Jun 2016 Unit 1 Flashcards

1
Q

Give one piece of evidence that supports the theory that mitochondria evolved from prokaryotic cells.

A

Circular DNA

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2
Q

What is the advantage to cells of having mitochondria?

A
  1. Able to respire aerobically;
  2. So make (more) ATP/ release (more)
    energy
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3
Q

Explain how the highest blood pressure is produced in the left ventricle.

A

stronger contractions as it has a thicker muscular wall

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4
Q

Some babies are born with a hole between the right and the left ventricles. These babies are unable to get enough oxygen to their tissues.
Suggest why.

A
  1. Blood flows from left ventricle to right ventricle/ mixing of oxygenated and deoxygenated blood;
  2. Lower volume of (oxygenated) blood leaves left ventricle/flows into aorta/C
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5
Q

Suggest one advantage of using a pH meter rather than a pH indicator in this experiment.

A

Greater accuracy

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6
Q

Explain why the pH decreases when the lipase is added to the milk.

A

Fatty acids produced

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7
Q

Suggest why the pH remained constant after 2 minutes.

A
  1. No more (fatty) acids produced;

2. All triglycerides/fat//lipids/substrate used up / enzyme denatured;

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8
Q

Trypsin is a protease. It is produced in an inactive form inside some of the cells of the pancreas.
Name the part of a pancreatic cell that produces the inactive form of trypsin.

A

Ribosome

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9
Q

Suggest the advantage of producing trypsin in an inactive form inside cells in the pancreas.

A
  1. Does not digest protein inside cells;

2. So (pancreatic) cell/tissue/function not destroyed/damaged;

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10
Q

Sometimes trypsin can become activated inside a pancreatic cell. A competitive inhibitor in the cell then binds to the trypsin and stops it working.
Explain how the competitive inhibitor stops trypsin working.

A
  1. Inhibitor is a similar shape to the substrate;
  2. (Inhibitor) blocks active site/is complementary to the active site/binds to the active site (of trypsin);
  3. Substrate can’t bind to active site / no/fewer ES complexes formed;
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11
Q

Explain the role of the diaphragm in breathing out.

A
  1. Diaphragm moves up /becomes dome shaped;
  2. Reduces volume of lungs / increase
    pressure in lungs;
  3. Pressure in lungs higher than outside (air);
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12
Q

Use the data shown in Figure 4 to compare the change in FEV1 of people who continued to smoke with those who stopped smoking.

A
  1. FEV1 of those who have stopped smoking increased after 1 year whereas the FEV1 of smokers decreased;
  2. (Between years 1 and 5, FEV1 of both decreases but) the rate of decrease in FEV1 of smokers is faster than those who stopped smoking;
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13
Q

Smoking causes changes in the lungs and airways of smokers.

Suggest two changes in the lungs of people who continue to smoke that could explain the change in their FEV1.

A
  1. Airways are narrowed/blocked;

2. Excess mucus (in airway);

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14
Q

Suggest how the scientists may have treated the milk to remove lactose.

A

Add lactase

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15
Q

The scientists told the volunteers to drink the milk first thing in the morning rather than at bedtime.
Suggest why.

A

able to record their symptoms during the day

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16
Q

Suggest one instruction that the scientists would have given the volunteers about what they should not eat or drink each day, during this investigation.

A

Eat no other foods containing lactose

17
Q

Suggest why the scientists changed the type of milk they gave each group after one week.

A

to compare effect of lactose on both groups;

18
Q

What can you conclude from the scientists’ results in Table 3?

A
  1. Drinking (untreated) milk causes (a little) bloating;
  2. Drinking (small amount)of untreated milk has little/no effect on pain/diarrhoea;
  3. Difference is small so may not be significant
19
Q

People who do not have the specific receptor protein in their cell-surface membranes may be infected with the Ebola virus but do not develop the disease (lines 1–5).
Explain why they do not develop the disease.

A
  1. Virus can’t bind (to receptor)/ can’t enter cells;

2. So can’t be replicated/ multiply;

20
Q

Explain the increase in specific plasma cells and antibody in people infected with the nEbola virus.

A
  1. Antigen/glycoprotein on Ebola binds to/stimulates (a specific) B cell;
  2. (Binding causes) replication/cloning of B cell;
  3. Plasma cells/B cells release/produce antibodies;
21
Q

Explain how a blood transfusion from a patient recently recovered from Ebola may be an effective treatment (lines 8–10).

A
  1. Lots of antibodies (against Ebola) in recovered patient;
  2. Transfusion/plasma contains antibodies;
  3. Antibodies (specific so) will bind with (Ebola) antigen;
  4. (In recipient) virus destroyed/cannot enter cell;
22
Q

A high mutation rate makes it difficult to develop a vaccine (line 11). Explain why.

A
  1. (High mutation rate leads to) antigens change/antigenic variability;
  2. Vaccine contains specific antigen;
  3. Antibodies not complementary to (changed) antigen / won’t bind to (changed) antigens;
23
Q

Glucose is absorbed from the lumen of the small intestine into epithelial cells.
Explain how the transport of sodium ions is involved in the absorption of glucose by epithelial cells.

A
  1. Na+ ions leave epithelial cell and enter blood;
  2. (Transport out is by) active transport / pump / via carrier protein using ATP;
  3. So, Na+ conc. in cell is lower than in lumen (of gut);
  4. Sodium/Na+ ions enter by facilitated diffusion;
  5. Glucose absorbed with Na+ ions against their concentration/diffusion gradient / glucose absorbed down an electrochemical gradient;
24
Q

Oxygen and chloride ions can diffuse across cell surface membranes. The diffusion of chloride ions involves a membrane protein. The diffusion of oxygen does not involve a membrane protein.
Explain why the diffusion of chloride ions involves a membrane protein and the diffusion of oxygen does not.

A
  1. Chloride ions water soluble/charged/polar;
  2. Cannot cross (lipid) bilayer (of membrane);
  3. Chloride ions transported by facilitated diffusion OR diffusion involving channel/carrier protein;
  4. Oxygen not charged/non-polar;
  5. (Oxygen) soluble in/can diffuse across (lipid) bilayer;