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This page provides review questions for [http://biology.kenyon.edu/courses/biol238/biol238syl09.html BIOL 238] (Spring 2009).  Answers may be posted by students.
This page provides review questions for [http://biology.kenyon.edu/courses/biol238/biol238syl11.html BIOL 238] (Spring 2011).  Answers may be posted by students.
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==Chapter 17, 18==
==Chapter 19==
==Chapter 20==
==Chapter 21==
==Chapter 22==
<b></b>


<br><br>
==Species to know==


<br><br>
<b>For each species of bacteria or archaea, state one or two broader categories of organism (such as gram-positive endospore-forming bacteria), the type of genome, type(s) of metabolism, habitat, and disease caused (if any).</b>
 
==Species to know for Test==
<br><br>
<b>For each species, state one or two broader categories of organism (such as gram-positive endospore-forming bacteria), the type of genome, type(s) of metabolism, habitat, and disease caused (if any).</b>
<br><br>
<br><br>
<b><i>Aeromonas hydrophila</i></b>
<b><i>Aeromonas hydrophila</i></b>
<br><br>
<br><br>
Broader Categories: Gram-negative, anaerobic
<br>Genome: Genes that contribute to its toxicity are cytotoxic enterotoxin gene (act), heat labile enterotoxins (Alt), and heat-stable cytotonic enterotoxins (Ast).
<br>Metabolism: Heterotrophic, ferments glucose, digests gelatin, hemoglobin, and elastin.
<br>Habitat: Exists in aerobic and anaerobic environments: aquatic environments, fish guts, food, human bloodstream and organs.
<br>Disease: Causes many diseases in fish and amphibians, since it exists in aquatic environments.  Can cause disease in humans, such as septiticemia, meningitis, pneumonia, and gastroenteritis.
<b><i>Anabaena</i> sp.</b>
<b><i>Anabaena</i> sp.</b>
<br><br>
<br><br>
<br>Broader Categories: Barrel-shaped cells.  Filamentous cyanobacteria (blue-green algae) found as plankton.
<b><i>Aquifex</i> sp.</b>
<br>Genome: 1 circular chromosome with 5368 protein-coding regions and 6 plasmids (from sequenced PCC 7120 strain).
<br>Metabolism: Photoautotrophic, perform oxygenic photosynthesis.  Form heterocysts (specialized nitrogen-fixing cells that convert nitrogen to ammonia) during nitrogen starvation.
<br>Habitat: Freshwater and damp soil.  Form symbiotic relationships with certain plants.
<br>Disease: Produce neurotoxins, such as anatoxins (neuromuscular poisons), that are harmful to wildlife and farm animals.
 
