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Latest revision as of 19:38, 18 September 2015

Team:BNU-CHINA - 2015.igem.org


Our Parts

iGEM 2015 BNU-CHINA Standard Biological Parts
BiobrickNameDescriptionLength
BBa_K1660000 K206000 (pBAD promoter) + B0034 + bace16 Encodes a serine protease in Bacillus nematocida target essential intestinal proteins and kill nematode under the control of pBAD promoter. 1305
BBa_K1660001 K206000 (pBAD promoter) + B0034 + pBAD + rMpL Encodes a nematotoxic lectin from the parasol mushroom
( Macrolepiota procera) under the control of pBAD promoter.
582
BBa_K1660002 J23100 + B0032 + l-limonene synthase Encodes l-limonene synthase to produce limonene in E. coli under a constitutive promoter. 1694
BBa_K1660003 J23100 + B0032 + d-limonene synthase Encodes d-limonene synthase to produce limonene in E. coli under a constitutive promoter. 1883
BBa_K1660004 pcyA + ho1 (BBa_I15008, BBa_I15009) Synthesizes PCB, which can form chromophore with Cph8. 1585
BBa_K1660005 PompC + rfp Expresses RFP under the OmpC promoter. 978
BBa_K1660006 J23100 + cph8 Expresses Cph1-EnvZ complex as a light sensor. 2299
BBa_K1660007 PompC + 6N + gp35 Expresses gp35 integrase with OmpC promoter. 1773
BBa_K1660008 J23100 + bace16 Encodes a serine protease in Bacillus nematocida target essential intestinal proteins and kill nematode with a constitutive promoter. 1210
BBa_K1660009 J23100 + rMpL Encodes a nematotoxic lectin from the parasol mushroom
( Macrolepiota procera) with a constitutive promoter.
487
BBa_K1660010 Bidirectional transcriptional circuit (Terminator + RFP + RBS + attB + J23110 + attP + RBS + GFP + Terminator) Recombined locus of attB and attP into the flanking sequences of a constitutive promotor 1897

Our Judging Criteria

  1. We have registered our team, spent a full summer, and plan to enjoy a feast of knowledge and culture at the Giant Jamboree.
  2. We have successfully completed and submitted the iGEM 2015 Judging form.
  3. Our story of Synthetic Intelligent Ranger E. coli for Nematodes (SIRENS) are described using the iGEM wiki. And we have designed, built and characterized several new functional standard biobricks including:
  4. Parts
  5. We made a poster and presentation, which is going to be presented at the Giant Jamboree.
  6. The attributions of our work is clear, and we have distinguished the work done by us and work down by others in the wiki.
  1. We have designed, built and experimentally validated six new functional biobricks (BBa_K1660000, BBa_K1660001, BBa_K1660002, and BBa_K1660003, BBa_K1660008, BBa_K1660009), and submitted characterization data to the Registry of Standard Biological Parts.
  2. Six new parts that we designed have been submitted to the Registry of Standard Biological Parts.
  3. Safety
    1. Laboratory safety: All of our laboratory members have receieved safety training before. We must fill out the log sheet of the laboratory safety after the inspection tour.
    2. Environmental safety: Firstly, we have evaluated the project feasibility and its relating security issue. In order to ensure that “Sirens” will work efficiently in the condition as we expect, we construct a photoinduced reverse promoter which can change direction to regulate the period of toxin release. In addition, a suicide switch designed for E. coli depending on quorum sensing so that after E.coli attracts and kills the nematodes, it will not spread into the environment. Also, we built a device which can restrict the spread of the nematodes.
    3. Proper usage of pesticide: We did a survey aiming at the application of pesticide in Ceyu village, Hebei province. The investigation object includes government staff, pesticide individual dealers, farmers and so on.
  1. Policy & Practice:
    1. Interview the specialist of nematodes research to improve our project: We interviewed prof. Liu Xingzhong and communicated with him to improve our design. We improved the method of verifying if compounds can attract nematodes under the suggestion of prof. Liu
    2. Consult specialist about laws and regulations: We interviewed Dr. Yan Houfu, from school of law, Beijing Normal University. We consulted him about the laws and regulation of bio-safety in China, the laws about protection of peasants’ rights and interests, governmental measures about popularizing agricultural technology.
    3. Survey about safety mechanism in different teams: We sent an e-mail to different teams in this track to get a general knowledge about safety mechanism in each team. We also summarized how to establish a safety mechanism according to the replies from different teams.
    4. The research in the country of Heibei province: We did a research which lasted 2 days in Jingxian in Heibei province. We interviewed some rural safety officers, pesticide sellers and farmers in order to know whether agricultural workers at the local level have knowledge about the nematodes.
    5. Soil nematodes screening and proposal: We tested the soil sample collecting from Hebei Province during our survey. We identified and counted the nematodes in the sample. We also drafted a proposal to Chinese government for precaution the nematodes according to the results of our survey.
    6. Voluntary educational service: We provided rural schools students with voluntary educational service during the survey and scientific propaganda, aiming at offering a scientific perspective for students there through our words and deeds.
    7. Conference: We took part in NCTU and CCiC conferences as well as gave a presentation in these conferences. We also improved our project during our communication in the conferences.
    8. Communication: We communicated and exchanged our ideas with BIT-CHINA, FAFU-China and ZJU-China. Through the collaboration with other teams, we all got improvement.
    9. Public scientific propaganda: we established our weChat public platform, gave scientific lectures for rural schools students and organized an open day of our BNU lab. It gave people a better understanding about our project.
  2. We offered BIT-China meticulous help in the expression of the membrane protein, NhaA and NhaB, and the modeling.
  3. We have characterized a previously existing BioBrick Part——the light sensor system (BBa_I15008, BBa_I15009, BBa_K592000 and BBa_R0082), and constructed a new biobrick BBa_K1660005, see the improvement page for more information.
  4. We have demonstrated a functional prototype of our project. We built a device based on the experiment and the data from modeling and wet lab. And we simulated the way of using our device in the laboratory.