Difference between revisions of "Part:BBa K896000"
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'''Gene construction and cloning''':<p></p> | '''Gene construction and cloning''':<p></p> | ||
− | 1. This gene is constructed by | + | 1. This gene is constructed by http://2012.igem.org/Team:NYMU-Taipei. |
− | 2. SQR gene came from Synechococcus elongatus PCC7002 because the hypersaline strain S. elongatus PCC 7002, which is already sequenced, is 96% similar to O.limnetica SQR gene. We got the whole gene sequence of SQR from NCBI web | + | 2. SQR gene came from Synechococcus elongatus PCC7002 because the hypersaline strain S. elongatus PCC 7002, which is already sequenced, is 96% similar to O.limnetica SQR gene. We got the whole gene sequence of SQR from NCBI web http://www.ncbi.nlm.nih.gov/gene/6054904<p></p> |
3. Figure showed the cloning result of SQR gene.<p></p> | 3. Figure showed the cloning result of SQR gene.<p></p> | ||
Figure 1[[Image:Cloning SQR.jpg]]<p></p> | Figure 1[[Image:Cloning SQR.jpg]]<p></p> | ||
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'''Methods and materials'''<p></p> | '''Methods and materials'''<p></p> | ||
− | Details described in | + | Details described in https://parts.igem.org/Part:BBa_K896000:Experience. |
'''Results''' | '''Results''' | ||
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(B)different concentration of H2S under 48 hrs[[Image:SQR_48hr.jpg]]<p></p> | (B)different concentration of H2S under 48 hrs[[Image:SQR_48hr.jpg]]<p></p> | ||
Figure 3<p></p> | Figure 3<p></p> | ||
− | [[Image: | + | [[Image:SQR_Na2S500mM.png]] |
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2.Other related parts for solving sulfide problems not only on earth but also on Venus<p></p> | 2.Other related parts for solving sulfide problems not only on earth but also on Venus<p></p> | ||
− | + | a.[https://parts.igem.org/Part:BBa_K896001 CysI(sulfite reductase)]:BBa_K896001<p></p> | |
− | + | b.[https://parts.igem.org/Part:BBa_K896002 Dsr(sulfite reductase)]:BBa_K896002<p></p> | |
+ | |||
+ | 3.We did a great job on sulfur metabolism.Above was the novelty of our engineered E.coli or cyanobacteria. | ||
+ | [[Image:S metabolism.png]]<p></p> | ||
===References=== | ===References=== | ||
− | 1.Facultative Anoxygenic Photosynthesis in the Cyanobacterium Oscillatoria limnetica | + | 1.Facultative Anoxygenic Photosynthesis in the Cyanobacterium Oscillatoria limnetica Yehuda Cohen,* Etana Padan, and Moshe Shilo Department of Microbiological Chemistry, The Hebrew University-Hadassah Medical School, Jerusalem, Israel Received for publication 9 May 1975 <p></p> |
2.Sulfide oxidation in gram-negative bacteria by expression of the sulfide–quinone reductase gene of Rhodobacter capsulatus and by electron transport to ubiquinone Hiroomi Shibata and Shigeki Kobayashi 2001 <p></p> | 2.Sulfide oxidation in gram-negative bacteria by expression of the sulfide–quinone reductase gene of Rhodobacter capsulatus and by electron transport to ubiquinone Hiroomi Shibata and Shigeki Kobayashi 2001 <p></p> | ||
3.Sulfur metabolism in Thiorhodoceae. I. Quantitative measurements on growing cells of Chromatium okenii. Antonie Leeuwenhoek, 30: 225–238 Trüper, H.G., and Schlegel, H.G. 1964. <p></p> | 3.Sulfur metabolism in Thiorhodoceae. I. Quantitative measurements on growing cells of Chromatium okenii. Antonie Leeuwenhoek, 30: 225–238 Trüper, H.G., and Schlegel, H.G. 1964. <p></p> |
Latest revision as of 16:36, 25 October 2012
SQR(sulfide quinone reductase),from Synechococcus sp. PCC 7002 plasmid pAQ7
(Cohen, Y., E. Padan, and M. Shilo, Facultative anoxygenic photosynthesis in the cyanobacterium Oscillatoria limnetica. J Bacteriol, 1975. 123(3): p. 855-61.)
1. This gene is constructed by http://2012.igem.org/Team:NYMU-Taipei.
2. SQR gene came from Synechococcus elongatus PCC7002 because the hypersaline strain S. elongatus PCC 7002, which is already sequenced, is 96% similar to O.limnetica SQR gene. We got the whole gene sequence of SQR from NCBI web http://www.ncbi.nlm.nih.gov/gene/6054904 3. Figure showed the cloning result of SQR gene. Figure 1Function analysis
Methods and materialsDetails described in https://parts.igem.org/Part:BBa_K896000:Experience.
Results
After establishing a H2S standard curve to quantify H2S concentration, different H2S concentration challenge SQR transformed E.coli and H2S consumption in 24hrs or 48hrs were tested. The result showed that SQR transformed E.coli consumed much more H2S compred to the blank control, Str transformed E.coli. Our SQR transformed E.coli depleted much more H2S in 48 hours than in 24 hours timepoint.(figure 2A,2B) And SQR transformed E.coli consumed H2S dramatically.(figure 3) Following were results in our experiment. Figure 2 (A)different concentration of H2S under 24 hrs (B)different concentration of H2S under 48 hrs Figure 3
Conclusion
Practical Usage
1. To further practical use, we believe our artificial creatures have high ability to convert hydrogen sulfide to sulfur.
2.Other related parts for solving sulfide problems not only on earth but also on Venus a.CysI(sulfite reductase):BBa_K896001 b.Dsr(sulfite reductase):BBa_K8960023.We did a great job on sulfur metabolism.Above was the novelty of our engineered E.coli or cyanobacteria.
References
1.Facultative Anoxygenic Photosynthesis in the Cyanobacterium Oscillatoria limnetica Yehuda Cohen,* Etana Padan, and Moshe Shilo Department of Microbiological Chemistry, The Hebrew University-Hadassah Medical School, Jerusalem, Israel Received for publication 9 May 1975 2.Sulfide oxidation in gram-negative bacteria by expression of the sulfide–quinone reductase gene of Rhodobacter capsulatus and by electron transport to ubiquinone Hiroomi Shibata and Shigeki Kobayashi 2001 3.Sulfur metabolism in Thiorhodoceae. I. Quantitative measurements on growing cells of Chromatium okenii. Antonie Leeuwenhoek, 30: 225–238 Trüper, H.G., and Schlegel, H.G. 1964.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 349