Difference between revisions of "Team:JiangnanU China/Parts"

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                 <b>BBa_K3137004</b>
+
                 <b>BBa_K3137004 : <a href="http://parts.igem.org/Part:BBa_K3137004" style="color:blue;"alt=""><i>mCherry</i></a></b>
 
             </div>
 
             </div>
 
             <br/>
 
             <br/>
 
             <div class="fm_22">
 
             <div class="fm_22">
                 <i>mCherry</i>      708bp report gene<br/>
+
                 708bp report gene<br/>
 
                 The <i>mCherry</i> can express red fluorescence protein and it is used as a report  gene in the process of
 
                 The <i>mCherry</i> can express red fluorescence protein and it is used as a report  gene in the process of
 
                 reporting the number of cells.
 
                 reporting the number of cells.
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             <div class="fb_48">
                 <b>BBa_K3137005</b>
+
                 <b>BBa_K3137005 : <a href="http://parts.igem.org/Part:BBa_K3137005" style="color:blue;"alt=""><i>gntR</i></a></b>
 
             </div>
 
             </div>
 
             <br/>
 
             <br/>
 
             <div class="fm_22">
 
             <div class="fm_22">
                 <i>gntR</i>      996bp<br/>
+
                 996bp<br/>
 
                 The Gluconate repressor <i>gntR</i>, is a transcription factor that negatively regulates the operon
 
                 The Gluconate repressor <i>gntR</i>, is a transcription factor that negatively regulates the operon
 
                 involved in
 
                 involved in
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                 <b>BBa_K3137006</b>
+
                 <b>BBa_K3137006 : <a href="http://parts.igem.org/Part:BBa_K3137006" style="color:blue;"alt=""><i>abpAB</i></a></b>
 
             </div>
 
             </div>
 
             <br/>
 
             <br/>
 
             <div class="fm_22">
 
             <div class="fm_22">
                 <i>abpAB</i>      3803bp anti-protein<br/>
+
                 3803bp anti-protein<br/>
 
                 Gene <i>abpAB</i> is from <i>E.coli</i> genome which express anti-proteins that are resistant to T2,T4,T7
 
                 Gene <i>abpAB</i> is from <i>E.coli</i> genome which express anti-proteins that are resistant to T2,T4,T7
 
                 and λ phages. We obtained <i>abpA</i> and <i>abpB</i> by PCR from the genome of <i>E.coli</i> BL21 and
 
                 and λ phages. We obtained <i>abpA</i> and <i>abpB</i> by PCR from the genome of <i>E.coli</i> BL21 and
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                 <b>BBa_K3137007</b>
+
                 <b>BBa_K3137007 : <a href="http://parts.igem.org/Part:BBa_K3137007" style="color:blue;"alt=""><i>rzpD</i> </a></b>
 
             </div>
 
             </div>
 
             <br/>
 
             <br/>
 
             <div class="fm_22">
 
             <div class="fm_22">
                 <i>rzpD</i>      462bp<br/>
+
                 462bp<br/>
 
                 Overexpression of <i>rzpD</i> causes an abnormal biofilm architecture.
 
                 Overexpression of <i>rzpD</i> causes an abnormal biofilm architecture.
 
             </div>
 
             </div>
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                 <b>BBa_K3137008</b>
+
                 <b>BBa_K3137008 : <a href="http://parts.igem.org/Part:BBa_K3137008" style="color:blue;"alt=""><i>yhjH</i> </a></b>
 
             </div>
 
             </div>
 
             <br/>
 
             <br/>
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                 <b>BBa_K3137009</b>
+
                 <b>BBa_K3137009 : <a href="http://parts.igem.org/Part:BBa_K3137009" style="color:blue;"alt=""><i>nuoE</i></a></b>
 
             </div>
 
             </div>
 
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             <br/>
 
             <div class="fm_22">
 
             <div class="fm_22">
                 <i>nuoE</i>      501bp<br/>
+
                 501bp<br/>
 
                 <i>NuoE</i> is part of the soluble fragment of NADH dehydrogenase I, which represents the electron input
 
                 <i>NuoE</i> is part of the soluble fragment of NADH dehydrogenase I, which represents the electron input
 
                 part
 
                 part
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                 <b>BBa_K3137010</b>
+
                 <b>BBa_K3137010 : <a href="http://parts.igem.org/Part:BBa_K3137010" style="color:blue;"alt="">T7 terminator</a></b>
 
             </div>
 
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             <div class="fm_22">
 
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                 T7 terminator      48bp terminator<br/>
+
                 48bp terminator<br/>
 
                 T7 terminator is used to quantify the level of expression in <i>E. coli</i>.
 
                 T7 terminator is used to quantify the level of expression in <i>E. coli</i>.
 
             </div>
 
             </div>
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                 <b>BBa_K3137011</b>
+
                 <b>BBa_K3137011 : <a href="http://parts.igem.org/Part:BBa_K3137011" style="color:blue;"alt=""><i>gfp</i></a></b>
 
             </div>
 
             </div>
 
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             <br/>
 
             <div class="fm_22">
 
             <div class="fm_22">
                 <i>gfp</i>      717bp reporter<br/>
+
                 717bp reporter<br/>
 
                 The <i>gfp</i> can express green fluorescent protein, which can be used as a report gene in the process
 
                 The <i>gfp</i> can express green fluorescent protein, which can be used as a report gene in the process
 
                 to report the number of cells.
 
                 to report the number of cells.

