Immunoadsorbent for the isolation of purine- specific antibodies.
Immunoadsorbent synthesis for isolating purine- specific antibodies from blood serum
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Immunoadsorbent synthesis for isolating purine- specific antibodies from blood serum
Paper chromatography and mass spectrometry for analyses of pyrimidine and purine bases
Absorption of pyrimidines, purines, and nucleosides by copper, nickel, cobalt, and iron montmorillonite
Absorption of purines, pyrimidines, and nucleoside in aqueous solution by montmorillionite occurring as cation exchange reaction
Free radicals formation in gamma irradiated pyrimidine-purine co-crystal complex, using electron spin resonance spectroscopy
Purines, pyrimidines and nucleosides absorption by Li-, Na-, Mg- and Ca-montmorillonite in aqueous solutions over range pH 2-12 by cation exchange
Absorption of nucleosides, purine and pyrimidine derivatives by Co-, Cu- and Ni-montmorillonite taking place by cation exchange process
Pyrimidine and purine bases analysis by time of flight mass spectrometry and paper chromatography
Pyrimidine polyribonucleotides or purine polyribonucleotides binding to lysine- or arginine-rich proteinoids considered for abiogenesis
Dilute (0.1 M) solutions of HCN condense to oligomers at pH 9.2, and hydrolysis of these oligomers yields 4,5-dihydroxypyrimidine, orotic acid, 5-hydroxyuracil, adenine, 4-aminoimidazole-5-carboxamide, and amino acids. It is suggested that the three main classes of nitrogen-containing biomolecules - purines, pyrimidines, and amino acids may have originated from HCN on the primitive earth. It is also suggested that the presence of orotic acid and 4-aminoimidazole-5-carboxamide might indicate that contemporary biosynthetic pathways for nucleotides evolved from the compounds released on hydrolysis of HCN oligomers.
Oligomerization of HCN (1 molar) in the presence of added formaldehyde (0.5 molar) produced an order of magnitude more 8-hydroxymethyladenine than adenine or any other biologically significant purine. This result suggests that on the prebiotic earth, nucleoside analogs may have been synthesized directly in more complex mixtures of HCN with other aldehydes.
The lack of pyrimidine diversity in meteorites remains a mystery since prebiotic chemical models and laboratory experiments have predicted that these compounds can also be produced from chemical precursors found in meteorites. Here we report the detection of nucleobases in three carbonaceous meteorites using state-of-the-art analytical techniques optimized for small-scale quantification of nucleobases down to the range of parts per trillion (ppt). In addition to previously detected purine nucleobases in meteorites such as guanine and adenine, we identify various pyrimidine nucleobases such as cytosine, uracil, and thymine, and their structural isomers such as isocytosine, imidazole-4-carboxylic acid, and 6-methyluracil, respectively. Given the similarity in the molecular distribution of pyrimidines in meteorites and those in photon-processed interstellar ice analogues, some of these derivatives could have been generated by photochemical reactions prevailing in the interstellar medium and later incorporated into asteroids during solar system formation. This study demonstrates that a diversity of meteoritic nucleobases could serve as building blocks of DNA and RNA on the early Earth.
Cytosine, adenine, guanine, thymine and uracil detection in core samples from experimental Mohole
With porous channels for ion transport, the electronic conductivity of MOFs can be tuned to realize outstanding memory operation and seamlessly integrated into devices emulating complex multi-terminal synaptic responses.
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Reactivity of deoxyribonucleic acid /DNA/ with antibody showing that salmon sperm DNA reacts with antipurinoyl antibody with or without heat denaturation
Hydrogen bonding of derivatives of guanosine and cytidine soluble in chloroform studied in IR, CONFIRMING geometrical specificity in two-stranded nucleic acids
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