Metabolism Flashcards

1
Q

How is energy stored in ATP

A

Through the phosphoanhydride bonds. When the bonds are broken the energy is released.

If more energy is needed to be released we break the phosphoanhydride bonds between the beta and alpha bonds releasing ppi ( pyrophosphate).

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2
Q

Substrate- level phosphorylation

A

The transfer of a phosphate from a molecule to ATP.

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3
Q

How is energy stored in NADH and FADH2?

A

Through their reduction potentials

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4
Q

Secondary v. Primary active transport

A

Secondary transport is when the energy released from a molecule moving down it’s concentration gradient powers the movement of molecule against their concentration gradients.

Primary active transport is when the hydrolysis of ATP moves molecules against their concentration gradients.

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5
Q

Catabolism v. Anabolism

A

Catabolism is the breakdown of molecules whereas anabolism is the creation of larger molecules from metabolites.

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6
Q

What happens when the free energy of a reaction is large?

A

Not all the energy is captured and therefore some of it is wasted and the reaction is irreversible.

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7
Q

Futile cycle

A

Unregulated recycling of substrates between catabolic and anabolic reactions .

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8
Q

Purpose of glucose in the cell

A

Primary energy source for the cell

it’s skeleton can be used to form other molecules
it’s byproducts can be used to protect cell against oxidative damage to build other molecules.

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9
Q

Net products of glycolysis

A

for every 1 molecule of glucose you get 2 ATP, 2 NADH, and 2 pyruvate

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10
Q

Energy- investment phase v. Energy- payoff phase of glycolysis

A

Energy- investment phase is the first five steps of glycolysis and uses ATP.

The energy- payoff phase is the last steps of glycolysis and is where the lost is recuperated and we gain net energy products.

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11
Q

Incorporation of mannose into the glycolytic cycle

A

Mannose is phosphorylated by hexokinase into mannose-6-phosphate.

Mannose-6- phosphate is converted to fructose-6-phosphate by phosphomannose isomerase.

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12
Q

Incorporation of fructose into the glycolytic cycle

A

Fructose is converted to fructose-6-phosphate by hexokinase.

In the liver it’s converted to fructose-1-phosphate by fructokinase. Fructose-1-phosphate is then converted to DHAP and glyceraldehyde via aldolase. Glycerol is converted to glyceraldehyde-3- phosphate by triose. These then go on to glycolysis.

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13
Q

Incorporation of galactose into the glycolytic cycle

A

Galactokinase converts galactose to galactose-1-phosphate. GALT transfers UDP from UDP- glucose to galactose creating UDP- galactose and glucose-1-phosphate.

The enzyme phosphoglucomutase converts the glucose-1-phosphate to glucose-6- phosphate.

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14
Q

Process of gluconeogenesis and the enzymes involved

A

Primarily happens in the liver and serves to make glucose via the reverse of glycolysis, using enzymes to bypass the irreversible steps.

pyruvate carboxylase converts pyruvate to oxaloacetate. Phosphenolpyruvate carboxykinase (PEPCK) converts oxaloacetate into phosphenolpyruvate.

fructose-1,6-bisphosphatase converts fructose-1,6- bisphosphate to fructose-6- phosphate.

glucose-6-phosphatase converts glucose-6-phosphate to phosphate.

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15
Q
A
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16
Q

How can alanine be ushered into gluconeogenesis?

A

By converting alanine to pyruvate via deamination.

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17
Q

How does lactic acid fermentation and gluconeogenesis are linked?

A

During lactic acid fermentation pyruvate is converted to lactate but in the liver it’s reversed so pyruvate can enter gluconeogenesis.

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18
Q

How can catabolism of triacylglycerol participate in gluconeogenesis?

A

Glycerol is produced by the breakdown of triacylglycerol which is phosphorylated to glycerol-3-phosphate. This is then oxidized to DHAP which can enter glycolysis directly.

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19
Q

Purpose of the Cori cycle?

A

It’s a method that allows humans to thrive in diverse environments.

In systems in hypoxic environments or that lack mitochondria lactic acid fermentation creates lactate which is then exported to the blood and to the liver where it’s converted back to pyruvate where it undergoes gluconeogenesis. The glucose is released by the liver into the bloodstream where it’s taken up by muscles that need it.

