Difference between revisions of "Part:BBa K592010:Experience"

Revision as of 03:44, 27 September 2012

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Applications of BBa_K592010

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UNIQ889c251052460853-partinfo-00000000-QINU UNIQ889c251052460853-partinfo-00000001-QINU

UNIQ889c251052460853-partinfo-00000002-QINU

BBa_K592010 iGEM Groningen 2012

Our team has managed to couple this biobrick part with our promoters: alsT, fnr, and sboA. The cloning was done in BBa_K818000 (plasmid backbone for B. subtilis, engineered by team Groningen 2012), to allow color expression in B. subtilis. We utilized a strong RBS BBa_B0034 for pigment expression in E. coli and B. subtilis.

The yellow colour was strongly visible in E.coli without any induction, while the expression in B. subtilis was more subtle (B. subtilis colony looks slightly yellow on the plate agar). However, under the induction of volatiles that were produced by the rotten meat, the expression of this part in B. subtilis was strongly visible by human naked eyes.

We also measured fluoresence of AmilGFP. For an elaborate characterization of our sboA-AmilGFP construct and the fluorescence data, look at BBa_K818600

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 The yellow colour was strongly visible in E.coli without any induction, while the expression in B. subtilis was more subtle (B. subtilis colony looks slightly yellow on the plate agar). However, under the induction of volatiles that were produced by the rotten meat, the expression of this part in B. subtilis was strongly visible by human naked eyes.
+We also measured fluoresence of AmilGFP. For an elaborate characterization of our sboA-AmilGFP construct and the fluorescence data, look at [[Part:BBa_K818600 | BBa_K818600]]
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