CH 10 Metabolism EXAM 1 Flashcards

Metabolism

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1
Q

Define metabolism.

A

Metabolism is the sum of all the chemical reactions in a cell.

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2
Q

Describe anabolism.

A

Anabolism is the buildup of small molecules to create large molecules, requiring energy (endergonic). Examples include photosynthesis, DNA synthesis, and protein synthesis.

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3
Q

Explain catabolism.

A

Catabolism is the breakdown of large molecules into small molecules, releasing energy (exergonic). Examples include glycolysis and the Krebs cycle.

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4
Q

How do anabolism and catabolism differ?

A

Anabolism involves the buildup of small molecules into large molecules and is endergonic, while catabolism involves the breakdown of large molecules into small molecules and is exergonic.

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5
Q

What role do enzymes play in metabolism?

A

Enzymes are needed in both anabolism and catabolism as they speed up chemical reactions.

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6
Q

Describe dehydration synthesis.

A

Dehydration synthesis is a reaction that synthesizes a polymer by losing water, resulting in a longer polymer.

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7
Q

Explain hydrolysis.

A

Hydrolysis is a reaction that breaks down a polymer by using water to break a bond, adding a water molecule in the process.

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8
Q

How does energy change in anabolism?

A

In anabolism, energy is required, making it an endergonic process.

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9
Q

How does energy change in catabolism?

A

In catabolism, energy is released, making it an exergonic process.

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10
Q

Describe hydrolysis in the context of polymers.

A

Hydrolysis is the process of breaking down a polymer by using a water molecule to break a bond.

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11
Q

How do enzymes affect chemical reactions in the body?

A

Enzymes speed up reactions by acting as organic catalysts and lowering the activation energy required for a chemical reaction.

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12
Q

Define the characteristics of enzymes.

A

Enzymes are primarily made of proteins, speed up reactions, lower activation energy, have a unique shape and specificity, possess an active site for substrate binding, are not used up in reactions, can be reused, can be regulated, and are subject to denaturation.

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13
Q

What is the role of an active site in an enzyme?

A

The active site is the region on the enzyme where the substrate binds, facilitating the chemical reaction.

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14
Q

Explain the difference between apoenzyme and holoenzyme.

A

An apoenzyme is the inactive protein component of an enzyme, while a holoenzyme is the active form, consisting of the apoenzyme plus a cofactor.

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15
Q

How do cofactors and coenzymes assist enzymes?

A

Cofactors are non-protein molecules, often metal ions like iron or zinc, that assist enzyme function, while coenzymes are organic molecules, often vitamins, that help enzymes work properly.

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16
Q

Describe how enzymes are generally named.

A

Enzymes are typically named based on their substrate or the reaction they catalyze, such as lactase for lactose or polymerase for DNA.

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17
Q

What are exoenzymes and endoenzymes?

A

Exoenzymes are enzymes that act outside the cell, while endoenzymes function within the cell.

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18
Q

How can enzymes be regulated?

A

Enzymes can be regulated through various mechanisms, including the presence of inhibitors or activators that affect their activity.

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19
Q

What happens to enzymes during denaturation?

A

During denaturation, enzymes lose their unique shape and functionality, often due to changes in temperature or pH.

20
Q

Describe the function of exoenzymes.

A

Exoenzymes are involved in breaking down large, complex molecules into smaller subunits that can be easily absorbed by the cell.

21
Q

Define endoenzymes and their role in cellular processes.

A

Endoenzymes are enzymes that function inside the cell, catalyzing reactions necessary for normal cellular processes.

22
Q

How do constitutive enzymes differ from regulated enzymes?

A

Constitutive enzymes, like those in glycolysis, are always present and ready to function, while regulated enzymes, such as the Lac operon in E. coli, are only produced or activated when needed.

23
Q

Explain feedback or end-product inhibition.

A

Feedback or end-product inhibition occurs when the final product of a metabolic pathway blocks an early reaction, shutting down the entire series to prevent waste.

24
Q

Describe competitive inhibition in enzyme activity.

A

In competitive inhibition, a normal substrate competes with a competitive inhibitor for the active site of an enzyme. If the substrate wins, the reaction proceeds; if the inhibitor wins, the reaction is blocked.

