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This lab was presented in the General Biology 103 Lab Manual by the Department of Biology, Fall 1999 edition on pages 106-118. In this lab we first used specific aseptic techniques to properly transfer bacteria from test tubes to petri dishes. The lab bench was cleaned with a 10% Clorox bleach solution and left to dry while my lab partners and myself washed our hands. A Bunsen burner was provided so the inoculating loop and the neck of the test tubes could be placed in the flame to kill off any bacteria that was on it. After the inoculating loop and test tube neck are cooled the loop is pl
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For the next part of the lab transformation will be studied. The cells were left on ice and then placed into a 49°C for 90 seconds and then placed back on ice. The temperature change creates a draft to carry the DNA into the cell. The nutrient broth is a combination of sugars, minerals and amino acids. Because of the growth on all three plates I came to the conclusion that the DNA was shared between both strains of bacteria. If the conjunction did not take place I would have expected the same results that were observed in table 1-1. In the first plate containing LB agar only we observed that the bacteria grew for both the streptomycin and ampicillin.
In the process of transformation there is an uptake of exogenous DNA to create a genetic trait that is stable and heritable. The dish with LB and ampicillin produced growth on both sides and finally the LB, ampicillin and Xgal produced growth on both sides. Growth on the mating plate proved to be a success because we were looking for growth and we got it. The Xgal is so identical to lactose that beta-galactosidase will recognize Xgal as lactose. The state before transformation is called competency.
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