Unit 6: Enzyme Activity - Practice Quiz

BTY301 — Biochemistry Laboratory 60 Questions
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1 Which enzyme in saliva helps digest starch?

Determination of salivary amylase enzyme activity Easy
A. Pepsin
B. Salivary amylase
C. Lipase
D. Trypsin

2 What is the main substrate of salivary amylase?

Determination of salivary amylase enzyme activity Easy
A. DNA
B. Starch
C. Protein
D. Fat

3 Which reagent is commonly used to test for the presence of starch?

Determination of salivary amylase enzyme activity Easy
A. Benedict's solution
B. Biuret reagent
C. Sudan III
D. Iodine solution

4 What color indicates the presence of starch after adding iodine?

Determination of salivary amylase enzyme activity Easy
A. Brick-red
B. Violet
C. Orange
D. Blue-black

5 What happens to the iodine color as salivary amylase digests starch?

Determination of salivary amylase enzyme activity Easy
A. It becomes lighter
B. It turns bright green
C. It becomes darker
D. It remains unchanged

6 Why is saliva diluted before testing its amylase activity?

Determination of salivary amylase enzyme activity Easy
A. To remove all starch
B. To destroy the enzyme
C. To increase the temperature
D. To obtain a measurable reaction

7 Which condition is generally suitable for salivary amylase activity?

Determination of salivary amylase enzyme activity Easy
A. Strongly acidic pH
B. Near-neutral pH
C. Extremely salty pH
D. Strongly alkaline pH

8 What is the purpose of incubating the starch and saliva mixture?

Determination of salivary amylase enzyme activity Easy
A. To allow enzyme action
B. To stop all reactions
C. To remove the substrate
D. To sterilize the iodine

9 What does enzyme activity describe?

Determination of salivary amylase enzyme activity Easy
A. The density of the reagent
B. The rate of substrate conversion
C. The color of the test tube
D. The volume of saliva used

10 Which substance is produced when amylase breaks down starch?

Determination of salivary amylase enzyme activity Easy
A. Maltose
B. Fatty acids
C. Amino acids
D. Nucleotides

11 Why is a control tube included in an amylase experiment?

Determination of salivary amylase enzyme activity Easy
A. To digest extra starch
B. To increase enzyme concentration
C. To provide a comparison
D. To change the pH automatically

12 What is the independent variable in a test comparing different saliva dilutions?

Determination of salivary amylase enzyme activity Easy
A. Saliva dilution
B. Iodine color
C. Final observation
D. Tube label

13 What is the dependent observation in an iodine-starch amylase test?

Determination of salivary amylase enzyme activity Easy
A. Saliva collection time
B. Volume of the test tube
C. Name of the enzyme
D. Remaining starch color

14 What is the effect of boiling saliva before the assay?

Determination of salivary amylase enzyme activity Easy
A. It creates more starch
B. It reduces enzyme activity
C. It changes starch into protein
D. It increases enzyme activity

15 What is denaturation of an enzyme?

Determination of salivary amylase enzyme activity Easy
A. Formation of additional substrate
B. Increase in its volume
C. Conversion into a vitamin
D. Loss of its functional shape

16 Why should the incubation time be kept constant for all tubes?

Determination of salivary amylase enzyme activity Easy
A. To make every enzyme inactive
B. To allow fair comparison
C. To remove the iodine reaction
D. To prevent saliva collection

17 What generally happens to enzyme activity when temperature is increased moderately toward the optimum?

Determination of salivary amylase enzyme activity Easy
A. It generally increases
B. It becomes independent of pH
C. It always becomes zero
D. It changes into starch

18 What may happen if salivary amylase is exposed to very high temperature?

Determination of salivary amylase enzyme activity Easy
A. It may produce iodine
B. It may be denatured
C. It may form more saliva
D. It may become starch

19 Which measurement can be used to compare amylase activity in a timed assay?

Determination of salivary amylase enzyme activity Easy
A. Mass of the test-tube rack
B. Color of the laboratory coat
C. Length of the test tube
D. Amount of starch remaining

20 What is the role of saliva in this experiment?

Determination of salivary amylase enzyme activity Easy
A. It provides the starch indicator
B. It provides the enzyme
C. It provides the iodine
D. It provides the water bath

21 A saliva sample is diluted before testing amylase activity. What is the main purpose of this dilution?

Determination of salivary amylase enzyme activity Medium
A. To convert maltose into starch
B. To stop starch hydrolysis immediately
C. To increase the enzyme concentration
D. To bring the reaction into a measurable range

