What are the products of maltose digestion?
Glucose.
What is the substrate that pepsin acts on?
Proteins.
1/537
p.5
Digestive Enzymes and Their Functions

What are the products of maltose digestion?

Glucose.

p.22
Digestive Enzymes and Their Functions

What is the substrate that pepsin acts on?

Proteins.

p.4
Digestive Enzymes and Their Functions

What is the source of Lingual lipase?

Lingual glands.

p.6
Lipid Digestion and Absorption

What is the product of triglyceride digestion by pancreatic lipase?

Fatty acids and monoacylglycerides.

p.11
Absorption Mechanisms in the Small Intestine

What is the fifth mechanism of absorption?

Endocytosis.

p.35
Digestive Disorders and Malabsorption Issues

What enzyme is deficient in lactose intolerance?

Lactase.

p.32
Nucleic Acid Digestion

How are the products of nucleic acid digestion absorbed?

Through the alimentary canal wall.

p.13
Absorption Mechanisms in the Small Intestine

How do water-soluble nutrients enter cells?

They use transport molecules embedded in the cell's plasma membrane.

p.11
Absorption Mechanisms in the Small Intestine

What is the first mechanism of absorption?

Active transport.

p.6
Digestive Enzymes and Their Functions

What do nucleases target in the digestive process?

Ribonucleic acids and deoxyribonucleic acids.

p.28
Lipid Digestion and Absorption

What role do bile salts play in lipid absorption?

They speed up lipid digestion and are essential for absorbing the end products of lipid digestion.

p.11
Absorption Mechanisms in the Small Intestine

What is the third mechanism of absorption?

Facilitated diffusion.

p.21
Protein Digestion and Absorption

What hormone is secreted into the blood when acidic stomach contents enter the small intestine?

Secretin.

p.25
Protein Digestion and Absorption

How are proteins absorbed in the small intestine?

Using an active transport mechanism, primarily in the duodenum and jejunum.

p.25
Protein Digestion and Absorption

What percentage of protein is digested and absorbed in the small intestine?

95 to 98 percent.

p.13
Absorption Mechanisms in the Small Intestine

What are lacteals?

Lymphatic capillaries in the small intestine that absorb dietary fats.

p.28
Lipid Digestion and Absorption

How do short-chain fatty acids enter the absorptive cells?

They are relatively water-soluble and can enter directly via simple diffusion.

p.1
Types of Digestion: Mechanical and Chemical

What is mechanical digestion?

A physical process where food is broken into smaller pieces without chemical change.

p.6
Digestive Enzymes and Their Functions

What is the function of trypsin in digestion?

To break down proteins into peptides.

p.18
Carbohydrate Digestion and Absorption

How is fructose absorbed and transported?

By facilitated diffusion alone.

p.1
Types of Digestion: Mechanical and Chemical

Where does mechanical digestion continue after chewing?

In the stomach.

p.19
Absorption Mechanisms in the Small Intestine

What is the function of glucose transporters (GLUTs)?

They enable glucose entrance and exit into cells.

p.34
Digestive Disorders and Malabsorption Issues

What is malabsorption?

A term used to characterize abnormalities of both digestion and absorption across the gastrointestinal tract.

p.33
Nucleic Acid Digestion and Absorption

What happens to the end products of nucleic acid digestion after they are absorbed?

They enter the bloodstream.

p.16
Carbohydrate Digestion and Absorption

What enzyme breaks down sucrose into glucose and fructose?

Sucrase.

p.35
Digestive Disorders and Malabsorption Issues

What is lactose intolerance?

A digestive disorder caused by the inability to digest lactose due to a deficiency of lactase.

p.2
Types of Digestion: Mechanical and Chemical

Which substances in food must be chemically digested?

Carbohydrates, proteins, lipids, and nucleic acids.

p.35
Digestive Disorders and Malabsorption Issues

What accumulates in the gut due to lactose intolerance?

Lactose.

p.39
Digestive Disorders and Malabsorption Issues

What is Hartnup disease also known as?

Pellagra.

p.38
Digestive Disorders and Malabsorption Issues

What are the treatment options for Irritable Bowel Syndrome?

Managing diet, lifestyle, and stress; in some cases, medication may be required.

p.5
Digestive Enzymes and Their Functions

What products result from the digestion of nucleotides?

Phosphates, nitrogenous bases, and pentoses.

p.38
Digestive Disorders and Malabsorption Issues

What is Crohn's disease?

A type of inflammatory bowel disease (IBD) that affects the large intestine.

p.39
Digestive Disorders and Malabsorption Issues

What amino acid absorption is primarily affected in Hartnup disease?

Nonpolar amino acids, specifically tryptophan.

p.10
Absorption Mechanisms in the Small Intestine

What is the primary goal of mechanical and chemical digestion?

To convert food into molecules small enough to be absorbed by epithelial cells of the intestinal villi.

p.3
Digestive Enzymes and Their Functions

Where are digestive enzymes secreted from?

Exocrine glands or the mucosal layer of epithelium lining the gastrointestinal tract.

p.1
Overview of Digestion

What is digestion a form of?

Catabolism.

p.21
Protein Digestion and Absorption

What is trypsinogen converted to?

Trypsin, its active form.

p.11
Absorption Mechanisms in the Small Intestine

What is the second mechanism of absorption?

Passive diffusion.

p.19
Absorption Mechanisms in the Small Intestine

Where is GLUT 2 predominantly found?

In the liver and pancreatic beta cells.

p.25
Protein Digestion and Absorption

What are dipeptides and tripeptides?

Short chains of two amino acids (dipeptides) or three amino acids (tripeptides) that are also transported actively.

p.19
Absorption Mechanisms in the Small Intestine

What signals an increase in GLUT 4 transporters in muscle and fat cells?

The presence of insulin.

p.1
Types of Digestion: Mechanical and Chemical

When does mechanical digestion begin?

With the first bite of food and continues as you chew.

p.23
Protein Digestion and Absorption

What is the function of rennin in milk digestion?

It coagulates milk to slow down its passage from the stomach.

p.2
Carbohydrate Digestion and Absorption

Into what must carbohydrates be broken down?

Simple sugars.

p.2
Nucleic Acid Digestion and Absorption

What do nucleic acids break down into?

Nitrogen bases and sugars.

p.10
Absorption Mechanisms in the Small Intestine

What is absorption in the context of digestion?

The process by which the end products of digestion pass through the intestinal mucosa into the blood or lymph.

p.32
Nucleic Acid Digestion

Where are dietary nucleic acids digested?

In the small intestine.

p.33
Nucleic Acid Digestion and Absorption

How are the end products of nucleic acid digestion transported across the villus epithelium?

By carriers via active transport.

p.19
Absorption Mechanisms in the Small Intestine

Which GLUT is responsible for basal glucose uptake in all mammalian cells?

GLUT 1 and GLUT 3.

p.34
Digestive Disorders and Malabsorption Issues

What are some causes of abnormalities in digestion and absorption?

Enzyme deficiencies (like lactose intolerance), digestive failure (like bile acid/bile salt malabsorption), and infective agents.

p.34
Digestive Disorders and Malabsorption Issues

What are common symptoms of digestion and absorption abnormalities?

Bleeding, bloating, constipation, diarrhea, heartburn, incontinence, nausea, vomiting, stomach cramps, swallowing problems, weight loss or gain.

p.4
Digestive Enzymes and Their Functions

What is the substrate for α-Dextrinase?

α-Dextrins.

p.32
Nucleic Acid Digestion

Which intestinal brush border enzymes further break down nucleotides?

Nucleosidase and phosphatase.

p.37
Digestive Disorders and Malabsorption Issues

What is galactosemia?

An inherited condition in which galactose cannot be converted to glucose.

p.35
Digestive Disorders and Malabsorption Issues

What are some common symptoms of lactose intolerance?

Abdominal cramps, diarrhea, flatulence, bloating, nausea, vomiting, and occasionally constipation.

p.36
Digestive Disorders and Malabsorption Issues

What are some symptoms of GGM in newborns?

Diarrhea, dehydration, difficulties in weight gain, and glucosuria.

p.30
Lipid Digestion and Absorption

What do lacteals form together?

Lymphatic vessels.

p.21
Protein Digestion and Absorption

What triggers the release of the hormone cholecystokinin in the duodenum?

The arrival of amino acids.

p.21
Protein Digestion and Absorption

What does cholecystokinin stimulate the secretion of?

Several pancreatic enzymes.

p.1
Absorption Mechanisms in the Small Intestine

What are the final products of digestion absorbed primarily?

From the digestive tract, primarily in the small intestine.

p.18
Carbohydrate Digestion and Absorption

What happens to monosaccharides after disaccharides are broken down?

They combine with transport proteins immediately.

p.2
Types of Digestion: Mechanical and Chemical

What is chemical digestion?

The biochemical process in which macromolecules in food are changed into smaller molecules that can be absorbed into body fluids.

p.4
Digestive Enzymes and Their Functions

Which enzyme is produced by Chief cells that acts on proteins?

Pepsin.

p.14
Absorption Mechanisms in the Small Intestine

What is the absorption mechanism for glucose?

Co-transport with sodium ions.

p.25
Protein Digestion and Absorption

How do amino acids enter the capillary blood after absorption?

Via diffusion after being broken down from dipeptides and tripeptides.

p.30
Lipid Digestion and Absorption

Where do chylomicrons enter after being released from the cell?

The large pores of lacteals.

p.5
Digestive Enzymes and Their Functions

What does dipeptidase break down?

Dipeptides into amino acids.

p.26
Lipid Digestion

What advantage do micelles provide during lipid digestion?

They increase surface area for lipase action and orient hydrophilic heads of fatty acids outward.

p.5
Digestive Enzymes and Their Functions

What enzyme breaks down sucrose in the small intestine?

Sucrase.

p.7
Digestive Enzymes and Their Functions

Where is pancreatic amylase sourced from?