<b><i>Aquifex</i></b>
<br><br>
 
<b><i>Aspergillus</i> sp.</b>
<br><br>
<br><br>
Broader Categories: Over 185 species of this genus
Genome: Largely incomplete
Metabolism: Highly aerobic.  Pathogenic species obtain nutrients from host, while non-pathogenic species obtain nutrients from soil, wood, and plant detritus.
Habitat: Grow as molds in oxygen-rich environments and carbon-sources.  Some species are capable of living in nutrient-depleted environments as well.
Disease: About 20 species are  pathogenic in humans and animals.  Aspergillus fumigatus and Aspergillus flavus cause invasive pulmonary aspergillosis and is often fatal.
<b><i>Bacillus anthracis</i></b>
<b><i>Bacillus anthracis</i></b>
<br><br>
<br><br>
Broader Categories: Gram-positive, rod-shaped, form endo-spores and biofilms
<br>Genome: 1 circular chromosome with over 5 million b.p.  2 circular plasmids: pxO1 and pxO2.  These plasmids encode main virulent factors.
<br>Metabolism: Facultative anaerobe and must grow in medium with essential nutrients including C and N sources.  Upon nutrient deprivation, endospores form (requires oxygen to form) and can live in inhospitable envrionments for many years.  Can grow into vegetative cells in aqueous environment with adequate nutrients.
<br>Habitat: Live in soils world-wide and is the main habitat.
<br>Disease: Anthrax disease.  Infectious endospores harm host by germinating for vegetative growth.  During growth the bacteria produce toxins in the body of humans and animals.  The slime capsule enables it to resist phagocytosis.  3 main forms of the disease: cutaneous, pulmonary, and gastrointestinal.  Can cause death in 2-48 hours.
<b><i>Bacillus subtilis</i></b>
<b><i>Bacillus subtilis</i></b>
<br><br>
<br><br>
Broader Categories: Gram-positive, rod-shaped, form stress-resistant endospores
Genome: 1 circular chromosome with 4100 genes coding for proteins.
Metabolism: Can grow in aerobic and anaerobic conditions.  Uses fermentation and nitrate ammonification to make ATP in the absence of oxygen.
Habitat: Soil and vegetation at mesophilic temperatures.
Disease: Non-pathogenic.  Responsible for spoilage of food, since contamination often results in decomposition, but it rarely causes food-poisoning.
<b><i>Bacillus thuringiensis</i></b>
<b><i>Bacillus thuringiensis</i></b>
<br><br>
<br><br>
Broader Categories: Gram-positive, spore-forming, rod-shaped
<b><i>Bacteroides thetaiotaomicron</i></b>
Genome: 1 circular chromosome with 5.2-5.8 Megabases. Contains many plasmids.
<br><br>
Metabolism: Facultative anaerobe (makes ATP by aerobic respiration if oxygen is present, but can switch to fermentation).
<b><i>Borrelia burgdorferi</i></b>
Habitat: Soil. It is used in 90% of pesticides. Fends off insects by producing crystal proteins (Cry proteins).
<br><br>
Disease: Species-specific, non-pathogenic to humans, making it an environmentally-friendly insecticide. Cry toxin grows and sporulates in alkaline gut o finsect, which aids in its ability to infect the insect gut. The gut breaks down and the insect eventually dies.
<b><i>Chlamydia</i> sp.</b>
<br><br>
<b><i>Clostridium botulinum</i></b>
<br><br>
<b><i>Chloroflexus</i> sp.</b>
<br><br>
<b><i>Corynebacterium diphtheriae</i></b>
<br><br>
<b><i>Deinococcus radiodurans</i></b>
<br><br>
<b><i>Enterococcus </i>sp.</b>
<br><br>
<b><i>Escherichia coli</i></b>
<br><br>
<b><i>Geobacter metallireducens</i></b>
<br><br>
<b><i>Halobacterium</i> sp.</b>
<br><br>
<b><i>Helicobacter pylori</i></b>
<br><br>
<b><i>Lactobacillus</i> sp.</b>
<br><br>
<b><i>Lactococcus</i> sp.</b>
<br><br>
<b><i>Leptospira</i> sp.</b>
<br><br>
<b><i>Methanococcus</i> sp.</b>
<br><br>
<b><i>Mycobacterium tuberculosis</i></b>
<br><br>
<b><i>Mycoplasma pneumoniae</i> sp.</b>
<br><br>
<b><i>Nitrospira</i> sp.</b>
<br><br>
<b><i>Prochlorococcus</i> sp.</b>
<br><br>
<b><i>Pseudomonas aeruginosa</i></b>
<br><br>
<b><i>Pyrococcus furiosus</i></b>
<br><br>
<b><i>Pyrodictium occultum</i></b>
<br><br>
<b><i>Rhodobacter</i> sp.</b>
<br><br>
<b><i>Rhodopseudomonas</i> sp.</b>
<br><br>
<b><i>Rhodospirillum rubrum</i></b>
<br><br>
<b><i>Rickettsia</i> sp.</b>
<br><br>
<b><i>Salmonella enterica</i></b>
<br><br>
<b><i>Serratia marcescens</i></b>
<br><br>
<b><i>Sinorhizobium meliloti</i></b>
<br><br>
<b><i>Staphylococcus epidermidis</i></b>
<br><br>
<b><i>Staphylococcus aureus</i></b>
<br><br>
<b><i>Streptomyces</i> sp.</b>
<br><br>
<b><i>Vibrio cholerae</i></b>
<br><br>
<b><i>Vibrio fischeri</i></b>
<br><br>


<b><i>Bacteroides thetaiotaomicron</i></b>
==Chapter 13==
<br>
<b>1. ATP and NADH are both energy carriers: What are the advantages of using one over the other?</b>
<br><br>
<br><br>
Broader Categories: Gram-negative, anaerobic, human-bacterial symbiosis model
Genome: 1 circular chromosome made of d.s. DNA, consists of 4776 proein-coding genes, 90% of which are essential in the binding and import of various polysaccharides.
Metabolism: Starch (all 3 forms) is primary carbohydrate used as its source of C and Energy.  Polysaccharides bind to the cell surface before undergoing hydrolysis.
Habitat: Adult intestine-allows humans to degrade plant polysaccharides
Disease: Serious infections include intra-abdominal sepsis and bacteremia.  It is resistant to many antimicrobial agents.


