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28 Apr 2019

Please answer both questions with good, long answers.

#1 .Describe the different methods of locomotion used by the live protists presented in this lab.

Protists:Amoeba, Apicomplexa, Ciliophora, Foraminifera, Kinetoplastans, Radiolaria

#2.Describe the methods of reproduction used by protists and illustrate the life histories of the parasites Trypanosoma brucei rhodesiense and Plasmodium vivax.

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Casey DurganLv2

29 Apr 2019

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Related questions

An area has two different Anopheles species, both of which can vector Plasmodium, although Plasmodiumdevelops best and is transmitted best by species B. Species A is dominant because its larvae outcompete species B in the main shared breeding sites, small lakes and ponds. Therefore the population of B is currently small. The small lakes and ponds are also the source for the main food source in the region, fish, grown in fish farms. There is grazing land, but other than chickens, the local population does not have livestock. Species A is largely endophagous and endophilic, species B is exophilic. In other sites, both species A and B will also feed on cattle, and B appears to prefer cattle. Both species also like to roost during the hot day in rock overhangs and small caves. To give some context to your answers use the IPM terminology considered in class.

A) The national malaria control agency sends in a new person to develop a malarial control strategy. (S)he recommends oiling the lakes and ponds, and intensive house spraying . Discuss why each of these two options would be a good or bad idea. In your answer consider effects on species A, species B, and malaria incidence. And remember, the idea is to help the local population.

B) Develop an alternative targeted strategy that might work well in this situation. Explain why this would be a good fit. Use only strategies that have been used successfully in the field, and avoid "just spray everything" strategies. Explain why your strategy should work.

After roughly 15 years we have the first malaria vaccine going into phase 4 trials. Meanwhile a Zika vaccine is starting phase 2b trials, only 2-3 years after the first major outbreak in Brazil.

A) Discuss in some detail why it is so much more difficult to develop a vaccine for malaria than for e.g. the Zika or rubella virus. I am looking for at least 2 reasons, and a brief explanation of those reasons. Just stating that one is complex and the other simple is insufficient. If that is what you want to say, back it up with facts.

B) Both the CRISPR bacterial defense system and the adaptive immune system in mammals have means to recognize âsignaturesâ of invading organisms. In what way are the two systems different?

The malaria control team in a given area has access to 5 different drugs, chloroquine, mefloquine, pyrimethamine, amodiaquine, and artimisinin. Nothing else will be available for the foreseeable future. Some resistance to all 5 is already observed.

A) Provide a strategy to maximize the time you can cure malaria using these 5 drugs. Explain why you want to use this strategy (what is the idea behind your plan), and be precise: when do you plan to use what drugs. What are the potential problems you can face and how do you plan to deal with them? Remember, you are working with humans, not robots.

B) Hypnozoites are forms of P. vivax and P. ovale that are dormant, with barely any metabolic activity. After long periods of time (months, a year), they can be re-activated start invading red blood cells, and causing malaria. Explain why artemisinin would or would not be a good drug for people suspected of carrying hyponozoites.

This experiment is about Affinity Purification of Green Fluorescent Protein (GFP)

please answer the below questions

1. What is a bacterial colony?

2. Why did you pick one green colony and one white colony from your agar plate(s)? Why do you think you picked one of each color? What could this prove?

3. How are these items helpful in this cloning experiment? a. ultraviolet (UV) light - b. incubator - c. shaking incubator

4. Explain how placing cloned cells in nutrient broth to multiply relates to your overall goal of purifying the fluorescent protein.

5. You have used a bacterium to propagate a gene that produces a green fluorescent protein. Identify the function of these items you need in this procedure. a. Centrifuge â b. Lysozyme â c. Freezer â

6. Can you explain why both liquid cultures fluoresce green?

7. Why did you discard the supernatant in this part of the protein purification procedure?

8. Can you explain why the bacterial cellsâ outer membrane ruptures when the cells are frozen. What happens to an unopened soft drink when it freezes?

9. What was the purpose of rupturing or lysing the bacteria?

10. Briefly describe hydrophobic interaction chromatography and identify its purpose in this lab.

This lab is about Crystal Growth of Hen Egg White Lysozyme so please answer the following question

1. What condition yielded the "best" crystals of lysozyme?

2. What changes did your group try to make, and what effect did they have on the crystals?

3. How many of your conditions yielded crystals? How many did the entire class get? Give the percentage (number of conditions that gave crystals/number of different conditions that were set up) for your attempts as well as for the entire class. What does this tell you about protein crystallization?

4. What methods can you think of to determine if the crystals are lysozyme and not salt (many salt crystals are colorless as well)? (Hint: think of protein properties and ways to assay and look at proteins).

5. Many protein crystals are formed at or near the pI of the protein being studied. Can you rationalize any reason why this observation might be made (in other words, why is the pI so good at helping form protein crystals).

You and your hypothetical lab partner each develop an experimental plan to test this hypothesis. The two experimental plans are presented below. Evaluate each plan for its pros and cons in the experimental design using the bullet points below. Both experimental plans have some good elements and areas that could be improved.

Experiment A) Mature 2 inch sections (sprigs) of Elodea will be used to measure oxygen production under different light conditions. 5 sprigs will be tested. One will be kept in the dark (no light). The others will be exposed to a light filtered with cellophane. One sprigâs light will be filtered through clear cellophane to receive all wavelengths of light, and the other sprigsâ light will be filtered through red, blue, and green cellophane, respectively. The no-light plant will be kept in a dark cabinet, while the other plants will be together on a counter. Each plant sprig will be placed in equal sized upside-down test tubes in 100ml of tap water so that oxygen bubbles produced by the plant will be trapped at the top of the test tube. A ruler will be used to measure the length of the oxygen pocket collected at the top of the test tube. The experiment will continue until one sprig produces 5 cm of oxygen in the tube.

Experiment B) 3 cm sections (sprigs) of Elodea of various ages will be used to measure oxygen production under different light conditions. 15 sprigs will be divided into 3 groups of 5 sprigs each. One group will receive natural sunlight, one group will be exposed to a blue light bulb under a box to block natural light, and the final group will be exposed to a red light bulb under a similar box to block natural light. Each group of plant sprigs will be trapped under a clear plastic funnel that is covered by an upside-down test tube to collect oxygen bubbles produced by all the sprigs in the group. All groups will be in 100ml of water of the same temperature and pH. The experiment will continue for 24 hours, and then the volume of oxygen gas produced will be measured by multiplying the length of the oxygen pocket by the circle described by the test tube, ?r². The average volume produced by all groups will be graphed and compared to determine which condition produced the most total volume of oxygen.

Consider the following questions to evaluate experimental plans A and B (DO NOT ANSWER THESE QESTIONS)

What is the independent variable suggested by the hypothesis? Do both plans test the independent variable equally well?

What is the dependent variable in each experiment? Which experimentâs dependent variable best matches the prediction in the hypothesis?

What are the experimental and control groups for each experiment? Which experiment gives the best opportunity to assess the effect of the independent variable?

How does each experiment account for standardized variables? Which experiment do you think is the better controlled experiment?

How is sample size addressed in each experiment? Which would you find to be more convincing?

Does either experiment describe any statistical analyses to be performed on the data?

ANSWER THIS QUESTION: BELOW

Considering your analysis of each of the questions above,write an improved experimental design to test the hypothesis âIf blue light is more effective at promoting photosynthesis, then more oxygen gas (O₂) will be produced when plants are exposed to blue-filtered light compared to other wavelengths.âYou may use elements of the above experiments