Team:SJTU-BioX-Shanghai/Project/project2.1

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(Violacein Biosynthetic Pathway)
(Membrane Rudder Sensing Light Signal)
 
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==Biosynthesis - Violacein==
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=Membrane Rudder <br><br> - Violacein & Deoxyviolacein Synthetic Pathway=
 +
{{Template:12SJTU_part_summary_head}}
 +
 
 +
*'''State of the art'''
 +
Dynamically and artificially regulating the direction of biochemical pathway ''in vivo'' has remained a challenge for scientists. We are now to achieve this goal through controlling the aggregation state of different enzymes in branched biological reactions based on Membrane Scaffold. We named this universal device ''Membrane Rudder''.
 +
 +
Violacein is a purple chromobacterial pigment synthesized from the basic amino acid tryptophan. Its biosynthetic pathway contains 3 branches and produces 3 final products, which are violacein, deoxyviolacein and deoxychromoviridans respectively. Thus it is incorporated to test the feasibility of ''Membrane Rudder''
 +
 
 +
 
 +
*'''Aims'''
 +
To switch the direction of Violacein and deoxyviolacein synthetic pathway through light signal
 +
 
 +
To switch the direction of Violacein and deoxyviolacein synthetic pathway through RNA signal
 +
 
 +
To justify the universality of ''Membrane Rudder''
 +
 
-
*'''State of the art'''
 
-
Violacein is a purple chromobacterial pigment produced from tryptophan. In its biosynthetic pathway there are 3 possible branches and 2 side products. The five key enzymes of ''Chromobacterium violaceum'' could be expressed in ''E.Coli'' and corresponding parts are available in the Registry. The Cambridge  2009 iGEM team had succesfully achieved the production of violacein.
 
-
*'''Aim'''
 
-
Our membrane rudder calls for a branched reaction to test its efficiency. We wanted to examine the advantages of membrane system in adjusting quantity of different products.
 
*'''Achievements'''
*'''Achievements'''
-
We modified the five vio parts and inserted them in the membrane assembly, producing a plasmid with violacein biosynthetic enzyme, light-inducing protein as well as a membrane protein. Analysis of bacteria extracts showed a satisfying decrease in side products between light-induced samples and the control group. These results demonstrate a rather promising way of using membrane rudder to switch the direction of reaction.
 
-
------------------------------------------------------------------------
+
''Direction switched'' successfully in Violacein synthetic pathway by light signal
-
===Background===
+
''8-fold yields decrease'' of side product deoxychromaviridans with ''Membrane Rudder'' compared to group with free cytoplasmic enzyme
-
Violacein is a pigment produced by several bacteria through pathway of 5 related genes, ''vioA'', ''vioB'', ''vioC'', ''vioD'' and ''vioE''. It was initially discovered in ''Chromobacterium violaceum''.  This metabolite of tryptophan has such special applications as antibacterial, anti-trypanocidal, anti-ulcerogenic, and anticancer drugs.
+
''A novel device constructed'' that connects post-translational Membrane Scaffold system to genetic circuits by recruiting RNA as a controlling signal.
 +
{{Template:12SJTU_part_summary_foot}}
-
There are two interesting branches in this pathway which could be utilized in service of verification of the ''membrane rudder''. We can identify the different end-products by means of separation, such as thin-layer chromatography (TLC), or high-performance liquid chromatography (HPLC). The product proportion change demonstrates the efficiency of alteration in reaction direction.
 
