Difference between revisions of "Part:BBa K3731000"
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− | == | + | ==iGEM2021_Nanjing-China Experiment== |
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− | <b>Group: Nanjing-China | + | <b>Group: Nanjing-China 2021</b> |
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− | <b>Author: | + | <b>Author: Haoru Song</b> |
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− | We | + | We |
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− | PolyP | + | PolyP |
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− | <h2> | + | <h2>iGEM2021_Nanjing China Experiment</h2> |
<p>This year our team develops a simple solo medium-copy plasmid-based polyphosphate kinase (PPK1) overexpression strategy for achieving maximum intracellular polyphosphate accumulation.</p> | <p>This year our team develops a simple solo medium-copy plasmid-based polyphosphate kinase (PPK1) overexpression strategy for achieving maximum intracellular polyphosphate accumulation.</p> | ||
− | <p>We test | + | <p>We test</p> |
<p>Ps: | <p>Ps: | ||
− | + | </p> | |
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<p>Reference: | <p>Reference: | ||
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Revision as of 14:28, 6 September 2021
ppk1 in E.Coli BL21
In bacteria, polyP is synthesized by polyphosphate kinase (PPK). PPK consists of PPK1 and PPK2. PPK1 can lengthen the polymer by using the γ-Pi phosphate bond of ATP, and its reversible reaction is to synthesize ATP from ADP and Pi. PPK2 can use polyP to synthesize GTP or ATP reversibly, and mainly synthesize GTP. The ppk1 codes PPK1, which can promote the synthesis(major function) and decomposition(minor function) of polyP with the residue of ATP.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
iGEM2021_Nanjing-China Experiment
Group: Nanjing-China 2021
Author: Haoru Song
We
PolyP
iGEM2021_Nanjing China Experiment
This year our team develops a simple solo medium-copy plasmid-based polyphosphate kinase (PPK1) overexpression strategy for achieving maximum intracellular polyphosphate accumulation.
We test
Ps:
Reference: