Project/Area Number |
11440239
|
Research Category |
Grant-in-Aid for Scientific Research (B).
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
植物生理
|
Research Institution | HIMEJI INSTITUTE OF TECHNOLOGY |
Principal Investigator |
SONOBE Seiji FACULTY OF SCIENCE, HIMEJI INSTITUTE OF TECHNOLOGY ASSOCIATE PROFESSOR, 理学部, 助教授 (30197024)
|
Project Period (FY) |
1999 – 2000
|
Project Status |
Completed (Fiscal Year 2000)
|
Budget Amount *help |
¥14,000,000 (Direct Cost: ¥14,000,000)
Fiscal Year 2000: ¥6,700,000 (Direct Cost: ¥6,700,000)
Fiscal Year 1999: ¥7,300,000 (Direct Cost: ¥7,300,000)
|
Keywords | plant cell / cytokinesis / phragmoplast / golgi apparatus / cell plate / microtubules / motor protein / tobacco BY-2 cells / タパコBY-2細胞 / ゴルジ小胞 / 細胞周期 / キシログルカン |
Research Abstract |
Isolation of golgi derived vesicles from tobacco BY-2 cells which had been synchronized in mitotic phase was carried out. The criteria for golgi derived vesicles were, 1) the diameter in electron microscopy was about 0.1 um, 2) it contained xyloglucan. As a result, we obtained a membrane fraction which contained golgi derived vesicles. Because golgi derived vesicles were thought to be transfered during cell plate formation in MT-dependent manner, we examined the interaction between isolated vesicles and MTs. About 30% of vescles was found to bind to MTs in vitro. In vitro motility assay too test motor activity which was predicted to exist on the vesicles did not support MT translocation on the glass to which isolated vesicles were attached. To investigate fusion activity of the isolated vesicles, they were added to the cytoplasmic extract prepared from BY-2 cells synchronized at anaphase. Aggregates which were stained with anilin blue were observed, although the frequency was very low. We are now trying to construct an advanced system by improving the system obtained in this project for investigation on cell plate formation in plant cells.
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