22 Why is starch commonly used as the substrate in a salivary amylase assay?

Determination of salivary amylase enzyme activity Medium
A. Starch directly produces iodine molecules
B. Amylase hydrolyzes starch into smaller sugars
C. Starch maintains a constant reaction temperature
D. Starch inhibits all salivary enzymes

23 In the iodine method, a decrease in the blue-black color of the reaction mixture indicates:

Determination of salivary amylase enzyme activity Medium
A. An increase in intact starch
B. An increase in iodine concentration
C. A decrease in intact starch
D. A decrease in enzyme temperature

24 A control tube contains starch and buffer but no saliva. Its purpose is to determine whether:

Determination of salivary amylase enzyme activity Medium
A. The substrate reacts without enzyme
B. The buffer increases enzyme synthesis
C. The saliva contains glucose
D. The iodine solution digests starch

25 Why should saliva and starch solutions be pre-equilibrated at the assay temperature before mixing?

Determination of salivary amylase enzyme activity Medium
A. To denature the amylase before timing
B. To convert starch into reducing sugar
C. To reduce the effect of temperature changes
D. To remove all substrate from the mixture

26 If the reaction temperature is increased well above the optimum for salivary amylase, the measured activity will most likely:

Determination of salivary amylase enzyme activity Medium
A. Decrease because the enzyme may denature
B. Become independent of substrate concentration
C. Remain unchanged because enzymes ignore temperature
D. Increase indefinitely with temperature

27 Salivary amylase usually shows reduced activity in a strongly acidic mixture because:

Determination of salivary amylase enzyme activity Medium
A. Acid changes the enzyme's active-site structure
B. Acid converts amylase into a carbohydrate
C. Acid prevents iodine from dissolving
D. Acid increases starch concentration

28 A buffer is included in the salivary amylase assay primarily to:

Determination of salivary amylase enzyme activity Medium
A. Maintain a relatively stable pH
B. Replace the need for enzyme
C. Supply starch for the reaction
D. Measure absorbance directly

29 Two assays use equal volumes of starch and saliva, but one is incubated twice as long. If the reaction remains linear, the longer assay should show:

Determination of salivary amylase enzyme activity Medium
A. Approximately twice the substrate hydrolysis
B. A complete loss of buffer capacity
C. No measurable change in starch
D. Exactly half the enzyme concentration

30 Why is enzyme activity preferably calculated from the initial reaction rate?

Determination of salivary amylase enzyme activity Medium
A. The enzyme is completely absent initially
B. The reaction has already reached equilibrium
C. The color reagent has fully decomposed
D. The substrate and product effects are minimized

31 If a saliva sample is accidentally heated to boiling before the assay, its amylase activity will most likely be:

Determination of salivary amylase enzyme activity Medium
A. Unchanged because starch protects enzymes
B. Lower because the protein is denatured
C. Higher because boiling activates iodine
D. Higher because collisions increase permanently

32 A reaction mixture gives a lighter iodine color than the control after the same incubation time. This result suggests that the sample:

Determination of salivary amylase enzyme activity Medium
A. Prevented the iodine reagent from reacting
B. Contains no hydrolyzable substrate
C. Has a higher starch concentration than control
D. Contains active starch-degrading enzyme

33 In a spectrophotometric assay, absorbance at the starch-iodine wavelength decreases over time. The decrease most directly represents:

Determination of salivary amylase enzyme activity Medium
A. Increase in enzyme molecular mass
B. Decrease in the cuvette path length
C. Loss of the starch-iodine complex
D. Formation of additional intact starch

34 If the saliva volume is doubled while substrate, temperature, and time remain suitable, the initial reaction rate is expected to:

Determination of salivary amylase enzyme activity Medium
A. Approximately double
B. Approximately become zero
C. Decrease by approximately half
D. Remain exactly unchanged

35 A student starts timing several seconds after mixing saliva with starch. The calculated activity will most likely be:

Determination of salivary amylase enzyme activity Medium
A. Invalid only if iodine is absent
B. Unaffected because timing is irrelevant
C. Overestimated because reaction time is recorded too long
D. Underestimated because reaction time is recorded too long

36 Why should saliva be collected under similar conditions when comparing amylase activity among samples?

Determination of salivary amylase enzyme activity Medium
A. Iodine reacts differently with each donor's glassware
B. Salivary composition can vary with collection conditions
C. Buffer pH is determined by the donor's identity
D. Starch concentration is fixed by saliva collection

