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Exam 4 Review Sheet AP Biology USE THIS SHEET AFTER YOU HAVE STUDIED AS A METHOD OF EVALUATING WHAT YOU STILL NEED TO WORK ON…OR DO WHAT YOU ARE LIKELY TO DO, WHICH IS WHATEVER YOU WANT. SERIOUSLY, STUDY FIRST AND THEN FLY THROUGH MOST OF THESE. Exam 4 will cover: Chapter 5 – ALL Make sure you look at ALL the questions in all chapters as well as bold words, headings and figures, the PowerPoint, and this review sheet. **I posted a macromolecule review chart online. CHAPTER 5 This question will be on the test: Explain The Central Dogma of molecular biology at the depth of information discussed in class starting with gene on a chromosome. Draw a picture to accompany your description. You must include the following terms: transcription, translation, mRNA, tRNA, ribosome, rRNA, nuclear pore, nuclear envelope, books, photocopy, library, chromosome, gene, RNA polymerase, amino acids, nucleus, mRNA genes, tRNA genes, rRNA genes, polypeptide. 1. What is meant by a macromolecule? List each and its general function in organisms. 2. Compare monomers to polymers. Know the terms dimer, trimer, tetramer, pentamer, etc… 3. Draw ATP as discussed in class and explain why this molecule has available energy. What is the role (function) of ATP in the cell? There are two obvious roles. 4. Explain the reactions in detail used to build (anabolic, synthesis) and break (catabolic, digest) the macromolecules. – you should be able to draw these using spheres. 5. You will need to be able to draw the monomers: any nucleotide, cysteine and two additional amino acids from the other two groups, glucose. You will also need to be able to draw dimers of these… 6. Compare and contrast monosaccharides, disaccharides and polysaccharides. In addition, be able to give examples of each. All together these are called what? 7. Be able to draw a chart indicating the various combinations of monosaccharides and their respective disaccharides (maltose, sucrose, lactose). 8. Be able to draw the ring structure of glucose as well as any glucose disaccharide like maltose. 9. Describe how two glucose molecules join together and the type of linkage that is formed. You should be able to draw this chemical reaction. 10. Describe the difference between alpha and beta glucose, and explain why these two different forms exist. 11. What does the word “carbohydrate” mean, literally and why do we use this word to describe the kinds of molecules that we do? 12. Discuss what is meant by the empirical formula [CH2O]n 13. Look at the structure of ANY monosaccharide. What functional group is attached to every carbon except one? What functional group is that other carbon a part of? 14. If I told you to draw C6H12O6, what would your response be to me… 15. Make sure you can identify different glycosidic linkages when looking at disaccharides. Ex. Beta 1,4 vs alpha 1,6 etc… 16. Compare and contrast the three polysaccharides discussed in class. Include their structures, why they have the same or different structures, where they are found in the world, their functions in organisms, how structure relates to function in this case, etc… 17. Cellulose is considered “fiber”. Like when the commercials on TV say that Cheerios is high in “fiber”. What is fiber? Why is cellulose called or at least part of what we call “fiber”? What is the benefit of insoluble fiber if we cannot digest it? 18. Why are most animals not able to hydrolyze cellulose, but can hydrolyze glycogen and starch when all three are just polymers of glucose? How are some animals able to hydrolyze cellulose? 19. Explain what happens to plant starch when you eat it (like if you eat a potato). 20. Why are some people considered to be lactose intolerant? What does this mean and why is it a problem? 21. Are glycogen, starch and cellulose the only three polysaccharides found in organisms? Explain. What is the fourth one discussed in class and where is it found? 22. What is the function of glucose? Basically, what do organisms use glucose monomers for? Why do we store them? Where do humans store them? 23. If there is too much glucose in your blood, how does your body handle this? Where does it end up? Where might this surge in glucose have come from? 24. For every polymer we eat (disaccharides, polysaccharides, polypeptides, etc…), we need to have a ___________________ somewhere in our digestive tract to hydrolyze it. This may seem obvious, but we eat cells (unless you are eating processed food, which case the cells have already been destroyed and broken apart) of other organisms. There we eat macromolecule or at least polymers for the most part. We need to hydrolyze them. Why? Why not just keep them together? 