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Thiamin
Vitamin B1 essential for energy metabolism, part of Kreb's Cycle, contains pyrimidine ring and thiazole moiety.
Niacin
Vitamin B3, works alongside thiamin and riboflavin in the Kreb's Cycle.
Riboflavin
Vitamin B2, works alongside thiamin and niacin in the Kreb's Cycle.
Kreb's Cycle
Metabolic pathway for ATP production, involving thiamin, niacin, and riboflavin.
Pyrimidine ring
Part of thiamin's structure, involved in energy metabolism.
Thiazole moiety
Part of thiamin's structure, involved in energy metabolism.
Methyl group
Found in the thiazole ring of thiamin, serves as the active site during enzyme interaction.
Enzymes
Biological catalysts, often requiring thiamin for activation.
Thiamin sources
Found in meat, whole grains, legumes, and yeast
frequently enriched in grain products.
Thiamin sensitivity
Sensitive to high temperatures and alkaline pH, protected by reducing reagents like vitamin C and citric acid.
Thiamin absorption
Only free form can be absorbed, phosphorylated forms must be dephosphorylated by intestinal phosphatases.
Thiamin storage
Absorbed into blood, taken up by the liver, phosphorylated to coenzyme form TDP/TPP.
TDP/TPP
Most metabolically active form of thiamin, involved in energy metabolism and coenzyme function.
Thiamin functions
Energy metabolism, pentose and NADPH synthesis, membrane and nerve conduction.
Decarboxylase reactions
Essential for energy transformation, involve TDP/TPP and specific enzymes like pyruvate dehydrogenase.
Pyruvate dehydrogenase
Enzyme complex involving TDP/TPP, responsible for converting pyruvate to acetyl CoA.
Transketolase
Enzyme involved in pentose phosphate pathway, loosely binds to TDP/TPP.
Thiamin in nerve conduction
TTP plays a role in nerve conduction, activates chloride transport and stimulates nerve impulses.
Thiamin deficiency
Uncommon in developed world, can occur in alcoholism, liver damage, and diseases impairing absorption.
Maple syrup urine disease
Genetic disease related to thiamin status, results in accumulation of branched-chain amino acids and keto acids in the blood.
Thiamin toxicity
Parenteral exposure can cause headaches, cardiac arrhythmia, and convulsions.
Thiamin assessment
Measured by urinary thiamin concentrations and red blood cell transketolase activity.
Pantothenic acid
Vitamin B5, metabolically active form of coenzyme A, comprised of beta-alanine and D-pantoic acid.
Pantothenic acid sources
Found in various foods, including brewer's yeast, corn, cauliflower, kale, egg yolk, organ meats, milk, and whole-grain breads.
Pantothenic acid digestion
Hydrolyzed to free form before absorption through the enterocytes.
Pantothenic acid absorption
Absorbed via sodium-dependent active multivitamin carrier in the jejunum.
Pantothenic acid functions
Carries out acetyl and acyl transfer reactions, important for macronutrient and lipid metabolism.
Biotin
Vitamin B7, composed of ureido and tetrahydrothiophene rings with a valeric acid side chain.
Biotin sources
Found in meat products, soybeans, cereal products, and synthesized by intestinal bacteria.
Biotin digestion and absorption
Requires digestion prior to absorption, absorbed in the small intestine via passive diffusion or carrier-mediated transport.
Biotin functions
Covalently attaches to carboxylases, regulates gene expression, and plays a role in cellular division.
Biotin deficiency
Can occur due to impaired absorption, inflammatory bowel diseases, alcoholism, or genetic mutations in biotin-dependent enzymes.
Biotin toxicity
No reported toxic side effects, used in large amounts in skin and hair products.
Biotin assessment
Blood and urine analysis, decreased urinary biotin excretion and greater excretion of 3-hydroxy isovaleric acid are markers of deficiency.