The pancreas.

p.30
Lipid Digestion and Absorption

What happens to the breakdown products of triglycerides after passing through capillary walls?

They are used for energy by cells or stored in adipose tissue as fat.

p.14
Lipid Digestion and Absorption

What is the absorption mechanism for short-chain fatty acids?

Simple diffusion.

p.9
Digestive Enzymes and Their Functions

What are the main functions of pancreatic enzymes?

To digest proteins, peptides, nucleic acids, and fats in the small intestine.

p.8
Digestive Enzymes and Their Functions

Which enzyme is responsible for lactose digestion?

Lactase.

p.47
Metabolism: Catabolism and Anabolism

What happens during the reactions of the TCA cycle?

Release of ATP, NADH, and FADH2.

p.8
Lipid Digestion and Absorption

What are the products of emulsified triglycerides digestion by pancreatic lipase?

Fatty acids and monoacylglycerides.

p.48
Metabolism: Catabolism and Anabolism

What is the role of ATP in metabolism?

ATP serves as the energy currency of the cell.

p.88
Metabolism: Catabolism and Anabolism

What are the reactants involved in Reaction 7 of glycolysis?

2 ATP and phosphoglycerate.

p.76
Metabolism: Catabolism and Anabolism

What is the effect of elevated ATP levels on PFK-1?

ATP inhibits PFK-1 allosterically, indicating an abundance of high-energy compounds.

p.61
Metabolism: Catabolism and Anabolism

What is metabolism composed of?

The catabolism and anabolism of an organism.

p.76
Metabolism: Catabolism and Anabolism

What triggers the activation of PFK-1?

High concentrations of AMP activate PFK-1, signaling depleted energy stores.

p.40
Overview of Digestion

What is a common way to express goodwill or positive sentiments?

By saying 'Best wishes.'

p.6
Digestive Enzymes and Their Functions

What is the role of pancreatic elastase?

To break down proteins into peptides.

p.1
Overview of Digestion

Where does digestion begin and end?

It begins in the mouth and ends in the small intestine.

p.23
Protein Digestion and Absorption

In what form is rennin present in the human body?

In its inactive form called prorennin.

p.1
Types of Digestion: Mechanical and Chemical

What are the two types of digestion in the digestive system?

Mechanical and chemical digestion.

p.16
Carbohydrate Digestion and Absorption

What is sucrose commonly known as?

Table sugar.

p.20
Protein Digestion and Absorption

What hormone is secreted by the gastric mucosa in response to dietary protein?

Gastrin.

p.38
Digestive Disorders and Malabsorption Issues

What is Irritable Bowel Syndrome (IBS)?

A condition involving irritation of the small intestine, leading to diarrhea or constipation.

p.16
Carbohydrate Digestion and Absorption

Where are glucose and fructose absorbed in the digestive system?

In the small intestine.

p.30
Lipid Digestion and Absorption

Why can't chylomicrons pass through the basement membranes of blood capillaries?

Because of their large size.

p.29
Lipid Digestion and Absorption

What happens to free fatty acids and monoacylglycerides once inside epithelial cells?

They are reincorporated into triglycerides to form chylomicrons.

p.14
Absorption Mechanisms in the Small Intestine

How do fructose molecules get absorbed?

Facilitated diffusion.

p.5
Digestive Enzymes and Their Functions

What type of enzymes are peptidases?

Brush border enzymes in the small intestine.

p.20
Protein Digestion and Absorption

What type of environment do trypsin and chymotrypsin require to work?

An alkaline environment.

p.38
Digestive Disorders and Malabsorption Issues

Can Crohn's disease be cured?

No, it cannot be cured.

p.20
Protein Digestion and Absorption

What neutralizes the acidic chyme as it enters the small intestine?

Bile from the liver and bicarbonate from the pancreas.

p.20
Protein Digestion and Absorption

What happens to proteins in the stomach during digestion?

They are broken down into smaller polypeptides by HCl and pepsin.

p.7
Digestive Enzymes and Their Functions

What substrate do brush border enzymes act on?

Disaccharides.

p.42
Metabolism: Catabolism and Anabolism

What is metabolism?

Metabolism refers to the set of life-sustaining chemical reactions in organisms that convert food into energy.

p.17
Digestive Enzymes and Their Functions

What enzyme is produced by the pancreas?

Pancreatic amylase.

p.44
Metabolism: Catabolism and Anabolism

What is the primary function of metabolism related to energy?

To obtain chemical energy from fuel molecules like carbohydrates, lipids, and proteins.

p.43
Metabolism: Catabolism and Anabolism

What is another name for metabolism that includes digestion and absorption?

Intermediary metabolism.

p.49
Metabolism: Catabolism and Anabolism

What do anabolic processes require?

Energy.

p.82
Overview of Digestion

What is the substrate for Reaction 4 in glycolysis?

Fructose 1,6-bisphosphate.

p.54
Metabolism: Catabolism and Anabolism

What connects the biochemical reactions in a metabolic pathway?

Intermediates.

p.13
Absorption Mechanisms in the Small Intestine

How do lipid-soluble nutrients enter cells?

They can diffuse directly through the plasma membrane.

p.13
Absorption Mechanisms in the Small Intestine

What happens to lipid-soluble nutrients once inside the cell?

They are packaged for transport and enter the lacteals of the villi.

p.29
Lipid Digestion and Absorption

What is a micelle?

A tiny sphere with polar ends facing the watery environment and hydrophobic tails turned inward, enabling absorption of long-chain fatty acids.

p.25
Protein Digestion and Absorption

What is the role of sodium in the absorption of amino acids?

Most carriers for amino acids are linked to the active transport of sodium.

p.11
Absorption Mechanisms in the Small Intestine

What is the fourth mechanism of absorption?

Co-transport (or secondary active transport).

p.5
Digestive Enzymes and Their Functions

What are the products of lactose digestion?

Glucose and galactose.

p.5
Digestive Enzymes and Their Functions

What enzyme breaks down maltose in the small intestine?

Maltase.

p.29
Lipid Digestion and Absorption

What is a chylomicron?

A water-soluble lipoprotein made of triglycerides, phospholipids, cholesterol, and surrounded by a protein coat.

p.19
Absorption Mechanisms in the Small Intestine

Where is GLUT 5 predominantly located and what does it transport?

In the small intestine, acting as a fructose transporter.

p.4
Digestive Enzymes and Their Functions

What are the products of Lingual lipase?

Free fatty acids, mono- and diglycerides.

p.39
Digestive Disorders and Malabsorption Issues

What type of disorder is Hartnup disease?

An autosomal recessive metabolic disorder.

p.15
Carbohydrate Digestion

What role does saliva play in carbohydrate digestion?

It lubricates food and provides alkaline conditions for amylase.

p.7
Digestive Enzymes and Their Functions

What end products are formed from the action of salivary amylase?

Disaccharides (maltose) and oligosaccharides.

p.35
Digestive Disorders and Malabsorption Issues

What is the treatment for lactose intolerance?

Removal of dairy products from the diet.

p.9
Digestive Enzymes and Their Functions

What enzyme activates trypsinogen to trypsin?

Enteropeptidase.

p.7
Digestive Enzymes and Their Functions

What substrate does sucrase act on?

Sucrose.

p.7
Digestive Enzymes and Their Functions

What are the end products of sucrase?

Glucose and fructose.

p.8
Digestive Enzymes and Their Functions

What enzyme digests emulsified triglycerides in the small intestine?

Pancreatic lipase.

p.77
Digestive Enzymes and Their Functions

How does fructose 2,6-bisphosphate affect gluconeogenesis?

It inhibits fructose 1,6-bisphosphatase, an enzyme of gluconeogenesis.

p.52
Metabolism: Catabolism and Anabolism

Which organ is a major site of metabolism?

Liver.

p.65
Metabolism: Catabolism and Anabolism

What does the aerobic pathway of glycolysis lead to?

Oxidative decarboxylation of pyruvate to acetyl CoA.

p.82
Digestive Enzymes and Their Functions

What enzyme catalyzes the cleavage of Fructose 1,6-bisphosphate?

Aldolase.

p.65
Metabolism: Catabolism and Anabolism

What is the result of alcoholic fermentation pathway?

Pyruvate is converted to ethanol and carbon dioxide.

p.94
Metabolism: Catabolism and Anabolism

What is the role of pyruvate kinase (PK) in glycolysis?

It catalyzes the conversion of PEP to pyruvate, which is the third irreversible reaction of glycolysis.

p.81
Digestive Enzymes and Their Functions

What are the two products of the cleavage of fructose 1,6-bisphosphate?

Dihydroxyacetone phosphate (DHAP) and glyceraldehyde 3-phosphate.

p.12
Absorption Mechanisms in the Small Intestine

What is active transport?

Movement of a substance across a cell membrane from lower concentration to higher concentration.

p.13
Absorption Mechanisms in the Small Intestine

Where do water-soluble nutrients go after entering the capillary blood in the villi?

They travel to the liver via the hepatic portal vein.

p.33
Nucleic Acid Digestion and Absorption

What are the end products of nucleic acid digestion?

Pentose sugars, nitrogenous bases, and phosphate ions.

p.32
Nucleic Acid Digestion

What types of enzymes are involved in the digestion of dietary nucleic acids?

Pancreatic enzymes and enzymes produced by the small intestine.

p.21
Protein Digestion and Absorption

What do trypsin and chymotrypsin do to proteins?

They break down proteins into peptides.

p.6
Carbohydrate Digestion and Absorption

What types of carbohydrates does pancreatic amylase act on?

Polysaccharides (starches), producing α-Dextrins, disaccharides, and trisaccharides.

p.29
Lipid Digestion and Absorption

What additional substances do micelles contain?

Cholesterol and fat-soluble vitamins.

p.5
Digestive Enzymes and Their Functions

What enzyme breaks down lactose in the small intestine?

