Difference between revisions of "Part:BBa K5291032"
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<partinfo>BBa_K5291032 short</partinfo> | <partinfo>BBa_K5291032 short</partinfo> | ||
− | As a plasmid, pBBR1MCS2-nadM-nadK-pntA-pntB can increase the intracellular level of NADPH by introducing four exogenous genes: nadM, nadK, pntA and pntB. | + | As a plasmid, pBBR1MCS2-<i>nadM-nadK-pntA-pntB</i> can increase the intracellular level of NADPH by introducing four exogenous genes: <i>nadM</i>, <i>nadK</i>, <i>pntA</i> and <i>pntB</i>. |
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===Usage and Biology=== | ===Usage and Biology=== | ||
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+ | To increase the intracellular level of NADPH, we constructed the pBBR1MCS2-<i>nadM-nadK-pntA-pntB</i> plasmid containing four exogenous genes, including nadM, nadK, pntA, and pntB.<br> | ||
+ | <html><img width = "600" src="https://static.igem.wiki/teams/5291/images/parts-lhs/pbbr1mcs2-pnta-pntb-nadm-nadk.png" /></html><br> | ||
+ | <b>Fig.1 The map of plasmid pBBR1MCS2-<i>nadM-nadK-pntA-pntB</i>.</b><br><br> | ||
+ | Since the efficiency of homologous recombination of multiple fragments was too low, we decided to ligate the two inserts first, and then ligate the inserts to the linearized vector.Here we have successfully concatenated the inserts.<br> | ||
+ | <html><img width = "300" src="https://static.igem.wiki/teams/5291/images/result/electropherogram-of-nadm-nadk-pnta-pntb-pcr-gel.png" /></html><html><img width = "500" src="https://static.igem.wiki/teams/5291/images/parts-lhs/nadm-nadk-pnta-pntb.png" /></html><br> | ||
+ | <b>Fig.2 Electropherogram of <i>nadM-nadK-pntA-pntB</i> PCR gel.</b> | ||
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Latest revision as of 03:36, 2 October 2024
pBBR1MCS2-nadM-nadK-pntA-pntB
As a plasmid, pBBR1MCS2-nadM-nadK-pntA-pntB can increase the intracellular level of NADPH by introducing four exogenous genes: nadM, nadK, pntA and pntB.
Usage and Biology
To increase the intracellular level of NADPH, we constructed the pBBR1MCS2-nadM-nadK-pntA-pntB plasmid containing four exogenous genes, including nadM, nadK, pntA, and pntB.
Fig.1 The map of plasmid pBBR1MCS2-nadM-nadK-pntA-pntB.
Since the efficiency of homologous recombination of multiple fragments was too low, we decided to ligate the two inserts first, and then ligate the inserts to the linearized vector.Here we have successfully concatenated the inserts.
Fig.2 Electropherogram of nadM-nadK-pntA-pntB PCR gel.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]