Difference between revisions of "Team:FAFU-CHINA/Notebook"

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<div> 2015.6.8</div>
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<div class="animate slideInLeft delay-3">Apiculture这个是标题,放大,居中</div>
<div> Today was the first day that we began our project in the lab after we made a scientific plan. Firstly, we extracted the whole RNA of CSBV by Trizol. As we all know, RNA is easy to be digested in the environment. Therefore although we did this quickly, there were still some samples without RNA fragment. But we did again and the result was satisfied at that time. It was encouraging! </div>
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                <img src=' https://static.igem.org/mediawiki/2015/2/24/FAFU-CHINA_Apiculture_%282%29.png'>
<div> 6.9</div>
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                <img src=' https://static.igem.org/mediawiki/2015/6/64/FAFU-CHINA_Apiculture_%281%29.png'>
<div> Today we made RT-PCR with four sets of reverse specific primers and the RNA of CSBV to synthesize homologous cDNA(CSBV Helicase、Protease、VP1 and RdRp respectively). Then dsDNAs was amplified with four sets of specific primers by PCR. It went through smoothly. So far, we got the target fragments successfully. Also,we used GFP F/R to amplify GFP gene. </div>
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                <div>Q:What is the influence of CSBV to your bee population?</div>
 +
                <div>A:This disease outbroke seriously in my bee farm located in Wuyi Mountain. It began from April this year with high Infectiousness and spread fast and strong.This disease is so difficult to cure that it resulted in economic loss. </div>
 +
                <div>Q:How do you combat this disease based on past experience? </div>
 +
<div>A:If this disease outbroke more serious in the past , then they could only be used some illicit chemicals to combat, such as oxytetracycline. Most of these drugs are expensive but the effect is good, so it has become a choice for traditional beekeepers. But now with the improvement of beekeeping technologies, as well as taking into account the impact of drugs on product quality .We seldom use the drugs. </div>
  
