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Introduction

Our project goal is to maximize the photosynthetic productivity of a series of photobioreactors containing Rhodobacter sphaeroides under both high and low light intensities by synthetically regulating the size of the light-harvesting antenna complex LH2. We chose to undertake such a project using R. sphaeroides due to its well-characterized photosynthetic and genetic system.

The antenna system functions to expand the spectrum of light available for photosynthesis by absorbing different wavelengths than that of the reaction center. Essentially, it is like the dish around the main receiver of any antenna. Marine bacteria, such as R. sphaeroides, evolved very large antenna complexes to absorb light in a natural environment, where there is great competition for photons. As a result, the photosynthetic machinery is saturated at low light intensities in a synthetic non-competitive environment, such as a photobioreactor. This causes up to 95% of incidental photons to be dissipated as heat or fluorescence by bacteria through a process called Non-Photochemical Quenching (NPQ) (Mussgnug et al., 2007). In essence, these photons are being wasted as NPQ reduces light penetration into and across bioreactors and starves the shaded cells for for photons. One method that has been shown to improve photosynthetic productivity in photobioreactors is the reduction of light-harvesting antenna sizes (Polle et al., 2002, Mussgnug et al., 2007). Though, current approaches to this end are difficult to precisely control from the perspective of biological engineering and synthetic biology.

Our intention is to create a dynamic system that varies antenna size, is dependent on incident light intensity, and can be readily optimized using bioengineering principles. This synthetic regulation of the LH2 complex should result in bacteria grown under high light intensities expressing fewer LH2 complexes than cells that are more shaded, leading to a reduction of wasted incident photons while maintaining a high overall absorbance across subsequent bioreactors. Consequently, we expect to see an increase in the total photosynthetic productivity of our mutant Rhodobacter sphaeroides when compared to the wild type grown under similar conditions.

Wild Type Energy Production in a series of Bioreactors

Synthetically Regulated Antenna Energy Production in Bioreactors

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Organism

Rhodobacter sphaeroides is a purple Alphaproteobacteria. It is metabolically flexible: it can grow heterotrophically, via aerobic and anaerobic respiration, as well as phototrophically under anaerobic conditions with light.

R. sphaeroides is one of the best understood photosynthetic organisms. The photosystem is located in intracytoplasmic membrane invaginations and the main components are the Light Haresting Complex 2 (LH2), Light Harvesting Complex 1 (LH1), and the Reaction Center (RC). These pigment-protein complexes non-covalently bind bacteriochlorophylls and carotenoids. LH1 and RC make up the core complex and are often found in the ratio of 1:1. LH2 is more peripheral and naturally ranges in the ratio to LH1/RC of 3.0:1 to 6.7:1 under varying light conditions (Scheuring et al., 2005). LH2 absorbs photons maximally at the wavelengths of 850 and 800 nm and funnels its energy to LH1 and the reaction center for photochemistry. (Scheuring et al., 2005).

The two subunits of LH2 are coded for by the pucB/A genes and are naturally promoted by the puc promoter.

ICM of R. sphaeroides

source:Sener et al.2007

LH2 Absorption Spectra

Plate of R. sphaeroides 2.4.1

source: Walz et al. 1998

Online Resources for R. sphaeroides

[http://www.kazusa.or.jp/codon/cgi-bin/showcodon.cgi?species=272943 Codon Usage Table for R. sphaeroides 2.41]
[http://www.ncbi.nlm.nih.gov/sites/entrez?db=genome&cmd=Retrieve&dopt=Overview&list_uids=18843 R. sphaeroides 2.41 NCBI Genome Tools]
[http://archaea.ucsc.edu/cgi-bin/hgPcr?wp_target=&db=0&org=Rhodobacter+sphaeroides+2+4+1&wp_f=&wp_r=&wp_size=2000&wp_perfect=15&wp_good=15&wp_showPage=true&hgsid=159191 In silico PCR of R. sphaeroides 2.41 genome]

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Regulation

The Natural System (Left) Under high oxygen tension, PpsR prevents transcription from the puc promoter of the pucBA genes, and thus prevents the expression of LH2(1st panel). Under low oxygen tension, this repression is removed by activated AppA, thus allowing expression of LH2 from pucBA(2nd panel).
Synthetic Regulation System (Right) Our system takes advantage of constitutive protein expression from the puc promoter at low oxygen tension, and replaces pucBA with Cph8 at this site. Placing pucBA expression under the control of the ompC promoter allows for Cph8/OmpR control of LH2 expression under varying light conditions. Under high intensity of incident light, Cph8 will not be autophosphorylated, preventing expression of pucBA (3rd panel). When light intensity is lower, Cph8 will autophosphorylate, thus phosphorylating and activating OmpR and promoting expression of LH2 from the ompC promoter.
This regulation system was designed such that light is able to penetrate deeper into and through photobioreactors where light is plentiful.

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Results

For methods, materials, and procedures regarding these results, please see Tissue Flask Experiment or Modeling

Figure 1

a Tissue Flask Position 1 Optical Density of Wild Type and DCBomega

b Tissue Flask Position 2 Optical Density of Wild Type and DCBomega

c Tissue Flask Position 3 Optical Density of Wild Type and DCBomega

d Tissue Flask Position 4 Optical Density of Wild Type and DCBomega

e Tissue Flask Position 5 Optical Density of Wild Type and DBComega

Figure 1a,b,c,d,e are the optical density of a tissue flask, as assessed at 600 nm, over the course of the 6 days of the experiment.

Figure 2

a The Change in the Optical Density of the Tissue Flasks for the WT

b The Change in the Optical Density of the Tissue Flasks for DBComega

Figure 2a and 2b display the growth of the tissue flasks as measured by OD assessed as absorbance at 600 nm. The graph is organized such that those closest to the "days" axis were closest to the light source (i.e. flask 1 is closer than flask 2).

Figure 3

a Cumulative Growth of Wild Type Tissue Flasks

b Cumulative Growth of the DBComega Tissue Flasks

Figure 3a and 3b display the cumulative growth of the tissue flasks as measured by the sum of the optical density of the respective cell type's tissue flasks at a given day. Furthermore, the contribution of a given tissue flask to cumulative growth is displayed.

