IGEM:Harvard/2006/Cyanobacteria: Difference between revisions
From OpenWetWare
Jump to navigationJump to search
JeffreyLau (talk | contribs) |
|||
| (19 intermediate revisions by 4 users not shown) | |||
| Line 4: | Line 4: | ||
==Introduction== | ==Introduction== | ||
Welcome to the lab notebook for the Cyanobacteria project! The goal of our team, composed of four members, is to reconstruct the cyanobacterial circadian oscillator system into E. coli. Three proteins, KaiA, B, and C, have been shown to have an in-vitro phosphorylation state oscillation (Nakajima et al. 2005) by transcriptional-translational independent methods. If this system can be reconstituted in E. coli, there are two important applications: | Welcome to the lab notebook for the Cyanobacteria oscillator project! The goal of our team, composed of four members, is to reconstruct the cyanobacterial circadian oscillator system into E. coli. Three proteins, KaiA, B, and C, have been shown to have an in-vitro phosphorylation state oscillation (Nakajima et al. 2005) by transcriptional-translational independent methods. If this system can be reconstituted in ''E. coli'', there are two important applications: | ||
#'''Synthetic Biology''': Creating a functional, oscillating set of proteins is the next logical step from the synthetic "repressilator" system engineered by Elowitz et al. (2000). Although a good proof of concept, the "repressilator" lacks the stability needed from a robust oscillator such as the naturally evolved cyanobacterial oscillator. This robust oscillator could prove useful in an eventual biocircuit. | #'''Synthetic Biology''': Creating a functional, oscillating set of proteins is the next logical step from the synthetic "repressilator" system engineered by Elowitz et al. (2000). Although a good proof of concept, the "repressilator" lacks the stability needed from a robust oscillator such as the naturally evolved cyanobacterial oscillator. This robust oscillator could prove useful in an eventual biocircuit. | ||
#'''Circadian Biology''': Cyanobacteria are the simplest model organisms for the study of circadian oscillation. Although circadian oscillation has been fairly well characterized, less is understood at the molecular level. By porting the oscillation system into E. coli, one can begin to understand more precisely the pathways involved in the genomic oscillation of cyanobacteria. | #'''Circadian Biology''': Cyanobacteria are the simplest model organisms for the study of circadian oscillation. Although circadian oscillation has been fairly well characterized, less is understood at the molecular level. By porting the oscillation system into ''E. coli'', one can begin to understand more precisely the pathways involved in the genomic oscillation of cyanobacteria. | ||
For more background information on the ciracadian system, please check out our "Literature" section. Otherwise, day-to-day work can be found under the "Lab Notebook" tab; we will post major results of our work and links to the days as they become available. If you have questions or comments, feel free to contact us: information is located at the main Harvard iGEM 2006 page. Thanks! | For more background information on the ciracadian system, please check out our "Literature" section. Otherwise, day-to-day work can be found under the "Lab Notebook" tab; we will post major results of our work and links to the days as they become available. If you have questions or comments, feel free to contact us: information is located at the main Harvard iGEM 2006 page. Thanks! | ||
| Line 14: | Line 14: | ||
Sincerely,<br> | Sincerely,<br> | ||
Zhipeng, Hetmann, Dave, and Jeff | Zhipeng, Hetmann, Dave, and Jeff | ||
'''Update 10/27/06:''' We believe we can express the three proteins into e. coli, and that there is interaction between A+C and possible interaction between B+C. See the Lab Notebook for more information. | |||
[[Image:102706_cyanoresult.jpg]] | |||
==Outline of Findings and Signifigant Dates== | ==Outline of Findings and Signifigant Dates== | ||
*07/05/06: The incubator for growing up our cyanobacteria is complete; we have cultures growing! | *07/05/06: The incubator for growing up our cyanobacteria is complete; we have cultures growing! [[IGEM:Harvard/2006/Cyanobacteria/Notebook/2006-7-5 | Link]] | ||
