstocks or input molecules into the reaction.[15] Self-organized autocatalytic networks, like the formose reaction, would allow for adaptation to changing prebiotic environmental conditions. As a proof-of-concept, Robinson and colleagues demonstrated how changing environmental conditions and catalyst availability can impact the resultant sugar products.[16]

In the past, many researchers have suggested the importance of this reaction for abiogenesis and the origins of metabolism because it can lead to ribose. Ribose is a building block of RNA and an important precursor in proto-metabolism. However, there are limitations for the formose reaction to be the chemical origin of sugars including the low chemoselectivity for ribose and high complexity of the final reaction mixture.[17] In addition, a direct joining together of ribose, a nucleobase, and phosphate to make a ribonucleotide (the building block of RNA) is not currently chemically feasible.[18] Alternative prebiotic mechanisms have been proposed including cyanosulfidic prebiotic chemistries.

HCN oligomerization

On Earth, hydrogen cyanide (HCN) is made in volcanos, lightning, and reducing atmospheres like the Miller-Urey experiment.[19] On the Hadean Earth, large impactor events and active hydrothermal processes likely contributed to widespread metal production and metal-based proto-metabolism.[20] Hydrogen cyanide has also been detected in meteorites and atmospheres in the outer solar system.[21] [22]

HCN-derived polymers are the oligomer or hydrolysis products of HCN.[23] These polymers can be synthesized from HCN or cyanide salts often in alkaline conditions, but they have been observed in a wide range of experimental conditions.[24] HCN readily reacts with itself[25] to produce many HCN polymers and biologically-relevant compounds like nucleobases,[26] amino acids,[27] and carboxylic acids.[28] The diversity of products could point to a plausible proto-metabolic network of HCN oligomerization reactions. Although, some groups point to low HCN concentrations in early Earth and low chemioselectivity of key biologically-relevant products, similar to the formose reaction.[29] Others have shown that abundant HCN is produced after large impacts[30] and that high specificity and yield can be achieved.

Formamide chemistry

Formamide (NH2CHO) is the simplest naturally-occurring amide. Similar to HCN, formamide can form naturally.[31] Formamide has specific physical and stability properties possibly suitable for a universal prebiotic precursor for early proto-metabolic networks. For example, it has four universal atomic elements ubiquitous to life: C, H, O, N. The presence of unique functional groups involving oxygen and nitrogen support reaction chemistries to build key biomolecules like amino acids, sugars, nucleosides and other key intermediates of other prebiotic reactions (e.g. the citric acid cycle).[32] In addition, early Earth geological features like hydrothermal pores might support formamide chemistry and synthesis of key prebiotic biomolecules with concentration requirements.[33]

Overall, formamide chemistry can support connections and substrates needed to support prebiotic biomolecule synthesis including the formose reaction, Strecker synthesis, HCN oligomerization, or the Fischer-Tropsch process.[34] In addition, formamide can be easily concentrated through evaporation reactions as it has a boiling point of 210C.[35] Although this reaction has high versatility across one-carbon atom precursors, the connections between different biosynthetic pathways are yet to be directly explored experimentally.

Experimental reconstruction

Many research groups are actively attempting experimental reconstruction of the interactions between prebiotic reactions. One major consideration is the ability for these reactions to operate in the same environmental conditions.[36] These one-pot syntheses would likely push the reaction towards specific subgroups of molecules. The key to building proto-metabolic scenarios involves coupling constructive and interconversion reactions. Constructive reactions use autocatalytic prebiotic chemistries to increase the structural complexity of the original molecule, while interconversion reactions connect different prebiotic chemistries by changing the functional groups appended to the original molecule. A functional group is a group of atoms that has similar properties whenever it appears in different molecules. These interconversion reactions and functional group transformations can lead to new prebiotic chemistries and precursor molecules.

