Published August 1995
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Amino acid chirality breaking by N-phosphorylation
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Description
The chirality breaking of amino acid is a focus issue in the origin of life. For chemists, there are some interesting chemical approaches to solve the symmetry breaking problem. Our previous experiments indicated that when amino acids were phosphorylated, there were many bio-mimic reactions happened. In this paper, it was found that there had significant difference between the N-phosphoryl L- and D- amino acids such as serine and threonine. The optical rotation tracing experiments of the racemic N-phosphoamino acids also showed the similar results. The chirality breaking of amino acids by N-phosphorylation was a novel phenomena. (author). 3 refs, 1 fig. Abstract only
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Additional details
Publishing Information
- Imprint Title
- Cyril Ponnamperuma Memorial. Trieste conference on chemical evolution, 4: Physics of the origin and evolution of life. Summaries
- Imprint Pagination
- 21 p.
- Journal Page Range
- p. 20.
- Report number
- IC--95/238
Conference
- Title
- Physics of the origin and evolution of life. Cyril Ponnamperuma memorial.
- Acronym
- 4. Trieste conference on chemical evaluation
- Dates
- 4-8 Sep 1995.
- Place
- Trieste (Italy).
INIS
- Country of Publication
- International Atomic Energy Agency (IAEA)
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 26075565
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Resource subtype / Literary indicator
- Conference
- Descriptors DEI
- AMINO ACIDS; CHIRAL SYMMETRY; CHIRALITY; PHOSPHORYLATION; SYMMETRY BREAKING
- Descriptors DEC
- CARBOXYLIC ACIDS; CHEMICAL REACTIONS; ORGANIC ACIDS; ORGANIC COMPOUNDS; PARTICLE PROPERTIES; SYMMETRY