Lactase.

p.29
Lipid Digestion and Absorption

How do micelles facilitate lipid absorption?

They squeeze between microvilli and allow lipid substances to exit via simple diffusion.

p.29
Lipid Digestion and Absorption

What are the components that enter epithelial cells from micelles?

Free fatty acids and monoacylglycerides.

p.14
Absorption Mechanisms in the Small Intestine

Where do carbohydrates like glucose and galactose enter after absorption?

Capillary blood in villi.

p.2
Protein Digestion and Absorption

Into what must proteins be broken down?

Amino acids.

p.15
Carbohydrate Digestion

Where does the chemical digestion of polysaccharides begin?

In the mouth, aided by amylase in saliva.

p.26
Lipid Digestion

What role does bile play in lipid digestion?

Bile emulsifies large globules of food lipids into smaller ones called micelles.

p.9
Digestive Enzymes and Their Functions

What is the primary function of pepsin?

To break down proteins into peptides.

p.15
Carbohydrate Digestion

What happens to salivary α-amylase in the stomach?

It is inactivated by the low pH.

p.30
Lipid Digestion and Absorption

What are the breakdown products of triglycerides once processed?

Free fatty acids and glycerol.

p.17
Digestive Enzymes and Their Functions

Where does salivary amylase act in the digestive system?

In the mouth.

p.42
Metabolism: Catabolism and Anabolism

What is anabolism?

The process of building up larger molecules from smaller ones, typically requiring energy.

p.50
Metabolism: Catabolism and Anabolism

Where do most metabolic reactions occur within a cell?

In the cytoplasm.

p.43
Metabolism: Catabolism and Anabolism

What aspects are involved in metabolism?

Production, storage, and utilization of metabolic energy.

p.51
Overview of Digestion

What are some examples of compartments involved in inter-compartmental crossing?

Cellular compartments such as the cytoplasm, nucleus, and organelles like mitochondria.

p.8
Lipid Digestion and Absorption

What are the products of triglycerides digestion by lingual lipase?

Free fatty acids, and mono- and diglycerides.

p.48
Metabolism: Catabolism and Anabolism

What is anabolism?

The synthesis of all compounds needed by the cells.

p.60
Metabolism: Catabolism and Anabolism

What is metabolism?

The set of life-sustaining chemical reactions in organisms.

p.65
Metabolism: Catabolism and Anabolism

What happens to pyruvate in the anaerobic pathway?

It is reduced to lactate.

p.78
Metabolism: Catabolism and Anabolism

What does PFK-1 stand for?

Phosphofructokinase-1.

p.81
Digestive Enzymes and Their Functions

What does aldolase cleave in Reaction 4?

Fructose 1,6-bisphosphate.

p.54
Metabolism: Catabolism and Anabolism

What is the relationship between the product of one reaction and the substrate of the next in a metabolic pathway?

The product of one reaction serves as the substrate for the subsequent reaction.

p.59
Metabolic Disorders and Malabsorption Issues

What is an example of a metabolic disease related to enzyme deficiency?

Albinism.

p.78
Metabolism: Catabolism and Anabolism

How does ATP affect PFK-1 activity?

High levels of ATP inhibit PFK-1 activity, indicating sufficient energy levels in the cell.

p.66
Overview of Digestion

Where do the reactions of glycolysis occur in the cell?

In the cytosolic compartment.

p.3
Digestive Enzymes and Their Functions

What are enzymes?

Proteins that catalyze, or speed up, biochemical reactions.

p.12
Absorption Mechanisms in the Small Intestine

What is co-transport?

Movement of one molecule from higher to lower concentration powering the movement of another from lower to higher concentration.

p.23
Protein Digestion and Absorption

What enzyme is responsible for milk digestion in infants?

Rennin.

p.18
Carbohydrate Digestion and Absorption

In what form are all carbohydrates absorbed?

As monosaccharides (Glucose, galactose, and fructose).

p.2
Types of Digestion: Mechanical and Chemical

What is the purpose of mechanical digestion?

To increase the surface area of food particles for more effective action by digestive enzymes.

p.20
Protein Digestion and Absorption

What must proteins be broken down into before absorption?

Their constituent amino acids.

p.26
Lipid Digestion

What are the most common dietary lipids?

Triglycerides, made up of a glycerol molecule and three fatty acid chains.

p.30
Lipid Digestion and Absorption

What are chylomicrons and where are they processed?

Chylomicrons are lipoproteins processed by the Golgi apparatus.

p.26
Lipid Digestion

Where does the chemical digestion of lipids begin?

In the mouth.

p.15
Carbohydrate Digestion

What process reduces the length of polysaccharides during digestion?

The breaking of bonds between glucose monomers.

p.36
Digestive Disorders and Malabsorption Issues

What symptoms can adults experience with GGM?

Bloating, nausea, diarrhea, abdominal cramps, and frequent urination.

p.20
Digestive Enzymes and Their Functions

What is required for pepsin to function?

HCl.

p.14
Absorption Mechanisms in the Small Intestine

What is the absorption mechanism for amino acids?

Co-transport with sodium ions.

p.37
Digestive Disorders and Malabsorption Issues

What long-term problems can occur despite treatment for Classic galactosemia?

Intellectual deficits, movement disorders, and premature ovarian failure (in females).

p.2
Digestive Enzymes and Their Functions

How is chemical digestion accomplished?

By digestive enzymes.

p.15
Carbohydrate Digestion

What enzyme is required to digest lactose found in milk?

Lactase.

p.8
Digestive Enzymes and Their Functions

What enzyme breaks down sucrose in the small intestine?

Sucrase.

p.17
Digestive Enzymes and Their Functions

What substrates does salivary amylase act on?

Polysaccharides (starch).

p.17
Digestive Enzymes and Their Functions

Where does pancreatic amylase act?

In the small intestine.

p.8
Lipid Digestion and Absorption

What are the products of triglyceride digestion by gastric lipase?

Fatty acids and monoacylglycerides.

p.45
Metabolism: Catabolism and Anabolism

What is the primary function of anabolic reactions?

To consume energy to build complex molecules.

p.17
Digestive Enzymes and Their Functions

What substrates do oligosaccharidases act on?

Disaccharides.

p.49
Metabolism: Catabolism and Anabolism

What is the primary function of anabolism?

To build up large molecules from smaller ones.

p.49
Metabolism: Catabolism and Anabolism

Which reducing equivalents are required for anabolism?

NADH, NADPH, FADH2.

p.10
Absorption Mechanisms in the Small Intestine

Where in the small intestine are the end products of digestion primarily absorbed?

In the jejunum and ileum regions.

p.12
Absorption Mechanisms in the Small Intestine

What characterizes facilitated diffusion?

Movement of substances from higher to lower concentration using a carrier protein in the cell membrane.

p.3
Digestive Enzymes and Their Functions

What part of the digestive system secretes enzymes besides the mouth?

The stomach lining and the small intestine lining.

p.12
Absorption Mechanisms in the Small Intestine

What is endocytosis?

A transportation process where the cell membrane engulfs material, requiring energy, usually in the form of ATP.

p.4
Digestive Enzymes and Their Functions

What substrates does Salivary amylase act on?

Polysaccharides.

p.25
Protein Digestion and Absorption

What happens to dipeptides and tripeptides once inside absorptive epithelial cells?

They are broken down into their amino acids before leaving the cell.

p.20
Protein Digestion and Absorption

What does Gastrin stimulate the secretion of?

HCl by parietal cells and pepsinogen by chief cells.

p.22
Digestive Enzymes and Their Functions

What enzyme is produced by the stomach?

Pepsin.

p.26
Digestive Enzymes and Their Functions

What are the three lipases responsible for lipid digestion?

Lingual lipase, gastric lipase, and pancreatic lipase.

p.7
Digestive Enzymes and Their Functions

What substrate does salivary amylase act on?

Polysaccharides (Starch).

p.36
Digestive Disorders and Malabsorption Issues

What sugar can be used as a substitute for glucose and galactose in patients with GGM?

Fructose.

p.15
Carbohydrate Digestion

What enzyme breaks down starch into smaller fragments in the small intestine?

Pancreatic amylase.

p.14
Lipid Digestion and Absorption

What is the absorption mechanism for glycerol?

Simple diffusion.

p.22
Digestive Enzymes and Their Functions

What enzyme is produced by the lining of the intestine?

Dipeptidase.

p.39
Digestive Disorders and Malabsorption Issues

How is steatorrhea treated?

By correcting the underlying cause and using digestive enzyme supplements.

p.7
Digestive Enzymes and Their Functions

What is the end product of α-Dextrinase?

Glucose.

p.17
Digestive Enzymes and Their Functions

What are the end products of salivary amylase activity?

Disaccharides (maltose) and oligosaccharides.

p.43
Metabolism: Catabolism and Anabolism

What role do enzymes play in metabolism?

Enzymes catalyze the chemical reactions, being highly specific and regulated.

p.47
Metabolism: Catabolism and Anabolism

What occurs in the second stage of catabolism?

Degradation of monomers to Acetyl-CoA.

p.17
Digestive Enzymes and Their Functions

Where do oligosaccharidases act in the digestive system?

In the small intestine at the brush border membrane.

p.48
Metabolism: Catabolism and Anabolism

What are the two main phases of metabolism?

Catabolism and Anabolism.

p.49
Metabolism: Catabolism and Anabolism

What is the nature of catabolic processes?

Oxidative.

p.65
Metabolism: Catabolism and Anabolism

What are the two main pathways glycolysis can lead to under different conditions?

Aerobic and anaerobic pathways.

p.74
Metabolism: Catabolism and Anabolism

What role does glucose-6-phosphate play in cellular metabolism?

It serves as a substrate for glycolysis and the pentose phosphate pathway.

p.52
Metabolism: Catabolism and Anabolism

Which organ is responsible for regulating metabolic waste?

Kidney.

p.66
Overview of Digestion

What are the two main phases of glycolysis?

