Genetic engineering is a technique used to modify the genetic material of a specific organism to change a characteristic. The production of insulin by genetic engineering involves the use of plasmids and the bacterium Escherichia coli. Multiple copies of a gene that codes for an insulin polypeptide are mixed with cut plasmids. During the process, only some of the plasmids that are taken up by host bacteria will lead to the expression of insulin polypeptides. Fig. 4.1 shows: - a cut plasmid and the gene coding for the insulin polypeptide - three different plasmids that have been formed as part of the genetic engineering process. Comment on whether a bacterium will produce the insulin polypeptide if it has either plasmid $$\(\mathbf{X}\)$$ or plasmid $$\(\mathbf{Y}\)$$ or plasmid $$\(\mathbf{Z}\)$$ and explain the reason for your choice. plasmid $$\(\mathbf{X}\)$$ plasmid $$\(\mathbf{Y}\)$$ plasmid Z
Exam No:9700_s24_qp_43 Year:2024 Question No:4(b)
Answer:

Knowledge points:
19.1.1 define the term recombinant DNA
19.1.10 outline how microarrays are used in the analysis of genomes and in detecting mRNA in studies of gene expression
19.1.11 outline the benefits of using databases that provide information about nucleotide sequences of genes and genomes, and amino acid sequences of proteins and protein structures
19.1.2 explain that genetic engineering is the deliberate manipulation of genetic material to modify specific characteristics of an organism and that this may involve transferring a gene into an organism so that the gene is expressed
19.1.3.1 extracted from the DNA of a donor organism
19.1.3.2 synthesised from the mRNA of a donor organism
19.1.3.3 synthesised chemically from nucleotides
19.1.4 explain the roles of restriction endonucleases, DNA ligase, plasmids, DNA polymerase and reverse transcriptase in the transfer of a gene into an organism
19.1.5 explain why a promoter may have to be transferred into an organism as well as the desired gene
19.1.6 explain how gene expression may be confirmed by the use of marker genes coding for fluorescent products
19.1.7 explain that gene editing is a form of genetic engineering involving the insertion, deletion or replacement of DNA at specific sites in the genome
19.1.8 describe and explain the steps involved in the polymerase chain reaction (PCR) to clone and amplify DNA, including the role of Taq polymerase
19.1.9 describe and explain how gel electrophoresis is used to separate DNA fragments of different lengths
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