| Project/Area Number |
16550141
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Chemistry related to living body
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| Research Institution | UNIVERSITY OF TOYAMA |
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Principal Investigator |
KANAMORI Hiroshi UNIVERSITY OF TOYAMA, FACULTY OF SCIENCE, PROFESSOR, 理学部, 教授 (00019001)
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| Co-Investigator(Kenkyū-buntansha) |
AIZAWA Sen-ichi UNIVERSITY OF TOYAMA, FACULTY OF ENGINEERING, ASSOCIATE PROFESSOR, 工学部, 助教授 (60231099)
MICHIBATA Hitoshi HIROSHIMA UNIVERSITY, GRADUATE SCHOOL OF SCIENCE, PROFESSOR, 大学院・理学研究科, 教授 (00111740)
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| Project Period (FY) |
2004 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥3,000,000 (Direct Cost: ¥3,000,000)
Fiscal Year 2005: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 2004: ¥1,900,000 (Direct Cost: ¥1,900,000)
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| Keywords | tunicate / vanadium / redox / タンパク / 錯体 |
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| Research Abstract |
Tunicates living in sea accumulate vanadium(V) ion from sea water and stores in their blood cells as vanadium(III) ion. However, this unique mechanism for vanadium accumulation and reduction has not been explored. In this project, we have obtained the basic knowledge concerning the vanadium in tunicates blood cells in order to explore the mechanism of accumulation and reduction of vanadium, using vanadium-binding protein and its small molecular model compounds.
1.Reduction of vanadium(V) to vanadium(IV) by NADPH : It has been suggested that NADPH might be involved in the reduction of vanadium(V) by tunicates. We have already reported NADPH can reduce vanadium(V) to vanadium(IV) in the existence of edta. In this project, we have studied whether amino acids and peptide can act as a promoter of the reduction of vanadium(V) by NADPH. We have found that amino acids and peptides that can bind to vanadium as a tridentate ligand can promote the reduction while those that can bind to vanadium only as a bidentate fashion can not.
2.Reduction of vanadium(IV) to vanadium(III) by thiol : We have shown that cystein methyl ester can promote the reduction of vanadium(IV) to vanadium(III) in the presence of edta. We have found that nta, glycylhistidine, and glycylaspartic acid can also promote the reduction of vanadium(IV) though partly. Lysine residue, which is rich in vanadium-binding protein, does not seem to relate to the reduction of vandium(V) and (IV).
3.Oxidation of vanadium-binding protein by vanadium(III) : In order to examine whether the dithio bond can be reduced by vanadium(III), we examined the reaction between vanadium(III) and cystine or glutathione (oxidiazed form) as a model compound of vanadium-binding protein. We found that the dithio bond in the model compounds was cleaved by vanadium(III). The reduction of vanadium-binding protein by vanadium(III) is now under investigation.
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