Team:Goettingen/week9-2

V06_25

• Experiment:
  In order to gain further plasmid material of the new vector pSB1C3 was transformed into E. coli (DH10B) as described in the protocol.
• Observations & Results:
  The transformation failed. Only the positive control featured colony formation. We found out that accidentally ampicillin containing plates were used whereas the plasmid obtains a chloramphenicol resistance. Thus, the out come is not surprising.

• Experiment:
  Since we received a new E. coli (DH10B) strain, over night cultures were prepared in order to produce new competent cells. The following protocol was considered.

V06_26

• Experiment:
  The preparation of the competent cells was performed according to the following protocol.
• Observations & Results:
  The performance of a test transformation proved the functionality of the new competent cells.

• Experiment:
  In order to test different E. coli strains competent cells of the recently received strains BL21, DH5α and XL1 Blue should be produced. On that account over night cultures of al strains were prepared.

V06_27

• Experiment:
  The preparation of the competent cells was performed according to the following protocol.

• Experiment:
  For the chemical transformation the standard protocol was considered. The following constructs were transferred into the cells:
  18O-fhlDC
  18M-fhlDC
  18C-fhlDC
  
• Observations & Results:
  The transformation of the DH10B cells functioned very well. Numerous colonies could be found at all plates except for the negative control. The other three strains did not lead to such good results. Here, now or low bacterial growth could be observed. Since the competent cells of DH10B worked so well, we suggested that the other strains were just too fresh, so the transformation should be repeated.

V06_28

• Experiment:
  For the chemical transformation the standard protocol was considered. The following constructs were transferred into the cells:
  18O-fhlDC
  18M-fhlDC
  18C-fhlDC
  
• Observations & Results:
  The transformation of BL21, DH5alpha and XL1 Blue was successful this time. All plates featured numerous colonies except the negative controls.
• Observations & Results:
  The transformation of the DH10B cells functioned very well. Numerous colonies could be found at all plates except for the negative control. The other three strains did not lead to such good results. Here, now or low bacterial growth could be observed. Since the competent cells of DH10B worked so well, we suggested that the other strains were just too fresh, so the transformation should be repeated.

• Experiment:
  For the chemical transformation the standard protocol was considered. The plasmid was used in its uncut form as well as restricted.
  
• Observations & Results:
  The transformation with the uncut DNA was successful whereas that using the restricted plasmid failed. This seems to be due to the fact that the restricted vector had not been religated by the cells.

• Experiment:
  Over night cultures of the four strains DH10B, BL21, DH5α and XL1 Blue hosting the three flhDC-promoter constructs were prepared.
  
• Observations & Results:
  The inoculation of the over night cultures failed. Perhaps something was wrong with the shaker.