-
===Violacein Biosynthetic Pathway===
+
==Background==
-
[[Image:12SJTU_VioPathway.png|thumb|250px|right|''Fig.1'' :The violacein biosynthetic pathway. The purple line indicates the biosynthetic flux of pigment deoxyviolacein and violet. The green line indicates the the biosynthetic flux of pigment deoxychromoviridans.]]
+
-
The violacein biosynthetic pathway includes 5 key enzymes which work in conjunction. VioA, a flavoenzyme and VioB, a heme protein, they work together to oxidize and dimerize tryptophen into IPA imine dimer. Then vioE induces a indole rearrangement,producing prodeoxyviolacein, also known as PVA.
+
Dynamically and artificially regulating the direction of biochemical pathway ''in vivo'' has remained a challenge for scientists. Based on Membrane Scaffold, we are now trying to achieve this goal through controlling the aggregation state of different enzymes in branched biological reactions. We named this universal device ''Membrane Rudder''. Theoretically this device could sense a large amount of signals. We chose blue light and rationally designed RNA molecule D0 as controlling signal. Branched violacein & deoxyviolacein synthetic pathway is recruited to verify the feasibility of ''Membrane Rudder''.
-
One key prerequisite in the metabolic flux is that: Automatically VioA, VioB and VioE can assemble and function to produce PVA. There exists one intrinsic E.coli enzyme that aids in an additional side reaction, further modifying PVA into a green pigment called deoxychromoviridans.  
+
There are three branches in violacein & deoxyviolacein synthetic pathway. We could identify amount of final products through high-performance liquid chromatography (HPLC). The change of products proportion will demonstrate the efficiency of direction alteration.
-
The last two proteins, VioC and VioD are flavin-dependent oxygenases. VioC alone transfers PVA into a purple pigment named deoxyviolacein, while vio C could also act sequentially with vioD.
 
-
vioD hydroxylates 5-position indole ring, then the other 2-position indole ring is processed by VioC to create the oxindole thus producing violacein, a violet pigment most well-studied.
 
-
===Design of Membrane Complex===
+
===Violacein & Deoxyviolacein Biosynthetic Pathway===
-
We chose violacein mainly because of the branching feature of its pathway. As demonstrated in the picture,vioA  was linked to membrane assembly 1, vio E was linked to membrane assembly 3, while vioC and vioD were linked to VIVID, the light-inducing-dimerizable protein. Then we inserted M1-vioA and VVD-vioC into pETduet, VVD-vioD and M3-vioE into pACYCduet. Since vioB and vioE normally function in dimer state, pRSFduet with rbs-vioB and rbs-vioE was also transformed into the bacterium, then all five functional enzymes could be expressed now.
+
-
//膜蛋白图片
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::[[Image:Figure1-SJTU violacein-pathway.png|thumb|600px|center|''Fig.1:'' :Details of violacein & deoxyviolacein biosynthetic pathway. The left pathway painted in purple indicates the synthetic pathway of purple pigment deoxyviolacein.The right pathway painted in violet indicates the synthetic pathway of purple pigment violacein. The green pathway indicates the nonenzymatic production of green pigment deoxychromoviridans.]]
-
As long as VVD is photo-induced and dimerized, they could act like magnets that pull vioC and vioD together, and thus make it easier for intermediate to undergo catalyzation of vioC and vioD.And in this case violacein should be the dominant product we expect.
+
-
===Results and Discussion===
+
The violacein & deoxyviolacein biosynthetic pathway includes 5 key enzymes which work in sequence: Vio A, B, C, D and E. VioA, a flavoenzyme and VioB, a heme protein, work together to oxidize and dimerize tryptophen into IPA imine dimer. Then VioE induces an indole rearrangement, producing prodeoxyviolacein acid, also known as PVA. In a word, enzyme VioA, VioB and VioE convert tryptophen into PVA. Then this biosynthetic pathway is about to branch.
-
Plasmids as designed has been successfully constructed and transformed into ''E. coli''. To ensure the efficiency of membrane switch, the bacteria culture was under bluelight during induction period. After 5h, there appeared to be visible pigments particles in the liquid. We further analyzed the extracts using more sensitive methods, e.g. High-performance liquid chromatography (HPLC) (for a detailed description of the protocols see the page "Protocal").  
+
-
'''图hplc进样图'''
+
In ''E.coli'', an additional side reaction could occur, and PVA is converted into a green pigment called deoxychromoviridans.
-
Results show that violacein is dominant from extracts of bacterial cultures with VIVID. Extracts of bacterial cultures without VIVID, however, contain much more deoxyviolacein than violacein.(Figure 1, compare lane 1 and 2) Moreover, a significant decrease of side products such as deoxychomoviridans was detected, when membrane system was present. (Figure 2, compare lane 1,2 and 3)
+
The last two enzymes, VioC and VioD are flavin-dependent oxygenases. VioC alone transforms PVA into a purple pigment called deoxyviolacein. VioC could also act cooperatively with VioD. VioD hydroxylates 5-position indole ring, and then the other 2-position indole ring is processed by VioC to create the oxindole. In this way, violacein is produced.
 +
==Design of Experiment==
-
[[Image:12SJTU_violacein products.jpg|thumb|300px|violacein biosynthetic pathway products]]
+
We tried to create ''Membrane Rudder'' controlled by light signal and RNA signal to switch direction of biochemical reaction dynamically and artificially in ''E.coli''.
-
These results fully confirm the idea of membrane protein assembly and the great role it plays in the switch of reaction. In addition to the anticipated realization of reaction switch, we were satisfied to observe significant suppression of the side products (deoxychromoviridans), which was primarily due to fact that PVA was instantly transferred to deoxyviolacein or violacein by adjacent Vio D and Vio C.
+
===Membrane Rudder Sensing Light Signal===
 +
Light is an intriguing signal to regulate E.coli activity because it is easy to obtain, highly tunable and nontoxic. A metabolite-coupled light-switchable system could be quite fascinating.
-
Although the theoretical production of violacein biosynthetic pathway composed of only three pigments, the separation result of HPLC depends on many different factors, including the purity of extraction, stationery phase type, the detector wavelength, etc. However, we did not have time to perform any optimizations with respect to extraction protocol, HPLC conditions etc., therefore the final result of HPLC could be much more legible with less interference of noise peak.   Despite that the experiment was repeated more than three times with similar results.
+
We constructed our device as demonstrated in ''Fig.2''. In light-sensing ''Membrane Rudder'', VioA, VioB, VioE and VioC with interacting Membrane Anchors constitutively aggregate. [https://2012.igem.org/Team:SJTU-BioX-Shanghai/Project/project1.2 VVD], a photoreceptor of ''Neurospora crassa'', can form dimer in the presence of blue light and disassociate as light is off. When blue light is present, VioD with VVD-coupled Membrane Anchor would aggregate with assembly of VioA, B, C and E, making violacein the dominant final product. But when blue light is off, VioD with VVD coupled Membrane Anchor will disassociate with VioA, B, C and E. Thus the biosynthetic pathway for deoxyviolacein is switched on.
-
===Reference===
+
[[File:12SJTU_VVD_Construction.png|center|500px|thumb|''Fig.2'' :Construction details of light-sensing ''Membrane Rudder''. VVD acts as a blue light sensor.]]
 +
 
