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Journal articles on the topic 'L-aspartic acid'

Author: Grafiati

Published: 3 June 2025

Last updated: 1 August 2025

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1

Sridhar, B., N. Srinivasan, and R. K. Rajaram. "L-Aspartic acid nitrate–L-aspartic acid (1/1)." Acta Crystallographica Section E Structure Reports Online 58, no. 12 (2002): o1372—o1374. http://dx.doi.org/10.1107/s1600536802020305.

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2

Umadevi, K., K. Anitha, B. Sridhar, N. Srinivasan, and R. K. Rajaram. "L-Aspartic acid monohydrate." Acta Crystallographica Section E Structure Reports Online 59, no. 7 (2003): o1073—o1075. http://dx.doi.org/10.1107/s1600536803014041.

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3

Meléndez-López, A., M. F. García-Hurtado, J. Cruz-Castañeda, A. Negrón-Mendoza, S. Ramos-Bernal, and A. Heredia. "Gamma Irradiation of Aqueos Solution of L-Aspartic Acid, L-Aspartic Acid in Solid State, and L-Aspartic Acid Adsorbed into Na-Montmorillonite: Its Relevance in Chemistry Prebiotic." Journal of Nuclear Physics, Material Sciences, Radiation and Applications 8, no. 2 (2021): 105–8. http://dx.doi.org/10.15415/jnp.2021.82012.

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Aspartic acid is an amino acid present in the modern proteins, however, is considered a primitive amino acid hence its importance in prebiotic chemistry experiments studies. In some works of prebiotic chemistry have been studied the synthesis and the stability of organic matter under high energy sources, and the role of clays has been highlighted due to clays that can affect the reaction mechanisms in the radiolytic processes. The present work is focused on the study of the role of Namontmorillonite in the gamma radiolysis processes of L-aspartic acid. Gamma radiolysis processes were carried o

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4

Appleton, Holly, and Kurt A. Rosentrater. "Sweet Dreams (Are Made of This): A Review and Perspectives on Aspartic Acid Production." Fermentation 7, no. 2 (2021): 49. http://dx.doi.org/10.3390/fermentation7020049.

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Aspartic acid, or “aspartate,” is a non-essential, four carbon amino acid produced and used by the body in two enantiomeric forms: L-aspartic acid and D-aspartic acid. The L-configuration of amino acids is the dominant form used in protein synthesis; thus, L-aspartic acid is by far the more common configuration. However, D-aspartic acid is one of only two known D-amino acids biosynthesized by eukaryotes. While L-aspartic acid is used in protein biosynthesis and neurotransmission, D-aspartic acid is associated with neurogenesis and the endocrine system. Aspartic acid production and use has been

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5

Jakusch, Tamás, Susana Marcão, Lígia Rodrigues, Isabel Correia, João Costa Pessoa, and Tamás Kiss. "Oxovanadium(iv) complexes of salicyl-l-aspartic acid and salicylglycyl-l-aspartic acid." Dalton Transactions, no. 18 (2005): 3072. http://dx.doi.org/10.1039/b506684k.

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6

Ward, P. F. V., and D. W. T. Crompton. "Features of amino acid metabolism in Moniliformis moniliformis (Acanthocephala) in vitro." Parasitology 94, no. 3 (1987): 533–41. http://dx.doi.org/10.1017/s0031182000055876.

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Experiments to investigate the metabolism of glycine, L-glutamic acid and L-aspartic acid by Moniliformis moniliformis were carried out by incubating adult worms aerobically for 3 h at 37°C in Tyrode's solution containing either [U-14C]glycine, L-[U-14C]glutamic acid, L-[U-14C]aspartic acid or L-[4-14C]aspartic acid. Much of the glycine and glutamic acid was absorbed by the worms, but little of either was metabolized. Aspartic acid was readily taken up and metabolized. After incubating with L[U-14C]aspartic acid, most radioactivity was found in ethanol and a volatile compound, presumed to be c

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7

Vukosav, Petra, and Marina Mlakar. "Speciation of biochemically important iron complexes with amino acids: L-aspartic acid and L-aspartic acid - glycine mixture." Electrochimica Acta 139 (September 2014): 29–35. http://dx.doi.org/10.1016/j.electacta.2014.07.006.

