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    • 62. 发明授权
    • Single use centrifuge system for highly concentrated and/or turbid feeds
    • 用于高度浓缩和/或混浊进料的单次离心机系统
    • US09222067B2
    • 2015-12-29
    • US13684051
    • 2012-11-21
    • Pneumatic Scale Corporation
    • Stephen B KesslerT. David Marro
    • C12M1/00C12N1/02B04B5/04
    • C12M47/02B04B5/0442B04B2005/0464C12M23/26C12M23/28C12M27/10C12M29/00C12M37/04C12N1/02
    • A method and apparatus for cell harvest of production scale quantities of cell cultures using single use components comprising a flexible membrane mounted on a rigid frame and is supported within a multiple use rigid centrifuge bowl, such single use components including a core with an increased diameter and an internal truncated cone shape in order to permit the system to maintain a sufficiently high angular velocity to create a settling velocity suited to efficiently processing highly concentrated cell culture streams. Features which minimize feed turbidity, and others which permit the continuous or semi-continuous discharge of cell concentrate, increase the overall production rate over the rate which can be achieved using current intermittent processing methods for large cell culture volumes. Injection of a diluent during the cell concentrate removal process permits more complete removal of viscous cell concentrates.
    • 一种用于使用单一使用部件的生产规模量的细胞培养物细胞收获的方法和装置,其包括安装在刚性框架上的柔性膜,并且被支撑在多用刚性离心机碗内,所述单一使用部件包括直径增加的芯和 内部截锥形,以便允许系统保持足够高的角速度以产生适于有效处理高度浓缩的细胞培养物流的沉降速度。 使进料浊度最小化的特征以及允许连续或半连续排出细胞浓缩物的其它特性使总生产率提高了超过使用目前间歇式处理大量细胞培养物体积的速率。 在细胞浓缩物移除过程期间注射稀释剂允许更完全地去除粘性细胞浓缩物。
    • 63. 发明授权
    • System for culturing and recovering micro algae
    • 微藻培养和回收系统
    • US08940531B2
    • 2015-01-27
    • US13300893
    • 2011-11-21
    • Kwang Mo Seong
    • Kwang Mo Seong
    • C12M1/42C12M1/00C12N1/12C12N1/02C12M1/26
    • C12M47/02C12M21/02C12M23/58C12M29/02C12M33/22C12N1/02C12N1/12
    • A system for culturing and recovering micro algae comprises a photo-bioreactor, a floatation separator, a centrifugal separator, and a micro bubble generator. The photo-bioreactor unit is configured to culture micro algae by a photochemical reaction to produce a micro algae precipitate. The precipitated micro algae is separated by the floatation separator. The separated micro algae is concentrated by the centrifugal separator. The micro bubble generator generates process water containing micro carbon dioxide bubbles and supplies the generated process water to the photo-bioreactor unit and the floatation separator. With this system, micro algae can be cultured and recovered in a simpler and more cost-effective manner.
    • 用于培养和回收微藻的系统包括光生物反应器,浮选分离器,离心分离器和微气泡发生器。 光生物反应器单元被配置为通过光化学反应培养微藻以产生微藻沉淀。 沉淀的微藻被浮选分离器分离。 分离的微藻被离心分离器浓缩。 微气泡发生器产生含有微量二氧化碳气泡的工艺水,并将生成的工艺水供应到光生物反应器单元和浮选分离器。 利用该系统,可以以更简单和更具成本效益的方式培养和回收微藻。
    • 65. 发明申请
    • CELL COLLECTION METHOD
    • 细胞收集方法
    • US20140335600A1
    • 2014-11-13
    • US14341543
    • 2014-07-25
    • TOYO SEIKAN GROUP HOLDINGS, LTD.
    • Satoshi TanakaRyo SuenagaMasahiro KuninoriKyohei Ota
    • C12N1/02
    • C12N1/02C12M23/14C12M33/18
    • A method for collecting cells that have been cultured by using a cell culture kit in which, at least, a culture container for cultivating cells, a cell collection container for collecting cells after cultivation and a waste liquid container for collecting a culture medium after cultivation are linked to one another through a conduit, the method including transferring a culture supernatant that has been cultured from the culture container to the waste liquid container, transferring a concentrated suspension of cells from the culture container to the cell collection container, returning part of the culture supernatant discharged in the waste liquid container to the culture container and allowing cells remaining in the culture container to be suspended in a suspension of cells, and transferring again a suspension of cells in which remaining cells are suspended from the culture container to the cell collection container.
    • 采用细胞培养试剂盒收集培养细胞的方法,其中至少培养细胞用培养容器,栽培后收集细胞的细胞收集容器和培养后收集培养基的废液容器, 该方法包括将从培养容器培养的培养上清液转移到废液容器,将细胞浓缩悬浮液从培养容器转移到细胞收集容器中,返回部分培养物 将废液容器中的上清液排出到培养容器中,使残留在培养容器中的细胞悬浮于细胞悬浮液中,再次将剩余细胞从培养容器悬浮的细胞悬浮液转移到细胞收集容器 。
    • 67. 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。
    • 69. 发明申请
    • METHOD FOR PRODUCTION OF INOCULUM OF MICROORGANISMS OPTIMIZED AS CATALYST FOR MULTIPLE PARALLEL MINERALIZATION
    • 优化作为多元平行矿化催化剂的微生物微生物生产方法
    • US20110126455A1
    • 2011-06-02
    • US13056120
    • 2009-07-16
    • Makoto Shinohara
    • Makoto Shinohara
    • A01G31/00C12N1/02C12N1/00C05F11/08A01G1/00A01G17/00
    • C05F17/00A01G22/00C05F3/00C05F11/10C12N1/14Y02A40/205Y02P20/145Y02W30/43
    • Provided is a method of producing an inoculum, which can drastically reduce a time to complete a reaction for mineralizing an organic material into nitrate nitrogen and can add a large amount of the organic material at one time in a multiple parallel mineralization for generating nitrate nitrogen as inorganic nutrients from the organic material, resulting in efficient generation of a high concentration of nitrate nitrogen and drastic reduction of the amount of a microorganism source added. The method of producing an inoculum comprises: placing water in a container that can store water therein, inoculating microorganisms capable of conducting a multiple parallel mineralization thereinto, and maintaining an environment that allows the multiple parallel mineralization to proceed in the water, thereby culturing the microorganisms capable of conducting a multiple parallel mineralization; forming a biofilm on a solid surface that contacts with the water and then collecting the biofilm; and utilizing the collected biofilm as an inoculum of the microorganisms optimized as a catalyst for the multiple parallel mineralization.
    • 提供一种生产接种物的方法,其可以显着减少完成将有机材料矿化成硝态氮的反应的时间,并且可以在多次平行的矿化中一次添加大量的有机材料以产生硝酸盐氮作为 来自有机材料的无机营养物质,导致有效产生高浓度的硝酸盐氮,并大大减少了加入的微生物源的量。 生产接种物的方法包括:将水放入容器中的水中,将容器内的水进行接种,接种能够进行多次平行矿化的微生物,并保持允许多次平行矿化在水中进行的环境,从而培养微生物 能够进行多次平行矿化; 在与水接触的固体表面上形成生物膜,然后收集生物膜; 并利用收集的生物膜作为微生物的接种物,其被优化为用于多次平行矿化的催化剂。