Difference between revisions of "Part:BBa K2092002"

Revision as of 15:24, 1 October 2016

PalcA, improved alcR inducible promoter from A. nidulans

The alcA promoter is one of the strongest inducible promoters in Aspergillus nidulans commonly used to overexpress proteins [1]. It has been shown that alcA promoter is also functional in monocotyledonous plant sugar cane [2] and Escherichia coli [3]. Its transciptional activation is dependent on the binding of its positive transcriptional regulator AlcR with various substrates that employ a hydroxyl group, for example ethanol and threonine. The native AlcA promoter consists of 3 AlcR binding sites. The number and position of the AlcR binding sites on the alcA promoter are crucial in determining its transcriptional activation strength. It has also been shown that each AlcR target in the alcA promoter contributes differently to the activation of the downstream protein expression.

This part is an improved BioBrick previously characterised by 2011 iGEM DTU-Denmark. Sequencing results showed that two Prefix/Suffix restriction sites XbaI and SpeI were absent in the original part. Hence the two missing restriction sites were added using PCR.

Sequence and Features

Assembly Compatibility:

10
COMPATIBLE WITH RFC[10]
12
COMPATIBLE WITH RFC[12]
21
INCOMPATIBLE WITH RFC[21]
Illegal BglII site found at 274
23
COMPATIBLE WITH RFC[23]
25
COMPATIBLE WITH RFC[25]
1000
COMPATIBLE WITH RFC[1000]

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 <partinfo>BBa_K2092002 short</partinfo>
-The alcA promoter is one of the strongest inducible promoters in Aspergillus nidulans.  Its transciptional activation is dependent on the binding of its positive transcriptional regulator AlcR with various substrates that employ a hydroxyl group, for example ethanol and threonine.  The native AlcA promoter consists of 3 AlcR binding sites.  The number and position of the AlcR binding sites on the alcA promoter are crucial in determining its transcriptional activation strength.  It has also been shown that each AlcR target in the alcA promoter contributes differently to the activation of the downstream protein expression.
+The alcA promoter is one of the strongest inducible promoters in Aspergillus nidulans commonly used to overexpress proteins [1].  It has been shown that alcA promoter is also functional in monocotyledonous plant sugar cane [2] and Escherichia coli [3]. Its transciptional activation is dependent on the binding of its positive transcriptional regulator AlcR with various substrates that employ a hydroxyl group, for example ethanol and threonine.  The native AlcA promoter consists of 3 AlcR binding sites.  The number and position of the AlcR binding sites on the alcA promoter are crucial in determining its transcriptional activation strength.  It has also been shown that each AlcR target in the alcA promoter contributes differently to the activation of the downstream protein expression.
 This part is an improved BioBrick previously characterised by 2011 iGEM DTU-Denmark. Sequencing results showed that two Prefix/Suffix restriction sites XbaI and SpeI were absent in the original part.  Hence the two missing restriction sites were added using PCR.