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8

Sadovnichii, Roman, Elena Kotelnikova, and Heike Lorenz. "Thermal Deformations of Crystal Structures in the L-Aspartic Acid/L-Glutamic Acid System and DL-Aspartic Acid." Crystals 11, no. 9 (2021): 1102. http://dx.doi.org/10.3390/cryst11091102.

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The method of temperature-resolved powder X-ray diffraction (TRPXRD) was used to determine the elevated temperature behavior of L-aspartic acid (L-asp), DL-aspartic acid (DL-asp), L-glutamic acid (L-glu), and an L-asp0.25,L-glu0.75 solid solution. These amino acids were not found to undergo any solid-phase (polymorph) transformations. When heated, they all experienced only thermal deformations. The corresponding parameters of the monoclinic cells of L-asp and DL-asp, and the orthorhombic cells of L-glu and L-asp0.25,L-glu0.75, were calculated for the entire range of studied temperatures (up to

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9

Chibata, Ichiro, Tetsuya Tosa, and Tadashi Sato. "Continuous production of L-aspartic acid." Applied Biochemistry and Biotechnology 13, no. 3 (1986): 231–40. http://dx.doi.org/10.1007/bf02798461.

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10

Ramakrishnan, B., and M. A. Viswamitra. "Structure of L-arginyl-L-aspartic acid dihydrate." Acta Crystallographica Section C Crystal Structure Communications 44, no. 11 (1988): 1959–61. http://dx.doi.org/10.1107/s0108270188007759.

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11

Whittem, T., K. Parton, and K. Turner. "Effect of polyaspartic acid on pharmacokinetics of gentamicin after single intravenous dose in the dog." Antimicrobial Agents and Chemotherapy 40, no. 5 (1996): 1237–41. http://dx.doi.org/10.1128/aac.40.5.1237.

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The effects of poly-L-aspartic acid on the pharmacokinetics of gentamicin were examined by using a randomized crossover trial design with the dog. When analyzed according to a three-compartment open model, poly-L-aspartic acid reduced some first-order rate equation constants (A3, lambda 1, and lambda 3), the deep peripheral compartment exit microconstant (k31), the elimination rate constant (k(el)), and the area under the concentration-time curve from 0 to 480 h (AUC0-480) (0.21-, 0.60-, 0.26-, 0.27-, 0.72-, and 0.76-fold, respectively; P < 0.05) but increased the volume of distribution at

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12

Röhm, Klaus H., та Robert L. van Etten. "Stereospecific synthesis of L-[1,4-13C2]aspartic acid, L-β-([13C]cyano)alanine and L-[4-13C]aspartic acid". Journal of Labelled Compounds and Radiopharmaceuticals 22, № 9 (1985): 909–15. http://dx.doi.org/10.1002/jlcr.2580220906.

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13

Castano, Ana M., and Antonio M. Echavarren. "L-aspartic acid bis(trimethylsilyl) ester: a convenient starting material for the acylation of L-aspartic acid." Tetrahedron 48, no. 16 (1992): 3377–84. http://dx.doi.org/10.1016/0040-4020(92)85013-5.

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14

Aboulmagd, Elsayed, Fred B. Oppermann-Sanio, and Alexander Steinbüchel. "Purification of Synechocystis sp. Strain PCC6308 Cyanophycin Synthetase and Its Characterization with Respect to Substrate and Primer Specificity." Applied and Environmental Microbiology 67, no. 5 (2001): 2176–82. http://dx.doi.org/10.1128/aem.67.5.2176-2182.2001.