Energy-investment phase and energy-generation phase.

p.75
Metabolism: Catabolism and Anabolism

What significant role does PFK-1 play in glycolysis?

It is the most important control point and the rate-limiting step.

p.53
Metabolism: Catabolism and Anabolism

What characterizes the fed state in metabolic conditions?

Increased energy storage.

p.69
Digestive Enzymes and Their Functions

What are the isoforms of hexokinase?

Hexokinases I–III.

p.91
Metabolism: Catabolism and Anabolism

How does the Rapoport-Luebering shunt affect hemoglobin's affinity for oxygen?

By increasing 2,3-BPG levels, it decreases hemoglobin's affinity for oxygen, facilitating oxygen delivery to tissues.

p.85
Metabolism: Catabolism and Anabolism

What is produced during the oxidation of Glyceraldehyde 3-phosphate?

NADH and 1,3-bisphosphoglycerate.

p.85
Metabolism: Catabolism and Anabolism

What enzyme catalyzes the oxidation of Glyceraldehyde 3-phosphate?

Glyceraldehyde 3-phosphate dehydrogenase.

p.91
Metabolism: Catabolism and Anabolism

What type of cells primarily utilize the Rapoport-Luebering glycolytic shunt?

Red blood cells (RBCs).

p.12
Absorption Mechanisms in the Small Intestine

What is passive diffusion?

The movement of substances from an area of higher concentration to an area of lower concentration.

p.28
Lipid Digestion and Absorption

What percentage of lipids are absorbed in the small intestine?

About 95 percent.

p.32
Nucleic Acid Digestion

What is the role of deoxyribonuclease?

It digests DNA.

p.32
Nucleic Acid Digestion

What is the role of ribonuclease?

It digests RNA.

p.18
Carbohydrate Digestion and Absorption

How are glucose and galactose transported into epithelial cells?

By common protein carriers via secondary active transport with sodium ions.

p.32
Nucleic Acid Digestion

What are the end products of nucleic acid digestion in the small intestine?

Pentoses, phosphates, and nitrogenous bases.

p.19
Absorption Mechanisms in the Small Intestine

What role does GLUT 4 play in the body?

It transports glucose into muscles and fat cells.

p.28
Lipid Digestion and Absorption

How do bile salts and lecithin assist in the absorption of long-chain fatty acids?

They enclose them in a micelle.

p.23
Protein Digestion and Absorption

What does rennin convert milk casein into?

Paracasein.

p.5
Digestive Enzymes and Their Functions

What enzymes are involved in the breakdown of nucleotides?

Nucleosidases and phosphatases.

p.37
Digestive Disorders and Malabsorption Issues

How many main types of galactosemia are there?

Three main types.

p.4
Digestive Enzymes and Their Functions

What type of enzymes are produced in the brush border of the small intestine?

Brush border enzymes.

p.38
Digestive Disorders and Malabsorption Issues

What are the symptoms of Crohn's disease?

Abdominal pain, severe diarrhea, fatigue, weight loss, and malnutrition.

p.39
Digestive Disorders and Malabsorption Issues

What does steatorrhea indicate?

A disorder of lipid absorption.

p.38
Digestive Disorders and Malabsorption Issues

What might a patient with Crohn's disease require if medications are not effective?

Surgery may be required.

p.7
Digestive Enzymes and Their Functions

What are the end products of pancreatic amylase?

Disaccharides (maltose) and monosaccharides.

p.15
Carbohydrate Digestion

What are the products of lactose digestion?

Glucose and galactose.

p.8
Carbohydrate Digestion and Absorption

What are the products of sucrose digestion?

Glucose and fructose.

p.45
Metabolism: Catabolism and Anabolism

What is anabolism?

Synthetic reactions that build up molecules.

p.45
Metabolism: Catabolism and Anabolism

What is the primary function of catabolic reactions?

To release energy by breaking down complex molecules.

p.8
Digestive Enzymes and Their Functions

Which enzyme begins fat digestion in the mouth?

Lingual lipase.

p.47
Metabolism: Catabolism and Anabolism

What is the final stage in catabolism?

ATP formation in the electron transport chain.

p.48
Metabolism: Catabolism and Anabolism

What is catabolism?

The breakdown of molecules to obtain energy.

p.49
Metabolism: Catabolism and Anabolism

Which oxidizing agents are required for catabolism?

NAD+, NADP+, FAD.

p.88
Metabolism: Catabolism and Anabolism

What is produced in Reaction 7 of glycolysis?

Phosphoglycerate synthesis.

p.77
Metabolism: Catabolism and Anabolism

What mechanism does fructose 2,6-bisphosphate employ to prevent futile cycles?

It activates glycolysis while inhibiting gluconeogenesis, ensuring both pathways are not fully active at the same time.

p.74
Carbohydrate Digestion and Absorption

What is glucose-6-phosphate?

A phosphorylated form of glucose that plays a key role in carbohydrate metabolism.

p.75
Metabolism: Catabolism and Anabolism

What is the product of the phosphorylation of fructose 6-phosphate?

Fructose 1,6-bisphosphate.

p.70
Digestive Enzymes and Their Functions

Which anomers of glucose can these isozymes act upon?

Both the α- and β-anomers of glucose.

p.60
Metabolism: Catabolism and Anabolism

What is anabolism?

The process of synthesizing larger molecules from smaller units.

p.73
Metabolism: Catabolism and Anabolism

Is the reaction of glucose 6-phosphate to fructose 6-phosphate reversible?

Yes, the reaction is readily reversible.

p.75
Metabolism: Catabolism and Anabolism

How many ATP molecules are consumed during the reaction catalyzed by PFK-1?

Two ATP molecules are consumed.

p.94
Metabolism: Catabolism and Anabolism

What is the high-energy substrate used to synthesize ATP from ADP in this reaction?

Enol phosphate in PEP.

p.3
Digestive Enzymes and Their Functions

Which glands in the mouth secrete digestive enzymes?

Salivary glands.

p.6
Digestive Enzymes and Their Functions

Where are pancreatic enzymes produced?

In the pancreatic acinar cells.

p.3
Digestive Enzymes and Their Functions

What organ secretes many digestive enzymes that are carried to the small intestine?

The pancreas.

p.3
Digestive Enzymes and Their Functions

How are digestive enzymes from the pancreas delivered to the small intestine?

By ducts.

p.34
Digestive Disorders and Malabsorption Issues

What can malabsorption lead to?

Malnutrition and a variety of anaemias.

p.4
Digestive Enzymes and Their Functions

What is the product of Gastric lipase?

Fatty acids and monoacylglycerides.

p.23
Protein Digestion and Absorption

What activates prorennin to produce active rennin?

Hydrochloric acid produced in the stomach.

p.28
Lipid Digestion and Absorption

What pathway do short-chain fatty acids take after absorption?

They enter the blood capillary of a villus, similar to monosaccharides and amino acids.

p.36
Digestive Disorders and Malabsorption Issues

What is Glucose-Galactose Malabsorption (GGM)?

An inherited metabolic disorder causing inability to absorb glucose and galactose.

p.28
Lipid Digestion and Absorption

Why can't long-chain fatty acids and glycerol be absorbed directly?

Because they are insoluble in water.

p.36
Digestive Disorders and Malabsorption Issues

What causes GGM?

A mutation in the gene responsible for the sodium/glucose cotransport protein I (SGLT1).

p.38
Digestive Disorders and Malabsorption Issues

What are common symptoms of Irritable Bowel Syndrome?

Abdominal pain, unpredictable bowel movements, variation in stool consistency, bloating, flatulence, nausea, headache, fatigue, depression, anxiety, and difficulty concentrating.

p.14
Absorption Mechanisms in the Small Intestine

What is the destination for absorbed carbohydrates?

Liver via hepatic portal vein.

p.35
Digestive Disorders and Malabsorption Issues

What are the two main types of lactose intolerance?

Primary and secondary lactose intolerance.

p.37
Digestive Disorders and Malabsorption Issues

What enzyme is completely deficient in Classic galactosemia (Type 1)?

Galactose-1-phosphate uridyl transferase (GALT).

p.30
Lipid Digestion and Absorption

Through what structure do chylomicrons empty into the circulatory system?

The thoracic duct.

p.38
Digestive Disorders and Malabsorption Issues

What medications are used to manage Crohn's disease?

Steroids and immunosuppressants are used to slow disease progression.

p.7
Digestive Enzymes and Their Functions

What enzymes are found at the brush border of the intestine?

Brush border enzymes.

p.42
Metabolism: Catabolism and Anabolism

What are the two main types of metabolism?

Catabolism and Anabolism.

p.47
Metabolism: Catabolism and Anabolism

What is the first stage of catabolism?

Hydrolysis of macromolecules to building blocks, such as polysaccharides to glucose and proteins to amino acids.

p.17
Digestive Enzymes and Their Functions

What are the end products of pancreatic amylase?

Disaccharides (maltose) and monosaccharides.

p.50
Metabolism: Catabolism and Anabolism

What metabolic process occurs in the nucleus?

DNA replication and transcription.

p.52
Metabolism: Catabolism and Anabolism

Where does metabolism primarily occur in the body?

In tissues and organs such as the blood, liver, muscle, adipose tissue, brain, kidney, and adrenals.

p.52
Metabolism: Catabolism and Anabolism

What role does the brain have in metabolism?

The brain is also involved in metabolic processes.

p.55
Metabolism: Catabolism and Anabolism

What does a reaction pathway illustrate?

The sequence of steps in a chemical reaction.

p.56
Metabolism: Catabolism and Anabolism

What is the starting substrate of the glycolytic pathway?

Glucose.

p.70
Digestive Enzymes and Their Functions

How do these isozymes respond to conditions like diabetes or insulin?

They are non-inducible enzymes and are not affected by diabetes or insulin.

p.78
Metabolism: Catabolism and Anabolism

What are the main allosteric regulators of PFK-1?

