Difference between revisions of "Part:BBa K3110007"
Line 24: | Line 24: | ||
<h3>Comparison between only O1PO2 and O1PO2 along with lldD</h3> | <h3>Comparison between only O1PO2 and O1PO2 along with lldD</h3> | ||
− | [[File:T--IISER Tirupati--compare.png|thumb|center|700px|Figure 1. Relative Expression of sfGFP under the control of only lldRO1-J23117-lldRO2([[Part:BBa_K1847008]])-strong RBS and lldRO1-J23117-lldRO2-strong RBS along with Medium Promoter-Strong RBS-lldD ([[BBa_K3110007]]). | + | [[File:T--IISER Tirupati--compare.png|thumb|center|700px|Figure 1. Relative Expression of sfGFP under the control of only lldRO1-J23117-lldRO2([[Part:BBa_K1847008]])-strong RBS and lldRO1-J23117-lldRO2-strong RBS along with Medium Promoter-Strong RBS-lldD ([[BBa_K3110007]]).]] |
Revision as of 06:33, 21 October 2019
Medium Promoter Strong RBS lldD
This construct has L-Lactate Dehydrogenase (lldD) under the control of a medium promoter and a strong RBS. lldD cleaves L-lactate to pyruvate. Our intention of using this part is to have control over the detection threshold of L-Lactate by the lldPRD regulatory region. We have also designed other parts which produce various higher and lower concentrations of lldD by varying the strength of the promoter and RBS controlling its production.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1202
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 639