The United Graduate School of Agricultural Sciences, Iwate University (Yamagata University)
Tadaomi OOZONE
Department of Bioresource Engineering, Faculty of Agriculture, Yamagata University
Tomoharu SUGAI
Department of Bioresource Engineering, Faculty of Agriculture, Yamagata University
Takeshi SASSA
The United Graduate School of Agricultural Sciences, Iwate University (Yamagata University) Department of Bioresource Engineering, Faculty of Agriculture, Yamagata University
The mass production of pure gibberellin A1 (GA1) by shake-culturing Phaeosphaeria sp. L487 was investigated. Its GA1 production was markedly influenced by natural nitrogen sources and NH4NO3. When the fungus was cultured in an 8% glucose−1.5% oatmeal−0.1% NH4NO3−0.5% KH2PO4−0.1% MgSO4·7H2O medium for 3 weeks, the amount of GA1 in the culture filtrate was up to ca. 200 μg/ml: the addition of safflower oil to the culture medium two weeks after inoculation prolonged the GA1-production period to produce 300 μg/ml. Further preparation of [U-13C]GA1 as a tool for the analysis of a complex of GA1 and its binding protein was attempted by using the fungus. The fungal culture in a [U-13C]glucose-oatmeal medium gave 6 mg of crystalline 13C-enriched GA1. Its 13C-enrichment of ca. 75% and 1JCC values were determined by NMR spectrometry.
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