<div> 6.10</div>
+
<div>Q: What were measures you taking to reduce the loss without drug treatment? </div>
<div> We utilized T7 RiboMAXTM Express RNAi System kit and dsDNAs as templates to synthesize dsRNAs(dsHelicase、dsProtease、dsVP1、dsRdRp and dsGFP), but there were only dsHelicase and dsGFP we could get. We tried again and still failed. It took our whole day to find the reason. Tomorrow we will ask our advisor for some solutions and do it one more time. </div>
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<div>A: Because the disease first breaks out in the general body of the bee larvae but he impact on adult bees are relatively small. Therefore, in the early stages, the hive of pest is more difficult to find. When honeycomb occurrence of disease was more serious on a board , we only could dispose of the pests on that board to prevent the transmission to other bees to reduce losses. </div>
<div> 6.12</div>
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<div> After figuring out the problem, we eventually got the all right dsRNAs.
+
Another part, we began to prepare the larvae of Chinese honeybee which was offered by our institute of bees. </div>
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<div> 6.13</div>
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<div> We put dsRNAs into fodder of the larvae of the honeybee to feed them. Then after 12h, we fed them another fodder with CSBV extracting solution. We did so twice before they got normal fodder. </div>
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<div> 6.17</div>
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<div> During three days, we observed the change of percentage of pupation and collect and analyse data. Meanwhile,RT-qPCR was done to detect the effect of different dsRNAs to CSBV. According to the result, we found that dsRdRp made a remarkable influence on the replication of CSBV. So we decided to use dsRdRp to inference CSBV. </div>
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<div> 6.19 </div>
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<div> We used cDNA of RdRp and specific primers(Not1-F/Pst1-R、EcoR1-F/Pst1-R) to synthesize RdRp gene. However, after agarose gel electrophoresis(AGE), we could not find our target fragment. </div>
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<div> 6.20</div>
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<div> We changed a better DNA polymerase and set the annealing temperature to 60℃. Finally we got the RdRp gene. </div>
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<div> 6.21</div>
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<div> We made RdRp gene link with T vector in 25℃, 15min and then transformed it into DH5α,a kind of competent cell, which was cultured in 37℃,overnight. </div>
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<div> 6.22</div>
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<div> We picked the colonies to do PCR and sent the positive sequencing(M13). </div>
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<div> 6.24</div>
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<div> Today we got the result of sequencing. After comparing with data in NCBI, we only had two 100 percent samples. </div>
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<div>We started to do double enzyme digestion(Not1 and Pst1、EcoR1 and Pst1) to cut vector L4440、pSB1C3 and RdRp-T recombinant plasmid. </div>
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<div>6.25</div>
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<div>The result of double enzyme digestion is terrible, because we could not get our target fragments successfully, which showed very dark stripes after AGE. </div>
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<div>We did again and at that time we took 8h to finish double enzyme digestion to make sure our target fragments were cut down completely. </div>
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<div>6.26</div>
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<div>We made it! And we immediately did gel recovery. Then we began to link RdRp with L4440 and pSB1C3 using T4 ligase, 4℃, overnight. </div>
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<div>6.27</div>
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<div>We did transformation. However,we forgot to make LB medium with CmRR. So the transformation of RdRp-pSB1C3 could only be done tomorrow. </div>
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<div>6.29</div>
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<div>Today there was two news. The good one was we successfully got recombinant plasmid RdRp-L4440 while the bad one was nothing grew on the plate with CmRR. We thought maybe it was because RdRp did not link with pSB1C3 successfully. Anyway we would do it again tomorrow. </div>
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<div>7.2</div>
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<div>On the one hand, we still could not link RdRp with pSB1C3 so that there still nothing on the plate. We wonder if it was because of the efficiency of ligase or anything. </div>
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<div>On the other hand, we prepared another competent cell,HT115,which included T7 RNAP gene in its genome. It was used as engineering bacteria for expressing dsRdRp. </div>
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<div>Also, considering the biosecurity of E.coli, we decided use yeast as the final transformation target. However, there is no T7 RNAP gene in yeast. So we would design T7 RNAP-pYES2 plasmid to express T7 RNAP. Meanwhile, because we do not know the effect of GAL1(which is one of promoters in pYES2) induced by different concentrations of galactose, we use pYES2 vector to express GFP protein firstly. Through measuring the fluorescence value under the induction of different concentrations of galactose and at different time intervals, we try to determine the GAL1 induced effect. </div>
