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    • 1. 发明授权
    • Method for isolating and culturing unculturable microorganisms
    • 分离和培养不可培养微生物的方法
    • US08158401B2
    • 2012-04-17
    • US12537646
    • 2009-08-07
    • Ariel KushmaroShimona GereshShaul Geresh, legal representative
    • Ariel KushmaroShimona Geresh
    • C12Q1/68C12N1/00C12N1/02C12N1/06C12N1/20C12N3/00
    • C12N1/00
    • The invention provides a method for isolating and culturing a previously unculturable microorganism, which comprises: (i) collecting a sample from an environmental source; (ii) counting/estimating the number of microorganisms in the sample; (iii) diluting the sample in an appropriate medium; (iv) adding a gelating agent such as to entrap one or more microorganisms within a sphere of the gelating agent; (v) coating the spheres containing the entrapped microorganism(s) with a natural or synthetic polymer to form a polymeric membrane; (vi) incubating the coated spheres in the original environment for an appropriate time; (vii) cutting the spheres and scanning for microorganisms colonies; and (viii) isolating the microorganisms, and repeating steps (iii) to (vii) until a pure clone of said previously unculturable microorganism is obtained.
    • 本发明提供了分离和培养以前不可培养的微生物的方法,其包括:(i)从环境来源收集样品; (ii)计数/估计样品中的微生物数量; (iii)将样品稀释在合适的培养基中; (iv)加入凝胶剂,例如在凝胶剂的球体内捕获一种或多种微生物; (v)用天然或合成聚合物涂覆含有捕获的微生物的球体以形成聚合物膜; (vi)将涂覆的球体在原始环境中孵育适当的时间; (vii)切割球体并扫描微生物菌落; 和(viii)分离微生物,并重复步骤(iii)至(vii),直到获得所述先前不可培养的微生物的纯克隆。
    • 2. 发明申请
    • METHOD FOR ISOLATING AND CULTURING UNCULTURABLE MICROORGANISMS
    • 用于分离和培养不可培养微生物的方法
    • US20100120037A1
    • 2010-05-13
    • US12537646
    • 2009-08-07
    • Ariel KushmaroShimona GereshShaul Geresh
    • Ariel KushmaroShimona GereshShaul Geresh
    • C12Q1/68C12N1/00C12N1/20C40B40/02
    • C12N1/00
    • The invention provides a method for isolating and culturing a previously unculturable microorganism, which comprises: (i) collecting a sample from an environmental source; (ii) counting/estimating the number of microorganisms in the sample; (iii) diluting the sample in an appropriate medium; (iv) adding a gelating agent such as to entrap one or more microorganisms within a sphere of the gelating agent; (v) coating the spheres containing the entrapped microorganism(s) with a natural or synthetic polymer to form a polymeric membrane; (vi) incubating the coated spheres in the original environment for an appropriate time; (vii) cutting the spheres and scanning for microorganisms colonies; and (viii) isolating the microorganisms, and repeating steps (iii) to (vii) until a pure clone of said previously unculturable microorganism is obtained.
    • 本发明提供了分离和培养以前不可培养的微生物的方法,其包括:(i)从环境来源收集样品; (ii)计数/估计样品中的微生物数量; (iii)将样品稀释在合适的培养基中; (iv)加入凝胶剂,例如在凝胶剂的球体内捕获一种或多种微生物; (v)用天然或合成聚合物涂覆含有捕获的微生物的球体以形成聚合物膜; (vi)将涂覆的球体在原始环境中孵育适当的时间; (vii)切割球体并扫描微生物菌落; 和(viii)分离微生物,并重复步骤(iii)至(vii),直到获得所述先前不可培养的微生物的纯克隆。
    • 3. 发明申请
    • Method for isolating and culturing unculturable microorganisms
    • 分离和培养不可培养微生物的方法
    • US20060240506A1
    • 2006-10-26
    • US10527076
    • 2003-09-03
    • Ariel KushmaroShimona GereshShaul Geresh
    • Ariel KushmaroShimona GereshShaul Geresh
    • C12Q1/04C12N1/20
    • C12N1/00
    • The invention provides a method for isolating and culturing a previously unculturable microorganism, which comprises: (i) collecting a sample from an environmental source; (ii) counting/estimating the number of microorganisms in the sample; (iii) diluting the sample in an appropriate medium; (iv) adding a gelating agent such as to entrap one or more microorganisms within a sphere of the gelating agent; (v) coating the spheres containing the entrapped microorganism(s) with a natural or synthetic polymer to form a polymeric membrane; (vi) incubating the coated spheres in the original environment for an appropriate time; (vii) cutting the spheres and scanning for microorganisms colonies; and (viii) isolating the microorganisms, and repeating steps (iii) to (vii) until a pure clone of said previously unculturable microorganism is obtained.
    • 本发明提供了分离和培养以前不可培养的微生物的方法,其包括:(i)从环境来源收集样品; (ii)计数/估计样品中的微生物数量; (iii)将样品稀释在合适的培养基中; (iv)加入凝胶剂,例如在凝胶剂的球体内捕获一种或多种微生物; (v)用天然或合成聚合物涂覆含有捕获的微生物的球体以形成聚合物膜; (vi)将涂覆的球体在原始环境中孵育适当的时间; (vii)切割球体并扫描微生物菌落; 和(viii)分离微生物,并重复步骤(iii)至(vii),直到获得所述先前不可培养的微生物的纯克隆。