Difference between revisions of "Part:BBa K2257000"
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<partinfo>BBa_K2257000 short</partinfo> | <partinfo>BBa_K2257000 short</partinfo> | ||
<p><font size="+1"><font face="Courier New, Courier, monospace"> | <p><font size="+1"><font face="Courier New, Courier, monospace"> | ||
− | + | A composite of hydrogen sensor full length sequence. The order of the elements is: HoxA-HoxB-HoxC-HoxJ-terminator-HoxP-EGFP. | |
The sequence of HoxABCJP comes from Ralstonia eutropha H16 megaplasmid pHG1. | The sequence of HoxABCJP comes from Ralstonia eutropha H16 megaplasmid pHG1. | ||
The hole sequence acts as an hydrogen sensor.</font> | The hole sequence acts as an hydrogen sensor.</font> | ||
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<p><font size="+1">Now we’ve succefully detected the protein expression by SDS-Page analysis and Western blot analysis.</font></p> | <p><font size="+1">Now we’ve succefully detected the protein expression by SDS-Page analysis and Western blot analysis.</font></p> | ||
[[File:T-Nanjing-China-h2-7.png|460px|thumb|left|Figure 1. Coomassie Brilliant Blue R-250-stained SDS-Page analysis of recombinant E.coli expressing hoxABCJ-terminator-hoxp-gfp]] | [[File:T-Nanjing-China-h2-7.png|460px|thumb|left|Figure 1. Coomassie Brilliant Blue R-250-stained SDS-Page analysis of recombinant E.coli expressing hoxABCJ-terminator-hoxp-gfp]] | ||
− | [[File:T-Nanjing-China-h2-8.png| | + | [[File:T-Nanjing-China-h2-8.png|380px|thumb|right|Fingure 2. Western blot analysis of recombinant E.coli expressing his-hoxA]]</div> |
<p></p> | <p></p> | ||
<p></p> | <p></p> | ||
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When the amount of hydrogen goes to a higher level Fluorescence intensity increases apparently. meaning the designed reporter pathway have worked. </font></p> | When the amount of hydrogen goes to a higher level Fluorescence intensity increases apparently. meaning the designed reporter pathway have worked. </font></p> | ||
[[File:T-Nanjing-China-h2-9.png|600px|thumb|center|Figure 3. Influence of H2 concentration on fluorescence expression]] | [[File:T-Nanjing-China-h2-9.png|600px|thumb|center|Figure 3. Influence of H2 concentration on fluorescence expression]] | ||
+ | <p>[[File:T-Nanjing-China-h2-Data_1.tif|600px|thumb|center|Figure 3. Influence of H2 concentration on fluorescence expression]]</p> | ||
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<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> |
Latest revision as of 04:11, 28 October 2017
hydrogen sensor sequence, HoxA-HoxB-HoxC-HoxJ-terminator-HoxP-EGFP
A composite of hydrogen sensor full length sequence. The order of the elements is: HoxA-HoxB-HoxC-HoxJ-terminator-HoxP-EGFP. The sequence of HoxABCJP comes from Ralstonia eutropha H16 megaplasmid pHG1. The hole sequence acts as an hydrogen sensor.
Usage and Biology
Design
This design is Inspired from Cupriavidusnecator H16.
Experiments
Now we’ve succefully detected the protein expression by SDS-Page analysis and Western blot analysis.
Fluorescence intensity remains stationary when IPTG is added.
And Fluorescence intensity increases in a low hydrogen atmosphere.
When the amount of hydrogen goes to a higher level Fluorescence intensity increases apparently. meaning the designed reporter pathway have worked.
File:T-Nanjing-China-h2-Data 1.tif
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 5912
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 6989
Illegal BamHI site found at 1
Illegal XhoI site found at 409
Illegal XhoI site found at 2562
Illegal XhoI site found at 2574
Illegal XhoI site found at 3102
Illegal XhoI site found at 3129
Illegal XhoI site found at 3876
Illegal XhoI site found at 4152 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 816
Illegal NgoMIV site found at 1767
Illegal NgoMIV site found at 1959
Illegal NgoMIV site found at 2074
Illegal NgoMIV site found at 2343
Illegal NgoMIV site found at 2751
Illegal NgoMIV site found at 3501
Illegal AgeI site found at 891
Illegal AgeI site found at 1476
Illegal AgeI site found at 3519 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 150
Illegal BsaI.rc site found at 3199
Illegal BsaI.rc site found at 3516
Illegal BsaI.rc site found at 4347
Illegal SapI.rc site found at 2304
Illegal SapI.rc site found at 4991