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ABSTRACT Synechocystis sp. strain PCC6308 cyanophycin synthetase was purified 72-fold in three steps by anion exchange chromatography on Q Sepharose, affinity chromatography on the triazine dye matrix Procion Blue HE-RD Sepharose, and gel filtration on Superdex 200 HR from recombinant cells of Escherichia coli. The native enzyme, which catalyzed the incorporation of arginine and aspartic acid into cyanophycin, has an apparent molecular mass of 240 ± 30 kDa and consists of identical subunits of 85 ± 5 kDa. The K m values for arginine (49 μM), aspartic acid (0.45 mM), and ATP (0.20 mM) indicated

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15

Hayashi, Toshio, and Makoto Iwatsuki. "Biodegradation of copoly(L-aspartic acid/L-glutamic acid) in vitro." Biopolymers 29, no. 3 (1990): 549–57. http://dx.doi.org/10.1002/bip.360290310.

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16

Yu, Hyo Gyeong, Hong Geun Ji, Ju Duck Kim, and Hye In Jang. "New Anti-Aging and Anti-Wrinkle Material: Properties and Activities of Nanoparticle Containing Poly(Aspartic Acid) Derivatives." Journal of Nano Research 59 (August 2019): 57–76. http://dx.doi.org/10.4028/www.scientific.net/jnanor.59.57.

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Polymers such as sodium polyacrylate; polysaccharides in starch; polyamino acids, which are the products of alpha-amino acid condensation; and polypeptides are widely used in cosmetics and pharmaceuticals. They are used as viscosity agent, emulsifying agent, and carriers for drug delivery. However, we studied the function of polymers as activity agent, especially that of synthesized poly(aspartic acid). Poly(aspartic acid) is a biocompatible synthetic polymer. It is a water-soluble polyamide containing carboxylic pendants prepared from polysuccinimide, the polycondensate of aspartic acid monom

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17

Azev, V. N., L. K. Baidakova, A. N. Chulin та ін. "Regiospecific Preparation of a Suitably Protected β-Branched Aspartic Acid Dipeptide". Биоорганическая химия 49, № 4 (2023): 411–21. http://dx.doi.org/10.31857/s0132342323040279.

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A new efficient synthetic approach for the preparation of Nα-protected β-L-aspartyl-L-aspartic acid dipeptide was elaborated. The distinctive features of the developed approach include utilization of readily available starting materials (Cbz-asparagine and dimethyl aspartate), aspartimide formation suppression employing electrostatic effect in a final deprotection step and an employment of a novel reagent (NaNO2/aqueous trifluoroacetic acid) for transformation of protected asparagine derivative into the corresponding aspartic acid. The developed method allowes preparation of aspartic acid deri

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18

Korovina, V. V. "STUDY OF ABNORMAL TOXICITY L-ASPARTIC ACID." International bulletin of Veterinary Medicine 1 (2021): 87–90. http://dx.doi.org/10.17238/issn2072-2419.2021.1.87.

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19

Ramakrishnan, B., and M. A. Viswamitra. "Structure ofL-arginyl-L-aspartic acid monohydrate." Acta Crystallographica Section C Crystal Structure Communications 45, no. 5 (1989): 822–24. http://dx.doi.org/10.1107/s0108270188012958.

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20

Paxton *, A. T., and J. B. Harper. "On the solvation of L-aspartic acid." Molecular Physics 102, no. 9-10 (2004): 953–58. http://dx.doi.org/10.1080/00268970410001711913.

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21

Paxton, A. T., and J. B. Harper. "On the solvation of L-aspartic acid." Molecular Physics 102, no. 18 (2004): 1981. http://dx.doi.org/10.1080/0026897042000297293.

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22

Alam, Md Mahmud, Abdullah M. Asiri, Mohammad A. Hasnat, and Mohammed M. Rahman. "Detection of L-Aspartic Acid with Ag-Doped ZnO Nanosheets Using Differential Pulse Voltammetry." Biosensors 12, no. 6 (2022): 379. http://dx.doi.org/10.3390/bios12060379.