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<div>7.3</div>
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We transformed RdRp-L4440 into HT115,culturing in 37 ℃. Overnight. And T7 RNAP gene and GFP gene were amplified by PCR(EcoR1-F/Xho1-R). </div>
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<div>7.4</div>
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<div>Today we used IPTG, which was divided into two groups with different concentrations(0.4mmol/ml、0.8mmol/ml), to induce the expression of dsRdRp in HT115 for 5h. Then we collected the bacteria to extract dsRdRp by CTAB. According to the result of AGE, dsRdRp had been expressed in HT115 successfully, even though its concentration was a little bit lower. It was really a good news for us! </div>
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<div>7.5</div>
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<div>We added engineering bacteria with expressed dsRdRp, which was divided into three groups with different concentrations(low、mediate and high), into the fodder of the infected swarms. And another infected swarm was fed normal fodder. Since now, we will obverse the change of population of them, the mortality, and the number of sealed brood and collect data every weeks until we get the obvious result. </div>
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<div>7.7</div>
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<div>Considering we have not gotten RdRp-pSB1C3 yet,we decided to link T7 RNAP gene to pSB1C3 first. So we used specific primers(EcoR1-F/Pst1-R) to synthesize T7 RNAP gene by PCR. </div>
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<div>7.8</div>
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<div>Transformation again! </div>
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<div>7.9</div>
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<div>As usual, picking the positive colonies, PCR and sequencing. We hope everything goes smoothly. </div>
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<div>7.11</div>
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<div>According to the result of sequencing, there was no sample 100 percent matching with T7 RNAP gene ,but some were matching with GFP gene. So we did transformation again and began to link GFP gene with pYES2. </div>
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<div>7.13</div>
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<div>The second sequencing was completely failed because the sequencing company could not get any plasmid. We thought maybe the replication of plasmid in competent cell(DH5α) was inefficient, so we changed another one,T1,bought from Transgene company. Besides, we got GFP-pYES2. </div>
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<div>7.14</div>
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<div>This time we sent plasmid rather than bacteria. Although the concentration of the plasmid was a little bit lower, it was enough to do sequencing. Meanwhile,we transformed GFP-pYES2 into yeast,30℃,culturing 48h. </div>
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<div>7.15</div>
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<div>Considering the lower fidelity of the enzyme used for T7 amplification before, we changed into a better one called KD Plus and restarted to PCR, linking and transformation. </div>
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<div>7.16</div>
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<div>The third sequencing still showed nothing right. We were a little disappointed, but we exactly knew that failure was a normal phenomenon in the lab. </div>
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<div>7.18</div>
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<div>Eventually, we got the matching sample after using KD Plus. Immediately, we began to do double enzyme digestion(EcoR1/Xho1、EcoR1/Pst1). Besides, we began to use galactose with different concentrations(2%,0.1%,0.02%) to induce the expression of GFP and measure the fluorescence value at different concentrations and time intervals. </div>
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<div>7.19</div>
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<div>After gel recovery, we linked our target fragments to relative vectors with T4 ligase, 4℃,overnight. </div>
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<div>Also, we began to make the diagrams of the fluorescence value at different concentrations and time intervals. </div>
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<div>Meanwhile, we collected data about the index of the condition of swarms again, which was used to analyze the effect of dsRdRp by Excel later. </div>
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<div>7.20</div>
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<div>Transformation, plate coating,37℃, overnight. </div>
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<div>7.21</div>
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<div>Picking the positive colonies, PCR detection, and then plasmid extraction. It was smooth! So, we got T7 RNAP-pYES2 and T7 RNAP-pSB1C3 successfully. We stored them in -20℃. </div>
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<div>7.23</div>
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<div>Today we went to observe the condition of swarms, and it was happy to see that the experimental groups turned to a healthier development comparing with control group. It meant that using dsRdRp expressed in E.coli to prevent and cure CSBV was working. Next, we would continue to collect more data until we draw the scientific conclusion. </div>
