Difference between revisions of "Part:BBa K316004"
Line 4: | Line 4: | ||
Standard constitutive E.coli promoter <bbpart>BBa_J23101</bbpart> combined with <bbpart>BBa_K316003</bbpart> for comparative characterisation of gene activity (catechol breakdown into 2,4 hydroxyaminobutane yellow product). | Standard constitutive E.coli promoter <bbpart>BBa_J23101</bbpart> combined with <bbpart>BBa_K316003</bbpart> for comparative characterisation of gene activity (catechol breakdown into 2,4 hydroxyaminobutane yellow product). | ||
+ | For more information about XylE, it's substrate and spectrophotometric assays, please see <bbpart>BBa_K316003</bbpart> or our wiki[http://2010.igem.org/Team:Imperial_College_London/Results] | ||
'''Safety''' | '''Safety''' |
Revision as of 09:35, 27 October 2010
Functional XylE under J23101 promoter, with double terminator
Standard constitutive E.coli promoter BBa_J23101 combined with BBa_K316003 for comparative characterisation of gene activity (catechol breakdown into 2,4 hydroxyaminobutane yellow product).
For more information about XylE, it's substrate and spectrophotometric assays, please see BBa_K316003 or our wiki[http://2010.igem.org/Team:Imperial_College_London/Results]
Safety
The substrate XylE works on is a chemical called catechol. It is classed as irritant in the EU but as toxic in the USA, as well as being a possible carcinogen. It should therefore be handled with care and proper safety equipment. More information is available on the Material Safety Data Sheet[http://www.sciencelab.com/msds.php?msdsId=9927131].
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 380
Illegal NgoMIV site found at 552
Illegal AgeI site found at 903 - 1000COMPATIBLE WITH RFC[1000]
Part Characterisation
Characterisation data was obtained using GFP-XylE constructs BBa_K316008 and XylE under two different promoters: B. subtilis derived Pveg BBa_K316005 and J23101 BBa_K316004 from E. coli. These are described in our wiki[http://2010.igem.org/Team:Imperial_College_London/Results] and the relevant parts pages.
References
<biblio>
- 1
</biblio>