Literature DB >> 501743

The formation of peptides from glycine thioesters.

A L Weber, L E Orgel.   

Abstract

The condensation products obtained from 0.01M S-glycyl-N-acetyl-cysteamine at different pH's were investigated. The highest yields of diketopiperazine (approx. 50%) were observed in phosphate buffers between pH 7.5 and 8.5. The highest yields of diglycine (46%), triglycine (10%) and tetraglycine (2%) were observed in carbonate buffers at pH 9.5. At pH 8.0, over 90% of the glycyl residues of 0.15M S-glycyl-N-acetylcysteamine were incorporated into condensation products, mainly DKP (60--70%). The yields of products from the condensation of S-glycyl-ethanethiol under similar conditions closely resembled those obtained with S-glycyl-N-acetylcysteamine.

Entities:  

Mesh:

Substances:

Year:  1979        PMID: 501743     DOI: 10.1007/bf01739479

Source DB:  PubMed          Journal:  J Mol Evol        ISSN: 0022-2844            Impact factor:   2.395


  6 in total

1.  Abiotic origin of biopolymers.

Authors:  J Oró; E Stephen-Sherwood
Journal:  Orig Life       Date:  1976-01

2.  Amino acid activation with adenosine 5'-phosphorimidazolide.

Authors:  A L Weber; L E Orgel
Journal:  J Mol Evol       Date:  1978-05-12       Impact factor: 2.395

3.  The formation of peptides from the 2'(3')-glycyl ester of a nucleotide.

Authors:  A L Weber; L E Orgel
Journal:  J Mol Evol       Date:  1978-08-02       Impact factor: 2.395

4.  A specific and sensitive assay for disulfides.

Authors:  W L Zahler; W W Cleland
Journal:  J Biol Chem       Date:  1968-02-25       Impact factor: 5.157

5.  The use of 2,2'-dithiobis-(5-nitropyridine) as a selective reagent for the detection of thiols.

Authors:  D R Grassetti; J F Murray
Journal:  J Chromatogr       Date:  1969-04-22

6.  The general synthetic route to amino acid esters of nucleotides and nucleoside-5'-triphosphates and some properties of these compounds.

Authors:  B P Gottikh; A A Krayevsky; N B Tarussova; P P Purygin; T L Tsilevich
Journal:  Tetrahedron       Date:  1970-09       Impact factor: 2.457

  6 in total
  21 in total

1.  Oligoglyceric acid synthesis by autocondensation of glyceroyl thioester.

Authors:  A L Weber
Journal:  J Mol Evol       Date:  1987       Impact factor: 2.395

2.  Alanine synthesis from glyceraldehyde and ammonium ion in aqueous solution.

Authors:  A L Weber
Journal:  J Mol Evol       Date:  1985       Impact factor: 2.395

3.  Sugars as the optimal biosynthetic carbon substrate of aqueous life throughout the universe.

Authors:  A L Weber
Journal:  Orig Life Evol Biosph       Date:  2000-02       Impact factor: 1.950

4.  The sugar model: catalytic flow reactor dynamics of pyruvaldehyde synthesis from triose catalyzed by poly-l-lysine contained in a dialyzer.

Authors:  A L Weber
Journal:  Orig Life Evol Biosph       Date:  2001-06       Impact factor: 1.950

5.  Selective emergence and survival of early polypeptides in water.

Authors:  A Brack
Journal:  Orig Life Evol Biosph       Date:  1987       Impact factor: 1.950

6.  The triose model: glyceraldehyde as a source of energy and monomers for prebiotic condensation reactions.

Authors:  A L Weber
Journal:  Orig Life Evol Biosph       Date:  1987       Impact factor: 1.950

7.  Hydrogels cross-linked by native chemical ligation.

Authors:  Bi-Huang Hu; Jing Su; Phillip B Messersmith
Journal:  Biomacromolecules       Date:  2009-08-10       Impact factor: 6.988

8.  Nonenzymatic formation of "energy-rich" lactoyl and glyceroyl thioesters from glyceraldehyde and a thiol.

Authors:  A L Weber
Journal:  J Mol Evol       Date:  1984       Impact factor: 2.395

9.  Diketopiperazine-mediated peptide formation in aqueous solution.

Authors:  M Nagayama; O Takaoka; K Inomata; Y Yamagata
Journal:  Orig Life Evol Biosph       Date:  1990       Impact factor: 1.950

10.  Formation of pyrophosphate, tripolyphosphate, and phosphorylimidazole with the thioester, n, s-diacetyl-cysteamine, as the condensing agent.

Authors:  A L Weber
Journal:  J Mol Evol       Date:  1981       Impact factor: 2.395

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.