Difference between revisions of "Part:BBa K2533054:Design"
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===References=== | ===References=== | ||
+ | 【1】:Henan journal of animal husbandry and veterinary medicine,by Wang yue xian ; Liu de hai | ||
+ | 【2】:The Capacity of Photosynthesis Bacteria Rhodopseudomonas palustris Assimilating to Phosphate, Bulletin of Science and Technology, 2002, issue 2, pp 142-146 | ||
+ | 【3】:KEGG, https://www.genome.jp/kegg/pathway.html | ||
+ | 【4】:Cloning and sequence analysis of the gene encoding Lactococcus lactis malolactic enzyme: relationships with malic enzymes FEMS Microbiol Lett. 1994 Feb 1;116(1):79-86 | ||
+ | 【5】:Fine tuning the transcription of ldhA for d-lactate production August 2012, Volume 39, Issue 8, pp 1209–1217 | ||
+ | 【6】:Transport of L-Lactate, D-Lactate, and Glycolate by the LldP and GlcA Membrane Carriers of Escherichia coli Volume 290, Issue 2, 18 January 2002, Pages 824-829 | ||
+ | 【7】:Enhancement of Hydrogen Production and Carbon Fixation in Purple Nonsulfur Bacterium Bacterium by Synthetic Biology Shou-Chen Lo | ||
+ | 【8】:Jcat, http://www.jcat.de/#opennewwindow |
Revision as of 16:14, 17 October 2018
RBS-ldhA-RBS-lldP
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1309
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 247
Illegal NgoMIV site found at 457
Illegal NgoMIV site found at 1065
Illegal NgoMIV site found at 1431
Illegal NgoMIV site found at 1503
Illegal NgoMIV site found at 1572
Illegal NgoMIV site found at 1706 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1802
Illegal BsaI.rc site found at 982
Illegal BsaI.rc site found at 1698
Design Notes
Compared with cyanobacteria, we find Rhodopseudomonas palustris is more suitable than cyanobacteria to provide Lactate to Shewenella due to its charactestics of Anaerobic respiration.Therefore, we decided to modify Rhodopseudomonas palustris so that it could produce lactate under the anaerobic condition and transport lactate to the extracellular. And we have found that if we want to enhance the production of lactate from Rhodopseudomonas palustris, we can promote the convertion efficiency of pyruvate to D-lactate and malate to L-lactate. Therefore, we decided to use this two genes, mleS and ldhA to help Rhodopseudomonas palustris to produce lactate. Also, Considering the necessity of helping Rhodopseudomonas palustris to transport lactate out of the membrane, we need to add a lldP gene. In this part, we switch the composition of lldp and ldha to detect the production of Lactate.
Source
Escherichia coli str. K-12 substr. MG1655 & Escherichia coli str. K-12 substr. MG1655
References
【1】:Henan journal of animal husbandry and veterinary medicine,by Wang yue xian ; Liu de hai 【2】:The Capacity of Photosynthesis Bacteria Rhodopseudomonas palustris Assimilating to Phosphate, Bulletin of Science and Technology, 2002, issue 2, pp 142-146 【3】:KEGG, https://www.genome.jp/kegg/pathway.html 【4】:Cloning and sequence analysis of the gene encoding Lactococcus lactis malolactic enzyme: relationships with malic enzymes FEMS Microbiol Lett. 1994 Feb 1;116(1):79-86 【5】:Fine tuning the transcription of ldhA for d-lactate production August 2012, Volume 39, Issue 8, pp 1209–1217 【6】:Transport of L-Lactate, D-Lactate, and Glycolate by the LldP and GlcA Membrane Carriers of Escherichia coli Volume 290, Issue 2, 18 January 2002, Pages 824-829 【7】:Enhancement of Hydrogen Production and Carbon Fixation in Purple Nonsulfur Bacterium Bacterium by Synthetic Biology Shou-Chen Lo 【8】:Jcat, http://www.jcat.de/#opennewwindow