Difference between revisions of "Part:BBa K1949000"
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===Characterization=== | ===Characterization=== | ||
− | <span style="margin-left: 10px;">RFU per turbidity was measured using cells cultured at 18℃ and 37℃ to confirm function of P<i>cold</i>. The cells had a plasmid which carries P<i>cold</i>-<i>gfp</i> or P<i>tet</i>-RBS-<i>gfp</i>. | + | <span style="margin-left: 10px;">RFU of GFP per turbidity was measured using cells cultured at 18℃ and 37℃ to confirm function of P<i>cold</i>. The cells had a plasmid which carries P<i>cold</i>-<i>gfp</i> or P<i>tet</i>-RBS-<i>gfp</i>. |
− | <span style="margin-left: 10px;"><i>E. coli</i> cells which carry the P<i>tet</i>-RBS-<i>gfp</i> plasmid was cultured at 18℃, and RFU was measured at indicated time points. Also, the same experiment was performed at 37℃. We thought this was because GFP is easy to fold for florescence at low temperature. By contrast, RFU of <i>E. coli</i> which included P<i>tet</i>-RBS-<i>gfp</i> at 18℃ was about eight times as much as it at 37℃. By this result, we confirm P<i>cold</i> activates gene expression at low temperature. | + | <span style="margin-left: 10px;"><i>E. coli</i> cells which carry the P<i>tet</i>-RBS-<i>gfp</i> plasmid was cultured at 18℃, and RFU of GFP was measured at indicated time points. Also, the same experiment was performed at 37℃. We thought this was because GFP is easy to fold for florescence at low temperature. By contrast, RFU of <i>E. coli</i> which included P<i>tet</i>-RBS-<i>gfp</i> at 18℃ was about eight times as much as it at 37℃. By this result, we confirm P<i>cold</i> activates gene expression at low temperature. |
Revision as of 13:54, 12 October 2016
cold inducible promoter (Pcold)
This promoter is used to effectively produce proteins at low temperatures. This new promoter, a cold inducible promoter (we call this Pcold) consists of the cspA promoter, Cold Box, 5’-UTR, RBS and DB. The combination (of cspA promoter which is active at both low and high temperature, Cold box which inhibits excessive gene expression, 5’UTR which is stable at only low temperature, and DB which function as an extra RBS) activates gene expression at low temperature.
Characterization
RFU of GFP per turbidity was measured using cells cultured at 18℃ and 37℃ to confirm function of Pcold. The cells had a plasmid which carries Pcold-gfp or Ptet-RBS-gfp.
E. coli cells which carry the Ptet-RBS-gfp plasmid was cultured at 18℃, and RFU of GFP was measured at indicated time points. Also, the same experiment was performed at 37℃. We thought this was because GFP is easy to fold for florescence at low temperature. By contrast, RFU of E. coli which included Ptet-RBS-gfp at 18℃ was about eight times as much as it at 37℃. By this result, we confirm Pcold activates gene expression at low temperature.
Biobrick Tips
This part is not able to be used for most common assembly, because restriction enzyme digestion with XbaI and SpeI generates an unexpected stop codon. Therefore, this part do not meet the criteria of basic parts construction. Our team generated a unique digestion site, BamHI at the upstream of the suffix. We recommend to use this BamHI site for cloning.
Reference
Famg L,Hou Y and Inoue M.1998. Role of Escherichia coli cspA promoter sequences and adaptation of translational apparatus in the cold shock response.
Goldenberg D,Azar I,Oppenheim AB,Brandi A,Pon CL,Gualerzi CO. Role of the cold-box region in the 5' untranslated region of the cspA mRNA in its transient expression at low temperature in Escherichia coli.
Nakashima N and Tamura T. 2004. Cell-free protein synthesis using cell extract of Pseudomonas fluorescens and CspA promoter. Biochemical and Biophysical Research Communications 319 (2004) 672 Yamanaka K.1999. Cold Shock Response in Escherichia coli. J. Mol. Microbiol. Biotechnol. (1999) 1(2): 193-202
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 308
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]