Lysis of transformed E. coli
- To retrieve the adenosine deaminase (ADA) from E.coli, the cell must be lysed. By lysing the cell, the cytoplasm will no longer isolate the macromolecules, such as the ADA for this instance, from the extracellular environment.
- Samples 1 and sample 2 which were placed below -80°C on 9/19/12 is taken out from the freezer to thaw to room temperature.
- There are different methods by which the cell can be lysed. These methods include heat shock, blender polytron, homogenization etc. For this procedure, sonication will be used to lyse the cell. By exposing the cells to high frequency sound waves of a sonicator, the cell membrane are sheared exposing the intracellular contents.
- The sonicator used is the Misonix XL-2000 series Ultrasonic Liquid Processors.
- When the samples were at room temperature, a bucket of ice was prepared.
- Sample 1 was uncapped and inserted through the nozzle of the sonicator for 30 sec. followed by a 30 sec. soak in an ice bath. The nozzle is wiped off with kim wipes. Cooling the sample in an ice bath is necessary to prevent the denaturing of proteins. Denaturation can occur due to the heat generated by the high frequency sound waves of the sonicator.
- While sample 1 is in the ice bath, sample 2 was inserted through the nozzle. These steps were repeated two more times with a total repetition of 3 for each sample.
- Upon finishing sonication of cells, the samples were transferred to centrifuge tubes. The rotor chosen for the tubes is the make of Fiberlite (Piramoon Technologies Inc.) rotor F21-8x50y max. 21,000 rpm.
- The samples contained in the centrifuge tubes were balanced on the rotor having one of the tubes contain water (total of four tubes). The centrifuge settings were fixed on 18,000 rpm at 4°C for 2 h.
Filtration of Buffers