25
Q

What is non-competitive inhibition?

A

Non-competitive inhibition occurs when an inhibitor binds to an allosteric site on the enzyme, changing its shape and preventing the substrate from binding to the active site.

26
Q

Define an allosteric site in the context of enzyme function.

A

An allosteric site is a unique region of an enzyme, distinct from the substrate binding site, that influences the enzyme’s catalytic activity.

27
Q

How does penicillin act as a competitive inhibitor?

A

Penicillin acts as a competitive inhibitor by competing with the normal substrate for the active site of the enzyme, blocking the reaction.

28
Q

What role do heavy metal ions play in non-competitive inhibition?

A

Heavy metal ions act as non-competitive inhibitors by binding to the allosteric site of an enzyme, altering its shape and preventing substrate binding.

29
Q

Explain the significance of PFK in glycolysis regarding feedback inhibition.

A

PFK (phosphofructokinase) is an example of feedback inhibition, where the final product binds allosterically to inhibit an early step in glycolysis, preventing wasteful reactions.

30
Q

Describe protein denaturation and its effects on proteins.

A

Protein denaturation refers to the loss of a protein’s native structure, resulting in a biologically inactive protein.

31
Q

Identify factors that can lead to protein denaturation.

A

Factors that can denature a protein include physical and chemical conditions such as pH, salt concentration, temperature, and other environmental factors.

32
Q

Define oxidation and reduction in terms of electron transfer.

A

Oxidation is the loss of electrons, while reduction is the gain of electrons.

33
Q

Explain the role of coenzymes NAD+ and FAD in electron transfer.

A

NAD+ and FAD are involved in electron transfer by stripping glucose of electrons and adding hydrogen, forming NADH and FADH2, which transfer H+ electrons to the electron transport system to produce ATP.

34
Q

How does ATP function as an energy molecule?

A

ATP is a good energy molecule because it packs a lot of energy, storing significant potential energy within the strong covalent bonds between its phosphate groups.

35
Q

Differentiate between substrate-level phosphorylation and oxidative phosphorylation.

A

Substrate-level phosphorylation is less efficient and involves directly transferring a phosphate group from a high-energy substrate molecule to ADP to produce ATP, as seen in glycolysis and the Krebs cycle.

36
Q

Describe the process of oxidative phosphorylation.

A

Oxidative phosphorylation uses the energy from electron transfer along the electron transport chain to create a proton gradient, which drives ATP synthesis through ATP synthase. It requires oxygen.

37
Q

Define glycolysis and its key characteristics.

A

Glycolysis is a metabolic process that starts with glucose (a 6-carbon molecule) and occurs in the cytoplasm. It produces a net of 2 ATP and 2 NADH, is anaerobic, and results in 2 pyruvate. It involves substrate-level phosphorylation.

38
Q

How many ATP and NADH are produced in glycolysis?

A

Glycolysis produces a net of 2 ATP and 2 NADH.

39
Q

Where does glycolysis occur in the cell?

A

Glycolysis occurs in the cytoplasm.

40
Q

What is the end product of glycolysis?

A

The end product of glycolysis is 2 pyruvate.

41
Q

Explain the transition reaction and Kreb’s cycle.

A

The transition reaction and Kreb’s cycle start with pyruvate and occur in the mitochondria. They produce a net of 2 ATP and 8 NADH, and involve substrate-level phosphorylation.

42
Q

How many ATP are produced in the transition reaction and Kreb’s cycle combined?

A

The transition reaction and Kreb’s cycle combined produce a net of 2 ATP.

43
Q

What type of phosphorylation occurs during glycolysis?

A

Glycolysis involves substrate-level phosphorylation.

44
Q

How many NADH are produced in the transition reaction and Kreb’s cycle?

A

The transition reaction and Kreb’s cycle produce a total of 8 NADH.

45
Q

Where does the transition reaction and Kreb’s cycle take place?

A

The transition reaction and Kreb’s cycle take place in the mitochondria.

46
Q

What is the starting material for the transition reaction?

A

The starting material for the transition reaction is pyruvate.

47
Q

Describe the role of oxygen in oxidative phosphorylation.

A

Oxygen acts as the final electron acceptor in oxidative phosphorylation.