Difference between revisions of "Part:BBa K3994011"
 
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<partinfo>BBa_K3994011 short</partinfo>
 
<partinfo>BBa_K3994011 short</partinfo>
  
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promoter
 
  
 
=== Profile ===
 
=== Profile ===
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HrpS is a key functional factor under PttB344 promoter. amilGFP is a fluorescent protein under PhrpL promoter. IL10 is an anti-inflammatory factor.
 
HrpS is a key functional factor under PttB344 promoter. amilGFP is a fluorescent protein under PhrpL promoter. IL10 is an anti-inflammatory factor.
  
−
[[File:T--Shanghai Metro Utd--BBa K4005001-figure2a.png|500px|thumb|center|Figure 1. Boolean gate logic circuit/AND circuit construction...]]
+
[[File:T--NOFLS YZ--BBa K3994011-Figure1.png|500px|thumb|center|Figure 1. Boolean gate logic circuit/AND circuit construction...]]
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 Part3: PhrpL_amilGFP_IL10_PJ23104_ttrS, will release fluorescence if sensing both the substances, R and S released from Part 1(HrpR) and Part 2 (HrpS) , respectively.
 
 Part3: PhrpL_amilGFP_IL10_PJ23104_ttrS, will release fluorescence if sensing both the substances, R and S released from Part 1(HrpR) and Part 2 (HrpS) , respectively.
  
