专利快速检索-快速检索全球专利，免费商用专利数据库-IPRDB

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

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

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

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。

7. 发明专利

JP2003274925A Apparatus for automatically preparing nucleic acid and method for detecting nucleic acid in sample using the same 审中-公开
标题翻译：用于自动制备核酸的装置和使用该样品检测样品中的核酸的方法
公开(公告)号：JP2003274925A
公开(公告)日：2003-09-30
申请号：JP2002086380
申请日：2002-03-26
申请人： Juki Corp , Tokyo Univ Of Agriculture & Technology , ジューキ株式会社 , 東京農工大学長
发明人： YODA SEI , UDAGAWA YUJI , NEMOTO ETSUO , MARUYAMA KOHEI , MATSUNAGA TADASHI
IPC分类号： C12N15/09 , C12M1/00 , C12M1/32 , C12M1/38 , C12M1/42 , C12Q1/68
摘要： PROBLEM TO BE SOLVED: To automate a hybridization process requiring much time for detecting nucleic acids and a large space for experiment by very simple operation, bring a small size to an apparatus at the same time and simply and quickly prepare a single chain nucleic acid.
SOLUTION: The apparatus for automatically preparing the nucleic acid is constituted by installing at least (A) a reaction part having a reaction vessel holder, a heating and cooling device and a magnetic force controller, (B) a chip rack/supernatant recovering part having a chip rack and a supernatant recovery vessel, (C) a reagent part having a reagent-holding vessel and (D) a plurality of chip nozzles, having a mechanism for attaching and detaching the chip to and from the nozzle and a mechanism for sucking and injecting a treatment solution by attached chip and installing a head part installed with an arm unit movable toward X-Z axis direction. The method for detecting the nucleic acid in a sample uses the apparatus.
COPYRIGHT: (C)2003,JPO
摘要翻译：要解决的问题：为了使通过非常简单的操作需要大量时间来检测核酸和大的实验空间的杂交方法自动化，同时将小尺寸的设备带到设备上，并且简单且快速地制备单链核酸。解决方案：用于自动制备核酸的装置通过至少安装（A）具有反应容器支架的反应部件，加热和冷却装置和磁力控制器，（B）芯片架/上清液具有芯片架和上清液回收容器的回收部分，（C）具有试剂保持容器的试剂部分和（D）多个芯片喷嘴，具有用于将芯片连接到喷嘴和从喷嘴分离的机构，以及通过安装芯片吸取和注入处理溶液的机构，并安装安装有能够朝向XZ轴方向移动的臂单元的头部。用于检测样品中核酸的方法使用该装置。版权所有（C）2003，JPO

8. 发明专利

JP2007089566A Microorganism separating device 有权
标题翻译：微生物分离装置
公开(公告)号：JP2007089566A
公开(公告)日：2007-04-12
申请号：JP2006195978
申请日：2006-07-18
申请人： Tokyo Univ Of Agriculture & Technology , Toshiba Corp , 国立大学法人東京農工大学 , 株式会社東芝
发明人： MATSUNAGA TADASHI , TAKEYAMA HARUKO , TAGUCHI TOMOYUKI , HARAGUCHI SATOSHI , YOSHINO MASATO , ISHIMORI YOSHIO , KANEKO MASAO , TOYODA HIROKAZU
IPC分类号： C12M1/26
CPC分类号： C12M47/02
摘要： PROBLEM TO BE SOLVED: To provide a microorganism separating device capable of selectively separating a target microorganism from sample water with good accuracy and recovering the microorganism.
SOLUTION: This microorganism separating device is equipped with a microchip 20 for capturing the target microorganism contained in the sample water, a sample water supply means 19 for supplying the sample water to the microchip 20, and a sample water suction means 21 for sucking the sample water from the microchip 20. The microchip 20 has a flat plate substrate 10 on which a flow channel 11 having a fluid supply port 13, a fluid suction port 15, and a fluid discharge port 14 are formed and a capturing part 12 positioned on the fluid suction port 15 of the flat plate substrate 10. The capturing part 12 of the microchips has a plurality of open holes 12a each having a diameter smaller than a minimum diameter of the target microorganism.
COPYRIGHT: (C)2007,JPO&INPIT
摘要翻译：要解决的问题：提供能够以良好的精度选择性地将目标微生物与样品水分离并回收微生物的微生物分离装置。解决方案：该微生物分离装置配备有用于捕获试样水中所含的目标微生物的微芯片20，将样品水供给到微芯片20的试样供水装置19，以及用于从微芯片20吸取样本水。微芯片20具有平板基板10，在其上形成有具有流体供给口13，流体吸入口15和流体排出口14的流路11，并且捕获部12 定位在平板基板10的流体吸入口15上。微芯片的捕获部分12具有多个直径小于目标微生物的最小直径的开孔12a。版权所有（C）2007，JPO＆INPIT

