2. Devise a strategy that could be used to combine the DNA parts in the plasmids below to create an "IS-AWESOME" plasmid. You need to use the Bg|Brick standard assembly method when creating your strategy. The new “IS-AWESOME" part should be made by moving the "AWESOME” part out of the plasmid that it is in and into the "IS" plasmid. This question should be answered using point form in a numbered list. Each point/step in your strategy should have two parts: a) What is being done in the step (be descriptive), and b) What the result of the step is (this should descriptive and include names of parts and any new or changed features and sizes - describe the new plasmid) Eg. Step 1. a) What is done in the first step... b) What is the result of the first step... EcoRI Bglll Length = 1450 base pairs BamHI Xhol GAATTCatgAGATCT AWESOME CTTAAGtacTCTAGA GGATCCtaaCTCGAG CCTAGGattGAGCTC Plasmid 2-AWESOME Xbal = Length 2350 base pairs TCTAGA AGATCT Length = 450 base pairs EcoRI Bglll Length = 950 base pairs GAATTCatgAGATCT CTTAAGtacTCTAGA IS Plasmid 1-IS AmpR Length = 950 base pairs BamHI Xhol GGATCCtaaCTCGAG CCTAGGattGAGCTC Length = 2200 base pairs Spel ACTAGTA TGATCAT KanR Length 1150 base pairs Length = 750 base pairs 3. Devise a strategy that could be used to combine the DNA part "IS-AWESOME" that you created in question 2 with the "BIOCHEMISTRY" part below to make the part "BIOCHEMISTRY-IS- AWESOME". You again need to use the Bg|Brick standard assembly method when creating your strategy. The new part should be made by moving the "BIOCHEMISTRY" part out of the plasmid that it is in and into the "IS-AWESOME" plasmid you made in the previous question. Answer this question using the same format described in question 2. EcoRI Bglll Length = 1700 base pairs BamHI Xhol GAATTCatgAGATCT CTTAAGtacTCTAGA GGATCCtaaCTCGAG BIOCHEMISTRY CCTAGGattGAGCTC Plasmid 3-BIOCHEMISTRY Length = 2100 base pairs Notl GCGGCCGCT CGCCGGCGA ChlorR Length 750 base pairs Length = 570 base pairs 4. Conduct a theoretical restriction mapping experiment on the "BIOCHEMISTRY-IS-AWESOME" plasmid you created in questions 2 and 3. You must select the minimum number of restriction enzyme(s) that will allow you to determine if your cloning steps from the previous questions have been successful. Draw the results of an agarose gel from your theoretical mapping experiment. You must label the size of all bands that you would see on your mapping gel and indicate what enzyme(s) generated the DNA in the bands. You should also indicate in your label what DNA parts might be contained in the band. Your figure should be made with drawing software such as Powerpoint and pasted into your answers, do not hand-draw. Base-pair lengths given in the plasmid maps above are from the center of one plasmid feature to the next plasmid feature. For example, the length of 750 bp on Plasmid 1-IS is from the center of Kan clockwise around the plasmid to the center of the nucleotide sequence given on the left of "IS" (Spel site). 5. Design PCR primers to amplify the "BIOCHEMISTRY-IS-AWESOME” DNA you have made in questions 2 and 3. Give the sequences of any primers you design. Any primers your design should have a melting point of 35 degrees Celsius or greater (there are online calculators you can use to check your primers)). Make sure you label the 5' and 3' ends of your primers. You also need to indicate where these primers anneal, both where in the plasmid and what DNA strand. Explain what the PCR product will be (give the names of any DNA component that is amplified in the product).