Cyanosulfidic scenario

Cyanosulfidic scenarios are mechanisms for proto-metabolism proposed by the Eschenmoser and Sutherland groups.[37] Research from the Eschenmoser group suggested that interactions between HCN and aldehydes can catalyze the formation of diaminomaleodinitrile (DAMN). Iterations of this cycle would generate multiple intermediate metabolites and key biomolecular precursors through functional group transformations by hydrolytic and redox processes. To expand upon this finding, the Sutherland group experimentally assessed the assembly of biomolecular building blocks from prebiotic intermediates and one-carbon feedstocks. They synthesized precursors of ribonucleotides, amino acids and lipids from the reactants of hydrogen cyanide, acetylene, acrylonitrile (product of cyanide and acetylene), and dihydroxyacetone (stable triose isomer of glyceraldehyde and phosphate). These reactions are driven by UV light and use hydrogen sulfide (H2S) as the primary reductant in these reactions. As each of these synthesis reactions was tested independently and some reactions require periodic input of additional reactants, these biomolecular precursors were not strictly generated through a one-pot synthesis expected of early Earth environments. In the same work, these authors argue that flow chemistry or the movement of reactants through water could generate the conditions favorable for the synthesis of these molecules.

Glyoxylate scenario

Eschenmoser also proposed a parallel scenario where the connections between prebiotic reactions would be connected by glyoxylate, a simple α-ketoacid, produced by HCN oligomerization and hydrolysis.[38] In this work, Eschenmoser proposes potential schemes to generate both informational oligomers and other key autocatalytic reactions from plausible one-carbon sources (HCN, CO, CO2).

The Krishnamurthy group at Scripps experimentally expanded on this theory.[39] In mild aqueous conditions, they demonstrated that the reaction of glyoxylate and pyruvate can produce a series of α-ketoacid intermediates constituting the reductive tricarboxylic acid (TCA) cycle. This reaction proceeded without metal or enzyme catalysts as glyoxylate acted as both the carbon source and reducing agent in the reaction. Similarly, the Moran group have also reported pyruvate and glyoxylate can react in warm iron-rich water to produce TCA intermediates and some amino acids.[40] [41] Their work has successfully reconstructed 9 out of 11 TCA intermediates and 5 universal metabolic precursors.[42] [43] Additional experimental analysis is needed to connect this scenario to modern metabolism.

Energy sources

Unlike proto-metabolism, the bioenergetic pathways powering modern metabolism are well understood. In early Earth conditions, there were mainly three kinds of energy to support early metabolic pathways: high energy sources to catalyze monomers, lower energy sources to support condensation or polymerization, and energy carriers that support transfer of energy from the environment to metabolic networks. Examples of high energy sources include photochemical energy from ultraviolet light, atmospheric electric discharge, and geological electrochemical energy. These energy sources would support synthesis of biological monomers or feedstocks for proto-metabolism. In contrast, examples of lower energy sources for assembly of more complex molecules include anhydrous heat, mineral-catalyzed synthesis, and sugar-driven reactions. Energy carrier molecules could allow for propagation of the energy through the metabolic networks likely resembled modern energy carriers including ATP and NADH. Both energy carriers are nucleotide-based molecules and likely originated early in metabolism.[44]

Metabolism-first hypothesis

Metabolism-first hypothesis suggests that autocatalytic networks of metabolic reactions were the first forms of life.[45] This is an alternative hypothesis to RNA-world, which is a genes-first hypothesis. It was first proposed by Martynas Ycas in 1955.[46] Many recent work in this area is focused in computational modeling of theoretical prebiotic networks.[47] [48] [49] [50]

Metabolism-first proponents postulate that replication and genetic machinery could not arise without the accumulation of the molecules needed for replication.[51] [6] Alone, simple connections between prebiotic synthesis reactions could form key organic molecules and once encapsulated by a membrane would constitute the first cells. These reactions could be catalyzed by various inorganic molecules or ions and stabilized by solid surfaces.[52] Molecular self-replicators and enzymes would emerge later, with these future metabolisms better resembling modern metabolism.

One critique for the metabolism-first hypothesis for abiogenesis is they would also need self-replicating abilities with a high degree of fidelity.[53] If not, the chemical networks with greater fitness in early Earth would not be preserved. There is limited experimental evidence for these theories, so additional exploration in this area is needed to determine the feasibility of a metabolism-first origins of life.