*07/10/06: Some computer modeling has been done to see the effect of multiple unsyncronized clocks on phosphorylation state output. [[IGEM:Harvard/2006/Cyanobacteria/Notebook/2006-7-10 | Link]] | |||
*07/10/06: Some computer modeling has been done to see the effect of multiple unsyncronized clocks on phosphorylation state output. | *07/21/06: Upon having trouble with site-specific mutagenesis on the KaiA and KaiBC operons from the cyanobacterial genome, we have decided to pursue synthesis of the constructs in parallel with continued extraction attempts. [[IGEM:Harvard/2006/Cyanobacteria/Notebook/2006-7-21 | Link]] | ||
*08/01/06: Preliminary success with site-specific mutagenesis. [[IGEM:Harvard/2006/Cyanobacteria/Notebook/2006-8-1 | Link]] | |||
*07/21/06: Upon having trouble with site-specific mutagenesis on the KaiA and KaiBC operons from the cyanobacterial genome, we have decided to pursue synthesis of the constructs in parallel with continued extraction attempts. | *08/05/06: Promoter leakness tests come out negative. May have to use low-copy plasmids if we want good control of protein expression in Top10F. [[IGEM:Harvard/2006/Cyanobacteria/Notebook/2006-8-5 | Link]] | ||
*08/11/06: We are moving to the synthetic KaiA, KaiB, and KaiC for future work. [[IGEM:Harvard/2006/Cyanobacteria/Notebook/2006-8-11 | Link]] | |||
*08/01/06: Preliminary success with site-specific mutagenesis. | *08/30/06: We successfully made the first construct, Lac+RBS+KaiC. [[IGEM:Harvard/2006/Cyanobacteria/Notebook/2006-8-30 | Link]] | ||
*09/01/06: Using the newly developed ligation protocol, we have successfully repeated Lac+RBS+KaiC from 08/30/06 and made Lac+RBS+KaiA. [[IGEM:Harvard/2006/Nicholas_Stroustrup%27s_Notebook#Results_Summary | | |||
*08/05/06: Promoter leakness tests come out negative. May have to use low-copy plasmids if we want good control of protein expression in Top10F. | Link]] | ||
*10/21/06: Successfully made Lac+RBS+KaiB and Lac+RBS+KaiA+Lac+RBS+KaiC. [[IGEM:Harvard/2006/Cyanobacteria/Notebook/2006-10-21 | Link]] | |||
*08/11/06: We are moving to the synthetic KaiA, KaiB, and KaiC for future work. | *10/24/06: Successfully made Lac+RBS+KaiB+Lac+RBS+KaiC. [[IGEM:Harvard/2006/Cyanobacteria/Notebook/2006-10-24 | Link]] | ||
*10/25/06: Constructs for Stage I have been completed; ready to move to Stage I of Western Blotting, to verify expression of KaiC and interaction of KaiA and KaiB with KaiC. [[IGEM:Harvard/2006/Cyanobacteria/Notebook/2006-10-24 | Link]] | |||
*08/30/06: We successfully made the first construct, Lac+RBS+KaiC. | *'''10/27/06: Preliminary data indicates that the Kai proteins are being expressed in e. coli and that there is interaction between the three proteins! [[IGEM:Harvard/2006/Cyanobacteria/Notebook/2006-10-27 | Link]]''' | ||
* | |||
*10/ | |||
* | |||
*10/25/06: Constructs for Stage I have been completed; ready to move to Stage I of Western Blotting, to verify expression of KaiC and interaction of KaiA and KaiB with KaiC. | |||
*10/27/06: Preliminary data indicates that the Kai proteins are being expressed in e. coli and that there is interaction between the three proteins! | |||
==Construct Planning== | ==Construct Planning== | ||
| Line 51: | Line 47: | ||
* KaiC + J04500: 2110 bp | * KaiC + J04500: 2110 bp | ||
==Agenda== | ==Agenda== | ||
''See image at right for our long-term project outline.'' | ''See image at right for our long-term project outline.'' | ||
[[Image:Cyanobacteria_Flowchart.png|thumb|Long-term project outline]] | [[Image:Cyanobacteria_Flowchart.png|thumb|Long-term project outline]] | ||
==BioBricks Used== | ==BioBricks Used== | ||
| Line 104: | Line 88: | ||
*''[[Media:final_presentation_draft2.ppt |Final Presentation (complete)]]'' --old | *''[[Media:final_presentation_draft2.ppt |Final Presentation (complete)]]'' --old | ||
*[[:Image:Cyano presentation.ppt | Jamboree presentation]] (in progress) | *[[:Image:Cyano presentation.ppt | Jamboree presentation]] (in progress) | ||
**[[:Image:Cyano_presentation_script.doc|Script]] (in progress) | |||
*[[:Image:Cyano poster.ppt | Cyano poster]] (in progress) | |||