<b><i>Borrelia burgdorferi</i></b>
<br><br>
<br><br>
Broader Categories: Sprial-shaped with 2 flagella
<b>2. When cells need to make glucose (gluconeogenesis), they "reverse glycolysis" because most steps are reversible.  However, there are a couple of steps that are not reversible. How do you think they get reversed for gluconeogenesis? </b>
Genome: A linear chromosome with 910,725 b.p. with 853 genes. 17 linear and circular plasmids.
<br><br>
Metabolism: Require specific nutritional requirements making it difficult to culture in vitro.
Habitat: Live extracellularly and adapts to various host animals (tick, rodents, birds) by regulating various lipoproteins on thier surface.
Disease: Lyme disease and recurring fever.


<b><i>Chlamydia</i> sp.</b>
<br><br>
<br><br>
Broader Categories: Gram-negative, aerobic, coccoid or rod-shaped
<b>3. There are 3 main pathways to form pyruvate- EMP, ED and PPS. How and why might a cell switch among these?</b>
Genome: C. trachomatis-1,042,519 b.p. with 894 protein-coding sequences (70 genes are not homologous to sequences on the C. pneumoniae genome).  C. pneumoniae- 1,230,230 b.p. (186 genes are not homologous to sequences on the C. trachomatis genome)
<br><br>
Metabolism: Cannot synthesize its own ATP, so they cannot be grown on artificial medium and require growing cells to remain viable.
Habitat: C. trachomatis-human host cells, C. suis- swine host cells, C. muridarum- mice and hamster host cells.  Infectious elementary body form induces endocytosis upon contact with host cell. Once inside, the elementary body germinates to vegetative form, and divides every 2-3 hrs.  It then reverts back to the elementary form and is released by the cell through exocytosis.
Disease: C. trahomatis causes chlamydia and is the most common STD in the world.  C. pneumoniae causes pneumonia and bronchitis


<b><i>Clostridium botulinum</i></b>
<br><br>
<br><br>
Broader Categories: Gram-positive, rod-shaped, anaerobic, spore-former
<b>4. Explain why most soil bacteria grow using energy-yielding reactions with very small delta-G.</b>
Genome: Genome size of 4039 kbp, which is larger than most Gram-positive genomes, indicating the extra genomic requirements needed for sporulation and pathogenic toxin production
<br><br>
Metabolism: Lie dormant in very adverse environments.  Spores can begin to grow in favorable conditions: non-halophilic salinity and anaerobic conditions.  Grows at mesophilic temps.
Habitat: Soils and improperly canned food products
Disease: A-G subtypes produce different botulin toxin- al except C and D subtypes are human pathogens.  The toxin prevents propagation of action potentials to the muscle fibers- causing paralysis by inhibiting muscle contraction.  Fatalities usually occur due to asphyxiation


<b><i>Chloroflexus</i></b>
<br><br>
<b>5. Why are glucose catabolism pathways ubiquitous, despite the fact that most bacterial habitats never provide glucose?  Explain several reasons.</b>
<br><br>
<br><br>


<b><i>Corynebacterium diphtheriae</i></b>
<br><br>
<b>6. In glycolysis, explain why bacteria have to return the hydrogens from NADH back onto pyruvate to make fermentation products.  Why can't NAD+ serve as a terminal electron acceptor, like O<sub>2</sub>?</b>
<br><br>
<br><br>


<b><i>Escherichia coli</i></b>
<br><br>
<br><br>
Broader Categories: Gram-negative, rod-shaped, aerobic
<b>7. Why do environmental factors regulate catabolism? Give examplesWhy are amino acids decarboxylated at low pH, and under anaerobiosis?</b>
Genome: 1 circular chromosome, (4300 coding sequences) with 1800 known proteinsSome contain circular plasmid.
<br><br>
Metabolism: Facultative anaerobeUses mixed-acid fermentation in anaerobic conditions.  Growth driven by aerobic or anaerobic respiration using a large variety of redox pairs: oxidation of pyruvic acid, formic acid, hydrogen, and amino acids and reduction of oxygen, nitrate, dimethyl sulfoxide, trimethylamine N-oxide.
Habitat: Lower intestines of human and mammals, where it aids in digestion processes: vitamin K production, food breakdown and absorption
Disease: E. coli O157:H7 (enterohemorrhagic strain) causes food poisoning- leading to bloody diarrhea and kidney failure due to its production of Shiga-like toxin.  Also can cause urinary tract infections by ascending infections of the urethra.


