Team:Kyoto/Discussion

• 
• Project
  • Description
  • Design
  　　　　
  • Results
  　　　　　　　　　
  • Demonstration
  • Discussion
• Modeling
• Lab Work
  • Notebook
  • Materials&Methods
  • Special Methods
  • Safety
• Parts
  • Basic Parts
  • Composite Parts
  • Improving parts
  • Parts Collection
• Human Practices
  • Human Practice/Silver
  • Integrated Human Practice/Gold
  • Collaborations
• Team
  • Members
  • Attributions

仲里　一応　訳中

• 1)Summary of our research
• 2)Performance and application of "Swallowmyces cerevisiae"
• 3)
• 4)

1)Summary of our research

We worked on the construction of the yeast “Swallowmyces cerevisiae” which absorbs NaCl from solution and adjusts the salt concentration of the solution. We created a gene-disrupted strain designed to make Na+ inside the cell, expressed the chaperone and produced the compatible solute to reduce the damage the cell receives from high salt concentration. And, we added a variety of genes for taking Na+ into the vacuole to the collection of BioBrick parts. With the help of mathematical modeling optimizing the system, eventually we produced a yeast that retains averagely 80mM of Na+ into the cell. Also, we performed the model experiment that this device really absorbed Na+ from all over the solution and demonstrated the decrease of Na+ in solution by it.

2)Performance and application of "Swallowmyces cerevisiae"

Our early purpose was to assist the operation of other devices by lowering the salt concentration of the aqueous solution in the test tube in this device.

Our pilot experiments showed the salt concentration in a solution of 1000mM of the solution and 500mM, differ in the repertory of proteins interacting nonspecifically with GFP.As can be inferred from this example, if we really aim the effect of helping functions of other devices, it is worth working on the desalination from solution of NaCl concentration 1000mM with a little up from the current salt concentration range. The current system is still the first prototype, and it seems to be necessary to add various improvements after this.

There are several possible suggestions for concrete improvement.

First of all, it will be necessary to raise the halotolerance of yeast. Since wild-type yeast has multiple pumps exhausting Na+ outside, yeast can grow even in the solution of NaCl concentration 1000mM (inhibition of growth is seen). However, in order to store Na+ inside of yeast, it is necessary to turn off these pumps. As seen in this study, in such strains, yeast becomes sensitive even to solution of very low NaCl concentrations. It is necessary to improve so that such susceptible yeast can grow with maintaining the ability to take Na + from the external solution, even if the salt concentration is higher than usual.

3)

4)

Reference

• [1]
• [2]
• [3]
• [4]
• [5]
• [6]
• [7]
• [8]