Team:Yale/Our Project/Methods
From 2010.igem.org
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(1) phsABC gene and vector | (1) phsABC gene and vector | ||
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<img src="https://static.igem.org/mediawiki/2010/thumb/f/f8/Phsplasmiddiagram.png/800px-Phsplasmiddiagram.png" " width="568" height="70" /> | <img src="https://static.igem.org/mediawiki/2010/thumb/f/f8/Phsplasmiddiagram.png/800px-Phsplasmiddiagram.png" " width="568" height="70" /> | ||
<div id="caption">phsABC in pSB74</div> | <div id="caption">phsABC in pSB74</div> | ||
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This central component encodes Thiosulfate Reductase. The gene phsABC was obtained from Dr. Jay Keasling laboratory at University of California, Berkeley. According to their results, Thiosulfate Reductase encoded in the plasmid pSB74 showed the highest activity, so we obtained phsABC from the plasmid pSB74. E. coli DH5α strain were used for plasmid manipulation. | This central component encodes Thiosulfate Reductase. The gene phsABC was obtained from Dr. Jay Keasling laboratory at University of California, Berkeley. According to their results, Thiosulfate Reductase encoded in the plasmid pSB74 showed the highest activity, so we obtained phsABC from the plasmid pSB74. E. coli DH5α strain were used for plasmid manipulation. | ||
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(2) Biobrick Promoter</b> <p>Promoter used was designed by Caitlin Conboy and was found within the parts registry. This promoter is a Quad Part Inverter: “that is, a PoPS-based inverter composed of four sub-parts: a ribosome binding site, a coding region for a repressor protein (e.g., lambda cI), a terminator, and the promoter (e.g., pLambda) regulated by the encoded repressor protein.” Research into promoter activity by previous groups has suggested that this promoter has a strong on state with a noticeable background in the off state .</p> | (2) Biobrick Promoter</b> <p>Promoter used was designed by Caitlin Conboy and was found within the parts registry. This promoter is a Quad Part Inverter: “that is, a PoPS-based inverter composed of four sub-parts: a ribosome binding site, a coding region for a repressor protein (e.g., lambda cI), a terminator, and the promoter (e.g., pLambda) regulated by the encoded repressor protein.” Research into promoter activity by previous groups has suggested that this promoter has a strong on state with a noticeable background in the off state .</p> | ||
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(3) Promoter B0034</b> | (3) Promoter B0034</b> | ||
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<br />Length 1370 bp | <br />Length 1370 bp | ||
<br />IPTG-induced (regulatory)</p> | <br />IPTG-induced (regulatory)</p> | ||
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(4) Terminator | (4) Terminator |
Revision as of 02:08, 28 October 2010
our project
experimental methods
Our plasmid is composed of three parts: a promoter and a terminator Biobrick as well as a novel addition to the biobrick library, the phsABC gene that is known to encode Thiosulfate Reductase.
(1) phsABC gene and vector
This central component encodes Thiosulfate Reductase. The gene phsABC was obtained from Dr. Jay Keasling laboratory at University of California, Berkeley. According to their results, Thiosulfate Reductase encoded in the plasmid pSB74 showed the highest activity, so we obtained phsABC from the plasmid pSB74. E. coli DH5α strain were used for plasmid manipulation.
Promoter used was designed by Caitlin Conboy and was found within the parts registry. This promoter is a Quad Part Inverter: “that is, a PoPS-based inverter composed of four sub-parts: a ribosome binding site, a coding region for a repressor protein (e.g., lambda cI), a terminator, and the promoter (e.g., pLambda) regulated by the encoded repressor protein.” Research into promoter activity by previous groups has suggested that this promoter has a strong on state with a noticeable background in the off state .
(3) Promoter B0034
Biobrick Part:BBa_Q04121.
Length 1370 bp
IPTG-induced (regulatory)
(4) Terminator
Restriction Enzyme Sites:
The digested sticky ends of the enzymes Xba I and Spe I are complimentary. Once two ends from different combine, neither Xba I nor Spe I can recognize its restriction site in the gene.
By using this ligation method, we added the promoter to phsABC:
Read more about the background of the PHS gene