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33 Cards in this Set

  • Front
  • Back
metabolism

-all of the reactions in the body that require energy transfer


-2 kinds: Anabolism and Catabolism

anabolism
-requires input of energy to synthesize larger molecules
catabolism
-releases energy by breaking down large molecules into smaller molecules
Catabolism drives anabolism
-catabolic reactions that break down glucose, fatty acids, and amino acids serve as energy sources for the anabolism of ATP
aerobic cellular respiration

-complete catabolism of glucose requires oxygen as final electron receptor


-breaking down glucose req many ensymaticly catalized steps- first are anaerobic

glycolysis
-conversion of glucose into two molecules of pyruvic acid
glycogenesis
-production of glycogen mostly in skeletal muscles and liver
glycogenolysis

-hydrolysis breakdown of glycogen


=glucose 6 phosphate for glycolysis(in liver only) or free glucose secreted in blood

gluconeogenesis
-production of glucose from noncarb molecules incl lactic acid and amino acids primarily in liver
aerobic respiration of glucose

3 steps


1.Glycolysis-occurs in cytoplasm;anaerobic


2.Citric Acid cycle(Krebs)-occurs in matrix of mitochondria;aerobic


3.electron transport-occurs on cristae of mitochondria inner membrane;aerobic


C6H12O6 + O2 >6 CO2 + 6 H2O + ATP

glycolysis

-first step in catabolism of glucose


occurs in cytoplasm of cell


-glucose splits into 2 pyruvic acid molecules

glycolysis formula

-6-carbon sugar >2 molecules of 3-carbon pyruvic acid


-C6H12O6>2 molecules C3H4O3


-Note loss of 4 hydrogen ions. These were used to reduce 2 molecules of NAD.


2NAD + 4H+ > 2NADH + H+ (2NADH)

glycolysis

-Glucose + 2 NAD + 2 ADP + 2 Pi> 2 pyruvic acid + 2 NADH + 2 ATP


- pyruvic acid will be used in a metabolic pathway called the citric acid cycle, and the NADH will be oxidized to make ATP.

Lactic Acid

-When there is no oxygen to complete the breakdown of glucose, NADH has to give its electrons to pyruvic acid


-results in the reformation of NAD and the conversion of pyruvic acid to lactic acid


-anaerobic metabolism/lactic fermentation

Lactic Acid Pathway

-Yields a net gain of 2 ATP


- Muscle cells can survive for awhile without oxygen by using lactic acid fermentation.


-RBCs can only use lactic acid fermentation because they lack mitochondria

Citric Acid Cycle

-TCA


-Acetyl CoA combines with oxaloacetic acid to form citric acid


-Citric acid starts the citric acid cycle and ‘moves’ through a series of reactions to produce oxaloacetic acid again



process of citric acid cycle

-One guanosine triphosphate (GTP) is produced, which donates a phosphate group to ADP to form ATP


-Three molecules NAD are reduced to NADH.-One molecule FAD is reduced to FADH2


-These events occur for each acetic acid, so it happens twice for each glucose molecule

For each glucose TCA

For each glucose:


-6 NADH


-2 FADH2


-2 ATP


-4 CO2

Electron transport and oxidative phosphoration

-In the folds or cristae of the mitochondria are molecules that serve as electron transporters. -Include FMN, coenzyme Q, and several cytochromes


-accept electrons from NADH and FADH2.


- hydrogens are not transported with the electrons.


-Oxidized FAD and NAD are reused

electron transport chain

-Electron transport molecules pass electrons down a chain, with each being reduced and then oxidized.


-exergonic reaction, and the energy produced is used to make ATP from ADP


-ADP is phosphorylated= oxidative phosphorylation.


-Process is not 100%; difference is released as heat

oxidative phosphorylation

1.Electron transport fuels proton pumps, pump H+ from the mitochondrial matrix to space between inner& outer membranes


2.sets up huge conc gradient betw membranes


3.H+ can only move thru inner membrane thru respiratory assemblies


4.Movement of H+ across membrane provides energy to enzyme ATP synthase converts ADP to ATP

oxygen

-Final electron acceptor


- citric acid cycle and electron transport require it to continue


-Water is formed in the following reaction:


O2 + 4 e- + 4 H+ >2 H2O

ATP

-Direct (substrate-level) phosphorylation in glycolysis and the citric acid cycle yields 4 ATP.


-Oxidative phosphorylation in electron transport yields varying amounts of ATP, depending on the cell and conditions.

ATP yields

-each NADH yields 3 ATP and each FADH2 yields 2 ATP; actual yield is 2.5 ATP per NADH and 1.5 ATP per FADH2


-36-38 per glucose, actual is 30-32 ATP per glucose; energy is needed to move ATP from mitochondria to cytoplasm

glycogenesis

-Cells can’t store much glucose because it will pull water into the cell via osmosis.


-Glucose is stored as a larger molecule called glycogen in the liver, skeletal muscles, and cardiac muscles.


-Glycogen is formed from glucose via glycogenesis

glycogenolysis

-When the cell needs glucose, it breaks glycogen down again.


-Produces glucose 1-phosphate


-Glycogen phosphorylase is the catalyst

glycongenolysis

-Glucose from glycogen is form glucose 1-phosphate, so cannot leave muscle or heart cells.

-liver has an enzyme called glucose 6-phosphatase that removes the phosphate so glucose can reenter the bloodstream


lipid and protein metabolism

-Lipids and proteins can also be used for energy via the same pathways used for the metabolism of pyruvic acid


-When more food energy is taken than needed for energy, we can’t store ATP for later


-glucose is converted into glycogen and fat, and ATP production is inhibited

lipid metabolism

-ATP levels rise after an energy-rich meal, production of ATP is inhibited

Glucose doesn’t complete glycolysis to form pyruvic acid, and acetyl CoA already formed is joined together to produce a variety of lipids, including cholesterol, ketone bodies, and fatty acids

-

lipogenesis
-Fatty acids combine with glycerol to form triglycerides in the adipose tissue and liver
fatty acid as energy source

-β-oxidation: Enzymes remove acetic acid molecules from fatty acids to form acetyl CoA.


-For every 2 carbons on the fatty acid chain, 1 acetyl CoA can be formed.Each acetyl CoA >10 ATP + 1 NADH + 1 FADH2

Amino acid metabolism

-Proteins provide nitrogen for the body


-from dietary proteins needed to replace proteins in the body


-If more consumed than needed,excess used for energy or converted into carb or fat


-Our bodies can make 12 of the 20 from other molecules. Eight of them (9 in children) must come from the diet (ess.)

energy sources

-Glucose and ketone bodies come from the liver-Fatty acids come from adipose tissue


-Lactic acid and amino acids come from muscle


and organs