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    • 4. 发明专利
    • Method for production of astaxanthin-containing lipid
    • 用于生产含有ASTAXANTHIN的脂质的方法
    • JP2004129504A
    • 2004-04-30
    • JP2002294420
    • 2002-10-08
    • Suntory Ltdサントリー株式会社
    • HIGASHIYAMA KENICHINISHIO NAOMICHIKAKIZONO SHIYUNEI
    • C12P7/64C12N1/12C12P23/00
    • PROBLEM TO BE SOLVED: To provide a method for efficiently producing an astaxanthin-containing lipid with which a method for culturing a green alga Haematococcus pluvialis is improved and a cyst is thereby formed and matured under dark conditions.
      SOLUTION: A method for producing an algal body of the green alga Haematococcus pluvialis in which astaxanthin is accumulated in an amount of ≥40-700 pg/cell in the cyst obtained by culturing the green alga Haematococcus pluvialis under conditions of 0.01-0.5 vvm relative volume of ventilation in the dark. Furthermore, there is provided the method for producing the astaxanthin-containing lipid consisting essentially of a component selected from the group consisting of free type astaxanthin, an astaxanthin fatty acid monoester, an astaxanthin fatty acid diester and a mixture thereof. The method is characterized by affording the astaxanthin-containing substance from the algal body.
      COPYRIGHT: (C)2004,JPO
    • 解决问题的方案:提供一种高效生产含有青海洋黄素的脂质的方法,通过该方法培养绿藻类红潮球菌的方法,由此在黑暗条件下形成囊泡并成熟。 解决方案:一种生产绿藻类红潮球菌的藻体的方法,其中在通过在0.01-0.1%的条件下培养绿藻红球藻获得的囊肿中,虾青素以≥40-700pg/ 0.5vvm相对体积的通风在黑暗中。 此外,提供了生产含有虾青素的脂质的方法,其基本上由选自游离型虾青素,虾青素脂肪酸单酯,虾青素脂肪酸二酯及其混合物的组分组成。 该方法的特征在于从藻体中提供含有虾青素的物质。 版权所有(C)2004,JPO
    • 9. 发明专利
    • Manufacturing method of highly unsaturated fatty acid using new cell body-treating method
    • 使用新的细胞体内处理方法制备高度不饱和脂肪酸的方法
    • JP2006219528A
    • 2006-08-24
    • JP2005031918
    • 2005-02-08
    • Suntory Ltdサントリー株式会社
    • HIGASHIYAMA KENICHINAKAJIMA TOSHIHARU
    • C11B1/10A23D9/00A23J7/00A23K1/16A23K1/18A23L1/30C05F11/00C11B11/00C11C3/00C12N1/14C12N1/16C12P7/64C12R1/645C12R1/785
    • A23D9/00A23K10/12A23K20/158A23L33/115A23V2002/00C11B1/10C12N1/005C12P7/6472C12P7/6481A23V2250/1882
    • PROBLEM TO BE SOLVED: To provide a new isolation method of biomass, that is, a new drying method by a combination of a plurality of methods, and a manufacturing method and a preservation method of PUFA (polyunsaturated fatty acid)-containing oils and fats (triglycerides) and/or a PUFA-containing phospholipid, or a PUFA-containing cell body comprising cooling and subsequently filling and packaging a dried cell body. SOLUTION: The method is one for isolating one or more kinds of compounds from a biomass-containing microorganism having produced such compounds and comprises the following steps; (a) a step for preparing or obtaining a wet cell body having an average water content of 30-80%; (b) a step for feeding the wet cell body to a primary drier followed by molding to obtain a molded cell body having an average water content of 5-50%; (c) a step for subjecting the molded cell body obtained in the step (b) to a secondary drying to obtain a dried cell body having an average water content of at most 10%; and (d) a step for purifying, extracting or isolating the compound or the compounds from the dried cell body obtained in the step (c). COPYRIGHT: (C)2006,JPO&NCIPI