37 If all tubes are not mixed equally after saliva is added, the main effect on the assay is:

Determination of salivary amylase enzyme activity Medium
A. Poor contact between enzyme and substrate
B. Conversion of amylase into starch
C. Permanent increase in buffer concentration
D. Complete prevention of iodine binding

38 A student obtains absorbance values outside the standard calibration range. The best response is to:

Determination of salivary amylase enzyme activity Medium
A. Add more iodine until the value fits
B. Change the wavelength after measuring
C. Dilute the sample and repeat the measurement
D. Report the value without qualification

39 A blank containing all reagents except saliva is used to correct for:

Determination of salivary amylase enzyme activity Medium
A. The temperature of the water bath
B. The enzyme concentration in saliva
C. Background absorbance from the reagents
D. The exact rate of starch hydrolysis

40 If substrate concentration is increased from a limiting level while enzyme concentration remains constant, the initial rate will usually:

Determination of salivary amylase enzyme activity Medium
A. Decrease immediately to zero
B. Remain zero at every concentration
C. Increase without any upper limit
D. Increase until the enzyme approaches saturation

41 A starch–iodine assay is calibrated so that the absorbance at 620 nm is 0.800 when 100% of the initial starch remains and 0.080 when no starch remains. A reaction mixture gives an absorbance of 0.350. What percentage of starch was hydrolyzed, assuming a linear relationship?

Determination of salivary amylase enzyme activity Hard
A. 61.1%
B. 38.9%
C. 72.5%
D. 50.0%

42 In a salivary amylase assay, the sample contains 0.20 mL saliva and the reaction volume is 2.00 mL. After 5 minutes, 0.30 μmol of reducing sugar is produced. What is the activity expressed as μmol min⁻¹ mL⁻¹ of saliva?

Determination of salivary amylase enzyme activity Hard
A. 1.50 μmol min⁻¹ mL⁻¹
B. 0.03 μmol min⁻¹ mL⁻¹
C. 0.15 μmol min⁻¹ mL⁻¹
D. 0.30 μmol min⁻¹ mL⁻¹

43 Two assays use identical substrate concentrations and incubation times. Assay A contains 0.10 mL saliva diluted 1:5 and produces 0.40 μmol reducing sugar. Assay B contains 0.20 mL saliva diluted 1:10 and produces 0.60 μmol. Which conclusion is justified?

Determination of salivary amylase enzyme activity Hard
A. B has 50% greater original activity than A
B. A and B have equal original activities
C. A has twice the original activity of B
D. The activities cannot be compared without starch concentration

44 A blank containing starch, buffer, and iodine has an absorbance of 0.920. The complete reaction has an absorbance of 0.410, while a reagent blank without starch has an absorbance of 0.070. Which corrected absorbance should be used to estimate starch hydrolysis?

Determination of salivary amylase enzyme activity Hard
A. 0.850
B. 0.510
C. 0.340
D. 0.410

45 A student doubles the saliva volume while keeping substrate, buffer, total volume, and incubation time unchanged. The reaction is already substrate-limited and shows a proportional increase in product formation. What is the most likely result?

Determination of salivary amylase enzyme activity Hard
A. The rate approximately doubles
B. The rate increases fourfold
C. The rate remains unchanged
D. The rate decreases by half

46 The initial rate of starch hydrolysis is 0.80 μmol min⁻¹ during the first 4 minutes. Between 4 and 8 minutes, the average rate falls to 0.35 μmol min⁻¹. Which interpretation is most appropriate?

Determination of salivary amylase enzyme activity Hard
A. Substrate depletion or product effects may occur
B. The enzyme becomes more active later
C. The assay remains strictly linear
D. The iodine reagent has increased enzyme concentration

47 A saliva sample is diluted 1:20. A 0.10 mL aliquot of this dilution produces 2.4 μmol reducing sugar in 6 minutes. What is the activity of the original saliva?

Determination of salivary amylase enzyme activity Hard
A. 80 μmol min⁻¹ mL⁻¹
B. 4.0 μmol min⁻¹ mL⁻¹
C. 8.0 μmol min⁻¹ mL⁻¹
D. 480 μmol min⁻¹ mL⁻¹

48 A calibration curve for maltose is , where is in μg mL⁻¹. A test tube has absorbance 0.390 after subtraction of a reagent blank. Its final assay volume is 3.0 mL, and incubation lasted 5 minutes. What is the product formation rate?

Determination of salivary amylase enzyme activity Hard
A. 180.0 μg min⁻¹
B. 18.0 μg min⁻¹
C. 6.0 μg min⁻¹
D. 60.0 μg min⁻¹

49 An assay is incubated at 37 °C, but the enzyme and substrate are mixed at room temperature and the timer is started 90 seconds later. Why can this create a systematic error?