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Here, a sensitive voltametric electrochemical sensor probe was fabricated to reliably trace the detection of L-aspartic acid in phosphate-buffered medium using a glassy carbon electrode (GCE) layered with a film of wet-chemically prepared Ag2O-doped ZnO nanosheets (NSs). EDS, FESEM, XPS, and X-ray diffraction analyses were implemented as characterizing tools of prepared NSs to confirm the structural and compositional morphology, binding energies of existing atoms, and the crystallinity of synthesized NSs. The differential pulse voltammetry (DPV) was applied to the trace detection of L-aspartic

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23

Munegumi, Toratane, and Takafumi Yamada. "Thermal Synthesis of Polypeptides from N-Butyloxycarbonyl Oligopeptides Containing Aspartyl Residue at C-Terminus." International Journal of Polymer Science 2017 (2017): 1–16. http://dx.doi.org/10.1155/2017/8364710.

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The thermal reactions of amino acids have been investigated for pure organic synthesis, materials preparation in industry, and prebiotic chemistry. N-t-Butyloxycarbonyl aspartic acid (Boc-Asp) releases 2-butene and carbon dioxide upon heating without solvents. The resulting mixture of the free molten aspartic acid was dehydrated to give peptide bonds. This study describes the thermal reactions of N-t-butyloxycarbonyl peptides (Boc-Gly-L-Asp, Boc-L-Ala-L-Asp, Boc-L-Val-L-Asp, and Boc-Gly-Gly-L-Asp) having an aspartic residue at the carboxyl terminus. The peptides were deprotected upon heating a

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24

Zhou, Jie, Hai-Tao Hou, Yu Song, et al. "Metabolomics Analysis Identifies Differential Metabolites as Biomarkers for Acute Myocardial Infarction." Biomolecules 14, no. 5 (2024): 532. http://dx.doi.org/10.3390/biom14050532.

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Myocardial infarction (MI), including ST-segment elevation MI (STEMI) and non-ST-segment elevation MI (NSTEMI), is still a leading cause of death worldwide. Metabolomics technology was used to explore differential metabolites (DMs) as potential biomarkers for early diagnosis of STEMI and NSTEMI. In the study, 2531 metabolites, including 1925 DMs, were discovered. In the selected 27 DMs, 14 were successfully verified in a new cohort, and the AUC values were all above 0.8. There were 10 in STEMI group, namely L-aspartic acid, L-acetylcarnitine, acetylglycine, decanoylcarnitine, hydroxyphenyllact

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25

Mahaney, William C., Michael G. Boyer, and Nathaniel W. Rutter. "Evaluation of Amino Acid Composition as a Geochronometer in Buried Soils on Mount Kenya, East Africa." Géographie physique et Quaternaire 40, no. 2 (2007): 171–83. http://dx.doi.org/10.7202/032637ar.

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ABSTRACT A sequence of surface and buried paleosols from the slopes of Mount Kenya, East Africa, has been identified and dated by radiocarbon and amino acid dating techniques in order to elucidate the Quaternary history of the area. Buried paleosols vary in radiocarbon age from 900 to > 40,000 yrs BP. They have developed in glacial and periglacial deposits of variable texture, consisting of a high percentage of clasts of phonolite, basalt and syenite. All but two paleosols are located in the Afroalpine zone (above 3200 m). D/L ratios of amino acids in Ab horizons were determined in order to

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26

Hosoya, Ken-ichi, Michiko Sugawara, Hiroshi Asaba, and Tetsuya Terasaki. "Blood-Brain Barrier Produces Significant Efflux of L-Aspartic Acid but Not D-Aspartic Acid." Journal of Neurochemistry 73, no. 3 (2001): 1206–11. http://dx.doi.org/10.1046/j.1471-4159.1999.0731206.x.

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27

Wang, Ling-ling, Yi-xian Wu, Ri-wei Xu, Guan-ying Wu, and Wan-tai Yang. "SYNTHESIS AND CHARACTERIZATION OF POLY(L-GLUTAMIC ACID-co-L-ASPARTIC ACID)." Chinese Journal of Polymer Science 26, no. 04 (2008): 381. http://dx.doi.org/10.1142/s0256767908003047.

