| Project/Area Number |
02660110
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
応用微生物学・発酵学
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| Research Institution | The University of Tokyo |
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Principal Investigator |
YOSHIMURA Etsuro The Univ. of Tokyo., Agric., Instructor, 農学部, 助手 (10130303)
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| Co-Investigator(Kenkyū-buntansha) |
OHKUBO Akira The Univ. of Tokyo., Agric., Asoc. prof., 農学部, 助教授 (20111479)
YAMAZAKI Sunao The Univ. of Tokyo., Agric., Professor, 農学部, 教授 (00011982)
戸田 昭三 東京大学, 農学部, 教授 (40011845)
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| Project Period (FY) |
1990 – 1991
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| Project Status |
Completed (Fiscal Year 1991)
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| Budget Amount *help |
¥1,900,000 (Direct Cost: ¥1,900,000)
Fiscal Year 1991: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 1990: ¥1,300,000 (Direct Cost: ¥1,300,000)
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| Keywords | Cadmium / Fission yeast / Phytochelatin / Cadystin |
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| Research Abstract |
1. Development of high sensitive determination of PC Phytochelatins were determined by such a way that each PC was separated by HPLC with ODS column, derivatized with DTNB and determined by absorption at 412 nm. It enables to determine glutathione and PCs about 15 sin per a sample.
2. Change in PC and its related compounds in culturing Concentrations of PC and its related compounds were measured when S. pombe cells were cultured in the absence of Cd. In the early culturing period the level of PC2 is increased with a concomitant decrease in glutathione. These indicate that PC is synthesized via glutathione.
3. Purification of PC-synthsizing enzyme
A crude extract solution was prepared from S. poebe cells which were cultured in the absence of Cd. The activity was purified by ammonium sulfate fractionation and hydrophobic chromatography. The fraction containing the synthetic enzyme was applied to a hydroxy appatite column. The activity was, however, lost. In addition the enzyme was found to be very unstable so that a straging method which prevent the enzyme from inactivating is now still on investigation.
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