 +
 +
[[File:T--NOFLS YZ--BBa K3994011-Figure2.png|500px|thumb|center|Figure 2. A. PyeaR_HrpR, sensing NO3- to release the substance R; B. PttB344_HrpS_PJ23105_ttrR, sensing S4O62- to release the substance S; C.  PhrpL_amilGFP_IL10_PJ23104_ttrS...]]
 +
 +
 +
The profiles of every basic part are as follows:
 +
 +
=== BBa_K3994003 ===
 +
 +
==== Name: HrpS ====
 +
==== Base Pairs: 912bp ====
 +
==== Origin: Pseudomonas syringae, genome ====
 +
==== Properties: A coding sequence of HrpS protein ====
 +
 +
=== Usage and Biology ===
 +
 +
This codes for HrpS protein. HrpR protein binds to HrpS protein forming a complex and then triggering the transcription of promoter hrpL. This functions like a AND logic gate.
 +
 +
=== BBa_K3994012 ===
 +
 +
==== Name: PttB344 ====
 +
==== Base Pairs: 85bp ====
 +
==== Origin: Synthetic ====
 +
==== Properties: A coding sequence of promoter ttB344. ====
 +
 +
=== Usage and Biology ===
 +
 +
This is a sequence of PttB344. PttrB185-269 is a minimal TtrR activated promoter when TtrR is phosphorylated by TtrS after TtrS sensing tetrathionate.
 +
 +
=== BBa_K3994005 ===
 +
 +
==== Name: PhrpL ====
 +
==== Base Pairs: 190bp ====
 +
==== Origin: Synthetic ====
 +
==== Properties: A coding sequence of promoter hrpL. ====
 +
 +
=== Usage and Biology ===
 +
 +
It is the sequence of inducible promoter PhrpL. HrpR protein binds to HrpS protein forming a complex and then triggering the transcription of induced promoter PhrpL. It functions like a AND logic gate to open a gene circuit. The hrpL promoter (PhrpL) contains a functional UAS relative to the transcription start-site, to which purified HrpR, HrpS and HrpRS bind in electrophoretic mobility shift assays.
 +
 +
 +
=== BBa_K3994006 ===
 +
 +
 +
==== Name: IL10 ====
 +
==== Base Pairs: 864bp ====
 +
==== Origin: Homo sapiens, genome ====
 +
==== Properties: A coding sequence of an immune regulatory cytokine ====
 +
 +
=== Usage and Biology ===
 +
 +
This is a coding sequence of IL10. This is a major immune regulatory cytokine that acts on many cells of the immune system where it has profound anti-inflammatory functions, limiting excessive tissue disruption caused by inflammation.
 +
 +
 +
=== Experimental approach ===
 +
 +
==== Recombinant Plasmid Construction ====
 +
 +
 +
[[File:T--NOFLS YZ--BBa K3994001-Figure1.png|500px|thumb|center|Figure 3. The electrophoresis results of enzyme digestion and PCR...]]
 +
 +
Lane 1 and 2: Plasmid pSU2718-p15A digested by Xba1 and BamH1.
 +
 +
Lane 3: Part 2, PttB344_HrpS_PJ23105_ttrR, got by PCR method with size of 2060bp.
 +
 +
This step is used to get the plasmids pSU2718-p15A digested by enzyme Xba1 and BamH1and gene PttB344_HrpS_PJ23105_ttrR by PCR method for later in the process. Therefore, channel 1 and 2 were plasmids pSU2718-p15A digested by enzyme Xba1 and BamH1. And channel 3 were gene PttB344_HrpS_PJ23105_ttrR got by PCR. Clean-up the product to obtain pSU2718-p15A backbone and PttB344_HrpS_PJ23105_ttrR-fragment.
 +
T4 DNA ligase is used to connect pSU2718-p15A backbone and PttB344_HrpS_PJ23105_ttrR-fragment to get plasmid pSU2718-part2.
 +
 +
[[File:T--NOFLS YZ--BBa K3994001-Figure2.png|500px|thumb|center|Figure 4 E-coil having the desired pSU2718-part2 (Left) and control (Right)...]]
 +
 +
 +
 +
[[File:T--NOFLS YZ--BBa K3994001-Figure3.png|500px|thumb|center|Figure 5. The electrophoresis result of enzyme digestion identification...]]
 +
 +
 +
Lane 1: Plasmid pSU2718-p15A digested by EcoR1.
 +
 +
Lane 2 to 5: Recombinant plasmid pSU2718-part2 digested by EcoRI. We got two bands with size of 2803bp and 1544bp.
 +
 +
The results show that we got the correct plasmid. And the plasmid was sent to sequence.
 +
 +
 +
[[File:T--NOFLS YZ--BBa K3994001-Figure4.png|500px|thumb|center|Figure 6 The result of sequencing for plasmid pSU2718-part2...]]
 +
 +
Sequencing feedback shows we have obtained the correct plasmids which is consistent with their DNA profiles.
 +
 +
[[File:T--NOFLS YZ--BBa K3994001-Figure5.png|500px|thumb|center|Figure 7 The electrophoresis results of enzyme digestion (Middle) and PCR (Right)...]]
 +
 +
Middle:
 +
 +
Lane 1 and 2: Plasmid pSU2718-part2 digested by HindIII.
 +
 +
