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Name Course/Section Date Professor/TA_____ Activity 4.1/5.1 How can you identify organic macromolecules? Refer to the figure (Some Simple Chemistry) on the next page when doing this activity. Part A. Answer the questions. Then use your answers to develop simple rules for identifying carbohydrates, lipids, proteins, and nucleic acids. 1. What is the approximate C:H:O ratio in each of the following types of macromolecules? 2. Which of the compounds listed in question 1 can often be composed of C, H, and 0 alone? 3. Which of the compounds can be identified by looking at the C:H:O ratios alone? 4. What other elements are commonly associated with each of these four types of macromolecules? Carbohydrates Lipids Proteins Nucleic acids Always contain P Generally contain no P Always contain N Generally contain noN Frequently contain S Generally contain noS Activity 4.1/5. 1 Copyright © 2011 Pearson Education. Inc. 7 9 5 Compound CarL’ohydraa . boars’tarches gtyc qc.n °‘ cilon I -. . LpLds: “ Ftsc c’ C’ WdXfl, r)o’tero! . - - -. -: I- I-..—, 3 &oteins: , to-’ yrve’ S - -. 0 r teine 4 Nucleic acids: 1 - £ R4 ‘3 4, t r a. .1’ f .. F S - Activity4.1/5J CopnhtO 2011 Peamor Iducation. Inc. Name__________________________ Course/Section________________________ 5. Functional groups can modify the properties of organic molecules, In the following table, indicate whether each functional group is polar or nonpolar and hydrophobic or hydrophilic. Which of these functional groups are found in proteins and lipids? Functional group —OH Polar or nonpolar Hydrophobic or hydrophilic Found in all proteins Found in many proteins Found in many lipids 2 —CH —COOH 2 —NH —SH 4 —P0 6. You want to use a radioactive tracer that will label only the protein in an RNA virus. Assume the virus is composed of only a protein coat and an RNA core. Which of the 9 Be sure to explain your answer. following would you use a. Radioactive P b. Radioactive N c. Radioactive S d. Radioactive C 7. Closely related macromolecules often have many characteristics in common. For example, they share many of the same chemical elements and functional groups. Therefore, to separate or distinguish closely related macromolecules, you need to determine how they differ and then target or label that difference, a. What makes RNA different from DNA? b. If you wanted to use a radioactive or fluorescent tag to label only the RNA in a cell and not the DNA. what compound(s) could you label that is/are specific for RNA? c. If you wanted to label only’ the DNA. what compound(s) could you label? Activity 4.l/5l Copyright © 2011 Pearson Education Inc 9 8. Based on your answers to questions 1—7, what simple rule(s) can you use to identify the following macromolecules? Carbohydrates Lipids Proteins Nucleic acids DNA versus RNA Part B. Carbohydrate, lipid, protein, or nucleic acid? Name that structure! Based on the rules you developed in Part A, identify the compounds below (and on the following page) as carbohydrates, lipids, amino acids, polypeptides, or nucleic acids, In addition, indicate whether each is likely to be polar or nonpolar, hydrophilic or hydrophobic. 0 H 1) OH H H C — 0 L,.7fI5 H Ho! 0\ ÷ OH H COH 17 C 3 H HO 0 35 H 7 C—C HO — ‘) C r1 7 C 0 C 0 17 C H H-C 0 C H, 7 C H 1:1 HC —N CH / C—N H CH! 2) HN—CC-O 3 OHCH -I 3) H--N H -- H C— II HO 10 CH H 9 2 CH C C—N—C—C- II HO H I HO vit4.l/5.l Copyright © 201 1 Pearson Education, Inc. Name Course/Section Part B. Continued 4) OH 2 CH /H0 H 6ase O%O 20 H0CH H HOO ‘OCHOH OH H 2 CF! H OH E3aee H O’ 2 CH E3aae 0 H OH N H 0 6) 2 CH —CH -CH C 3 H — 4, OH ç HO—P—O—CH 7) 2 /N &: tH1 0 c=O 6) NH —C—NH 2 2 —CHCH —CH — CH NH OH 2 CH OH 3 CH OH 2 CH OH 2 CH HHHH i.\ 9) Q “t_?”o 4 Hd’ OH OH Activity 4.1/5.1 Copyright © 2011 Pearson Education, Inc. ‘QL?’o OH /<tOH OH 10) H -C—C—C—C—C I I ‘4 / I OH OH OH OH 11 L4.115.1 Test Your Understanding A student, Mary, is given four samples and told they are lysine (an amino acid), lactose (a disaccharide), insulin (a protein hormone), and RNA. The samples are in test tubes marked 1. 