发明授权
US08008040B2 Process for production of 5-ene-3-one or 3,6-dione derivatives of sterols, processes for production of lipid metabolism improvers, foods, drinks, and animal feeds, and analytical method 有权
甾醇的5-烯-3-酮或3,6-二酮衍生物的制备方法,脂质代谢改进剂的生产方法,食品,饮料和动物饲料,以及分析方法

  • 专利标题: Process for production of 5-ene-3-one or 3,6-dione derivatives of sterols, processes for production of lipid metabolism improvers, foods, drinks, and animal feeds, and analytical method
  • 专利标题(中): 甾醇的5-烯-3-酮或3,6-二酮衍生物的制备方法,脂质代谢改进剂的生产方法,食品,饮料和动物饲料,以及分析方法
  • 申请号: US11632072
    申请日: 2005-07-12
  • 公开(公告)号: US08008040B2
    公开(公告)日: 2011-08-30
  • 发明人: Kunio SuzukiTadashi NagashimaShinya Nagahashi
  • 申请人: Kunio SuzukiTadashi NagashimaShinya Nagahashi
  • 申请人地址: JP Aichi
  • 专利权人: Toyo Hakko Co., Ltd.
  • 当前专利权人: Toyo Hakko Co., Ltd.
  • 当前专利权人地址: JP Aichi
  • 代理机构: Morgan, Lewis & Bockius LLP
  • 优先权: JP2004-207885 20040714
  • 国际申请: PCT/JP2005/012869 WO 20050712
  • 国际公布: WO2006/006608 WO 20060119
  • 主分类号: C12P33/00
  • IPC分类号: C12P33/00
Process for production of 5-ene-3-one or 3,6-dione derivatives of sterols, processes for production of lipid metabolism improvers, foods, drinks, and animal feeds, and analytical method
摘要:
An object of the present invention is to provide a process according to which 5-ene-3-one or 3,6-dione derivatives of sterols can be synthesized with a better yield, as well as a process for production of lipid metabolism improvers, foods, drinks, and animal feeds containing the 5-ene-3-one or 3,6-dione derivatives of sterols.The process for production of 5-ene-3-one or 3,6-dione derivatives of sterols of the present invention involves preparing a culturing solution containing an Arthrobacter bacterium, which is a microorganism exhibiting a cholesterol oxidase activity, and then, adding to the culturing solution an equivalent amount of hexane so as to prepare a bilayer solution consisting of an aqueous layer and a hydrocarbon-based solvent layer. Thereafter, sterol, or a derivative thereof, is made as a substrate contained therein, a reaction performed with cholesterol oxidase at 30° C. for 2 days, and, ethanol then added to separate a hydrocarbon-based solvent layer. Thereafter, the layer is dried to a state of dryness by means of a vacuum dryer so as to obtain 5-ene-3-one or 3,6-dione derivatives.
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