Coding

Part:BBa_K863005:Experience

Designed by: Isabel Huber   Group: iGEM12_Bielefeld-Germany   (2012-09-18)
Revision as of 15:30, 25 September 2012 by Sednanalien (Talk | contribs) (User Reviews)

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UNIQc8477fbac9d9aeca-partinfo-00000000-QINU UNIQc8477fbac9d9aeca-partinfo-00000001-QINU

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University College London 2012

As part of our collaboration with Bielefeld-Germany, we have characterised their Laccase BioBrick utilising a Syringaldazine assay to determine their Laccase activity. Syringaldazine is oxidised by Laccase, causing a colourmetric change that can be observed by a spectrophotometer at 530nm. As seen in the graph below, the highest rate of Laccase production is in transformed BL21 cells - this is to be expected due to the T7 promoter, which requires the T7 RNA polymerase that BL21 produces. However, expression in transformed W3110, which does not produce T7 RNA polymerase, is still elevated above that of untransformed E. coli, though not at the level of expression of transformed BL21. We hence conclude that Bielefeld-Germany's Laccase BioBrick is working as expected.

UniversityCollegeLondon CollaborationLaccase.png
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