Chapter 25 Flashcards
Metabolism
All the chemical reactions that occur in the body
Catabolism
Exergonic reactions that produce more energy than they consume releasing the chemical energy stored in organic molecules
Anabolism
Chemical reactions that combine simple molecules and monomers to form the bodies complex structural and functional components; endergonic reactions Consuming more energy than they produce
What happens to the energy released in catabolism?
40% is used for cellular functions
The rest is converted to heat which helps maintain normal body temperature
Oxidation
Removal of electrons from an atom or molecule the result being a decrease in the potential energy of the atom or molecule
Dehydrogenation reactions
The loss of hydrogen atoms, which happens in most biological oxidation reactions
Reduction
Addition of electrons to a molecule, result in an increase in the potential energy of the molecules
What are the two enzymes that are commonly used by animal cells to carry hydrogen atoms?
- Nicotinamide adenine dinucleotide (NAD), Derivative of the B vitamin niacin
- Flavin adenine dinucleotide (FAD), Derivative of B2 (riboflavin)
Oxidation-reduction or redox reactions are what?
Paired reactions that are coupled such as: When one substance is oxidized (exergonic reaction) another is simultaneously reduced
Phosphorylation
The addition of a phosphate group to a molecule which increases its potential energy
What are the three mechanisms of phosphorylation that organisms use to generate ATP
- Substrate level phosphorylation
- Oxidative phosphorylation
- Photophosphorylation
Substrate level phosphorylation
Generate ATP by transferring a high energy phosphate group from an intermediate phosphorylated metabolic compound-a substrate-directly to ADP. in human cells this process occurs in the cytosal
Oxidative phosphorylation
Removes electrons from organic compounds and passes them through a series of electron acceptors called electron transport chain, to molecules of oxygen. this process occurs in the inner mitochondrial membrane of the cells
Photophosphorylation
Occurs only in the chlorophyll-containing plant cells or in certain bacteria that contain other light- absorbing pigment
What is the body’s preferred source for synthesizing ATP
Glucose
What are the different fates of glucose?
- ATP production - Body cells that require immediate energy glucose is oxidized to produce ATP
- Amino acid synthesis - Cells throughout the body can use glucose to form several amino acids which can then be incorporated into proteins
- Glycogen synthesis - hepatocytes and muscle fibres can perform glycogenesis in which hundreds of glucose monomers are combine to form the polysaccharide glycogen
- Triglyceride synthesis - When glycogen storage areas are filled up hepatocytes can transform the glucose to glycerol and fatty acids that can be used for lipogenesis the synthesis of triglycerides, triglycerides are then deposited in adipose tissue which has virtually unlimited storage capacity
What are the four sets of reactions in cellular respiration?
- Glycolysis - in which one glucose molecule is oxidized and then two molecules of pyruvic acid are produced the reactions also produce two molecules of ATP in to energy containing NADH + H+
- Formation of acetyl Coenzyme A - A transition step that prepares pyruvic acid for entrance into the Krebs cycle also produces energy containing NADH + H+ plus carbon dioxide
- Krebs cycle reactions these reactions oxidize acetyl CoA and produce CO2, ATP, NADH + H +, and FADH2
- Electron transport chain reactions - these reactions oxidize NADH + H+ and FADH2 and transfer the electrons through a series of electron carriers
Aerobic
With oxygen
Anaerobic
Without oxygen
Aerobic respiration
Reactions that require oxygen such as the Krebs cycle and electron transport chain
Glycolysis does not require oxygen which makes it what kind of reaction?
It can occur under aerobic or anaerobic conditions
Anaerobic glycolysis
When glycolysis occurs by itself under anaerobic conditions
Glycolysis
Chemical reactions split a six carbon molecule of glucose into two 3 carbon molecules of pyruvic acid, Consumes to ATP molecules it produces for ATP molecules for a net gain of two ATP molecules for each glucose molecule that is oxidized
What is the fate of pyruvic acid?
- If oxygen is scarce, Then pyruvic acid is reduced via an anaerobic pathways by the addition of two hydrogen atoms to form lactic acid. Lactic acid rapidly diffuses out of the cell and enters the blood the hepatocytes remove lactic acid from the blood and convert it back to pyruvic acid
- In aerobic conditions most cells convert pyruvic acid to acetyl coenzyme A, this molecule links glycolysis which occurs in the cytosol with the Krebs cycle which occurs in the matrix of the mitochondria pyruvic acid enters the mitochondrial matrix with the help of a special transporter protein
How can red blood cells produce ATP because they lack mitochondria?
