| Project/Area Number |
04304049
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| Research Category |
Grant-in-Aid for Co-operative Research (A)
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| Allocation Type | Single-year Grants |
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| Research Field |
医学一般
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| Research Institution | Niigata University |
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Principal Investigator |
SATAKE Mei Niigata University, Brain Research Institute, Professor, 脳研究所, 教授 (70018589)
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| Co-Investigator(Kenkyū-buntansha) |
YAMASHITA Mitsuji Shizuoka University, Faculty of Engineering, Associate Professor, 工学部, 助教授 (60110748)
SETO Haruo Tokyo University, Institute of Modecular and Cellular Science, Professor, 分子細胞生物学研究所, 教授 (10013335)
HAYASHI Akira Kinki University, Faculty of Science and Technology, Professor, 理工学部, 教授 (20088313)
SUGITA Mutsumi Siga University, Faculty of Liberal Arts and Education, Professor, 教育学部, 教授 (20024937)
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| Project Period (FY) |
1992 – 1993
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| Project Status |
Completed (Fiscal Year 1993)
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| Budget Amount *help |
¥8,000,000 (Direct Cost: ¥8,000,000)
Fiscal Year 1993: ¥4,000,000 (Direct Cost: ¥4,000,000)
Fiscal Year 1992: ¥4,000,000 (Direct Cost: ¥4,000,000)
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| Keywords | C-P compounds / Glycolipids / Nervous tissues / Antibiotics / Enzymatic synthesis of C-P bond / Genes / Chemical synthesis of C-P compounds |
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| Research Abstract |
Since Horiguchi and Kandatsu first isolated natural C-P compound, 2-aminoethyl-phosphonate, much work has been carried out in Japan. Theme of the present 2-years project were (1) isolation and identification, (2) tissue distribution, (3) biological activities, (4) biosynthesis and (5) chemical synthesis of the C-P compounds.
Following results were obtaied : (Theme 1) Several new C-P sphingoglycolipids were isolated from protostomia. Their carbohydrate and oligosaccharide structures were different from those of deuterostomia. A glycolipid had one mole each of 2-aminoethylphosphonate (C-P) and phosphoethanolamine (C-O-P) which suggests a way of molecular evolution of sphingoglycolipid species. (Theme 2) antiphosphonoglycocerebroside antisera specifically stain nervous tissues of crustacea. (Theme 3) C-P sphingoglycolipids isorated from Aplysia activated cAMP-dependent protein kinase by binding to the catalytic subunit of the enzyme. (theme 4) Genes of phosphoenolpyruvic acid (PnPy) phosphomutase and PnPy decarboxylase which were key enzymes for the synthesis of fosfomycin were cloned and a gene of p-methylating enzyme for the synthesis of C-P-C bond of bialaphos was cloned. (Theme 5) Oxygen of hemiacetal ring of sugar was replaced by phosphorus by sophisticated methods and many novel C-P compounds were chemically synthesized. Some of them were biologically active.
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