9. 发明专利

JP2014140313A Capturing device for circulating cancer cells 有权
标题翻译：用于循环癌细胞的捕获装置
公开(公告)号：JP2014140313A
公开(公告)日：2014-08-07
申请号：JP2013009450
申请日：2013-01-22
申请人： Hitachi Chemical Co Ltd , 日立化成株式会社 , Tokyo Univ Of Agriculture & Technology , 国立大学法人東京農工大学
发明人： UEHARA TOSHISHIGE , KANETOMO MASABUMI , HOSOKAWA MASATO , YOSHINO TOMOKO , MATSUNAGA TADASHI
IPC分类号： C12M1/34 , C12N5/09 , C12Q1/04
摘要： PROBLEM TO BE SOLVED: To realize efficient capturing work of circulating cancer cells in blood by suppressing contamination of air into a flow path.SOLUTION: The capturing device for circulating cancer cells comprises a construction in which liquid to be supplied to a filter unit is selected by selection means and, based on the result, blood or processing solution is supplied to the filter unit by liquid supplying means, resulting in that efficient capturing work for circulating cancer cells in blood is performed when being compared to conventional device. In addition, a deaeration means is arranged at upstream side of the filter for capturing air in blood and discharging the air outside, thereby it is avoided that blood into which air is contaminated passes the filter, resulting in that reduction in processing efficiency due to air contamination is suppressed and high measurement precision may be maintained.
摘要翻译：要解决的问题：通过抑制空气进入流路的污染来实现血液循环癌细胞的有效捕获工作。解决方案：用于循环癌细胞的捕获装置包括其中选择供给到过滤器单元的液体通过选择手段，根据结果，通过液体供给装置向过滤器单元供给血液或加工溶液，从而与常规装置进行比较，进行用于循环血液中的癌细胞的高效捕获工作。此外，在过滤器的上游侧设置有除气装置，用于捕获血液中的空气并将空气排出到外部，从而避免被污染空气的血液通过过滤器，导致由于空气而导致的处理效率的降低污染被抑制，并且可以保持高的测量精度。

10. 发明专利

JP2013226063A Method for cultivating microalgae, biofilm formed on liquid surface by the method, biomass and oil obtained from the biofilm, method for retrieving the biofilm, and method for producing biomass fuel 有权
标题翻译：用于通过方法，生物质和生物质获得的生物质和油获得微生物，在液体表面上形成的生物膜的方法，用于检索生物膜的方法和用于生产生物质燃料的方法
公开(公告)号：JP2013226063A
公开(公告)日：2013-11-07
申请号：JP2012099189
申请日：2012-04-24
申请人： Fujifilm Corp , 富士フイルム株式会社 , Tokyo Univ Of Agriculture & Technology , 国立大学法人東京農工大学
发明人： KANEHARA HIDEYUKI , MATSUNAGA TADASHI , TANAKA TAKESHI , TANAKA SUKEYOSHI
IPC分类号： C12N1/12 , C07G99/00 , C10L5/44 , C11B1/00 , C12N15/09 , C12R1/89
CPC分类号： Y02E50/10 , Y02E50/30 , Y02P20/582
摘要： PROBLEM TO BE SOLVED: To provide a method for cultivating microalgae, capable of cutting cost of producing microalgae-derived biomass.SOLUTION: A method for cultivating microalgae is provided, comprising cultivating microalgae capable of forming biofilm on liquid surface so as to form biofilm on the liquid surface of a liquid medium.
摘要翻译：要解决的问题：提供一种培养微藻的方法，能够降低产生微藻衍生生物的成本。解决方案：提供一种培养微藻的方法，包括培养能够在液面上形成生物膜的微藻，以形成生物膜液体介质的液体表面。

你已经成功收藏专利！

检索式保存成功!

IPRDB

热门服务

关于我们

友情链接

联系方式