Difference between revisions of "Part:BBa K1974022"
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<h1>'''Experiment'''</h1>
 
<h1>'''Experiment'''</h1>
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<p style="padding:1px;"><b>1. Cloning </b>:<br>After assembling the DNA sequences from the basic parts, we recombined each P<sub>T7</sub>+B0034+Sf1a+ linker + snowdrop -lectin +linker+ 6X His-Tag gene to pSB1C3 backbones and conducted a PCR experiment to check the size of each part. The DNA sequence length of these parts is around 500-700 b.p. In this PCR experiment, the toxin product's size should be near at 800-1000 b.p.Proved that we successfully ligated the toxin sequence onto an ideal backbone.
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<p style="padding:1px;"><b>1. Cloning </b>:<br>After assembling the DNA sequences from the basic parts, we recombined each P<sub>T7</sub>+B0034+Sf1a+ linker + snowdrop -lectin +linker+ 6X His-Tag gene to pSB1C3 backbones and conducted a PCR experiment to check the size of each part. The DNA sequence length of these parts is around 600~700 b.p. In this PCR experiment, the toxin product's size should be near at 850-950 b.p.Proved that we successfully ligated the toxin sequence onto an ideal backbone.
 
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<H1>'''Results'''</H1>
 
<H1>'''Results'''</H1>
 
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Pantide-expressed E. coli Rosetta gami strain and diluted it with the three concentration.We applied the sample onto the leaf disks and put five cutworms into the separate cabinets for feeding assays. The positive control in the experiment was to apply Bacillus thuringiensis, which is the most widely-used bioinsecticide. We preserved all the result of the remained leaves sealing with the glass paper and calculated the ratio of the remained area on the leaves. The collected data were analyzed by t – test. Here are the feeding assay results.
 
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Pantide-expressed E. coli Rosetta gami strain and diluted it with the three concentration.We applied the sample onto the leaf disks and put five cutworms into the separate cabinets for feeding assays. The positive control in the experiment was to apply Bacillus thuringiensis, which is the most widely-used bioinsecticide. We preserved all the result of the remained leaves sealing with the glass paper and calculated the ratio of the remained area on the leaves. The collected data were analyzed by t – test. Here are the feeding assay results.
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[[File:NCTU_DOSE_SL_1.png|400px|thumb|center|'''Figure 6.''' Below are leaves with of Negative control ( DDwater ), Positive control ( Bacillus thuringiensis bacteria ), Sf1a+linker+His-Tag, Sf1a+linker+snowdrop-lectin+linker+His-Tag]]
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[[File:NCTU_DOSE_SL_1.png|400px|thumb|center|'''Figure 6.''' Above is leaves remaining area of Negative control ( DDwater ), Positive control ( Bacillus thuringiensis bacteria ), Hv1a+linker+6XHis-Tag, Hv1a+linker+snowdrop-lectin+linker+6XHis-Tag]]
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[[File:NCTU_leaves_sl.png|400px|thumb|center|'''Figure 7.''' Below are leaves with of Negative control ( DDwater ), Positive control ( Bacillus thuringiensis bacteria ), Sf1a+linker+snowdrop-lectin+linker+His-Tag,]]
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[[File:NCTU_leaves_sl.png|400px|thumb|center|'''Figure 7.''' Above are leaves with of Negative control ( DDwater ), Positive control ( Bacillus thuringiensis bacteria ), Hv1a+linker+6X His-Tag]]
  
  

Revision as of 01:11, 20 October 2016


T7Promoter+RBS+Sf1a+linker+snowdrop-lectin+linker+6X His-Tag


Introduction:

Figure 1. PT7+RBS+Sf1a+linker+snowdrop-lectin+linker+6X His-Tag

       By ligating the IPTG induced PT7(BBa_ I712074), strong ribosome binding site (BBa_B0034), Sf1a, linker, snowdrop lectin (BBa K1974020) and the 6X His-Tag (BBa_ K1223006), we can express Sf1a, the toxin by IPTG induction
       This year we create a revolutionary system that integrates biological pesticides, automatic detector, sprinkler, and IoT. We made a database that contains most of the spider toxins and selected the target toxins by programming. μ-segestritoxin-Sf1a is coded for the venom of a spider, Hadronyche versuta.
       It is under the control of the strong PT7. Snowdrop-lectin acts as a carrier that could transport the toxin to insect’s nervous system, hemolymph and can improve the oral activity. A 6X His-Tag is added for further protein purification.
       According to reference, snowdrop-lectin is resistant to high temperature and would not be degraded by digestive juice. The species-specificity is based on the toxin, and the snowdrop lectin is the role of the carrier.


Mechanism of Sf1a:

      According to reference, μ-segestritoxin-Sf1a has a structure called ICK(inhibitor cysteine knot).[1] This kind of structure contains three disulfide bonds and beta-sheet. With this structure, μ-segestritoxin-Sf1a can resist the high temperature, acid-base solution and the digest juice of insect gut. μ-segestritoxin-Sf1a can bind on insect voltage-gated Calcium channels (CaV1) in the central nervous system, making it paralyze and die eventually.