Right:
 +
 +
Lane 1: Part 1, PyeaR_HrpR, got by PCR method with size of 1293bp.
 +
This step is used to get the plasmids pSU2718-part2 digested by enzyme and gene PyeaR_HrpR by PCR method for later in the process. Therefore, channel 1 and 2 (Middle) were plasmids pSU2718--part2 digested by enzyme HindIII. And channel 1 (Right) was gene PyeaR_HrpR got by PCR. Clean-up the product to obtain pSU2718-part2 backbone and PyeaR_HrpR-fragment.
 +
T4 DNA ligase is used to connect pSU2718-part2 backbone and PyeaR_HrpR-fragment to get plasmid pSU2718-part2-part1.
 +
 +
 +
 +
[[File:T--NOFLS YZ--BBa K3994001-Figure6.png|500px|thumb|center|Figure 8 E-coil having the desired pSU2718-part2-part1 (Left) and control (Right)...]]
 +
 +
[[File:T--NOFLS YZ--BBa K3994001-Figure7.png|500px|thumb|center|Figure 9 The electrophoresis result of enzyme digestion...]]
 +
 +
 +
Lane 1: Recombinant plasmid pSU2718-part2-part1 without enzyme digestion.
 +
 +
Lane 2: Recombinant plasmid pSU2718-part2-part1 digested by EcoR1.
 +
 +
The result shows that we got the correct plasmid. And the plasmid was sent to sequence.
 +
 +
[[File:T--NOFLS YZ--BBa K3994001-Figure8.png|500px|thumb|center|Figure 10 The result of sequencing for plasmid pSU2718-part2-part1...]]
 +
 +
Sequencing feedback shows we have obtained the correct plasmids which is consistent with their DNA profiles.
 +
 +
 +
=== Proof of function ===
 +
 +
==== Attempt 1 ====
 +
 +
[[File:T--NOFLS YZ--BBa K3994001-Figure9.jpg|500px|thumb|center|Figure 11 Genetic Construction of IBD Distinguisher...]]
 +
 +
 +
Sample 1: NO3- + S4O62-
 +
 +
Sample 2: S4O62-
 +
 +
Sample 3: NO3-
 +
 +
Sample 4: Blank Control
 +
 +
 +
As shown above, there is obvious fluorescence in sample 1 and sample 2; for sample 3 and sample 4, there also a slight fluorescence produced in the tubes. In order to scientifically quantify the result, we used ELIASA to read the accurate fluorescence intensity, respectively.
 +
 +
[[File:T--NOFLS YZ--BBa K3994001-table1.png|500px|thumb|center|Table 1...]]
 +
 +
 +
 +
[[File:T--NOFLS YZ--BBa K3994001-Figure10.png|500px|thumb|center|Figure 12. Histogram of the fluorescence intensity of samples in Table 1...]]
 +
 +
According to the histogram above, we can see that Sample 1 (NO3-+ S4O62-) presents obvious higher fluorescence intensity than the rest three samples which means our design working. But we do realize that Sample 2 (S4O62-) also presents fluorescence than the blank control which confused us a lot. According to our design, if we only add S4O62- without NO3-, this AND gate wouldn’t allow to pass into the reporter (Part 3) as there is a closed door of the NO3- sensor (Part 1). Therefore, we thought there was something wrong in Part 1.
 +
 +
 +
In order to figure out the reason, we did several literature research and find out that in Part 1 we didn’t build the NarX-NarL two-component regulator (Figure 13), which shall be the first one to sense nitrate and that is why Part 1 didn’t work fine as we expected.
 +
 +
 +
[[File:T--NOFLS YZ--BBa K3994001-Figure11.png|500px|thumb|center|Figure 13. Genetic construction design map...]]
 +
 +
Ref. Woo, Seung-Gyun, et al. "A designed whole-cell biosensor for live diagnosis of gut inflammation through nitrate sensing." Biosensors and Bioelectronics 168 (2020): 112523.
 +
 +
 +
==== Attempt 2 ====
 +
 +
[[File:T--NOFLS YZ--BBa K3994003-Figure5.jpg|500px|thumb|center|Figure 14...]]
 +
 +
Sample 1: Negative Control (E. coli)
 +
 +
Sample 2: Positive Control (E. coli/amilGFP)
 +
 +
Sample 3: E. coli/pUC-57_Part 3
 +
 +
Sample 4: E.coli/pSU2718-Part 1_Part 2+pUC-57_Part 3
 +
 +
 +
In order to further analyze the performance of Part 2, we also designed the control groups as showing above where Sample 1 and Sample 2 were presented as the comparison of the fluorescence phenomenon. We can see that there was no fluorescence in Sample 3 (the report part, Part 3). According to the result of Sample 3 and Sample 4 (Figure 14), we could infer that the AND gate design works (HrpR_HrpS, PhrpL) as the Part 3 didn’t respond when there is no Part 1 and Part 2.
 +
Of course, we also repeated the experiments and measured the fluorescence intensity by ELIASA.  The data is given below.
