Difference between revisions of "Part:BBa K4090010"
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<partinfo>BBa_K4090010 short</partinfo>
 
<partinfo>BBa_K4090010 short</partinfo>
  
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A kind of fusion protein that helps to form silicon dioxide outside the membrane.
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=Introduction=
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INP could not be produced by E.coli itself, but it could be successfully express on the plasma membrane of E.coli. The co-expression of the INP and other genes could bring the proteins that other genes encode to the cell surface. This biobrick contains the sequence of INP gene after the codon optimization base on the codon bias of E.coli. Silicatein is a protein from the demosponge. It could induce the precipitation of the silica with the presence of silicic acid or TMOS. This biobrick could induce the precipitation of the silica.  
  
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<!-- Add more about the biology of this part here -->
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==Usage and Viability==
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[[File:T--SDSZ China--result inpsilicatein.png|700px|thumb|center|Fig.1]]
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We designed the part as below.
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[[File:T--SDSZ China--result 1-3parts.png|700px|thumb|center|Fig.2]]
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[[File:T--SDSZ China--result 1-3parts.png|500px|thumb|center|Fig.1]]
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==Data==
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<br><br>
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[[File:T--SDSZ_China--result_1-2parts.png|700px|thumb|center|Fig.3]]
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Gibson Assembly was used to transform the gene. Then, the gel electrophoresis was used to test whether plasmids were constructed successfully. Since the gene that inserted is too long to detect as a whole, which is about 2000bp, our team decided to detect sequences of two connections (one connected the silicatein with the vector and the other connected the INP with silicatein) , both of which are approximately 600bp. From the graph below, we could see that the result was positive, proving that the plasmids are successfully constructed.  
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According to Fig.1, all the fragments designed have been successfully made, including S1&S2, which are Silicatein combined with INP, and P1&P2, which are S010_pET28b-csgA-linker-mfp5-7His(pET).
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[[File:T--SDSZ China--result 1-4parts.png|500px|thumb|center|Fig.2]]
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[[File:T--SDSZ China--result 1-4parts.png|700px|thumb|center|Fig.4]]
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Fig.2 represents the results of gel electrophoresis to test the fragment after Gibson Assembly. The length is about 600bp, which, together with the results from sequencing, indicates a positive outcome.
 
Fig.2 represents the results of gel electrophoresis to test the fragment after Gibson Assembly. The length is about 600bp, which, together with the results from sequencing, indicates a positive outcome.
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[[File:T--SDSZ China--result 1-6parts.png|700px|thumb|center|Fig.5]]
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<br><br>
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After using the Gibson Assembly to transform the INP-silicatein gene in the E.coli and cultured them under appropriate environment, controlled experiment is performed. In order to know whether the silicatein was also expressed inside the cell, part of the E.coli were homogenized by ultrasonic comminution and added to the sample. The graph below showed that the experimental groups present higher OD values, and the group with homogenization has higher OD values than the group without homogenization. The result showed that this part could induce the precipitation effectively, though there is still a small amount of silicatein could not be expressed on the surface.
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[[File:T--SDSZ China--result 1-6parts.png|500px|thumb|center|Fig.3]]
 
Fig.3 represents qualitative OD values, showing that there is sufficient amount of silicatein produced, since:  
 
Fig.3 represents qualitative OD values, showing that there is sufficient amount of silicatein produced, since:  
 
•Both NC Control are darker (NC1 remain as yellow which indicates that it needs MORE NaOH to turn blue, it contains more acids).
 
•Both NC Control are darker (NC1 remain as yellow which indicates that it needs MORE NaOH to turn blue, it contains more acids).
 
•Both silicatein mixture (with / without homogenization) have higher OD810nm, meaning that there are more bacteria inside the test tube (the solution is thicker / not as clear as NCs).
 
