| Project/Area Number |
61470129
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| Research Category |
Grant-in-Aid for General Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Research Field |
発酵・醸造
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| Research Institution | Faculty of Agriculture, The University of Tokyo |
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Principal Investigator |
TAKAGI Masamichi Faculty of Agriculture, The University of Tokyo, 農学部, 助教授 (50018339)
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| Project Period (FY) |
1986 – 1987
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| Project Status |
Completed (Fiscal Year 1987)
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| Budget Amount *help |
¥4,400,000 (Direct Cost: ¥4,400,000)
Fiscal Year 1987: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1986: ¥3,600,000 (Direct Cost: ¥3,600,000)
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| Keywords | Candida maltosa / Saccharomyces cerevisiae / cycloheximide / gene cloning / protein syntesis / ribosome modification / Saccharomyses cerevisiae / リボソーム / 抗生物質耐性 / 耐性化遺伝子 / クローニング |
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| Research Abstract |
1. We isolated a gene designated the RIM-C gene (ribosome-modification by cycloheximide) from the genome of Candida maltosa by using a host-vector system of Sachharomyces cerevisiae, which is sensitive to cycloheximide (CYH). When this gene was introduced to S. cerevisiae, its ribosomes were modified to be resistant to CYH.
2. We determined the nucleotide sequence of DNA region containing the RIM-C gene.
3. By using the dot-hybridization technique, we found that the modified ribosomes did not contain a RNA product of the gene. An RNA product of this gene was found to contain poly(A)-tail. These data indicate that the gene encode a mRNA and not a new species of rRNA.
4. By using the two-dimensional gel electrophoresis, we did not found a new ribosomal protein in the modified ribosomes. It is suggested that the gene does not code for a new ribosomal protein, but codes for a modification enzymes of a component of ribosomes.
5. We determined the transcription strand of the gene and the transcription start-point.
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