Difference between revisions of "Part:BBa K620000"
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[[Image:Ddtspb1c3.png|frame|center|Plasmid map of K620000 in pSB1C3 (submission plasmid)]] | [[Image:Ddtspb1c3.png|frame|center|Plasmid map of K620000 in pSB1C3 (submission plasmid)]] | ||
[[Image:Ddtpet11a.png|frame|center|Plasmid map of K620000 in pET11-a to amplify and purify the protein.]] | [[Image:Ddtpet11a.png|frame|center|Plasmid map of K620000 in pET11-a to amplify and purify the protein.]] | ||
− | [[Image:Ddtreact.png|frame|center|DDT reaction with DDT Dehydrochlorinase analyzed with GCMS. There is a | + | [[Image:DDT_blank.jpg|frame|center|DDT in reaction buffer, original peak at 235g/mol]] |
+ | [[Image:Ddtreact.png|frame|center|DDT reaction with DDT Dehydrochlorinase analyzed with GCMS. There is a peak at 191g/mol and a peak at 206 g/mol]] | ||
[[Image:Ddt.png|frame|center|DDT Molecular Structure]] | [[Image:Ddt.png|frame|center|DDT Molecular Structure]] | ||
[[Image:MS1DDT235.png|frame|center|DDT structure after GCMS with a molecular weight of 235 g/mole]] | [[Image:MS1DDT235.png|frame|center|DDT structure after GCMS with a molecular weight of 235 g/mole]] |
Revision as of 03:29, 29 September 2011
DDT Dehydrochlorinase
Also known as Glutathione S-transferase 1-1, this protein is supposed to degrade DDT, an endocrine disruptor and persistent organic pollutant. The protein was identified from the Anopheles dirus mosquito by [http://www.sciencedirect.com/science/article/pii/0965174895000909 Prapanthadara et al] and the gene was assembled from the protein's amino acid sequence, taken from [http://www.ncbi.nlm.nih.gov/protein/Q93113.1 NCBI's protein database], via PIPE cloning.
Usage and Biology
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]