Erstellt von Hannah Tribe
vor mehr als 10 Jahre
|
||
Frage | Antworten |
What is catabolism? | Breakdown of complex molecules into smaller ones, releasing energy |
What is anabolism? | Sythesis of new complex molecules from its smaller constituents, using energy |
Why should we study metabolism? | Often the basis of disease - therefore we need to know how the body NORMALLY uses nutrients. In a disease state, metabolism can change (e.g. cancer) |
The body needs to re-synthesise ____ from ____ to meet demand, as the body only has ____g - this is one fifth of the required amount during exercise. | ATP, ADP, 100 |
How is most ATP in the body synthesised? | Through oxidative phosphorylation in the mitochondria |
Name 4 major oxidative pathways | 1. glycolysis 2. fatty acid oxidation 3. TCA cycle (Krebs cycle) 4. Electron transport chain and oxidative phosphorylation |
Glycolysis is an _________ process converting _________ to 2 x _________. It occurs in the ___________ | anaerobic, glucose, pyruvate, cytoplasm |
1. Glucose is _________ using ____ by __________ (or in the liver, ___________). This maintains a _______ _______. | phosphorylated, ATP, hexokinase, glucokinase, concentration gradient. |
2. G-6-P is then converted to _________ __ ________ and then phosphorylated again using ____ by _____________________. This is the ____ _______ ____ of glycolysis. | Fructose 6 phosphate, ATP, phosphofructokinase, rate limiting step |
3. The resulting ________ __ __ _________ splits into 2 x 3 carbon compounds, which undergo dephosphorylation to produce _________. | fructose 1,6 bisphosphate, pyruvate |
How many ATP molecules are used and gained in glycolysis, and what is the resultant net gain? | 2 used, 4 made = 2 gained |
How many molecules of NAD+ are used in glycolysis, and at what stage? | 2, in the conversion of the unstable 3 carbon compound to pyruvate. |
Which enzyme converts phosphoenol pyruvate to pyruvate? | Pyruvate kinase |
What inhibits the action of hexokinase? | G-6-P (it's own product) |
What inhibits the action of phosphofructokinase? | ATP, Citrate and H+ (low pH) = (the products of oxidative phosphorylation) |
What stimulates the action of phosphofructokinase? | AMP and Fructose 6 phosphate |
What inhibits the action of pyruvate kinase? | ATP |
How does ATP inhibit phosphofructokinase? | Lowers the affinity of PFK for fructose 6 phosphate |
What does inhibiting PFK lead to? | Build up of G-6-P and therefore also inhibition of hexokinase |
In the liver, there is _________ as well as hexokinase. It is not inhibited by a build up of ___ ___ ___ like hexokinase. | glucokinase, G-6-P |
In muscles and tumours, most energy is gained through glycolysis, which is ________. | anaerobic |
In anaerobic glycolysis in muscle and tumours, there needs to be a supply of NAD+ for formation of pyruvate. As there is no oxidative phosphorylation, where does it come from? | Pyruvate is converted to lactate, which also converts NADH to NAD+ which is used in the earlier stages of glycolysis. |
What are 2 dangers in a build up of lactate? | 1. Lactate is toxic - it must be broken down in the liver 2. It is acidic so causes fall in pH, which inhibits PFK |
Tumours exist in a _______ environment, which activates __ __ __ __. This stimulates ______ _______ to grow and an increase in ___________ _______ so tumours can overcome the usual regulatory processes and survive. | hypoxic, HIF1, blood vessels, glycolytic enzymes |
Apart from lactate, what is the other fate of pyruvate? | Acetyl CoA |
What is an advantage and disadvantage of this? | Advantage = yields more ATP Disadvantage = requires O2 |
Where does aerobic respiration take place? | The mitochondria |
Where does the TCA cycle take place? | Mitochondrial matrix |
Pyruvate is converted to ________ ___ in the presence of ______. It is a __ carbon compound, and the by-products of the reaction are ______ and ______ | Acetyl CoA, oxygen, 2, CO2, NADH |
What does Acetyl CoA react with on its entry to the TCA cycle? | Oxaloacetate (4C) |
What does this form? | Citrate (6C) |
Citrate undergoes 3 main reactions: 1. a 5C compound is obtained by the loss of ____ and _____. 2. a 4C compound is obtained by the loss of ____ and _____. 3. The 4C compound is converted back to oxaloacetate, losing a molecule each of ____, _____ and _____. | CO2 and NADH, CO2 and NADH, GTP, NADH and FADH2 |