Figure 4

a Wild Type Tissue Flasks

b The DBComega Tissue Flasks

Figure 4A and 4B display the appearance of the tissue flasks for both strains on day 6. They are arranged from left to right with left being closed to the light source (flask 1) and right furthest (flask 5)

Figure 5

a R. sphaeroides Spectrum by Flask Distance from Source

bDBComega Spectrum by Flask Distance from Source

Contour of Absolute Irradiance by Flash distance from Source

c R. Sphaeroides 2.4.1

d DBComega

e Wild Type Absolute Irradiance Behind Flask 1: Day 6

Figure 5 shows the results of the absolute irradiance data taken using the sprectroradiomter. A and B shows absolute irradiance on a given flask at each wavelength. Figure C and D represent the data for the same days as A and B in two dimensions. Figure E is the absolute irradiance behind only flask 1 on day 6.

Figure 6

Figure 7

Nonlinear least-squares estimation of WT LH2 saturation curve

Simulated Optical Density of Mutant and Wild Type Bioreactors
Layers One and Two Layers Three, Four and Five

Figure 6 derived from absolute irradiance data from WT tissue flask experiment

Figure 7 shows the results of modeling the WT vs. mutant regulation system

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Analysis

Though we were not able to have our mutant functionally express our system, the tissue flask experiment was an interesting way to observe the effects of a full knockout of the Light Harvesting Antenna Complex 2 (LH2) vs the Wild Type on an array of consecutive photobioreactors. A couple of conclusions can be drawn from this data that can be used in modeling our synthetic regulation system for LH2 and in the future design of systems for the optimization of Light Harvesting Antenna size for photobioreactors .

The most striking difference between the Wild Type Rhodobacter Sphaeroides 2.41 and DBCOmega (LH2 knockout) growth patterns is that the first flask in the WT (closest to the light source) grew less than the second flask, while the converse was true in DBCOmega (figure 2a and 2b). This can be attributed to the photosystem saturation curves for the respective cultures. The Wild Type has an LH2 complex, meaning that their antenna size is inherently larger and that their photosystem will be saturated at lower light intensities than the LH2 deficient mutant. We observed that the incident light intensity used in this experiment led to oversaturation for the first WT tissue flask and resulted in growth-inhibiting photodamage, as is evidenced by its lesser growth relative to the second culture. In contrast, photodamage was not observed in DBCOmega as is evidenced by the first tissue flask that grew at the fastest respective rate. Furthermore, it appears that this photodamage slowed the growth of the first WT tissue flask to the point that the OD of this tissue flask was nearly equal to that of DBCOmega after 5 days of growth(.987 vs. .967) (figure 1a). As such, the contribution of LH2 to the growth of the WT in flask 1 can be assessed to be little after day 3 when the growth curve slows- though, this light (at 800 and 850 nm) was still greatly absorbed by flask 1 (Figure 5e). It is likely that much of this light was then wasted through Non-Photochemical Quenching (NPQ), depleting the flasks behind flask 1 of photons at the LH2 absorbtion peaks and decreasing the cumulative productivity of flasks 1-5. This effect of wasting photons though NPQ under high light intensities is one that we sought to minimize in the design of our synthetic regulation for the pucB/A genes.

A further a comparison of the WT and DBCOmega experiments reveals that the 3rd tissue flask in each had almost identical growth rates (figure 1c), while the DBCOmega 4th and 5th tissue flask outperformed that of the WT (figure 1d and 1e). This can simply be attributed to the higher density of cells in the 2nd flask of the WT that led to an overall lesser quantity of photons passing through to the 4th and 5th flasks in the WT experiment and likely resulting in heterotrophic growth (though this will need to be confirmed with a "dark control" experiment that should be completed in time for the Jamboree). This decrease in available photons for the WT can be seen by viewing the absolute irradiance data (incident light intensity at a given wavelength) after the third culture for the WT (figure 5a and 5c). This decrease in irradiance is the most pronounced for the LH2 absorption bands at 800 and 850 nm, as was expected. Our synthetic regulation system for pucB/A was designed with the intention of allowing greater penetration of light through the first couple of flasks at the LH2 wavelengths, as expression of pucB/A is inversely correlated to incident light intensity.

Overall, the cumulative culture growth of the WT exceeded that of DBCOmega (figure 3) due to the performance of the second tissue flask of the WT relative to that of DBCOmega (figure 1b) despite the photodamage that occurred in tissue flask 1 for the WT. This cumulative culture growth can be considered photosynthetic productivty and is proportional to the amount of energy/desired product that can be obtained from these cultures.

It is an interesting exercise to model how our mutant system would perform under these same conditions. To do so, the LH2 saturation curve for the WT (figure 6) and the relative contribution of LH1/LH2 light absorbance to growth was derived from our empirical data and applied to a model that took into account incident light and gave the relative growth in terms of optical density as an output. In this model, our synthetic regulation system of pucB/A allowed our mutant to outperform the wild type species (figure 7). This was due to the performance of the 3rd, 4th, and 5th tissue flask relative to those of the wild type (see figure 7 layers 1,2 vs 1-5). The reason for this is that the wild type LH2 light saturation curve does not vary with changes in incident light intensity as the wild type expresses pucB/A at a uniform level under low oxygen conditions. As a result, the first two layers of Wild Type bioreactors absorb nearly all the available light and starve the bioreactors behind them for photons.

Conversely, our mutant was modeled to have a dynamic expression of pucB/A based on the incident light intensity. This light response curve was modeled as an inverse exponential for the Cph8/OmpR ompC Promoter system and the saturation curve changes for each tissue flask in accordance with the incident light intensity- as light intensity decreases, the expression pucB/A increases. This results in more light passing through the first 2 flasks and facilitating greater growth in flasks 3, 4 and 5 as they express large antenna complexes. Nonetheless, we believe that growth across the bioreactors could be further maximized by increasing antenna size in the first 2 bioreactors and sacrificing growth in the 4th and 5th. This could be achieved with a feedback mechanism that sets a minimum level for LH2 expression.

Conclusion

Though we were not able to conduct the tissue flask growth experiment on our mutant, the results of this experiment on our controls (WT and DBComega) match the assumptions that we had laid out at the beginning of the project, allowed us to draw further conclusions about the efficiency of light-based growth for a series of bioreactors, and to create a model for our mutant based on empirical data.

Based on this model, we have concluded that it would be favorable to have a feedback regulation mechanism that sets a minimum expression level for pucB/A to further improve photosynthetic productivity.

We intend to conduct the tissue flask w DBComega+prkcbc3 before jamboree and compare/interpret these results using our characterization data for the pucB/A and the puc promoter.

We will conduct the tissue flask experiment with our functioning mutant in future and compare the results to our model

Finally, we would like to characterize the puc promoter under various light conditions and additional oxygen tensions.

