Amino Acids (AA)

<p>L-Lysine L-malate is a chemical compound that is used in wastewater treatment. It inhibits the activity of enzymes such as carbon disulphide oxidase, copper complexes, and cationic surfactants. L-Lysine L-malate can be synthesized from sodium citrate and malonic acid by reacting with hydrogen peroxide to form a bicyclic heterocycle. This compound has been shown to have biological effects on metabolic disorders in animal studies, which may be due to its ability to inhibit the synthesis of fatty acids and proteins. The adsorption mechanism for this product is unknown.</p>

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<p>L-phenylalanine is an amino acid that has a sweet taste. It is one of the 20 amino acids encoded by the universal genetic code, and is classified as a polar amino acid because it has a hydroxyl group on its side chain. L-Phenylalanine is used in the food industry as a sweetener and to enhance salty or acidic flavors. Phenylalanine has been shown to be an important precursor for several important neurotransmitters in the brain. This includes serotonin, dopamine, and norepinephrine. Phenylalanine also plays a role in protein metabolism and enzyme activity, including aminopeptidases and racemases, which are enzymes that catalyze reactions involving racemic mixtures.</p>

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<p>Z-Ala-Arg-OH is a low molecular weight carboxylate that has an acidic, hydrophobic side chain. The chemical formula for Z-Ala-Arg-OH is C11H18N4O6. The chemical structure of Z-Ala-Arg-OH can be found in the figure below:<br>Z-Ala-Arg-OH is an ionizable, acidic compound with a pKa of 3.5. The functional groups on Z-Ala-Arg-OH are shown in the figure below:<br>The carboxylate group and the amine group are present in this molecule.<br>Z-Ala-Arg-OH is a transpeptidase, which catalyses the posttranslational modification of proteins by transferring amino acids from one protein to another during translation or after translation. Transpeptidases are important enzymes in bacterial cell wall synthesis because they catalyze peptide bond formation between two amino acid</p>