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

JP2009072144A Method for saccharifying celluloses 有权
标题翻译：用于分离细胞的方法
公开(公告)号：JP2009072144A
公开(公告)日：2009-04-09
申请号：JP2007245455
申请日：2007-09-21
申请人： Mitsui Eng & Shipbuild Co Ltd , Univ Nagoya , 三井造船株式会社 , 国立大学法人名古屋大学
发明人： KOBAYASHI SHINSUKE , TAKAOKA KAZUE , TOYAMA MASAYUKI , KATAGIRI MANABU
IPC分类号： C12P19/14
摘要： PROBLEM TO BE SOLVED: To provide a method capable of efficiently promoting hydrolysis of celluloses by an enzyme while keeping lignin in a system without carrying out oxidative decomposition of lignin.
SOLUTION: The method for saccharifying the celluloses comprises saccharifying celluloses contained in biomass such as a non-edible part of farm products and ligneous unused material or waste material by using a hydrolase. The method for saccharifying the celluloses is characterized in that a substance having high affinity for lignin is previously added to celluloses and then, hydrolysis reaction of the celluloses is started by the hydrolase.
COPYRIGHT: (C)2009,JPO&INPIT
摘要翻译：待解决的问题：提供一种能够有效地促进酶的纤维素水解，同时将木质素保持在体系中而不进行木质素的氧化分解的方法。糖化纤维素的方法包括通过使用水解酶来糖化生物质中包含的纤维素，例如农产品的不可食用部分和木质未使用的材料或废料。糖化纤维素的方法的特征在于，预先将对木质素具有高亲和力的物质加入到纤维素中，然后通过水解酶开始纤维素的水解反应。版权所有（C）2009，JPO＆INPIT

2. 发明专利

JP2009201389A New microorganism 有权
标题翻译：新型微生物
公开(公告)号：JP2009201389A
公开(公告)日：2009-09-10
申请号：JP2008045185
申请日：2008-02-26
申请人： Kyushu Univ , Mitsui Eng & Shipbuild Co Ltd , 三井造船株式会社 , 国立大学法人九州大学
发明人： TOYAMA MASAYUKI , TAKAOKA KAZUE , YOSHINO SADAZO
IPC分类号： C12N1/20
摘要： PROBLEM TO BE SOLVED: To provide a new microorganism having ability for producing ethanol.
SOLUTION: The new microorganism belonging to Veillonella has ability for producing ethanol in an anaerobic environment into which carbon monoxide, or a synthetic gas comprising carbon dioxide and hydrogen is introduced as a substrate, and is deposited as Veillonella sp. Strain M9 (Accession number NITE P-472) in Patent Organisms Depositary in National Institute of Technology and Evaluation.
COPYRIGHT: (C)2009,JPO&INPIT
摘要翻译：待解决的问题：提供具有生产乙醇能力的新微生物。解决方案：属于维雷诺氏菌属的新微生物具有在厌氧环境中生产乙醇的能力，其中一氧化碳或包含二氧化碳和氢气的合成气体作为基质被引入，并作为Veillonella sp沉积。国家技术与评估研究所专利生物保藏中的菌株M9（登录号NITE P-472）。版权所有（C）2009，JPO＆INPIT

3. 发明专利

JP2008253153A Method for producing alcohol 有权
标题翻译：生产醇的方法
公开(公告)号：JP2008253153A
公开(公告)日：2008-10-23
申请号：JP2007095733
申请日：2007-03-30
申请人： Mitsui Eng & Shipbuild Co Ltd , 三井造船株式会社
发明人： TOYAMA MASAYUKI , KATAGIRI MANABU , TAKAOKA KAZUE
IPC分类号： C12P7/10
CPC分类号： Y02E50/16
摘要： PROBLEM TO BE SOLVED: To provide a method for producing an alcohol, by which saccharification using an enzyme and alcohol fermentation using a yeast can efficiently be performed in one reaction tank.
SOLUTION: This method for producing the alcohol, comprising saccharifying cellulose originated from wood-based biomass into glucose by an enzymatic reaction and then supplying the glucose to a yeast comprising Saccharomyces cerevisiae AM12 strain to subject the glucose to alcohol fermentation, is such that by controlling the temperature in the reaction tank to 40 to 45°C, when the saccharification reaction for saccharifying the cellulose with the enzyme and the alcohol fermentation using the yeast comprising the AM12 strain are performed simultaneously.
COPYRIGHT: (C)2009,JPO&INPIT
摘要翻译：待解决的问题：提供一种生产醇的方法，通过该方法，可以在一个反应槽中有效地使用使用酵母的酶和醇发酵进行糖化。解决方案：用于生产醇的方法包括通过酶反应将源自木质生物质的纤维素糖化为葡萄糖，然后将葡萄糖供应到包含酿酒酵母AM12菌株的酵母以使葡萄糖进行酒精发酵，通过将反应罐中的温度控制在40〜45℃，同时进行使用含有AM12菌株的酵母进行酶的纤维素糖化和醇发酵的糖化反应。版权所有（C）2009，JPO＆INPIT