25. Describe structure of chitin and where it is found in nature. 26. Know the kingdoms with organisms that have cell walls and the composition of these walls in each: Monera (prokaryotes/bacteria) – peptidoglycan cell walls Fungi – chitin cell walls Plants – cellulose cell walls 41. What is the monomer of the protein, how many are there, what makes each of these different, how are they similar and how are they grouped (the three groups)? Can you draw any two of them yet and connect them via dehydration synthesis (condensation reaction)?...you need to be able to do this. 42. Where does the “amino acid” get its name from? 43. Why do I feel that proteins are the most important class of macromolecules (they are all important of course)? 44. Compare an amino acid, dipeptide, polypeptide, and protein. 45. Describe how a dipeptide is formed (Figure 3.13). What do we call the bond that links them? How is this analogous to what happens with carbohydrates? 46. Describe the three groups of amino acids. Which group has the acidic and basic ones? 47. What determines the structure of a particular protein? Explain why. Of course, the structure then determines the… 48. Explain why a change in the DNA might lead to problems. 48.5 Know sickle-cell anemia example really well. You should be able to use this example to convince to me that mutations can be both positive and negative. Really well! 49. Describe in general terms what happens to a polypeptide (or any polymer for that matter) when you eat it. What happens to it, what do you do with it, etc… 50. Describe the four levels of protein structure. I could ask another 15 questions about each level… Know all the details we went over in class like when the side chains come into play or when only the backbone is involved, hydrophobic vs hydrophilic side chains, where different types of side chains are located in proteins typically, etc… 50.5. All alpha helices are right or left handed? This is because they are made with… 51. Explain why the levels of structure have little to do with actual protein folding in the cytoplasm. 52. Explain, starting with a gene, how a protein is formed (The Central Dogma). Make sure you include items like mRNA, tRNA, ribosome, nuclear pore, RNA polymerase, amino acids, nucleus, etc… Basically, describe the central dogma. 53. Be able to identify the various secondary structure elements in a protein and circle them if presented with a ribbon diagram. 54. Explain how a ribbon diagram is generated. What are you looking at when you view a ribbon diagram of a protein – (these are the colorful diagrams with sheets shown as arrows and helices are cartoon-like spirals)? 55. Compare and contrast a polypeptide to a protein. When are they the same and when would they be different? 56. What is meant by a subunit in a protein? 57. Explain what is meant by denature and renature. How and why do proteins denature? You must be very specific. You cannot just say a lower pH than the protein evolved in will cause it to denature…the question is WHY. 58. Know the functions of proteins. Know examples like hemoglobin, myosin, insulin, insulin receptor, ATP synthase, photosystem II, antibodies, HIV protease, etc… and under what category they would fall. 59. How small is a protein relative to the size of a cell? (use the analogy) How many hemoglobin proteins are packed into a single red blood cell? How many red blood cells do you have on average? How many oxygens can your blood carry if it were completely saturated with oxygen? 65. Know who Linus Pauling was and what he did… 68. Describe what 3.6 and n+4 mean in terms of alpha helices. 66. Describe the structure of a nucleotide. 67. How many different nucleotides are there that will build RNA and DNA? Be able to draw them all the way we discussed in class. For example, I could ask you to draw dAMP or AMP or dCMP etc… or I could ask you to draw an RNA nucleotide containing a purine base, etc… 68. How do the purines differ structurally from the pyrimidines in general? Know the names of the bases and to which group they belong, purine or pyrimidine. 69. Draw the ester, diester, and phosphdiester functional group. 70. Explain how two nucleotides can be connected together to form a dinucleotide and so on. You should be able to draw this. What type of linkage is formed? Why do we give it this name? 71. Compare and contrast a DNA nucleotide to an RNA nucleotide (how are they the same/different?). 