Difference between revisions of "Part:BBa K2533051"
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<h1>'''Usage and biology'''</h1> | <h1>'''Usage and biology'''</h1> | ||
− | + | It encodes malate dehydrogenase and L-lactate permease, which could produce and transport lactate. mleS could convert malic acid to L-lactate. lldP could transport lactate out of the cell. In this way, Rhodopseudomonas palustris could efficiently transport produced lactate out of the cell, which later will be used by Shewanella. | |
<h1>'''Characterization'''</h1> | <h1>'''Characterization'''</h1> | ||
− | This is one section for lactate | + | This is one section for lactate production and transportation part. |
[[File:T--HUST-China--2018-tonglu-mles-lldp.png |400px|thumb|center|Figure1:mleS-lldP-TT]] | [[File:T--HUST-China--2018-tonglu-mles-lldp.png |400px|thumb|center|Figure1:mleS-lldP-TT]] | ||
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<h2>Electrogenesis</h2> | <h2>Electrogenesis</h2> | ||
− | By detecting the production of lactate after expressing | + | By detecting the production of lactate after expressing, we might find out whether mleS-lldP-TT could effectively help Rhodopseudomonas palustris transport produced lactate out of the cell. |
[[File:T--HUST-China--2018-expression of lactate.png |400px|thumb|center|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.]] | [[File:T--HUST-China--2018-expression of lactate.png |400px|thumb|center|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 | + | It could be demonstrated that the target genes could be expressed in the engineered cells. More lactate has been produced and transported by engineered bacteria. |
<!-- Uncomment this to enable Functional Parameter display | <!-- Uncomment this to enable Functional Parameter display | ||
===Functional Parameters=== | ===Functional Parameters=== | ||
<partinfo>BBa_K2533030 parameters</partinfo> | <partinfo>BBa_K2533030 parameters</partinfo> | ||
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Revision as of 16:41, 17 October 2018
mleS-lldP-TT
Same as BBa_K2533048
Usage and biology
It encodes malate dehydrogenase and L-lactate permease, which could produce and transport lactate. mleS could convert malic acid to L-lactate. lldP could transport lactate out of the cell. In this way, Rhodopseudomonas palustris could efficiently transport produced lactate out of the cell, which later will be used by Shewanella.
Characterization
This is one section for lactate production and transportation part.
DNA Gel Electrophoretic
To make sure that we get the target gene, we did DNA gel electrophoretic for verification. And here is the result.
Our target genes are 3372bp, and as the marker is DS5000, we could be sure that the bright bands in this picture are our target genes.
Electrogenesis
By detecting the production of lactate after expressing, we might find out whether mleS-lldP-TT could effectively help Rhodopseudomonas palustris transport produced lactate out of the cell.
It could be demonstrated that the target genes could be expressed in the engineered cells. More lactate has been produced and transported by engineered bacteria.