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Revision as of 16:41, 17 October 2018
Collaboration with DUOT
Our two teams have held a meeting to discuss some question about the whole project.
During the meeting, we solved some problems of our projects.
Question from NEU
Quiz1:The idea of your team is very novel and has important practical value. But as a medicine that enters the
human body, how to control it does not harm the intestinal flora?
Answer: We have reviewed a group quantity control system of Imperial College of Science and Technology in 2016.
We have made improvements in light of our own situation. Simply put, the concentration of signal substances
controlled by the bacteria itself controls the opening and closing of the suicide system, thereby regulating the
number of bacteria.
Quiz2:Your final product is a bacterial preparation. There are great potential threats to the environment. Have
you thought about any suicide mechanism? We are doing a cold lethal system, and if you are interested we can
cooperate.
Answer:Thank you very much for your proposal. We also checked the information and found the Blu-ray lethal
system, etc., but I am still very happy to work with you. You can provide our plasmids. We can help you to
characterize and provide relevant data.
Question from DUOT
Quiz1: As a system for detecting lactic acid, what are the advantages of your products with lactic acid detection
products on the market?
Answer: Compared with the normal detection of lactic acid products, we have more use of biological related
technologies. By referring to some of the design experience of the 2015-year team at the ETH Zurich, we used the
group sensing system of E. coli and used fiber optic circuitry for detection,. It is low cost and ease of use.
Quiz2: How do you ensure that E. coli in your system does not pollute the fermentation industry? Answer: We intend to paste our product into a portable device, and the part that touches the fermentation liquid is only the probe. The E. coli inside the unit does not pollute the fermentation broth.
Collaboration with SCAU-China
Our team conducted an exchange discussion with NEU_China_B in August 2018. This meeting is mainly to share the
two team's projects main content and two teams each encountered in the experiment problem. The Q&A are as follow.
NEU_China_B: How do you ensure that the integrative vector in transformants will not lose?
SCAU-China: The integrative vector we used is pFQ20 provided by the Qingdao Institute of Bioenergy and Bioprocess
Technology, Chinese Academy of Sciences. The homology arms in integrative vector for homologous recombination allows
the target genes to be stably transferred into the genome of Microcoleus vaginatus. It has been verified through our
experiment results.
SCAU-China: How to match the concentration of AI-2 expressed by the first plasmid pCFDuet-1 with the GFP
concentration expressed by pet28a(+).
NEU_China_B: Our experiment was to release the AI-2 signal molecule after the pCFDuet-1 expression plasmid
induction of lactic acid concentration, and AI-2 signal molecule can inhibit the lldr sequence on the second plasmid
pet28a(+).
The lldr sequence is capable of producing GFP-deterring proteins. In the experiment, we verified that two plasmid
copies were more similar, and that the o1o2 sequence could be started normally when the lactic acid concentration was
lower (less than 1m mol), and then the GFP gene could be produced fluorescent signal.
Therefore, the expression of two plasmids is more matched, and the experimental results are not affected in this
project.
Collaboration with Fujian normal university
1. Online meeting.
Our two teams focused on the problems encountered in the experiment, including some enzymes that we did not use like Gibson enzymes. Our team mainly raised the problem of the actual operation of importing two plasmids into bacteria. In response to this problem, the students of Fujian Normal University gave us a solution. They tell us that we need to import the first plasmid and then the second plasmid. In addition, they also provide us with some experience about fermentation industry.
2. Plasmid construction
We have two teams in the construction of the plasmid also carried out a certain level of cooperation. The students of Fujian Normal University helped us to construct plasmid p-LsrA-GFP. We helped them to measure the fluorescence value of proU-GFP and construct the plasmid proU-GFP. (http://parts.igem.org/Part:BBa_K2570020)
3. Visiting beer factory
Under the guidance of the students of Fujian Normal University, we have visited the beer factory inside the college to learn about the whole production line of beer production and the function of each step. In the course of the visit, we retrieved a portion of the beer fermentation liquid to observe the experiment, and used chemical methods to detect the lactic acid content in the fermentation process.
(photos of fermentation tanks in FJNU)