发明公开
EP1609868A1 METHOD OF COLLECTING HIGHLY PURE POLYHYDROXYALKANOATE FROM MICROBIAL CELLS
有权
VERFAHREN ZUR ENTNAHME VON HOCHREINEM POLYHYDROXYALKANOAT AUS MIKROBIELLEN ZELLEN
- 专利标题: METHOD OF COLLECTING HIGHLY PURE POLYHYDROXYALKANOATE FROM MICROBIAL CELLS
- 专利标题(中): VERFAHREN ZUR ENTNAHME VON HOCHREINEM POLYHYDROXYALKANOAT AUS MIKROBIELLEN ZELLEN
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申请号: EP04703505.0申请日: 2004-01-20
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公开(公告)号: EP1609868A1公开(公告)日: 2005-12-28
- 发明人: YANAGITA, Yoshifumi 1-701, Saususukuea , OGAWA, Noriko , UEDA, Yasuyoshi , OSAKADA, Fumio , MATSUMOTO, Keiji
- 申请人: KANEKA CORPORATION
- 申请人地址: 2-4, Nakanoshima 3-chome Kita-ku Osaka-shi, Osaka 530-8288 JP
- 专利权人: KANEKA CORPORATION
- 当前专利权人: KANEKA CORPORATION
- 当前专利权人地址: 2-4, Nakanoshima 3-chome Kita-ku Osaka-shi, Osaka 530-8288 JP
- 代理机构: Vossius & Partner
- 优先权: JP2003011099 20030120
- 国际公布: WO2004065608 20040805
- 主分类号: C12P7/62
- IPC分类号: C12P7/62
摘要:
The present invention has an object to provide a method for separating and purifying a PHA without causing a serious decrease of the molecular weight to obtain a highly pure PHA in a high yield, which comprises efficiently removing cell components other than PHA particles from a cultured PHA-containing microbial cell. Another object of the present invention is to provide a method for obtaining an agglomerate of PHA particles.
The method for recovering a PHA according to the present invention is a method which comprises efficiently disrupting a cell to recover the PHA by carrying out a physical disruption treatment and an alkali addition at low temperature for an aqueous suspension of the PHA-containing microbial cell, and then treating the PHA with an enzyme and/or a surfactant. Moreover, the particle diameter of the PHA may be enlarged by suspending the PHA in a hydrophilic solvent and/or water, and stirring at a temperature equal to or below the boiling point of said suspension, to agglomerate said PHA.
The method for recovering a PHA according to the present invention is a method which comprises efficiently disrupting a cell to recover the PHA by carrying out a physical disruption treatment and an alkali addition at low temperature for an aqueous suspension of the PHA-containing microbial cell, and then treating the PHA with an enzyme and/or a surfactant. Moreover, the particle diameter of the PHA may be enlarged by suspending the PHA in a hydrophilic solvent and/or water, and stirring at a temperature equal to or below the boiling point of said suspension, to agglomerate said PHA.
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