Difference between revisions of "Part:BBa K855000:Experience"
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'''Figure 2:''' Fresh samples of (1)Sonication supernatant, (2) Sonication Pellet and (3) Whole cells are mixed with 15ug AHL as well as their boiled fractions for 4 hours at 30 degree celsius. Also, each sample in incubated alone without AHL to adjusted their coresponding Background absorbance value. | '''Figure 2:''' Fresh samples of (1)Sonication supernatant, (2) Sonication Pellet and (3) Whole cells are mixed with 15ug AHL as well as their boiled fractions for 4 hours at 30 degree celsius. Also, each sample in incubated alone without AHL to adjusted their coresponding Background absorbance value. | ||
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[[Image:Ahl data (800x783).jpg]] | [[Image:Ahl data (800x783).jpg]] | ||
Latest revision as of 04:47, 6 October 2012
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Applications of BBa_K855000
BBa_K855000 is inserted into commercial expression vector pET-21(a) whose transcription is under the control of T7 promoter and a modified lac operon system. The recombinant vector is transformed into BL21 expression host cell. After the culture reaches an OD of 0.6, the protein expression is induced using 0.5mM IPTG.
The bacteria harvested is divided into two groups undergo sonication and osmotic shock which give three samples, (1)Sonication Supernatant(2)Sonication Pellet(3)Osmotic Shock Fluid. IPTG induced BL21 without plasmid is used as negative control.
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Figure 1: Developed X-ray Film of Western Blot Transfer to Evaluate pvdQ Expression The pvdQ protein is subject to posttranslational processing resulting in its autocatalytic cleavage into an alpha subunit (18kDa) and a beta subunit (60kDa). As the alpha subunit does not contain the HisTag, its expression is not visible through this method. The positive controls are two HisTag standard proteins of 50 and 80 kDa. The negative control is the IPTG induced BL21 without the plasmid (the whole cell bacterium). As the 60kDa band is absent from the negative control lane but present in the sonication supernatant and pellet, the pvdQ protein was successfully expressed in the commercial vector and exits in both a soluble and insoluble state. Moreover, the osmotic shock fraction that is the periplasmic portion of the cell also exhibits a 60kDa band. This confirms that the signal peptide on pvdQ functions to translocate it to the periplasm of the host cell as well
C12-AHL Assay
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Figure 2: Fresh samples of (1)Sonication supernatant, (2) Sonication Pellet and (3) Whole cells are mixed with 15ug AHL as well as their boiled fractions for 4 hours at 30 degree celsius. Also, each sample in incubated alone without AHL to adjusted their coresponding Background absorbance value.
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Figure 3：PBS acts at a negative control to monitor the natural degradation of AHL molecules. Boiling of each of the respective samples denatures the proteins and decreases their activity as an AHL acylase. Therefore, compared to the unboiled, intact samples, more AHL remained after 4 hours of incubation in the boiled samples for each graph. A greater degree of AHL degradation was observed for the sonication supernatant than the pellet. This might imply that most of the pvdQ enzyme is present in the soluble form or the activity of pvdQ in the supernatant is greater.
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