 +
For VioB and VioE only function normally in dimeric state, free VioB and free VioE were coexpressed with membrane anchored VioA, B, C, D and E (''Fig.2'')to ensure the normal function of the whole system.
 +
 
 +
Bacteria in experimental group were induced at a L-Arabinose concentration of 0.1%. One group of bacteria expressing full set of light-sensing ''Membrane Rudder'' is incubated under blue light. The other group of bacteria expressing full set of light-sensing ''Membrane Rudder'' are incubated in the dark. In each comparative group, bacteria prepared for light induction and dark incubation are taken from the same sample.
 +
 
 +
The BioBrick Part VVD-MA5-vioC and VVD-MA6-vioD is [http://partsregistry.org/Part:BBa_K771205 Part:BBa_K771205] and [http://partsregistry.org/Part:BBa_K771206 Part:BBa_K771206], respectively. For MA2-VioA, MA3-VioB, MA4-VioE, the corresponding part is [http://partsregistry.org/Part:BBa_K771201 Part:BBa_K771201], [http://partsregistry.org/Part:BBa_K771202 Part:BBa_K771202], [http://partsregistry.org/Part:BBa_K771203 Part:BBa_K771203], respectively.
 +
 
 +
===Membrane Rudder Sensing RNA Signal===
 +
 
 +
Membrane Accelerator and Membrane Rudder are both post-translational controlling device to regulate metabolic flux of the host cell. To connect this relatively isolated post-translational control system to genetic circuits, we employed RNA signal, which is present in cytoplasm. Rationally designed RNA D0 with MS2 and PP7 aptamer domain is recruited. When RNA molecule with this two aptamer domains is present in cells, their cognate aptamer binding proteins can thus aggregate together. Furthermore, if we place RNA D0 (with PP7 and MS2 aptamer domains) under various promoters regulated by different signals, approaches to induce dimerization would be expanded sharply. Thus, Membrane Rudder could sense much more signals.
 +
 