Overall- our project has demonstrated the potential for a synthetically regulated light harvesting antenna to improve photosynthetic productivity for a series of photobioreactors vs. the wild type.

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References

"2007-2008 Catalog & Technical Reference." New England BioLabs Inc. (2007).
Alon, Uri. Introduction to systems biology and the design principles of biological networks. Boca Raton, FL: Chapman & Hall, 2006.
Ausubel, Fred et al. Short Protocols in Molecular Biology: Third Edition. Canada: John Wiley and Sons, Inc., 1999.
"BioBrick Assembly Help." Registry of Standard Biological Parts. 2009. 6 July 2009. <http://partsregistry.org/Main_Page>.
Bower, James M. Computational Modeling of Genetic and Biochemical Networks (Computational Molecular Biology). New York: M.I.T. PRESS, 2001.
Braatsch, Stephan et al. "A single Flavoprotein AppA, Integrates Both Redox and Light Signals in Rhodobacter sphaeroides." Molecular Microbiology. Vol. 45.3 (2002): 827-836.
Brown, Stanley B. et al. "Bile Pigment Synthesis in Plants: Incorporation of Haem into Phycocyanobilin and Phycocyanobiliproteins in Cyanidium Caldarium." Biochemistry. Vol. 194 (1981): 137-147.
Dragnea, Vladimira et al. "Time-Resolved Spectroscopic Studies of the AppA Blue-Light Receptor BLUF Domain from Rhodobacter sphaeroides Biochemistry. Vol. 44 (2005): 15,978-15,985.
"Entrez Nucleotide Search." National Center for Biotechnology Information. 2009. 6 June 2009 <http://www.ncbi.nlm.nih.gov/nuccore/49175990?from=3533887&to=3534606&report=gbwithparts>.
Fowler, Gregory J. S. and C. Neil Hunter. "The Synthesis and Assembly of Functional High and Low Light LH2 Antenna Complexes from Rhodopseudomonas palustris in Rhodobacter sphaeroides." The Journal of Biological Chemistry. Vol. 271.23 (1996): 13,356-13,361.
Gabrielsen, Mads et al. "Peripheral Complexes of Purple Bacteria." The Purple Phototropic Bacteria. (2009): 135-153.
"GenElute HP Plasmid Miniprep Kit: User Guide." Sigma-Aldrich. (2008).
Harwood, Caroline S. "Nitrogenase-Catalyzed Hydrogen Production by Purple Nonsulfur Photosynthetic Bacteria." Bioenergy. (2008): 259-271.
Jager, Andreas et al. "The AppA and PpsR Proteins from Rhodobacter sphaeroides Can Establish a Redox-Dependent Signal Chain but Fail to Transmit Blue-Light Signals in Other Bacteria." Journal of Bacteriology. Vol. 189.6 (2007): 2,274-2,282.
Jones, M. R. et al. "Mutants of Rhodobacter sphaeroides Lacking One or More Pigment-Protein Complexes and Complementation with Reaction-Centre, LH1, and LH2 Genes." Molecular Microbiology. Vol. 6.9 (1992): 1,173-1,184.
Kondo, Toshihiko et al. "Enhancement of Hydrogen Production by a Photosynthetic Bacterium Mutant with Reduced Pigment." Journal of Bioscience and Bioengineering. Vol. 93.2 (2002): 145-150.
Lagarias, J. Clark. PCB from Spirulina. Personal Communication. June 2009.
Laible, Philip D. "Foreign Gene Expression in Photosynthetic Bacteria." The Purple Phototropic Bacteria. (2009): 839-860.
Lee, Jeong K. and Samuel Kaplan. "Transcriptional Regulation of puc Operon Expression in Rhodobacter sphaeroides." Journal of Biological Chemistry. Vol. 270.35 (1995): 20,453-20,458.
Levskaya, Anselmetal et al. "Engineering Escherichia coli to See Light." Nature. Vol. 438 (2005): 441-442.
"Life Sciences Catalog 2009-2010." National Diagnostics. (2009).
Melis, Anastasios. "Solar Energy Conversion Efficiencies in Photosynthesis: Minimizing the Chlorophyll Antennae to Maximize Efficiency." Plant Science. (2009).
Mizuno, Takeshi and Shoji Mizushima. "Characterization by Deletion and Localized Mutagenesis in Vitro of the Promoter Region of the Escherichia coli OmpC Gene and Importance of the Upstream DNA Domain in Positive Regulation by the OmpR Protein." Journal of Bacteriology. Vol. 168.1 (1986): 86-95.
Moskvin, Oleg V. et al. "Transcriptome Analysis of the Rhodobacter sphaeroides PspR Regulon: PspR as a Master Regulator of Photosystem Development." Journal of Bacteriology. Vol. 187.6 (2005): 2,148-2,156.
Mussgnug, Jan H. et al. "Engineering photosynthetic light capture: impacts on improved solar energy to biomass conversion." Plant Biotechnology Journal Vol. 5 Issue 6. (2007) pp. 802-814
"NEBCutter V2.0." New England BioLabs. 2009. 6 June 2009 <http://tools.neb.com/NEBcutter2/index.php>.
"OligoAnalyzer 3.1." Integrated DNA Technologies. 2009. 6 June 2009. <http://www.idtdna.com/analyzer/Applications/OligoAnalyzer/>
Sambrook, Joseph and David W. Russell. Molecular Cloning: A Laboratory Manual. Vol. 1-3. New York: Cold Springs Harbor Laboratory Press, 2001.
Scheuring, Simon and Sturgis, James N. "Chromatic Adaptation of Photosynthetic Membranes" Science Vol. 309 (2005) pp.484-487
Sener, Melih K. et al. "Atomic-level structural and functional model of a bacterial photosynthetic membrane vesicle" Proceedings of the National Academy of Sciences of the United States of America. Vol. 104, Number 40,pp. 15723-15728
Shimizu-Sato, Sae et al. "A Light-Switchable Gene Promoter System." Nature Publishing Group. Vol. 20 (2002): 1,041-1044.
Smith, Harry and M. Geoffrey Holmes. Techniquies in Photomorphogenesis. London: Academic Press, Inc., 1984.
System modeling in cellular biology from concepts to nuts and bolts. Cambridge, MA: MIT P, 2006.
Terry, Matthew J. "Biosynthesis and Analysis of Bilins." Heme, Chlorophyll, and Bilins: Methods and Protocols. (2002) 273-291.
Wang, Wanneng et al. "Heterologous Synthesis and Assembly of Functional LHII Antenna Complexes from Rhodovulum sulfidophilum in Rhodobacter sphaeroides Mutant." Molecular Biology Reports. Vol. 12.3 (2008).
Walz, Thomas et al. "Projection Structures of Three Photosynthetic Complexes from Rhodobacter sphaeroides: LH2 at 6 A, LH1 and RC-LH1 at 25 A" Journal of Molecular Biology Vol. 282 pp. 833-845
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@@ Line 6: / Line 6: @@
 == '''Introduction''' ==
 <font size="2">
-Our project goal is to maximize the photosynthetic productivity for a series of photobioreactors containing ''Rhodobacter sphaeroides'' under both high and low light intensities by synthetically regulating the size of the light-harvesting antenna complex LH2.   We chose to undertake such a project in ''R. sphaeroides'' due to its well-characterized photosynthetic and genetic system.