Which enzyme helps convert pyruvate to Acetyl CoA? | pyruvate dehydrogenase |
How does it control entry to the TCA cycle? | Build up of NADH and Acetyl CoA causes production of a kinase which phosphosylates pyruvate dehydrogenase and makes it inactive |
When a muscle in exercising, there is increased ____. This stimulates a _________ enzyme which activates __________ __________ and allows conversion of ________ to ______ ___. | Ca++, phosphatase, pyruvate dehydrogenase, pyruvate, Acetyl CoA |
Which enzyme helps make citrate from acetyl CoA and oxaloacetate? | Citrate synthase |
Which enzymes helps convert citrate into the 5C compound (alpha-ketogluterate)? | Isocitrate dehydrogenase |
Which enzyme helps convert the 5C alpha ketogluterate into the 4C Succinyl CoA? | alpha ketogluterate dehydrogenase |
What is beriberi and what does it do? | Deficiency of vitamin B1 (thiamine). Thiamine is a prosthetic group in pyruvate and alpha-ketogluterate dehydrogenase - lack of these causes difficulties in generating energy from glucose so causes cardiac and neurological symptoms |
The FADH2 and NADH produced in the TCA cycle then goes to the ________ ___________ ________ to take part in the _________ __________ _________. | inner mitochondrial membrane, electron transport chain |
NADH is oxidised by _____ ____________ to give _____ + ____ + ___. The ______ enter the chain at complex I and travel through complexes II, III and IV, gradually losing ______. They are then used in a reduction reaction to form _____ at complex IV. | NADH dehydrogenase, NAD+, H+, 2e-, electrons, energy, H2O |
The FADH2 is oxidised by ________ ________ and the _______ enter the chain at complex II, taking the same course as those from NADH. | succinate dehydrogenase, electrons |
As the electrons pass along the chain, their ______ allows ___ ions across the membrane into the ____________ _____. This creates an ____________ _______. | energy, H+, intermembrane space, electrochemical gradient |
For each NADH molecule, ___ H+ ions are pumped out. For every FADH2 molecule, ___ H+ ions are pumped out. | 10, 6 |
____ ______ molecules exist on the membrane, which are molecular motors. They have a channel which allows ____ ions into the matrix down the __________ _________. This movement causes a rotation of part of the protein, and the synthesis of ____ from ___ + ___. | ATP synthase, H+, electrochemical gradient, ATP, ADP + Pi |
If the protein is uncoupled, ___ ions enter the matrix without synthesising ____. This generates _____ (used in newborns in brown fat molecules, as they cannot shiver). | H+, ATP, heat |
What is the main regulator of the electron transport chain? | ATP - when there is excess, electron flow can be scaled down, but when there is need for ATP it can be increased. |
What processes provide the energy for a 100m sprint? (4) | 1. ATP stores in muscle 2. Glycolysis 3. Glycogenolysis 4. Creatine phosphate + ADP --> ATP + creatine |
Why can creatine phosphate and glycolysis only be used for short bursts of exercise? | We only have small stores of creatine phosphate, and glycolysis produces lactate and therefore a fall in pH. |
What substances provide energy while running a marathon? | Glycogen and fatty acids |
In the fed state, where are most nutrients going? | 1. From gut to liver 2. From liver to adipose stores 3. From liver to muscle 4. From liver to kidneys 5. From liver to brain |
Which pathways are stimulated in the fed state? (3) | 1. Glycolysis 2. Glycogenesis 3. Lipogenesis |
Which pathways are inhibited in the fed state? (3) | 1. Glycogenolysis 2. Lipolysis 3. Gluconeogenesis |
Which molecules are abundant in the fed state? | 1. Glycogen 2. Fatty acids |
Which molecules are few in the fed state? | 1. Glucose 2. Ketones |
In starvation, where are most nutrients going? | 1. From muscle to liver 2. From adipose stores to liver 3. From liver to brain 4. From liver to kidneys |
Which pathways are stimulated in the starved state? (4) | 1. Glycogenolysis 2. Gluconeogenesis 3. Lipolysis 4. Ketogenesis |
What pathways are inhibited in the starved state? (3) | 1. Glycolysis 2. Glycogenesis 3. Lipogenesis |
Which molecules are abundant in the starved state? (2) | 1. Glucose 2. Ketones |
Which molecules are few in the starved state? (2) | 1. Glycogen 2. Fatty acids |
Möchten Sie mit GoConqr kostenlos Ihre eigenen Karteikarten erstellen? Mehr erfahren.