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Biochemistry is the study of the chemicals and reactions that occur in living things.

Section 1 Carbohydrates and Lipids. Chapter 23. Biochemistry is the study of the chemicals and reactions that occur in living things. Biochemical compounds are often large and complex organic molecules, but their chemistry is similar to that of the smaller organic molecules.

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Biochemistry is the study of the chemicals and reactions that occur in living things.

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  1. Section 1 Carbohydrates and Lipids Chapter 23 • Biochemistry is the study of the chemicals and reactions that occur in living things. • Biochemical compounds are often large and complex organic molecules, but their chemistry is similar to that of the smaller organic molecules

  2. Section 1 Carbohydrates and Lipids Chapter 23 Carbohydrates • Carbohydratesare molecules that are composed of carbon, hydrogen, and oxygen atoms in a 1:2:1 ratio, and provide nutrients to the cells of living things. • sugars, starches,and cellulose • Carbohydrates are produced by plants through a process called photosynthesis. • Carbohydrates provide nearly all of the energy that is available in most plant-derived food.

  3. Section 1 Carbohydrates and Lipids Chapter 23 Carbohydrates, continued Monosaccharides • A monosaccharideis a simple sugar that is the basic subunit of a carbohydrate. • A single monosaccharide molecule contains three to seven carbon atoms. • Monosaccharide compounds are • typically sweet-tasting • white solids at room temperature • water soluble

  4. Section 1 Carbohydrates and Lipids Chapter 23 Carbohydrates, continued Monosaccharides, continued • The most common monosaccharides are glucose (also called dextrose) and fructose. • Both have the formula C6(H2O)6. • Their structural formulas differ.

  5. Section 1 Carbohydrates and Lipids Chapter 23 Carbohydrates, continued Disaccharides • A disaccharideis a sugar that consists of two monosaccharide units that are joined together. • sucrose, C12H22O11 • A molecule of sucrose forms when a glucose molecule bonds to a fructose molecule. • lactose • Lactose is made up of a sugar called galactose and glucose.

  6. Section 1 Carbohydrates and Lipids Chapter 23 Carbohydrates, continued Carbohydrate Reactions • Carbohydrates undergo two important kinds of reactions: condensation reactions and hydrolysis reactions. • A condensation reactionis a reaction in which two molecules or parts of the same molecule combine.

  7. Section 1 Carbohydrates and Lipids Chapter 23 Carbohydrates, continued Carbohydrate Reactions, continued • Hydrolysisis a chemical reaction between water and another substance to form two or more new substances. • Disaccharides and longer-chain polysaccharides can be broken down into smaller sugar units by hydrolysis.

  8. Section 1 Carbohydrates and Lipids Chapter 23 Carbohydrates, continued Polysaccharides • When many monosaccharides or disaccharides combine in a series of condensation reactions, they form a polysaccharide. • A polysaccharideis a carbohydrate made up of long chains of simple sugars. • Cellulose, starch, and glycogen are polymersof glucose. • Sheets of cellulose make up plant cell walls. • Starch is the storage form of glucose in plants.

  9. Section 1 Carbohydrates and Lipids Chapter 23 Carbohydrates, continued Polysaccharides, continued • Glycogen, cellulose, and starch differ in their arrangement of glucose monomers.

  10. Section 1 Carbohydrates and Lipids Chapter 23 Lipids • A lipidis a type of biochemical that does not dissolve in water, has a high percentage of C and H atoms, and is soluble in nonpolar solvents. • As a class, lipids are not nearly as similar to each other as carbohydrates are. • Long-chain fatty acids, phospholipids, steroids, and cholesterol are lipids.

  11. Section 1 Carbohydrates and Lipids Chapter 23 Lipids, continued Fatty Acids and Triglycerides • Fatty acidsconsist of a long, nonpolar hydrocarbon “tail” and a polar carboxylic acid functional group at the “head.” • They have hydrophilic polar heads, but their hydrocarbon chains make them insoluble in water.

