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Chemistry of aminoacylation of 5'-AMO and the origin of protein synthesisMuch of our recent work has been a study of aminoacyl AMP derivatives. Elucidation of the character of aminoacyl AMP derivatives has made it obvious that AMP has characteristics which should allow it to preferentially catalyze the synthesis of L-amino acid peptides. The essential features which lead to this conclusion are that all l-amino acids (but not all D amino acids) when esterified to 5'-AMP preferentially (65 percent) distribute to the 3' position of the 5'-AMP; that esterification is predominantly at the 2' position; that 2', 3' diaminoacyl esters are readily formed; and that a peptide bond can be formed between adjacent 2',3' aminoacyl esters.
Document ID
19920004403
Acquisition Source
Legacy CDMS
Document Type
Conference Paper
Authors
Lacey, J. C., Jr.
(Alabama Univ. Birmingham, AL, United States)
Date Acquired
September 6, 2013
Publication Date
October 1, 1991
Publication Information
Publication: NASA, Washington, Fourth Symposium on Chemical Evolution and the Origin and Evolution of Life
Subject Category
Space Biology
Accession Number
92N13621
Distribution Limits
Public
Copyright
Work of the US Gov. Public Use Permitted.
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