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. Lipase
B. Pepsin
C. Trypsin
D. Salivary amylase

2 What is the main substrate of salivary amylase?

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

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. Sudan III
C. Biuret reagent
D. Iodine solution

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

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

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

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

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 remove the substrate
B. To stop all reactions
C. To allow enzyme action
D. To sterilize the iodine

9 What does enzyme activity describe?

Determination of salivary amylase enzyme activity Easy
A. The color of the test tube
B. The density of the reagent
C. The rate of substrate conversion
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. Amino acids
C. Fatty 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 provide a comparison
C. To increase enzyme concentration
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. Name of the enzyme
B. Volume of the test tube
C. Saliva collection time
D. Remaining starch color

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

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

15 What is denaturation of an enzyme?

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

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 remove the iodine reaction
C. To prevent saliva collection
D. To allow fair comparison

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 changes into starch
C. It always becomes zero
D. It becomes independent of pH

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

Determination of salivary amylase enzyme activity Easy
A. It may be denatured
B. It may form more saliva
C. It may produce iodine
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. Color of the laboratory coat
B. Amount of starch remaining
C. Length of the test tube
D. Mass of the test-tube rack

20 What is the role of saliva in this experiment?

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

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 stop starch hydrolysis immediately
B. To increase the enzyme concentration
C. To bring the reaction into a measurable range
D. To convert maltose into starch

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

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

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 enzyme temperature
D. A decrease in intact starch

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 iodine solution digests starch
B. The buffer increases enzyme synthesis
C. The saliva contains glucose
D. The substrate reacts without enzyme

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

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. Increase indefinitely with temperature
B. Decrease because the enzyme may denature
C. Remain unchanged because enzymes ignore temperature
D. Become independent of substrate concentration

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 prevents iodine from dissolving
C. Acid increases starch concentration
D. Acid converts amylase into a carbohydrate

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

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

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

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

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

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. Higher because boiling activates iodine
B. Unchanged because starch protects enzymes
C. Lower because the protein is denatured
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. Contains active starch-degrading enzyme
B. Contains no hydrolyzable substrate
C. Has a higher starch concentration than control
D. Prevented the iodine reagent from reacting

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. Loss of the starch-iodine complex
C. Decrease in the cuvette path length
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 become zero
B. Remain exactly unchanged
C. Approximately double
D. Decrease by approximately half

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. Underestimated because reaction time is recorded too long
C. Unaffected because timing is irrelevant
D. Overestimated 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. Starch concentration is fixed by saliva collection
C. Salivary composition can vary with collection conditions
D. Buffer pH is determined by the donor's identity

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. Complete prevention of iodine binding
C. Permanent increase in buffer concentration
D. Conversion of amylase into starch

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

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

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

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

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. Increase until the enzyme approaches saturation
B. Remain zero at every concentration
C. Increase without any upper limit
D. Decrease immediately to zero

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. 72.5%
C. 38.9%
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. 0.30 μmol min⁻¹ mL⁻¹
B. 1.50 μmol min⁻¹ mL⁻¹
C. 0.03 μmol min⁻¹ mL⁻¹
D. 0.15 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. A and B have equal original activities
B. A has twice the original activity of B
C. B has 50% greater original activity than A
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. 0.410
B. 0.340
C. 0.510
D. 0.850

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 remains unchanged
B. The rate decreases by half
C. The rate approximately doubles
D. The rate increases fourfold

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. The iodine reagent has increased enzyme concentration
B. The enzyme becomes more active later
C. The assay remains strictly linear
D. Substrate depletion or product effects may occur

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. 8.0 μmol min⁻¹ mL⁻¹
B. 4.0 μmol min⁻¹ mL⁻¹
C. 80 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. 60.0 μg min⁻¹
D. 6.0 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 changes starch into protein
B. It eliminates all pipetting variation
C. It omits part of the reaction period
D. It increases the iodine wavelength

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. Altered collection volume or flow rate
B. Conversion of amylase into DNA
C. Contamination with oral food residues
D. Hemoconcentration of saliva

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. 48.00 μmol min⁻¹
C. 0.75 μmol min⁻¹
D. 3.00 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 is precipitated by buffer
B. Iodine permanently activates amylase
C. Iodine primarily detects residual starch
D. Maltose always absorbs at 280 nm

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 saliva dilution factor becomes zero
B. The cuvette path length becomes shorter
C. The enzyme's catalytic rate may change during incubation
D. The starch concentration becomes exactly constant

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 contains no active enzyme
B. It proves the first assay was contaminated
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. 0–6 minutes
B. 4–6 minutes
C. 2–4 minutes
D. 0–2 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. Report the absorbance as enzyme units directly
B. Dilute the sample and repeat within range
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 assay proves complete hydrolysis
B. The enzyme necessarily denatured
C. The iodine must be absent
D. The substrate may remain largely unhydrolyzed

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. 12.0 μmol min⁻¹ mL⁻¹
B. 9.0 μmol min⁻¹ mL⁻¹
C. 3.0 μmol min⁻¹ mL⁻¹
D. 1.5 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. Iodine cannot react with any starch concentration
B. Different substrate concentrations alter reaction conditions
C. Amylase activity is independent of substrate concentration
D. Higher starch concentration always destroys the enzyme

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 product concentration is overestimated
B. The enzyme concentration is doubled
C. The incubation time becomes negative
D. The product concentration is underestimated