Notes and References

  1. Web site: 2022-04-04 . 'Impossible' chemistry may reveal origins of life on Earth . 2024-01-02 . Science . en.
  2. Islam . Saidul . Powner . Matthew W. . April 2017 . Prebiotic Systems Chemistry: Complexity Overcoming Clutter . Chem . 2 . 4 . 470–501 . 10.1016/j.chempr.2017.03.001 . 2451-9294. free .
  3. McCollom . Thomas M. . Ritter . Gilles . Simoneit . Bernd R. T. . 1999 . Lipid Synthesis Under Hydrothermal Conditions by Fischer- Tropsch-Type Reactions . Origins of Life and Evolution of the Biosphere . 29 . 2 . 153–166 . 10.1023/a:1006592502746 . 10227201 . 1999OLEB...29..153M . 25687489 . 0169-6149.
  4. Benner . Steven A. . Kim . Hyo-Joong . Carrigan . Matthew A. . 2012-03-28 . Asphalt, Water, and the Prebiotic Synthesis of Ribose, Ribonucleosides, and RNA . Accounts of Chemical Research . 45 . 12 . 2025–2034 . 10.1021/ar200332w . 22455515 . 0001-4842.
  5. Oro . J. . Kimball . A. P. . August 1961 . Synthesis of purines under possible primitive earth conditions. I. Adenine from hydrogen cyanide . Archives of Biochemistry and Biophysics . 94 . 2 . 217–227 . 10.1016/0003-9861(61)90033-9 . 0003-9861 . 13731263.
  6. Scossa . Federico . Fernie . Alisdair R. . 2020 . The evolution of metabolism: How to test evolutionary hypotheses at the genomic level . Computational and Structural Biotechnology Journal . 18 . 482–500 . 10.1016/j.csbj.2020.02.009 . 2001-0370 . 7063335 . 32180906.
  7. Web site: Metabolism First as Evidence of Evolution . 2024-01-02 . www.labxchange.org.
  8. Web site: Cowing . Keith . 2023-08-15 . Scientists Outline A New Strategy For Understanding The Origin Of Life . 2024-01-02 . Astrobiology . en-US.
  9. Web site: Rutgers Researchers Identify the Origins of Metabolism . 2024-01-02 . www.rutgers.edu . en.
  10. Hordijk . Wim . Steel . Mike . 2018-12-08 . Autocatalytic Networks at the Basis of Life's Origin and Organization . Life . en . 8 . 4 . 62 . 10.3390/life8040062 . 2075-1729 . 6315399 . 30544834 . 2018Life....8...62H . free .
  11. Cleaves II . H. James . 2008-07-30 . The prebiotic geochemistry of formaldehyde . Precambrian Research . en . 164 . 3–4 . 111–118 . 10.1016/j.precamres.2008.04.002. 2008PreR..164..111C .
  12. Butlerow . A. . January 1861 . Bildung einer zuckerartigen Substanz durch Synthese . Justus Liebigs Annalen der Chemie . en . 120 . 3 . 295–298 . 10.1002/jlac.18611200308 . 0075-4617.
  13. Masuda . Saeka . Furukawa . Yoshihiro . Kobayashi . Takamichi . Sekine . Toshimori . Kakegawa . Takeshi . April 2021 . Experimental Investigation of the Formation of Formaldehyde by Hadean and Noachian Impacts . Astrobiology . 21 . 4 . 413–420 . 10.1089/ast.2020.2320 . 33784199 . 2021AsBio..21..413M . 232429925 . 1531-1074.
  14. Delidovich . Irina V. . Simonov . Alexandr N. . Taran . Oxana P. . Parmon . Valentin N. . July 2014 . Catalytic Formation of Monosaccharides: From the Formose Reaction towards Selective Synthesis . ChemSusChem . en . 7 . 7 . 1833–1846 . 10.1002/cssc.201400040 . 24930572 . 2014ChSCh...7.1833D . 1864-5631.
  15. Nogal . Noemí . Sanz-Sánchez . Marcos . Vela-Gallego . Sonia . Ruiz-Mirazo . Kepa . de la Escosura . Andrés . 2023 . The protometabolic nature of prebiotic chemistry . Chemical Society Reviews . en . 52 . 21 . 7359–7388 . 10.1039/D3CS00594A . 0306-0012 . 10614573 . 37855729.
