Difference between revisions of "Part:BBa K1642002"

Revision as of 12:31, 16 September 2015

PcpcG2

Figure1. Green light sensing expression system.

CcaS phosphorylates CcaR under green light and phosphorylated CcaR binds to promoter of cpcG2 to induce expression of cpcG2.

There is an EcoRI recognition site(GAATTC)in the orginal sequence of PcpcG2 from 14bp to 20bp. In our plasmid for transformation of PCC 6803, we maintained the orginal sequence. After we cloned our composite part BBa_K1642010 which contained PcpcG2, we did site-directed mutagenesis by PCR. And the present sequence from 14bp to 20bp is GAATAC.

Sequence and Features

Assembly Compatibility:

10
COMPATIBLE WITH RFC[10]
12
COMPATIBLE WITH RFC[12]
21
COMPATIBLE WITH RFC[21]
23
COMPATIBLE WITH RFC[23]
25
INCOMPATIBLE WITH RFC[25]
Illegal NgoMIV site found at 481
1000
COMPATIBLE WITH RFC[1000]

Revision as of 12:15, 9 September 2015 (view source) EvaJiang (Talk \| contribs) ← Older edit		Revision as of 12:31, 16 September 2015 (view source) Yincan518 (Talk \| contribs) Newer edit →
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	CcaS phosphorylates CcaR under green light and phosphorylated CcaR binds to promoter of cpcG2 to induce expression of cpcG2.		CcaS phosphorylates CcaR under green light and phosphorylated CcaR binds to promoter of cpcG2 to induce expression of cpcG2.

−		+	There is an EcoRI recognition site(GAATTC)in the orginal sequence of PcpcG2 from 14bp to 20bp. In our plasmid for transformation of PCC 6803, we maintained the orginal sequence. After we cloned our composite part BBa_K1642010 which contained PcpcG2, we did site-directed mutagenesis by PCR. And the present sequence from 14bp to 20bp is GAATAC.
−		+