Difference between revisions of "Part:BBa K2533048"

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<h2>DNA Gel Electrophoretic</h2>
 
<h2>DNA Gel Electrophoretic</h2>
 
To make sure that we get the target gene, we did the DNA gel electrophoretic to separate different gene. And here is the result.
 
To make sure that we get the target gene, we did the DNA gel electrophoretic to separate different gene. And here is the result.
[[File:T--HUST-China--2018-jiaotu-ldha and lldp.png|400px|thumb|center|Figure2:Verification of successful transformation of pSB1C3-RBS-ldhA]]
+
[[File:T--HUST-China--2018-jiaotu-mles-lldp.png|400px|thumb|center|Figure2:Verification of successful transformation of pSB1C3-RBS-mleS-RBS-lldP]]
Our target genes are 1047bp, and as the marker is DS5000, we could be sure that the bright bands in this picture are our target genes.
+
Our target genes are 3370bp, and as the marker is DS5000, we could be sure that the bright bands in this picture are our target genes.
  
 
<h2>Electrogenesis</h2>
 
<h2>Electrogenesis</h2>

Revision as of 15:06, 17 October 2018


RBS-mleS-RBS-lldP

Production of lactate and transport lactic acid

Usage and biology

dld refers to FAD-dependent D-lactate dehydrogenase which could catalyze D-lactate’s transformation into pyruvate. With the overexpression of dld, Shewanella could utilize D-lactate more efficiently, which brings more electricity being produced.

Characterization

This is one section for lactate utilization part.

Figure1:RBS-mleS-RBS-lldP

DNA Gel Electrophoretic

To make sure that we get the target gene, we did the DNA gel electrophoretic to separate different gene. And here is the result.

Figure2:Verification of successful transformation of pSB1C3-RBS-mleS-RBS-lldP

Our target genes are 3370bp, and as the marker is DS5000, we could be sure that the bright bands in this picture are our target genes.

Electrogenesis

By comparing the ability of producing electricity, we might find out whether dld could effectively help Shewanella to produce more electricity.

Figure3:shows that our modification is effective. Every gene circuits can help strains produce lactate, and mleS-lldP-ldhA is the most efficient one. Therefore, our construction of gene circuits achieve the goal to help strains produce lactate.

It could be demonstrated that targeted genes could be expressed in the engineered cells. More NADH has been produced by engineered bacteria, which helps to produce more electricty.