Analyses of secondary metabolism gene promoters activated by combined-culture
| Project/Area Number |
26850044
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| Research Category |
Grant-in-Aid for Young Scientists (B)
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| Allocation Type | Multi-year Fund |
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| Research Field |
Applied microbiology
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| Research Institution | The University of Tokyo |
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Principal Investigator |
ASAMIZU Shumpei 東京大学, 農学生命科学研究科, 助教 (90709057)
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| Project Period (FY) |
2014-04-01 – 2016-03-31
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| Project Status |
Completed (Fiscal Year 2015)
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| Budget Amount *help |
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2015: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2014: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
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| Keywords | 放線菌 / ミコール酸含有細菌 / 二次代謝 / 共培養 / 微生物間相互作用 / 遺伝子プロモーター / 遺伝子発現 / 複合培養 / 二次代謝活性化 / 抗生物質生産 / 細菌間相互作用 / 生合成 |
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| Outline of Final Research Achievements |
Secondary metabolites (SMs) produced by actinomycetes are great resources for therapeutic application. Actinomycetes are suggested to possess more than 20 of cryptic gene clusters for SMs production. Our study focus on co-culture method between actinomycetes and mycolic acid-containing bacteria (MACB), that had been shown to activate the cryptic gene clusters of actinomycetes. We used biosynthetic gene cluster of a ribosomal synthesized peptide antibiotic as a model to elucidate the mechanism of activation by stimulation of MACB.
Within this specific research project, godA promoter (PgodA) was identified using genetic analyses and colorimetric reporter assay. The sequence of PgodA showed consensus of HrdB. Transcriptomic analyses of co-culture between Streptomyces coelicolor and MACB showed global variations of gene expression by S. coelicolor, suggesting a possibility that overproduction of SMs are as the result of flux balance variations of whole cell metabolism.
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Report
(3 results)
Research Products
(17 results)
