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  • 1
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1980-06-27
    Description: The Pb2+ and Zn2+ ions are efficient catalysts for the polycytidylic acid-directed polymerization of an activated guanylic acid derivative, guanosine 5'-phosphorimidazolide. The products include oligomers of 30 to 40 units in length. The nucleotide residues are predominantly 2'-5' linked when Pb2+ is the catalyst, and predominantly 3'-5' linked in the presence of Zn2+. The significance of these results in the context of the prebiotic evolution of RNA polymerase is discussed.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lohrmann, R -- Bridson, P K -- Orgel, L E -- New York, N.Y. -- Science. 1980 Jun 27;208(4451):1464-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6247762" target="_blank"〉PubMed〈/a〉
    Keywords: DNA-Directed RNA Polymerases ; Guanine Nucleotides/*chemical synthesis ; Guanosine Monophosphate/analogs & derivatives/*chemical synthesis ; *Lead ; Pancreas/enzymology ; *Poly C ; *Polyribonucleotides ; Ribonucleases ; Templates, Genetic ; *Zinc
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1983-02-18
    Description: Polynucleotide templates containing C (cytidine) as the major component facilitate the synthesis of oligonucleotides from mixtures of the activated mononucleotide derivatives (as indicated by structure 1 in the text). A nucleotide is incorporated into oligomeric products if and only if its complement is present in the template. The reaction has a high fidelity and produces products with mean chain lengths of six to ten nucleotides. Bases other than guanosine are incorporated within oligomers or at their 3' termini, but rarely at their 5' termini.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Inoue, T -- Orgel, L E -- GM-13435/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1983 Feb 18;219(4586):859-62.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6186026" target="_blank"〉PubMed〈/a〉
    Keywords: Base Sequence ; DNA-Directed RNA Polymerases/*metabolism ; Hydrogen Bonding ; Models, Chemical ; RNA/*chemical synthesis ; Templates, Genetic
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1985-05-03
    Description: In studying the origins of life, it is important to examine reactions of substrate mixtures that could plausibly have accumulated on the primitive earth. Nucleoside diphosphates would probably have been synthesized along with the standard nucleotides under prebiotic conditions. For these reasons, the template-directed reactions of activated derivatives of these diphosphates, alone or mixed with activated nucleotides, were investigated. An activated derivative of deoxyguanosine 3',5'-diphosphate condensed efficiently on a polycytidylate template to give oligonucleotide analogues in which each 3',5'-phosphodiester bond was replaced by a pyrophosphate linkage. Oligomers were formed even in the absence of a template, but much more slowly. Template-directed condensation occurred also with an analogous deoxyadenosine derivative on polyuridylic acid and with an analogous acycloguanosine derivative on polycytidylic acid.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schwartz, A W -- Orgel, L E -- New York, N.Y. -- Science. 1985 May 3;228:585-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Salk Insitute for Biological Sciences, San Diego, California 92138, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11541994" target="_blank"〉PubMed〈/a〉
    Keywords: Cytosine/chemistry ; Deoxyguanine Nucleotides/chemistry ; Evolution, Molecular ; Guanine/chemistry ; Nucleic Acids/*chemical synthesis ; Oligonucleotides/*chemical synthesis ; *Origin of Life ; Poly C/chemistry ; Poly U/chemistry ; Templates, Genetic
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 2011-08-12
    Description: Nucleoside synthesis under potentially prebiotic conditions
    Keywords: BIOSCIENCES
    Format: text
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  • 5
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    Unknown
    In:  Other Sources
    Publication Date: 2011-08-16
    Description: Questions regarding the combination of amino acids and ribonucleotides to polypeptides and polynucleotides are investigated. Each of the reactions considered occurs in the solid state in plausible prebiotic conditions. Together they provide the basis for a unified scheme of amino acid and nucleotide activation. Urea, imidazole and Mg(++) are essential catalytic components of the reaction mixtures. However, these compounds could probably be replaced by other organic molecules.
    Keywords: BIOSCIENCES
    Type: Nature; 244; Aug. 17
    Format: text
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  • 6
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    Unknown
    In:  Other Sources
    Publication Date: 2019-06-27
    Description: It is suggested that the earliest coding polynucleotides contained a high proportion of alternating sequences of purines and pyrimidines, and that these sequences coded for polypeptides in which hydrophobic and hydrophylic amino acids alternated. Structural properties of such alternating polypeptides are discussed.
    Keywords: BIOSCIENCES
    Type: Israel Journal of Chemistry; 10; 1972
    Format: text
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  • 7
    Publication Date: 2019-06-27
    Description: The phosphorylation of thymidine is described for a variety of conditions at 65 C to demonstrate that the reaction could readily take place in deserts at the present time. This might be used as an indication that urea-phosphate mixtures could have been important as phosphorylating agents on the primitive earth. Reaction products were identified by comparing their chromatographic and electrophoretic mobilities with those of authentic materials and by enzymatic degradation. The results show that good yields of nucleotides are obtained when nucleosides are heated with urea-phospate mixtures at 65 C. Reactions proceed more rapidly at moderate humidities than in a stream of dry nitrogen. Occasional wetting results in even faster and more extensive reactions. There was no reaction for a mixture of urea and trimetaphosphate.
    Keywords: BIOSCIENCES
    Type: Nature; 237; May 19
    Format: text
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