Determination of salivary amylase enzyme activity Hard
A. It increases the iodine wavelength
B. It omits part of the reaction period
C. It eliminates all pipetting variation
D. It changes starch into protein

50 A saliva sample gives lower apparent amylase activity after vigorous exercise, although the subject's enzyme production is unchanged. Which preanalytical factor most plausibly explains the result?

Determination of salivary amylase enzyme activity Hard
A. Hemoconcentration of saliva
B. Contamination with oral food residues
C. Conversion of amylase into DNA
D. Altered collection volume or flow rate

51 The measured activity is 12.0 μmol min⁻¹ mL⁻¹. The assay used 0.25 mL saliva, but the saliva had been diluted 1:4 before use. What total activity was present in the original saliva volume used?

Determination of salivary amylase enzyme activity Hard
A. 12.00 μmol min⁻¹
B. 3.00 μmol min⁻¹
C. 0.75 μmol min⁻¹
D. 48.00 μmol min⁻¹

52 A student uses iodine color intensity as though it were directly proportional to maltose concentration. What is the principal conceptual error?

Determination of salivary amylase enzyme activity Hard
A. Maltose always absorbs at 280 nm
B. Iodine primarily detects residual starch
C. Iodine permanently activates amylase
D. Maltose is precipitated by buffer

53 A reaction mixture is incubated at pH 6.8, but the buffer capacity is very low. Hydrolysis causes the pH to fall to 5.2. What is the strongest reason this can distort the calculated activity?

Determination of salivary amylase enzyme activity Hard
A. The starch concentration becomes exactly constant
B. The saliva dilution factor becomes zero
C. The cuvette path length becomes shorter
D. The enzyme's catalytic rate may change during incubation

54 A 1.00 mL assay contains 0.20 mL saliva and produces 0.50 μmol product in 2 minutes. A second assay contains 0.10 mL saliva and produces 0.28 μmol in 2 minutes. Which result best indicates the second assay?

Determination of salivary amylase enzyme activity Hard
A. It proves the first assay was contaminated
B. It contains no active enzyme
C. It has greater activity per saliva volume
D. It has exactly half the enzyme activity

55 In a time-course experiment, absorbance values for residual starch are 0.80, 0.62, 0.45, and 0.31 at 0, 2, 4, and 6 minutes. Which interval is most suitable for estimating the initial rate?

Determination of salivary amylase enzyme activity Hard
A. 4–6 minutes
B. 0–2 minutes
C. 0–6 minutes
D. 2–4 minutes

56 A sample's absorbance lies above the highest standard in a starch–iodine calibration curve. Which action gives the most defensible quantitative result?

Determination of salivary amylase enzyme activity Hard
A. Dilute the sample and repeat within range
B. Report the absorbance as enzyme units directly
C. Replace the value with the highest standard
D. Extrapolate far beyond the calibration range

57 In an iodine endpoint method, the test color is still strongly blue after incubation, but a no-enzyme control is also blue. Which conclusion is most appropriate?

Determination of salivary amylase enzyme activity Hard
A. The iodine must be absent
B. The enzyme necessarily denatured
C. The substrate may remain largely unhydrolyzed
D. The assay proves complete hydrolysis

58 An assay contains 0.15 mL saliva and is diluted 1:3. It produces 1.8 μmol product in 4 minutes. If the original saliva volume represented is used for normalization, what activity is obtained?

Determination of salivary amylase enzyme activity Hard
A. 3.0 μmol min⁻¹ mL⁻¹
B. 1.5 μmol min⁻¹ mL⁻¹
C. 9.0 μmol min⁻¹ mL⁻¹
D. 12.0 μmol min⁻¹ mL⁻¹

59 A student compares two saliva samples using different starch concentrations: sample X is measured at 0.5% starch and sample Y at 2.0% starch. Why is a direct comparison of absorbance changes potentially invalid?

Determination of salivary amylase enzyme activity Hard
A. Higher starch concentration always destroys the enzyme
B. Iodine cannot react with any starch concentration
C. Different substrate concentrations alter reaction conditions
D. Amylase activity is independent of substrate concentration

60 A reaction is stopped by adding acid before iodine is added. If the acid volume is not included in the final-volume calculation for a reducing-sugar assay, what type of error results?

Determination of salivary amylase enzyme activity Hard
A. The enzyme concentration is doubled
B. The incubation time becomes negative
C. The product concentration is overestimated
D. The product concentration is underestimated