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Burton’s Microbiology for the Health Sciences Chapter 7. Microbial Physiology and Genetics

Burton’s Microbiology for the Health Sciences Chapter 7. Microbial Physiology and Genetics. Chapter 7 Outline. Microbial Physiology Introduction Microbial Nutritional Requirements Categorizing Microorganisms According to Their Energy and Carbon Sources Metabolic Enzymes

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Burton’s Microbiology for the Health Sciences Chapter 7. Microbial Physiology and Genetics

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  1. Burton’s Microbiologyfor the Health SciencesChapter 7. Microbial Physiology and Genetics

  2. Chapter 7 Outline Microbial Physiology Introduction Microbial Nutritional Requirements Categorizing Microorganisms According to Their Energy and Carbon Sources Metabolic Enzymes Biologic Catalysts Factors That Affect the Efficiency of Enzymes Metabolism Catabolism Anabolism Bacterial Genetics Mutations Ways in Which Bacteria Acquire New Genetic Information Genetic Engineering Gene Therapy

  3. Microbial PhysiologyIntroduction Physiology is the study of the vital life processes of organisms. Microbial physiology concerns the vital life processes of microorganisms. Scientists can learn about human cells by studying the nutritional needs of bacteria, their metabolic pathways, and why they live, grow, multiply, or die under certain conditions. Bacteria, fungi, and viruses are used extensively in genetic studies because they produce generation after generation so rapidly.

  4. Microbial PhysiologyMicrobial Nutritional Requirements All living protoplasm contains six major chemical elements: carbon, hydrogen, oxygen, nitrogen, phosphorus, and sulfur. Combinations of these and other elements make up vital macromolecules of life, including carbohydrates, lipids, proteins, and nucleic acids. Materials that organisms are unable to synthesize, but are required for building macromolecules and sustaining life, are termed essential nutrients (e.g., certain essential amino acids and essential fatty acids).

  5. Microbial PhysiologyCategorizing Microorganisms According to Their Energy and Carbon Sources Terms relating to an organism’s energy source: Phototrophs use light as an energy source. Chemotrophs use either inorganic or organic chemicals as an energy source. Chemolithotrophs use inorganic chemicals as an energy source. Chemoorganotrophs use organic chemicals as an energy source.

  6. Microbial PhysiologyCategorizing Microorganisms According to Their Energy and Carbon Sources (cont.) Terms relating to an organism’s carbon source: Autotrophs use carbon dioxide (CO2) as their sole source of carbon. Heterotrophs use organic compounds other than CO2 as carbon sources. Terms that combine both energy and carbon source: Photoautotrophs use light as an energy source and CO2 as a carbon source. Photoheterotrophs use light as an energy source and organic compounds other than CO2 as a carbon source. Chemoautotrophs use chemicals as an energy source and CO2 as a carbon source. Chemoheterotrophs use chemicals as an energy source and organic compounds other than CO2 as a carbon source.

  7. Microbial PhysiologyCategorizing Microorganisms According to Their Energy and Carbon Sources (cont.) Ecology is the study of the interactions between living organisms and the world around them. Ecosystem refers to the interactions between living organisms and their nonliving environment. Interrelationships among the different nutritional types are of prime importance in the functioning of the ecosystem. Example: Phototrophs, such as algae and plants, are the producers of food and oxygen for chemoheterotrophs, such as animals.

  8. Decomposition of a Fallen Tree

  9. Metabolic Enzymes Metabolism refers to all of the chemical reactions that occur in a cell. The chemical reactions are referred to as metabolic reactions. Metabolic reactions are enhanced and regulated by enzymes known as metabolic enzymes. Biologic Catalysts Enzymes are biologic catalysts; they are proteins that either cause a particular chemical reaction to occur or accelerate it.

