Enzyme Function and Carbohydrate Chemistry

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114 Terms

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Enzyme

Biological catalyst increasing reaction rates without change.

<p>Biological catalyst increasing reaction rates without change.</p>
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Activation Energy

Energy required to initiate a chemical reaction.

<p>Energy required to initiate a chemical reaction.</p>
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Carbonic Anhydrase

an enzyme that converts CO2 and H2O into carbonic acid and then turns into bicarbonate +hydrogen ions

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Substrate

Molecule that binds to an enzyme's active site.

<p>Molecule that binds to an enzyme's active site.</p>
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Active Site

Region on enzyme where substrates bind for reaction.

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Enzyme-Substrate Complex

Combination of enzyme and substrate during catalysis.

<p>Combination of enzyme and substrate during catalysis.</p>
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Enzyme-Product Complex

Intermediate formed after substrate conversion in enzyme.

<p>Intermediate formed after substrate conversion in enzyme.</p>
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Lactase

Enzyme that catalyzes lactose hydrolysis into monosaccharides.

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Quaternary Structure

Protein structure with multiple subunits, like lactase.

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Absolute Specificity

Enzymes catalyzing only one specific substrate reaction.

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Lock-and-Key Model

Rigid substrate fits rigid enzyme like a key.

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Induced-Fit Model

Flexible enzyme adapts to substrate shape for catalysis.

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Phosphorylation

Covalent modification activating or deactivating an enzyme.

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Kinase

Enzyme that activates others by adding phosphate groups.

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Phosphatase

Enzyme that removes phosphate groups to activate enzymes.

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Allosteric Enzymes

Enzymes regulated by binding at sites other than active site.

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Positive Regulator

Molecule enhancing substrate binding to the active site.

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Negative Regulator

Molecule preventing substrate binding, decreasing reaction rate.

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Feedback Control

Regulatory mechanism using end product to control enzyme activity.

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Regulatory Enzymes

Enzymes controlling reaction rates based on substrate levels.

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Hydrogen Bonds

Weak interactions stabilizing enzyme-substrate complexes.

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Salt Bridges

Ionic interactions contributing to enzyme structure stability.

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Hydrophobic Interactions

Nonpolar interactions aiding enzyme-substrate binding.

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Feedback control

End product binds to allosteric enzyme, regulating synthesis.

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Allosteric enzyme

First enzyme in a reaction sequence, regulated by end product.

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Noncompetitive inhibitor

Does not resemble substrate; binds elsewhere on enzyme.

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Inhibitors

Molecules causing loss of catalytic activity in enzymes.

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Reversible inhibition

Loss of enzyme activity that can be restored.

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Competitive inhibitor

Competes with substrate for the active site.

<p>Competes with substrate for the active site.</p>
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Antimetabolites

Competitive inhibitors used to treat bacterial infections.

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Sulfanilamide

Competes with PABA, inhibiting(preventing) bacterial growth.

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Irreversible inhibition

Enzyme activity destroyed by covalent bond with inhibitor.

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Covalent modification

Enzyme activity modified by forming or breaking covalent bonds.

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Zymogens

Inactive enzyme precursors activated by covalent modification.

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Proteases

Digestive enzymes that hydrolyze proteins from inactive forms.

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Trypsinogen

Zymogen activated to trypsin for protein digestion.

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Proinsulin

Inactive form of insulin, activated by peptide removal.

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Cofactor

Non-protein molecule required for enzyme activity.

<p>Non-protein molecule required for enzyme activity.</p>
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Coenzyme

Small organic molecule, often a vitamin, aiding enzymes.

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Carboxypeptidase

Enzyme requiring Zn2+ cofactor for peptide bond hydrolysis.

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Vitamins

Organic molecules essential for health, required in trace amounts.

<p>Organic molecules essential for health, required in trace amounts.</p>
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Optimum pH

pH level where enzymes function best, around 7.4.

<p>pH level where enzymes function best, around 7.4.</p>
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Carbohydrates

Major energy source, made of carbon, hydrogen, oxygen.

<p>Major energy source, made of carbon, hydrogen, oxygen.</p>
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Photosynthesis

Process plants use to produce glucose from CO2 and H2O.

<p>Process plants use to produce glucose from CO2 and H2O.</p>
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Saccharides

Another term for sugars, referring to carbohydrate structure.

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C-terminal aromatic amino acid

Target of carboxypeptidase during peptide bond hydrolysis.

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Monosaccharides

Simple carbohydrates, single sugar units.

<p>Simple carbohydrates, single sugar units.</p>
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Disaccharides

Two monosaccharides linked together.

<p>Two monosaccharides linked together.</p>
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Polysaccharides

Many monosaccharides linked together.