  16. Robinson . William E. . Daines . Elena . van Duppen . Peer . de Jong . Thijs . Huck . Wilhelm T. S. . June 2022 . Environmental conditions drive self-organization of reaction pathways in a prebiotic reaction network . Nature Chemistry . en . 14 . 6 . 623–631 . 10.1038/s41557-022-00956-7 . 35668214 . 2022NatCh..14..623R . 238709887 . 1755-4330. 2066/250891 . free .
  17. Zhao . Ze-Run . Wang . Xiao . December 2021 . A plausible prebiotic selection of ribose for RNA - formation, dynamic isolation, and nucleotide synthesis based on metal-doped-clays . Chem . 7 . 12 . 3292–3308 . 10.1016/j.chempr.2021.09.002 . 240543960 . 2451-9294. free .
  18. Banfalvi . Gaspar . 2021-04-08 . Prebiotic Pathway from Ribose to RNA Formation . International Journal of Molecular Sciences . 22 . 8 . 3857 . 10.3390/ijms22083857 . free . 1422-0067 . 8068141 . 33917807.
  19. Bada . Jeffrey L. . 2023-04-10 . Volcanic Island lightning prebiotic chemistry and the origin of life in the early Hadean eon . Nature Communications . en . 14 . 1 . 2011 . 10.1038/s41467-023-37894-y . 2041-1723 . 10086016 . 37037857. 2023NatCo..14.2011B .
  20. Kitadai . Norio . Nakamura . Ryuhei . Yamamoto . Masahiro . Takai . Ken . Yoshida . Naohiro . Oono . Yoshi . 2019-06-07 . Metals likely promoted protometabolism in early ocean alkaline hydrothermal systems . Science Advances . en . 5 . 6 . eaav7848 . 10.1126/sciadv.aav7848 . 2375-2548 . 6584212 . 31223650. 2019SciA....5.7848K .
  21. Smith . Karen E. . House . Christopher H. . Arevalo . Ricardo D. . Dworkin . Jason P. . Callahan . Michael P. . 2019-06-25 . Organometallic compounds as carriers of extraterrestrial cyanide in primitive meteorites . Nature Communications . en . 10 . 1 . 2777 . 10.1038/s41467-019-10866-x . 2041-1723 . 6592946 . 31239434. 2019NatCo..10.2777S .
  22. Rimmer . P. B. . Rugheimer . S. . 2019-09-01 . Hydrogen cyanide in nitrogen-rich atmospheres of rocky exoplanets . Icarus . 329 . 124–131 . 10.1016/j.icarus.2019.02.020 . 1902.08022 . 2019Icar..329..124R . 119208979 . 0019-1035.
  23. Ruiz-Bermejo . Marta . de la Fuente . José Luis . Pérez-Fernández . Cristina . Mateo-Martí . Eva . April 2021 . A Comprehensive Review of HCN-Derived Polymers . Processes . en . 9 . 4 . 597 . 10.3390/pr9040597 . 2227-9717 . free . 10261/343108 . free .
  24. Cleaves . H. James . September 2012 . Prebiotic Chemistry: What We Know, What We Don't . Evolution: Education and Outreach . en . 5 . 3 . 342–360 . 10.1007/s12052-012-0443-9 . 255493640 . 1936-6434. free .
  25. Deamer . D. . Weber . A. L. . 2010-02-01 . Bioenergetics and Life's Origins . Cold Spring Harbor Perspectives in Biology . en . 2 . 2 . a004929 . 10.1101/cshperspect.a004929 . 1943-0264 . 2828274 . 20182625.
  26. Oró . J. . June 1960 . Synthesis of adenine from ammonium cyanide . Biochemical and Biophysical Research Communications . 2 . 6 . 407–412 . 10.1016/0006-291x(60)90138-8 . 0006-291X.
  27. ORÓ . J. . KAMAT . S. S. . April 1961 . Amino-acid Synthesis from Hydrogen Cyanide under Possible Primitive Earth Conditions . Nature . 190 . 4774 . 442–443 . 10.1038/190442a0 . 13731262 . 1961Natur.190..442O . 4219284 . 0028-0836.
  28. Negrón-Mendoza . A. . Draganić . Z. D. . Navarro-González . R. . Draganić . I. G. . Negron-Mendoza . A. . Draganic . Z. D. . Navarro-Gonzalez . R. . Draganic . I. G. . August 1983 . Aldehydes, Ketones, and Carboxylic Acids Formed Radiolytically in Aqueous Solutions of Cyanides and Simple Nitriles . Radiation Research . 95 . 2 . 248 . 10.2307/3576253 . 3576253 . 1983RadR...95..248N . 0033-7587.
