TY - JOUR
T1 - Cation exchange to montmorillonite induces selective adsorption of amino acids
AU - Millman, Emily
AU - Chatterjee, Anamika
AU - Parker, Kimberly M.
AU - Catalano, Jeffrey G.
N1 - Publisher Copyright:
© 2024 Elsevier Ltd
PY - 2024/5/1
Y1 - 2024/5/1
N2 - Concentrating simple organic molecules, such as amino acids, in the adsorbed phase could have been an early step in prebiotic evolution towards more complex bio-macromolecules on the early Earth. Smectite clay minerals represent potential selective sorbents for prebiotic molecules because of their negative structural charge and high surface area. This study evaluated the adsorption behavior of amino acids to montmorillonite, a well-characterized smectite, at varying pH and fluid compositions. At both pH 5 and 7 in a sodium chloride fluid, amino acids with basic sidechains (L-arginine and L-lysine), which are primarily cationic under these conditions, were selectively adsorbed to montmorillonite with Langmuir constants much greater than amino acids that were predominantly zwitterionic or anionic in solution. On average, the Langmuir constants for the cationic amino acids were 30 (pH 5) and 50 (pH 7) times greater than the constants for zwitterionic amino acids and 120 (pH 5) and 80 (pH 7) times greater than the constants for L-glutamic acid. Under the same pH conditions in a magnesium chloride solution, the adsorption of L-arginine and L-lysine was substantially inhibited with Langmuir constants ∼ 10 times smaller. These observations suggest that cation exchange is the dominant adsorption mechanism for amino acids on montmorillonite. X-ray diffraction and infrared spectroscopy indicate that L-arginine and L-lysine enter the smectite interlayer where the protonated amino sidechain has the strongest interactions with the mineral surface, further supporting adsorption driven primarily through electrostatic interactions. Therefore, smectites on the early Earth may have selectively concentrated cationic amino acids, providing a potential template for the polymerization of α-amine linked peptides.
AB - Concentrating simple organic molecules, such as amino acids, in the adsorbed phase could have been an early step in prebiotic evolution towards more complex bio-macromolecules on the early Earth. Smectite clay minerals represent potential selective sorbents for prebiotic molecules because of their negative structural charge and high surface area. This study evaluated the adsorption behavior of amino acids to montmorillonite, a well-characterized smectite, at varying pH and fluid compositions. At both pH 5 and 7 in a sodium chloride fluid, amino acids with basic sidechains (L-arginine and L-lysine), which are primarily cationic under these conditions, were selectively adsorbed to montmorillonite with Langmuir constants much greater than amino acids that were predominantly zwitterionic or anionic in solution. On average, the Langmuir constants for the cationic amino acids were 30 (pH 5) and 50 (pH 7) times greater than the constants for zwitterionic amino acids and 120 (pH 5) and 80 (pH 7) times greater than the constants for L-glutamic acid. Under the same pH conditions in a magnesium chloride solution, the adsorption of L-arginine and L-lysine was substantially inhibited with Langmuir constants ∼ 10 times smaller. These observations suggest that cation exchange is the dominant adsorption mechanism for amino acids on montmorillonite. X-ray diffraction and infrared spectroscopy indicate that L-arginine and L-lysine enter the smectite interlayer where the protonated amino sidechain has the strongest interactions with the mineral surface, further supporting adsorption driven primarily through electrostatic interactions. Therefore, smectites on the early Earth may have selectively concentrated cationic amino acids, providing a potential template for the polymerization of α-amine linked peptides.
KW - Adsorption
KW - Amino acids
KW - Montmorillonite
KW - Prebiotic chemistry
KW - Selectivity
UR - http://www.scopus.com/inward/record.url?scp=85188012469&partnerID=8YFLogxK
U2 - 10.1016/j.gca.2024.02.020
DO - 10.1016/j.gca.2024.02.020
M3 - Article
AN - SCOPUS:85188012469
SN - 0016-7037
VL - 372
SP - 181
EP - 195
JO - Geochimica et Cosmochimica Acta
JF - Geochimica et Cosmochimica Acta
ER -