    • 要解决的问题:为了提供生物质的新的分离方法,即通过多种方法的组合的新的干燥方法以及含有PUFA(多不饱和脂肪酸)的制造方法和保存方法 油和脂肪(甘油三酸酯)和/或含PUFA的磷脂或含PUFA的细胞体,其包括冷却并随后填充和包装干细胞体。 解决方案:该方法是用于从生产这种化合物的含生物质的微生物中分离一种或多种化合物的方法,包括以下步骤: (a)制备或获得平均含水量为30-80%的湿细胞体的步骤; (b)将湿细胞体供给到初级干燥器中,随后成型以获得平均含水量为5-50%的模制电池体的步骤; (c)使步骤(b)中获得的模制电池体进行二次干燥以获得平均含水量为至多10%的干燥电池体的步骤; 和(d)从步骤(c)获得的干燥细胞体中纯化,提取或分离化合物或化合物的步骤。 版权所有(C)2006,JPO&NCIPI
    • 10. 发明专利
    • Method for culturing fungal cell body
    • 培养真菌细胞体的方法
    • JP2006067964A
    • 2006-03-16
    • JP2004258151
    • 2004-09-06
    • Suntory Ltdサントリー株式会社
    • HIGASHIYAMA KENICHI
    • C12N1/14C12P7/64
    • C12P7/6472C12N1/14C12P7/6427
    • PROBLEM TO BE SOLVED: To provide a method for culturing fungal cell bodies, capable of keeping good productivity of a highly unsaturated fatty acid or a compound containing the highly unsaturated fatty acid as a constituent fatty acid, without requiring to actually seek an oxygen-transfer coefficient (KLa) when scaling-up thereof is conducted. SOLUTION: This method for culturing the fungal cell bodies comprises using a culturing apparatus of aeration and agitation type, wherein agitation power and a maximum aeration amount of the culturing apparatus are adjustable and controllable, so that mechanical agitation of the apparatus is conducted by keeping the agitation power per unit amount of a liquid at 269 (W/m 3 ) or less, until a prescribed time has elapsed since culturing started, and then the maximum aeration amount and a maximum agitation power requirement of the apparatus are increased to ranges satisfying: the KLa expressed by (P/V) 0.95 /Vs 0.67 [P is an agitation power requirement (W); V is an amount of the liquid (m 3 ); and Vs is an aeration linear velocity (m/sec)] is not less than 59; an aeration linear velocity parameter expressed by Vs 0.67 [(m/sec) 0.67 ] is not less than 0.075; and an agitation power requirement parameter expressed by (P/V) 0.95 [(W/m 3 ) 0.95 ] is not less than 203, after the prescribed time has elapsed. COPYRIGHT: (C)2006,JPO&NCIPI
    • 待解决的问题:提供一种培养真菌细胞体的方法,其能够保持高度不饱和脂肪酸或含有高度不饱和脂肪酸的化合物作为构成脂肪酸的生产率,而不需要实际寻求 氧气传递系数(KLa)在进行放大时。 解决方案:用于培养真菌细胞体的方法包括使用通气和搅拌类型的培养装置,其中培养装置的搅拌功率和最大通气量是可调节和可控的,从而进行设备的机械搅拌 通过将每单位量的液体的搅拌功率保持在269(W / m 3 / SP>)以下,直到从培养开始经过规定时间,然后将最大通气量和最大搅拌功率 将装置的要求提高到满足以下范围:由(P / V) 0.95表示的KLa / Vs 0.67 [P是搅拌功率要求(W) V是液体的量(m 3 ); 而Vs是曝气线速度(m / sec)]不小于59; 由Vs 0.67表示的曝气线速度参数[(m / sec) 0.67 ]不小于0.075; 并且由(P / V) 0.95 [(W / m 3 0.95 表示的搅拌功率要求参数不小于203, 经过规定的时间。 版权所有(C)2006,JPO&NCIPI