  12. Section 1 Carbohydrates and Lipids Chapter 23 Lipids, continued Fatty Acids and Triglycerides, continued • Triglycerides are formed by condensation reactions in which three fatty acid molecules bond to one glycerol (a type of alcohol) molecule. • Fats and oils that are the most common group of lipids in your diet. • Because they have a large amount of saturated fatty acids, fats are solids at room temperature. • Oils have more unsaturated fatty acids than fats, and are liquids • Fat is stored in adipose tissue until it is needed as an energy source.

  13. Section 1 Carbohydrates and Lipids Chapter 23 Lipids, continued Fatty Acids and Triglycerides, continued • When a fat combines with NaOH, an acid-base reaction called saponificationoccurs, and a salt and water form. • This salt is made up of molecules that have long carboxylic acid chains and is called soap. • Lipids that react with a base to form soap are called saponifiable lipids, which include fats, oils, and fatty acids.

  14. Section 1 Carbohydrates and Lipids Chapter 23 Lipids, continued Other Important Lipids • Compound saponifiable lipidsplay an important role in biochemical processes. • These lipids are structurally similar to triglycerides in that at least one fatty acid is bonded to the central glycerol or glycerol-like unit. • These molecules may also have phosphate groups, sugar units, or nitrogen containing groups. • Phospholipids, are compound saponifiable lipids and are the main structural component of cell membranes.

  15. Section 1 Carbohydrates and Lipids Chapter 23 Lipids, continued Other Important Lipids, continued • Nonsaponifiablelipids are nonpolar compounds that do not form soap. • steroids, many vitamins, and bile acids • Cholesterolis a steroid present in animal cell membranes and is a precursor of many hormones.

  16. Section 2 Amino Acids and Proteins Chapter 23 • Amino acid molecules are the basic building blocks of proteins. • More than 700 types of amino acids occur in nature. • Only 20 types of amino acids are found in human proteins. • The human body can synthesize only 11 of the 20 amino acids as needed. • The other nine, called the essential amino acids,have to be supplied by the food that we eat.

  17. Section 2 Amino Acids and Proteins Chapter 23 Amino Acids • Amino acidsare organic molecules that contain two functional groups: a basic —NH2 amino group and an acidic —COOH carboxylic acid group. or • The R-groups of the amino acids present in a protein determine the protein’s biological activity.

  18. Section 2 Amino Acids and Proteins Chapter 23 Amino Acids, continued Amino Acid Reactions • Two amino acids can react with each other in an acid-base reaction. • The basic amino group of one amino acid reacts with the acidic carboxylic acid group of another amino acid to form a peptide,and a molecule of water is lost. • This reaction is classified as a condensation reaction • The bond formed is called a peptide bond. • The product is a dipeptide.

  19. Section 2 Amino Acids and Proteins Chapter 23 Amino Acids, continued Amino Acid Reactions • Longer chains of amino acids are called polypeptides. • Chains of 50 or more amino acids are called proteins. • Peptide bonds can be broken, or hydrolyzed,by enzymes called proteases.

  20. Section 2 Amino Acids and Proteins Chapter 23 Proteins • Proteins are the most complex and varied class of biochemical molecules. • A proteinis an organic biological polymer that is made up of polypeptide chains of 50 or more amino acids and is an important building block of all cells. • Proteins are made up of specific sequences of amino acids. • They have molecular masses that range from 6000 to more than 9 million atomic mass units. • About 9000 different protein molecules are found in cells in the human body.

  21. Section 2 Amino Acids and Proteins Chapter 23 Proteins, continued • Nitrogen accounts for about 15% of the mass of a protein molecule. Most proteins also contain sulfur. Some contain phosphorus or other elements, such as iron, zinc, and copper. • Proteins have many important catalytic, structural, regulatory, and antibody defense functions. • Keratinis the main component of hair and fingernails. • Enzymes catalyze biochemical reactions. • Hemoglobin carries oxygen in the blood. • Insulinregulates glucose levels. • Antibodies protect the body from foreign substances.

  22. Section 2 Amino Acids and Proteins Chapter 23 Proteins, continued Arrangement of Amino Acids in Peptides and Proteins • Each peptide, polypeptide, or protein is made up of a special sequence of amino acids. • A simple set of three-letter abbreviations is used to represent each amino acid in these kinds of molecules. • The tripeptide made up of valine, asparagine, and histidine would be written as Val–Asp–His. • Polypeptide and protein function depend not only on the kinds and number of amino acids but also on their order.

