Difference between revisions of "Part:BBa K1824003"

 
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<partinfo>BBa_K1824003 short</partinfo>
 
<partinfo>BBa_K1824003 short</partinfo>
  
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This is a composite regulatory part that consisting of pBAD promoter and RNA Thermometer A1 BBa_K1824556 for temperature induced gene expression at 42 degrees. The possible secondary structure of A1 was simulated by RNAstructure (Fig.1). This combination is compatible with the assembly method that XJTLU-CHINA promoted.
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This is a composite regulatory part that consisting of pBAD <partinfo>BBa_I13453</partinfo> promoter and RNA Thermometer A1 <partinfo>BBa_K1824557</partinfo> for temperature induced gene expression at 42 degrees. The possible secondary structure of A1 was simulated by RNAstructure (Fig.1). This combination is compatible with the assembly method that XJTLU-CHINA promoted.
  
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===Usage and Biology===
 
  
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[[Image:A1 RNA Thermometer.jpg|360px]]
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<span class='h3bb'>Sequence and Features</span>
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<br>'''Figure 1:''' Possible secondary structure of RNAT A1.
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<partinfo>BBa_K1824003 SequenceAndFeatures</partinfo>
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===Characterization===
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===Functional Parameters===
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[[File:pBad.jpg]]
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<partinfo>BBa_K1824003 parameters</partinfo>
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<br>'''Figure 2:''' The fluorescence of pBad+A1 with different dilution ratio at 30℃ and 37℃(Control and Arabinose).
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<br>eGFP protein was used as report protein to show the function of ribothermometer. The bacteria were centrifuged and observed under UV light by eyes directly. Then the bacteria were sonicated and plate reader was used to measure the fluorescence of eGFP.
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<br>The result of A1 ribothermometer with pBad promoter is showed in Figure 2. The result is not optimistic. Except the result of ½ dilution ratio, all the fluorescence of the samples at 30℃ is higher than the fluorescence of the samples at 37℃.
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<br>The unsatisfactory result of pBad+A1 may be because of the misleading during the disruption.

Latest revision as of 13:06, 17 September 2015

pBAD + RNA Thermometer A1

This is a composite regulatory part that consisting of pBAD BBa_I13453 promoter and RNA Thermometer A1 BBa_K1824557 for temperature induced gene expression at 42 degrees. The possible secondary structure of A1 was simulated by RNAstructure (Fig.1). This combination is compatible with the assembly method that XJTLU-CHINA promoted.


A1 RNA Thermometer.jpg
Figure 1: Possible secondary structure of RNAT A1.


Characterization

PBad.jpg
Figure 2: The fluorescence of pBad+A1 with different dilution ratio at 30℃ and 37℃(Control and Arabinose).


eGFP protein was used as report protein to show the function of ribothermometer. The bacteria were centrifuged and observed under UV light by eyes directly. Then the bacteria were sonicated and plate reader was used to measure the fluorescence of eGFP.
The result of A1 ribothermometer with pBad promoter is showed in Figure 2. The result is not optimistic. Except the result of ½ dilution ratio, all the fluorescence of the samples at 30℃ is higher than the fluorescence of the samples at 37℃.
The unsatisfactory result of pBad+A1 may be because of the misleading during the disruption.