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1. 发明专利

JP2003310288A Method for producing ethanol and biological carrier 审中-公开
标题翻译：生产乙醇和生物载体的方法
公开(公告)号：JP2003310288A
公开(公告)日：2003-11-05
申请号：JP2002127690
申请日：2002-04-26
申请人： Electric Power Dev Co Ltd , Tokyo Univ Of Agriculture & Technology , Toshiba Corp , 東京農工大学長 , 株式会社東芝 , 電源開発株式会社
发明人： SUZUKI NOBUKAZU , MATSUNAGA KENTARO , MORIYAMA HIDESHIGE , ONODA HIROKO , OHATA HIROSUKE , MATSUMOTO TERUBUMI , MATSUNAGA TADASHI
IPC分类号： C12P7/06 , C12R1/645
CPC分类号： Y02E50/17
摘要： PROBLEM TO BE SOLVED: To provide a method for efficiently producing ethanol from algae grown in the sea and marine plants and recycling waste ash, and obtain a biological carrier.
SOLUTION: The method for producing ethanol is to separate and take out the algae from the biological carrier in a process 1 for taking out algae or marine plants, take out starch from the taken out algae by heating the algae or the marine plant grown in the sea in a process 2 for taking out starch and send them to a process 3 for producing sugar. The process 3 for producing sugar produces the sugar by adding amylase-producing marine bacteria to the starch and produce ethanol by subsequently adding a salt resistant yeast.
COPYRIGHT: (C)2004,JPO
摘要翻译：要解决的问题：提供一种从海洋和海洋植物生长的藻类中有效生产乙醇的方法，并回收废灰，并获得生物载体。解决方案：用于生产乙醇的方法是在用于取出藻类或海洋植物的方法1中从生物载体中分离和取出藻类，通过加热藻类或海洋植物从取出的藻类中取出淀粉在用于取出淀粉的方法2中在海中生长并将其送到生产糖的方法3中。用于生产糖的方法3通过向淀粉中加入产淀粉酶的海洋细菌产生糖，然后通过加入耐盐酵母产生乙醇。版权所有（C）2004，JPO

2. 发明专利

JP2014135906A Transgenic fine algae and culture method thereof 审中-公开
标题翻译：转基因小麦及其培养方法
公开(公告)号：JP2014135906A
公开(公告)日：2014-07-28
申请号：JP2013004703
申请日：2013-01-15
申请人： Tokyo Univ Of Agriculture & Technology , 国立大学法人東京農工大学 , Electric Power Dev Co Ltd , 電源開発株式会社
发明人： MATSUNAGA TADASHI , TANAKA TSUYOSHI , YOSHINO TOMOKO , TANAKA SUKEYOSHI , MUTO MASAKI , MATSUMOTO TERUBUMI
IPC分类号： C12N1/13 , C12N9/12 , C12N15/09 , C12P7/62 , C12P7/64 , C12R1/89
CPC分类号： Y02P20/52
摘要： PROBLEM TO BE SOLVED: To introduce a specific gene to fine algae capable of high accumulation of oil, thereby improving glycerol assimilation properties.SOLUTION: A glycerol kinase gene is introduced to fine algae having oil accumulation capacity, e.g. Fistulifera sp. JPCC DA0580 strain.
摘要翻译：要解决的问题：将特定基因引入能够高度积聚油的精细藻类，从而提高甘油同化特性。解决方案：将甘油激酶基因导入具有油积累能力的细藻类，例如，瘘管 JPCC DA0580菌株。