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20
Q

How does glycolysis and gluconeogenesis regulate in the cell?

What’s unique about this regulation in the liver?

A

Through allosteric inhibition of the enzymes that catalyze irreversible steps.

In the liver glucokinase is used instead of hexokinase and so it doesn’t participate in allosteric inhibition because it acts as a glucose sensor.

21
Q

How is pyruvate kinase inhibited?

A

Largely through it’s products. It can be inhibited by pyruvate, ATP, long chain fatty acids, or acetyl-coa.

22
Q

How is PFK-1 inhibited?

A

It’s inhibited by ATP (meaning the cell has enough energy and glycolysis doesn’t need to continue).

Activated by ADP and AMP. When the levels rise it relieves the inhibition acted on by ATP.

It’s also inhibited by citrate which is shuttled from the mitochondria in times of energy excess.

23
Q

Role of fructose-2,6- bisphosphate

A

It’s the most potent activator of PFK-1.

Phosphofructokinase-2 converts fructose-6- phosphate to fructose-2,6- bisphosphate and is converted to fructose-6- phosphate by fructose-2,6-phosphatase.

24
Q

Role of glucagon, insulin, and epinephrine in the liver?

A

Glucagon and insulin act on the liver on both cycles of glycolysis and gluconeogenesis.

GPCR acts on GPCR receptors and it’s effects are similar to glucagon.

25
Q

How does glucagon and insulin regulate glycolysis and gluconeogenesis?

A

Glucagon activates PKA which phosphorylates many enzymes involved in those processes.
Glucagon phosphorylates PFK-1 inhibiting it and activates FBpase-2 ( both on same proteins). This makes glycolysis slow down. PKA phosphorylates pyruvate kinase further slowing down the cycle.

Insulin dephosphorylates PKA and so prevents phosphorylation of enzymes involved in those processes.

Insulin dephosphorylates PFK-2 which acts of PFK-1 stimulating the enzyme. It inhibits FBpase-1 which prevents gluconeogenesis which prevents the futile cycle.

26
Q

Purpose of glycogen formation

A

Allows the cell to use glucose quickly without disrupting the osmolarity of the cell

27
Q

Describe the process of glycogenesis? What’s the first step of UDP- glucose formation?

A

Glycogenesis is the process of creating glycogen as a easily accessible form of glucose storage.

Glucose is incorporated into the cell and is phosphorylated to glucose-6- phosphate by hexokinase. Phosphoglucomutase then converts it to glucose-1- phosphate by moving phosphate from carbon 6 to carbon 1 thereby activating the reducing end.

UDP is transferred from UTP via UDP- glucose phosphorylase to carbon 6 of the glucose-1- phosphate, this creates UDP-glucose.

Reaction with phosphoglucomutase is reversible and reaction with UDP- glucose phosphorylase is irreversible.

28
Q

Role of glycogen synthase

A

Enzyme that breaks apart the UDP- glucose and adds the glucose to the nonreducing end of the glycogen chain via an alpa-1,4- glycosidic bond.

Net gain is 1 UTP which is equivalent to 1 ATP.

29
Q

Role of glycogenin in glycogenesis?

A

It’s the core of the glycogen chain and catalyzes the attachment of the glycogen chains to itself via an alpha-1,4- tyr glycosidic bonds.

30
Q

Role of glycogen branching enzyme

A

It serves to form branches of glycogen chains by removing an oligosaccharide from the main chain and add it to a carbon-6 of a more interior sugar via an alpha-1,6- glycosidic bond.

This creates an additional nonreducing end which glycogen synthase can add on more glucose monors.

31
Q

What is the purpose of glycogenolysis?

A

It serves to break apart the glucose subunits from the glycogen so it can be used for energy.

Instead of hydrolyzation to break apart the glucose we use phosphorolysis.

32
Q

Role of glycogen phosphorylase?

A

It breaks apart the glucose from the glycogen chain in the form of glucose-1- phosphate (at the alpha-1,4- glycosidic bond). Then phosphoglucomutase converts it to glucose-6- phosphate.

33
Q

What releases glucose-6- phosphate into the bloodstream during glycogenolysis?

A

Glycogen phosphatase removes the phosphate.

34
Q

Role of debranching enzyme?