The only way for red blood cells to produce ATP because their lack of mitochondria is through glycolysis
Coenzyme A
Derived from pantothenic acid a B vitamin
Acetyl CoA
Formed when the acetyl group attaches to the Coenzyme A After pyruvic acid has undergone decarboxylation
Krebs cycle
Known as the citric acid cycle, occurs in the matrix of mitochondria and consists of a series of oxidation reduction reactions and decarboxylation reactions that release CO2.
Electron transport chain
A series of electron carriers, integral membrane proteins in the inner mitochondrial membrane, cristae that increases its surface area accommodating thousands of copies of the transport chain in each mitochondrion each carrier in the chain is reduced as it picks up electrons and is oxidized as it gives up electrons
Chemiosmosis
The mechanism of ATP generation links chemical reactions with the pumping of hydrogen ions
Oxidative phosphorylation
Chemiosmosis and the electron transport chain together
What are the different electron carriers?
- Flavin mononucleotide (FMN) - Flavoprotein derived from riboflavin (vitamin B2)
- Cytochromes - Proteins with an iron containing group capable of existing alternately in a reduced form and then oxidized form
the cytochromes involved in the electron transport chain includes cytochrome b, cytochrome C1, cytochrome C, cytochrome a, and cytochrome a3 - Iron and sulphur centres - contain either two or four iron atoms bound to sulphur atoms that form an electron transfer centre within a protein
- Copper atoms - bound to two proteins in the chain also participate in electron transfer
- Coenzyme Q - is a non-protein low molecular weight carrier that is mobile in the lipid bilayer of the inner membrane
Glucose anabolism reactions
Glycogen and new glucose molecules from some of the products of protein and lipid breakdown
Glucose storage: glycogenesis
If glucose is not needed immediately for ATP production it combines with other molecules of glucose to form glycogen: the only stored form of carbohydrate in the body
insulin from pancreatic beta cells stimulates hepatocytes and skeletal muscle cells to carry out glycogenesis
The body can store 500 g of glycogen 75% in skeletal muscle fibres and the rest in the liver
Glucose release: glycogenolysis
When ATP is required glycogen stored in hepatocytes is broken down into glucose and released into the blood to be transported to cells where it will be catabolized by the process of cellular respiration
Formation of glucose from proteins and fats: gluconeogenesis
 When the glycerol part of triglycerides , lactic acid, and certain amino acids are converted in the liver to glucose it is called gluconeogenesis (when glucose is formed from non-carbohydrate sources)
Glucose is not converted back from glycogen but is newly formed
60% of the amino acids in the body can be used for gluconeogenesis
Stimulated by cortisol and by glucagon from the pancreas
Lipids
Nonpolar and therefore very hydrophobic
such as triglycerides
they do not dissolve in water
can combine with proteins produced by the liver and intestine which can create Lipo proteins
Lipoproteins
Spherical particles with an outer shell of proteins, phospholipids, and cholesterol molecules surrounding an inner core of triglycerides and other lipids
Each has a different function but all are essentially transport vehicles
Four major classes of lipoproteins are chylomicrons, Very low density lipoproteins (VLDL’s), low density lipoproteins (LDL’s), and high density Lipo proteins (HDL’s)
Apoproteins (apo)
Proteins in the outer shell of Lipo proteins that are designated by the letters a A, B, C, D, and E plus a number
they help solubilized the lipoprotein
Chylomicrons
form in mucosal epithelial
ells of the small intestine,
transport dietary (ingested) lipids to adipose tissue for storage.
They contain about 1-2% proteins, 85% triglycerides, 7% phospholipids, and 6-7% cholesterol, plus a small amount of fat soluble vitamins
Enter lacteals of intestinal villi and are carried by lymph intervenous blood and then into the systemic circulation
Very low density lipoprotein
form in hepatocytes,
contain mainly endogenous (made in the body) lipids.
Contain about 10% proteins, 50% triglycerides, 20% phospholipids,
d 20% cholesterol.
transport triglycerides synthesized in
patocytes to adipocytes for storage. Like chylomicrons, they lose
glycerides as their apo C-2 activates endothelial lipoprotein lipase,
the resulting fatty acids are taken up by adipocytes for storage
by muscle cells for ATP production.
As they deposit some of their
glycerides in adipose cells, VLDLs are converted to LDLs.