 +
We constructed our device as demonstrated in ''Fig.3''. In RNA-sensing ''Membrane Rudder'', VioA, VioB, VioE and VioC with interacting Membrane Anchors constitutively aggregate. [https://2012.igem.org/Team:SJTU-BioX-Shanghai/Project/project1.2 RNA D0], can aggregate with RNA aptamer binding protein MS2 and PP7. So when RNA D0 is present, VioD with MS2-coupled Membrane Anchor would aggregate with assembly of VioA, B, C and E, making violacein the dominant final product. But when RNA D0 is absent, VioD with MS2-coupled Membrane Anchor will disassociate with VioA, B, C and E. Thus the biosynthetic pathway for deoxyviolacein is switched on.
 +
 
 +
[[File:12SJTU_RNA_construction.png|center|500px|thumb|''Fig.3'' :Construction details of RNA-sensing ''Membrane Rudder''. RNA aptamer binding protein MS2 and PP7 act as an RNA signal sensors.]]
 +
 
 +
Free VioB and free VioE were coexpressed with membrane anchored VioA, B, C, D and E to ensure the normal function of the whole system.
 +
 
 +
Bacteria in experimental group were induced at a L-Arabinose concentration of 0.1%. One group of bacteria expressing full set of RNA-sensing ''Membrane Rudder'' are incubated under blue light. The other group of bacteria expressing full set of RNA-sensing ''Membrane Rudder'' are incubated in the dark. In each comparative group, bacteria prepared for light induction and dark incubation are taken from the same sample.
 +
 
 +
==Results and Discussion==
 +
===Membrane Rudder Sensing Light Signal===
 +
 
 +
'''Overview'''
 +
 
 +
By attaching Enzymes VioA, B, C, D and E to Membrane Anchors as shown in ''Fig.2'', we managed to change the proportion of final products by switching on or off blue light signal. When blue light is on, VioA, B, C, D and E aggregate together, making violacein the dominant final product. When blue light is off, VioD with Membrane Anchor will disassociate with VioA, B, C and E. Thus the biosynthetic pathway for deoxyviolacein is switched on.
 +
 
 +
Moreover, a significant decrease of side products such as deoxychomoviridans was observed when ''Membrane Rudder'' system was present.
 +
 
 +
 
 +
 
 +
'''Direction Alteration'''
 +
 
 +
Altering direction of violacein & deoxyviolacein synthetic pathway can be realized by dynamically controlling the aggregation state of crucial enzymes. Through the blue light induction, all five enzymes aggregate together. Thus branch pathway producing deoxyviolacein by VioA, B, E and C is inhibited because PVA is more preferably hydroxylated by VioD. On the other hand, as long as blue light is absent from the bacteria, VioD will disassociate with assembling VioA, B, E and C, leading to the production of deoxyviolacein.
 +
 
 +
[[Image:P1000998.JPG|thumb|400px|center|''Fig.4'' :Collections of different peaks in HPLC results, ready to undergo MS for molecule construction verification.]]
 +
 
 +
We ran an HPLC (SHIMADZU LC-20AP, C18 reversed column) test with the purple samples extracted from the bacteria culture. Then we ran mass spectrometry (Thermo Ultra GC-ISQ) test and thus further confirmed the molecular constitution of main peaks in HPLC results.
 +
 
 +
The HPLC results perfectly fit our prediction.
 +
 
 +
[[Image:12SJTU_vio_propotion4.jpg|thumb|700px|center|''Fig.5'' :HPLC result (right) and the ratio(left) of deoxyviolacein in sample group with blue light induction and group without blue light induction. Red column stands for yield of deoxyviolacein; Blue column stands for yield of violacein.  Fig. B shows the HPLC result from sample without blue light induction. Fig. C shows the HPLC result from sample with from sample under blue light induction.The HPLC results show that the peak of deoxyviolacein appears at about 9 minutes after the injection. The peak of deoxyviolacein is identified according to previously published research. Results indicate that the amount of the deoxyviolacein from the sample without blue light induction is tremendously larger than that from light induced sample]]
 +
 
 +
 
 +
Under the induction of blue light, production of deoxyviolacein was inhibited (to almost 0%) while most products were violacein, which is predicted above. Without blue light induction, however, the pathway leading to the production of deoxyviolacein was turned on and thus considerable amount of deoxyviolacein was produced. All results confirmed the feasibility of our light-sensing ''Membrane Rudder''. Besides, it indicated that by replacing signal sensors and functioning enzymes, we could regulate direction of various branched reactions through diversified signals.
 +
<br>
 +
 