+Our project goal is to maximize the photosynthetic productivity of a series of photobioreactors containing ''Rhodobacter sphaeroides'' under both high and low light intensities by synthetically regulating the size of the light-harvesting antenna complex LH2.   We chose to undertake such a project using ''R. sphaeroides'' due to its well-characterized photosynthetic and genetic system.
-The antenna system functions to expand the spectrum of light available for photosynthesis by absorbing different wavelengths than that of the reaction center.  Essentially, it is like the dish around the main receiver of any antenna.  Marine bacteria, such as ''R. sphaeroides'', evolved very large antenna complexes to absorb light in a natural environment where there is great competition for photons.  As a result, the photosynthetic machinery is saturated at low light intensities in a synthetic non-competitive environment, such as a photobioreactor.  This causes up to 95% of incidental photons to be dissipated as heat or fluorescence by bacteria through a process called Non-Photochemical Quenching (NPQ) (Mussgnug et al., 2007). In essence, these photons are being wasted as NPQ reduces light penetration into and across bioreactors and starves the shaded cells for for photons.  One method that has been shown to improve photosynthetic productivity in photobioreactors is the reduction of light-harvesting antenna sizes (Polle et al., 2002, Mussgnug et al., 2007).  Though, current approaches to this end are difficult to precisely control from the perspective of biological engineering and synthetic biology.
+The antenna system functions to expand the spectrum of light available for photosynthesis by absorbing different wavelengths than that of the reaction center.  Essentially, it is like the dish around the main receiver of any antenna.  Marine bacteria, such as ''R. sphaeroides'', evolved very large antenna complexes to absorb light in a natural environment, where there is great competition for photons.  As a result, the photosynthetic machinery is saturated at low light intensities in a synthetic non-competitive environment, such as a photobioreactor.  This causes up to 95% of incidental photons to be dissipated as heat or fluorescence by bacteria through a process called Non-Photochemical Quenching (NPQ) (Mussgnug et al., 2007). In essence, these photons are being wasted as NPQ reduces light penetration into and across bioreactors and starves the shaded cells for for photons.  One method that has been shown to improve photosynthetic productivity in photobioreactors is the reduction of light-harvesting antenna sizes (Polle et al., 2002, Mussgnug et al., 2007).  Though, current approaches to this end are difficult to precisely control from the perspective of biological engineering and synthetic biology.
-Our intention is to create a dynamic system to vary antenna size that is dependent on incident light intensity and that can be readily optimized using bioengineering principles. This synthetic regulation of the LH2 complex should result in the bacteria grown under high light intensities expressing fewer LH2 complexes than the cells that are more shaded, leading to a reduction of wasted incident photons while maintaining a high overall absorbance across subsequent bioreactors.  Consequently, we expect to see an increase in the total photosynthetic productivity for our mutant ''Rhodobacter sphaeroides'' when compared to the wild type grown under similar conditions.
+Our intention is to create a dynamic system that varies antenna size, is dependent on incident light intensity, and can be readily optimized using bioengineering principles. This synthetic regulation of the LH2 complex should result in bacteria grown under high light intensities expressing fewer LH2 complexes than cells that are more shaded, leading to a reduction of wasted incident photons while maintaining a high overall absorbance across subsequent bioreactors.  Consequently, we expect to see an increase in the total photosynthetic productivity of our mutant ''Rhodobacter sphaeroides'' when compared to the wild type grown under similar conditions.
+<div style="text-align: center;">
+{|style="background-color:#ffefd5; width:100%" <font size="2">
+|
+|
+|
+|<font size="2" style="color:black;">'''Wild Type Energy Production in a series of Bioreactors'''
+|
+|
+|
+|<font size="2" style="color:black;">'''Synthetically Regulated Antenna Energy Production in Bioreactors'''
+|
+|
+|
+|}
-[[Image:Slide10.jpg| 450 px]] [[Image:Slide09.jpg| 450 px]]
+[[Image:Slide09b.jpg| 450px | left]][[Image:Slide10 a.jpg| 450px | right]]
+<br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br>
+<div style="text-align: left;">
+[https://2009.igem.org/Team:Wash_U/Project Back To Top]
-<br>[https://2009.igem.org/Team:Wash_U/Project Back To Top]
@@ Line 23: / Line 38: @@
 == '''Organism''' ==
 <font size="2">
-''Rhodobacter sphaeroides'' is a purple Alphaproteobacteria.  It is flexible metabolically and can grow heterotrophically via aerobic and anaerobic respiration, as well as phototrophically under anaerobic conditions with light.
+''Rhodobacter sphaeroides'' is a purple Alphaproteobacteria.  It is metabolically flexible: it can grow heterotrophically, via aerobic and anaerobic respiration, as well as phototrophically under anaerobic conditions with light.
 <br> <br>
-''R.  sphaeroides'' is one of the best understood photosynthetic organisms.  The photosystem is located in intracytoplasmic membrane invaginations and the main components are the Light Haresting Complex 2 (LH2), Light Harvesting Complex 1 (LH1), and the Reaction Center (RC).  These pigment-protein complexes non-covalently bind bacteriochlorophylls and carotenoids.  LH1 and RC make up the core complex and are often found in the ratio 1:1. LH2 is more peripheral and naturally ranges in the ratio to LH1/RC of 3.0:1 to 6.7:1 under varying light conditions (Scheuring et al., 2005). LH2 absorbs photons maximally at the wavelengths of 850 and 800 nm and funnels its energy to LH1 and the reaction center for photochemistry. (Scheuring et al., 2005).
+''R.  sphaeroides'' is one of the best understood photosynthetic organisms.  The photosystem is located in intracytoplasmic membrane invaginations and the main components are the Light Haresting Complex 2 (LH2), Light Harvesting Complex 1 (LH1), and the Reaction Center (RC).  These pigment-protein complexes non-covalently bind bacteriochlorophylls and carotenoids.  LH1 and RC make up the core complex and are often found in the ratio of 1:1. LH2 is more peripheral and naturally ranges in the ratio to LH1/RC of 3.0:1 to 6.7:1 under varying light conditions (Scheuring et al., 2005). LH2 absorbs photons maximally at the wavelengths of 850 and 800 nm and funnels its energy to LH1 and the reaction center for photochemistry. (Scheuring et al., 2005).