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28

Greiner, Edward, Kartik Kumar, Madhuresh Sumit та ін. "Adsorption of l-glutamic acid and l-aspartic acid to γ-Al2O3". Geochimica et Cosmochimica Acta 133 (травень 2014): 142–55. http://dx.doi.org/10.1016/j.gca.2014.01.004.

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29

CASTANO, A. M., and A. M. ECHAVARREN. "ChemInform Abstract: L-Aspartic Acid Bis(trimethylsilyl) Ester: A Convenient Starting Material for the Acylation of L-Aspartic Acid." ChemInform 23, no. 34 (2010): no. http://dx.doi.org/10.1002/chin.199234272.

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30

SZYMAŃSKA, GRAŻYNA, BOGUSŁAW SOBIERAJSKI, and ALEKSANDER CHMIEL. "Immobilized Cells of Recombinant Escherichia coli Strain for Continuous Production of L-aspartic Acid." Polish Journal of Microbiology 60, no. 2 (2011): 105–12. http://dx.doi.org/10.33073/pjm-2011-014.

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For L-aspartic acid biosynthesis, high production cells of Escherichia coli mutant B-715 and P1 were immobilized in chitosan gel using a technique developed in our laboratory. The immobilization process reduced initial activity of the intact cells, however, the biocatalyst produced was very stabile for long-term use in multi-repeated batch or continuous processes. Temperature influence on the conversion of ammonium fumarate to L-aspartic acid was investigated. In long-term experiments, over 603 hours, the temperature 40 degrees C was found to be the best for both biocatalyst stability and high

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31

Hanessian, Stephen, and Benoit Vanasse. "Novel access to (3R)- and (3S)-3-hydroxy-L-aspartic acids, (4S)-4-hydroxy- L-glutamic acid, and related amino acids." Canadian Journal of Chemistry 71, no. 9 (1993): 1401–6. http://dx.doi.org/10.1139/v93-181.

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32

RATNA, DODKE, and KHAN FARID. "Effects of Size, Basicity and Steric Hindrance on the Solution Stability of Binary and Ternary Complexes of Cadmium(II) with some Amino Acids and Formic Acid : A Polarographic Study." Journal of Indian Chemical Society Vol. 70, Jan 1993 (1993): 14–18. https://doi.org/10.5281/zenodo.5910422.

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Department of Chemistry, Dr. Hari Singh Gour University, Sagar-470 003 <em>Manuscript rceived 15 July 1992, revised 15 October 1992, accepted 5 November 1992</em> Polarographic technique was used to determine the values of stability constants (log β) or binary and ternary complexes of Cd<sup>ll </sup>with L-lysine, L-ornithine, L-threonine, L-serine, L-phenylglycine, L-phenylalanine, L·glutamic acid and L-aspartic acid as primary ligands and formic acid as secondary ligand at pH= 8.50 and ionic strength µ = 1.0 <em>M</em> (KNO<sub>3</sub>) at 25<sup>º</sup> Cd<

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33

Uzar, Horst C. "Improved Synthesis of L-Homoserine Derivatives from L-Aspartic Acid." Synthesis 1991, no. 07 (1991): 526–28. http://dx.doi.org/10.1055/s-1991-26507.

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34

Wang, Xiao-Lin, Ai-Ling Ying, and Wei-Ning Wang. "Nanofiltration of l-phenylalanine and l-aspartic acid aqueous solutions." Journal of Membrane Science 196, no. 1 (2002): 59–67. http://dx.doi.org/10.1016/s0376-7388(01)00570-1.

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35

Amgoth, Chander, Shuai Chen, Tirupathi Malavath, and Guping Tang. "Block copolymer [(l-GluA-5-BE)-b-(l-AspA-4-BE)]-based nanoflower capsules with thermosensitive morphology and pH-responsive drug release for cancer therapy." Journal of Materials Chemistry B 8, no. 40 (2020): 9258–68. http://dx.doi.org/10.1039/d0tb01647k.

