Difference between revisions of "Part:BBa K1884009"

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Ferredoxin-NADP+ reductase (FNR) is the key enzyme catalyzing the reaction of electron transfer from ferredoxin (Fd) to NADP+, leading to production of NADPH mainly used for carbon dioxide (CO2) fixation in photosynthesis. Under anaerobic condition, FNR has been proposed to be one of the components competing for photosynthetic electrons from Fd with hydrogenases in Chlamydomonas [1]. Recent data from an in vitro experiment indicated that, under anaerobic condition supporting H2 production, there is a significant loss of photosynthetic electrons toward NADPH formation [2]. Using a proteomic approach, we have previously identified FNR as one of the differentially expressed proteins in Chlamydomonas that undergo sulfur-deprived H2 photoproduction process [3].  
 
Ferredoxin-NADP+ reductase (FNR) is the key enzyme catalyzing the reaction of electron transfer from ferredoxin (Fd) to NADP+, leading to production of NADPH mainly used for carbon dioxide (CO2) fixation in photosynthesis. Under anaerobic condition, FNR has been proposed to be one of the components competing for photosynthetic electrons from Fd with hydrogenases in Chlamydomonas [1]. Recent data from an in vitro experiment indicated that, under anaerobic condition supporting H2 production, there is a significant loss of photosynthetic electrons toward NADPH formation [2]. Using a proteomic approach, we have previously identified FNR as one of the differentially expressed proteins in Chlamydomonas that undergo sulfur-deprived H2 photoproduction process [3].  
  
PSAD terminator is a plant specific Terminator, and serves to increase expression of a gene placed upstream. It works in collaboration with PSAD promoter(BBa_K1547005). Both of these parts are activated by sunlight.
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PSAD terminator is a plant specific Terminator, and serves to increase expression of a gene placed upstream. It works in collaboration with PSAD promoter(BBa_K1547005). Both of these parts are activated by sunlight.<b>(Fig 1)</b>
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<figure style="text-align: center"><img style="width:70%" src="https://static.igem.org/mediawiki/2016/d/df/AD-CRY2FNRzhili.png"/><figcaption style="text-align:center"><b>Figure 1.</b> The diagram of this composite part in pSB1C3 Backbone. </figcaption></figure>
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===Usage===
 
===Usage===

Revision as of 19:44, 17 October 2016


PSAD Promoter+GalAD-CRY2+UAS+FNR(fumarate and nitrate reduction)+PSAD Terminator

The device we constructed this year is one of the functional plasmids in the light-mediated expression system,followed the example of yeast two-hybrid system. With BD-CIB1 which is constructed in the other device(BBa_K1884007), light-mediated expression system, followed the example of yeast two-hybrid system, will be activated and starting to transcript Ferredoxin-NADP(+)Reductase(BBa_K1884006) which is on the 3 prime end of Upstream activating sequence(BBa_K1884004) in green algae

Biology

PASD promoter(BBa_K1547005) is a plant promoter from the green algae Chlamydomonas reinhardtii. It is a high expression promoter that encodes for a ferrodoxin-binding protein of photosystem I.This year we decided to built the light-mediate-controlled system in green algae Chlamydomonas reinhardtii.Based on the origin of PSAD promoter, we thought it would be fully competible in our project.

AD-CRY2, a fusion protein, is for use in a yeast-two-hybrid system, and a VP16 DNA activating domian fused to its N terminus.In order to control DNA transcription by blue light, the system is based on a two-hybrid interaction in which a light-mediated protein brings together two halves of a split transcription factor. CRY2 will disconnected with CIB1 in the dark and halt the DNA transcription

Upstream activating sequence(UAS) is a cis-acting regulatory sequence which is a region of non-coding DNA, regulating the transcription of nearby genes. It is distinct from the promoter and increases the expression of a neighbouring gene. Due to its essential role in activating transcription, the upstream activating sequence is often considered to be analogous to the function of the enhancer in multicellular eukaryotes

Ferredoxin-NADP+ reductase (FNR) is the key enzyme catalyzing the reaction of electron transfer from ferredoxin (Fd) to NADP+, leading to production of NADPH mainly used for carbon dioxide (CO2) fixation in photosynthesis. Under anaerobic condition, FNR has been proposed to be one of the components competing for photosynthetic electrons from Fd with hydrogenases in Chlamydomonas [1]. Recent data from an in vitro experiment indicated that, under anaerobic condition supporting H2 production, there is a significant loss of photosynthetic electrons toward NADPH formation [2]. Using a proteomic approach, we have previously identified FNR as one of the differentially expressed proteins in Chlamydomonas that undergo sulfur-deprived H2 photoproduction process [3].

PSAD terminator is a plant specific Terminator, and serves to increase expression of a gene placed upstream. It works in collaboration with PSAD promoter(BBa_K1547005). Both of these parts are activated by sunlight.(Fig 1)

Figure 1. The diagram of this composite part in pSB1C3 Backbone.

Usage

This device will work with BBa_K1884007 in our system, following photographs will show the level of hydrogen production when the light-mediate controlled yeast-two-hybrid system works.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 3123
    Illegal NotI site found at 3221
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 1560
    Illegal BglII site found at 2019
    Illegal BamHI site found at 2498
    Illegal XhoI site found at 3052
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 1444
    Illegal AgeI site found at 2173
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 1796
    Illegal BsaI.rc site found at 1205
    Illegal SapI.rc site found at 1313
    Illegal SapI.rc site found at 3384