Biotechnology: Genetic Engineering Techniques (College Board AP® Biology): Exam Questions

16 mins14 questions
1
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Which of the following best describes the purpose of the polymerase chain reaction (PCR)?

  • Creating recombinant plasmids.

  • Separating DNA fragments by mass.

  • Making more copies of specific DNA fragments for analysis.

  • Determining the order of bases in a DNA molecule.

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2
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Figure 1 shows part of a genetic engineering technique.

Diagram shows DNA electrophoresis in agarose gel with wells labelled CS, 1, 2, 3. DNA bands visible, negative and positive electrodes marked.
Figure 1. A genetic engineering technique.

Which of the following descriptions can be correctly applied to Figure 1?

  • The DNA bands each contain a different type of nucleotide.

  • The DNA bands represent fragments of different size.

  • The DNA bands show that all of the DNA fragments are the same size.

  • Figure 1 shows the polymerase chain reaction.

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3
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Which of the following best describes the process of bacterial transformation?

  • Cutting DNA into smaller fragments for analysis.

  • Amplifying DNA.

  • The production of human proteins by bacteria.

  • Introducing new DNA sequences into bacteria.

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41 mark

Which of the following correctly describes a genetic engineering technique?

  • Gel electrophoresis separates DNA fragments by size.

  • PCR creates new DNA molecules from scratch.

  • Bacterial transformation removes genes from bacterial cells.

  • DNA sequencing is used to alter the sequence of DNA bases.

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5
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A forensic expert isolated a small DNA sample at the scene of a crime. In order to analyze the DNA they needed to:

  • produce more copies of the DNA

  • determine the order of nucleotide bases in the DNA

Which of the following lists the DNA manipulation techniques that the forensic expert would need to use?

  • PCR and bacterial transformation

  • PCR and DNA sequencing

  • gel electrophoresis and DNA sequencing

  • DNA sequencing only

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A researcher investigated whether a patient carried a genetic mutation linked to a hereditary disease. They used a small DNA sample from the patient and the polymerase chain reaction (PCR).

Which of the following is the most likely predicted outcome from the PCR process?

  • The DNA sample will remain unchanged and there will not be enough DNA to analyze.

  • The DNA will be amplified, allowing the researcher to analyze the mutation more easily.

  • The genome will be sequenced, revealing the mutations present in the patient's DNA.

  • The PCR process will repair the mutation in the patient's DNA sample.

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A restriction enzyme is an enzyme used in biotechnology to cut DNA wherever a specific sequence of bases occurs. A restriction enzyme was used to cut a sample of DNA from a wild boar. The resulting genetic fingerprint can be seen in Figure 1.

Vertical black rectangle with five horizontal grey bars evenly spaced. The image resembles a simplified ruler or scale design.
Figure 1. Electrophoretegram of wild boar DNA

Which of the following states the number of times that the enzyme made a cut in the DNA sample?

  • Five

  • Four

  • Six

  • Twelve

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3
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BRCA1 is a tumor suppressor gene involved in the repair of damaged DNA. In an investigation researchers used PCR to amplify the BRCA1 gene from DNA samples taken from 50 individuals with a family history of breast cancer. After sequencing the amplified gene regions they found that 10 individuals carried mutations associated with an increased risk of cancer.

Which of the following conclusions can be drawn from this study?

  • All individuals with a family history of breast cancer will carry mutations in the BRCA1 gene.

  • Only individuals with BRCA1 mutations are at risk of developing breast cancer.

  • Some individuals with a family history of breast cancer may carry mutations in the BRCA1 gene, increasing their risk.

  • The absence of BRCA1 mutations means individuals have no risk of developing breast cancer.

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4
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The run-off from nitrogen-rich fertilizer applied to farmland creates major ecological problems. Plants such as legumes have symbiotic nitrogen-fixing bacteria which can help them to gain nitrogen from the soil without the need for adding fertilizer. However, these symbionts are not associated with crops such as corn. Scientists have developed a strain of nitrogen-fixing bacteria that can associate with corn roots.

Which of the following describes the method used by the scientists to synthesize this bacteria?

  • Polymerase chain reaction used to amplify the required gene fragments which can then be inserted into the cells of the host plant.

  • A plasmid vector with the required genes for corn association and nitrogen fixation is used to transform bacteria.

  • Cross-breeding of nitrogen-fixing bacteria from legumes with bacteria from corn plants to obtain the desired characteristics.