 +
'''Decrease in Side Products'''
 +
 
 +
We also found membrane anchored enzymes could help to reduce the amount of side-product(deoxychromaviridans) by 8 fold compared to diffusing cytoplasmic enzymes. This is because rationally designed enzyme assembly facilitate and improve the metabolic flux of biosynthesis. Intermediate PVA is more preferably processed by adjacent membrane anchored VioD or VioC rather than converted into deoxychromaviridans. Actually this is one of the advantages of Membrane Scaffold.
 +
 
 +
[[Image:12SJTU_Virdrans_before_after.jpg|thumb|400px|center|''Fig.5'' :The HPLC peak area of deoxychromoviridans from sample with free VioABCDE(denoted as ''Free'')  and membrane anchored VioABCDE(denoted as Complex). Construction detail of membrane anchored VioABCDE is shown in ''Fig.2''. Bacteria are incubated under light for 6 hours in ''Complex'' group.]]
 +
 
 +
==Reference==
1. Balibar, C. J. and C. T. Walsh (2006). "In vitro biosynthesis of violacein from L-tryptophan by the enzymes VioA-E from Chromobacterium violaceum." Biochemistry 45(51): 15444-57.
1. Balibar, C. J. and C. T. Walsh (2006). "In vitro biosynthesis of violacein from L-tryptophan by the enzymes VioA-E from Chromobacterium violaceum." Biochemistry 45(51): 15444-57.
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3. Shrode, L. B., Z. A. Lewis, et al. (2001). "vvd is required for light adaptation of conidiation-specific genes of Neurospora crassa, but not circadian conidiation." Fungal Genet Biol 32(3): 169-81.
3. Shrode, L. B., Z. A. Lewis, et al. (2001). "vvd is required for light adaptation of conidiation-specific genes of Neurospora crassa, but not circadian conidiation." Fungal Genet Biol 32(3): 169-81.
 +
 +
 +
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{{Template:12SJTU_footer}}
{{Template:12SJTU_footer}}

Latest revision as of 03:55, 27 October 2012

Membrane Rudder

- Violacein & Deoxyviolacein Synthetic Pathway

  • State of the art

Dynamically and artificially regulating the direction of biochemical pathway in vivo has remained a challenge for scientists. We are now to achieve this goal through controlling the aggregation state of different enzymes in branched biological reactions based on Membrane Scaffold. We named this universal device Membrane Rudder.

Violacein is a purple chromobacterial pigment synthesized from the basic amino acid tryptophan. Its biosynthetic pathway contains 3 branches and produces 3 final products, which are violacein, deoxyviolacein and deoxychromoviridans respectively. Thus it is incorporated to test the feasibility of Membrane Rudder


  • Aims

To switch the direction of Violacein and deoxyviolacein synthetic pathway through light signal

To switch the direction of Violacein and deoxyviolacein synthetic pathway through RNA signal

To justify the universality of Membrane Rudder


  • Achievements

Direction switched successfully in Violacein synthetic pathway by light signal

8-fold yields decrease of side product deoxychromaviridans with Membrane Rudder compared to group with free cytoplasmic enzyme

A novel device constructed that connects post-translational Membrane Scaffold system to genetic circuits by recruiting RNA as a controlling signal.


Background

Dynamically and artificially regulating the direction of biochemical pathway in vivo has remained a challenge for scientists. Based on Membrane Scaffold, we are now trying to achieve this goal through controlling the aggregation state of different enzymes in branched biological reactions. We named this universal device Membrane Rudder. Theoretically this device could sense a large amount of signals. We chose blue light and rationally designed RNA molecule D0 as controlling signal. Branched violacein & deoxyviolacein synthetic pathway is recruited to verify the feasibility of Membrane Rudder.

There are three branches in violacein & deoxyviolacein synthetic pathway. We could identify amount of final products through high-performance liquid chromatography (HPLC). The change of products proportion will demonstrate the efficiency of direction alteration.