  29. Das . Tamal . Ghule . Siddharth . Vanka . Kumar . 2019-09-25 . Insights Into the Origin of Life: Did It Begin from HCN and H 2 O? . ACS Central Science . en . 5 . 9 . 1532–1540 . 10.1021/acscentsci.9b00520 . 2374-7943 . 6764159 . 31572780.
  30. Wogan . Nicholas F. . Catling . David C. . Zahnle . Kevin J. . Lupu . Roxana . 2023-09-01 . Origin-of-life Molecules in the Atmosphere after Big Impacts on the Early Earth . The Planetary Science Journal . 4 . 9 . 169 . 10.3847/PSJ/aced83 . free . 2307.09761 . 2023PSJ.....4..169W . 2632-3338.
  31. Bizzarri . Bruno Mattia . Saladino . Raffaele . Delfino . Ines . García-Ruiz . Juan Manuel . Di Mauro . Ernesto . 2021-01-18 . Prebiotic Organic Chemistry of Formamide and the Origin of Life in Planetary Conditions: What We Know and What Is the Future . International Journal of Molecular Sciences . en . 22 . 2 . 917 . 10.3390/ijms22020917 . 1422-0067 . 7831497 . 33477625 . free .
  32. Saladino . Raffaele . Ciambecchini . Umberto . Crestini . Claudia . Costanzo . Giovanna . Negri . Rodolfo . Di Mauro . Ernesto . 2003-06-06 . One-Pot TiO 2 -Catalyzed Synthesis of Nucleic Bases and Acyclonucleosides from Formamide: Implications for the Origin of Life . ChemBioChem . en . 4 . 6 . 514–521 . 10.1002/cbic.200300567 . 12794862 . 2349609 . 1439-4227.
  33. Niether . Doreen . Afanasenkau . Dzmitry . Dhont . Jan K. G. . Wiegand . Simone . 2016-04-04 . Accumulation of formamide in hydrothermal pores to form prebiotic nucleobases . Proceedings of the National Academy of Sciences . 113 . 16 . 4272–4277 . 10.1073/pnas.1600275113 . 27044100 . 4843465 . 2016PNAS..113.4272N . 0027-8424 . free .
  34. Andersen . Jakob . Andersen . Tommy . Flamm . Christoph . Hanczyc . Martin . Merkle . Daniel . Stadler . Peter . 2013-09-25 . Navigating the Chemical Space of HCN Polymerization and Hydrolysis: Guiding Graph Grammars by Mass Spectrometry Data . Entropy . en . 15 . 12 . 4066–4083 . 10.3390/e15104066 . 2013Entrp..15.4066A . 1099-4300 . free .
  35. Saladino . Raffaele . Crestini . Claudia . Pino . Samanta . Costanzo . Giovanna . Di Mauro . Ernesto . 2012-03-01 . Formamide and the origin of life . Physics of Life Reviews . 9 . 1 . 84–104 . 10.1016/j.plrev.2011.12.002 . 22196896 . 2012PhLRv...9...84S . 2108/85168 . 1571-0645. free .
  36. Patel . Bhavesh H. . Percivalle . Claudia . Ritson . Dougal J. . Duffy . Colm D. . Sutherland . John D. . April 2015 . Common origins of RNA, protein and lipid precursors in a cyanosulfidic protometabolism . Nature Chemistry . en . 7 . 4 . 301–307 . 10.1038/nchem.2202 . 1755-4330 . 4568310 . 25803468. 2015NatCh...7..301P .
  37. Koch . Klemens . Schweizer . W. Bernd . Eschenmoser . Albert . April 2007 . Reactions of the HCN-Tetramer with Aldehydes . Chemistry & Biodiversity . en . 4 . 4 . 541–553 . 10.1002/cbdv.200790049 . 17443870 . 38695557 . 1612-1872.
  38. Eschenmoser . Albert . December 2007 . The search for the chemistry of life's origin . Tetrahedron . 63 . 52 . 12821–12844 . 10.1016/j.tet.2007.10.012 . 0040-4020.
  39. Stubbs . R. Trent . Yadav . Mahipal . Krishnamurthy . Ramanarayanan . Springsteen . Greg . November 2020 . A plausible metal-free ancestral analogue of the Krebs cycle composed entirely of α-ketoacids . Nature Chemistry . en . 12 . 11 . 1016–1022 . 10.1038/s41557-020-00560-7 . 1755-4330 . 8570912 . 33046840. 2020NatCh..12.1016S .
