scholarly journals Acetic Acid Can Catalyze Succinimide Formation from Aspartic Acid Residues by a Concerted Bond Reorganization Mechanism: A Computational Study

2015 ◽  
Vol 16 (1) ◽  
pp. 1613-1626 ◽  
Author(s):  
Ohgi Takahashi ◽  
Ryota Kirikoshi ◽  
Noriyoshi Manabe
1968 ◽  
Vol 107 (3) ◽  
pp. 335-340 ◽  
Author(s):  
D. K. J. Tommel ◽  
J. F. G. Vliegenthart ◽  
T. J. Penders ◽  
J F Arens

1. Peptides and α-amino acids, occurring in mixtures from various sources, can be separated into one fraction containing the amino acids and several peptide fractions. This is achieved by chelation of the mixture with Cu2+ ions and subsequent chromatography of these chelates over the acetate form of diethylaminoethylcellulose or triethylaminoethylcellulose. 2. The amino acid fraction is obtained by elution with 0·01m-collidine–acetate buffer, pH8·0. 3. Peptide fractions are eluted with 0·01m-collidine–acetate buffer, pH4·5, 0·17n-acetic acid and 0·1n-hydrochloric acid respectively. 4. With the exception of aspartic acid and glutamic acid, which are partly found in the acidic peptide fraction, the amino acids are completely separated from the peptides. 5. Contamination of the acidic peptide fraction with glutamic acid and aspartic acid can be largely avoided by previous addition of an excess of arginine. 6. Copper is removed from the eluates by extraction with 8-hydroxyquinoline in chloroform.


1987 ◽  
Vol 35 (10) ◽  
pp. 4203-4207 ◽  
Author(s):  
RYOTA KUROKI ◽  
NAOE KANESAKA ◽  
HIDENORI YAMADA ◽  
TAIJI IMOTO
Keyword(s):  

2019 ◽  
Vol 37 (9) ◽  
pp. 883-886 ◽  
Author(s):  
Xin Yue ◽  
Longfei Li ◽  
Pengjie Li ◽  
Chenguang Luo ◽  
Min Pu ◽  
...  

2012 ◽  
Vol 24 (2) ◽  
pp. 762-777 ◽  
Author(s):  
Rocío González-Lamothe ◽  
Mohamed El Oirdi ◽  
Normand Brisson ◽  
Kamal Bouarab

2017 ◽  
Vol 5 (43) ◽  
pp. 8498-8505 ◽  
Author(s):  
Taehoon Sim ◽  
Chaemin Lim ◽  
Ngoc Ha Hoang ◽  
Jae Eun Kim ◽  
Eun Seong Lee ◽  
...  

Poly(aspartic acid-graft-imidazole)-poly(ethylene glycol) was applied as a pH-sensitive nanocarrier of the photosensitizer indole-3-acetic acid for treatment of skin cancer.


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