Citrate (inhibitor) and AMP (activator).

p.73
Metabolism: Catabolism and Anabolism

Is the isomerization of glucose 6-phosphate a rate-limiting step?

No, it is not a rate-limiting or regulated step.

p.59
Metabolic Disorders and Malabsorption Issues

What is G6PD deficiency?

A metabolic disease caused by a genetic enzyme deficiency.

p.71
Digestive Enzymes and Their Functions

What role does glucokinase play in hypothalamic neurons?

It serves as a glucose sensor, key in the adrenergic response to hypoglycemia.

p.63
Metabolism: Catabolism and Anabolism

Where does glycolysis occur in the cell?

In the cytoplasm.

p.21
Protein Digestion and Absorption

What enzymes do the cells of the brush border secrete to further break down peptides?

Aminopeptidase and dipeptidase.

p.13
Absorption Mechanisms in the Small Intestine

What does the absorption of most nutrients through the intestinal villi require?

Active transport fueled by ATP.

p.21
Protein Digestion and Absorption

What is the final result of protein digestion in the small intestine?

Molecules small enough to enter the bloodstream.

p.16
Carbohydrate Digestion and Absorption

What are the simple sugars produced from carbohydrate digestion?

Glucose, fructose, and galactose.

p.15
Carbohydrate Digestion

What is the main component of dietary carbohydrates?

The plant polysaccharide amylose and animal polysaccharide glycogen.

p.34
Digestive Disorders and Malabsorption Issues

What factors can impair the absorption of nutrients?

Single or multiple nutrient abnormalities depending on the condition.

p.4
Digestive Enzymes and Their Functions

What role does Enteropeptidase serve in digestion?

It activates Trypsinogen to Trypsin.

p.20
Digestive Enzymes and Their Functions

What are the three primary enzymes involved in protein digestion?

Pepsin, trypsin, and chymotrypsin.

p.15
Carbohydrate Digestion

Which enzyme is required to chemically digest amylose and glycogen?

Amylase.

p.2
Lipid Digestion and Absorption

What are lipids broken down into?

Fatty acids and glycerol.

p.7
Digestive Enzymes and Their Functions

What type of enzyme is salivary amylase?

Salivary enzyme.

p.22
Digestive Enzymes and Their Functions

What are the end products of pepsin's action?

Peptides.

p.39
Digestive Disorders and Malabsorption Issues

What are some symptoms of Hartnup disease?

Failure to thrive, photosensitivity, intermittent ataxia, nystagmus, and tremor.

p.37
Digestive Disorders and Malabsorption Issues

What is characteristic of Galactokinase deficiency (Type 2)?

A deficiency of the enzyme galactokinase 1, typically causing only cataracts.

p.22
Digestive Enzymes and Their Functions

What enzyme is responsible for breaking down peptides into amino acids?

Aminopeptidase.

p.9
Digestive Enzymes and Their Functions

What are brush border enzymes?

Enzymes present in the small intestine that break down peptides and nucleotides.

p.7
Digestive Enzymes and Their Functions

What does α-Dextrinase act on?

α-Dextrins.

p.45
Metabolism: Catabolism and Anabolism

What is catabolism?

Degradative reactions that break down molecules.

p.44
Metabolism: Catabolism and Anabolism

What macromolecules are assembled from building blocks in metabolism?

Carbohydrates, proteins, lipids, nucleic acids, and other cell components.

p.49
Metabolism: Catabolism and Anabolism

What is the nature of anabolic processes?

Reductive.

p.52
Metabolism: Catabolism and Anabolism

Which tissue contributes to metabolism alongside muscle tissue?

Adipose tissue.

p.58
Metabolism: Catabolism and Anabolism

What is the purpose of regulating metabolic pathways?

To control metabolism.

p.61
Metabolism: Catabolism and Anabolism

In which living things does metabolism occur?

In bacteria, plants, animals, and humans.

p.55
Metabolism: Catabolism and Anabolism

What are the key components of a reaction pathway?

Reactants, intermediates, and products.

p.56
Metabolism: Catabolism and Anabolism

What is the end product of glycolysis under aerobic conditions?

Pyruvate.

p.85
Metabolism: Catabolism and Anabolism

What is Glyceraldehyde 3-phosphate (G3P)?

A three-carbon sugar involved in glycolysis and the Calvin cycle.

p.71
Digestive Enzymes and Their Functions

What is the primary function of glucokinase in β cells?

To act as a glucose sensor and determine the threshold for insulin secretion.

p.83
Digestive Enzymes and Their Functions

What does triose phosphate isomerase do?

It interconverts dihydroxyacetone phosphate (DHAP) and glyceraldehyde 3-phosphate.

p.59
Metabolic Disorders and Malabsorption Issues

What metabolic condition results from the inability to digest lactose?

Lactose intolerance.

p.92
Metabolism: Catabolism and Anabolism

What role does 3-Phosphoglycerate play in the Calvin cycle?

It is formed from ribulose bisphosphate and carbon dioxide.

p.67
Carbohydrate Digestion and Absorption

Which enzymes catalyze the phosphorylation of glucose?

Hexokinase or glucokinase.

p.87
Metabolism: Catabolism and Anabolism

Which enzyme catalyzes the conversion of 1,3-BPG to 3-phosphoglycerate?

Phosphoglycerate kinase.

p.67
Carbohydrate Digestion and Absorption

Why do phosphorylated sugar molecules not readily penetrate cell membranes?

There are no specific transmembrane carriers, and they are too polar to diffuse through the lipid bilayer.

p.18
Carbohydrate Digestion and Absorption

How do monosaccharides leave epithelial cells?

Via facilitated diffusion and then enter capillaries through intercellular clefts.

p.26
Lipid Digestion

Where does most lipid digestion occur?

In the small intestine.

p.22
Digestive Enzymes and Their Functions

Where is trypsin produced?

In the pancreas.

p.20
Protein Digestion and Absorption

Where does protein digestion first begin?

In the stomach.

p.2
Types of Digestion: Mechanical and Chemical

Where does most chemical digestion occur?

In the first part of the small intestine (duodenum).

p.14
Lipid Digestion and Absorption

How do long-chain fatty acids enter intestinal cells?

Diffusion, combined with proteins to create chylomicrons.

p.22
Digestive Enzymes and Their Functions

What are the end products of carboxypeptidase's action?

Amino acids and peptides.

p.7
Digestive Enzymes and Their Functions

What does pancreatic amylase act on?

Polysaccharides (Starch).

p.9
Digestive Enzymes and Their Functions

What does aminopeptidase primarily act on?

Amino acids at the amino end of peptides.

p.9
Digestive Enzymes and Their Functions

What does chymotrypsin do?

Breaks down proteins and peptides in the small intestine.

p.9
Digestive Enzymes and Their Functions

What do ribonuclease and deoxyribonuclease target?

Ribonucleic acids and deoxyribonucleic acids, respectively.

p.46
Metabolism: Catabolism and Anabolism

Can you give an example of an amphibolic pathway?

The TCA Cycle reactions.

p.8
Digestive Enzymes and Their Functions

What enzyme breaks down triglycerides in the stomach?

Gastric lipase.

p.17
Digestive Enzymes and Their Functions

What are the monosaccharides produced by oligosaccharidases?

Glucose, fructose, and galactose.

p.77
Digestive Enzymes and Their Functions

What is the role of fructose 2,6-bisphosphate in glycolysis?

It is the most potent activator of PFK-1.

p.68
Metabolism: Catabolism and Anabolism

What is glucose converted into during glucose phosphorylation?

Glucose-6-phosphate.

p.58
Metabolism: Catabolism and Anabolism

How does the metabolic status affect metabolic regulation?

It distinguishes between fed or starved states, influencing metabolism control.

p.54
Metabolism: Catabolism and Anabolism

What is a metabolic pathway?

A sequence of chemical reactions occurring within a cell.

p.75
Digestive Enzymes and Their Functions

Which enzyme phosphorylates fructose 6-phosphate?

Phosphofructokinase-1 (PFK-1).

p.74
Metabolism: Catabolism and Anabolism

What are the main pathways that utilize glucose-6-phosphate?

Glycolysis and the pentose phosphate pathway.

p.66
Metabolism: Catabolism and Anabolism

What occurs during the energy-investment phase of glycolysis?

Phosphorylated forms of intermediates are synthesized at the expense of ATP.

p.56
Metabolism: Catabolism and Anabolism

How many ATP molecules are produced in the glycolytic pathway per glucose molecule?

A net gain of 2 ATP molecules.

p.85
Metabolism: Catabolism and Anabolism

What process involves the oxidation of Glyceraldehyde 3-phosphate?

Glycolysis.

p.54
Metabolism: Catabolism and Anabolism

Can reaction steps in a metabolic pathway be reversible?

Yes, a reaction step may be reversible or irreversible.

p.83
Metabolism: Catabolism and Anabolism

Why must dihydroxyacetone phosphate (DHAP) be isomerized?

It must be isomerized to glyceraldehyde 3-phosphate for further metabolism by the glycolytic pathway.

p.63
Metabolism: Catabolism and Anabolism

What is the main product of glycolysis?

Pyruvate.

p.69
Digestive Enzymes and Their Functions

What does a low Km indicate for hexokinase?

A high affinity for glucose.

p.79
Metabolism: Catabolism and Anabolism

What causes PFK-2 to be active in the well-fed state?

Dephosphorylation of PFK-2 due to increased fructose 2,6-bisphosphate.

p.72
Metabolism: Catabolism and Anabolism

How does glucokinase help minimize hyperglycemia during the absorptive period?

By preventing large amounts of glucose from entering the systemic circulation after a meal.

p.80
Regulation of Glycolysis

What inhibitors affect PFK-1?

Citrate and ATP.

p.86
Metabolism: Catabolism and Anabolism

What is linked to carbon 1 of the 1,3-BPG product?

