Dietary factors potentially impacting thiaminase I-mediated thiamine deficiency

• Published in: Scientific reports Vol. 13; no. 1; pp. 7008 - 17
• Main Authors: Edwards, Katie A., Randall, Eileen A., Wolfe, Patricia C., Angert, Esther R., Kraft, Clifford E.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 28.04.2023; Nature Publishing Group; Nature Portfolio
• Subjects: 631/158; 631/326/41; 631/45/607; 692/700/2814; Alkyl and Aryl Transferases; Animals; Ascorbic acid; Copper; Degradation; Enzymatic activity; Enzymes; Fish populations; Fishes - metabolism; Fluorescence; Fluorescence in situ hybridization; Humanities and Social Sciences; Hydrolases - metabolism; multidisciplinary; Nicotinic acid; Nutrient deficiency; Population decline; Prey; Pyridoxine; Science; Science (multidisciplinary); Substrates; Thiaminase; Thiamine; Thiamine - metabolism; Thiamine Deficiency; Vitamin B; Vitamin B6
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-023-34063-5

Fish population declines from thiamine (vitamin B1) deficiency have been widespread in ecologically and economically valuable organisms, ranging from the Great Lakes to the Baltic Sea and, most recently, the California coast. Thiamine deficiencies in predatory fishes are often attributed to a diet of prey fishes with high levels of thiamine-degrading (e.g., thiaminase) enzymes, such as alewives, rainbow smelt, and anchovies. Since their discovery, thiaminase I enzymes have been recognized for breaking down thiamine into its pyrimidine and thiazole moieties using various nucleophilic co-substrates to afford cleavage, but these studies have not thoroughly considered other factors that could modify enzyme activity. We found the thiaminase I enzyme from Clostridium botulinum efficiently degrades thiamine in the presence of pyridoxine (vitamin B6) as a co-substrate but has relatively limited activity in the presence of nicotinic acid (vitamin B3). Using fluorescence measurements, thiamine degradation in an over-the-counter complete multivitamin formulation was inhibited, and a B-complex formulation required co-substrate supplementation for maximal thiamine depletion. These studies prompted the evaluation of specific constituents contributing to thiaminase I inhibition by both chromatography and fluorescence assays: Cu 2+ potently and irreversibly inhibited thiamine degradation; ascorbic acid was a strong but reversible inhibitor; Fe 2+ , Mn 2+ and Fe 3+ modulated thiamine degradation to a lesser degree. The enhancement by pyridoxine and inhibition by Cu 2+ extended to thiaminase-mediated degradation from Burkholderia thailandensis , Paenibacillus thiaminolyticus , and Paenibacillus apiarius in tryptic soy broth supernatants. These co-substrate limitations and the common presence of inhibitory dietary factors complement recent studies reporting that the intended function of thiaminase enzymes is to recycle thiamine breakdown products for thiamine synthesis, not thiamine degradation.