3. 发明专利

JP2010187645A Microalga belonging to scenedesmus, oil manufacturing method including process for culturing the microalgae, and oil collected from microalga 有权
标题翻译： MICROALGA相关文献，油制造方法，包括微藻培养方法和从MICROALGA收集的油
公开(公告)号：JP2010187645A
公开(公告)日：2010-09-02
申请号：JP2009038477
申请日：2009-02-20
申请人： Electric Power Dev Co Ltd , Tokyo Univ Of Agriculture & Technology , 国立大学法人東京農工大学 , 電源開発株式会社
发明人： MATSUMOTO TERUBUMI , MATSUNAGA TADASHI , TANAKA TAKESHI
IPC分类号： C12N1/12 , C12P5/00
摘要： PROBLEM TO BE SOLVED: To provide a method for manufacturing microalga capable of producing a large amount of 14-22C aliphatic hydrocarbon and a method, containing a process for culturing the microalga, for manufacturing oil, the oil collected from the microalga, dried algous bodies obtained by drying the microalga, fuel obtained from the microalga, and a carbon dioxide fixation method including a process for culturing the microalga. SOLUTION: There are provided: (1) the microalga belonging to scenedesmus, (2) the method, containing a process for culturing the microalga described in (1), for manufacturing the oil, (3) the oil manufactured by the method for manufacturing the oil described in (2), (4) the dried algous bodies obtained by drying the microalga described in (1), (5) the fuel obtained from the microalga described in (1), and (6) the carbon dioxide fixation method including the process for culturing the microalga described in (1). COPYRIGHT: (C)2010,JPO&INPIT
摘要翻译：要解决的问题：提供一种能够生产大量14-22C脂族烃的微藻的方法，以及含有用于培养微藻的方法，用于制造油的方法，从微藻收集的油，通过干燥微藻，从微藻获得的燃料获得的干燥的algos体以及包括培养微藻的方法的二氧化碳固定方法。提供：（1）属于西葫芦的微藻，（2）该方法，含有（1）所述的微藻的培养方法，用于制造油，（3）由（2），（4）中所述的制造油的方法通过干燥由（1），（5）中描述的微藻获得的干燥的含水体，由（1）中所述的微藻获得的燃料和（6）包括用于培养（1）中描述的微藻的方法的二氧化碳固色方法。版权所有（C）2010，JPO＆INPIT

4. 发明专利

JP2010022218A New microorganism and method for producing glucosylceramide 有权
标题翻译：新型微生物和生产葡萄球蛋白的方法
公开(公告)号：JP2010022218A
公开(公告)日：2010-02-04
申请号：JP2008184034
申请日：2008-07-15
申请人： Electric Power Dev Co Ltd , Tokyo Univ Of Agriculture & Technology , 国立大学法人東京農工大学 , 電源開発株式会社
发明人： MATSUMOTO TERUBUMI , MATSUNAGA TADASHI , TANAKA TAKESHI
IPC分类号： C12N1/16 , C12P13/00 , C12R1/72
摘要： PROBLEM TO BE SOLVED: To provide a new microorganism having a glucosylceramide-producing ability: and to provide a method for producing the glucosylceramide utilizing the microorganism. SOLUTION: There are provided the microorganism belonging to Candida JPCCY0024 strain (NITE P-571); the microorganism whose 26S rDNA-D1/D2 base sequence has a homology of ≥96% based on a specific base sequence, and which has a glucosylceramide-producing ability, and belongs to genus Candida; Candida JPCCY0024 strain (NITE P-571); and a method for producing glucosylceramide, having a process for culturing the microorganism. COPYRIGHT: (C)2010,JPO&INPIT
摘要翻译：待解决的问题：提供具有葡萄糖神经酰胺生产能力的新微生物，并提供利用该微生物生产葡糖基酰胺的方法。
解决方案：提供属于JPCCY0024假丝酵母菌株（NITE P-571）的微生物; 其26S rDNA-D1 / D2碱基序列基于特定碱基序列具有≥96％的同源性且具有葡萄糖基神经酰胺生产能力的微生物，属于假丝酵母属; 假丝酵母JPCCY0024菌株（NITE P-571）; 以及具有培养微生物的方法的葡糖基神经酰胺的制造方法。版权所有（C）2010，JPO＆INPIT