A phosphate group by a high-energy bond.

p.57
Metabolism: Catabolism and Anabolism

What is the first step in cellular respiration that breaks down glucose?

Glycolysis.

p.57
Metabolism: Catabolism and Anabolism

What cycle is also known as the Krebs cycle?

The TCA cycle reactions.

p.36
Digestive Disorders and Malabsorption Issues

What is the role of SGLT1 in glucose and galactose absorption?

It carries both sugars into the intestines.

p.23
Protein Digestion and Absorption

Which enzyme further degrades paracasein?

Pepsin.

p.23
Protein Digestion and Absorption

What role does calcium play in the milk digestion process?

It helps rennin change casein into paracasein and forms calcium paracaseinate.

p.26
Lipid Digestion

What does pancreatic lipase do to triglycerides?

It breaks them down into two free fatty acids and a monoglyceride.

p.26
Lipid Digestion

What types of fatty acids are included in lipid digestion?

Both short-chain (less than 10 to 12 carbons) and long-chain fatty acids.

p.39
Digestive Disorders and Malabsorption Issues

What causes steatorrhea?

A deficit in bile secretion or pancreatic juice into the intestine.

p.39
Digestive Disorders and Malabsorption Issues

What is the manifestation of steatorrhea?

Presence of excess fats in feces.

p.46
Metabolism: Catabolism and Anabolism

What is amphibolism?

It involves reaction processes that include both synthesis and breakdown of molecules.

p.46
Metabolism: Catabolism and Anabolism

What are pathways that play both anabolic and catabolic roles called?

Amphibolic pathways.

p.8
Carbohydrate Digestion and Absorption

What are the products of lactose digestion?

Galactose and glucose.

p.50
Metabolism: Catabolism and Anabolism

Which organelle is responsible for protein synthesis?

Ribosomes.

p.50
Metabolism: Catabolism and Anabolism

What is the role of the endoplasmic reticulum in metabolism?

It is involved in the synthesis of lipids and proteins.

p.48
Metabolism: Catabolism and Anabolism

In which phase of metabolism is energy consumed?

Anabolism.

p.48
Metabolism: Catabolism and Anabolism

How do catabolism and anabolism interact?

Catabolism provides the energy and building blocks for anabolic processes.

p.60
Metabolism: Catabolism and Anabolism

What are the two main types of metabolism?

Catabolism and Anabolism.

p.60
Metabolism: Catabolism and Anabolism

What is catabolism?

The process of breaking down molecules to obtain energy.

p.82
Carbohydrate Digestion and Absorption

What are the products of the cleavage of Fructose 1,6-bisphosphate?

Dihydroxyacetone phosphate (DHAP) and glyceraldehyde 3-phosphate (G3P).

p.65
Metabolism: Catabolism and Anabolism

Which organisms primarily utilize the alcoholic fermentation pathway?

Mainly prokaryotes, such as yeast and some strains of bacteria.

p.94
Metabolism: Catabolism and Anabolism

What type of phosphorylation occurs during the conversion of PEP to pyruvate?

Substrate-level phosphorylation.

p.55
Metabolism: Catabolism and Anabolism

What is the significance of activation energy in a reaction pathway?

It is the energy required to initiate a chemical reaction.

p.64
Metabolism: Catabolism and Anabolism

Is glycolysis used by all tissues?

Yes, all tissues use glycolysis for glucose oxidation.

p.94
Metabolism: Catabolism and Anabolism

What is the end product of glycolysis under aerobic conditions?

Pyruvate.

p.71
Digestive Enzymes and Their Functions

How does glucokinase differ from other hexokinases regarding inhibition?

Glucokinase activity is not directly inhibited by glucose 6-phosphate.

p.85
Metabolism: Catabolism and Anabolism

What is the role of NAD+ in the oxidation of Glyceraldehyde 3-phosphate?

It acts as an electron carrier, being reduced to NADH.

p.79
Metabolism: Catabolism and Anabolism

What is the effect of low fructose 2,6-bisphosphate during fasting?

It inhibits glycolysis and activates gluconeogenesis.

p.87
Metabolism: Catabolism and Anabolism

How is the reaction catalyzed by phosphoglycerate kinase unique?

It is physiologically reversible, unlike most other kinases.

p.63
Metabolism: Catabolism and Anabolism

What happens to pyruvate after glycolysis under aerobic conditions?

It enters the mitochondria for further oxidation in the citric acid cycle.

p.72
Metabolism: Catabolism and Anabolism

What is the specificity of glucokinase?

Glucokinase has absolute specificity for glucose.

p.86
Metabolism: Catabolism and Anabolism

What role does the high-energy phosphate play in glycolysis?

It drives ATP synthesis in the next reaction.

p.86
Digestive Disorders and Malabsorption Issues

What additional effect does arsenate have besides harming glycolysis?

It inhibits ATP synthase in the electron transport chain (ETC).

p.35
Digestive Disorders and Malabsorption Issues

What causes primary lactose intolerance?

A decrease in lactase production with age.

p.37
Digestive Disorders and Malabsorption Issues

What are early signs and symptoms of Classic galactosemia?

Liver dysfunction, susceptibility to infections, failure to thrive, and cataracts.

p.35
Digestive Disorders and Malabsorption Issues

What causes secondary lactose intolerance?

Illnesses such as a stomach bug or celiac disease, leading to inflammation in the gut wall.

p.9
Digestive Enzymes and Their Functions

What type of cells produce gastric enzymes?

Chief cells.

p.5
Digestive Enzymes and Their Functions

What does carboxypeptidase do?

Breaks down amino acids at the carboxyl end of peptides.

p.5
Digestive Enzymes and Their Functions

What is chymotrypsin's role in digestion?

Breaks down proteins into peptides.

p.14
Nucleic Acid Digestion and Absorption

How are nucleic acid digestion products absorbed?

Active transport via membrane carriers.

p.8
Digestive Enzymes and Their Functions

Which enzyme breaks down maltose in the small intestine?

Maltase.

p.43
Metabolism: Catabolism and Anabolism

What does the term 'metabolism' mean?

It comes from the Greek word 'metabole,' which means change.

p.43
Metabolism: Catabolism and Anabolism

What does metabolism comprise?

All the chemical reactions that take place in a living system.

p.44
Metabolism: Catabolism and Anabolism

What do metabolic processes convert exogenous nutrients into?

Building blocks or precursors of macromolecular cell components.

p.44
Metabolism: Catabolism and Anabolism

What roles do metabolic processes play in relation to biomolecules?

They form and degrade biomolecules required for specialized functions in cells.

p.48
Metabolism: Catabolism and Anabolism

In which phase of metabolism is energy released?

Catabolism.

p.49
Metabolism: Catabolism and Anabolism

What is the primary function of catabolism?

To break down large molecules to form smaller ones.

p.36
Digestive Disorders and Malabsorption Issues

How is GGM treated?

By avoiding milk, milk products, and foods containing glucose and galactose.

p.22
Digestive Enzymes and Their Functions

What enzyme acts on peptides in the small intestine?

Carboxypeptidase.

p.39
Digestive Disorders and Malabsorption Issues

What dietary treatment is recommended for Hartnup disease?

A high protein diet.

p.14
Lipid Digestion and Absorption

Where do long-chain fatty acids go after absorption?

Lacteals of villi to systemic circulation via lymph entering thoracic duct.

p.37
Digestive Disorders and Malabsorption Issues

What enzyme deficiency causes Galactose epimerase deficiency (Type 3)?

UDP-galactose-4-epimerase.

p.37
Digestive Disorders and Malabsorption Issues

What is the most common treatment for galactosemia?

A low-galactose diet.

p.22
Digestive Enzymes and Their Functions

What substrate does dipeptidase act on?

Peptides.

p.7
Digestive Enzymes and Their Functions

What are the end products of the brush border enzymes?

Monosaccharides (e.g., glucose, fructose, galactose).

p.42
Metabolism: Catabolism and Anabolism

What is catabolism?

The process of breaking down molecules to obtain energy.

p.17
Digestive Enzymes and Their Functions

What substrates does pancreatic amylase act on?

Polysaccharides (starch).

p.51
Metabolism: Catabolism and Anabolism

Why is inter-compartmental crossing important?

It allows for the exchange of nutrients and waste products between compartments, supporting various metabolic processes.

p.47
Metabolism: Catabolism and Anabolism

What is the nature of catabolism?

Catabolism is convergent in nature.

p.49
Metabolism: Catabolism and Anabolism

What do catabolic processes release?

Energy.

p.68
Metabolism: Catabolism and Anabolism

What is the first step in the metabolism of glucose?

Glucose phosphorylation.

p.58
Metabolism: Catabolism and Anabolism

What are the main factors that regulate metabolic pathways?

Enzymes, hormones, compartmentalization, specialized products, and metabolic status.

p.76
Metabolism: Catabolism and Anabolism

How does citrate affect PFK-1 activity?

Citrate inhibits PFK-1, favoring glucose use for glycogen synthesis.

p.73
Digestive Enzymes and Their Functions

What enzyme catalyzes the isomerization of glucose 6-phosphate?

Phosphohexoseisomerase (phosphoglucoseisomerase).

p.64
Metabolism: Catabolism and Anabolism

What is the primary purpose of the glycolytic pathway (EMP pathway)?

To oxidize glucose to provide energy (as ATP) and intermediates for other metabolic pathways.

p.61
Metabolism: Catabolism and Anabolism

When does metabolism begin and end in an organism?

It starts at conception and stops at death.

p.71
Digestive Enzymes and Their Functions

Where is glucokinase predominantly found?

In liver parenchymal cells and pancreatic β cells.

p.54
Metabolism: Catabolism and Anabolism

What catalyzes each reaction step in a metabolic pathway?

An enzyme.

p.56
Metabolism: Catabolism and Anabolism

What is produced during glycolysis besides ATP?

NADH.

p.53
Metabolism: Catabolism and Anabolism

What is the main challenge during the diseased state?