Violacein & Deoxyviolacein Biosynthetic Pathway

Fig.1: :Details of violacein & deoxyviolacein biosynthetic pathway. The left pathway painted in purple indicates the synthetic pathway of purple pigment deoxyviolacein.The right pathway painted in violet indicates the synthetic pathway of purple pigment violacein. The green pathway indicates the nonenzymatic production of green pigment deoxychromoviridans.

The violacein & deoxyviolacein biosynthetic pathway includes 5 key enzymes which work in sequence: Vio A, B, C, D and E. VioA, a flavoenzyme and VioB, a heme protein, work together to oxidize and dimerize tryptophen into IPA imine dimer. Then VioE induces an indole rearrangement, producing prodeoxyviolacein acid, also known as PVA. In a word, enzyme VioA, VioB and VioE convert tryptophen into PVA. Then this biosynthetic pathway is about to branch.

In E.coli, an additional side reaction could occur, and PVA is converted into a green pigment called deoxychromoviridans.

The last two enzymes, VioC and VioD are flavin-dependent oxygenases. VioC alone transforms PVA into a purple pigment called deoxyviolacein. VioC could also act cooperatively with VioD. VioD hydroxylates 5-position indole ring, and then the other 2-position indole ring is processed by VioC to create the oxindole. In this way, violacein is produced.

Design of Experiment

We tried to create Membrane Rudder controlled by light signal and RNA signal to switch direction of biochemical reaction dynamically and artificially in E.coli.

Membrane Rudder Sensing Light Signal

Light is an intriguing signal to regulate E.coli activity because it is easy to obtain, highly tunable and nontoxic. A metabolite-coupled light-switchable system could be quite fascinating.

We constructed our device as demonstrated in Fig.2. In light-sensing Membrane Rudder, VioA, VioB, VioE and VioC with interacting Membrane Anchors constitutively aggregate. VVD, a photoreceptor of Neurospora crassa, can form dimer in the presence of blue light and disassociate as light is off. When blue light is present, VioD with VVD-coupled Membrane Anchor would aggregate with assembly of VioA, B, C and E, making violacein the dominant final product. But when blue light is off, VioD with VVD coupled Membrane Anchor will disassociate with VioA, B, C and E. Thus the biosynthetic pathway for deoxyviolacein is switched on.

Fig.2 :Construction details of light-sensing Membrane Rudder. VVD acts as a blue light sensor.

For VioB and VioE only function normally in dimeric state, free VioB and free VioE were coexpressed with membrane anchored VioA, B, C, D and E (Fig.2)to ensure the normal function of the whole system.

Bacteria in experimental group were induced at a L-Arabinose concentration of 0.1%. One group of bacteria expressing full set of light-sensing Membrane Rudder is incubated under blue light. The other group of bacteria expressing full set of light-sensing Membrane Rudder are incubated in the dark. In each comparative group, bacteria prepared for light induction and dark incubation are taken from the same sample.

The BioBrick Part VVD-MA5-vioC and VVD-MA6-vioD is [http://partsregistry.org/Part:BBa_K771205 Part:BBa_K771205] and [http://partsregistry.org/Part:BBa_K771206 Part:BBa_K771206], respectively. For MA2-VioA, MA3-VioB, MA4-VioE, the corresponding part is [http://partsregistry.org/Part:BBa_K771201 Part:BBa_K771201], [http://partsregistry.org/Part:BBa_K771202 Part:BBa_K771202], [http://partsregistry.org/Part:BBa_K771203 Part:BBa_K771203], respectively.

Membrane Rudder Sensing RNA Signal

Membrane Accelerator and Membrane Rudder are both post-translational controlling device to regulate metabolic flux of the host cell. To connect this relatively isolated post-translational control system to genetic circuits, we employed RNA signal, which is present in cytoplasm. Rationally designed RNA D0 with MS2 and PP7 aptamer domain is recruited. When RNA molecule with this two aptamer domains is present in cells, their cognate aptamer binding proteins can thus aggregate together. Furthermore, if we place RNA D0 (with PP7 and MS2 aptamer domains) under various promoters regulated by different signals, approaches to induce dimerization would be expanded sharply. Thus, Membrane Rudder could sense much more signals.