  10. Metabolic EnzymesBiologic Catalysts (cont.) Enzymes are specific, in that they catalyze only one particular chemical reaction. A particular enzyme can exert its effect on only one particular substance, known as the substrate for that enzyme. The unique three-dimensional shape of an enzyme enables it to fit the combining site of the substrate like a key fits into a lock. An enzyme does not become altered during the chemical reaction it catalyzes. (They don’t last forever, however!)

  11. Action of a Specific Enzyme (E1)Breaking Down a Substrate (S1) Molecule

  12. Metabolic EnzymesBiologic Catalysts (cont.) Endoenzymes are enzymes produced within a cell that remain within the cell to catalyze reactions. Example: digestive enzymes within phagocytes Exoenzymes are produced within a cell and then released outside of the cell to catalyze extracellular reactions. Examples: cellulase and pectinase, which are secreted by saprophytic fungi to break down cellulose and pectin, respectively Hydrolases and polymerases are examples of metabolic enzymes.

  13. Metabolic EnzymesFactors That Affect the Efficiency of Enzymes Many factors can affect the efficiency or effectiveness of enzymes; for example, each enzyme has an optimum pH and optimum temperature range at which it functions at peak efficiency. Optimum pH rangeefficiency can be adversely affected if too acidic or too alkaline. Optimum temperature rangeefficiency can be affected if too hot or too cool. Optimum concentration of enzyme and/or substrate – concentration might be too high or too low. Presence of inhibitors (e.g., heavy metals such as lead, zinc, mercury, and arsenic) can affect efficiency.

  14. Metabolism As previously stated, metabolism refers to all of the chemical reactions within a cell. These reactions known as metabolic reactions. A metabolite is any molecule that is a nutrient, an intermediary product, or an end product in a metabolic reaction. Metabolic reactions fall into two categories: catabolism and anabolism. Catabolism refers to all catabolic reactions in a cell. Anabolism refers to all anabolic reactions in a cell.

  15. Metabolism (cont.) Catabolic reactions involve the breaking down of larger molecules into smaller ones. Whenever chemical bonds are broken, energy is released. Catabolic reactions are a cell’s major source of energy. Anabolic reactions involve the assembly of smaller molecules into larger molecules, requiring the formation of bonds. Once formed, the bonds represent stored energy. Much of the energy released during catabolic reactions is used to drive anabolic reactions.

  16. Anabolic and Catabolic Reactions

  17. Differences betweenCatabolism and Anabolism

  18. Metabolism (cont.) Energy can be temporarily stored in high-energy bonds in special molecules, usually adenosine triphosphate (ATP). ATP molecules are the major energy-storing or energy-carrying molecules in a cell. ATP molecules are found in all cells because they are used to transfer energy from energy-yielding molecules, such as glucose, to energy-requiring reactions. When ATP is used as an energy source, it is hydrolyzed to adenosine diphosphate (ADP). If necessary, ADP can be used as an energy source by hydrolysis to adenosine monophosphate (AMP).

  19. Interrelationships between ATP, ADP, and AMP Molecules

  20. Metabolism (cont.) Energy is required not only for metabolic pathways but also for growth, reproduction, sporulation, and movement of the organism, as well as active transport of substances across membranes. Some organisms (e.g., marine dinoflagellates) use energy for bioluminescence. Cellular mechanisms that release small amounts of energy as the cell needs it usually involve a sequence of catabolic and anabolic reactions.

  21. MetabolismCatabolism Catabolic reactions release energy (by breaking bonds) and are a cell’s major source of energy. Some energy is lost as heat in catabolic reactions. Biochemical pathways are a series of linked biochemical reactions occurring in a stepwise manner, from a starting material to an end product. Think of nutrients as energy sources for organisms and think of chemical bonds as stored energy. Glucose, for example, can be catabolized by one of two common biochemical pathways: aerobic respiration and fermentation.

  22. A Biochemical Pathway with Four Steps Compound A is ultimately converted to compound E. Four enzymes are required in this biochemical pathway. Compound A is the substrate for Enzyme 1, Compound B for Enzyme 2, etc.