 +
 +
 +
[[File:T--NOFLS YZ--BBa K3994003-table2.png|500px|thumb|center|Table 2...]]
 +
 +
[[File:T--NOFLS YZ--BBa K3994003-Figure6.png|500px|thumb|center|Figure 15. Histograms of the fluorescence intensity of samples in Table 2...]]
 +
 +
[[File:T--NOFLS YZ--BBa K3994003-Figure7.png|500px|thumb|center|Figure 16. Trend Contrast of the fluorescence intensity between that under OD600=0.8 and that under OD600=1...]]
 +
 +
According to the trend in Figure 16, the fluorescence intensity of pUC57-Part 3 presents the similar level as that of blank control and group NO3-, which means the “gate keeper” promoter, PhrpL works well and this conclusion also back up the conclusion that the AND gate design works well (HrpR_HrpS, PhrpL).
 +
 +
As the group S4O62 did present higher fluorescence intensity than that of group NO3- whenever OD600 equals to 0.8 or 1, it indicates that Part 2 and Part 3 both works well as Part 2 did show “green light” to the thiosulfate to finally “light” the Part 3.
 +
 +
 +
=== Improvement of an existing part ===
 +
 +
The group NEU_CHINA 2020 designed a composite part BBa_K3611009. They connected a secondary amplifier in series on the basis of the original hrp amplifier. The extracytoplasmic functional (ECF) sigma factor ECF11_987 and promoter ECF11_3726, which were proved as a higher-gain amplifier combination, were selected to build secondary amplifier.
 +
 +
Our team design the new composite part BBa_K3994011, with sequence different from the old one BBa_K3611009 (Figure 17). When and only when S2O32-/S4O62- and NO3- are present at the same time, the fluorescent gene is expressed. The fluorescent gene can be replaced with a gene that produce the interleukin-10 (anti-inflammatory factor). Our new composite part BBa_K3994011 was given a completely new function, producing the interleukin-10 (anti-inflammatory factor) for the treatment of IBD.
 +
 +
[[File:T--NOFLS YZ--BBa K3994011-Figure17.jpg|500px|thumb|center||Figure 17 The blast results about the sequence of our new part BBa_K3994011 and the old one BBa_K3611009...]]
 +
 +
 +
In addition, our project can serve General Public, Hospital and Biotechnology Firms lots of industrial biofactory companies. If our IBD biosensor may enter the market, it is possible to distribute it to ordinary people who want to have a test of IBD at home. IBD diagnosis has been a challenge for hospital because of its complex and various clinical symptoms. Thus, it should always be good to equip doctors with additional methods to help them better evaluate patients’ IBD related symptoms, which may help doctors enhance their diagnosis efficiency and efficacy. If we treat our development technique as a product, it is also possible to identify biotechnology firms as our potential clients. The biotechnology firms may be willing to buy our techniques and make further optimization
 +
 +
=== Future plan ===
 +
 +
 +
So far, we have ensured that Part 2, Part 3 and also the AND gate design work, we need to improve the design of Part 1 which is used to sense nitrate so that we could fully complete the whole biosensor construction to diagnose IBD.
 +
Besides, we also have concerns about the biosensor carrier, E. coli. Firstly, we need ensure that our engineered bacteria would not be immediately degraded or eliminated by other enteric microorganism. Secondly, E.coli may have adverse effects such as septicemia in patients with immune deficiency to the gut microbiome. In the future, safer bacteria like lactobacillus should be found as carrier receptors for transformation.
 +
 +
 +
=== References ===
 +
 +
 +
==== 1 CDC -What is inflammatory bowel disease, available at: https://www.cdc.gov/ibd/what-is-ibd.htm ====
 +
==== 2炎症性肠病 百度百科available at: https://baike.baidu.com/item/%E7%82%8E%E6%80%A7%E8%82%A0%E7%97%85/5296499?fr=aladdin ====
 +
==== 3 Data and StatisticsInflammatory Bowel Disease (IBD) in the United StatesAvailable at: https://www.cdc.gov/ibd/data-statistics.htm ====
 +
==== 4. Wang, Baojun, et al. "Engineering modular and orthogonal genetic logic gates for robust digital-like synthetic biology." Nature communications 2.1 (2011): 1-9. ====
  
