Difference between revisions of "Part:BBa K2123201"
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<partinfo>BBa_K2123201 short</partinfo> | <partinfo>BBa_K2123201 short</partinfo> | ||
− | + | ===Overview== | |
+ | This composite part was developed to turn available two <i>mer</i> operon enzymes, related to Hg metabolism: organomercurial lyase (MerB) and mercury reductase (MerA), as you can see below. | ||
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+ | https://parts.igem.org/File:UFAM_MERBA_1.png | ||
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+ | With this part, you can switch: I) promoter sequences, regulating (or not) by what you want; II) transporters protein, using the preferential one for your chassis; III) and whatever you want related to mercury metabolism! These two enzymes together increase the mercury metabolism spectrum in bacteria, improving bioremediation process. Check how the enzymatic pathway works on “Structure and mechanism” and it’s results in “Usage, Methodology and Experiments”. | ||
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<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 19:45, 27 October 2016
Strong RBS + MerB (Organomercurial Lyase) + Strong RBS + MerA (Mercuric Reductase) + B0015
=Overview
This composite part was developed to turn available two mer operon enzymes, related to Hg metabolism: organomercurial lyase (MerB) and mercury reductase (MerA), as you can see below.
https://parts.igem.org/File:UFAM_MERBA_1.png
With this part, you can switch: I) promoter sequences, regulating (or not) by what you want; II) transporters protein, using the preferential one for your chassis; III) and whatever you want related to mercury metabolism! These two enzymes together increase the mercury metabolism spectrum in bacteria, improving bioremediation process. Check how the enzymatic pathway works on “Structure and mechanism” and it’s results in “Usage, Methodology and Experiments”.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 458
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 56
Illegal NgoMIV site found at 630 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 49