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Phenylthiocarbamide Lab Report

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The phenylthiocarbamide (PTC) gene allows us to taste compounds that are bitter. Students are given two strips, one being coated with PTC and the other uncoated, and are asked to record how they respond to both strips. Nonetheless, the methods of DNA extraction and amplification are explained, and how students predicted their genotypes along with how it compared to their actual genotypes. INTRODUCTION The singular phenylthiocarbamide (PTC) bitter taste receptor gene codes for taste receptors on the tongue, thus allowing individuals to taste PTC. The taste buds on our tongue are filled with tasting cells called gustatory cells, which are filled with a variety of bitter taste receptors to detect a multitude of compounds. The common forms …show more content…

Nonetheless, these changes may occur in the regions that regulate these genes and have an effect on their functions, thus allowing multiple alleles to be formed. There are three common SNPs that are correlated to PTC sensitivity, and each one of them causes a change to the amino acid sequences of the PTC receptor (Sullivan, n.d). These SNPs in terms of base pair positions are 145, 785 and 886, and the subsequent SNP-containing codons are proline or alanine; alanine or valine or valine and isoleucine. The SNP haplotypes for the PTC gene include PAV (taster), AVI (non-taster) and …show more content…

The primary purpose is to identify a genetic marker or study the function of a specific gene. There are three steps involved in this process which are as follows: denaturation, annealing and elongation. Denaturation involves heating the DNA to agitate the hydrogen bonds, and annealing allows the temperature to be lowered so that the primers can be “annealed” to the single-stranded DNA template. The last step requires DNA polymerase to synthesize a new strand of DNA that is complementary to the RNA strand in the 5’ to 3’ direction (Amplifying DNA: The Polymerase Chain Reaction, 2016). The forward and reverse primers are needed to start the replication process by providing the appropriate nucleotides to the new strand. On the contrary, sanger sequencing makes copies of a target DNA, and the the DNA strand that will be sequenced is separated into two strands, so they can be copied through chemically altered bases. The altered bases cause the process of copying to terminate each time a particular letter is added to the growing DNA chain, which happens to all four bases until the fragments are put together to reveal the original sequence of the original DNA. The aforementioned processes are thoroughly explained to give an overview of the steps involved in providing the end products of the experiment, so an individual can manually decipher

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