5. 发明专利

JP2010022217A Method for producing glucosylceramide 审中-公开
标题翻译：生产葡糖酰胺的方法
公开(公告)号：JP2010022217A
公开(公告)日：2010-02-04
申请号：JP2008184033
申请日：2008-07-15
申请人： Electric Power Dev Co Ltd , Tokyo Univ Of Agriculture & Technology , 国立大学法人東京農工大学 , 電源開発株式会社
发明人： MATSUMOTO TERUBUMI , MATSUNAGA TADASHI , TANAKA TAKESHI
IPC分类号： C12P19/44 , A61K8/99 , A61Q19/00 , C12N15/09
摘要： PROBLEM TO BE SOLVED: To provide a method for producing glucosylceramide with a yeast in high productivity. SOLUTION: Provided is the method for producing glucosylceramide, characterized by having a process for culturing a microorganism belonging to Cadida. The microorganism belonging to the Cadida is preferably Candida tropicalis JPCCY0004 strain (NITE P-570). COPYRIGHT: (C)2010,JPO&INPIT
摘要翻译：待解决的问题：提供以高生产率用酵母生产葡糖基神经酰胺的方法。解决方案：提供生产葡糖基神经酰胺的方法，其特征在于具有培养属于卡达达的微生物的方法。属于Cadida的微生物优选为热带念珠菌JPCCY0004菌株（NITE P-570）。版权所有（C）2010，JPO＆INPIT

6. 发明专利

JP2006191919A Method for producing carotenoid pigment, sphingoglycolipid, ubiquinone q-10 有权
标题翻译：生产CAROTENOID颜料的方法，SPHINGOGLYCOLIPID，UBIQUINONE Q-10
公开(公告)号：JP2006191919A
公开(公告)日：2006-07-27
申请号：JP2005112481
申请日：2005-04-08
申请人： Electric Power Dev Co Ltd , Tokyo Univ Of Agriculture & Technology , 国立大学法人東京農工大学 , 電源開発株式会社
发明人： MATSUNAGA TADASHI , TANAKA TAKESHI , MATSUMOTO TERUBUMI
IPC分类号： C12N1/20 , A01K61/00 , A23K1/16 , A23K1/18 , C12N15/09 , C12P7/66 , C12P19/44 , C12P23/00 , C12R1/01
CPC分类号： Y02A40/81
摘要： PROBLEM TO BE SOLVED: To provide a novel microorganism which simultaneously produces carotenoid pigments and sphingoglycolipids and furthermore produces ubiquinone Q-10, and a method for producing the pigment, glycolipid and ubiquinone Q-10 using the microorganism. SOLUTION: The novel Sphingomonus, JPCCMB0017, has production ability of both carotenoid pigments and sphingoglycolipids, and furthermore has production ability of ubiquinone Q-10. The carotenoid pigments, sphingoglycolipids and ubiquinone Q-10 can be produced by culturing the bacterial strain. COPYRIGHT: (C)2006,JPO&NCIPI
摘要翻译：要解决的问题：提供一种同时产生类胡萝卜素颜料和鞘糖脂并进一步产生泛醌Q-10的新型微生物，以及使用微生物制备颜料，糖脂和泛醌Q-10的方法。解决方案：新型鞘氨醇单胞菌，JPCCMB0017具有类胡萝卜素和鞘糖脂的生产能力，并具有泛醌Q-10的生产能力。类胡萝卜素颜料，鞘糖脂和泛醌Q-10可以通过培养细菌菌株来制备。版权所有（C）2006，JPO＆NCIPI