  23. MetabolismCatabolism (cont.) Catabolism of glucose by aerobic respiration occurs in three phases (each is a biochemical pathway): Glycolysis The Krebs cycle The electron transport chain The first phase (glycolysis) is actually anaerobic, but the other two phases are aerobic. Glycolysis (also called the glycolytic pathway, the Embden–Meyerhof pathway and the Meyerhof–Parnas pathway) is a nine-step biochemical pathway. Each step requires a specific enzyme.

  24. Glycolysis (First Step in the Aerobic Respiration of Glucose)

  25. CatabolismAerobic Respiration of Glucose (cont.) The Krebs cycle (also known as the citric acid cycle, the tricarboxylic acid cycle, and the TCA cycle): A biochemical pathway consisting of eight separate reactions, each controlled by a different enzyme. Only two ATP molecules are produced, but a number of products (e.g., NADH, H+, FADH2) are formed, which enter the electron transport chain. In eukaryotes, the TCA cycle and the electron transport chain occur in mitochondria. In prokaryotes, both occur at the inner surface of the cell membrane.

  26. The Krebs Cycle

  27. CatabolismAerobic Respiration of Glucose (cont.) The electron transport chain (also referred to as the electron transport system or respiratory chain): A series of oxidation–reduction reactions, whereby energy is released as electrons which are transferred from one compound to another. Many enzymes are involved in the electron transport chain, including cytochrome oxidase, which transfers electrons to oxygen (the final acceptor). A large number of ATP molecules are produced by oxidative phosphorylation. Aerobic respiration is very efficient!

  28. Number of ATP Molecules Produced from One Molecule of Glucose by Aerobic Respiration aVaries depending on the number of NADH molecules produced during glycolysis that enter the mitochondria.

  29. CatabolismFermentation of Glucose Fermentation reactions do not involve oxygen. They take place in anaerobic environments. There are many industrial applications of fermentation reactions. First step is glycolysis (anaerobic). The next step is conversion of pyruvic acid into an end product. The end product varies from one organism to another. For example, yeasts are used to make wine and beer; the end product is ethanol. Fermentation reactions produce very little energy (~2 ATP molecules).

  30. CatabolismOxidation–Reduction (Redox) Reactions Oxidation–reduction reactions are paired reactions in which electrons are transferred from one compound to another. Oxidation occurs whenever an atom, ion, or molecule loses one or more electrons in a reaction, in which case, the molecule is said to be oxidized. The gain of one or more electrons by a molecule is called reduction,and the molecule is said to be reduced. Within a cell, an oxidation reaction is always paired with a reduction reaction, hence the term oxidation–reduction reaction.

  31. CatabolismOxidation–Reduction (Redox) Reactions (cont.) • In a redox reaction, the electron donor (compound A) is the reducing agent, and the electron acceptor (compound B) is the oxidizing agent. • Many biologic oxidations are referred to as dehydrogenation reactions because hydrogen ions, as well as electrons, are removed.

  32. Anabolism Anabolic reactions require energy because chemical bonds are being formed. The energy that is required comes from catabolic reactions, which are occurring simultaneously. Anabolic reactions are also called biosynthetic reactions. Biosynthesis of organic compounds requires energy. The energy may be obtained through photosynthesis (from light) or chemosynthesis (from chemicals). Photosynthetic reactions trap the radiant energy of light and convert it into chemical bond energy in ATP and carbohydrates (e.g., glucose).

  33. Bacterial Genetics Genetics is the study of heredity. An organism’s genotype (or genome) is its complete collection of genes. An organism’s phenotype refers to its physical traits (e.g., hair and eye color in humans). An organism’s phenotype is the manifestation of that organism’s genotype. Genes direct all functions of the cell. A particular segment of the chromosome constitutes a gene.