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<div>7.26</div>
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<div>With the development of our project, we gradually have realized that even if using yeast can solve the problem of biosecurity, there are still other troubles, such as less expression of dsRdRp in yeast, easier to loss plasmids in yeast and harder to digest the cytoderm of yeast for Chinese honeybees. </div>
+
<div>So we need a better plan to deal with these to make a more practical production. That was what we would consider deeply in future work. </div>
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<div>7.27</div>
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<div>Today we decided to constract RdRp-pSB1C3 again, because we thought T7 RNAP-pSB1C3 may be not a new part any more. So, we did linking. We decided if it is failed just like before this time. We had to change T4 into a faster ligase. </div>
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<div>7.29</div>
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<div>As predicted, there was still nothing on the plate.(please tell us why you cannot grow out, bacteria!) </div>
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<div>8.1</div>
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<div>We got the preliminary result of index of swarms. Next few days we would detect the expression quantity of CSBV in offspring. </div>
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<div>8.2</div>
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<div>We made the figure of the effect of dsRdRp on the number of sac-like larvae. It showed that the number of infected larvae which were fed with HT115-dsRdRp in mediate and high concentration was remarkably less than the control group. </div>
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<div>8.5</div>
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<div>Other two figures were made out, which showed the effect of dsRdRp on the number of sealed brood and the population of a colony respectively. They demonstrated the similar conclusion. </div>
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<div>8.8</div>
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<div>We detected the CSBV-carried rate of offspring by RT-PCR. After AGE, it showed that the CSBV-carried rate of first and second filial generation was 30% and 20% respectively, which was obviously declined. </div>
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<div>8.12</div>
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<div>We detected the expression quantity of CSBV in offspring by RT-qPCR. We found with the decreasing of CSBV. The expression quantity of RdRp gene declined either, which meant that dsRdRp really could inhibit the replication of CSBV. </div>
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<div>Last final month</div>
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<div>Even though we were succeed in using dsRdRp expressed in proeukaryotic system to prevent and cure CSBV, we still had to take care of some problem we met. So next stage we will try to constract another plasmid with suicide gene to control the concentration of engineering bacteria. Further more, we want to use CRISPR-Cas9 system to make RdRp gene inserted into the genome of E.coli. So that we can solve the problem of biosecurity. </div>
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<div>Q: Our project is to create a gene medicine that can inhibit viral replication and add E. coli bacteria to the syrup to feed bees.It will use bees’ habits of feeding each other to achieve the effect of prevention and treatment of disease.Then we want to know whether the E. coli we add will have effects on honey quality and safety ? </div>
 +
<div>A: Actually, unprocessed honey contains various active microbes, such as yeast, E. coli and other bacteria. So there is a specified index for honey products. But our production of honey bee is essentially non-pasteurized. First, because the honey itself contains a certain amount of lysozyme, it has a bactericidal effect. Second, the quality honey which is sterilized will decline. In addition, E. coli is not the dominant bacteria in honey, so basically you can not consider security issues. </div>
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<div>Q: If we made gene medicine products, compared with traditional chemical drugs in the market what are our competitive advantages? </div>
 +
<div>A: Your generic drugs can effectively treat CSBV and has small food safety risks to human as opposed to the traditional hazards of drugs on security issues. If it is put into the market, it will certainly have a incomparable advantages with other drugs. But you have to take into account the cost and the use of generic drugs. Because to the beekeepers, what they pursue are economic benefits. So if you can effectively solve these problems, it will be promising. </div>
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<div>Q: How Chinese bee population develops in China how? </div>
 +
<div>A: Nowadays most bees Chinese beekeepers raise are Italian bees. Because Italian honey bee produce high volume honeey and has relatively cheap price to have a higher economic efficiency. While the population of Chinese bees is relatively small and product less honey.So people seldom farm them.These factors slowly caused the population of Italian bee  rapidly expanding.However, the relative reduction was in Chinese bees population. </div>
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<div>Education这个是标题,放大,居中</div>
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<img src=' https://static.igem.org/mediawiki/2015/8/85/FAFU-CHINA_Education_%281%29.png'>
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<img src=' https://static.igem.org/mediawiki/2015/3/3d/FAFU-CHINA_Education_%282%29.png'>
  
