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to the lowest OD<sub>600</sub> of the three samples to standardize OD<sub>600</sub>. This was necessary growth at pH 8.0 and 8.5 was significant slower than at pH 7.0. This diluted samples | to the lowest OD<sub>600</sub> of the three samples to standardize OD<sub>600</sub>. This was necessary growth at pH 8.0 and 8.5 was significant slower than at pH 7.0. This diluted samples | ||
where used to measure fluorescence (extinction 490 nm, absorbance 520 nm) and again OD<sub>600</sub> with our plate reader. Three aliquots of each sample where measured (n=3), fluorescence was divided | where used to measure fluorescence (extinction 490 nm, absorbance 520 nm) and again OD<sub>600</sub> with our plate reader. Three aliquots of each sample where measured (n=3), fluorescence was divided | ||
− | by OD | + | by OD<sub>600</sub> and average of the three aliquots where taken to obtain the data shown in Figure 3.</p> |
− | + | ||
</div> | </div> | ||
<div class=" container"> | <div class=" container"> | ||
<img class="section-image" src="https://static.igem.org/mediawiki/2017/d/dd/Asr_res.png" alt="[Diagramm_alx.xlsx]"> | <img class="section-image" src="https://static.igem.org/mediawiki/2017/d/dd/Asr_res.png" alt="[Diagramm_alx.xlsx]"> | ||
<div class="section-sub-text container"> | <div class="section-sub-text container"> | ||
− | <b>Fig 1.</b> | + | <b>Fig 1.</b> alx-promtor controlled mNeonGreen expression: Culture media was bufferd to pH 7, 8 and 8.5 and inoculated |
to an OD<sub>600</sub> of 0.2. After 20 and 40 minutes, aliquotes where taken and fluorescence (extinction 490 nm, absorbance | to an OD<sub>600</sub> of 0.2. After 20 and 40 minutes, aliquotes where taken and fluorescence (extinction 490 nm, absorbance | ||
520 nm) and OD<sub>600</sub> were measured with the plate reader (n=3).</font> | 520 nm) and OD<sub>600</sub> were measured with the plate reader (n=3).</font> |
Revision as of 23:04, 31 October 2017
RESULTS
pH-Sensing
To test if our pH sensitive constructs express the fluorescence proteins we cultivated the bacteria hosting the plasmids in LPM with pH 7 overnight. For expression control for our alx-mNeonGreen construct, we inoculated 20 ml LPM with pH 7.0, 8.0 and 8.5 to an OD600 of 0.2 using the overnight culture. After 20 and 40 minutes 1 ml of each culture where taken and adjusted to the lowest OD600 of the three samples to standardize OD600. This was necessary growth at pH 8.0 and 8.5 was significant slower than at pH 7.0. This diluted samples where used to measure fluorescence (extinction 490 nm, absorbance 520 nm) and again OD600 with our plate reader. Three aliquots of each sample where measured (n=3), fluorescence was divided by OD600 and average of the three aliquots where taken to obtain the data shown in Figure 3.