72. What is the overall charge of DNA and why? 73. Describe the ink and the paper analogy for nucleic acid. 74. Describe the backbone of DNA. What do we call the backbone? 75. What are the optimum temperature, pH and salt concentration of proteins? (Explain why this is a trick question). 76. How would the optimal pH of a protein in the stomach differ from that of a protein in the blood? 76.5. Explain how changing the pH, temperature or salt actually disrupts the protein/polypeptide on the molecular level. 77. Explain what happens to the polymers we are constantly eating. Where did most the monomers that make up these polymers ultimately come from? (This will require some logical thinking) 78. Make sure you can describe the nucleus/library analogy down to the ink. 75. Make sure you can explain the technique of chromatography as well as the experiment done by Erwin Chargaff. What was the conclusion of Chargaff’s study? How did this help Watson and Crick solve the structure of DNA? 76. What is the function of DNA? Genes code for ___________________. 78. How would you define a lipid? 79. How are lipids chemically different from the other three classes of macromolecules? 80. Identify the four types of lipids discussed in class. Be able to draw each type as we discussed in class. 81. How do unsaturated and saturated fatty acids differ structurally? How does this change how they behave relative to each other? How do trans fats differ from cis fats? Make sure you can draw a trans or cis fatty acid. Which are found in plants, cis or trans? Make sure you can draw any triglyceride (saturated, mono-, or polyunsaturated) 81.5. Make sure you can explain how soap is made and how soap works, and the similarities between soap and phospholipids. 82. Where does one find unsaturated fats in nature? What about saturated fats? 83. What does the term “hydrogenated vegetable oil” refer to? Give an example of hydrogenated vegetable oil that you might find in the supermarket. 84. Describe why saturated fats tend to be solid at room temperature while unsaturated fats tend to be liquid. 85. Identify the functions of triglycerides in nature. Where are they found (what type of cell and what location in humans)? What is the name given to the two general types of fat in humans? Which is more prevalent in males? Females? 86. Compare and contrast a phospholipid to a triglyceride (What is similar and what is different?). Make sure you can draw a phospholipid. 87. Describe the function of phospholipids in nature. 88. Why do phospholipids tend to always have one kinked fatty acid (one kinked tail)? Is this kink cis or trans? Explain why. 89. Define the term amphiphilic. 90. How does the term amphiphilic relate to phospholipids and why is this an important property of these molecules? What other molecules have we discussed that are amphiphilic? 91. Be able to draw the two structures discussed in class that will result if you take moles of phospholipids and add them to water. Know the names of the two resulting structures. Which of these structures would be similar to a cell membrane? 91.5. Explain why phospholipids assume the above described structures in aqueous solution…hint…water cage and random motion should be in the explanation. 91.7 Be able to draw a simple cell membrane containing phospholipids and cholesterol. 92. Describe the general function of cell membranes in the cell. 94. Describe the general structure of a steroid and give at least four examples in humans. 95. One example of a steroid is cholesterol. Describe the two functions of cholesterol in our cells that we spoke about in class, and indicate how the structure of this molecule determines its function. 95.25. In what organ do you synthesize cholesterol and in what organelle? 95.5 Explain in detail how cholesterol maintains the integrity of the cell membrane throughout a wide range of temperatures. Why is it called a membrane buffer? 96. What is a hormone? What type of molecules act as hormones in the body? 98. We learned that steroids can act as hormones (so now you know that protein amino acid based molecules and steroids can act as hormones - signaling molecules that allow cells to “talk” to each other that are not typically located near each other). Indicate the two types of steroid hormones we discussed in class and describe their function in the body. 98.5. Discuss the function of the corticoids. Where are they synthesized? Why are they called glucocorticoids and mineralcorticoids? 