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Explain why microbes are useful biotechnology, using examples of specific fungi (cerevisae) and bacteria (E.coli)
Microbes are used in biotechnology because they:
Grow fast and are easy to culture in large quantities.
Have simple genetics, making it easy to insert or remove genes.
Can produce useful substances like enzymes, hormones, and antibiotics.
Examples:
Fungus – Saccharomyces cerevisiae (yeast):
Used in baking and brewing (ferments sugars → ethanol + CO₂).
Used in biotechnology to produce human insulin, hepatitis B vaccine, and other recombinant proteins.
Bacterium – E. coli:
Used as a model organism for genetic engineering.
Can carry plasmids with foreign genes (e.g., human insulin gene).
Used for mass production of proteins like insulin, growth hormone, enzymes for detergents, etc.
Explain what a plasmid is, and define the roles of different kinds of plasmids in nature and in biotechnology
A plasmid is a small circular DNA molecule found in bacteria, separate from chromosomal DNA.
In nature:
Plasmids carry extra genes (not essential for survival).
These genes can provide advantages:
Antibiotic resistance (R-plasmids)
Toxin production
Metabolic abilities (break down unusual substances)
In biotechnology:
Plasmids are used as vectors ( carriers of foreign DNA)
Scientists insert desired genes into plasmids, then put them into bacteria (like E. coli).
The bacteria then replicate, producing copies of the recombinant DNA and expressing the new protein (e.g., insulin, enzymes).
Define the terms “DNA cloning” “recombinant DNA” “GMO”
DNA cloning:
The process of making many identical copies of a DNA fragment, gene, or entire organism.
Recombinant DNA:
DNA that has been artificially combined from two or more different sources (e.g., human gene + bacterial plasmid).
GMO (Genetically Modified Organism):
Any organism whose genetic material has been altered using biotechnology to include a foreign or modified gene.
Explain how recombinant DNA and GMOs are made, and especially which enzymes do which jobs in this process
Target gene is cut out using a restriction enzyme (cuts DNA at specific sites).
Plasmid is cut open with the same restriction enzyme to make matching sticky ends.
DNA ligase joins the gene and plasmid → forms recombinant DNA.
The recombinant plasmid is put into a bacterium (e.g., E. coli) = GMO.
The bacterium copies the plasmid and produces the protein from the inserted gene.
Main enzymes and their jobs:
Restriction enzyme: Cuts DNA.
DNA ligase: Joins DNA pieces.
DNA polymerase: Copies DNA (e.g., in PCR or when the bacterium replicates).
Discuss why vaccines are important, and how recombinant DNA methods can be used to make
Why vaccines are important:
They stimulate the immune system to produce antibodies without causing disease.
They provide immunity and help prevent epidemics.
They can even help eradicate diseases (e.g., smallpox).
How recombinant DNA is used to make vaccines:
The gene coding for an antigen (a surface protein from a pathogen) is identified.
The antigen gene is inserted into a plasmid.
The plasmid is placed into yeast or bacteria, which then produce large amounts of the antigen protein.
The purified antigen is used as a subunit vaccine, safe because no live virus is used.