 
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===Usage and Biology===
 
===Usage and Biology===
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Latest revision as of 04:15, 20 October 2021


PyeaR_HrpR+PttB344_HrpS_PJ23105_ttrR+PhrpL_amilGFP_IL10_PJ23104_ttrS


Profile

Name: PyeaR_HrpR+PttB344_HrpS_PJ23105_ttrR+PhrpL_amilGFP_IL10_PJ23104_ttrS

Base Pairs: 7494 bp

Origin: Synthetic

Properties: A biosensor releasing fluorescence only when detecting the IBD marker.

Usage and Biology

Background

Inflammatory bowel disease (IBD) is a chronic intestinal inflammatory disease of unknown etiology, including ulcerative colitis (CD) and Crohn’s disease (CD). This chronic disease, which is prone to repeated deterioration, currently lacks unified diagnostic and treatment standards, and is posing a great threat to public health. Drug therapy (anti-inflammatory drugs) is the preferred treatment for IBD. However, studies in the past 10 years have found that 30-50% of IBD patients do not respond to anti-TNF treatment. In addition, after long-term use of anti-inflammatory drugs, the patient's intestinal microbial status changes over time, and the effect may be lost due to drug resistance. Therefore, we need to seek help from other treatments for IBD.


Construct design

We can build Boolean logic circuits to combine thiosulfate/tetrasulfate and nitrate biosensors to optimize performance, improve sensor accuracy and enhance robustness, and optimize intestinal inflammation detection (Figure 1). When and only when S2O32-/S4O62- and NO3- are present at the same time, the fluorescent gene is expressed (Figure 1). The fluorescent gene can be replaced with a gene that produce the interleukin-10 (anti-inflammatory factor) for the treatment of IBD. HrpS is a key functional factor under PttB344 promoter. amilGFP is a fluorescent protein under PhrpL promoter. IL10 is an anti-inflammatory factor.

Figure 1. Boolean gate logic circuit/AND circuit construction...



 Part1: PyeaR_HrpR, sensing NO3- then release the substance R;

 Part2: PttB344_HrpS_PJ23105_ttrR, sensing S4O62- then release the substance S;

 Part3: PhrpL_amilGFP_IL10_PJ23104_ttrS, will release fluorescence if sensing both the substances, R and S released from Part 1(HrpR) and Part 2 (HrpS) , respectively.


Figure 2. A. PyeaR_HrpR, sensing NO3- to release the substance R; B. PttB344_HrpS_PJ23105_ttrR, sensing S4O62- to release the substance S; C. PhrpL_amilGFP_IL10_PJ23104_ttrS...


The profiles of every basic part are as follows:

BBa_K3994003

Name: HrpS

Base Pairs: 912bp

Origin: Pseudomonas syringae, genome

Properties: A coding sequence of HrpS protein

Usage and Biology

This codes for HrpS protein. HrpR protein binds to HrpS protein forming a complex and then triggering the transcription of promoter hrpL. This functions like a AND logic gate.

BBa_K3994012

Name: PttB344

Base Pairs: 85bp

Origin: Synthetic

Properties: A coding sequence of promoter ttB344.

Usage and Biology

This is a sequence of PttB344. PttrB185-269 is a minimal TtrR activated promoter when TtrR is phosphorylated by TtrS after TtrS sensing tetrathionate.

BBa_K3994005

Name: PhrpL

Base Pairs: 190bp

Origin: Synthetic

Properties: A coding sequence of promoter hrpL.

Usage and Biology

It is the sequence of inducible promoter PhrpL. HrpR protein binds to HrpS protein forming a complex and then triggering the transcription of induced promoter PhrpL. It functions like a AND logic gate to open a gene circuit. The hrpL promoter (PhrpL) contains a functional UAS relative to the transcription start-site, to which purified HrpR, HrpS and HrpRS bind in electrophoretic mobility shift assays.


BBa_K3994006

Name: IL10

Base Pairs: 864bp

Origin: Homo sapiens, genome

Properties: A coding sequence of an immune regulatory cytokine

Usage and Biology

This is a coding sequence of IL10. This is a major immune regulatory cytokine that acts on many cells of the immune system where it has profound anti-inflammatory functions, limiting excessive tissue disruption caused by inflammation.


Experimental approach

Recombinant Plasmid Construction

Figure 3. The electrophoresis results of enzyme digestion and PCR...

Lane 1 and 2: Plasmid pSU2718-p15A digested by Xba1 and BamH1.

Lane 3: Part 2, PttB344_HrpS_PJ23105_ttrR, got by PCR method with size of 2060bp.

This step is used to get the plasmids pSU2718-p15A digested by enzyme Xba1 and BamH1and gene PttB344_HrpS_PJ23105_ttrR by PCR method for later in the process. Therefore, channel 1 and 2 were plasmids pSU2718-p15A digested by enzyme Xba1 and BamH1. And channel 3 were gene PttB344_HrpS_PJ23105_ttrR got by PCR. Clean-up the product to obtain pSU2718-p15A backbone and PttB344_HrpS_PJ23105_ttrR-fragment. T4 DNA ligase is used to connect pSU2718-p15A backbone and PttB344_HrpS_PJ23105_ttrR-fragment to get plasmid pSU2718-part2.

Figure 4 E-coil having the desired pSU2718-part2 (Left) and control (Right)...


Figure 5. The electrophoresis result of enzyme digestion identification...


Lane 1: Plasmid pSU2718-p15A digested by EcoR1.

Lane 2 to 5: Recombinant plasmid pSU2718-part2 digested by EcoRI. We got two bands with size of 2803bp and 1544bp.

The results show that we got the correct plasmid. And the plasmid was sent to sequence.


Figure 6 The result of sequencing for plasmid pSU2718-part2...

