Part:BBa_K864001:Experience
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Applications of BBa_K864001
This part has been used as a low copy backbone by iGEM Team Uppsala University 2012.
User Reviews
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iGEM Team Uppsala University 2012 The copy number of the pSB4x15 series, especially the pSB4C15, has been estimated by three methods all pointing to it being maintained at a consistent low copy number in E coli cells.
Flow cytometry E coli MG1655 was transformed with plasmids of different backbones with the J04450 standard RFP cassette. Liquid cultures were analysed by fluorescence with a Fluorescence activated cell sorter (FACS), quantitivly measuring the fluorescence of individual cells. Due to the active native lacI repression system in the bacteria, the experiment was performed with and without IPTG for promoter induction. It can be expected that a native lacI system represses a low copy plasmid more than a high copy plasmid. The experiment was conducted very similar to our promoter characterization. Quadruplicates (for +IPTG) or triplicates (-IPTG) of E coli MG1655 strains carrying pSB3C5-red, pSB4C5-red, pSB4C15-red, and a DH5alpha strain carrying pSB1C3 with a non-coding construct, were inoculated in 2 mL LB media with chloramphenicol (12 µg/mL) and with or without IPTG (0.5 mM). Cultures were grown shaking at 37° C for 15 hours (+IPTG) or 19 hours (-IPTG), and were visibly confirmed to have grown at steady state for at least 4 hours. Samples were equilibrated in PBS solution at 1:160 dilution for 2 hours, and then measured by a BD Biosciences FACSaria II. 10^5 cells of each sample were individually measured and averaged, with dead and other non-flourescent cells excluded.
Results indicate that that the pSB4C5 has similar or higher copy number than the low to medium copy number plasmid pSB3C5. The pSB4C15 strain shows a lower fluorescence by more than an order of magnitude. In the +IPTG experiment, it expresses less than 1/20 of the flourescence of the other strains, and even is lower without induction. Plasmid yieds The cultures of the +IPTG flow cytometry experiment were also plasmid prepped using the Sigma-Aldrich GenElute Miniprep kit, according to the manufacturers instructions. The order of the cultures was randomized during prepping, and elution was done with 100 µL elution buffer. Concentrations were measured with a Nanodrop 1000 spectrofotometer. All measurements yielded good curves.
Significantly higher plasmid yields were observed in pSB3C5 and pSB4C5 than in pSB4C15, suggesting a higher copy number. The variance in yield is however large. Color development on plates E coli MG1655 carrying pSB4C5-red, pSB4C15 and pSBC15 was plated on on LA plates with chloramphenicol (12 µl/mL) and incubated at 30° C or 37° C for two days. Color expression was assed visually. Strong RFP expression was observed in pSB4C5-red strains, weak color in pSB8C15-red strains and no color in pSB4C15-red strains. This points to higher plasmid copy number in pSB4C5 than of the other plasmids. The native lacI system of MG1655 likely repressed the lacI promoter well, inhibiting color development. Conclusions Results of fluorescence measurments, plasmid yield and color development on plates all point to pSB4C15 being a true low copy backbone. It is strongly suggested that this result is also valid for the whole pSB4x15 series, since they only differ in their resistance cassette. The results also show that pSB4C5 has a significantly higer copy number than specified, of the same magnitude as pSB3C5. We are confident to conclude that the copy number regulation of pSB4C5 is broken. This conclusion can also be expanded to the other pSB4x5 backbones, since they an identical origin of replication. Casual observations also support this result. Thus, we recommend replacing the pSB4C5 for the pSB4C15 for all low copy applications
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