| Project/Area Number |
25630372
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| Research Category |
Grant-in-Aid for Challenging Exploratory Research
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| Allocation Type | Multi-year Fund |
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| Research Field |
Biofunction/Bioprocess
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| Research Institution | Tokyo University of Agriculture and Technology |
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Principal Investigator |
TANAKA Tsuyoshi 東京農工大学, 工学(系)研究科(研究院), 教授 (20345333)
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| Project Period (FY) |
2013-04-01 – 2015-03-31
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| Project Status |
Completed (Fiscal Year 2014)
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| Budget Amount *help |
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2014: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2013: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
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| Keywords | オルガネラ回収 / 微細藻類 / 細胞破砕 / バイオディーゼル / 顕微ラマン分光法 / 微細孔アレイ / 単一細胞ライブイメージング / オルガネラ / 中性脂質 / 葉緑体 / 有用珪藻 |
|---|
| Outline of Final Research Achievements |
The cell disruption method to extract intact organelle from the cells, including hard plant cells, was developed in this study. The diatom species were used as model samples, and captured on the micro-cavity array, followed by addition of aspiration pressure. Another strategy for cell disruption is chemical method, such as acidic treatments. As comparing these two, an acidic treatment was demonstrated to be better way to achieve efficient and benign cell disruption. Furthermore, live imaging system for the micro-cavity array was developed, and further analysis and characterization were carried out using Raman microscope on the imaging system. These techniques can contribute to development of a quantitative and efficient cell disruption method.
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