Metabolic struggle for survival.

p.69
Digestive Enzymes and Their Functions

What important regulatory role does hexokinase play?

It is a regulatory enzyme of glycolysis, inhibited by glucose-6-phosphate.

p.93
Metabolism: Catabolism and Anabolism

What type of reaction is Reaction 8 considered?

Freely reversible.

p.63
Metabolism: Catabolism and Anabolism

What are the two phases of glycolysis?

The energy investment phase and the energy payoff phase.

p.72
Metabolism: Catabolism and Anabolism

What effect does glucokinase's high Vmax have on glucose metabolism?

It allows the liver to effectively remove the flood of glucose delivered by the portal blood.

p.80
Regulation of Glycolysis

What activates PFK-1 in the liver?

Fructose-2,6-bisphosphate (F-2,6-bisP).

p.84
Digestive Enzymes and Their Functions

Why must NADH be oxidized back to NAD+?

To allow glycolysis to continue due to limited NAD+ in the cell.

p.57
Metabolism: Catabolism and Anabolism

What process breaks down fatty acids into acetyl-CoA?

β-oxidation.

p.30
Lipid Digestion and Absorption

What enzyme breaks down triglycerides from chylomicrons in the bloodstream?

Lipoprotein lipase.

p.5
Digestive Enzymes and Their Functions

What are the products of sucrose digestion?

Glucose and fructose.

p.15
Carbohydrate Digestion

What does the brush border enzyme α-dextrinase do?

It breaks off one glucose unit at a time from α-dextrin.

p.14
Lipid Digestion and Absorption

How are monoacylglycerides absorbed?

Diffusion into intestinal cells, combined with proteins to create chylomicrons.

p.9
Digestive Enzymes and Their Functions

What is the function of dipeptidase?

To break down dipeptides into amino acids.

p.17
Digestive Enzymes and Their Functions

What enzyme is produced by the salivary glands?

Salivary amylase.

p.9
Digestive Enzymes and Their Functions

What are nucleosidase and phosphatase responsible for?

Breaking down nucleotides into phosphates, nitrogenous bases, and pentoses.

p.8
Carbohydrate Digestion and Absorption

What are the products of maltose digestion?

Glucose.

p.51
Absorption Mechanisms in the Small Intestine

What does inter-compartmental crossing refer to?

The process of substances moving between different compartments in a biological system.

p.50
Metabolism: Catabolism and Anabolism

What intracellular organelle is primarily involved in energy production?

Mitochondria.

p.51
Absorption Mechanisms in the Small Intestine

How is inter-compartmental crossing regulated?

Through specific transport proteins and channels that facilitate the movement of molecules across compartment membranes.

p.70
Digestive Enzymes and Their Functions

What is the characteristic of these isozymes regarding maximal velocity (Vmax) for glucose?

They have a low maximal velocity (Vmax) for glucose, limiting glucose phosphorylation to what the cell can use.

p.82
Carbohydrate Digestion and Absorption

What occurs during the cleavage of Fructose 1,6-bisphosphate?

It is split into two three-carbon molecules: dihydroxyacetone phosphate (DHAP) and glyceraldehyde 3-phosphate (G3P).

p.56
Metabolism: Catabolism and Anabolism

What is the main function of the glycolytic pathway?

To convert glucose into pyruvate, producing energy.

p.66
Overview of Digestion

What is the overall process of glycolysis?

The conversion of glucose to pyruvate in two stages.

p.58
Metabolism: Catabolism and Anabolism

Which macromolecules play a significant role in the regulation of metabolic pathways?

Enzymes and hormones.

p.59
Metabolic Disorders and Malabsorption Issues

What are errors in metabolic pathways primarily responsible for?

Metabolic diseases.

p.78
Metabolism: Catabolism and Anabolism

What role does PFK-1 play in glycolysis?

It is a key regulatory enzyme that catalyzes the conversion of fructose-6-phosphate to fructose-1,6-bisphosphate.

p.92
Metabolism: Catabolism and Anabolism

What is the significance of 3-Phosphoglycerate in metabolic reactions?

It serves as an intermediate in glycolysis and the Calvin cycle.

p.55
Digestive Enzymes and Their Functions

What role do enzymes play in reaction pathways?

Enzymes act as catalysts, speeding up the reaction steps.

p.60
Metabolism: Catabolism and Anabolism

Why is metabolism important?

It provides energy for vital processes and helps in the growth and repair of tissues.

p.64
Metabolism: Catabolism and Anabolism

Where does glycolysis occur within the cell?

In the cell cytosol.

p.66
Metabolism: Catabolism and Anabolism

What happens during the energy-generation phase of glycolysis?

A net of two molecules of ATP are formed by substrate-level phosphorylation per glucose molecule metabolized.

p.53
Metabolism: Catabolism and Anabolism

What happens during the starved state?

Increased energy release.

p.75
Metabolism: Catabolism and Anabolism

What is formed from fructose 6-phosphate by phosphofructokinase-2 (PFK-2)?

Fructose 2,6-bisphosphate.

p.81
Digestive Enzymes and Their Functions

Is the cleavage reaction regulated?

No, it is not regulated.

p.69
Digestive Enzymes and Their Functions

Where is hexokinase found?

In all cells/tissues (ubiquitous).

p.91
Metabolism: Catabolism and Anabolism

In which pathway does the Rapoport-Luebering shunt operate?

It operates within the glycolytic pathway.

p.81
Digestive Enzymes and Their Functions

What does Aldolase B do in addition to cleaving fructose 1,6-bisphosphate?

It also cleaves fructose 1-phosphate and functions in dietary fructose metabolism.

p.91
Metabolism: Catabolism and Anabolism

What is the significance of 2,3-bisphosphoglycerate (2,3-BPG) in RBCs?

It plays a crucial role in modulating oxygen release from hemoglobin.

p.83
Metabolism: Catabolism and Anabolism

What is the net production of glyceraldehyde 3-phosphate from the cleavage products of fructose 1,6-bisphosphate?

Two molecules of glyceraldehyde 3-phosphate.

p.70
Digestive Enzymes and Their Functions

What does the broad substrate specificity of these isozymes mean?

They can phosphorylate several hexoses, such as fructose, mannose, and galactose, though at a slower rate.

p.74
Carbohydrate Digestion and Absorption

How is glucose-6-phosphate formed?

By the phosphorylation of glucose, catalyzed by the enzyme hexokinase.

p.73
Digestive Enzymes and Their Functions

What is the product of the isomerization of glucose 6-phosphate?

Fructose 6-phosphate.

p.64
Metabolism: Catabolism and Anabolism

What are the end products of glycolysis?

Pyruvate, energy (ATP), and NADH.

p.92
Metabolism: Catabolism and Anabolism

What reactions are associated with 3-Phosphoglycerate?

Reactions 8, 9, and 10 in the glycolytic pathway.

p.60
Metabolism: Catabolism and Anabolism

What role do enzymes play in metabolism?

They act as catalysts to speed up chemical reactions.

p.55
Digestive Disorders and Malabsorption Issues

How can a reaction pathway be affected by inhibitors?

Inhibitors can slow down or halt the reaction by affecting enzyme activity.

p.92
Metabolism: Catabolism and Anabolism

Which enzyme catalyzes the conversion of 3-Phosphoglycerate in glycolysis?

Phosphoglycerate kinase.

p.59
Metabolic Disorders and Malabsorption Issues

What metabolic condition is associated with the inability to metabolize galactose?

Galactosemia.

p.79
Metabolism: Catabolism and Anabolism

What happens to fructose 2,6-bisphosphate during fasting?

It decreases due to elevated glucagon and low insulin levels.

p.80
Regulation of Glycolysis

Which enzyme is considered the major regulatory enzyme of glycolysis?

PFK-1 (Phosphofructokinase-1).

p.79
Metabolism: Catabolism and Anabolism

What happens to PFK-2 during fasting?

PFK-2 is phosphorylated, making it inactive.

p.84
Digestive Enzymes and Their Functions

What is the first oxidation-reduction reaction of glycolysis?

The oxidation of glyceraldehyde 3-phosphate to 1,3-bisphosphoglycerate.

p.80
Regulation of Glycolysis

What activates pyruvate kinase?

AMP and F-1,6-bisP.

p.86
Digestive Disorders and Malabsorption Issues

How does pentavalent arsenic (arsenate) affect glycolysis?

It prevents net ATP and NADH production by competing with Pi as a substrate for glyceraldehyde 3-phosphate dehydrogenase.

p.59
Metabolic Disorders and Malabsorption Issues

What mainly causes metabolic diseases or inborn errors of metabolism?

Genetic enzyme deficiencies.

p.74
Metabolism: Catabolism and Anabolism

What can glucose-6-phosphate be converted into?

It can be converted into glucose, glycogen, or enter the pentose phosphate pathway.

p.81
Digestive Enzymes and Their Functions

Is the cleavage reaction catalyzed by aldolase reversible?

Yes, the reaction is reversible.

p.79
Metabolism: Catabolism and Anabolism

What hormones are elevated during the well-fed state?

Insulin levels are elevated, and glucagon levels are decreased.

p.93
Metabolism: Catabolism and Anabolism

What occurs in Reaction 8 of glycolysis?

The phosphate group shifts from carbon 3 to carbon 2 of phosphoglycerate, forming 2-Phosphoglycerate.

p.93
Metabolism: Catabolism and Anabolism

Which enzyme catalyzes the shift of the phosphate group in Reaction 8?

Phosphoglycerate mutase.

p.89
Metabolism: Catabolism and Anabolism

What is the Rapoport Luebering Glycolytic Shunt?

A modified glycolysis pathway in RBCs that includes shunt reactions.

p.69
Digestive Enzymes and Their Functions

Why is a high affinity for glucose beneficial for hexokinase?