 <br><br>
 The two subunits of LH2 are coded for by the pucB/A genes and are naturally promoted by the puc promoter.
-ICM of ''R. sphaeroides'' [[Image:R sphaeroides photosystem.png| 500 px]] source:Sener et al.2007<br>
+<br><div style="text-align: center;">'''ICM of ''R. sphaeroides'' '''[[Image:R sphaeroides photosystem.png| 500 px | center]]<center>source:Sener et al.2007
-LH2 Absorption Spectra [[Image:R sphaeroides aborbance.png| 500 px]] source: Walz et al. 1998<br>
+<br>
-A Plate of ''R. sphaeroides'' 2.4.1 [[Image:R sphaeroides 0986.png| 500 px]]
-<br>[https://2009.igem.org/Team:Wash_U/Project Back To Top]
+<div style="text-align: center;">
+{|style="background-color:#ffefd5; width:100%" <font size="2">
+|
+|
+|
+|<font size="2" style="color:black;">'''LH2 Absorption Spectra'''
+|
+|
+|
+|<font size="2" style="color:black;">'''Plate of ''R. sphaeroides'' 2.4.1'''
+|
+|
+|
+|}
+[[Image:R sphaeroides aborbance.png| 450px | left]][[Image:R sphaeroides 0986.png| 450px | right]]<br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br>source: Walz et al. 1998<br>
+<div style="text-align: left;">
 <font size="2">
@@ Line 41: / Line 71: @@
 <br> [http://www.ncbi.nlm.nih.gov/sites/entrez?db=genome&cmd=Retrieve&dopt=Overview&list_uids=18843 ''R. sphaeroides'' 2.41 NCBI Genome Tools]
 <br> [http://archaea.ucsc.edu/cgi-bin/hgPcr?wp_target=&db=0&org=Rhodobacter+sphaeroides+2+4+1&wp_f=&wp_r=&wp_size=2000&wp_perfect=15&wp_good=15&wp_showPage=true&hgsid=159191 ''In silico'' PCR of ''R. sphaeroides'' 2.41 genome]
+[https://2009.igem.org/Team:Wash_U/Project Back To Top]
 <font size="4">
@@ Line 47: / Line 81: @@
 <font size="2">
 [[Image:pucregulation-fullpanels.png|950px]]
 '''The Natural System (Left)''' Under high oxygen tension, PpsR prevents transcription from the puc promoter of the pucBA genes, and thus prevents the expression of LH2(1st panel). Under low oxygen tension, this repression is removed by activated AppA, thus allowing expression of LH2 from pucBA(2nd panel).<br>
-'''Synthetic Regulation System (Right)''' Our system takes advantage of constitutive protein expression from the puc promoter at low oxygen tension, and replaces pucBA with Cph8 at this site. Placing pucBA expression under the control of the ompC promoter  allows for Cph8/OmpR control of LH2 expression under varying light conditions. Under high intensity of incident light, Cph8 will not be autophosphorylated, preventing expression of pucBA (3rd panel). When light intensity is lower, Cph8 will autophosphorylate, thus phosphorylating and activating OmpR and promoting expression of LH2 from the ompC promoter.
+'''Synthetic Regulation System (Right)''' Our system takes advantage of constitutive protein expression from the puc promoter at low oxygen tension, and replaces pucBA with Cph8 at this site. Placing pucBA expression under the control of the ompC promoter  allows for Cph8/OmpR control of LH2 expression under varying light conditions. Under high intensity of incident light, Cph8 will not be autophosphorylated, preventing expression of pucBA (3rd panel). When light intensity is lower, Cph8 will autophosphorylate, thus phosphorylating and activating OmpR and promoting expression of LH2 from the ompC promoter.<br>
+This regulation system was designed such that light is able to penetrate deeper into and through photobioreactors where light is plentiful.
 <br>[https://2009.igem.org/Team:Wash_U/Project Back To Top]
 <font size="4">
@@ Line 56: / Line 94: @@
 == '''Results''' ==
 <font size="2">
-'''Figure 1'''<br>
+For methods, materials, and procedures regarding these results, please see [https://2009.igem.org/Team:Wash_U/Protocol#Tissue_Flask_Experiment Tissue Flask Experiment] or [https://2009.igem.org/Team:Wash_U/Biological_Parts#Modeling Modeling]
-'''a''' Tissue Flask Position 1 Optical Density of WT and DBComega                             '''b''' Tissue Flask Position 2 Optical Density of WT and DBComega[[Image:Tissue Flask 1b.png| 450 px]]
-[[Image:Tissue Flask 2b.png| 450 px]]<br>
-'''c''' Tissue Flask Position 3 Optical Density of WT and DBComega '''d''' Tissue Flask Position 4 Optical Density of WT and DBComega[[Image:Tissue Flask 3b.png| 450 px]]
-[[Image:Tissue Flask 4b.png| 450 px]]<br>
-'''e''' Tissue Flask Position 5 Optical Density of WT and DBComega <br>[[Image:Tissue Flask 5b.png| 450 px]] Figure 1a,b,c,d,e are the optical density of a tissue flask, as assessed at 600 nm, over the course of the 6 days of the experiment.  <br><br>
-'''Figure 2'''<br> '''a''' The Change in the Optical Density of the Tissue Flasks for the WT '''b''' The Change in the Optical Density of Tissue Flasks for DBComega[[Image:3D 241.png| 450 px]]
-[[Image:3D DBCOmega2.png| 450 px]]<br> Figure 2a and 2b display the growth of the tissue flasks as measured by OD assessed as absorbance at 600 nm. The graph is organized such that those closest to the "days" axis were closest to the light source (i.e. flask 1 is closer than flask 2).
- <br><br>
-'''Figure 3'''<br>'''a''' Cumulative Growth of the WT Tissue Flasks '''b''' Cumulative Growth of the DBComega Tissue Flasks[[Image:Bar 241 b.png| 450 px]]
-[[Image:Bar DBCOmega b.png| 450 px]]<br> Figure 3a and 3b display the cumulative growth of the tissue flasks as measured by the sum of the optical density of the respective cell type's tissue flasks at a given day.  Furthermore, the contribution of a given tissue flask to cumulative growth is displayed.<br>
-'''Figure 4'''
+<div style="text-align: center;">
-'''A''' The WT tissue flasks '''B''' The DBComega tissue flasks<br>
+'''Figure 1'''
-[[image:sphaeroides tissue flask.jpg|450 px|]][[image:dbc tissue flask.jpg|450px|]]<br>
-Figure 4A and 4B display the appearance of the tissue flasks for both strains on day 6.  They are arranged from left to right with left being closed to the light source (flask 1) and right furthest (flask 5)<br>
-'''Figure 5''' Relative growth of DBComega to WT in Flask 2 at OD 600 <br>[[Image:relative growth.png| 600 px]]<br>
+{|style="background-color:#ffefd5; width:100%" <font size="2">