7. 发明专利

JP2005323515A Method for producing hydrogen by microorganism 审中-公开
标题翻译：通过微生物生产氢的方法
公开(公告)号：JP2005323515A
公开(公告)日：2005-11-24
申请号：JP2004142803
申请日：2004-05-12
申请人： Electric Power Dev Co Ltd , 電源開発株式会社
发明人： MATSUMOTO TERUBUMI
IPC分类号： C12P3/00 , C02F3/00
摘要： PROBLEM TO BE SOLVED: To provide a method for producing hydrogen, capable of producing the hydrogen with high energy conversion efficiency and capable of making facilities small as a whole.
SOLUTION: This method for producing the hydrogen comprises culturing anaerobic bacteria having ability of forming the hydrogen by using an organic acid as a substrate, or facultative anaerobic bacteria having the ability, in a culture medium containing the organic acid, so as to make the bacteria form the hydrogen.
COPYRIGHT: (C)2006,JPO&NCIPI
摘要翻译：解决的问题：提供能够以高能量转换效率制造氢并且能够使整体设施小的氢气的制造方法。解决方案：这种生产氢的方法包括通过使用有机酸作为底物培养具有形成氢能力的厌氧细菌，或者在含有有机酸的培养基中具有能力的兼性厌氧细菌，以便使细菌形成氢。版权所有（C）2006，JPO＆NCIPI

8. 发明专利

JP2009112228A New microorganism, selenium oxyanion absorbent and method for removing selenium oxyanion 有权
标题翻译：新型微生物，硒氧化物吸收剂和去除氧化亚铁的方法
公开(公告)号：JP2009112228A
公开(公告)日：2009-05-28
申请号：JP2007287716
申请日：2007-11-05
申请人： Electric Power Dev Co Ltd , 電源開発株式会社
发明人： MATSUMOTO TERUBUMI
IPC分类号： C12N1/16 , B01J20/24 , C02F1/28 , C12N15/09
摘要： PROBLEM TO BE SOLVED: To provide a new microorganism having excellent adsorption ability of a selenium oxyanion, to provide a selenium oxyanion adsorbent using the microorganism as an active ingredient, and to provide a method for removing the selenium oxyanion using the microorganism.
SOLUTION: Provided are a microorganism belonging to a species to which Cryptococcus JPCCY0075 strain (NITE P-414) belongs; a microorganism belonging to the Cryptococcus in which the base sequence of 18SrDNA has ≥96% homology with a specific base sequence, and has the selenium oxyanion-adsorbing ability; Cryptococcus JPCCY0075 strain(NITE P-414); the selenium oxyanion adsorbent containing the microorganisms as active ingredients; and the method for removing the selenium oxyanion using such the microorganisms.
COPYRIGHT: (C)2009,JPO&INPIT
摘要翻译：待解决的问题：提供一种具有优异的硒氧阴离子吸附能力的新微生物，以提供使用微生物作为活性成分的硒氧阴离子吸附剂，并提供使用该微生物除去硒氧阴离子的方法。解决方案：提供属于JPCCY0075菌株（NITE P-414）所属物种的微生物; 属于隐球菌属的微生物，其中18SrDNA的碱基序列与特定碱基序列具有≥96％的同源性，并具有硒氧阴离子吸附能力; 密码子JPCCY0075菌株（NITE P-414）; 含有微生物作为活性成分的硒氧阴离子吸附剂; 以及使用这些微生物除去硒氧阴离子的方法。版权所有（C）2009，JPO＆INPIT