4. 发明专利

JP2008092819A Method for continuous production of alcohol 有权
标题翻译：连续生产醇的方法
公开(公告)号：JP2008092819A
公开(公告)日：2008-04-24
申请号：JP2006275850
申请日：2006-10-06
申请人： Mitsui Eng & Shipbuild Co Ltd , 三井造船株式会社
发明人： TOYAMA MASAYUKI , TAKAOKA KAZUE
IPC分类号： C12P7/06 , C12R1/865
CPC分类号： Y02E50/17
摘要： PROBLEM TO BE SOLVED: To provide a method for continuously producing alcohol with high continuous ethanol productivity, under aerobic conditions.
SOLUTION: The method for continuous production of the alcohol comprises feeding a yeast culture solution cultured by using a yeast comprising Saccharomyces cerevisiae AM12 strain and an alcohol raw material to a fermentation vessel 2, carrying out alcohol fermentation, taking out the resultant alcohol culture solution from the fermentation vessel 2, and conducting the continuous fermentation of the alcohol. The method for continuous production of the alcohol maintains the interior of the fermentation vessel 2 under an aerobic condition and continuously ferments the alcohol.
COPYRIGHT: (C)2008,JPO&INPIT
摘要翻译：待解决的问题：提供一种在有氧条件下连续生产具有高连续乙醇生产率的醇的方法。解决方案：连续生产醇的方法包括将通过使用包含酿酒酵母AM12菌株和酒精原料的酵母培养的酵母培养溶液进料到发酵容器2中，进行酒精发酵，取出所得醇来自发酵容器2的培养液，进行醇的连续发酵。连续生产醇的方法将发酵容器2的内部保持在需氧条件下并连续发酵酒精。版权所有（C）2008，JPO＆INPIT

5. 发明专利

JP2008048605A Method for decomposing dioxins 审中-公开
标题翻译：分解二氧化硅的方法
公开(公告)号：JP2008048605A
公开(公告)日：2008-03-06
申请号：JP2006099396
申请日：2006-03-31
申请人： Mitsui Eng & Shipbuild Co Ltd , 三井造船株式会社
发明人： TOYAMA MASAYUKI , TAKAOKA KAZUE , IWAI TOMOKO , NAKATANI TATSUO
IPC分类号： C12N1/20 , A62D3/02 , A62D101/08 , B09C1/10 , C02F11/00 , C02F11/02
CPC分类号： B09C1/10
摘要： PROBLEM TO BE SOLVED: To provide a method for decomposing dioxins in a short time by mixing dioxin contaminants with a compost comprising microorganisms capable of decomposing dioxins.
SOLUTION: The method for decomposing dioxins contained in dioxin contaminants comprises making a microaerobic condition having 0.1-1.0 vol.% ratio of oxygen contained in a gas in a container shielded from contact with the air, feeding a compost containing microorganisms having decomposition ability of at least dioxins and dioxin contaminants to the container, when the number of the microorganisms contained in the mixture is 1.0×10
10 -1.0×10
12 per g based on the dry weight of the mixture, adding ≥0.008g based on 1 g of the dry weight of the mixture to the mixture daily.
COPYRIGHT: (C)2008,JPO&INPIT
摘要翻译：要解决的问题：提供一种通过将二恶英污染物与包含能够分解二恶英的微生物的堆肥混合的短时间分解二恶英的方法。解决方案：分解二恶英污染物中所含二恶英的方法包括制备微生物条件，其中容纳在与空气接触的容器中的气体中所含的氧含量为0.1-1.0体积％，将含有分解的微生物的堆肥当混合物中含有的微生物数量为1.0×10×SP×10 / SP / g时，至少二恶英和二恶英污染物对容器的能力基于混合物的干重，每天向混合物中加入≥0.008g，基于混合物的干重1克。版权所有（C）2008，JPO＆INPIT

