Revision as of 11:37, 21 October 2016

Omega-hexatoxin-hv1a

Introduction:

Figure 1. Omega-hexatoxin-Hv1a

      This year we create a revolutionary system that integrates biological pesticide, an automatic detector, a sprinkler, and IoT. We made a database that contains most of the spider toxins and selected the target toxins by programming. Omega-hexatoxin-Hv1a is coded for the venom of a spider, Hadronyche versuta.

Figure 2. Omega-hexatoxin-Hv1a structure

Mechanism of Hv1a:

      According to the reference, Omega-hexatoxin-Hv1a has a structure called ICK(inhibitor cysteine knot). This kind of structure contains three disulfide bonds and beta-sheet. With this structure, Hv1a can resist the high temperature, acid base solution and the digest juice of insect gut. Hv1a can bind on insect voltage-gated Calcium channels (CaV1) in the central nervous system, making it paralyze and die eventually.

Features of Hv1a:

">1. Non-toxic

2. Biodegradable

: Omega-hexatoxin-Hv1a 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, Omega-hexatoxin-Hv1a has specificity to Lepidopteran (moths), Dipteran (flies) and Orthopteran (grasshoppers).

4. Eco-friendly: Compare with chemical pesticides, Omega-hexatoxin-Hv1a will not remain in soil and water so that it will not pollute the environment and won’t harm the ecosystem.

      Altogether, using Omega-hexatoxin-Hv1a is totally an environmentally friendly way for solving harmful insect problems by using this ion channel inhibitor as a biological pesticide.

Target insect:

Figure 3. Hv1a target insect

House cricket (Acheta domesticus) Musca domestica Amblyomma americanum Heliothis virescens

Experiment

1. Cloning :
After assembling the DNA sequences from the basic parts, we recombined toxin 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 100-150 bp. In this PCR experiment, the toxin product's size should be near at 350-450 bp.

Figure 4.Hv1a,
The DNA sequence length of Hv1a is around 100-150 b.p. In this PCR experiment, the product’s size should be close to 350-450 b.p.

Application of the part

1. 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 Hv1a with 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 Hv1a and make it a linear form. The other one adding sample buffer is the native form of Hv1a 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 Hv1a is smaller than linear one because the disulfide bonds in Hv1a make the whole structure a globular shape.

Figure 5.Protein electrophoresis of P_T7 + RBS + Hv1a+linker+6X His-Tag (control: Without constructed plasmid)
We can see the band of Hv1a at 5-6 kDa.
A: add β-mercaptoethanol and sample buffer
B: add sample buffer

Figure 6.Protein electrophoresis of P_T7 + RBS + Hv1a+linker+Lectin+linker+6X His-Tag (control: Without constructed plasmid)
We can see the band of Hv1a-Lectin at 5-6 kDa.
A: add β-mercaptoethanol and sample buffer
B: add sample buffer

2.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 Hv1a.

Figure 7.Protein electrophoresis of Hv1a-6X His-Tag purification
A is the sonication product. B is the elution product of purification.

Figure 8.Protein electrophoresis of Hv1a-linker-lectin-linker-6X His-Tag purification
A is the sonication product. B is the elution product of purification.

3.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 modified the program in our device.Therefore, Pantide was tested under the ultraviolet light. The protein electrophoresis was shown below.

Figure 9. SDS-PAGE gel and the concentrations of UV radiolytic oxidation test to native ω-hexatoxin-Hv1a (Hv1a, 5.3 kDa). The samples are marked on the top of gel.

4. Device:
We designed a device that contains detector, sprinkler, and integrated hardware with users by APP through IoT talk. We use an 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 10.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 11.Above are leaves with of Negative control ( DDwater ), Positive control ( Bacillus thuringiensis bacteria ), Hv1a+linker+6X His-Tag

Sequence and Features