| Project/Area Number |
02660079
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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 |
応用生物化学・栄養化学
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| Research Institution | The University of Tokyo (1991)
Saitama University (1990) |
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Principal Investigator |
OHTA Akinori The University of Tokyo, Department of Agriculture Associate Professor., 農学部, 助教授 (30125885)
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| Co-Investigator(Kenkyū-buntansha) |
TAKAGI Masamichi The University of Tokyo, Department of Agriculture Professor., 農学部, 教授 (50018339)
SHIBUYA Isao Saitama University, Department of Biochemistry, Professor., 理学部, 教授 (60013306)
松崎 博 埼玉大学, 理学部, 助手 (80008870)
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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 | Saccharomyces cerevisiae / Phosphatidylserine / Phosphatidylethanolamine / Yeast / Phosphatidylserine synthase / Vacuole / Phospholipid / Biomembrane / Phosphatidylethanolamine / Saccharomyces cerevisiae / Phosphatidylserine synthase / Biomembrane / Phosphatidylinositol |
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| Research Abstract |
(1) Analysis of role of nitrogen-containing phospholipids in yeast cell growth.
(1) Response to various environmental conditions of a yeast mutant that were deficient in phosphatidylserine (PS) synthesis were examined. Even in the presence of choline or ethanolamine which enables the mutant to grow, only 10% cells were viable at mid-stationary phase, judging by Malachite green staining. Sensitivity to high concentration of Ca^<2+>, Zn^<2+>, Mn^<2+>, or basic amino acids was increased. Central vacuoles were not observed by Nomarski optics and fluorescence microscopy of quinacrine-stained cells. These results suggest that PS aynthesis is necessary for the function of intracellular membraneous structures and for cellular adaptation to environmental conditions.
(2) A strain of which chromosomal CHO1 gene that encoded PS synthase was disrupted but that carried it downstream of GAL7 promoter on a centromere plasmid was constructed. When the strain was transferred from a medium with galactose to the one with glucose as a carbon source, the amount of PS was decreased to 0.3% of total phospholipids and that of phosphatidylethanolamine was also decreased, but that of posphatidylinositol was increased up to 47% at 9 hours after C-source change. Increase in culture turbidity was continued for 9 hours after medium change, but the increase in cell number did not continue over 6 hours, when 80% to 90% of cells were unbudded cells. This result suggests that the cessation of PS synthesis blocked entry from G1 to S phase of cell division cycle.
(2) Analysis of upstream region of the CHO1 gene
(1) Expression of a CHO1-lacZ fusion gene was examined after heat shock. Since stimulation of reporter enzyme activity was not observed, role of an HSE-like sequence in 5'-upstream region was not clear.
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