-This data illustrates the contribution of LH1 to growth relative to that of LH2 <br>
+|
+|
+|
+|
+|<font size="2" style="color:#black;">'''a'''  Tissue Flask Position 1 Optical Density of Wild Type and DCBomega
+|
+|
+|
+|
+|<font size="2" style="color:#black;">'''b'''  Tissue Flask Position 2 Optical Density of Wild Type and DCBomega
+|
+|
+|
+|
+|}
-'''Figure 6''' Various Irradiance Graphs<br>
+<div style="text-align: left;">
-[[Image: WT irradiance 3d.png| 450 px]][[Image: DBComega irradiance 3d.png| 450 px]]
+[[Image:Tissue Flask 2b.png| 450 px| left]][[Image:Tissue Flask 1b.png| 450px | right]]<br><br><br><br><br><br><br><br><br><br><br><br><br><br><br>
+<div style="text-align: center;">
+{|style="background-color:#ffefd5; width:100%" <font size="2">
+|
+|
+|
+|
+|<font size="2" style="color:#black;">'''c'''  Tissue Flask Position 3 Optical Density of Wild Type and DCBomega
+|
+|
+|
+|
+|<font size="2" style="color:#black;">'''d'''  Tissue Flask Position 4 Optical Density of Wild Type and DCBomega
+|
+|
+|
+|
+|}
-'''Figure 7''' WT LH2 saturation curve as inferred from data<br>
+<div style="text-align: left;">
-[[Image: saturation for WT as inferred.png| 450 px]]
+[[Image:Tissue Flask 3b.png| 450px | left]][[Image:Tissue Flask 4b.png| 450px | right]]
+<br><br><br><br><br><br><br><br><br><br><br><br><br><br><div style="text-align: center;">
+'''e''' Tissue Flask Position 5 Optical Density of Wild Type and DBComega
+[[Image:Tissue Flask 5b.png| 450px | center]]<br>
+Figure 1a,b,c,d,e are the optical density of a tissue flask, as assessed at 600 nm, over the course of the 6 days of the experiment.
+<div style="text-align: center;">
+'''Figure 2'''
+<div style="text-align: left;">
+{|style="background-color:#ffefd5; width:100%" <font size="2">
+|
+|
+|
+|
+|<font size="2" style="color:#black;">'''a''' The Change in the Optical Density of the Tissue Flasks for the WT
+|
+|
+|
+|
+|<font size="2" style="color:#black;">'''b''' The Change in the Optical Density of the Tissue Flasks for DBComega
+|
+|
+|
+|
+|}
+[[Image:3D 241.png| 450 px | left]][[Image:3D DBCOmega2.png| 450 px | right]]
+<br><br><br><br><br><br><br><br><br><br><br><br><br><br><br>
+Figure 2a and 2b display the growth of the tissue flasks as measured by OD assessed as absorbance at 600 nm. The graph is organized such that those closest to the "days" axis were closest to the light source (i.e. flask 1 is closer than flask 2).
+<div style="text-align: center;">
+'''Figure 3'''
+{|style="background-color:#ffefd5; width:100%" <font size="2">
+|
+|
+|
+|
+|<font size="2" style="color:#black;">'''a''' Cumulative Growth of Wild Type Tissue Flasks
+|
+|
+|
+|
+|<font size="2" style="color:#black;">'''b''' Cumulative Growth of the DBComega Tissue Flasks
+|
+|
+|
+|
+|}
+<div style="text-align: left;">
+[[Image:Bar 241 b.png| 450px | left]][[Image:Bar DBCOmega b.png| 450px | right]]
+<br><br><br><br><br><br><br><br><br><br><br><br><br><br><br>
+Figure 3a and 3b display the cumulative growth of the tissue flasks as measured by the sum of the optical density of the respective cell type's tissue flasks at a given day.  Furthermore, the contribution of a given tissue flask to cumulative growth is displayed.<br>
+<div style="text-align: center;">
+'''Figure 4'''
+{|style="background-color:#ffefd5; width:100%" <font size="2">
+|
+|
+|
+|
+|<font size="2" style="color:#black;">'''a''' Wild Type Tissue Flasks
+|
+|
+|
+|
+|<font size="2" style="color:#black;">'''b''' The DBComega Tissue Flasks
+|
+|
+|
+|
+|}
+<div style="text-align: left;">
+[[image:sphaeroides tissue flask.jpg|450 px|left|]][[image:dbc tissue flask.jpg|450px|right]]
+<br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br>
+Figure 4A and 4B display the appearance of the tissue flasks for both strains on day 6.  They are arranged from left to right with left being closed to the light source (flask 1) and right furthest (flask 5)
+<div style="text-align: center;">
+'''Figure 5'''
+{|style="background-color:#ffefd5; width:100%" <font size="2">
+|
+|
+|
+|
+|<font size="2" style="color:#black;">'''a'''  R. sphaeroides Spectrum by Flask Distance from Source
+|
+|
+|
+|
+|<font size="2" style="color:#black;">'''b'''DBComega Spectrum by Flask Distance from Source
+|
+|
+|
+|
+|}
+[[Image: WT irradiance 3d.png| 450 px | left]][[Image: DBComega irradiance 3d.png| 450 px | right]]
+<br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br>
+Contour of Absolute Irradiance by Flash distance from Source
+{|style="background-color:#ffefd5; width:100%" <font size="2">
+|
+|
+|
+|
+|<font size="2" style="color:#black;">'''c''' R. Sphaeroides 2.4.1
+|
+|
+|
+|
+|<font size="2" style="color:#black;">'''d''' DBComega
+|
+|
+|
+|
+|}
+<div style="text-align: left;">
+[[Image: r sphaeroides day 2 a.jpg| 450px | left]][[Image: dbc day 4b.jpg| 450px | right]]
+<br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br>
+<div style="text-align: center;">
+'''e''' Wild Type Absolute Irradiance Behind Flask 1: Day 6
+[[Image: irradiance WT flask 1 day6.png| 450px | center]]
+Figure 5 shows the results of the absolute irradiance data taken using the sprectroradiomter.  A and B shows absolute irradiance on a given flask at each wavelength.  Figure C and D represent the data for the same days as A and B in two dimensions.  Figure E is the absolute irradiance behind only flask 1 on day 6.  <br>
+<div style="text-align: center;">
+{|style="background-color:#ffefd5; width:100%" <font size="2">
+|
+|
+|
+|
+|<font size="2" style="color:#black;">'''Figure 6'''
+|
+|
+|
+|
+|<font size="2" style="color:#black;">'''Figure 7'''
+|
+|
+|
+|
+|}
+{|style="background-color:#ffefd5; width:100%" <font size="2">
+|
+|
+|
+|
+|<font size="2" style="color:#black;">Nonlinear least-squares estimation of WT LH2 saturation curve
+|
+|
+|
+|
+|<font size="2" style="color:#black;">Simulated Optical Density of Mutant and Wild Type Bioreactors<br>Layers One and Two Layers Three, Four and Five
+|
+|
+|
+|
+|}
+[[Image: saturation for WT as inferred.png| 450px | left]][[Image: OD after 3,4, and 5.jpg| 215px |right]][[Image: OD after flask 1 and 2.jpg| 215px | center]]
+{|style="background-color:#ffefd5; width:100%" <font size="2">
+|
+|
+|
+|
+|<font size="2" style="color:#black;">Figure 6 derived from absolute irradiance data from WT tissue flask experiment
+|
+|
+|
+|