<b><i>Geobacter metallireducens</i></b>
<br><br>
<br><br>
Broader Categories: Gram-negative, rod-shaped, possesses flagella, and pili
<b>8. Why does catabolism of benzene derivatives yield less energy than sugar catabolism? Why is benzene-derivative catabolism nevertheless widespread among soil bacteria?</b>
Genome: 1 circular chromosome encoding 3621 genesPlasmid encodes 13 genes, 1 of which is addiction module toxin (gives resistance to bacteria and another encoding plasmid stabilization system protein (allows bacteria to adapt to new environmental conditions)
<br><br>
Metabolism: First organism with the ability to oxidize organic compounds and metals (iron, radioactive metals like Uranium, and petroleum compounds) into environmentally benign carbon dioxide while using iron oxide and other available metals an electron acceptors.
Habitat: anaerobic conditions in soils and aquatic sediments
Disease: Non-pathogenic


<b><i>Pseudomonas aeruginosa</i></b>
<br><br>
<br><br>
Broader categories: Gram-negative, rod-shaped, does not produce spores. Habitat: due to its capability to synthesize arginine, P. aeruginosa proliferates in anaerobic conditions. It can be found in environments such as soil, water, humans, animals, plants, sewage, and hospitals. Metabolism: Aerobic respiration. P. aeruginosa can metabolize on hundreds of other things besides arginine, and can respire on nitrate (although it does much better on O2).Genome: a single and supercoiled circular chromosome in the cytoplasm. Disease(s) caused: Causes disease in immuno-compromised patients, such as those with cystic fibrosis, cancer, or AIDS. It further weakens the patient, allowing the patient to become more susceptible to other diseases. Usually this kills the patient. P. aeruginosa forms biofilms in the lung of cystic fibrosis patients; it is the major cause of death in these individuals.


<b><i>Halobacterium</i> sp.</b>
==Chapter 14==
<br>
<b>1. Explain how bacteria and archaea switch among various electron acceptors depending on environmental conditions.</b>
<br><br>
<br><br>
Broader categories: rod-shaped, halophilic, candidate for life on Mars. Genome: 1 large chromosome and 2 plasmids (3 circular replicons). Metabolism: aerobic, but not glucose degradation. Habitat: highly saline lakes. Disease: non-pathogenic


<b><i>Helicobacter pylori</i></b>
<br><br>
<b>2. Explain how cell processes such as ATP synthesis can be powered by either the transmembrane pH difference or by the charge difference across the membrane.  Which form of energy is likely to be used at low external pH?  At high external pH?</b>
<br><br>
<br><br>


<b><i>Lactobacillus</i></b>
<br><br>
<b>3. For phototrophy, discuss the relative advantages and limitations of using PS I versus PS II.</b>
<br><br>
<br><br>


<b><i>Lactococcus</i> sp.</b>
<br><br>
<br><br>
Broader categories: spherical, gram positive. Genome: 1 circular chromosome with 2, 365, 589 bp, where 86 % of the genome code for protein, 1.4 % for RNA, and 12.6 % for noncoding region. 64.2 % of the genes code for known functional proteins, and 20.1 % of the genes for known protein with unknown function. Metabolism: aerobic or anaerobic, often use lactic acid fermentation. Habitat: plant surfaces, digestive tract of cows. Disease: non-pathogenic.
<b>4. What environments favor oxygenic photosynthesis, versus sulfur phototrophy and photoorganotrophy? Explain.</b>
<br><br>


<b><i>Leptospira</i></b>
<br><br>
<b>5. Explain why certain lithotrophs acidify their environments, to more extreme levels than fermentation.  What are some practical consequences for human industry?</b>
<br><br>
<br><br>


<b><i>Methanococcus</i> sp.</b>
<br><br>
<br><br>
Broader categories: gram-negative, cocci-shaped, archaea domain, thermophilic and mesophilic. Genome: 1 circular chromosome with 1 large extra-chromosomal element and 1 small extra-chromosomal element. Metabolism: autotrophic, anaerobic, reduces carbon dioxide with hydrogen gas to generate methane. Habitat: can grow up to pressures of 200 atm, temperature ranges between 48-94 degrees C, with optimal growth at 85 degrees C. Disease: non-pathogenic.
<b>6. Is it surprising that an organism may switch between lithotrophy and organotrophy? What enzymes would have to be replaced, and what enzymes could be used in common for both kinds of metabolism?</b>
<br><br>


<b><i>Mycobacterium tuberculosis</i></b>
<br><br>
<b>7. What kind of environments favor methanogenesis?  Why are methanogens widespread, despite the low delta-G of their energy-yielding metabolism?</b>
<br><br>
<br><br>


<b><i>Mycoplasma pneumoniae</i> sp.</b>
<br><br>
<br><br>
Broader categories: spherical without a cell wall, highly pathogenic--osmotic instability. Genome: 1 small circular chromosome. Metabolism: major nutrients come from mucosal epithelial cells of the host, many proposed metabolic pathways. Habitat: not found in the environment but can be cultured in medium-rich agar. Disease: highly pathogenic; parasitizes epithelial cells in the respiratory tract.
==Chapter 15==
<br><br>
<b>1. Why does biosynthesis need both ATP and NADPH?  Why couldn't biosynthetic pathways use just ATP, or just NADPH?</b>
<br><br>


