Results 231 to 240 of about 15,313,595 (281)
Some of the next articles are maybe not open access.
Synthesis of Deuterium Derivatives of L-Aspartic Acid
The Journal of Biochemistry, 1962All the possibie deuterium derivatives of L-aspartic acid were prepared by combining various enzymic and chemical reactions. Deuterium analysis by mass spectrometry showed the syntheses proceeded as expected. A comparison of the infrared absorption spectra of the 16 preparations showed they were all different and not contaminated with each other ...
N, TAMIYA, T, OSHIMA
openaire +2 more sources
L-ASPARTIC ACID FORMATION PROM N-ACETYL-L-ASPARTIC ACID IN THE BRAIN
Psychiatry and Clinical Neurosciences, 1961Summary 1. Radioactive L-aspartic acid was produced by incubating C i*-N-acetyl-L-aspartic acid with a mouse brain homogenate. 2. Glutathione and Co++ must co-exist to activate this reaction. However, the reaction could be performed more or less by using Fe++, Cu++, Ca++, and Zn*+ instead of Co*H. 3.
openaire +2 more sources
Applied Biochemistry and Biotechnology, 2016
Aspartase (L-aspartate ammonia lyase, EC 4.3.1.1) catalyses the reversible amination and deamination of L-aspartic acid to fumaric acid which can be used to produce important biochemical. In this study, we have explored the characteristics of aspartase from Pseudomonas aeruginosa PAO1 (PA-AspA).
Arti T, Patel +4 more
openaire +2 more sources
Aspartase (L-aspartate ammonia lyase, EC 4.3.1.1) catalyses the reversible amination and deamination of L-aspartic acid to fumaric acid which can be used to produce important biochemical. In this study, we have explored the characteristics of aspartase from Pseudomonas aeruginosa PAO1 (PA-AspA).
Arti T, Patel +4 more
openaire +2 more sources
2001
(l) [56-84-8] C4H7NO4 (MW 133.10) (d) [1783-96-6] (dl) [617-45-8] InChI = 1S/C4H7NO4/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H,6,7)(H,8,9)/t2-/m1/s1 InChIKey = CKLJMWTZIZZHCS-UWTATZPHSA-N InChI = 1S/C4H7NO4/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H,6,7)(H,8,9)/t2-/m1/s1 InChIKey = CKLJMWTZIZZHCS-UWTATZPHSA-N InChI = 1S/C4H7NO4/c5-2(4(
openaire +1 more source
(l) [56-84-8] C4H7NO4 (MW 133.10) (d) [1783-96-6] (dl) [617-45-8] InChI = 1S/C4H7NO4/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H,6,7)(H,8,9)/t2-/m1/s1 InChIKey = CKLJMWTZIZZHCS-UWTATZPHSA-N InChI = 1S/C4H7NO4/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H,6,7)(H,8,9)/t2-/m1/s1 InChIKey = CKLJMWTZIZZHCS-UWTATZPHSA-N InChI = 1S/C4H7NO4/c5-2(4(
openaire +1 more source
The Acidulant Properties of L‐aspartic Acid
Journal of Food Science, 1965SUMMARY Preliminary studies suggest L‐aspartic acid possesses acidulant properties of potential use in foods. Present costs are not competitive with citric acid, though special application may exist. The concept of using amino acids as flavoring materials is suggested, with a second role in improving nutritional quality.
openaire +1 more source
Mutagenicity studies with N-acetyl-l-aspartic acid
Food and Chemical Toxicology, 2009Analytical studies have reported that N-acetyl-L-aspartic acid (NAA) is present at low concentrations in many foods. The current studies were conducted to assess the mutagenicity of NAA using standard OECD guideline in vitro bacterial and in vivo mammalian mutagenicity studies.
Sule, Karaman +4 more
openaire +2 more sources
Active transport of l-aspartic acid in Neurospora crassa
Biochimica et Biophysica Acta (BBA) - Biomembranes, 1971Abstract Transport of l -aspartic acid in Neurospora crassa conidia is shown to be mediated by neutral and general amino acid transport systems. The transport activity is dependent on pH and results in accumulation of l -aspartic acid against a gradient. Mutants deficient in transport of l -aspartic acid are described.
L, Wolfinbarger +2 more
openaire +2 more sources
Thermodynamics of the conversion of aqueous l-aspartic acid to fumaric acid and ammonia
Biophysical Chemistry, 1986The thermodynamics of the conversion of aqueous L-aspartic acid to fumaric acid and ammonia have been investigated using both heat conduction microcalorimetry and high-pressure liquid chromatography. The reaction was carried out in aqueous phosphate buffer over the pH range 7.25-7.43, the temperature range 13-43 degrees C, and at ionic strengths ...
R N, Goldberg +3 more
openaire +2 more sources
Archives of Pharmacal Research, 2005
Polyene macrolide amphotericin B (AmB) is the drug of choice for the treatment of disseminated fungal infections. However, because of its pronounced side effects, the drug has limited applicability. There are few interesting reports, which state that co-administration of the drug with homo-peptide of polyaspartic acid reduces the side effects of the ...
Bong K, Yoo +3 more
openaire +2 more sources
Polyene macrolide amphotericin B (AmB) is the drug of choice for the treatment of disseminated fungal infections. However, because of its pronounced side effects, the drug has limited applicability. There are few interesting reports, which state that co-administration of the drug with homo-peptide of polyaspartic acid reduces the side effects of the ...
Bong K, Yoo +3 more
openaire +2 more sources