It allows efficient phosphorylation and metabolism of glucose even at low tissue concentrations.

p.93
Metabolism: Catabolism and Anabolism

What characterizes phosphoenolpyruvate (PEP)?

It contains a high-energy enol phosphate.

p.67
Carbohydrate Digestion and Absorption

What is the consequence of the irreversible phosphorylation of glucose?

It traps glucose as cytosolic glucose-6-phosphate, committing it to further metabolism.

p.89
Metabolism: Catabolism and Anabolism

Why is 2,3-BPG present at high concentrations in RBCs?

Because it plays a crucial role in oxygen delivery, unlike most cells where it is found in trace amounts.

p.80
Regulation of Glycolysis

How does PFK-II relate to F-2,6-bisP?

PFK-II synthesizes F-2,6-bisP and is regulated by phosphorylation.

p.57
Metabolism: Catabolism and Anabolism

What pathway generates NADPH and ribose-5-phosphate for nucleotide synthesis?

Pentose phosphate shunt pathway.

p.91
Metabolism: Catabolism and Anabolism

What is the primary function of the Rapoport-Luebering glycolytic shunt in red blood cells (RBCs)?

To generate 2,3-bisphosphoglycerate (2,3-BPG), which regulates oxygen release from hemoglobin.

p.92
Metabolism: Catabolism and Anabolism

What is produced from 3-Phosphoglycerate during glycolysis?

Pyruvate is ultimately produced after further conversion.

p.78
Metabolism: Catabolism and Anabolism

What is the effect of fructose-2,6-bisphosphate on PFK-1?

It acts as a potent activator of PFK-1.

p.66
Overview of Digestion

How many steps are involved in the glycolytic pathway?

Ten (10) steps.

p.67
Carbohydrate Digestion and Absorption

What is the first reaction in the glycolytic pathway involving glucose?

The phosphorylation of glucose to glucose-6-phosphate.

p.87
Metabolism: Catabolism and Anabolism

What is produced during the conversion of 1,3-BPG to 3-phosphoglycerate?

ATP is synthesized from ADP.

p.63
Metabolism: Catabolism and Anabolism

Which coenzyme is reduced during glycolysis?

NAD+ is reduced to NADH.

p.93
Metabolism: Catabolism and Anabolism

Is the reaction forming PEP reversible?

Yes, despite the high-energy nature of the product.

p.87
Metabolism: Catabolism and Anabolism

What type of phosphorylation is described in this reaction?

Substrate-level phosphorylation.

p.80
Regulation of Glycolysis

What inhibits pyruvate kinase?

ATP, acetyl CoA, and phosphorylation.

p.57
Metabolism: Catabolism and Anabolism

What process occurs in the mitochondria to produce ATP using electron transport?

Oxidative phosphorylation.

p.63
Metabolism: Catabolism and Anabolism

What is glycolysis?

A metabolic pathway that converts glucose into pyruvate, generating ATP and NADH.

p.79
Metabolism: Catabolism and Anabolism

What effect does a carbohydrate-rich meal have on fructose 2,6-bisphosphate?

It increases the levels of hepatic fructose 2,6-bisphosphate.

p.79
Metabolism: Catabolism and Anabolism

What is the role of fructose 2,6-bisphosphate in the well-fed state?

It acts as an intracellular signal of glucose abundance, increasing glycolysis and inhibiting gluconeogenesis.

p.83
Metabolism: Catabolism and Anabolism

What is dihydroxyacetone phosphate (DHAP) used for?

It is used for the synthesis of glycerol-3-phosphate utilized in triacylglycerol synthesis.

p.93
Metabolism: Catabolism and Anabolism

What role does enolase play in the conversion of 2-Phosphoglycerate?

Enolase catalyzes the dehydration of 2-Phosphoglycerate to form PEP.

p.80
Regulation of Glycolysis

What activators affect hexokinase?

AMP, ADP, Pi.

p.89
Metabolism: Catabolism and Anabolism

Why is the lack of ATP production advantageous for RBCs?

It allows the accumulation of 2,3-BPG and enables glycolysis to proceed when ATP needs are minimal.

p.72
Metabolism: Catabolism and Anabolism

How is glucokinase regulated in the body?

Its synthesis is induced by insulin and repressed in diabetes.

p.86
Digestive Disorders and Malabsorption Issues

What does arsenate form when it competes with Pi?

A complex that spontaneously hydrolyzes to form 3-phosphoglycerate.

p.56
Metabolism: Catabolism and Anabolism

In which cellular location does glycolysis occur?

In the cytoplasm.

p.56
Metabolism: Catabolism and Anabolism

What are the two major phases of glycolysis?

The energy investment phase and the energy payoff phase.

p.63
Metabolism: Catabolism and Anabolism

How many ATP molecules are produced during glycolysis?

A net gain of 2 ATP molecules per glucose molecule.

p.72
Metabolism: Catabolism and Anabolism

What is the function of glucokinase in the liver following a carbohydrate-rich meal?

It requires a higher glucose concentration for half-saturation, functioning effectively when intracellular glucose levels are elevated.

p.63
Metabolism: Catabolism and Anabolism

What happens to pyruvate after glycolysis under anaerobic conditions?

It is converted to lactic acid or ethanol, depending on the organism.

p.72
Metabolism: Catabolism and Anabolism

What role does GLUT-2 play in glucose metabolism?

It ensures that blood glucose equilibrates rapidly across the hepatocyte membrane.

p.84
Digestive Enzymes and Their Functions

What is required as the oxidizing agent in the oxidation of glyceraldehyde 3-phosphate?

NAD+.

p.84
Metabolism: Catabolism and Anabolism

What are the two major mechanisms for oxidizing NADH to NAD+?

Reduction of pyruvate to lactate by lactate dehydrogenase and the electron transport chain.

p.57
Metabolism: Catabolism and Anabolism

What metabolic processes involve the formation and breakdown of glycogen?

Glycogenesis and glycogenolysis.

p.69
Digestive Enzymes and Their Functions

What is the function of glucose-6-phosphate in relation to hexokinase?

It inhibits hexokinase to control glucose uptake in extrahepatic tissues.

p.93
Metabolism: Catabolism and Anabolism

What happens in Reaction 9 of glycolysis?

2-Phosphoglycerate undergoes dehydration to form phosphoenolpyruvate (PEP).

p.67
Carbohydrate Digestion and Absorption

How many isozymes of hexokinase do mammals have?

Four isozymes (I–IV).

p.89
Metabolism: Catabolism and Anabolism

What is the ATP production status when glycolysis takes the Rapoport Luebering Shunt pathway?

There is no production of ATP.

p.84
Digestive Enzymes and Their Functions

What enzyme catalyzes the oxidation of glyceraldehyde 3-phosphate?

Glyceraldehyde 3-phosphate dehydrogenase.

p.84
Digestive Enzymes and Their Functions

What is produced as NAD+ is reduced during the reaction?

NADH.

p.86
Digestive Disorders and Malabsorption Issues

What is arsenate poisoning in the context of glycolysis?

It bypasses the synthesis of 1,3-BPG, depriving the cell of energy normally obtained from glycolysis.

p.80
Regulation of Glycolysis

What primarily controls the rate of glycolysis?

Allosteric regulation of three key enzymes: hexokinase, PFK-1, and pyruvate kinase.

p.89
Metabolism: Catabolism and Anabolism

What is the primary role of 2,3-BPG in RBCs?

To increase oxygen delivery by enabling the unloading of oxygen from oxyhemoglobin.

p.87
Metabolism: Catabolism and Anabolism

How many molecules of 1,3-BPG are formed from each glucose molecule?

Two molecules of 1,3-BPG.

p.89
Metabolism: Catabolism and Anabolism

What enzyme converts 1,3-BPG to 2,3-BPG in RBCs?

Bisphosphoglycerate mutase.

p.80
Regulation of Glycolysis

What inhibitors affect hexokinase?

G-6-P.

p.93
Metabolism: Catabolism and Anabolism

What is the purpose of fluoride/oxalate bottles in blood collection?

To preserve the carbons of glucose for estimation.

p.57
Metabolism: Catabolism and Anabolism

Which metabolic pathway is responsible for the synthesis of glucose from non-carbohydrate precursors?

Gluconeogenesis.

p.67
Carbohydrate Digestion and Absorption

What is the role of ATP in glucose phosphorylation?

ATP is used to phosphorylate glucose, converting it to glucose-6-phosphate.

p.89
Metabolism: Catabolism and Anabolism

How is 2,3-BPG converted back to an intermediate in glycolysis?

It is hydrolyzed by a phosphatase to 3-phosphoglycerate.

p.87
Metabolism: Catabolism and Anabolism

What does the kinase reaction replace regarding ATP usage?

It replaces the two ATP molecules consumed by the earlier formation of glucose 6-phosphate and fructose 1,6-bisphosphate.

p.86
Metabolism: Catabolism and Anabolism

What happens to the aldehyde group of glyceraldehyde 3-phosphate during oxidation?

It is oxidized to a carboxyl group, coupled with the attachment of Pi.

p.57
Metabolism: Catabolism and Anabolism

Which metabolic pathway synthesizes fatty acids?

Fatty acid synthesis.

p.57
Metabolism: Catabolism and Anabolism

Which cycle is responsible for converting ammonia into urea for excretion?

Urea cycle.

p.93
Metabolism: Catabolism and Anabolism

How does fluoride affect enolase?

Fluoride inhibits enolase.

p.87
Metabolism: Catabolism and Anabolism

Where does the energy for ATP production come from in substrate-level phosphorylation?

From a high-energy substrate rather than from the electron transport chain (ETC).

p.80
Regulation of Glycolysis

What hormone inhibits glycolysis?

Glucagon, by repressing the synthesis of F-2,6-bisP.

p.57
Metabolism: Catabolism and Anabolism

What is the process of breaking down and synthesizing amino acids called?

Amino acid degradation and synthesis.

Study Smarter, Not Harder
Study Smarter, Not Harder