Features of Sf1a

1. Non-toxic: μ-segestritoxin-Sf1a is non-toxic to mammals and Hymenoptera (bees). Since the structure of the target ion channel is different, μ-segestritoxin-Sf1a does not harm mammals and bees. So it is safe to use it as a biological pesticide.


2. Biodegradable: μ-segestritoxin-Sf1a is a polypeptide so it must degrade over time. After degradation, the toxin will become nutrition in the soil.


3. Species-specific: According to reference, μ-segestritoxin-Sf1a has specificity to Lepidopteran (moths), Dipteran (flies) and Orthopteran (grasshoppers).


4. Eco-friendly: Compare with chemical pesticides, μ-segestritoxin-Sf1a will not remain in soil and water so that it will not pollute the environment and won’t harm the ecosystem.

       Together, using μ-segestritoxin-Sf1a is totally an environmentally friendly way for solving harmful insect problems by using this ion channel inhibitor as a biological pesticide.


Target insect:

Figure 2. Target insects


Experiment

1. Cloning :
After assembling the DNA sequences from the basic parts, we recombined each PT7+B0034+Sf1a+ linker + snowdrop -lectin +linker+ 6X His-Tag gene to pSB1C3 backbones and conducted a PCR experiment to check the size of each part. The DNA sequence length of these parts is around 600~700 b.p. In this PCR experiment, the toxin product's size should be near at 850-950 b.p.Proved that we successfully ligated the toxin sequence onto an ideal backbone.

Figure 3. PT7 + RBS + Sf1a+linker+Lectin+linker+6X His-Tag
The DNA sequence length of PT7 + RBS + Sf1a+linker+6X His-Tag is around 600~700 b.p. In this PCR experiment, the product’s size should be close to 850-950 b.p.

2. Expressing:
We chose E.coli Rosetta gami strain, which can form the disulfide bonds in the cytoplasm to express the protein. To verify the E.coli express the PT7 + RBS + Sf1a+linker+Lectin+linker+6X His-Tag which contains disulfide bonds, we treated the sample in two different ways. A means adding β-mercaptoethanol and sample buffer. β-mercaptoethanol can break the disulfide bonds of PT7 + RBS + Sf1a+linker+Lectin+linker+6X His-Tag and make it a linear form. The other one adding sample buffer is the native form of PT7 + RBS + Sf1a+linker+Lectin+linker+6X His-Tag which maintains its structure. B is adding only sample buffer. The two samples are treated in boiling water for 15 mins. The SDS-PAGE shows that the native PT7 + RBS+Sf1a+linker+Lectin+linker+6X His-Tag is smaller than linear one because the disulfide bonds in PT7 + RBS + Sf1a+linker+Lectin+linker+6X His-Tag make the whole structure a globular shape.

Figure 4. Protein electrophoresis of PT7 + RBS + Sf1a+linker+Lectin+linker+6X His-Tag (control: Without constructed plasmid)
We can see the band of PT7 + RBS + Sf1a+linker+Lectin+linker+6X His-Tag at 17-18 kDa.
A: add β-mercaptoethanol and sample buffer
B: add sample buffer

3. Purification:We sonicated the bacteria and purified the protein by 6X His-Tag behind the peptide using Nickel resin column. Then we ran the SDS-PAGE to verify the purification and analyze the concentration of PT7 + RBS + Sf1a+linker+Lectin+linker+6X His-Tag.


Figure 5. Protein electrophoresis of PT7 + RBS + Sf1a+linker+Lectin+linker+6X His-Tag purification.
A is the sonication product. B is the elution product of purification.

4.Modeling:
According to reference, the energy of Ultraviolet will break the disulfide bonds and the toxicity is also decreased. To take the parameter into consideration for our automatic system, we modeled the degradation rate of the protein and modify the program in our device.


5. Device:
We designed a device that contains detector, sprinkler, and integrated hardware with users by APP through IoT talk. We use infrared detector to detect the number of the pest and predict what time to spray the farmland. Furthermore, other detectors like temperature, humidity, lamination, pressure of carbon dioxide and on also install in our device. At the same time, the APP would contact the users that all the information about the farmland and spray biological pesticides automatically. This device can make farmers control the farmland remotely.


Results

       Pantide-expressed E. coli Rosetta gami strain and diluted it with the three concentration.We applied the sample onto the leaf disks and put five cutworms into the separate cabinets for feeding assays. The positive control in the experiment was to apply Bacillus thuringiensis, which is the most widely-used bioinsecticide. We preserved all the result of the remained leaves sealing with the glass paper and calculated the ratio of the remained area on the leaves. The collected data were analyzed by t – test. Here are the feeding assay results.

Figure 6. Above is leaves remaining area of Negative control ( DDwater ), Positive control ( Bacillus thuringiensis bacteria ), Hv1a+linker+6XHis-Tag, Hv1a+linker+snowdrop-lectin+linker+6XHis-Tag
Figure 7. Above are leaves with of Negative control ( DDwater ), Positive control ( Bacillus thuringiensis bacteria ), Hv1a+linker+6X His-Tag



Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]