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Lab Work - 07/09/09

Metal Sensing Team

Introduction

In last week's lab session, we had received some BBa_J33206 + pSB1A2 DNA in it's original form by Chris French (the person who submitted the BioBrick to the Parts Registry) as well as both PCR and Sequencing primers. Whilst we used the sequencing primers to determine the sequence of the midi-prepped BBa_J33206 DNA derived from the Parts Registry, we also attempted to transform some DH5-alpha E. coli bacteria with the original BBa_J33206 BioBrick sent to us.

In today's lab session, the plates on which the transformed cells were placed will be examined for colonies; if colonies should be present then they will be used to inoculate LB media in preparation for mini-preps.

Observations

Both of the LB+amp plates (one with 200ul of transformants and one with 500ul of transformants) used to grow the transformant DH5-alpha E. coli cells were covered in hundreds of colonies - almost like a lawn of bacteria could be seen on the plates. This suggests that the transformation rate was very high; this is expected considering we were sent pure DNA. The only thing to note was that the 500ul plate seemed to contain dense, large round colonies in addition to the E. coli cells; this may be contamination.

Procedure

In light of these observations, a total of 6 tubes of 5ml LB solution were innoculated with the transformed E. coli cells. The first three tubes were inoculated by 3 cultures found on the 200ul LB+agar plate and the next three tubes were inoculated with 3 cultures found on the 500ul LB+agar plate. This was all done under aspetic conditions. Theese tubes were then placed in the orbital shaking incubator at 37C in the morning of inoculations. The tubes were as follows:

• Tube 1 - culture 1 from 200ul transformants on LB+amp plate
• Tube 2 - culture 2 from 200ul transformants on LB+amp plate
• Tube 3 - culture 3 from 200ul transformants on LB+amp plate
• Tube 4 - culture 1 from 500ul transformants on LB+amp plate
• Tube 5 - culture 2 from 500ul transformants on LB+amp plate
• Tube 6 - culture 3 from 500ul transformants on LB+amp plate

Further Observations

When the tubes in the orbital incubator were observed in the afternoon, it was found that all of them had gone cloudy. This opacity meant that the E. coli cells had grown sufficiently within the space of a day.

Further Procedure

Inoculating 50ml LB flasks

Because it is likely that the Metal Sensing Team will be using BBa_J33206 in plasmid pSB1A2 DNA in further project work it is a good idea that midi-preps of the DNA are made. 3 flasks, each containing 50ml of LB solution (+ ampicillin), were innoculated each with 50ul from a chosen 5ml LB-grown E.coli culture.

The three 5ml cultures chosen to inoculate the three 50ml LB+amp flasks were taken from Tube 1 (culture 1 from the 200ul plate), Tube 2 (culture 2 from the 200ul plate) and Tube 5 (culture 2 from the 500ul plate). This was all done under aseptic conditions. The resulting inoculated flasks were placed in the orbital shaking incubator at 37C for overnight growth.

Attempting mini-prep

Seen as the six tubes containing LB+amp appeared to all contain sufficient amounts of transformed DH5-alpha E. coli cells, mini-preps of the samples were attempted. This was done using Phil Aldridge's mini-prep protocol and there were no changes to the protocol. However the procedure had to be called off at step 6 due to a problem with the samples.

The problem was the online wiki protocol was correct except for one thing; it missed out the 'shake rigourously' step which comes immediately after the addition of isopropanol.

Conclusions