We constructed our device as demonstrated in Fig.3. In RNA-sensing Membrane Rudder, VioA, VioB, VioE and VioC with interacting Membrane Anchors constitutively aggregate. RNA D0, can aggregate with RNA aptamer binding protein MS2 and PP7. So when RNA D0 is present, VioD with MS2-coupled Membrane Anchor would aggregate with assembly of VioA, B, C and E, making violacein the dominant final product. But when RNA D0 is absent, VioD with MS2-coupled Membrane Anchor will disassociate with VioA, B, C and E. Thus the biosynthetic pathway for deoxyviolacein is switched on.

Fig.3 :Construction details of RNA-sensing Membrane Rudder. RNA aptamer binding protein MS2 and PP7 act as an RNA signal sensors.

Free VioB and free VioE were coexpressed with membrane anchored VioA, B, C, D and E to ensure the normal function of the whole system.

Bacteria in experimental group were induced at a L-Arabinose concentration of 0.1%. One group of bacteria expressing full set of RNA-sensing Membrane Rudder are incubated under blue light. The other group of bacteria expressing full set of RNA-sensing Membrane Rudder are incubated in the dark. In each comparative group, bacteria prepared for light induction and dark incubation are taken from the same sample.

Results and Discussion

Membrane Rudder Sensing Light Signal

Overview

By attaching Enzymes VioA, B, C, D and E to Membrane Anchors as shown in Fig.2, we managed to change the proportion of final products by switching on or off blue light signal. When blue light is on, VioA, B, C, D and E aggregate together, making violacein the dominant final product. When blue light is off, VioD with Membrane Anchor will disassociate with VioA, B, C and E. Thus the biosynthetic pathway for deoxyviolacein is switched on.

Moreover, a significant decrease of side products such as deoxychomoviridans was observed when Membrane Rudder system was present.


Direction Alteration

Altering direction of violacein & deoxyviolacein synthetic pathway can be realized by dynamically controlling the aggregation state of crucial enzymes. Through the blue light induction, all five enzymes aggregate together. Thus branch pathway producing deoxyviolacein by VioA, B, E and C is inhibited because PVA is more preferably hydroxylated by VioD. On the other hand, as long as blue light is absent from the bacteria, VioD will disassociate with assembling VioA, B, E and C, leading to the production of deoxyviolacein.

Fig.4 :Collections of different peaks in HPLC results, ready to undergo MS for molecule construction verification.

We ran an HPLC (SHIMADZU LC-20AP, C18 reversed column) test with the purple samples extracted from the bacteria culture. Then we ran mass spectrometry (Thermo Ultra GC-ISQ) test and thus further confirmed the molecular constitution of main peaks in HPLC results.

The HPLC results perfectly fit our prediction.

Fig.5 :HPLC result (right) and the ratio(left) of deoxyviolacein in sample group with blue light induction and group without blue light induction. Red column stands for yield of deoxyviolacein; Blue column stands for yield of violacein. Fig. B shows the HPLC result from sample without blue light induction. Fig. C shows the HPLC result from sample with from sample under blue light induction.The HPLC results show that the peak of deoxyviolacein appears at about 9 minutes after the injection. The peak of deoxyviolacein is identified according to previously published research. Results indicate that the amount of the deoxyviolacein from the sample without blue light induction is tremendously larger than that from light induced sample


Under the induction of blue light, production of deoxyviolacein was inhibited (to almost 0%) while most products were violacein, which is predicted above. Without blue light induction, however, the pathway leading to the production of deoxyviolacein was turned on and thus considerable amount of deoxyviolacein was produced. All results confirmed the feasibility of our light-sensing Membrane Rudder. Besides, it indicated that by replacing signal sensors and functioning enzymes, we could regulate direction of various branched reactions through diversified signals.

Decrease in Side Products

We also found membrane anchored enzymes could help to reduce the amount of side-product(deoxychromaviridans) by 8 fold compared to diffusing cytoplasmic enzymes. This is because rationally designed enzyme assembly facilitate and improve the metabolic flux of biosynthesis. Intermediate PVA is more preferably processed by adjacent membrane anchored VioD or VioC rather than converted into deoxychromaviridans. Actually this is one of the advantages of Membrane Scaffold.

Fig.5 :The HPLC peak area of deoxychromoviridans from sample with free VioABCDE(denoted as Free) and membrane anchored VioABCDE(denoted as Complex). Construction detail of membrane anchored VioABCDE is shown in Fig.2. Bacteria are incubated under light for 6 hours in Complex group.

Reference

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