99. Why does one not need to ingest cholesterol to survive? 99.5 Why are the androgens like testosterone also called anabolic steroids, while the other steroid hormones are not? 99.7. Compare anabolic reactions to catabolic reactions and give examples of each. 100. How is cholesterol linked to the steroid hormones? 101. Describe Chargaff’s experiments and why the results were critical in determining the three-dimensional structure of DNA. 102. Chargaff used a technique known in general terms as paper chromatography. Describe how to do and the purpose of paper chromatography in general. For example, if I gave you a solution containing a mixture of various food colorings, how might you separate them? Explain how paper chromatography works. 103. Describe the three-dimensional structure of DNA. 104. Why is it important that the base pairs of DNA be held together by hydrogen bonds as opposed to using covalent or ionic bonds? 105. One of the DNA strands is typically called the “complementary” strand. Why do you think this strand was given this name? 106. What do I mean when I say that the strands of DNA are anti-parallel? 107. Be able to label the ends of the DNA strands (5’ and 3’) and be able to explain why the ends are given these names. 108. Describe the function of DNA in organisms. 109. Explain the charge of DNA. 110. How does the structure of DNA compare to that of RNA? (Three major differences) 111. Identify the three types of RNA discussed in class and give their function. 112. Describe how the cell is able to make polypeptides using the information that is encoded in the DNA. Be able to describe it both using the analogy and using the actual terms. Be sure to include the following words: DNA, mRNA, tRNA, rRNA, protein, RNA polymerase (why is this enzyme called RNA polymerase?), ribosome, polypeptide, amino acids, library, paper, transcribe, translate, nuclear pores, nuclear membrane, guards. You should be able to make a sketch of this process. 113. The process described above is known as “The Central Dogma” of molecular biology. What does this mean? (google it) 114. Why is the nucleus NOT NOT NOT (just incase you didn’t see the first NOT) the control center/brain of the cell? 115. We discussed the RNA world hypothesis in class. Describe why it is logical to hypothesize that RNA was used by the most primitive of cells before the evolution of DNA and protein. What specific evidence do we have that supports this? (I discussed two major pieces of observational evidence) Why couldn’t protein have come first or DNA have come first? 116. Why do you think protein and DNA exist today? Why aren’t organisms still solely based on RNA? Use the term natural selection in your answer to these questions. 117. What is the name given to a stretch of DNA that codes (stores the information for) for mRNA, tRNA or rRNA? 118. How are tRNA’s and rRNA’s made? 119. Describe the structure of the ribosome. What is it made of? 120. Where do the amino acids that our cells use to build polypeptides come from? Yes, I know they are in the cytoplasm, but before that… 121. List each macromolecule class and identify where you would find each in a cell. The next step is going to be to put these molecules together and build a cell. You should have the basic location and function down before we start getting into details. 122. How many pieces of DNA (“books”) are found in a human nucleus? If you attached all those pieces end to end, how long would the DNA be? Discuss the size of DNA in terms of actual size and the MSG analogy. What do we call each piece (“book”)? How many unique books are there? Explain. 123. Describe the Madison square garden analogy and be sure to include every macromolecule class (the rope, the straight pin (a phospholipid), the baseball, the head of a pin (a glucose molecule)) 124. Explain why hydrophilic molecules like proteins, amino acids, carbohydrates, nucleic acids, etc… are NOT able to move through a plasma membrane, while small hydrophobic molecules can. (Why do you think large hydrophobic molecules have trouble crossing?) 125. Why do think amino acid based hormones require a cell surface receptor protein to tell the cell what to do (talk to the cell), while steroid hormones typically have protein receptors inside the cell, in the cytoplasm? 126. Compare a phospholipid bilayer to a phospholipid monolayer. Which would make up a cell membrane and why is this a logical choice (why would the other not work as a cell membrane?).