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Carbon Compounds In Cells Chapter 3. Producers Capture Carbon Using photosynthesis, plants and other producers turn carbon dioxide and water into carbon-based.

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Presentation on theme: "Carbon Compounds In Cells Chapter 3. Producers Capture Carbon Using photosynthesis, plants and other producers turn carbon dioxide and water into carbon-based."— Presentation transcript:

1 Carbon Compounds In Cells Chapter 3

2 Producers Capture Carbon Using photosynthesis, plants and other producers turn carbon dioxide and water into carbon-based compounds

3 Atmospheric Carbon Dioxide Researchers have studied concentration of CO 2 in air since the 1950s Concentration shifts with season –Declines in spring and summer when producers take up CO 2 for photosynthesis

4 CO 2 and Global Warming Seasonal swings in CO 2 increasing Spring decline starting earlier Temperatures in lower atmosphere increasing Warming may be promoting increased photosynthesis

5 Humans and Global Warming Fossil fuels are rich in carbon Use of fossil fuels releases CO 2 into atmosphere Increased CO 2 may contribute to global warming

6 Organic Compounds Hydrogen and other elements covalently bonded to carbon Carbohydrates Lipids Proteins Nucleic Acids

7 Carbon’s Bonding Behavior Outer shell of carbon has 4 electrons; can hold 8 Each carbon atom can form covalent bonds with up to four atoms

8 Bonding Arrangements Carbon atoms can form chains or rings Other atoms project from the carbon backbone

9 Functional Groups Atoms or clusters of atoms that are covalently bonded to carbon backbone Give organic compounds their different properties

10 Examples of Functional Groups Hydroxyl group - OH Amino group- NH 3 + Carboxyl group- COOH Phosphate group- PO 3 - Sulfhydryl group- SH

11 Types of Reactions Functional group transfer Electron transfer Rearrangement Condensation Cleavage

12 Condensation Reactions Form polymers from subunits Enzymes remove -OH from one molecule, H from another, form bond between two molecules Discarded atoms can join to form water

13 Fig. 3.4a, p. 37 enzyme action at functional groups CONDENSATION

14 Hydrolysis A type of cleavage reaction Breaks polymers into smaller units Enzymes split molecules into two or more parts An -OH group and an H atom derived from water are attached at exposed sites

15 enzyme action at functional groups HYDROLYSIS Fig. 3.4b, p. 37

16 Carbohydrates Monosaccharides (simple sugars) Oligosaccharides (short-chain carbohydrates) Polysaccharides (complex carbohydrates)

17 Monosaccharides Simplest carbohydrates Most are sweet tasting, water soluble Most have 5- or 6-carbon backbone Glucose (6 C)Fructose (6 C) Ribose (5 C)Deoxyribose (5 C)

18 Two Monosaccharides glucosefructose

19 Disaccharides Type of oligosaccharide Two monosaccharides covalently bonded Formed by condensation reaction + H 2 O glucosefructose sucrose

20 Polysaccharides Straight or branched chains of many sugar monomers Most common are composed entirely of glucose –Cellulose –Starch (such as amylose) –Glycogen

21 Cellulose & Starch Differ in bonding patterns between monomers Cellulose - tough, indigestible, structural material in plants Starch - easily digested, storage form in plants

22 Cellulose and Starch

23 Glycogen Sugar storage form in animals Large stores in muscle and liver cells When blood sugar decreases, liver cells degrade glycogen, release glucose

24 Chitin Polysaccharide Nitrogen-containing groups attached to glucose monomers Structural material for hard parts of invertebrates, cell walls of many fungi

25 Most include fatty acids –Fats –Phospholipids –Waxes Sterols and their derivatives have no fatty acids Tend to be insoluble in water Lipids

26 Fatty Acids Carboxyl group (-COOH) at one end Carbon backbone (up to 36 C atoms) –Saturated - Single bonds between carbons –Unsaturated - One or more double bonds

27 Three Fatty Acids stearic acidoleic acidlinolenic acid

28 Fats Fatty acid(s) attached to glycerol Triglycerides are most common

29 Phospholipids Main components of cell membranes

30 Sterols and Derivatives No fatty acids Rigid backbone of four fused-together carbon rings Cholesterol - most common type in animals

31 Waxes Long-chain fatty acids linked to long chain alcohols or carbon rings Firm consistency, repel water Important in water-proofing

32 Amino Acid Structure amino group carboxyl group R group

33 Properties of Amino Acids Determined by the “R group” Amino acids may be: –Non-polar –Uncharged, polar –Positively charged, polar –Negatively charged, polar

34 Protein Synthesis Protein is a chain of amino acids linked by peptide bonds Peptide bond –Type of covalent bond –Links amino group of one amino acid with carboxyl group of next –Forms through condensation reaction

35 Primary Structure Sequence of amino acids Unique for each protein Two linked amino acids = dipeptide Three or more = polypeptide Backbone of polypeptide has N atoms: -N-C-C-N-C-C-N-C-C-N-

36 Protein Shapes Fibrous proteins –Polypeptide chains arranged as strands or sheets Globular proteins –Polypeptide chains folded into compact, rounded shapes

37 Primary structure influences shape in two main ways: –Allows hydrogen bonds to form between different amino acids along length of chain –Puts R groups in positions that allow them to interact Primary Structure & Protein Shape

38 Secondary Structure Hydrogen bonds form between different parts of polypeptide chain These bonds give rise to coiled or extended pattern Helix or pleated sheet

39 Examples of Secondary Structure

40 Tertiary Structure Folding as a result of interactions between R groups heme group coiled and twisted polypeptide chain of one globin molecule

41 Quaternary Structure Some proteins are made up of more than one polypeptide chain Hemoglobin

42 Polypeptides With Attached Organic Compounds Lipoproteins –Proteins combined with cholesterol, triglycerides, phospholipids Glycoproteins –Proteins combined with oligosaccharides

43 Denaturation Disruption of three-dimensional shape Breakage of weak bonds Causes of denaturation: –pH –Temperature Destroying protein shape disrupts function

44 A Permanent Wave hair wrapped around cuticles different bridges form bridges broken

45 Sugar –Ribose or deoxyribose At least one phosphate group Base –Nitrogen-containing –Single or double ring structure Nucleotide Structure

46 Nucleotide Functions Energy carriers Coenzymes Chemical messengers Building blocks for nucleic acids

47 ATP - A Nucleotide three phosphate groups sugar base

48 Composed of nucleotides Single- or double-stranded Sugar-phosphate backbone Nucleic Acids Adenine Cytosine

49 DNA Double-stranded Consists of four types of nucleotides A bound to T C bound to G

50 RNA Usually single strands Four types of nucleotides Unlike DNA, contains the base uracil in place of thymine Three types are key players in protein synthesis

51 Normal metabolic products of one species that can harm or kill a different species Natural pesticides –Compounds from tobacco –Compounds from chrysanthemum Natural Toxins

52 Synthetic Toxins atrazine DDT malathion

53 Negative Effects of Pesticides May be toxic to predators that help fight pests May be active for weeks to years Can be accidentally inhaled, ingested, or absorbed by humans Can cause rashes, headaches, allergic reactions


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