Difference between revisions of "Part:BBa K737024:Experience"

Revision as of 16:05, 28 October 2013

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Applications of BBa_K737024

User Reviews

UNIQce955ecdc1182c5e-partinfo-00000000-QINU UNIQce955ecdc1182c5e-partinfo-00000001-QINU

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Tokyo-Tech iGEM 2013

1. Sequence
No NotI restriction site in prefix and suffix.
1bp deletion and 2bp mutation exist between the promoter and RBS.

2. Result of our experiment
We improved this OUC-China’s phosphate sensor part including the phoB promoter, by amplifying the phoA promoter region of E. coli (MG1655) and ligating it upstream of GFP part (BBa_K1139200)

Fig. 1. Our phoA promoter assay result

Fig. 2. OUC-China 2012’s phoB promoter assay result (converted to bar chart)

Compared to OUC-China’s phosphate sensor part including phoB promoter (Fig. 2), our phosphate sensor part shows clearer result (Fig. 1) (BBa_K1139200, BBa_K1139201).

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 <b>1. Sequence</b><br>
 No NotI restriction site in prefix and suffix. <br>
-bp deletion and 2bp mutation exist between promoter and RBS. (They are not fatal to the function)<br>
+bp deletion and 2bp mutation exist between the promoter and RBS.<br>
 <b>2. Result of our experiment</b><br>
-We improved this OUC-China’s phosphate sensor part including <i>phoB</i> promoter by amplifying the <i>phoA</i> promoter region of <i>E. coli</i> (MG1655) and ligating it upstream of GFP part (<partinfo>BBa_K1139200</partinfo>)<br>
+We improved this OUC-China’s phosphate sensor part including the <i>phoB</i> promoter, by amplifying the <i>phoA</i> promoter region of <i>E. coli</i> (MG1655) and ligating it upstream of GFP part (<partinfo>BBa_K1139200</partinfo>)<br>
 [[Image:Titech2013_parts_K1139201_Fig4.jpg|thumb|left|500px|'''Fig. 1.''' Our <i>phoA</i> promoter assay result]]