Revision as of 14:31, 21 October 2019

JiangNan

Basic Parts
BBa_K3137000 : rsmH

250bp constitutive promoter
RsmH can detect the intensity of the fluorescence of gfp.
BBa_K3137002 : PputA

250bp inducible promoter
PputA is an inducible promoter. When E.coli is infected by a phage, both report and respond gene circuits are induced to express at the same time. When a phage infects Escherichia coli into the latent period (about 5 min), PputA will induce the bacteria to express anti-protein and display green fluorescence.
BBa_K3137003 : PglcF

250bp inducible promoter
PglcF is an inducible promoter that works when phages infect bacterial for around 20 min. If the anti-proteins successfully resist phage infection, the inducible promoter PglcF will not induce the expression of downstream gene. If the anti-proteins cannot kill phages, the phages will continue to infect. When phages infect bacteria into the burst period (about 20 min), the inducible promoter PglcF will induce expression of the red fluorescence protein gene mCherry and the downstream toxic protein gene protegrin-1, which will make the bacteria display red fluorescence and lyse cells before the assembly of phages.
BBa_K3137004 : mCherry

708bp report gene
The mCherry can express red fluorescence protein and it is used as a report gene in the process of reporting the number of cells.
BBa_K3137005 : gntR

996bp
The Gluconate repressor gntR, is a transcription factor that negatively regulates the operon involved in the catabolism of d-gluconate via the Entner-Doudoroff pathway and represses genes involved in the different systems related to d-gluconate uptake: gluconate I and gluconate II.
BBa_K3137006 : abpAB

3803bp anti-protein
Gene abpAB is from E.coli genome which express anti-proteins that are resistant to T2,T4,T7 and λ phages. We obtained abpA and abpB by PCR from the genome of E.coli BL21 and constructed recombinant plasmid that connected abpA and abpB at the same time. Then we used IPTG to induce the expression of anti-protein and verified the resistant function of the protein.
BBa_K3137007 : rzpD

462bp
Overexpression of rzpD causes an abnormal biofilm architecture.
BBa_K3137008 : yhjH

yhjH 768bp
YhjH protein contains a EAL domain to catalyze c-di-GMP into GMP, so as to regulate the levels of c-di-GMP.
BBa_K3137009 : nuoE

501bp
NuoE is part of the soluble fragment of NADH dehydrogenase I, which represents the electron input part of the enzyme.
BBa_K3137010 : T7 terminator

48bp terminator
T7 terminator is used to quantify the level of expression in E. coli.
BBa_K3137011 : gfp

717bp reporter
The gfp can express green fluorescent protein, which can be used as a report gene in the process to report the number of cells.
BBa_K3137011

codes forprotegrin-1 (anti-microbial peptide) 60bp antibacterial peptides
Protegrin-1 coding region. Protegrin-1 is an 18-residue beta-sheet peptide isolated from porcine leukocytes with antimicrobial activity against a broad range of microorganisms. It performs its effect by pore membrane disruption and possibly also by effects such as activation of membrane-damaging proteases and has anti-microbial activity against E. coli.
Composite Part
BBa_K3137013

report circuit 1666bp
1666bp
The report gene circuit consists of two periods of phage infection. In incubation period (about 5 min), there is an inducible promoter PputA and a green fluorescent protein gene gfp. In outbreak period (about 20 min), there is an inducible promoter PglcF, and a red fluorescent protein gene mCherry. When E. coli is infected by a phage, both report and respond gene circuits are induced to express at the same time. When a phage infects E. coli into the incubation period (about 5 min), the inducible promoter PputA will induce the bacteria to express the anti-proteins and the green fluorescent protein gene gfp. If the anti-protein successfully resists phage infection, the inducible promoter PglcF will not induce the expression of downstream gene. If the anti-protein fails to kill phages, it means that phages will continue to infect bacteria. And when it comes to the burst period (around 20 min) of phage infection, the inducible promoter PglcF will activate the red fluorescent protein gene mCherry and the downstream toxic protein gene so that the bacteria will display red fluoresce and lyse cells before the assembly of phages.
BBa_K3137014

respond circuit 5097bp
5097bp
The respond gene circuit is composed of an inducible promoter PputA and anti-phage protein genes of the latent period (about 5 min), and an inducible promoter PglcF and a toxic protein gene protegrin-1 of the burst period (about 20 min). When E. coli is infected by a phage, both report and respond gene circuits are induced to express at the same time. When a phage infects E. coli into the latent period (about 5 min), the inducible promoter PputA will induce the bacteria to express the resistant protein abpAB and gntR, and the green fluorescent protein gene gfp. If the resistant proteins successfully resist phage infection, the inducible promoter PglcF will not induce the expression of downstream gene. If the anti-proteins fail to kill phages, it means that phages will continue to infect bacteria, when it comes to the burst period (around 20 min) of phage infection, the inducible promoter PglcF will activate the red fluorescent protein gene mCherry and downstream toxic protein gene protegrin-1 so that the bacteria will display red fluoresce and lyse cells before the assembly of phages.
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