Published August 1995 | Version v1
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Amino acid chirality breaking by N-phosphorylation

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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Part of:
Cyril Ponnamperuma Memorial. Trieste conference on chemical evolution, 4: Physics of the origin and evolution of life. Summaries

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

Optional Information