Sequencing feedback shows we have obtained the correct plasmids which is consistent with their DNA profiles.

Figure 7 The electrophoresis results of enzyme digestion (Middle) and PCR (Right)...

Middle:

Lane 1 and 2: Plasmid pSU2718-part2 digested by HindIII.

Right:

Lane 1: Part 1, PyeaR_HrpR, got by PCR method with size of 1293bp. This step is used to get the plasmids pSU2718-part2 digested by enzyme and gene PyeaR_HrpR by PCR method for later in the process. Therefore, channel 1 and 2 (Middle) were plasmids pSU2718--part2 digested by enzyme HindIII. And channel 1 (Right) was gene PyeaR_HrpR got by PCR. Clean-up the product to obtain pSU2718-part2 backbone and PyeaR_HrpR-fragment. T4 DNA ligase is used to connect pSU2718-part2 backbone and PyeaR_HrpR-fragment to get plasmid pSU2718-part2-part1.


Figure 8 E-coil having the desired pSU2718-part2-part1 (Left) and control (Right)...
Figure 9 The electrophoresis result of enzyme digestion...


Lane 1: Recombinant plasmid pSU2718-part2-part1 without enzyme digestion.

Lane 2: Recombinant plasmid pSU2718-part2-part1 digested by EcoR1.

The result shows that we got the correct plasmid. And the plasmid was sent to sequence.

Figure 10 The result of sequencing for plasmid pSU2718-part2-part1...

Sequencing feedback shows we have obtained the correct plasmids which is consistent with their DNA profiles.


Proof of function

Attempt 1

Figure 11 Genetic Construction of IBD Distinguisher...


Sample 1: NO3- + S4O62-

Sample 2: S4O62-

Sample 3: NO3-

Sample 4: Blank Control


As shown above, there is obvious fluorescence in sample 1 and sample 2; for sample 3 and sample 4, there also a slight fluorescence produced in the tubes. In order to scientifically quantify the result, we used ELIASA to read the accurate fluorescence intensity, respectively.

Table 1...


Figure 12. Histogram of the fluorescence intensity of samples in Table 1...

According to the histogram above, we can see that Sample 1 (NO3-+ S4O62-) presents obvious higher fluorescence intensity than the rest three samples which means our design working. But we do realize that Sample 2 (S4O62-) also presents fluorescence than the blank control which confused us a lot. According to our design, if we only add S4O62- without NO3-, this AND gate wouldn’t allow to pass into the reporter (Part 3) as there is a closed door of the NO3- sensor (Part 1). Therefore, we thought there was something wrong in Part 1.


In order to figure out the reason, we did several literature research and find out that in Part 1 we didn’t build the NarX-NarL two-component regulator (Figure 13), which shall be the first one to sense nitrate and that is why Part 1 didn’t work fine as we expected.


Figure 13. Genetic construction design map...

Ref. Woo, Seung-Gyun, et al. "A designed whole-cell biosensor for live diagnosis of gut inflammation through nitrate sensing." Biosensors and Bioelectronics 168 (2020): 112523.


Attempt 2

Figure 14...

Sample 1: Negative Control (E. coli)

Sample 2: Positive Control (E. coli/amilGFP)

Sample 3: E. coli/pUC-57_Part 3

Sample 4: E.coli/pSU2718-Part 1_Part 2+pUC-57_Part 3


In order to further analyze the performance of Part 2, we also designed the control groups as showing above where Sample 1 and Sample 2 were presented as the comparison of the fluorescence phenomenon. We can see that there was no fluorescence in Sample 3 (the report part, Part 3). According to the result of Sample 3 and Sample 4 (Figure 14), we could infer that the AND gate design works (HrpR_HrpS, PhrpL) as the Part 3 didn’t respond when there is no Part 1 and Part 2. Of course, we also repeated the experiments and measured the fluorescence intensity by ELIASA. The data is given below.


Table 2...
Figure 15. Histograms of the fluorescence intensity of samples in Table 2...
Figure 16. Trend Contrast of the fluorescence intensity between that under OD600=0.8 and that under OD600=1...

According to the trend in Figure 16, the fluorescence intensity of pUC57-Part 3 presents the similar level as that of blank control and group NO3-, which means the “gate keeper” promoter, PhrpL works well and this conclusion also back up the conclusion that the AND gate design works well (HrpR_HrpS, PhrpL).