•Both silicatein mixture (with / without homogenization) have higher OD810nm, meaning that there are more bacteria inside the test tube (the solution is thicker / not as clear as NCs).
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[[File:T--SDSZ China--result 1-7parts.jpeg|700px|thumb|center|Fig.6]]
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<br><br>
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TEM testing is also utilized in order to verify its function. Five drips of bacteria mixture of different concentration were added onto the five pieces of carbon film, and were put into the 80 degree Celsius dryer. After they are completely dry, TEM testing was carried out. The dark particles on the surface of cells, which are the silcia particles, further verified that the part could induce the precipitation of the silica.
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[[File:T--SDSZ China--result 1-7parts.jpeg|300px|thumb|center|Fig.4]]
 
Fig.4 shows the results from TEM testing. Dark proportions represent silicon dioxide produced on the surface of cells.
 
Fig.4 shows the results from TEM testing. Dark proportions represent silicon dioxide produced on the surface of cells.
  

Revision as of 19:08, 21 October 2021


INP-Silicatein

Introduction

INP could not be produced by E.coli itself, but it could be successfully express on the plasma membrane of E.coli. The co-expression of the INP and other genes could bring the proteins that other genes encode to the cell surface. This biobrick contains the sequence of INP gene after the codon optimization base on the codon bias of E.coli. Silicatein is a protein from the demosponge. It could induce the precipitation of the silica with the presence of silicic acid or TMOS. This biobrick could induce the precipitation of the silica.

Usage and Viability

We designed the part as below.

Fig.1



Gibson Assembly was used to transform the gene. Then, the gel electrophoresis was used to test whether plasmids were constructed successfully. Since the gene that inserted is too long to detect as a whole, which is about 2000bp, our team decided to detect sequences of two connections (one connected the silicatein with the vector and the other connected the INP with silicatein) , both of which are approximately 600bp. From the graph below, we could see that the result was positive, proving that the plasmids are successfully constructed.

Fig.2

Fig.2 represents the results of gel electrophoresis to test the fragment after Gibson Assembly. The length is about 600bp, which, together with the results from sequencing, indicates a positive outcome.

After using the Gibson Assembly to transform the INP-silicatein gene in the E.coli and cultured them under appropriate environment, controlled experiment is performed. In order to know whether the silicatein was also expressed inside the cell, part of the E.coli were homogenized by ultrasonic comminution and added to the sample. The graph below showed that the experimental groups present higher OD values, and the group with homogenization has higher OD values than the group without homogenization. The result showed that this part could induce the precipitation effectively, though there is still a small amount of silicatein could not be expressed on the surface.

Fig.3

Fig.3 represents qualitative OD values, showing that there is sufficient amount of silicatein produced, since: •Both NC Control are darker (NC1 remain as yellow which indicates that it needs MORE NaOH to turn blue, it contains more acids). •Both silicatein mixture (with / without homogenization) have higher OD810nm, meaning that there are more bacteria inside the test tube (the solution is thicker / not as clear as NCs).

TEM testing is also utilized in order to verify its function. Five drips of bacteria mixture of different concentration were added onto the five pieces of carbon film, and were put into the 80 degree Celsius dryer. After they are completely dry, TEM testing was carried out. The dark particles on the surface of cells, which are the silcia particles, further verified that the part could induce the precipitation of the silica.

Fig.4

Fig.4 shows the results from TEM testing. Dark proportions represent silicon dioxide produced on the surface of cells.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1392
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 321
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 63
    Illegal NgoMIV site found at 396
    Illegal AgeI site found at 498
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 229

References

[1] Pamirsky, Igor E., and Kirill S. Golokhvast. "Silaffins of diatoms: from applied biotechnology to biomedicine." Marine drugs 11.9 (2013): 3155-3167.
[2] Park, Jeong Chan, et al. "R5 Peptide-based Biosilicification Using Methyltrimethoxysilane." Biotechnology & Bioprocess Engineering 23.1 (2018).
[3] Müller, Werner EG, et al. "Bioencapsulation of living bacteria (Escherichia coli) with poly (silicate) after transformation with silicatein-α gene." Biomaterials 29.7 (2008): 771-779.
[4] ZHU T, PAULO C, MERROUN, M L, et al. Potential application of biomineralization by Synechococcus PCC8806 for concrete restoration[J]. Sedimentology, 2013,61(1):1-21.
[5] Lechner, Carolin C., and Christian FW Becker. "A sequence‐function analysis of the silica precipitating silaffin R5 peptide." Journal of Peptide Science 20.2 (2014): 152-158.