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<div>Philosophy: </div>
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<div>Play is a way of being, a way of learning, and a way of doing science. </div>
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<div>Play is the most fundamental and best way of learning. </div>
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<div>Description: </div>
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<div>To remove the barrier between science and normal people’s life, It is our responsibility to lead people into the wonderland of science. This is a lofty ideal, and thousands of people in many fields have already been working for it for years. But this time, we need some innovations, perhaps some funs too. </div>
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<div>Play is not only a simple process. We believe that play is actually a way of being, a way of learning, a way of doing science. So now If u ever watched the TED of Beau Lotto .  You’ll know that play provides everything you need in oder to be a scientist, and that is what motivates us. If we add rules to play, we have a game which is actually what project is. And who can be better than children to play? Then we tried to spread the idea that everyone has the potential to be scientist as long as being offered an opportunity. Instead of giving a dull lesson about biology, this year FAFU-China decided to teach children how to play correctly, how to play with principles from science, and finally they will find their own way to science. </div>
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<div>We cooperated with a semi-profit social organization Fanshu Park. Part of the reason is that they are very experienced with holding activities for children. But most important of all, we actually have a common philosophy——Playing is the best way of learning. Over the past 4 years, Fanshu Park has successfully explored a new field in Fuzhou city and organized a bunch of children and parents on it’s back. They can definitely teach us how to play with kids and give us some lessons. But we were not simply trying to teach children something. We aimed to inspire their interest in science, and make it clear that they all have a talent of doing science, for they all have a talent of playing and learning. </div>
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<div>Fanshu Park gave us a few training so that we know how to deal with kids, besides they helped us organized ten children and provided us an activity space and facilities needed. </div>
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<div>In 28th of August, we held an half-day activity. During the activity, we taught them everything we know about honeybees, and they did show a great interest in the small charming creature.</div>
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<div>We taught them the structure of honeybees and they were required to use a way they want to show us what they have learned. Some kids tried to draw a picture of honeybee and some even tried to made a shape of honeybee by using plasticene. </div>
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<div>We also taught them the difference between real honey and fakes, so that in future they won’t make a terrible purchase. This part may be a bit dull for kids, but when they were required to distinguish out real honey from fakes on their own, it seemed rather practical instead. </div>
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<div>To illustrate that everyone has a potential of being a scientist, or a engineer, we helped them to design their own project. We helped children to solve their question on their own. Why will the honeybees die after biting a person? What is the relationship between honeybees and bumblebees? Something like that. The process of doing their project is more like a game, but we tried to add some rules in this game. We told them that they need four basic different sections to do their project, an objective, a procedure, an expectancy, and a discussion. The objective says what is the question? and why. The procedure tells you how you are going to solve the question. Expectancy is what do you think the answer for the question would be. And the discussion is, who cares? </div>
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<div>We successfully taught them the how to play correctly and scientifically by doing this way. And we believe that in their future, the principle of playing will have a long-lasting effect in many aspects of their life. </div>
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<div>Interview 这个是标题,放大,居中</div>
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<img src=' https://static.igem.org/mediawiki/2015/7/7f/FAFU-CHINA_interview.png'>
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<div>Professor  Susong Kun:He was awarded Special Economic Animals (including Silkworm, Honeybees) PhD by Zhejiang University . </div>
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<div>Now he is the vice president of bee faculty in Fujian Agriculture and Forestry University and he is Professor, doctoral tutor; positions bee scientist of modern industrial technology system , "Minjiang scholar" Professor; Deputy Secretary-General of China Institute of beekeeping, executive director of China Institute of beekeeping bee biology,deputy director of the professional Committee of three bee breeding, vice president and the Secretary-General of apiculture Zhejiang Association. He Mainly engaged in research work of bee genetics and breeding, behavior and molecular biology and other fields. </div>
