10007124Molecular Biology 1
Course Information
Description
This is the first course of a two-part series.  This course will teach modern molecular biology techniques including: basic recombinant DNA techniques and DNA analysis and purification.  The polymerase chain reaction and DNA fingerprinting will also be introduced.  This course will include classroom instruction to appreciate the importance of these techniques in life sciences research.
Total Credits
3

Course Competencies
  1. 1.1 Describe the historical developments that led to modern recombinant DNA technology
    Assessment Strategies
    Written Product, Exam
    Criteria
    describe the work of scientists discussed in their textbook and in computer animations

  2. 2.1 Apply basic concepts of recombinant DNA technology
    Assessment Strategies
    Formal Lab Report, Exam
    Criteria
    diagram the relationship between DNA, RNA and protein
    explain the basic Boyer-Cohen cloning experiment
    define all basic components of cloning including vectors, restriction enzymes, host transformation and electrophoresis
    apply these concepts to a simulated application

  3. 2.2 Perform a DNA cloning exercise
    Assessment Strategies
    Lab Activities, Written Product
    Criteria
    clone a gene for antibiotic resistance into a vector so that transformed E. coli acquire antibiotic resistance
    prepare written documentation (report) on cloning exercise
    correctly answer questions in DNA Science text

  4. 2.3 Perform a DNA mapping exercise
    Assessment Strategies
    Lab Activities, Written Product
    Individual Proficiency Project
    Criteria
    transform plasmid DNA into an E.coli strain
    perform plasmid purification from a transformed E. coli strain
    perform restriction digest and electrophoresis
    prepare a graph
    use results to correctly determine the molecular weights of fragments

  5. 3.1 Perform exercises involving PCR to study forensic analysis
    Assessment Strategies
    Lab Activities, Written Product
    Criteria
    DNA is successfully isolated from cheek cell swabs
    gel is prepared with correct pattern
    explain gel correctly in a written report

  6. 3.2 Perform an exercise involving PCR to study genetic modification of foods
    Assessment Strategies
    Lab Activities, Written Product
    Criteria
    DNA is successfully isolated from food products
    gel is prepared with correct pattern
    explain gel correctly in a written report

  7. 4.1 Apply PCR to a cloning exercise
    Assessment Strategies
    Lab Activities, Written Report
    Criteria
    DNA is successfully amplified from a bacteriophage genome
    amplified DNA is successful inserted into a plasmid vector
    recombinant plasmid is successfully transformed into E. coli
    colony screening and PCR amplification is used to verify successful insertion
    explain results in a written report

  8. 4.2 Apply the concepts of screening, genetic expression, expression vectors, and genetic libraries
    Assessment Strategies
    Group Oral Presentation
    Criteria
    explain concepts in the context of a commercial molecular biology kit