  23. Section 2 Amino Acids and Proteins Chapter 23 Proteins, continued Amino Acid Side-Chain Reactions • The properties of amino acids—and ultimately polypeptides and proteins—depend on the properties of the side chains present. • The side chain of glutamic acid is acidic. • The side chain of histidine is basic. • The side chains of asparagine and several other amino acids are polar. • Some amino acid side chains can form ionic or covalent bonds with other side chains.

  24. Section 2 Amino Acids and Proteins Chapter 23 Proteins, continued Amino Acid Side-Chain Reactions, continued • Cysteine is a unique amino acid, because the —SH group in cysteine can form a covalent bond with another cysteine side chain to form a disulfide bridge.

  25. Section 2 Amino Acids and Proteins Chapter 23 Proteins, continued Amino Acid Substitution • A single substitution of one amino acid for another can change the shape and function of a protein. • The genetic disease sickle cell anemia can happen when glutamic acid—is replaced by valine.

  26. Section 2 Amino Acids and Proteins Chapter 23 Proteins as Enzymes • An enzyme is a protein that catalyzes a biochemical reaction. • Enzymes make up the largest and most highly specialized class of proteins. • Most enzymes are water-soluble, globular proteins. • The amino acid side chains and the three-dimensional shape of enzymes play a very important role in the enzymatic activity.

  27. Section 2 Amino Acids and Proteins Chapter 23 Proteins as Enzymes, continued • An enzyme also does not change the amount of product that is formed in a reaction; it only decreases the time it takes to form the product. • Enzymes catalyze both decomposition and synthesis reactions. • Enzymes are very efficient. • A single molecule of carbonic anhydrase can break down 36 million carbonic acid molecules in 1 minute.

  28. Section 2 Amino Acids and Proteins Chapter 23 Proteins as Enzymes, continued Enzyme Specificity • Enzymes are very specific and often catalyze just a single reaction. • Enzymes act by binding to a specific substrate molecule. • The shape of the enzyme is such that the substrate can fit into the enzyme at a specific part of the enzyme molecule, called the active site.

  29. Section 2 Amino Acids and Proteins Chapter 23 Proteins as Enzymes, continued Enzyme Specificity • The resulting compound is called the enzyme-substrate complex. • This model of enzyme action is called the lock and key model.

  30. Section 2 Amino Acids and Proteins Chapter 23 Proteins as Enzymes, continued Enzymes and Reaction Rates • The presence of an enzyme in a chemical reaction can increase the rate of a reaction by a factor of up to 1020. • Only collisions that have enough energy to overcome the activation energy and have the proper orientation change reactants into products. • Enzymes lower the activation energy by forming the enzyme-substrate complex, which makes breaking bonds in the reactants and forming new bonds in the products easier.

  31. Section 2 Amino Acids and Proteins Chapter 23 Proteins as Enzymes, continued Temperature and Enzyme Activity • Enzymes typically have maximum activity within a relatively narrow range of temperatures. • Enzymes in the human body work optimally at the normal body temperature of 37°C (98.6°F).

  32. Section 2 Amino Acids and Proteins Chapter 23 Proteins as Enzymes, continued Temperature and Enzyme Activity • High heat can denature, or alter, the shape of a protein, which in turn alters the protein’s function. • Denaturationis a change in a protein’s characteristic three-dimensional shape due to changes of its secondary, tertiary, and quaternary structure. • example: cooking an egg

  33. Section 2 Amino Acids and Proteins Chapter 23 Proteins as Enzymes, continued pH and Enzyme Activity • The optimal pH for normal cell enzyme functions is almost neutral, about 7.3 to 7.4. • Changes in pH can cause changes in protein structure and shape. • Most enzymes become inactivated, or no longer work, because of denaturation when the pH changes.

  34. Section 2 Amino Acids and Proteins Chapter 23 Proteins as Enzymes, continued pH and Enzyme Activity, continued • Pre-enzymes,inactive forms of protein-digesting enzymes, become activated by the stomach’s low pH of 1.5 to 2.0. This prevents the active form of the enzymes from digesting the stomach lining. • Pepsin is a stomach enzyme found in adults.

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