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Herein, the synthesis of an amino-acid-based di-block copolymer (di-BCP) in-between an l-glutamic acid-5-benzyl ester and L-aspartic acid-4-benzyl ester [(l-GluA-5-BE)-b-(l-AspA-4-BE)] has been reported.

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36

Takaishi, Tomohiro, Minoru Izumi, Ryo Ota, Chieri Inoue, Hiromasa Kiyota, and Koichi Fukase. "Product Selectivity of Esterification of L-Aspartic Acid and L-Glutamic Acid Using Chlorotrimethylsilane." Natural Product Communications 12, no. 2 (2017): 1934578X1701200. http://dx.doi.org/10.1177/1934578x1701200227.

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TMSCl works as an acid catalyst precursor for selective esterification of L-aspartic and L-glutamic acids in the presence of primary, secondary and tertiary alcohols. Although excess TMSCl was required for the completion of esterification, the resulting alkyl TMS ether could be azeotropically removed by simple evaporation with alcohol.

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37

Beri, Aashima, Gagandeep Kaur, Palwinder Singh, Parampaul K. Banipal, and Tarlok S. Banipal. "Volumetric, acoustic, viscometric, calorimetric and spectroscopic studies to elucidate the effects of citrate and tartrate based food preservatives on the solvation behaviors of acidic amino acids at different temperatures." Food & Function 11, no. 1 (2020): 1006–26. http://dx.doi.org/10.1039/c9fo00872a.

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38

Liu, Yizhi, Xinpei Gao, Mingwei Zhao, Fei Lu, and Liqiang Zheng. "Formation of supermolecular chiral gels from l-aspartic acid-based perylenebisimides and benzene dicarboxylic acids." New Journal of Chemistry 41, no. 15 (2017): 7643–49. http://dx.doi.org/10.1039/c7nj01107e.

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39

Yoo, Bong K., M. A. Jalil Miah, Eung-Seok Lee, and Kun Han. "Synthesis of decapeptide ofl-aspartic acid and benzyl-l-aspartic acid by solid phase peptide synthesis." Archives of Pharmacal Research 28, no. 7 (2005): 756–60. http://dx.doi.org/10.1007/bf02977338.

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40

Henjum, Sigrun, Livar Frøyland, Margaretha Haugen, et al. "Risk Assessment of "Other Substances" – L-aspartic Acid." European Journal of Nutrition & Food Safety 9, no. 1 (2018): 36–38. http://dx.doi.org/10.9734/ejnfs/2019/45633.

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41

Sham, Hing L., Cheryl A. Rempel, Herman Stein, and Jerome Cohen. "Novel statine analogue synthesized from L-aspartic acid." Journal of the Chemical Society, Chemical Communications, no. 9 (1987): 683. http://dx.doi.org/10.1039/c39870000683.

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42

Maeda, Hidekatsu, Shu-Ichi Suzuki, Masanao Ikeguchi, Tsuyoshi Sakai, and Kunihiko Shibata. "Enzymatic synthesis of l-[4-13C]aspartic acid." Journal of Bioscience and Bioengineering 89, no. 4 (2000): 392–95. http://dx.doi.org/10.1016/s1389-1723(00)88966-5.

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43

MORIMOTO, Tomoaki, Yoshimi NAKAGAWA, Masaru SENUMA, and Tetsuya TOSA. "Microbial sensors for L-aspartic acid and urea." Bunseki kagaku 39, no. 11 (1990): 735–39. http://dx.doi.org/10.2116/bunsekikagaku.39.11_735.

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44

Karaman, Sule, Abby Myhre, E. Maria Donner, Susan M. Munley, and Bryan Delaney. "Mutagenicity studies with N-acetyl-l-aspartic acid." Food and Chemical Toxicology 47, no. 8 (2009): 1936–40. http://dx.doi.org/10.1016/j.fct.2009.05.005.

