The risk associated with doing gene splicing experiment by an amateur in middle and high school biology courses. Introduction: RDT (Recombinant DNA technology) is the manipulation of DNA by cutting, joining, and ligation process. It follows to create a combination of DNA sequences from different sources. By analyzing, sequencing, and manipulation of the gene at the genetic level, promotes the success of creating recombinant clones. Moreover, the use of RDT proves as an effective measure to treat different genetic disorders, identification of novel genes, vaccine formation, and crop improvement by genetically modified organisms (GMOs).

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Chapter 17, Problem 3CS

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The risk associated with doing gene splicing experiment by an amateur in middle and high school biology courses.

Introduction:

RDT (Recombinant DNA technology) is the manipulation of DNA by cutting, joining, and ligation process. It follows to create a combination of DNA sequences from different sources. By analyzing, sequencing, and manipulation of the gene at the genetic level, promotes the success of creating recombinant clones. Moreover, the use of RDT proves as an effective measure to treat different genetic disorders, identification of novel genes, vaccine formation, and crop improvement by genetically modified organisms (GMOs).

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1A) Which of the following best explains Griffith’s transformation experiments? Two strains of S. pneumoniae were used for the experiment. Griffith injected a mouse with heat-inactivated S strain (pathogenic) and living R strain (non-pathogenic). The mouse died and living S strain was recovered from the dead mouse. From this, it was later concluded that that mutation occurred in the DNA of the R-strain cells thus transforming them into a pathogenic S strain. Two strains of S. pneumoniae were used for the experiment. Griffith injected a mouse with heat-inactivated S strain (pathogenic) and living R strain (non-pathogenic). The mouse died and living S strain was recovered from the dead mouse. From this observation, it was later concluded that external DNA from the inactivated S strain was taken up by the R-strain cells thus transforming them into a pathogenic S strain. Two strains of S. pneumoniae were used for the experiment. Griffith injected a mouse…