<b><i>Nitrospira</i></b>
<br><br>
<b>2. Compare and contrast fatty acid biosynthesis and amino acid biosynthesis.  Which pathway requires more reduction?  Which requires a greater number of different enzymes?  Why?</b>
<br><br>
<br><br>


<b><i>Paramecium</i> sp.</b>
<br><br>
<b>3. What forms of nitrogen are available to microbes for assimilation?  When fertilizer is spread on farmland to nourish crops, what problem is caused by microbes?</b>
<b>What are the other oxidized forms that bacteria and plants take up and reduce to ammonia and ammonium ion?
What about N from reduced organic compounds?</b>
<br><br>
<b>4. How are the pathways of amino acid biosynthesis organized?  What common routes flow from which core pathways?</b>
<br><br>
<br><br>


Broader categories: Eukaryotic ciliated unicellular organisms. Genome: Linear. Metabolism: Paramecium eject trichocyts to help capture their prey. They commonly eat bacteria, yeasts, algae, and small protozoa. Paramecium are also heterotrophs.  Habitat: Aquatic environments, usually in stagnant warm water. Some Paramecium species form symbiotic relationships with green algae or bacteria. The bacteria/algae live in the cytoplasm of the Paramecium and perform photosynthesis. Disease: Non-pathogenic
<br><br>
<b>5. How and why do bacteria make "secondary products"?  What are their functions?</b>
<br><br>


<br><br>
<b>6. How can we manipulate bacterial secondary product formation to develop new pharmaceutical agents?</b>
<br><br>
<br><br>
==Chapter 17==
<b>1. Explain why the first kinds of metabolism on Earth involved electron donors from the sediment reacting with electron receptors from above.  What geolotical and outer-space processed generated these electron donors and electron acceptors?</b>
<br><br>


<b><i>Plasmodium falciparum</i></b>
<br><br>
<br><br>
Broader Categories: Protazoan parasite Genome: It contains a 23-megabase nuclear genome consisting of 14 chromosomes, encoding about 5,300 genes, and is the most A/T rich genome sequenced to date
<br><br>
Metabolism: Uses intracellular hemoglobin as a food source.  Anaerobic glycolisis with pyruvate being converted to lactate.
<b>2. What evidence supports the "RNA world" aspect of the origin of life?  What are evolutionary and medical implications of the RNA world model?</b>
Habitat: Requires both human and mosquito hosts
<br><br>
Pathogenicity: Causative agent of malaria


<b><i>Prochlorococcus</i> sp.</b>
<br><br>
<br><br>
Broader Categories: Single-celled cyanobacteria
<b>3. What is our modern definition of a microbial species?  Explain the strengths and limitations of defining microbial species based on common ancestry of DNA sequence.</b>
Genome: It is about 1.67 Mega-base pairs long with 1,694 predicted protein-coding regions
<br><br>
Metabolism: photoautotrophic
<br><br>
Habitat: Oceans
<b>4. Explain the evolutionary origins of mitochondria and chloroplasts. What evidence do we see in the structures of modern microbes?</b>
Pathogenicity: Non-pathogenic
<br><br>
<br><br>
<b>5. What is a virulence gene?  How do virulence genes evolve?  How can we analyze the relationship between virulent and nonvirulent strains of a bacterium?</b>
<br><br>


<b><i>Pseudomonas aeruginosa</i></b>
==Chapter 18==
<b>1. Compare and contrast the major divisions of bacteria.  State an example of a species of each major division.</b>
<br><br>
<br><br>
Broader Categories: Gram-negative, rod-shaped, and contains 1 flagella
Genome: It contains a 5.2 to 7 million base pairs and a single, supercoiled circular chromosome in the cytoplasm with many plasmids contributing to its pathogenicity.
Metabolism: Facultative aerobe, with its preferred metabolism being aerobic respiration by transferring electrons from glucose to oxygen. 
Habitat: Ubiquitous in that it can live in both human and inanimate environments.  This is possible mainly because of the vast array of enzymes that allow uptake of diverse forms of nutrients.
Pathogenicity: Disease-causing agent to immuno-compromised individuals (cystic fibrosis patients) or indivuals in a trauma (burn victims).  It tends to form biofilms and cause tissue damage through its virulence factors.


