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    • 94. 发明公开
    • 포괄고정화 담체의 보관방법 및 제조방법
    • 沉积固定介质的储存和制造方法
    • KR1020070064280A
    • 2007-06-20
    • KR1020060128296
    • 2006-12-15
    • 가부시키가이샤 히타치플랜트테크놀로지
    • 아오야마,코우타로우아베,나오키스미노,타츠오에모리,히로요시
    • C02F3/10C12N11/04C12N11/08
    • C12N11/04C02F3/108C12N11/08Y02W10/15
    • Storage and production methods of encapsulated immobilization carrier which can stably store and transport a carrier block, and can obtain encapsulated immobilization carrier having high quality stability are provided. In a method for storing encapsulated immobilization carrier(30) in which microorganisms are encapsulated and immobilized in an immobilizing material until the encapsulated immobilization carrier is used in a treatment tank, the method comprises: storing a large-sized carrier block(28) in water of 15 deg.C or less or in the atmosphere with a relative humidity of 90% or more and a temperature of 15 deg.C or less before cutting the carrier block into a used size of the encapsulated immobilization carrier until the encapsulated immobilization carrier is used. A method for producing encapsulated immobilization carrier(30) in which microorganisms are encapsulated and immobilized in an immobilizing material, the method comprises: polymerizing a liquid mixture in which the microorganisms are mixed with the immobilizing material into a gel to form a carrier block(28) with a size larger than a use size of the encapsulated immobilizing carrier; storing the carrier block in water at 15 deg.C or less or in the atmosphere with a relative humidity of 90% or more and a temperature of 15 deg.C or less until the encapsulated immobilization carrier is used; and cutting the stored carrier block into the use size of the encapsulated immobilization carrier when the encapsulated immobilization carrier is used.
    • 提供了可以稳定地储存和运输载体块的封装的固定载体的储存和生产方法,并且可以获得具有高质量稳定性的封装的固定载体。 在包封的固定化载体(30)的存储方法中,将微生物包封并固定在固定材料中,直到将封装的固定化载体用于处理槽中,该方法包括:将大尺寸载体块(28)储存在水中 在15℃以下或在相对湿度为90%以上且温度为15℃以下的气氛中,将载体块切割成胶囊固定化载体的使用尺寸,直到胶囊化固定载体为 用过的。 一种生产包封的固定化载体(30)的方法,其中将微生物包封并固定在固定材料中,该方法包括:将其中微生物与固定材料混合的液体混合物聚合成凝胶以形成载体块(28 ),其尺寸大于胶囊固定载体的使用尺寸; 将载体块储存在15℃或更低的水中或在相对湿度为90%以上且温度为15摄氏度以下的气氛中,直到使用胶囊化固定载体为止; 并且当使用封装的固定载体时,将储存的载体块切割成胶囊固定载体的使用尺寸。
    • 95. 发明公开
    • 초미립 고정화 발광미생물의 제조방법 및 이를 이용한 유독물질 모니터링 방법
    • 微阵列固定辐射微波及其制造方法和使用有毒材料监测方法
    • KR1020060132265A
    • 2006-12-21
    • KR1020050052512
    • 2005-06-17
    • 주식회사 엔바이져코리아
    • 박경순
    • C12N11/04C12N11/00C12N11/02
    • A luminous microorganism immobilized in microsomes, a manufacturing method thereof and a monitoring method of poisonous materials by using the same microorganism are provided to enhance sensitivity of the monitoring by reducing the size of microsomes, and improve monitoring accuracy by minimizing the errors caused by a control group. The luminous microorganism immobilized in microsomes having diameter of 0.01-0.03 mm is provided, wherein the luminous microorganism is Vibrio fischeri, and shows reduced luminescence in proportion to concentration of poisonous materials in a sample; and the immobilization material is alginic acid, agar, carrageenan or polyacrylamide. The method for manufacturing the luminous microorganism immobilized in microsomes comprises the steps of: mixing the luminous microorganism with the immobilization material, and culturing the mixture in seawater complete medium at 22-27 deg. C for 45-50 hours; suspending the recovered luminous microorganism cells with 0.5-0.8% physiological saline solution, centrifuging the cells and resuspending them with 2-3% physiological saline solution; and mixing the suspended microorganism solution with the immobilization material, adding dropwise of the mixture to calcium salt or strontium salt solution, and maintaining the solution at 0-5 deg. C for 1-3 hours to obtain gel type microbeads.
    • 提供固定在微粒体中的发光微生物,其制造方法和通过使用相同微生物的有害物质的监测方法,以通过减小微粒体的尺寸来提高监测的灵敏度,并通过最小化由控制引起的误差来提高监测精度 组。 提供了固定在直径为0.01-0.03mm的微粒体中的发光微生物,其中发光微生物是弧菌,并且与样品中有毒物质的浓度成比例地显示出降低的发光; 固定物为藻酸,琼脂,角叉菜胶或聚丙烯酰胺。 用于制造固定在微粒体中的发光微生物的方法包括以下步骤:将发光微生物与固定化材料混合,并在22-27度的海水完全培养基中培养该混合物。 C为45-50小时; 将回收的发光微生物细胞悬浮在0.5-0.8%生理盐水溶液中,离心细胞并用2-3%生理盐水重新悬浮; 并将悬浮的微生物溶液与固定化材料混合,将混合物滴加到钙盐或锶盐溶液中,并将溶液保持在0-5℃。 C 1-3小时得到凝胶型微珠。