Difference between revisions of "Part:BBa K2055369"
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This construct codes for intermembrane protein Na(+)/H(+) antiporter NhaA, which is a proton pump from E. coli capable of excreting one intracellular Na(+) ion in exchange for two H(+) external protons. This protein is active at alkaline pH. This construct is regulated by weak constitutive promoter and its objective is to augment bacterial resistance to alkaline pH. | This construct codes for intermembrane protein Na(+)/H(+) antiporter NhaA, which is a proton pump from E. coli capable of excreting one intracellular Na(+) ion in exchange for two H(+) external protons. This protein is active at alkaline pH. This construct is regulated by weak constitutive promoter and its objective is to augment bacterial resistance to alkaline pH. | ||
| − | + | https://static.igem.org/mediawiki/parts/c/c7/T--Tec-Monterrey--protonpump-final.png | |
We transformed E. coli BL21 with three different constructs, one coding for the proton pump, and the other two for GolS and TetH, which were used as control parameters to compare their growth rate at a constant alkaline pH adjusted with KOH. We measured OD600 of three replicates in approximate intervals of 60 minutes for 8 hours. We calculated an average of the three replicates for each transformed strain and graphed the data in order to determine if the proton pump had a significant effect on the survivability of the bacteria. As it is shown in the graphic, the strain transformed with the proton pump had an exponential growth, while the other two couldn’t resist the alkaline pH and had minimal growth. This modification to bacterial cell membrane may increase stress resistance under alkaline conditions | We transformed E. coli BL21 with three different constructs, one coding for the proton pump, and the other two for GolS and TetH, which were used as control parameters to compare their growth rate at a constant alkaline pH adjusted with KOH. We measured OD600 of three replicates in approximate intervals of 60 minutes for 8 hours. We calculated an average of the three replicates for each transformed strain and graphed the data in order to determine if the proton pump had a significant effect on the survivability of the bacteria. As it is shown in the graphic, the strain transformed with the proton pump had an exponential growth, while the other two couldn’t resist the alkaline pH and had minimal growth. This modification to bacterial cell membrane may increase stress resistance under alkaline conditions | ||
Revision as of 18:15, 30 October 2016
Na(+)/H(+) antiporter NhaA generator
This construct codes for intermembrane protein Na(+)/H(+) antiporter NhaA, which is a proton pump from E. coli capable of excreting one intracellular Na(+) ion in exchange for two H(+) external protons. This protein is active at alkaline pH. This construct is regulated by weak constitutive promoter and its objective is to augment bacterial resistance to alkaline pH.
We transformed E. coli BL21 with three different constructs, one coding for the proton pump, and the other two for GolS and TetH, which were used as control parameters to compare their growth rate at a constant alkaline pH adjusted with KOH. We measured OD600 of three replicates in approximate intervals of 60 minutes for 8 hours. We calculated an average of the three replicates for each transformed strain and graphed the data in order to determine if the proton pump had a significant effect on the survivability of the bacteria. As it is shown in the graphic, the strain transformed with the proton pump had an exponential growth, while the other two couldn’t resist the alkaline pH and had minimal growth. This modification to bacterial cell membrane may increase stress resistance under alkaline conditions (by maintaining the pH within the cell at a constant level, this is done by the entrance of two protons and exit of a sodium cation.)
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 415
Illegal BamHI site found at 1120 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 382
- 1000COMPATIBLE WITH RFC[1000]