==Team Members== | ==Team Members== | ||
Latest revision as of 04:28, 3 November 2006
<html><style type='text/css'> .tabs {
font-size:80%;
font-weight:none;
width: 100%;
color: #FFFFFF;
background:#FFFFFF url("/images/5/54/DarkgreenTab-bg.gif") repeat-x bottom;
}
.tabs li {
background:url("/images/3/36/DarkgeenTab-left.gif") no-repeat left top;
}
.tabs a,.tabs strong {
background:url("/images/d/d3/DarkgreenTab-right.gif") no-repeat right top;
color:#FFFFFF;
padding: 3px 10px 3px 4px;
}
.tabs strong{
color:#CCFF00;
background-image:url("/images/b/b1/DarkgreenTab-right_on.gif");
}
.tabs a:hover{
color:#66FF00;
}
</style></html>
Introduction
Welcome to the lab notebook for the Cyanobacteria oscillator project! The goal of our team, composed of four members, is to reconstruct the cyanobacterial circadian oscillator system into E. coli. Three proteins, KaiA, B, and C, have been shown to have an in-vitro phosphorylation state oscillation (Nakajima et al. 2005) by transcriptional-translational independent methods. If this system can be reconstituted in E. coli, there are two important applications:
- Synthetic Biology: Creating a functional, oscillating set of proteins is the next logical step from the synthetic "repressilator" system engineered by Elowitz et al. (2000). Although a good proof of concept, the "repressilator" lacks the stability needed from a robust oscillator such as the naturally evolved cyanobacterial oscillator. This robust oscillator could prove useful in an eventual biocircuit.
- Circadian Biology: Cyanobacteria are the simplest model organisms for the study of circadian oscillation. Although circadian oscillation has been fairly well characterized, less is understood at the molecular level. By porting the oscillation system into E. coli, one can begin to understand more precisely the pathways involved in the genomic oscillation of cyanobacteria.
For more background information on the ciracadian system, please check out our "Literature" section. Otherwise, day-to-day work can be found under the "Lab Notebook" tab; we will post major results of our work and links to the days as they become available. If you have questions or comments, feel free to contact us: information is located at the main Harvard iGEM 2006 page. Thanks!
Sincerely,
Zhipeng, Hetmann, Dave, and Jeff
Update 10/27/06: We believe we can express the three proteins into e. coli, and that there is interaction between A+C and possible interaction between B+C. See the Lab Notebook for more information.
Outline of Findings and Signifigant Dates
- 07/05/06: The incubator for growing up our cyanobacteria is complete; we have cultures growing! Link
- 07/10/06: Some computer modeling has been done to see the effect of multiple unsyncronized clocks on phosphorylation state output. Link
- 07/21/06: Upon having trouble with site-specific mutagenesis on the KaiA and KaiBC operons from the cyanobacterial genome, we have decided to pursue synthesis of the constructs in parallel with continued extraction attempts. Link
- 08/01/06: Preliminary success with site-specific mutagenesis. Link
- 08/05/06: Promoter leakness tests come out negative. May have to use low-copy plasmids if we want good control of protein expression in Top10F. Link
- 08/11/06: We are moving to the synthetic KaiA, KaiB, and KaiC for future work. Link
- 08/30/06: We successfully made the first construct, Lac+RBS+KaiC. Link
- 09/01/06: Using the newly developed ligation protocol, we have successfully repeated Lac+RBS+KaiC from 08/30/06 and made Lac+RBS+KaiA. Link
- 10/21/06: Successfully made Lac+RBS+KaiB and Lac+RBS+KaiA+Lac+RBS+KaiC. Link
- 10/24/06: Successfully made Lac+RBS+KaiB+Lac+RBS+KaiC. Link
- 10/25/06: Constructs for Stage I have been completed; ready to move to Stage I of Western Blotting, to verify expression of KaiC and interaction of KaiA and KaiB with KaiC. Link
- 10/27/06: Preliminary data indicates that the Kai proteins are being expressed in e. coli and that there is interaction between the three proteins! Link
Construct Planning
Lengths
From VF2 to VR (BioBrick primers):
- KaiA + J04500: 1406 bp
- KaiB + J04500: 859 bp
- KaiC + J04500: 2110 bp
Agenda
See image at right for our long-term project outline.