+|<font size="2" style="color:#black;">Figure 7 shows the results of modeling the WT vs. mutant regulation system
+|
+|
+|
+|
+|}
+<br>
+<div style="text-align: left;">
+[https://2009.igem.org/Team:Wash_U/Project Back To Top]
-<br>[https://2009.igem.org/Team:Wash_U/Project Back To Top]
 <font size="4">
@@ Line 89: / Line 334: @@
 == '''Analysis''' ==
 <font size="2">
-The tissue flask experiment was an interesting way to observe the effects of a full knockout of the Light Harvesting Antenna Complex 2 (LH2) vs the Wild Type on an array of conseuctive photobioreactors.  A couple of conclusions can be drawn from this data that can be used in modeling our synthetic regulation system for LH2 and in the future design of systems for the optimization of Light Harvesting Antenna size for photobioreactors .  <br><br>
-The most striking difference between the Wild Type Rhodobacter Sphaeroides 2.41 and DBCOmega (LH2 knockout) growth patterns is that the first flask in the WT (closest to the light source) grew less than the second flask, while the converse was true in DBCOmega (figure 2a and 2b).  This can be attributed to the photosystem saturation curves for the respective cultures.  The Wild Type has an LH2 complex, meaning that their antenna size is inherently larger and that their photosystem will be saturated at lower light intensities than the LH2 deficient mutant.  We observed that the incident light intensity used in this experiment led to oversaturation for the first WT tissue flask and resulted in growth-inhibiting photodamage, as is evidenced by its lesser growth relative to the second culture.  In contrast, photodamage was not observed in DBCOmega as is evidenced by the first tissue flask that grew at the fastest respective rate.  Furthermore, it appears that this photodamage slowed the growth of the first WT tissue flask to the point that the OD of this tissue flask was nearly equal to that of DBCOmega after 5 days of growth(.987 vs. .967) (figure 1a).  As such, the contribution of LH2 to the growth of the WT in flask 1 can be assessed to be little after day 3 when the growth curve slows- though, this light (at 800 and 850 nm) was still greatly absorbed by flask 1 ('''see irradiance figure for wt flask 1 day 6''').  It is likely that much of this light was wasted through Non-Photochemical Quenching (NPQ), thereby depleting the flasks behind flask 1 of photons at the LH2 absorbtion peaks and decreasing the cumulative productivity of flasks 1-5. This effect of wasting photons though NPQ under high light intensities is one that we sought to minimize in the design of our synthetic regulation for the pucB/A genes.   <br><br>
-'''Thomas- add stuff here about the second flasks and approaching 20% contribution of LH1 to growth'''
+Though we were not able to have our mutant functionally express our system, the tissue flask experiment was an interesting way to observe the effects of a full knockout of the Light Harvesting Antenna Complex 2 (LH2) vs the Wild Type on an array of consecutive photobioreactors.  A couple of conclusions can be drawn from this data that can be used in modeling our synthetic regulation system for LH2 and in the future design of systems for the optimization of Light Harvesting Antenna size for photobioreactors .  <br><br>
+The most striking difference between the Wild Type Rhodobacter Sphaeroides 2.41 and DBCOmega (LH2 knockout) growth patterns is that the first flask in the WT (closest to the light source) grew less than the second flask, while the converse was true in DBCOmega (figure 2a and 2b).  This can be attributed to the photosystem saturation curves for the respective cultures.  The Wild Type has an LH2 complex, meaning that their antenna size is inherently larger and that their photosystem will be saturated at lower light intensities than the LH2 deficient mutant.  We observed that the incident light intensity used in this experiment led to oversaturation for the first WT tissue flask and resulted in growth-inhibiting photodamage, as is evidenced by its lesser growth relative to the second culture.  In contrast, photodamage was not observed in DBCOmega as is evidenced by the first tissue flask that grew at the fastest respective rate.  Furthermore, it appears that this photodamage slowed the growth of the first WT tissue flask to the point that the OD of this tissue flask was nearly equal to that of DBCOmega after 5 days of growth(.987 vs. .967) (figure 1a).  As such, the contribution of LH2 to the growth of the WT in flask 1 can be assessed to be little after day 3 when the growth curve slows- though, this light (at 800 and 850 nm) was still greatly absorbed by flask 1 (Figure 5e).  It is likely that much of this light was then wasted through Non-Photochemical Quenching (NPQ), depleting the flasks behind flask 1 of photons at the LH2 absorbtion peaks and decreasing the cumulative productivity of flasks 1-5. This effect of wasting photons though NPQ under high light intensities is one that we sought to minimize in the design of our synthetic regulation for the pucB/A genes.   <br><br>
+A further a comparison of the WT and DBCOmega experiments reveals that the 3rd tissue flask in each had almost identical growth rates (figure 1c), while the DBCOmega 4th and 5th tissue flask outperformed that of the WT (figure 1d and 1e).  This can simply be attributed to the higher density of cells in the  2nd flask of the WT that led to an overall lesser quantity of photons passing through to the 4th and 5th flasks in the WT experiment and likely resulting in heterotrophic growth (though this will need to be confirmed with a "dark control" experiment that should be completed in time for the Jamboree).   This decrease in available photons for the WT can be seen by viewing the absolute irradiance data (incident light intensity at a given wavelength) after the third culture for the WT (figure 5a and 5c).   This decrease in irradiance is the most pronounced for the LH2 absorption bands at 800 and 850 nm, as was expected.  Our synthetic regulation system for pucB/A was designed with the intention of allowing greater penetration of light through the first couple of flasks at the LH2 wavelengths, as expression of pucB/A is inversely correlated to incident light intensity.<br><br>
