Difference between revisions of "Team:NAWI Graz/Results"

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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>
            <sub>600</sub> and average of the three aliquots where taken to obtain the data shown in Figure 3.</p>
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     <div class=" container">
 
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         <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> Alx controlled mNeonGreen Expression: Culture media was bufferd to pH 7, 8 and 8.5 and inoculated
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             <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.

[Diagramm_alx.xlsx]
Fig 1. alx-promtor controlled mNeonGreen expression: Culture media was bufferd to pH 7, 8 and 8.5 and inoculated to an OD600 of 0.2. After 20 and 40 minutes, aliquotes where taken and fluorescence (extinction 490 nm, absorbance 520 nm) and OD600 were measured with the plate reader (n=3).
As shown in figure 1. Expression of mNeonGreen is increased at pH 8 and 8.5 compared to standard pH 7. Cultures at pH 7, but also cultures without the mNeonGreen plasmid (data not shown) show a high basic fluorescence, leading to the conclusion that the cells naturally show emission at 520 nm. Still, fluorescence is increased twofold at pH 8.5 after 20 and 40 minutes and fluorescence is significantly increased at pH 8 at both measuring points