<b><i>Rhodobacter</i> sp.</b>
<br><br>
<br><br>
Broader categories: quorum-sensing bacteria, flagella motility. Genome: unique complexities-2 chromosomes, 1 large and 1 small, circular chromosomes. Metabolism: photosynthesis mostly, also capable of lithotrophy, aerobic, and anaerobic respiration pathways. Habitat: aquatic and marine environments. Disease: non-pathogenic.<br><b>Which photosystem does it use?  Does it conduct phototrophy anaerobically, or in the presence of oxygen?</b>
<b>2. Explain an example of a major division of bacteria whose species show nearly uniform metabolism but differ widely in form. Explain a different example of a division showing a common, distinctive form, but variety of metabolism.</b>
<br><br>


<b><i>Rhodopseudomonas</i></b>
<br><br>
<b>3. Compare and contrast three different types of phototrophy found in bacteria.</b>
<br><br>
<br><br>


<b><i>Rhodospirillum rubrum</i></b>
<br><b>Which photosystem does it use?</b><br>
<b><i>Rickettsia</i> sp.</b>
<br><br>
<br><br>
<b><i>Saccharomyces cerevesiae</i></b>
<b>4. Explain the pathology of three different gram-positive pathogens.</b>
<br><br>
<br><br>
<b><i>Salmonella enterica</i></b>
 
<br><br>
<br><br>
<b><i>Serratia marcescens</i></b>
<b>5. Explain two different examples of bacterial-host mutualism.</b>
<br><br>
<br><br>
<b><i>Sinorhizobium meliloti</i></b>
 
<br><br>
<br><br>
<b><i>Staphylococcus epidermidis</i></b>
 
<br><br>
<br><br>
<b><i>Staphylococcus aureus</i></b>
<b>6. Identify these kinds of bacteria based on their descriptions:</b>
 
<br>a. This bacteria is irregularly shaped with peptidoglycan cell walls and a cytoskeleton containing tubulin (previously thought to only be present in Eukaryotes). They are heterotrophs living in variable environments that are usually low in salt, and most are oligotrophs.
<br>b. This bacteria has a nucleus similar to that of a eukaryotic organism.  It is most notable for its unique membrane structure.  It has multiple internal membranes, with a double membrane functioning to surround the nucleoid.  What am I?!
<br>c. Bacteria in this group are filamentous photoheterotrophs.  In the presence of oxygen they conduct nonphotosynthetic heterotrophy.  They can be found in microbial mats together with thermophilic cyanobacteria.  Some species contain chlorosomes.  They are also known as green nonsulfur bacteria.
<br>d. These bacteria are photolithotrophs that deposit sulfur on the cell surface.  They use H<sub>2</sub>S as an electron donor and are known as green sulfur bacteria.  These bacteria also live in strictly anaerobic conditions below the water surface.
<br>e. This bacterium is gram positive but has permanently lost its cell wall and S-layer due to reductive/degenerative evolution.  It also has the smallest genome(580 kbp) and it is parasitic.
<br>f. This bacterial species ferments complex carbohydrates and serves as one of the major mutualists of the human gut.  Has a Gram-negative structure and is an obligate anaerobe.
<br>g. These bacteria are deep branching and come in a multitude of forms.  They can be found living independently or in colonies. Often times, these different forms allow them to fix nitrogen.  While these organisms can be found in both aquatic and terrestrial habitats, many species contain gas vesicles to maintain a favorable position in the water column.
 
<br><br>
<br><br>
Broader categories: gram positive, spherical, immobile. Genome: 1 circular genome, resistance for antibiotics are encoded by a transposon. Metabolism: EMP and Pentose-Phosphate pathways. Lactate is the end product of anaerobic glucose metabolism. Acetate and carbon dioxide are the end products of aerobic metabolism. Habitat: skin, mucous membranes of animals. Disease: skin infections, invasive diseases, toxic shock syndrome (TSS).


<b><i>Streptococcus </i>sp.</b>
==Chapter 19==
<b>1. Compare and contrast the different major groups of archaea.  Which ones grow in extreme heat or cold?  Extreme salt?  Produce methane?</b>
<br><br>
<br><br>
<b>2. Explain how archaea growing in extreme environments require specialized equipment for study.</b>
<br><br>
<br><br>
Broader Categories: Gram positive, spherical, can be found in chains or in pairs, immobile. Genome: 1 circular chromosome. Metabolism: Many species of Streptococcus are facultative anaerobes, while others are obligate anaerobes. Habitat: Part of normal animal flora. Can become pathogenic and infect humans and other animals. They often imitate aspects of their host organism to avoid being detected. Disease: Can cause step throat, necrotizing fasciitis, scarlet fever, rheumatic fever, postpartum fever, and streptococcal toxic shock syndrome. Some species of Streptococcus can cause pneumonia.


