Difference between revisions of "Team:SUSTech Shenzhen/Composite Part"

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! '''Feature'''
 
! '''Feature'''
 
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| '''BBa_K1943000'''
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| '''<partinfo>BBa_K592012</partinfo>'''
 
| fwYellow, yellow chromoprotein reporter system (Strong Promoter, Strong RBS)
 
| fwYellow, yellow chromoprotein reporter system (Strong Promoter, Strong RBS)
 
| 912bp
 
| 912bp

Revision as of 08:12, 18 October 2016

Team SUSTC-Shenzhen

Composite Parts

Contribution

This year, we constructed 12 composite Parts, including functional pigment proteins and fluorescence proteins driven by bacterial promoters. Our aim is to construct plasmids express proteins that can be seen by naked eyes without special devices, and thus are friendly to all labs without limitation on conditions. More importantly, our collections are convenient to use as backbones for construction of Biobricks and other plasmids.

1. Chromoprotein collection

We successfully constructed 8 plasmids with various pigment coding sequence, including eforRed, gfasPurple, Fw Yellow and SpisPink.

Name Description Length Feature
<partinfo>BBa_K592012</partinfo> fwYellow, yellow chromoprotein reporter system (Strong Promoter, Strong RBS) 912bp 205x59px
BBa_K1943001 fwYellow, yellow chromoprotein reporter system (medium Promoter , weak RBS) 914bp 221x67px
BBa_K1943002 gfasPurple, purple chromoprotein reporter system (Strong Promoter, Strong RBS) 867bp 224x58px
BBa_K1943003 gfasPurple, purple chromoprotein reporter system (medium Promoter , weak RBS) 869bp 227x58px
BBa_K1943004 eforRed, Red chromoprotein reporter system (Strong Promoter, Strong RBS) 879bp 204x58px
BBa_K1943005 eforRed, Red chromoprotein reporter system (medium Promoter , weak RBS) 881bp 217x62px
BBa_K1943006 spisPink, Pink chromoprotein reporter system (Strong Promoter, Strong RBS) 876bp 214x57px
BBa_K1943007 spisPink, Pink chromoprotein reporter system (medium Promoter , weak RBS) 878bp 212x55px

Compared to the common used fluorescence protein such as GFP, RFP, chromoproteins are obviously more useful reporter genes. In our parts, the coding sequences of these pigments are all among 700bp long, and the expression efficiency is high according to our experiment results.

We contributed this series of the chromoprotein plasmid for the reason that they have significant advantages to be used as backbones. The length of 700bp is easy to be distinguished from the original backbone (around 2000bp) by gel electrophoresis when constructing new expression system. Additionally, this kind of backbones are superior because we are able to directly observe the expression results by using naked eyes. It will be much more convenient for the laboratory with limited conditions and also save our time. In the tests, the color of colonies were easy to recognize after 18 hours of incubation.

Our plasmid can also be a substitute for J04450, which kindly recommended to be used in plasmid construction by replacing the RFP gene. For the same reason, we provide these pigment sequence to make the construction process more efficiently.

T--SUSTech Shenzhen--33A6D9B0-BC38-47A6-94B6-F0F45784B8F4.png
T--SUSTech Shenzhen--7C27533D-0B9E-4B9D-97D8-D127ABF417FE.png
The expression of 8 plasmids.

Source

The following list is the Biobricks we’ve used in construction and their detailed design information.

Part Type Description Backbone Location on the plate
BBa_K880005 Promoter + RBS Strong Promoter + Strong RBS pSB1C3 3F 2016 Kit Plate 2
BBa_K608007 Promoter + RBS Medium Promoter + Weak RBS pSB1C3 5G 2016 Kit Plate 1
BBa_K592012 Chromoprotein eforRed, red chromoprotein pSB1C3 15I 2016 Kit Plate 6
BBa_K1033919 Chromoprotein gfasPurple, purplr chromoprotein pSB1C3 9K 2016 Kit Plate 6
BBa_K1033910 Chromoprotein fwYellow, yellow chromoprotein pSB1C3 6K 2016 Kit Plate 4
BBa_K1033932 Chromoprotein spisPink, pink chromoprotein pSB1C3 11K 2016 Kit Plate 6
BBa_B0015 Terminator Double terminator pSB1C3 3F 2016 Kit Plate 3

2. sfGFP collection

We submitted this part of super folder GFP (sfGFP) with a strong promoter J23116. Under this expression system, a very bright blue-green fluorescence will be observed after 6 hours of incubation. Its excited wavelength is close to the UV light. We commonly manipulate it by using the UV in super clean bench. The fluorescence is strong enough to be observed by naked eyes. For this reason, sfGFP is always used as reporter gene under the plasmid construction.

This plasmid can be used as a vector. After ligation, it is easy to pick up the single colony without blue-green fluorescence.

On the other part we submitted mutated sfGFP (msfGFP). It has one base-pair difference with the original sfGFP on its 165th site. We changed the base pair from AT to GC by using whole plasmid mutagenesis to remove KpnI restriction site. We kindly hope the little effort can bring convenience to the following iGEMers.

In addition, we also constructed the sfGFP expression system with a terminator following the coding sequence. While the two groups (with and without terminator) showed no significant difference in our experience. We hope these parts can be provided as comparable experimental groups to quantify the efficiency of bacterial terminators.

T--SUSTech Shenzhen--430C12E0-3CD8-4086-B73C-B6A18929C527.png
The expression of mutated sfGFP (the middle and right tube) under UV.

Name Description Length Feature
BBa_K1943008 Strong promoter+ strong RBS+ sfGFP 778bp 133x52px
BBa_K1943009 Strong promoter+ strong RBS+ sfGFP+ terminator 918bp 206x49px
BBa_K1943010 Strong promoter+ strong RBS+ msfGFP 781bp 145x50px
BBa_K1943011 Strong promoter+ strong RBS+ msfGFP+ terminator 915bp 215x50px

Made by from the iGEM team SUSTech_Shenzhen.

Licensed under CC BY 4.0.