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用核糖体工程技术开拓海洋微生物药用资源的研究
引用本文:于志斌,崔承彬,朱天骄,卢克刚,顾谦群,方玉春,刘红兵. 用核糖体工程技术开拓海洋微生物药用资源的研究[J]. 高技术通讯, 2005, 15(5): 87-90
作者姓名:于志斌  崔承彬  朱天骄  卢克刚  顾谦群  方玉春  刘红兵
作者单位:教育部海洋药物重点实验室,中国海洋大学海洋药物与食品研究所,青岛,266003;教育部海洋药物重点实验室,中国海洋大学海洋药物与食品研究所,青岛,266003;军事医学科学院毒物药物研究所,北京,100850
基金项目:国家自然科学基金 (3 0 17110 2 ),863计划项目 (2 0 0 1AA62 40 2 0 ),山东省科技攻关计划项目 (0 12 110 0 10 7),山东省自然科学基金重点 (Z2 0 0 1C0 1),国家教育部长江学者奖励计划相关基金资助项目
摘    要:
利用核糖体工程技术对海洋中无活性的放线菌B3054进行诱导,获得了突变菌株B3054/M,其形态、菌丝体颜色都与母体菌株有显著的差异,发酵液经HPLC分析发现,代谢产物有明显的变化,特别是突变株产生了能抑制小鼠乳腺癌tsFT210细胞周期活性的活性代谢产物。这是首次利用核糖体工程技术诱变得到的具有细胞周期抑制活性的海洋放线菌菌株,这一研究结果表明,利用该技术对自然界的无活性微生物进行诱导来拓展微生物药用资源是可行的。

关 键 词:海洋放线菌  核糖体工程  细胞周期抑制活性

Studies on exploiting marine microbial resources for medicinal usage by using ribosome-engineering technology
Yu Zhibin,CUI Chengbin,ZHU Tianjiao,Lu Kegang,Gu Qianqun,FANG Yuchun,Liu Hongbing. Studies on exploiting marine microbial resources for medicinal usage by using ribosome-engineering technology[J]. High Technology Letters, 2005, 15(5): 87-90
Authors:Yu Zhibin  CUI Chengbin  ZHU Tianjiao  Lu Kegang  Gu Qianqun  FANG Yuchun  Liu Hongbing
Abstract:
In order to obtain active mutant strains, the ribosome-engineering technology was applied to inducing the non-active marine actinomycete strain B3054. An active mutant strain B3054/M was obtained, which showed obvious difference in the morphology and color from its parent strain B3054. The HPLC analyses of the fermentation products showed that the secondary metabolites of the mutant strain B3054/M were much different from that of the parent strain B3054. Especially, the new metabolites of the B3054/M showed cell cycle inhibitory activity on mammalian cancer tsFT210 cells. This experiment first presented the method to obtain the active marine strains with the cell cycle inhibitory activity by using the ribosome-engineering technology. It indicated that it is feasible to exploit new microbial resources for medicinal usage by the ribosome-engineering technology of inducing non-active actinomycetes in nature.
Keywords:marine actinomycetes   ribosome engineering   cell cycle inhibitory activity
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