<b><i>Streptomyces</i> sp.</b>
<br><br>
<br><br>
<b><i>Vibrio cholerae</i></b>
<b>3. What kinds of archaea grow in "average" environment such as the soil? Or an animal digestive tract?</b>
<br><br>
<br><br>
Broader Categories: Gram-negative, bent rod shaped, one polar flagellum.  Genome:  Two circular chromosomes.  Metabolism:  Fermentative and respiratory.  Habitat:  Aquatic environments.  Disease:  Responsible for cholera in humans, which is characterized by diarrhea and vomiting leading to dehydration.  The bacteria secrete a toxin that ultimately causes an increase in cyclic AMP levels that stimulates ion transport in the cells lining the intestine.  This is followed by water leaving the intestinal cells to compensate for the change in osmolarity. 


<b><i>Vibrio fischeri</i></b>
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Broader Categories:  Rod shaped, gram-negative. Genome: Two circular chromosomes with 2,284,050 bp and a plasmid.  The lux operon controls bioluminescence.  Metabolism:  Heterotrophic.  Habitat:  Found in marine environments in a symbiotic relationship or as free-livingIt can also be parasitic and saprophyticOften found in the Hawaiian squid, Euprymna scolopes, where the bacteria bioluminesce in the light organThe squid protects the bacteria from predators and provides nutrients, while the bacteria’s light eliminates the squid’s shadow, protecting it from predators. Disease: Other Vibrio species can cause human infections.
<b>4. Archaea identification: What is it?</b>
<br>These archaea were once thought to be extremophiles, but it turns out they are the most abundant archaea in the oceanNonetheless, the thermophiles responsible for giving this false impression are found at temperatures of 113degreesOthers are found living in sulfuring springsWhen gram stained, these archaea appear gram-negative.
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[[Category:Pages edited by students of Joan Slonczewski at Kenyon College]]

Latest revision as of 14:53, 23 July 2011

This page provides review questions for BIOL 238 (Spring 2011). Answers may be posted by students.


Species to know

For each species of bacteria or archaea, state one or two broader categories of organism (such as gram-positive endospore-forming bacteria), the type of genome, type(s) of metabolism, habitat, and disease caused (if any).

Aeromonas hydrophila

Anabaena sp.

Aquifex sp.

Bacillus anthracis

Bacillus subtilis

Bacillus thuringiensis

Bacteroides thetaiotaomicron

Borrelia burgdorferi

Chlamydia sp.

Clostridium botulinum

Chloroflexus sp.

Corynebacterium diphtheriae

Deinococcus radiodurans

Enterococcus sp.

Escherichia coli

Geobacter metallireducens

Halobacterium sp.

Helicobacter pylori

Lactobacillus sp.

Lactococcus sp.

Leptospira sp.

Methanococcus sp.

Mycobacterium tuberculosis

Mycoplasma pneumoniae sp.

Nitrospira sp.

Prochlorococcus sp.

Pseudomonas aeruginosa

Pyrococcus furiosus

Pyrodictium occultum

Rhodobacter sp.

Rhodopseudomonas sp.

Rhodospirillum rubrum

Rickettsia sp.

Salmonella enterica

Serratia marcescens

Sinorhizobium meliloti

Staphylococcus epidermidis

Staphylococcus aureus

Streptomyces sp.

Vibrio cholerae

Vibrio fischeri

Chapter 13


1. ATP and NADH are both energy carriers: What are the advantages of using one over the other?



2. When cells need to make glucose (gluconeogenesis), they "reverse glycolysis" because most steps are reversible. However, there are a couple of steps that are not reversible. How do you think they get reversed for gluconeogenesis?



3. There are 3 main pathways to form pyruvate- EMP, ED and PPS. How and why might a cell switch among these?



4. Explain why most soil bacteria grow using energy-yielding reactions with very small delta-G.



5. Why are glucose catabolism pathways ubiquitous, despite the fact that most bacterial habitats never provide glucose? Explain several reasons.



6. In glycolysis, explain why bacteria have to return the hydrogens from NADH back onto pyruvate to make fermentation products. Why can't NAD+ serve as a terminal electron acceptor, like O2?



7. Why do environmental factors regulate catabolism? Give examples. Why are amino acids decarboxylated at low pH, and under anaerobiosis?



8. Why does catabolism of benzene derivatives yield less energy than sugar catabolism? Why is benzene-derivative catabolism nevertheless widespread among soil bacteria?



Chapter 14


1. Explain how bacteria and archaea switch among various electron acceptors depending on environmental conditions.



2. Explain how cell processes such as ATP synthesis can be powered by either the transmembrane pH difference or by the charge difference across the membrane. Which form of energy is likely to be used at low external pH? At high external pH?