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<div>When we met professor Su we exhaustively introduced igem and our team to him. Then we told him about the project and the process of experiment. Next we started the interview. </div>
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<div>Q:According to reports, the number of bees is now declining every year.But we do not know the accurate reasons for it.We would like to ask your views on this matter, as well as the impact on the apiculture in China? </div>
 +
<div>A:Yes, this problem is more serious in Europe and America. American  bee colonies began baffling death with a large quantity in 2006, which was terrible for beekeepers. Europe also has a similar situation. But for China, the problem is not that serious. The reason may be the unique Chinese bees followed by domestic beekeeping long history and rich experience. Meanwhile beekeeping has also imposed a fine management. These factors make China has not been a big impact. </div>
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<div>Q:OK,please tell us your opinions about what results in this situation? </div>
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<div>A:The reason for this problem is unknow , I think the reason is multifaceted and comprehensive. Such as environmental factors, electromagnetic, viruses, pesticides, etc., it is a common effect of these factors make reduction in the number of bees. Where a large number of use of pesticides will be a very important affecting factor. </div>
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 +
<div>Q:We aim to cure Sacbrood disease which is caused by Chinese Sacbrood Virus. In recent years, This disease has been controlled under a certain level in some ways . What is the traditional method we have to control this disease and what are the advantages of our technology? </div>
 +
<div>A:In early times this virus is very serious indeed, resulting in enormous loss of bees . And this virus is very hard to be cured. I have been to bee farm in Wuyi Mountain , where the honeybees are infected by CSBV. And only 2 boxes in 100 boxes of bees survived after last epidemic outbreaks , resulting in heavy losses to beekeepers. But beekeepers have trained that two boxes of bees from the perspective of disease resistance, thanks to resistance to disease, and that two boxes of bees now develop into hundreds of boxes. The RNA-interference is an innovational idea , if you succeess,it will be a great news to all beekeepers in China. Oxytetracycline is the most widely used medicine in China for it’s cheap and effective, but it can not be guaranteed that there will be no infection. And Oxytetracycline is also harmful to human beings. So this medicine is urgently needed to be replaced. This technique is equivalent to cure from the root , more direct thorough. </div>
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<div>Q:In the experiment, we paid special attention to bio-safety issues. One of the biggest problems is that we used E. coli to be the carrier, but we feared that these E. coli is a potential pathogen, resulting in intestinal infections and other diseases. For this, we want to hear your views and suggestions? </div>
 +
<div>A:E.coli is indeed harmful and you also relates to a transgenic.So security  of products in question must be paid attention to. Suggestion, I think you can pass some security tests to verify. </div>
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<div>Q:In order to solve the security problems, we made two programs. One is turning Prokaryotic expression into eukaryotic expression , replaced with harmless yeast as carrier. Another is that suicide gene is introduced into E. coli. Do you have any ideas or suggestions for our two programs ? </div>
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 +
<div>A:The program of import suicide gene in E. coli ,effect of suicide gene  may not be as good as that in theory, in the end it may not effectively solve the security problems .So it remains to be confirmed,which you need to do experimental test . Yeast program sounds good, but I did not study in this regard, I can not give you any advice. </div>
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<div>Q:Our idea is to make this technology into patents and product, we want to hear your views and suggestions on our industrial prospects of this technology. </div>
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<div>A:Now there is no direct treatment to the virus, if the RNA interference technology is successful, I think the outlook is still very good. But before that there are several issues you need to address, the first one is the safety of the products , this was just been mentioned before. After all, the honey will be marketed, and goes to public. The safety problems must be solved. The second one is the effect of the product, you must reach a certain level of effect. Because now through artificial breeding, we have been able to reduce the harm caused by CSBV, so your products must have a better result. The final prices of product and costs are also important issues, if you can solve these problems, I think it will be a dramatic product in apiculture. </div>
  