BioBricks Used
- <bbpart>BBa_J04450</bbpart>
- RFP device
- Insert size: 1069bp
- [pSB1A2]
- High-copy, AmpR
- Size: 2079bp
- <bbpart>BBa_J04500</bbpart>
- Lac promoter + RBS
- Insert size: 220bp
- [pSB1AK3]
- High-copy, AmpR, KanR
- Insert size: 3189bp
- [pSB4A3]
- Low-copy, AmpR
- Insert size: 3339 bp
- <bbpart>BBa_R0010</bbpart> + <bbpart>BBa_E0241</bbpart>
- GFP device
- Insert size: 995 bp
- <bbpart>BBa_J04450</bbpart>
Presentations
- Project proposal (week 2)
- Week 3 progress update
- Built incubator and obtained WH8102, PCC7942, and PCC6803 strains
- Week 4 progress update
- Week 5 progress update, upd. 10:10 7/17
- Week 6 progress update, upd. 10:02 7/24 HH
- Week 7 progress update
- Week 8 progress update
- Week 9 progress update
- Week 10 progress update, 50% complete
- Final Presentation (incomplete) --old
- Final Presentation (complete) --old
- Jamboree presentation (in progress)
- Script (in progress)
- Cyano poster (in progress)
Team Members
- Hetmann Hsieh (talk, edits)
- Jeffrey Lau (talk, edits)
- Zhipeng Sun (talk, edits)
- David Ramos (talk, edits)
Recent Changes
List of abbreviations:
- N
- This edit created a new page (also see list of new pages)
- m
- This is a minor edit
- b
- This edit was performed by a bot
- (±123)
- The page size changed by this number of bytes
6 May 2024
|
|
12:59 | BioMicroCenter:Covaris 11 changes history +450 [Noelani Kamelamela (11×)] | |||
|
|
12:59 (cur | prev) −17 Noelani Kamelamela talk contribs (→R230) | ||||
|
|
12:58 (cur | prev) −1 Noelani Kamelamela talk contribs (→R230) | ||||
|
|
12:57 (cur | prev) +1 Noelani Kamelamela talk contribs (→R230) | ||||
|
|
12:57 (cur | prev) +6 Noelani Kamelamela talk contribs (→R230) | ||||
|
|
12:56 (cur | prev) +2 Noelani Kamelamela talk contribs (→R230) | ||||
|
|
12:55 (cur | prev) +6 Noelani Kamelamela talk contribs (→R230) | ||||
|
|
12:54 (cur | prev) −1 Noelani Kamelamela talk contribs (→R230) | ||||
|
|
12:54 (cur | prev) +64 Noelani Kamelamela talk contribs (→R230) | ||||
|
|
12:49 (cur | prev) +49 Noelani Kamelamela talk contribs (→R230) | ||||
|
|
12:22 (cur | prev) +221 Noelani Kamelamela talk contribs (→R230) | ||||
|
|
11:55 (cur | prev) +120 Noelani Kamelamela talk contribs (→R230) | ||||
| 11:41 | Paper Microfluidic Device for Archiving Breast Epithelial Cells diffhist −89 Xning098 talk contribs (→Paper Microfluidics) | ||||
5 May 2024
|
|
21:12 | (Upload log) [Xning098 (3×)] | |||
|
|
21:12 Xning098 talk contribs uploaded File:Whatman® FTA® cards.png | ||||
|
|
21:03 Xning098 talk contribs uploaded File:Diagram-Shows-the-Technique-of-FNAC.png | ||||
|
|
20:18 Xning098 talk contribs uploaded File:Guthrie test .png | ||||
