Decomposition and adsorption of peptides in Alaskan coastal marine sediments

Dissertation (Ph.D.) University of Alaska Fairbanks, 1994In organic-rich coastal sediments, hydrolyzable amino acids make up a substantial fraction of the sedimentary content of organic nitrogen. How this organic nitrogen resists decomposition and is preserved in sediments is poorly understood. In order to investigate the factors controlling mineralization and preservation of hydrolyzable amino acids, decomposition and adsorption of peptides were studied in suboxic and anoxic pore water and sediments from Resurrection Bay (RB) and Skan Bay (SB), Alaska. Five tritium-labeled peptides, basic di-lysine, acidic di-glutamic acid, and neutral di-alanine, tri-alanine and hexa-alanine, were used as tracers. In filtered pore water, the hydrolysis rates were usually low. The exception was that the initial enzymatic hydrolysis of di-alanine and di-glutamic acid was rapid in SB pore water. The hydrolysis rates of both peptides increased with concentration. In sediments, hydrolysis was found to be the rate-limiting step of peptide decomposition. Alanyl and glutamyl peptides were hydrolyzed faster than lysyl peptide, and the hydrolysis rates among alanyl peptides decreased with increasing molecular weight. Peptide hydrolysis was affected more by molecular structure than by oxic or anoxic conditions. Adsorption of lysyl peptide to sediments was greater than that of other peptides. Basicity enhanced peptide adsorption more than increased molecular weight. Sedimentary organic matter was mainly responsible for peptide adsorption. The different patterns of peptide adsorption in RB and SB sediments were related to the greater total organic carbon concentration in SB sediment. Some of the peptide adsorption was irreversible. Adsorbed peptides were more resistant to biological decomposition than dissolved peptides. Adsorption may be an important step in the process of peptide preservation in sediments, and thus the preservation of sediment organic matter during early diagenesis