  

Revision as of 15:50, 16 September 2015

谷歌Material Design侧边栏特效 - A5源码
Apiculture这个是标题,放大,居中
Q:What is the influence of CSBV to your bee population?
A:This disease outbroke seriously in my bee farm located in Wuyi Mountain. It began from April this year with high Infectiousness and spread fast and strong.This disease is so difficult to cure that it resulted in economic loss.
Q:How do you combat this disease based on past experience?
A:If this disease outbroke more serious in the past , then they could only be used some illicit chemicals to combat, such as oxytetracycline. Most of these drugs are expensive but the effect is good, so it has become a choice for traditional beekeepers. But now with the improvement of beekeeping technologies, as well as taking into account the impact of drugs on product quality .We seldom use the drugs.
Q: What were measures you taking to reduce the loss without drug treatment?
A: Because the disease first breaks out in the general body of the bee larvae but he impact on adult bees are relatively small. Therefore, in the early stages, the hive of pest is more difficult to find. When honeycomb occurrence of disease was more serious on a board , we only could dispose of the pests on that board to prevent the transmission to other bees to reduce losses.
Q: Our project is to create a gene medicine that can inhibit viral replication and add E. coli bacteria to the syrup to feed bees.It will use bees’ habits of feeding each other to achieve the effect of prevention and treatment of disease.Then we want to know whether the E. coli we add will have effects on honey quality and safety ?
A: Actually, unprocessed honey contains various active microbes, such as yeast, E. coli and other bacteria. So there is a specified index for honey products. But our production of honey bee is essentially non-pasteurized. First, because the honey itself contains a certain amount of lysozyme, it has a bactericidal effect. Second, the quality honey which is sterilized will decline. In addition, E. coli is not the dominant bacteria in honey, so basically you can not consider security issues.
Q: If we made gene medicine products, compared with traditional chemical drugs in the market what are our competitive advantages?
A: Your generic drugs can effectively treat CSBV and has small food safety risks to human as opposed to the traditional hazards of drugs on security issues. If it is put into the market, it will certainly have a incomparable advantages with other drugs. But you have to take into account the cost and the use of generic drugs. Because to the beekeepers, what they pursue are economic benefits. So if you can effectively solve these problems, it will be promising.
Q: How Chinese bee population develops in China how?
A: Nowadays most bees Chinese beekeepers raise are Italian bees. Because Italian honey bee produce high volume honeey and has relatively cheap price to have a higher economic efficiency. While the population of Chinese bees is relatively small and product less honey.So people seldom farm them.These factors slowly caused the population of Italian bee rapidly expanding.However, the relative reduction was in Chinese bees population.
Education这个是标题,放大,居中
Philosophy:
Play is a way of being, a way of learning, and a way of doing science.
Play is the most fundamental and best way of learning.
Description:
To remove the barrier between science and normal people’s life, It is our responsibility to lead people into the wonderland of science. This is a lofty ideal, and thousands of people in many fields have already been working for it for years. But this time, we need some innovations, perhaps some funs too.
Play is not only a simple process. We believe that play is actually a way of being, a way of learning, a way of doing science. So now If u ever watched the TED of Beau Lotto . You’ll know that play provides everything you need in oder to be a scientist, and that is what motivates us. If we add rules to play, we have a game which is actually what project is. And who can be better than children to play? Then we tried to spread the idea that everyone has the potential to be scientist as long as being offered an opportunity. Instead of giving a dull lesson about biology, this year FAFU-China decided to teach children how to play correctly, how to play with principles from science, and finally they will find their own way to science.
We cooperated with a semi-profit social organization Fanshu Park. Part of the reason is that they are very experienced with holding activities for children. But most important of all, we actually have a common philosophy——Playing is the best way of learning. Over the past 4 years, Fanshu Park has successfully explored a new field in Fuzhou city and organized a bunch of children and parents on it’s back. They can definitely teach us how to play with kids and give us some lessons. But we were not simply trying to teach children something. We aimed to inspire their interest in science, and make it clear that they all have a talent of doing science, for they all have a talent of playing and learning.
Fanshu Park gave us a few training so that we know how to deal with kids, besides they helped us organized ten children and provided us an activity space and facilities needed.
In 28th of August, we held an half-day activity. During the activity, we taught them everything we know about honeybees, and they did show a great interest in the small charming creature.
We taught them the structure of honeybees and they were required to use a way they want to show us what they have learned. Some kids tried to draw a picture of honeybee and some even tried to made a shape of honeybee by using plasticene.
We also taught them the difference between real honey and fakes, so that in future they won’t make a terrible purchase. This part may be a bit dull for kids, but when they were required to distinguish out real honey from fakes on their own, it seemed rather practical instead.
To illustrate that everyone has a potential of being a scientist, or a engineer, we helped them to design their own project. We helped children to solve their question on their own. Why will the honeybees die after biting a person? What is the relationship between honeybees and bumblebees? Something like that. The process of doing their project is more like a game, but we tried to add some rules in this game. We told them that they need four basic different sections to do their project, an objective, a procedure, an expectancy, and a discussion. The objective says what is the question? and why. The procedure tells you how you are going to solve the question. Expectancy is what do you think the answer for the question would be. And the discussion is, who cares?