  34. Bacterial GeneticsMutations A change in a DNA molecule (genetic alteration) that is transmissible to offspring is called a mutation. There are three categories of mutations: Beneficial mutations Harmful mutations (some are lethal mutations) Silent mutations Mutation rate (the rate at which mutations occur) can be increased by exposing cells to physical or chemical agents called mutagens. The organism containing the mutation is called a mutant.

  35. Bacterial GeneticsWays in Which Bacteria AcquireNew Genetic Information Ways in which bacteria acquire new genetic information (i.e., acquire new genes): Lysogenic conversion Transduction Transformation Conjugation An extrachromosomal DNA molecule is called a plasmid. An organism that acquires a plasmid acquires new genes. A plasmid that can either exist by itself or integrate into the chromosome is called an episome.

  36. Plasmids (A) A disrupted Escherichia coli cell, in which the DNA has spilled out. A plasmid can be seen slightly to the left of top center (arrow). (B) Enlargement of a plasmid.

  37. Bacterial GeneticsWays in Which Bacteria Acquire New Genetic Information (cont.) Lysogenic conversion Temperate phages (or lysogenic phages) inject their DNA into a bacterial cell. The phage DNA integrates into the bacterial chromosome but does not cause the lytic cycle to occur. This is known as lysogeny. A phage is called a prophage when all that remains of it is its DNA. The bacterial cell containing the prophage is referred to as a lysogenic cell. The bacterial cell exhibits new properties, directed by the viral genes. This is referred to as lysogenic conversion.

  38. Bacterial GeneticsWays in Which Bacteria Acquire New Genetic Information, cont. Transduction (“to carry across”): This involves bacteriophages. In transduction, bacterial genetic material is “carried across” from one bacterial cell to another by a bacterial virus; thus, in transduction, bacteria acquire new bacterial genes. Note how this differs from lysogenic conversion, wherein bacteria acquire new genetic information in the form of viral genes. Only small amounts of genetic material are transferred by transduction.

  39. GeneralizedTransduction

  40. Bacterial GeneticsWays in Which Bacteria Acquire New Genetic Information (cont.) Transformation A bacterial cell becomes genetically transformed following the uptake of DNA fragments (“naked DNA”) from its environment. The ability to absorb naked DNA into the cell is called competence and bacteria capable of absorbing naked DNA are said to be competent bacteria. Transformation is probably not widespread in nature.

  41. Transformation

  42. Bacterial GeneticsWays in Which Bacteria Acquire New Genetic Information (cont.) Conjugation This involves a specialized type of pilus called a sex pilus. A bacterial cell with a sex pilus (called the donor cell) attaches by means of the sex pilus to another bacterial cell (called the recipient cell). Some genetic material (usually a plasmid) is transferred from the donor cell to the recipient cell through a conjugative pore. A plasmid that contains multiple genes for antibiotic resistance is known as a resistance factor or R-factor. A bacterial cell that receives an R-factor becomes a “superbug.”

  43. Conjugation

  44. Conjugation in E. coli

  45. Genetic Engineering Genetic engineering or recombinant DNA technology involves techniques to transfer eukaryotic genes (particularly human genes) into easily cultured cells to manufacture important gene products (mostly proteins). Plasmids are frequently used as vehicles for inserting genes into cells. There are many industrial and medical benefits from genetic engineering. Examples: synthesis of antibodies, antibiotics, drugs, and vaccines, as well as synthesis of important enzymes and hormones for treatment of diseases.

  46. Recombinant DNA Technology and Genetic Engineering

  47. Gene Therapy Gene therapy of human diseases involves the insertion of a normal gene into cells to correct a specific genetic disorder caused by a defective gene. Viral delivery is the most common method for inserting genes into cells; specific viruses are selected to target the DNA of specific cells. Genes may someday be regularly prescribed as “drugs” in the treatment of diseases (e.g., autoimmune diseases, sickle cell anemia, cancer, cystic fibrosis, heart disease, etc.)

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