3. For phototrophy, discuss the relative advantages and limitations of using PS I versus PS II.



4. What environments favor oxygenic photosynthesis, versus sulfur phototrophy and photoorganotrophy? Explain.



5. Explain why certain lithotrophs acidify their environments, to more extreme levels than fermentation. What are some practical consequences for human industry?



6. Is it surprising that an organism may switch between lithotrophy and organotrophy? What enzymes would have to be replaced, and what enzymes could be used in common for both kinds of metabolism?



7. What kind of environments favor methanogenesis? Why are methanogens widespread, despite the low delta-G of their energy-yielding metabolism?



Chapter 15



1. Why does biosynthesis need both ATP and NADPH? Why couldn't biosynthetic pathways use just ATP, or just NADPH?



2. Compare and contrast fatty acid biosynthesis and amino acid biosynthesis. Which pathway requires more reduction? Which requires a greater number of different enzymes? Why?



3. What forms of nitrogen are available to microbes for assimilation? When fertilizer is spread on farmland to nourish crops, what problem is caused by microbes? What are the other oxidized forms that bacteria and plants take up and reduce to ammonia and ammonium ion? What about N from reduced organic compounds?



4. How are the pathways of amino acid biosynthesis organized? What common routes flow from which core pathways?



5. How and why do bacteria make "secondary products"? What are their functions?



6. How can we manipulate bacterial secondary product formation to develop new pharmaceutical agents?



Chapter 17

1. Explain why the first kinds of metabolism on Earth involved electron donors from the sediment reacting with electron receptors from above. What geolotical and outer-space processed generated these electron donors and electron acceptors?





2. What evidence supports the "RNA world" aspect of the origin of life? What are evolutionary and medical implications of the RNA world model?



3. What is our modern definition of a microbial species? Explain the strengths and limitations of defining microbial species based on common ancestry of DNA sequence.



4. Explain the evolutionary origins of mitochondria and chloroplasts. What evidence do we see in the structures of modern microbes?



5. What is a virulence gene? How do virulence genes evolve? How can we analyze the relationship between virulent and nonvirulent strains of a bacterium?

Chapter 18

1. Compare and contrast the major divisions of bacteria. State an example of a species of each major division.



2. Explain an example of a major division of bacteria whose species show nearly uniform metabolism but differ widely in form. Explain a different example of a division showing a common, distinctive form, but variety of metabolism.



3. Compare and contrast three different types of phototrophy found in bacteria.



4. Explain the pathology of three different gram-positive pathogens.



5. Explain two different examples of bacterial-host mutualism.





6. Identify these kinds of bacteria based on their descriptions:


a. This bacteria is irregularly shaped with peptidoglycan cell walls and a cytoskeleton containing tubulin (previously thought to only be present in Eukaryotes). They are heterotrophs living in variable environments that are usually low in salt, and most are oligotrophs.
b. This bacteria has a nucleus similar to that of a eukaryotic organism. It is most notable for its unique membrane structure. It has multiple internal membranes, with a double membrane functioning to surround the nucleoid. What am I?!
c. Bacteria in this group are filamentous photoheterotrophs. In the presence of oxygen they conduct nonphotosynthetic heterotrophy. They can be found in microbial mats together with thermophilic cyanobacteria. Some species contain chlorosomes. They are also known as green nonsulfur bacteria.
d. These bacteria are photolithotrophs that deposit sulfur on the cell surface. They use H2S as an electron donor and are known as green sulfur bacteria. These bacteria also live in strictly anaerobic conditions below the water surface.
e. This bacterium is gram positive but has permanently lost its cell wall and S-layer due to reductive/degenerative evolution. It also has the smallest genome(580 kbp) and it is parasitic.
f. This bacterial species ferments complex carbohydrates and serves as one of the major mutualists of the human gut. Has a Gram-negative structure and is an obligate anaerobe.
g. These bacteria are deep branching and come in a multitude of forms. They can be found living independently or in colonies. Often times, these different forms allow them to fix nitrogen. While these organisms can be found in both aquatic and terrestrial habitats, many species contain gas vesicles to maintain a favorable position in the water column.



Chapter 19

1. Compare and contrast the different major groups of archaea. Which ones grow in extreme heat or cold? Extreme salt? Produce methane?



2. Explain how archaea growing in extreme environments require specialized equipment for study.



3. What kinds of archaea grow in "average" environment such as the soil? Or an animal digestive tract?



4. Archaea identification: What is it?
These archaea were once thought to be extremophiles, but it turns out they are the most abundant archaea in the ocean. Nonetheless, the thermophiles responsible for giving this false impression are found at temperatures of 113degrees. Others are found living in sulfuring springs. When gram stained, these archaea appear gram-negative.