As the group S4O62 did present higher fluorescence intensity than that of group NO3- whenever OD600 equals to 0.8 or 1, it indicates that Part 2 and Part 3 both works well as Part 2 did show “green light” to the thiosulfate to finally “light” the Part 3.


Improvement of an existing part

The group NEU_CHINA 2020 designed a composite part BBa_K3611009. They connected a secondary amplifier in series on the basis of the original hrp amplifier. The extracytoplasmic functional (ECF) sigma factor ECF11_987 and promoter ECF11_3726, which were proved as a higher-gain amplifier combination, were selected to build secondary amplifier.

Our team design the new composite part BBa_K3994011, with sequence different from the old one BBa_K3611009 (Figure 17). When and only when S2O32-/S4O62- and NO3- are present at the same time, the fluorescent gene is expressed. The fluorescent gene can be replaced with a gene that produce the interleukin-10 (anti-inflammatory factor). Our new composite part BBa_K3994011 was given a completely new function, producing the interleukin-10 (anti-inflammatory factor) for the treatment of IBD.

Figure 17 The blast results about the sequence of our new part BBa_K3994011 and the old one BBa_K3611009...


In addition, our project can serve General Public, Hospital and Biotechnology Firms lots of industrial biofactory companies. If our IBD biosensor may enter the market, it is possible to distribute it to ordinary people who want to have a test of IBD at home. IBD diagnosis has been a challenge for hospital because of its complex and various clinical symptoms. Thus, it should always be good to equip doctors with additional methods to help them better evaluate patients’ IBD related symptoms, which may help doctors enhance their diagnosis efficiency and efficacy. If we treat our development technique as a product, it is also possible to identify biotechnology firms as our potential clients. The biotechnology firms may be willing to buy our techniques and make further optimization

Future plan

So far, we have ensured that Part 2, Part 3 and also the AND gate design work, we need to improve the design of Part 1 which is used to sense nitrate so that we could fully complete the whole biosensor construction to diagnose IBD. Besides, we also have concerns about the biosensor carrier, E. coli. Firstly, we need ensure that our engineered bacteria would not be immediately degraded or eliminated by other enteric microorganism. Secondly, E.coli may have adverse effects such as septicemia in patients with immune deficiency to the gut microbiome. In the future, safer bacteria like lactobacillus should be found as carrier receptors for transformation.


References

1 CDC -What is inflammatory bowel disease, available at: https://www.cdc.gov/ibd/what-is-ibd.htm

2炎症性肠病 百度百科available at: https://baike.baidu.com/item/%E7%82%8E%E6%80%A7%E8%82%A0%E7%97%85/5296499?fr=aladdin

3 Data and StatisticsInflammatory Bowel Disease (IBD) in the United StatesAvailable at: https://www.cdc.gov/ibd/data-statistics.htm

4. Wang, Baojun, et al. "Engineering modular and orthogonal genetic logic gates for robust digital-like synthetic biology." Nature communications 2.1 (2011): 1-9.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal XbaI site found at 1248
    Illegal XbaI site found at 1398
    Illegal XbaI site found at 3288
    Illegal XbaI site found at 3438
    Illegal PstI site found at 1236
    Illegal PstI site found at 3276
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 2062
    Illegal NheI site found at 2085
    Illegal NheI site found at 5496
    Illegal NheI site found at 5519
    Illegal PstI site found at 1236
    Illegal PstI site found at 3276
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 3116
    Illegal BamHI site found at 1254
    Illegal BamHI site found at 3294
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal XbaI site found at 1248
    Illegal XbaI site found at 1398
    Illegal XbaI site found at 3288
    Illegal XbaI site found at 3438
    Illegal PstI site found at 1236
    Illegal PstI site found at 3276
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal XbaI site found at 1248
    Illegal XbaI site found at 1398
    Illegal XbaI site found at 3288
    Illegal XbaI site found at 3438
    Illegal PstI site found at 1236
    Illegal PstI site found at 3276
    Illegal NgoMIV site found at 669
    Illegal AgeI site found at 142
    Illegal AgeI site found at 256
    Illegal AgeI site found at 262
    Illegal AgeI site found at 901
    Illegal AgeI site found at 1776
    Illegal AgeI site found at 2329
    Illegal AgeI site found at 2335
  • 1000
    COMPATIBLE WITH RFC[1000]