2, 3, and 4, but Mary doesn’t know which compound is in which tube. She is instructed to identify the contents of each tube, a. In her first test, she tries to hydrolyze a portion of the contents of each tube. Hydrolysis occurs in all tubes except tube 3. b. In Mary’s next test, she finds that tubes 1, 2, and 3 are positive for nitrogen but only tube 2 gives a positive result for the presence of sulfur. c. The last test Mary performs shows that the compound in tube 1 contains a high percentage of phosphate. Based on these data, fill in the following table and explain your answers. Tube number Contents Explanation 2 3 4 12 viy4/ Copyright © 2011 Pearson Education, Inc. Name________________________ Course/Section________________________ Date________________________ Professor/TA_________________________ Activity 4.2/5.2 What predictions can you make about the behavior of organic macromolecules if you know their structure? 1. Twenty amino acids are commonly utilized in the synthesis of proteins. These amino acids differ in the chemical properties of their side chains (also called R groups). What properties does each of the following R groups have? (Note: A side chain may display more than one of these properties.) R group Basic, acidic, or neutral Polar or nonpolar Hydrophilic or hydrophobic a. CH CH — CH,, Cf-I, ‘_% b. CH2 o-C,o C. 2 CH CH2 CII2 CH2 t4H, d. CHc OH Activity 4.2/5.2 Copyright © 2011 Pearson Education, Inc. 13 2. Polypeptides and proee’ns are made up of linear sequences of amino acids, In its functional form, each piotern has a specific threedimensiona1 structure or shape. Interactions among the individual amino acids and their side chains play a major role in determining thi shape a. How are amino acids linked together to form polypeptides or proteins? What is this type of bond called What kinds of bonds hold each of these structures together? b. Define the Primary: Secondary’ Tertiary: Quaternary: 3. Lipids as a group are defined as be ng hydrophobic, or insoluble in water. As a result, this group includes fairly ide r’ nge of compoundsfor example fats, oils, waxes, and steroids like a. How are fatty aciu id glycei i ked together to form fats (triglycerides)? b. What functions do I e. How do phospho 14 i — Actify42I2 ( pyright 0 2011 Pcir. Eduation, Inc L4.215.2_Test Your Understanding Use your understanding of the chemical characteristics of the four major types of macromolecules in living organisms to predict the outcome of the following experiments. Be sure to explain your reasoning. Experiment 1: You stir 10 g of glucose and 10 mL of phospholipids in a 500-mL beaker that contains 200 mL of distilled water, Draw a diagram to show where and how the glucose and phospholipids wuuld be distributed aftei you let the mixture settle for about 30 minutes. Experiment 2: You repeat Experiment I again, but this time you stir 10 g of glucose and 10 mL of phospholipids in a different 500mL beaker that contains 200 mL of distilled water and 100 mL of oil. Draw a diagram to show where and how the glucose, phospholipids, and oil would be distributed after you let the solution settle for about 30 minutes Experiment 3: To completely fill a sealed 500mL glass container that contains 490 mL of distilled water, you inJect 10 mL of phospholipids into it. (A small gasket allows the air to leave as you inject the phospho1ipids) You shake this mixture vigorously and then let it settle for an hour or morc Draw a diagram to show how the phospholipids would be distributed in the container vit4.2/5 Copyright © 2011 Pearson Fducation inc. Experiment 4: A globular protein that is ordinarily found in aqueous solution has these amino acids in its primary structure: glutamic acid, lysine, leucine, and tryptophan. Predict where you would find each amino acid: in the interior portion of the protein (away from water) or on the outside of the protein (facing water). (Refer to Figure 5.16, page 79.) Experiment 5: Drawn below is part of the tertiary structure of a protein showing the positions of two amino acids (aspartic acid and lysine), Replacing lysine with another amino acid in the protein may change the shape and function of the protein. Replacing lysine with which type(s) of amino acid(s) would lead to the least amount of change in the tertiary structure of this protein? (Refer to Figure 5.16, page 79,) Ionic bond I Q CH CH YjCH 2 2 -CH4NH O}cH 2 Lyirc 16 Aipartic acid ivit4,2I5,2 Copyright © 2011 Pearson Education, Inc.