We successfully taught them the how to play correctly and scientifically by doing this way. And we believe that in their future, the principle of playing will have a long-lasting effect in many aspects of their life.
Interview 这个是标题,放大,居中
Professor Susong Kun:He was awarded Special Economic Animals (including Silkworm, Honeybees) PhD by Zhejiang University .
Now he is the vice president of bee faculty in Fujian Agriculture and Forestry University and he is Professor, doctoral tutor; positions bee scientist of modern industrial technology system , "Minjiang scholar" Professor; Deputy Secretary-General of China Institute of beekeeping, executive director of China Institute of beekeeping bee biology,deputy director of the professional Committee of three bee breeding, vice president and the Secretary-General of apiculture Zhejiang Association. He Mainly engaged in research work of bee genetics and breeding, behavior and molecular biology and other fields.
When we met professor Su we exhaustively introduced igem and our team to him. Then we told him about the project and the process of experiment. Next we started the interview.
Q:According to reports, the number of bees is now declining every year.But we do not know the accurate reasons for it.We would like to ask your views on this matter, as well as the impact on the apiculture in China?
A:Yes, this problem is more serious in Europe and America. American bee colonies began baffling death with a large quantity in 2006, which was terrible for beekeepers. Europe also has a similar situation. But for China, the problem is not that serious. The reason may be the unique Chinese bees followed by domestic beekeeping long history and rich experience. Meanwhile beekeeping has also imposed a fine management. These factors make China has not been a big impact.
Q:OK,please tell us your opinions about what results in this situation?
A:The reason for this problem is unknow , I think the reason is multifaceted and comprehensive. Such as environmental factors, electromagnetic, viruses, pesticides, etc., it is a common effect of these factors make reduction in the number of bees. Where a large number of use of pesticides will be a very important affecting factor.
Q:We aim to cure Sacbrood disease which is caused by Chinese Sacbrood Virus. In recent years, This disease has been controlled under a certain level in some ways . What is the traditional method we have to control this disease and what are the advantages of our technology?
A:In early times this virus is very serious indeed, resulting in enormous loss of bees . And this virus is very hard to be cured. I have been to bee farm in Wuyi Mountain , where the honeybees are infected by CSBV. And only 2 boxes in 100 boxes of bees survived after last epidemic outbreaks , resulting in heavy losses to beekeepers. But beekeepers have trained that two boxes of bees from the perspective of disease resistance, thanks to resistance to disease, and that two boxes of bees now develop into hundreds of boxes. The RNA-interference is an innovational idea , if you succeess,it will be a great news to all beekeepers in China. Oxytetracycline is the most widely used medicine in China for it’s cheap and effective, but it can not be guaranteed that there will be no infection. And Oxytetracycline is also harmful to human beings. So this medicine is urgently needed to be replaced. This technique is equivalent to cure from the root , more direct thorough.
Q:In the experiment, we paid special attention to bio-safety issues. One of the biggest problems is that we used E. coli to be the carrier, but we feared that these E. coli is a potential pathogen, resulting in intestinal infections and other diseases. For this, we want to hear your views and suggestions?
A:E.coli is indeed harmful and you also relates to a transgenic.So security of products in question must be paid attention to. Suggestion, I think you can pass some security tests to verify.
Q:In order to solve the security problems, we made two programs. One is turning Prokaryotic expression into eukaryotic expression , replaced with harmless yeast as carrier. Another is that suicide gene is introduced into E. coli. Do you have any ideas or suggestions for our two programs ?
A:The program of import suicide gene in E. coli ,effect of suicide gene may not be as good as that in theory, in the end it may not effectively solve the security problems .So it remains to be confirmed,which you need to do experimental test . Yeast program sounds good, but I did not study in this regard, I can not give you any advice.
Q:Our idea is to make this technology into patents and product, we want to hear your views and suggestions on our industrial prospects of this technology.
A:Now there is no direct treatment to the virus, if the RNA interference technology is successful, I think the outlook is still very good. But before that there are several issues you need to address, the first one is the safety of the products , this was just been mentioned before. After all, the honey will be marketed, and goes to public. The safety problems must be solved. The second one is the effect of the product, you must reach a certain level of effect. Because now through artificial breeding, we have been able to reduce the harm caused by CSBV, so your products must have a better result. The final prices of product and costs are also important issues, if you can solve these problems, I think it will be a dramatic product in apiculture.

Communication Design

Communication design is a mixed discipline between design and information-development which is concerned with how media intermission such as printed, crafted, electronic media or presentations communicate with people.

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Communication Design

Communication design is a mixed discipline between design and information-development which is concerned with how media intermission such as printed, crafted, electronic media or presentations communicate with people.

Communication Design

Communication design is a mixed discipline between design and information-development which is concerned with how media intermission such as printed, crafted, electronic media or presentations communicate with people.

Communication Design

Communication Design

Communication design is a mixed discipline between design and information-development which is concerned with how media intermission such as printed, crafted, electronic media or presentations communicate with people.