  40. Muchowska . Kamila B. . Varma . Sreejith J. . Chevallot-Beroux . Elodie . Lethuillier-Karl . Lucas . Li . Guang . Moran . Joseph . 2017-10-02 . Metals promote sequences of the reverse Krebs cycle . Nature Ecology & Evolution . 1 . 11 . 1716–1721 . 10.1038/s41559-017-0311-7 . 28970480 . 5659384 . 2017NatEE...1.1716M . 2397-334X.
  41. Mayer . Robert J. . Kaur . Harpreet . Rauscher . Sophia A. . Moran . Joseph . 2021-11-03 . Mechanistic Insight into Metal Ion-Catalyzed Transamination . Journal of the American Chemical Society . 143 . 45 . 19099–19111 . 10.1021/jacs.1c08535 . 34730975 . 242937134 . 0002-7863.
  42. Mayer . Robert J. . Moran . Joseph . 2022-11-25 . Quantifying Reductive Amination in Nonenzymatic Amino Acid Synthesis . Angewandte Chemie International Edition . en . 61 . 48 . e202212237 . 10.1002/anie.202212237 . 1433-7851 . 9828492 . 36121198.
  43. Rauscher . Sophia A. . Moran . Joseph . 2022-12-19 . Hydrogen Drives Part of the Reverse Krebs Cycle under Metal or Meteorite Catalysis . Angewandte Chemie International Edition . en . 61 . 51 . e202212932 . 10.1002/anie.202212932 . 1433-7851 . 10100321 . 36251920.
  44. Pinna . Silvana . Kunz . Cäcilia . Halpern . Aaron . Harrison . Stuart A. . Jordan . Sean F. . Ward . John . Werner . Finn . Lane . Nick . 2022-10-04 . A prebiotic basis for ATP as the universal energy currency . PLOS Biology . en . 20 . 10 . e3001437 . 10.1371/journal.pbio.3001437 . 1545-7885 . 9531788 . 36194581 . free .
  45. Web site: What Is The Metabolism-First Hypothesis For The Origin Of Life? • Stated Clearly . 2024-01-02 . Stated Clearly . en.
  46. Yčas . Martynas . 1955-10-15 . A Note on the Origin of Life . Proceedings of the National Academy of Sciences . en . 41 . 10 . 714–716 . 10.1073/pnas.41.10.714 . free . 0027-8424 . 528169 . 16589734 . 1955PNAS...41..714Y .
  47. Lindahl . Paul A. . August 2004 . Stepwise Evolution of Nonliving to Living Chemical Systems . Origins of Life and Evolution of the Biosphere . 34 . 4 . 371–389 . 10.1023/b:orig.0000029880.76881.f5 . 15279172 . 2004OLEB...34..371L . 36069513 . 0169-6149.
  48. Yaman . Tolga . Harvey . Jeremy N. . 2021-12-04 . Computational Analysis of a Prebiotic Amino Acid Synthesis with Reference to Extant Codon–Amino Acid Relationships . Life . en . 11 . 12 . 1343 . 10.3390/life11121343 . 2075-1729 . 8707928 . 34947874 . 2021Life...11.1343Y . free .
  49. Sharma . Siddhant . Arya . Aayush . Cruz . Romulo . Cleaves II . Henderson . 2021-10-26 . Automated Exploration of Prebiotic Chemical Reaction Space: Progress and Perspectives . Life . en . 11 . 11 . 1140 . 10.3390/life11111140 . 2075-1729 . 8624352 . 34833016 . 2021Life...11.1140S . free .
  50. Web site: Yates . Diana . Study tracks evolutionary history of metabolic networks . 2024-01-02 . news.illinois.edu . en-US.
  51. Tessera . Marc . January 2018 . Is pre-Darwinian evolution plausible? . Biology Direct . en . 13 . 1 . 18 . 10.1186/s13062-018-0216-7 . 1745-6150 . 6151046 . 30241560 . free .
  52. Kocher . Charles . Dill . Ken A. . January 2023 . Origins of life: first came evolutionary dynamics . QRB Discovery . en . 4 . e4 . 10.1017/qrd.2023.2 . 37529034 . 10392681 . 2633-2892.
  53. Anet . Frank AL . 2004-12-01 . The place of metabolism in the origin of life . Current Opinion in Chemical Biology . 8 . 6 . 654–659 . 10.1016/j.cbpa.2004.10.005 . 15556411 . 1367-5931.

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