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AP Intermediate 2nd Year Biotechnology and Applications — practice questions

Explore 167 free Biotechnology and Applications questions in AP Intermediate 2nd Year Biology. Open each question or exercise to read its content, reference answers and available explanation.

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Biotechnology and Applications questions and exercises with answers

Showing questions 1–30 of 167.

Restriction enzymes are best described as:Read the answer and worked solution →In recombinant DNA technology, plasmids are commonly used as:Read the answer and worked solution →The three sequential steps of one PCR cycle are:Read the answer and worked solution →Taq DNA polymerase used in PCR is obtained from:Read the answer and worked solution →In gel electrophoresis, DNA fragments move toward the:Read the answer and worked solution →The standard PLANT cell transformation method uses:Read the answer and worked solution →The first MAJOR recombinant DNA pharmaceutical, released commercially in 1982, was:Read the answer and worked solution →Bt cotton is resistant to BOLLWORM pests because it carries a gene from:Read the answer and worked solution →Match each biotechnology term to its meaning.Read the answer and worked solution →Match each biotechnology term to its meaning.Read the answer and worked solution →NEET · Biology · Biotech — Medical or AgriculturalRead the answer and worked solution →Run one PCR cycle in orderRead the answer and worked solution →Which enzyme joins two cut DNA ends to make recombinant DNA?Read the answer and worked solution →The first restriction endonuclease to be isolated was:Read the answer and worked solution →Hind II cuts DNA on recognising a specific sequence of:Read the answer and worked solution →Restriction enzymes are popularly called:Read the answer and worked solution →Nucleases that remove nucleotides from DNA ends are:Read the answer and worked solution →In gel electrophoresis DNA fragments move towards the:Read the answer and worked solution →Which matrix is most commonly used to separate DNA fragments?Read the answer and worked solution →In an agarose gel the fragment that travels farthest is the:Read the answer and worked solution →Separated DNA bands become visible after staining with:Read the answer and worked solution →Cutting a stained DNA band out of the gel and recovering it is:Read the answer and worked solution →The vector sequence from which replication begins is the:Read the answer and worked solution →An antibiotic resistance gene on a vector serves mainly as a:Read the answer and worked solution →A foreign gene ligated at the BamH I site of pBR322 destroys:Read the answer and worked solution →Colonies whose beta galactosidase gene carries an insert appear:Read the answer and worked solution →Loss of gene function caused by a DNA insert inside it is:Read the answer and worked solution →Which plasmid was reworked into a cloning vector for plants?Read the answer and worked solution →Bacterial cells are made competent by treating them with a divalent:Read the answer and worked solution →Recombinant DNA uptake is helped by a brief heat shock at:Read the answer and worked solution →

Worked practice questions

Restriction enzymes are best described as:

  1. Enzymes that join DNA fragments together
  2. Enzymes that cut DNA at specific sequences
  3. Enzymes that replicate DNA in the cell
  4. Enzymes that unwind DNA helices
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Correct answer: B. Enzymes that cut DNA at specific sequences

Restriction endonucleases cut DNA at specific sequences (restriction sites, often 4-8 bp palindromes). Joining is done by DNA ligase. Replication by DNA polymerase. Unwinding by helicase.

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In recombinant DNA technology, plasmids are commonly used as:

  1. Restriction enzymes for cutting DNA
  2. Selection markers for antibiotic resistance
  3. Vectors for carrying foreign genes into hosts
  4. Primers used in PCR amplification
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Correct answer: C. Vectors for carrying foreign genes into hosts

Plasmids are small circular extra-chromosomal DNA molecules in bacteria. They are commonly used as VECTORS to carry foreign genes into host cells (typically E. coli). Plasmid pBR322 is a textbook example.

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The three sequential steps of one PCR cycle are:

  1. Mixing, heating, cooling repeatedly
  2. Cutting, joining, amplifying again
  3. Replication, transcription, translation
  4. Denaturation, annealing, extension
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Correct answer: D. Denaturation, annealing, extension

**One PCR cycle:** (1) DENATURATION at 94°C (DNA strands separate) (2) ANNEALING at 50-60°C (primers bind) (3) EXTENSION at 72°C (Taq polymerase extends). 30 cycles ≈ 10⁹ fold amplification.

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