Answer 14. As per given data 2.15 microgram of DNA is extracted which means 2.15 X10-6 grams. Average molecular weight of DNA base pair is 650 dalton and one dalton equals to 1.67X10-24 grams. Then 650 X 1.67X10-24 = 1086 X10-24 or
Then 2.15 X10-6 grams / 1.09 X10-22 grams = 1.97 X1016 cells. Hence the number of cell in 1 ml of culture is 1.97 X1016 cells.
Answer 15 if E.coli has length of 10,000 bases then fragments presents are 1.97 X1016 . because there are approx 1.97 X1016 cells which means each cell have individual genome which is considered as different fragment. So 1.97 X1016 fragments will be there.
14. You inoculated a 1 mL tube of sterile LB broth with E. coli, and let...
Suppose your professor handed you a test tube with 2.0 ml of an E. Coli broth culture in it and told you to make a 10 -1 dilution of the entire culture. Explain howyou would do this. Show your calculations.
E. coli strain BL21(DE3) was transformed with the pET30a+ plasmid containing the ilvC gene that encodes for E. coli KARI. The starter culture was incubated overnight in LB broth containing 50 µg/mL kanamycin at 37°C. The sample were already added IPTG and the OD600 reaches the 0.6-0.7 range. How to improve the purity and yield ?
Please explain why for 3&4 our diferent-richuring antibic Data Analysis: Tube (Broth) Dilution Test The following data were obtained for four different antibiotics (Doom, K.O., Mortum and Steril) by incubating Pseudomonas aeruginosa in a nutrient-rich medium with various concentrations of each antibiotic for 24 hours. This was followed by a subculturing step where each initial culture was used to inoculate a sterile nutrient-rich medium that contained NO antibiotic. Please use the following table to answer questions #1-4 below. (5 points...
A. You have been given a tube of E. coli. You are asked to make 1 mL total volume of 10-1 dilution of the bacterial culture. Explain how you would do this. Show all necessary calculations. ____ ml cells + _____ ml water = 1 ml (total volume) B. Next, you were asked to make a 10-2 dilution of the bacterial sample. Explain how you would perform this. Show all necessary calculations. You have bacteria at a concentration of 2...
En (2 points) You isolated your mitochondrial DNA in Part I. In step 6, you discard the supernatant, but keep the pellet. In step 15, you discard the pellet, but keep the supernatant. Explain why the pattern is different between the two steps and the consequence of mixing up these two steps. Procedure Part 1: mt DNA Isolation from your cheek cells. Lysis solution is used to breakdown the cells in this step, you will isolate MEONA from cheek cells....