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Question 6
6 (a) Yeast cells can be genetically modified to produce a painkiller. This painkiller is usually obtained from opium poppies. One method for genetically modifying a... show full transcript
Step 1
Answer
To insert a gene into a plasmid, the following steps are generally involved:
Cutting the DNA: The plasmid is first cut open at a specific location using a restriction enzyme. This creates sticky ends that are complementary to the gene of interest.
Inserting the gene: The desired gene is also cut with the same restriction enzyme, ensuring that it has matching sticky ends that will align with those in the plasmid.
Ligation: The gene is then inserted into the cut plasmid using an enzyme called ligase, which joins the sugar-phosphate backbone of the DNA strands, effectively sealing the gene within the plasmid.
Step 2
Answer
Producing painkillers from genetically modified yeast cells has several potential benefits:
Rapid Growth and Yield: Yeast can grow rapidly, allowing for increased production of the painkiller in a shorter timeframe.
Less Resource Intensive: Yeast cultivation can be more efficient as it occupies less space compared to growing opium poppies, which require significant agricultural land.
Consistency: Genetically modified yeast can provide consistent quality and potency of the painkiller as it is produced in controlled environments.
However, there are also risks involved:
Health Concerns: There might be doubts about the safety and efficacy of genetically modified painkillers compared to their natural counterparts from poppies.
Environmental Risks: There is concern regarding the accidental release of genetically modified organisms into the environment, which can disrupt local ecosystems.
Regulatory Challenges: The production and commercialization of genetically modified products may face stringent regulations and public resistance, impacting availability.
Step 3
Answer
Variations in DNA sequences among individuals can lead to differences in phenotypes and may affect various aspects of health. Here’s how:
Genetic Diseases: Changes in the DNA sequence can result in mutations that may predispose individuals to genetic disorders. Understanding these mutations helps identify at-risk individuals.
Risk Assessment: Knowing the specific genetic variations can help individuals evaluate their risk of developing certain conditions, enabling proactive health measures.
Personalized Medicine: The sequencing of a person’s genome allows for a tailored approach to medical treatment. Healthcare providers can select medications that align better with a patient’s genetic makeup, improving efficacy and minimizing adverse reactions.
Preventative Strategies: Knowledge of genetic predispositions enables individuals to adopt lifestyle changes to mitigate risks, such as dietary adjustments or increased monitoring for specific diseases.
Research and Development: Sequencing contributes to a deeper understanding of how specific genes influence disease and can drive innovation in drug development and treatment protocols.
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