Difference between revisions of "Part:BBa K5034206:Design"
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===Design Notes=== | ===Design Notes=== | ||
In order to improve the efficiency of energy production and phosphorus accumulation of Shewanella, this element of E. coli was migrated to Shewanella. We believe that the introduction of NADP can promote electron transport in Shewanella. | In order to improve the efficiency of energy production and phosphorus accumulation of Shewanella, this element of E. coli was migrated to Shewanella. We believe that the introduction of NADP can promote electron transport in Shewanella. | ||
− | + | This part is obtained by using a chemical synthesis method, with the aim of expressing the protein in Shewanella and regulating cellular phosphorus metabolism and electron transfer. | |
− | + | ||
===Source=== | ===Source=== |
Revision as of 07:09, 29 September 2024
Poly P -> NADP
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
In order to improve the efficiency of energy production and phosphorus accumulation of Shewanella, this element of E. coli was migrated to Shewanella. We believe that the introduction of NADP can promote electron transport in Shewanella. This part is obtained by using a chemical synthesis method, with the aim of expressing the protein in Shewanella and regulating cellular phosphorus metabolism and electron transfer.
Source
Inorganic polyphosphate/ATP-NAD kinase(PPNK) from Mycobacterium tuberculosis H37Rv. NCBI reference sequence: NC_000962.3:1918746-1919669
References
Itoh, H., & Shiba, T. (2004). Polyphosphate synthetic activity of polyphosphate:AMP phosphotransferase in Acinetobacter johnsonii 210A. Journal of Bacteriology, 186(15), 5178-5181. doi:10.1128/jb.186.15.5178-5181.2004