-A further a comparison of the WT and DBCOmega experiments reveals that the 3rd tissue flask in each had almost identical growth rates (figure 1c), while the DBCOmega 4th and 5th tissue flask outperformed that of the WT (figure 1d and 1e).  This can simply be attributed to the higher density of cells in the  2nd flask of the WT that led to an overall lesser quantity of photons passing through to the 4th and 5th flasks in the WT experiment and likely resulting in heterotrophic growth (though this will need to be confirmed with a "dark control" experiment that should be completed in time for the Jamboree).   This decrease in available photons for the WT can be seen by viewing the absolute irradiance data (incident light intensity at a given wavelength) after the third culture for the WT '''(after flask 2 WT Irradiance day 3)'''.   This decrease in irradiance is the most pronounced for the LH2 absorption bands at 800 and 850 nm, as was expected.  Our synthetic regulation system for pucB/A was designed with the intention of allowing greater penetration of light through the first couple of flasks at the LH2 wavelengths, as expression of pucB/A is inversely correlated to incident light intensity.<br><br>
-'''Thomas, add in some further comments about the sprectroradiometer stuff.  Specifically about how it changes in the WT vs. that of DBCOmega using some specific examples on the graphs'''<br><br>
 Overall, the cumulative culture growth of the WT exceeded that of DBCOmega (figure 3) due to the performance of the second tissue flask of the WT relative to that of DBCOmega (figure 1b) despite the photodamage that occurred in tissue flask 1 for the WT.  This cumulative culture growth can be considered photosynthetic productivty and is proportional to the amount of energy/desired product that can be obtained from these cultures.  <br><br>
-'''It is an interesting exercise to model how our mutant system would perform under these same conditions: Thomas add in some comments about referencing that diagram and what we took from this tissue flask experiment to construct that (and upload it when you are done with it).'''
-<br><br>
+It is an interesting exercise to model how our mutant system would perform under these same conditions.  To do so, the LH2 saturation curve for the WT (figure 6) and the relative contribution of LH1/LH2 light absorbance to growth was derived from our empirical data and applied to a model that took into account incident light and gave the relative growth in terms of optical density as an output.  In this model, our synthetic regulation system of pucB/A allowed our mutant to outperform the wild type species (figure 7).  This was  due to the performance of the 3rd, 4th, and 5th tissue flask relative to those of the wild type (see figure 7 layers 1,2 vs 1-5).  The reason for this is that the wild type LH2 light saturation curve does not vary with changes in incident light intensity as the wild type expresses pucB/A at a uniform level under low oxygen conditions.  As a result, the first two layers of Wild Type bioreactors absorb nearly all the available light and starve the bioreactors behind them for photons.  <br><br>
+Conversely, our mutant was modeled to have a dynamic expression of pucB/A based on the incident light intensity. This light response curve was modeled as an inverse exponential for the Cph8/OmpR ompC Promoter system and the saturation curve changes for each tissue flask in accordance with the incident light intensity- as light intensity decreases, the expression pucB/A increases.  This results in more light passing through the first 2 flasks and facilitating greater growth in flasks 3, 4 and 5 as they express large antenna complexes.  Nonetheless, we believe that growth across the bioreactors could be further maximized by increasing antenna size in the first 2 bioreactors and sacrificing growth in the 4th and 5th.  This could be achieved with a feedback mechanism that sets a minimum level for LH2 expression.
-<br><br><font size="2">
+<br><br>
-=='''Conclusion and Future Work'''==
-Based on model, should have had feedback mechanism- should be something that sets a minimum expression level for LH2, that is...<br>
--tissue flask w prkcbc3 before jamboree and compare/interpret using characterization data<br>
+<font size="2">
--tissue flask w. full mutant in future- if this doesn't reveal cph8 to responding in an exponentially decaying fashion to light intensity, try w. a system that would
--characterize puc promoter under light conditions and additional oxygen tensions
--complete other characterization work
+<font size="4">
+='''Conclusion'''=
 <font size="2">
-* What we tried to do?
-# What actually happened?
+Though we were not able to conduct the tissue flask growth experiment on our mutant, the results of this experiment on our controls (WT and DBComega) match the assumptions that we had laid out at the beginning of the project, allowed us to draw further conclusions about the efficiency of light-based growth for a series of bioreactors, and to create a model for our mutant based on empirical data. <br>
-* Ways to improve, redo parts of our experiment differently
-* What further should be done to our end product to further its development, related back to what we initially tried to do?
+*Based on this model, we have concluded that it would be favorable to have a feedback regulation mechanism that sets a minimum expression level for pucB/A to further improve photosynthetic productivity.  <br>
-* What are possible biofuel applications and how could our system be used to improve existing biofuels?
-<br>[https://2009.igem.org/Team:Wash_U/Project Back To Top]
+*We intend to conduct the tissue flask w DBComega+prkcbc3 before jamboree and compare/interpret these results using our characterization data for the pucB/A and the puc promoter.
+*We will conduct the tissue flask experiment with our functioning mutant in future and compare the results to our model
+*Finally, we would like to characterize the puc promoter under various light conditions and additional oxygen tensions.   <br>
+'''Overall- our project has demonstrated the potential for a synthetically regulated light harvesting antenna to improve photosynthetic productivity for a series of photobioreactors vs. the wild type.'''
+[https://2009.igem.org/Team:Wash_U/Project Back To Top]
 <font size="4">

Team:Wash U/Project

From 2009.igem.org

Latest revision as of 00:48, 10 November 2009

Introduction

Organism

Online Resources for R. sphaeroides

Regulation

Results

Analysis

Conclusion

References