  • Cloning nitrogen-fixing genes from animals and inserting them into the corn, allowing the plant to produce its own nitrogen.

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5
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DNA samples were taken from five individuals and analyzed using gel electrophoresis to produce a DNA profile. Figure 1 below shows the results for a single gene.

Electrophoresis gel diagram showing five individuals with DNA bands at varying positions. Bands are darker on the left, indicating higher molecular weights.
Figure 1. Electrophoresis results.

Which of the following can be concluded from the profile shown in Figure 1?

  • There are equal frequencies of two alleles in the sample population.

  • There are 3 different alleles for the gene.

  • There are two alleles, and the frequency of one of the alleles is 0.75.

  • There are three homozygous individuals in the sample population.

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11 mark

PCR is a process used to amplify DNA. It is possible to monitor the progress of a PCR reaction using quantitative PCR, or qPCR. qPCR involves the addition of a dye that emits fluorescence, meaning that as DNA is produced, fluorescence increases; this fluorescence can be plotted on a graph known as an amplification curve. The PCR cycle at which fluorescence can be detected above background levels is known as Cq. Figure 1 shows the point at which Cq is reached in PCR reactions that start with different numbers of DNA fragments.

PCR amplification graph showing fluorescence vs. cycle number for DNA samples; red, blue, and green lines represent 10,000,000, 1,000,000, and 100,000 fragments.
Figure 1. The impact of DNA starting sample size on Cq during qPCR.

Which of the following correctly describes the data in Figure 1?

  • Cq is reached more quickly when the original DNA sample is smaller.

  • When the starting sample contains 100 000 fragments, Cq is reached during cycle 22.

  • When the starting sample contains 10 000 000 DNA fragments, Cq is reached between qPCR cycles 16 and 18.

  • Reducing the size of the starting sample by a factor of 10 increases the number of PCR cycles required to reach Cq by approximately 6 cycles.

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Fragile X syndrome is a genetic disorder caused by the presence of an increased number of CGG-CCG repeats in the FMR1 gene. The FMR1 gene is located on the X chromosome.

  • Alleles with 55-200 additional CGG-CCG repeats are said to have a premutation status

  • Alleles with more than 200 additional CGG-CCG repeats can cause Fragile X syndrome

Figure 1 shows the results of a gel electrophoresis test used to determine whether an individual has any alleles for Fragile X syndrome. Note that individual 2 is a biological female with two unmutated copies of the FMR1 allele.

Gel electrophoresis image with five lanes, showing DNA bands of varying sizes and positions, labelled 1 to 5, with negative and positive ends.
Figure 1. The results of a gel electrophoresis test for Fragile X syndrome.

Which of the following contains a correct conclusion from Figure 1?

  • Individual 1 is a biological male with an unmutated FMR1 allele and individual 4 is a biological male with an allele that has premutation status.

  • None of the individuals have Fragile X syndrome.

  • Individual 2 is the only biological female in the sample.

  • Individuals 4 and 5 have Fragile X syndrome.

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31 mark

There are many factors that can influence the efficiency of the bacterial transformation process. A group of researchers studied the impact of bacterial cell storage method on transformation efficiency using the following procedure:

  • bacterial cells were stored in a freezer set to a temperature (-4 °C, -20 °C or -70 °C) for a set period of time (1 hour, overnight, 1 day, 2 days, 3 days, 5 days, 7 days, 10 days, 15 days or 20 days)

  • bacterial cultures were removed from the freezer and allowed to return to room temperature

  • a plasmid vector, specifically a pAHC25 plasmid, was used to transfer DNA into bacterial cells

  • the researchers assessed transformation efficiency by looking at the number of transformed cells.

Their results are shown in Figure 1 below.

Bar chart comparing transformation efficiency over various storage periods at temperatures of -4, -20, and -70 degrees Celsius.
Figure 1. The effect of storage temperature and time on transformation efficiency in bacteria.

Which of the following claims is most likely to be appropriate for the data in Figure 1?

  • pAHC25 transformation efficiency decreases when cells have been stored for longer time periods.

  • Storing cells at lower temperatures increases pAHC25 transformation efficiency.

  • Storing cells for a shorter time period reduces the effect of storage temperature on pAHC25 transformation efficiency.

  • Vectors cannot transform bacteria that have been stored at -4 °C for longer than 15 days.

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