<p>Many monosaccharides linked together.</p>
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Aldoses

Monosaccharides with an aldehyde group.

<p>Monosaccharides with an aldehyde group.</p>
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Ketoses

Monosaccharides with a ketone group.

<p>Monosaccharides with a ketone group.</p>
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Triose

Monosaccharide with three carbon atoms.

<p>Monosaccharide with three carbon atoms.</p>
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Tetrose

Monosaccharide with four carbon atoms.

<p>Monosaccharide with four carbon atoms.</p>
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Pentose

Monosaccharide with five carbon atoms.

<p>Monosaccharide with five carbon atoms.</p>
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Hexose

Monosaccharide with six carbon atoms.

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Aldopentose

Five-carbon saccharide with an aldehyde group.

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Ketohexose

Six-carbon saccharide with a ketone group.

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d-Glucose

Most common hexose, known as blood sugar.

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d-Galactose

Aldohexose obtained from lactose in milk.

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Galactosemia

Condition due to missing enzyme for galactose conversion.

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d-Fructose

Ketohexose, sweetest carbohydrate, found in fruits.

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High-fructose corn syrup

Sweetener made from sucrose hydrolysis.

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Haworth structures

Cyclic forms of sugars from carbonyl and hydroxyl reaction.

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Fischer projection

2D representation of carbohydrates showing stereochemistry.

<p>2D representation of carbohydrates showing stereochemistry.</p>
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α-anomer

Cyclic form with -OH group below the ring.

<p>Cyclic form with -OH group below the ring.</p>
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β-anomer

Cyclic form with -OH group above the ring.

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Sugar alcohols

Reduced carbohydrates used as sweeteners in products.

<p>Reduced carbohydrates used as sweeteners in products.</p>
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Glucose tolerance test

Measures blood glucose after glucose ingestion.

<p>Measures blood glucose after glucose ingestion.</p>
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Aldehyde group

Functional group with a carbonyl and hydrogen.

<p>Functional group with a carbonyl and hydrogen.</p>
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Hydroxyl group

Functional group containing an -OH group.

<p>Functional group containing an -OH group.</p>
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Sugar acids

Carbohydrates(H) oxidized to carboxylic(0H) acids.

<p>Carbohydrates(H) oxidized to carboxylic(0H) acids.</p>
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Benedict's solution

Oxidizing agent for reducing sugars.

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Reducing sugar

Carbohydrate that reduces another substance.

<p>Carbohydrate that reduces another substance.</p>
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Fructose

Ketohexose with a ketone group.

<p>Ketohexose with a ketone group.</p>
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Ketohexose

Hexose with a ketone functional group.

<p>Hexose with a ketone functional group.</p>
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Glucose

Aldose that can be oxidized easily.

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Sugar alcohols

Reduced monosaccharides, also called alditols.

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D-sorbitol

Sugar alcohol derived from D-glucose.

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D-xylitol

Sugar alcohol derived from D-xylose.

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D-mannitol

Sugar alcohol derived from D-mannose.

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Disaccharide

Carbohydrate formed from two monosaccharides.

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Glycosidic bond

Covalent bond linking monosaccharides.

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Lactose

Disaccharide of galactose and glucose.

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Maltose

Disaccharide known as malt sugar.

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α-(1→4)-glycosidic bond

Bond between carbon 1 and 4 of glucose.

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β-(1→4)-glycosidic bond

Bond in lactose between galactose and glucose.

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Sucrose

Disaccharide of glucose and fructose.

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α,β-(1→2)-glycosidic bond

Bond between glucose and fructose in sucrose.

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Sucralose

Chlorinated derivative of sucrose, artificial sweetener.

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Aspartame

Noncarbohydrate sweetener made from amino acids.

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Sweetness scale

Sucrose assigned a sweetness value of 100.

<p>Sucrose assigned a sweetness value of 100.</p>
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Neotame

Artificial sweetener 10,000 times sweeter than sucrose.

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Saccharin

Noncarbohydrate sweetener, banned in Canada.

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Lactose

Disaccharide of α-D-Glucose and β-D-Galactose.

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Maltose

Disaccharide of two α-D-Glucose units.

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Sucrose

Disaccharide of α-D-Glucose and β-D-Fructose.

<p>Disaccharide of α-D-Glucose and β-D-Fructose.</p>
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Melibiose

Disaccharide of α-D-Galactose and α-D-Glucose.

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Glycosidic bond

Covalent bond linking monosaccharides in carbohydrates.

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α-(1→6)-glycosidic bond

Bond linking α-D-Glucose and α-D-Galactose in melibiose.

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Cellulose

Polysaccharide of glucose with β-(1→4)-glycosidic bonds. >>> humans lack cellulose