9. 发明专利

JP2008259452A Astaxanthin-producing bacterium, bacterial culture product, astaxanthin-containing composition and method for producing astaxanthin 有权
标题翻译：产生氨酪蛋白的细菌，细菌培养物产品，含阿斯汉敏素的组合物及其生产方法
公开(公告)号：JP2008259452A
公开(公告)日：2008-10-30
申请号：JP2007104822
申请日：2007-04-12
申请人： Electric Power Dev Co Ltd , 電源開発株式会社
发明人： MATSUMOTO TERUBUMI
IPC分类号： C12N1/20 , C12P23/00
CPC分类号： C12P23/00 , C12R1/01
摘要： PROBLEM TO BE SOLVED: To provide a bacterium capable of producing astaxanthin and free from thick cell wall such as yeast and algae, a bacterial culture product produced by using the bacterium, an astaxanthin-containing composition and a method for producing astaxanthin by using the bacterium.
SOLUTION: The invention provides an Erythrobacter genus bacterium capable of producing a composition containing ≥35 mass% astaxanthin; Erythrobacter JPCC M strain having a 16SrDNA base sequence comprising a specific base sequence or a base sequence having ≥96% homology to the above base sequence; a bacterial culture product obtained by culturing the bacterium; an astaxanthin-containing composition collected from the bacterium; and an astaxanthin producing method having a step to culture the bacterium belonging to Erythrobacter genus, wherein the bacterium has an astaxanthin productivity to give an astaxanthin content of ≥35 mass% in the total pigments produced by the bacterium.
COPYRIGHT: (C)2009,JPO&INPIT
摘要翻译：待解决的问题：提供能够生产虾青素并且不含酵母和藻类等厚细胞壁的细菌，通过使用该细菌产生的细菌培养物，含虾青素的组合物和通过以下方法生产虾青素的方法：使用细菌。解决方案：本发明提供能够生产含有≥35质量％虾青素的组合物的红细菌属细菌; 具有包含特定碱基序列或与上述碱基序列具有≥96％同源性的碱基序列的16SrDNA碱基序列的红细菌JPCC M菌株; 通过培养细菌获得的细菌培养物; 从细菌收集的含有虾青素的组合物; 以及具有培养属于红细菌属细菌的步骤的虾青素的制造方法，其特征在于，所述细菌具有虾青素的生产性，以使细菌产生的总颜料中的虾青素含量≥35质量％。版权所有（C）2009，JPO＆INPIT

10. 发明专利

JP2008228709A New microorganism, new microorganism for feed of crassostrea gigas and method for culturing crassostrea gigas by using this new microorganism 审中-公开
标题翻译：新型微生物，新型微生物饲料用于饲养动物和使用这种新型微生物培养核动物的方法
公开(公告)号：JP2008228709A
公开(公告)日：2008-10-02
申请号：JP2007077273
申请日：2007-03-23
申请人： Electric Power Dev Co Ltd , Kaki Kenkyusho , 財団法人かき研究所 , 電源開発株式会社
发明人： MATSUMOTO TERUBUMI , NISHIMURA YASUHIKO
IPC分类号： C12N1/12 , A23K1/16 , A23K1/18 , C12N15/09
CPC分类号： Y02P60/877
摘要： PROBLEM TO BE SOLVED: To provide a new microorganism and the new microorganism for feed of Crassostrea gigas and to provide a method for culturing Crassostrea gigas by using the new microorganism. SOLUTION: There are provided a Pavlova sp. JPCC42D strain (hereinafter referred to as Pavlova sp. JPCC42D), Pavlova sp. JPCC42D used for culture of Crassostrea gigas having ≥1.5 mm shell height and a method for culturing Crassostrea gigas having ≥1.5 mm shell height by using Pavlova sp. JPCC42D alone or a mixture of Pavlova sp. JPCC42D with Chaetoceros calcitrans. The amount of Pavlova sp. JPCC42D occupied in the mixture is preferably 1/4 to 3/4. COPYRIGHT: (C)2009,JPO&INPIT
摘要翻译：待解决的问题：提供一种新的微生物和用于饲养克拉斯克氏菌的新微生物，并提供通过使用新的微生物培养克拉斯克氏菌的方法。
解决方案：提供了一个Pavlova sp。 JPCC42D菌株（以下称为Pavlova sp.JPCC42D），Pavlova sp。 JPCC42D用于培养具有≥1.5mm壳高的Crassostrea gigas和使用Pavlova sp。培养具有≥1.5mm壳高的Crassostrea gigas的方法。单独的JPCC42D或Pavlova sp。 JPCC42D与Chaetoceros calcitrans。 Pavlova sp。混合物中的JPCC42D优选为1/4〜3/4。版权所有（C）2009，JPO＆INPIT

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