A

Glycogen phosphorylase cannot break apart the bonds at the branching points and the linear chains past four oligosaccharides.

Debranching enzyme removes a trisaccharide from the branch point and attaches it to the linear chain so that glycogen phosphorylase can continue phosphorolysis. Alpha-1,6- glucosidase catalyzes the formation of the alpha-1,4- glycosidic bond via hydrolyzation. We get a free glucose as a result.

35
Q

What is the rate-limiting step in glycogenolysis?

A

Phosphorolysis. Regulated by allosteric and covalent means.

36
Q

What is the general trend on PKA phosphorylation for glycogenolysis and glycogenesis?

A

PKA phosphorylation activates proteins involved in glycogenolysis while it inhibits enzymes involved in glycogenesis.

37
Q

Role of epinephrine and glucagon bind to GPCR? Insulin?

A

When epinephrine and glucagon it leads to glycogenolysis.

When insulin binds to receptor tyrosine kinase it leads to glycogenesis.

38
Q

How is a futile cycle between regulated between glycogenesis and glycogenolysis?

A

Signals are removed via protein phosphatases.

39
Q

Describe each complex of the electron transport chain.

A

Complex 1 ( NADH- COQ Oxidoreductase)- iron sulfur core transfers electrons from NADH to FMN ( flavin mononucleotide) and then to Coq to form CoQH2. 4 H+ are released

Complex 2 ( Succinate- CoQ oxidoreductase)- iron sulfur group transfers electrons from succinate to FAD to succinate and from succinate to CoQ to form CoQH2. No H+ are released.

Complex 3 (CoQH2 cytochrome C Oxidoreductase) - iron sulfur group transfers electrons from CoQH2 to heme and from heme it enters the Q cycle to form cytochrome C. 4 H+ are released.

Complex 4 ( cytochrome c oxidoreductase)- Cu2+ and cytochromes transfer electrons in form of H+ from cytochrome C to oxygen. Releases 2 protons. Also forms water.

40
Q

Glycerol-3- phosphate shuttle

A

Method to shuttle electrons in form of NADH across membrane for electron transport chain.

NADH gives electrons to DHAP to glycerol-3- phosphate. From here electrons are transferred to FAD which forms FADH2.

41
Q

Malate- aspartate shuttle

A

Method to shuttle electrons in form of NADH across membrane for electron transport chain.

Electrons are transferred from NADH to oxaloacetate to form malate. The electrons are then transferred to NAD+ forming NADH.

42
Q

Proton- motive force

A

The electrochemical gradient caused by the electron transport chain shuttling electrons across the membrane.

Protons are in the intermembrane space and flow down their concentration gradient through the ATP Synthase.

F0 region is the region where the H+ flow down their concentration gradients and the F1 region is where ADP + Pi is combined to form ATP.

43
Q

Chemiosmotic coupling

A

The coupling the H+ flowing down their gradients and the formation of ATP.

44
Q

Short- chain fatty acids v. Long - chain fatty acids

A

Short- chain fatty acids can be directly absorbed whereas long- chain fatty acids must be packaged into chylomicrons.

45
Q

What’s the overall purpose of the pentose phosphate pathway?

A

Creates pentose phosphate which is used to make nucleotides and nucleosides.

NADPH whose reducing potential is used by the cell for energy. Also used against oxidative damage.

46
Q

What is the oxidative phase of the pentose phosphate pathway?

A

Oxidative phase and non-oxidative phases work independently and can make pentose phosphate pathway but also work together ( one makes it while the other uses it). Characteristic

The end product of the oxidative phase is ribulose-5- phosphate which exists in equilibrium with ribose-5- phosphate and xyulose-5- phosphate.

47
Q

Reversible v. Irreversible steps of the pentose phosphate pathway?

A

All steps of the oxidative phase are irreversible.

All steps of the non-oxidative phase reversible.

48
Q

What are the end products of non-oxidative phase?

A

The non-oxidative phase creates pentose phosphates but cannot make NADPH.

This phase can recycle carbons of pentose phosphates back to glycolysis.

49
Q

What’s the benefit having both phases of pentose phosphate pathway independent of each other?

A

The cell can control if it wants to make both pentose phosphate and NADPH or just NADPH.