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45

Levin, E. D., L. A. Lyublinskaya, E. A. Timokhina, and V. M. Stepanov. "N-formyl-L-aspartic acid synthesis and characterization." Chemistry of Natural Compounds 27, no. 4 (1991): 517–18. http://dx.doi.org/10.1007/bf00636593.

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46

Downing, J. A., J. Joss, and R. J. Scaramuzzi. "The effects of N-methyl-d,l-aspartic acid and aspartic acid on the plasma concentration of gonadotrophins, GH and prolactin in the ewe." Journal of Endocrinology 149, no. 1 (1996): 65–72. http://dx.doi.org/10.1677/joe.0.1490065.

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Abstract Aspartic acid is a neurotransmitter in the central nervous system that acts via the glutamate receptor and the analogue, N-methyl-d,l-aspartic acid (NMA) is an agonist that stimulates GnRH secretion. Under normal dietary conditions, the plasma concentration of aspartic acid in ewes is low and if increased by improved nutrition may increase the brain concentration of aspartic acid leading to increased gonadotrophin secretion. In two experiments we investigated the effects of NMA on pituitary hormone concentrations and the effects of aspartic acid on ovulation rate and pituitary hormone

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47

Singh, Jasdeep, Ankit Srivastava, Pravin Jha, Kislay K. Sinha, and Bishwajit Kundu. "l-Asparaginase as a new molecular target against leishmaniasis: insights into the mechanism of action and structure-based inhibitor design." Molecular BioSystems 11, no. 7 (2015): 1887–96. http://dx.doi.org/10.1039/c5mb00251f.

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48

Khan, Farid, and Afroza Khanam. "Study of complexes of cadmium with some L-amino acids and vitamin-C by voltammetric technique." Eclética Química Journal 33, no. 2 (2018): 29. http://dx.doi.org/10.26850/1678-4618eqj.v33.2.2008.p29-36.

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Voltammetric technique was used to study the binary and ternary complexes of cadmium with L-amino acids and vitamin-C (L-ascorbic acid) at pH =7.30 ± 0.01, μ = 1.0M KNO3 at 25ºC and 35ºC. Cd (II) formed 1:1:1, 1:1:2 and 1:2:1 complexes with L-lysine, L-ornithine, L-threonine, L-serine, L-phenylglycine, L-phenylalanine, L-glutamic acid and L-aspartic acid used as primary ligands and L-ascorbic acid used as secondary ligand. The trend of stability constant of complexes was Llysine < L-ornithine < L-threonine < L-serine < L-phenylglycine < L-phenylalanine < L-glutamic acid <

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Abbas Kareem, Adel, Hayder Abdul-Hussain Mohsen Al- Mughair, and Qassim A. S. Al-Zayadi. "Influence of phosphorous treatment and aspartic acid spray on a few aspects of oat Avena sativa L. growth and production." Sumer 3 8, CSS 3 (2023): 1–5. http://dx.doi.org/10.21931/rb/css/2023.08.03.7.

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The experiment was carried out in the Abu Al-Fadl Forest Nursery, the Plant Production Department, Al-Diwaniyah Agriculture Directorate (3 km north-east of Al-Diwaniyah city) during the winter season 2021-2022 to determine the effect of four levels of phosphate fertilizer (0, 30, 60 and 90 kg P ha-1 ) and two concentrations of aspartic acid spray (0 and 200 mg aspartic L -1 ), on the growth and yield of oats Avena sativa L. Shifa cultivar. The experiment was applied according to a Randomized Complete Block Design (RCBD) by a split plot with three replicates. The levels of phosphate fertilizer

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Shen, Hai-Min, Wen-Jie Zhou, Wu-Bin Yu, et al. "Metal-free chemoselective oxidation of sulfides to sulfoxides catalyzed by immobilized l-aspartic acid and l-glutamic acid in an aqueous phase at room temperature." New Journal of Chemistry 40, no. 6 (2016): 4874–78. http://dx.doi.org/10.1039/c6nj00854b.

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