Weekly Study Guide 5
Last revised: Tuesday, October 1, 2002

A. Overview for this week.

This week’s main focus is metabolism, which can be defined as “the sum of all chemical reactions in a cell”. A broad topic, surely! Metabolism can be separated into two broad categories: Anabolism = reactions that build new molecules needed for cell growth and maintenance, and Catabolism = reactions by which cells extract the energy needed to make anabolic reactions proceed exergonically.

ATP is a key molecule in metabolism. Phosphate groups are readily released from ATP (and ADP), along with lots of energy. Most anabolic reactions are coupled to an ATP reaction – we will see this in more detail when we study protein synthesis in a couple of weeks. Our main focus here will be on the resulting problem of regenerating new ATP supplies. Every breath we take, for example, has only one metabolic role – to bring in new Oxygen molecules used in ATP synthesis, and to get rid of CO2 molecules produced as a byproduct of ATP synthesis.

Key concepts for this week: ATP, Oxidation, Glycolysis, Fermentation, Respiration.

Our second focus this week will be to examine how cells respond to specific signals. Each cell in a multicellular organism is, in many ways, an island. Its membrane barrier insulates it from the activities of surrounding cells, and each cell is entirely responsible for expressing selected genes and controlling its biochemical and structural activities. These activities must be regulated with great precision in order for the organism to function, and cells are constantly exposed to chemical signals that arrive in the form of hormones, neutrotransmitters, and other signals to change behavior minute by minute. We shall study in some detail the marvelous machinery by which these chemical signals are detected, transduced, and amplified to create rapid and dramatic changes inside the receiving cell.

B. Lecture Topics and Assigned Reading.

Fri. 27 Sept.
Metabolism
Review ATP
Ch. 9
Ch. 6 (pp. 94-96)
Mon. 30 Sept.
Metabolism
Ch. 9
Wed. 2 Oct.
Metabolism
Cell Communication
Ch. 9
Ch. 11

C. Take the online Self-Quizzes associated with these lectures.

See the link at bottom of each page of lecture notes.

D. Visit Campbell Website. Do assigned activities.

Ch. 9 Ch. 11
  • Activity 11A: Activation of Cell Signalling (4 pages)
  • Activity 11B: Receptors (1 page)
  • Activity 11C: Signal Transduction Pathways (5 pages)
  • Activity 11D: Cellular Responses (1 page)
  • Activity 11E: Build a signal pathway (5 pages) – build at least one pathway using a G-protein transducer (either screen 2 or screen 4) – Strongly recommended!!
E. Take Online WebCT Quiz 5 – covers text Chapters 9 and 11.

Online quiz 5 will become available at 8 a.m. on Tuesday, Oct. 1, and remain available until 8 a.m. on Wednesday, Oct. 2. At some time during this 24 hour time window you must log in to your WebCT account and take the quiz. Quiz deadlines are firm and will not be extended for any reason, so please don’t ask – consult the syllabus if you have any questions about timing, grades, and number of quizzes you are required to take.

You will be allowed 12 minutes to complete the 10 questions. The quiz is “open book” – you are allowed to use your text and notes. However, you must take the quiz by yourself, not with the assistance of another person. Once you have completed your quiz, you will be able to see your grade. If you wish to retake a quiz on this material, you may do so once, as long as you are still within the 24 hour time window – in that case, your quiz grade will be the higher of the two quiz grades.

Each quiz is generated randomly from a large database of questions. As a result, no two quizzes will be identical, and it is quite possible that many if not all of the questions you would see in comparing two different quizzes will be entirely different. Each quiz will cover only the material from the assigned chapters – e.g., Quiz 5 will be based entirely of questions drawn from chapters 9 and 11 (more from 9, since this has more material).

F. Consult the study questions below as you read the text.

Chapter 9.
  1. Be able to recognize the structure of ATP, ADP, and AMP (see fig. 6.8). Why is ATP so useful in cell metabolism?
  2. What are “redox reactions”? Why are they important in biology?
  3. Explain why removal of a hydrogen atom (H) is called an oxidation. Where’s the electron? (Hint: what is a hydrogen atom made of?)
  4. What is the difference between an electron carrier and a terminal electron acceptor? Give examples of each.
  5. What does NAD+ do in biological systems? Relative to other biological molecules, how much NAD+is there in a cell? Choose from: (a) a lot; (b) comparable to the concentration of amino acids; (c) extremely little. What happens to a cell when all its NAD+becomes reduced to NADH? How can the cell get more NAD+? What happens to the hydrogen atoms?
  6. Be familiar with the process by which cells break down glucose sugar (glycolysis followed by respiration). How much energy does this process yield aerobically? anaerobically? How efficient are these two processes?
  7. Where does glycolysis occur? What are the end products? How many oxidation reactions are involved?
  8. What does the TCA (Krebs) cycle accomplish? What is the starting material? What are the final products?
  9. How is a mitochondrion organized? Be able to identify the matrix, the cristae, and the intermembrane space in which H+ ions accumulate during proton gradient formation. What kinds of molecules make up the electron transport chain? Where do electrons entering this chain originate? Where do they end up?
  10. What is a proton gradient? How is it generated? Once made, how can a cell use it to make ATP? What is the role of ATP synthase?
  11. Note that the term “chemiosmosis” refers to the coupling of enzyme reactions to the generation of transmembrane proton gradient. Are the terms “chemiosmotic phosphorylation” and “oxidative phosphorylation” interchangeable?
  12. What is meant by the term “fermentation”? Identify two organisms that can ferment. Identify two characteristic fermentation products. Are these edible? Identify common food/beverage in which you would find each of these two products.
  13. Contrast fermentation with respiration in each of the following respects: (1) what happens to electrons in NADH? (2) how efficient is the process? (3) where do the electrons made available in oxidation reactions wind up?
Chapter 11.
  1. Give at least two examples of situations in which cells alter their activity in response to external signals.
  2. What does the term "signal transduction" mean? What are the 3 stages of cell signaling?
  3. We will concentrate on "G-proteins" as our major example of signal transduction mechanisms. Draw a diagram of a simple G-protein signal pathway, indicating how each of the following components is situated relative to the cell membrane: receptor protein, G protein, effector enzyme. What does the "G" stand for? Which of these components (receptor protein, G protein, effector enzyme) are allosteric proteins, capable of alternating between active ("on") and inactive ("off") configurations?
  4. How common are G-protein linked signaling pathways? Are they related to health/disease states?
  5. We won't have time to talk about tyrosine-kinase receptors and ion-channel receptors (pp. 202-204 in text) during class.
  6. What is a protein kinase? What result does it bring about?
  7. Many signaling pathways involve multiple kinases, each of which activates another kinase, which activates yet another, etc., until the final target enzyme is activated. What is the advantage of such a scheme?
  8. What is a "second messenger"? How does it differ from a "first messenger"?
  9. What is cyclic AMP? [Note that the enzyme "adenyl cyclase", which makes cyclic AMP, is often the membrane-bound target of a G-protein.] What role does cyclic AMP perform in most cells? Be able to recognize the structure of cyclic AMP (see Fig. 11.12)
  10. Ca++ ion is widely used as a second messenger that controls different events than those controlled by cAMP. How does the intracellular and extracellular concentration of Ca++ compare? On which side of the cell membrane is most Ca++? What happens inside a cell when Ca++ suddenly increases? Examine Figs. 11.14 and 11.15 to see how Ca++ can serve to regulate various cell activities.
  11. What is the role of inositol triphosphate?


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