6. 发明专利

JP2009225756A Method for continuously producing alcohol 有权
标题翻译：连续生产醇的方法
公开(公告)号：JP2009225756A
公开(公告)日：2009-10-08
申请号：JP2008077765
申请日：2008-03-25
申请人： Mitsui Eng & Shipbuild Co Ltd , 三井造船株式会社
发明人： TOYAMA MASAYUKI , TAKAOKA KAZUE
IPC分类号： C12P7/06 , C12R1/865
CPC分类号： Y02E50/17
摘要： PROBLEM TO BE SOLVED: To provide a method for continuously producing a high concentration alcohol capable of making full use of the ability to produce an alcohol of yeast having a property of coagulation and sedimentation by preventing the outflow of yeast cells and improving the contact efficiency between alcohol raw materials and the yeast.
SOLUTION: The method for continuously producing an alcohol by which an alcohol is produced by forcibly causing a liquid flow to occur in a lower side of a fermentation tank when alcohol fermentation is performed by supplying alcohol raw materials to the fermentation tank in the presence of the yeast having the property of coagulation and sedimentation, characterized by controlling a liquid flow in the lower side of the fermentation tank such that yeast cell concentrations d1, d2 and d3 are measured at different positions in the vertical direction of the alcohol fermentation liquid in the fermentation tank and a ratio of d1 to d2 (d2/d1) becomes 1.7 or more and a ratio of d1 to d3 (d3/d1) becomes 7.6 or less.
COPYRIGHT: (C)2010,JPO&INPIT
摘要翻译：要解决的问题：提供一种连续制备能够充分利用通过防止酵母细胞流出而产生具有凝结和沉淀性质的酵母醇的能力的高浓度醇的方法，酒精原料与酵母的接触效率。解决方案：当通过向发酵罐中提供酒精原料进行酒精发酵时，连续生产醇的方法是通过强制引发发酵罐下侧发生液体流而产生醇的方法存在具有凝结和沉淀性质的酵母，其特征在于控制发酵罐下侧的液体流动，使得在酒精发酵液体的垂直方向上的不同位置测量酵母细胞浓度d1，d2和d3 在发酵槽中，d1〜d2（d2 / d1）的比例为1.7以上，d1〜d3（d3 / d1）的比为7.6以下。版权所有（C）2010，JPO＆INPIT

7. 发明专利

JP2008237055A Method for producing rice saccharified liquid 有权
标题翻译：生产米汁液体的方法
公开(公告)号：JP2008237055A
公开(公告)日：2008-10-09
申请号：JP2007079573
申请日：2007-03-26
申请人： Mitsui Eng & Shipbuild Co Ltd , 三井造船株式会社
发明人： TOYAMA MASAYUKI , TAKAOKA KAZUE
IPC分类号： C12P19/02 , A23L7/104
摘要： PROBLEM TO BE SOLVED: To provide a method for producing a rice saccharified liquid for remarkably improving the saccharification efficiency of rice, by carrying out a pretreatment with an acid and a high-temperature and a high-pressure when the rice saccharified liquid is produced with a normal enzyme. SOLUTION: The method for producing the rice saccharified liquid is carried out by introducing rice flour and water in 1:(1.5-2.5) mixing ratio (weight ratio) into a vessel, mixing and stirring both, then adding hydrochloric acid to the mixture liquid in the vessel, regulating the pH to 1.5-2.5, subsequently conducting a pretreatment of heating the mixture liquid, after the acid treatment in a pressurized vessel at a temperature within the range of 100-130°C for 15-25 min, and then carrying out saccharification with the enzyme. COPYRIGHT: (C)2009,JPO&INPIT
摘要翻译：待解决的问题：为了提供一种用于制造米糖化液的方法，用于显着提高米的糖化效率，通过在水分糖化液体中进行酸和高温高压的预处理用正常酶产生。解决方案：通过将米粉和水以1：（1.5-2.5）的混合比（重量比）引入容器中进行，混合搅拌，然后加入盐酸至在容器中的混合液体中，将pH调节至1.5-2.5，随后在加压容器中在100-130℃的温度下酸处理15-25分钟后进行加热混合液体的预处理，然后用酶进行糖化。版权所有（C）2009，JPO＆INPIT

8. 发明专利

JP2006280262A Method for measuring contaminant-degrading ability of microorganism 有权
标题翻译：测定微生物污染物降解能力的方法
公开(公告)号：JP2006280262A
公开(公告)日：2006-10-19
申请号：JP2005103710
申请日：2005-03-31
申请人： Mitsui Eng & Shipbuild Co Ltd , Toyohashi Univ Of Technology , 三井造船株式会社 , 国立大学法人豊橋技術科学大学
发明人： HIRAISHI AKIRA , TOYAMA MASAYUKI , NAKATANI TATSUO , TAKAOKA KAZUE , IWAI TOMOKO
IPC分类号： C12Q1/02 , B09C1/10
摘要： PROBLEM TO BE SOLVED: To provide a method for quickly monitoring the cleanup status in the process for the cleanup of an object contaminated with organic matter utilizing the microbial reaction in the object, without conducting a high-sensitivity contaminant analysis needing long time and high cost.
SOLUTION: The method comprises the pretreatment step of removing microorganism-undigested organic matter from a microorganism-containing contaminated object, the step of constructing, from the pretreated contaminated object, a contaminant culture system provided with only organic matter as contamination source as a respiratory substrate and a universal culture system provided with living organic matter free of the above organic matter, and the step of measuring the respiratory activity of the microorganisms in each of the above culture systems. By comparing the respiratory activity of the contaminant culture system with that of the universal culture system, the ability of the microorganisms in the contaminated object to degrade the contamination source is measured.
COPYRIGHT: (C)2007,JPO&INPIT
摘要翻译：要解决的问题：提供一种用于在物体中利用微生物反应清洁被有机物污染的物体的过程中快速监测清洁状态的方法，而不需要长时间的高灵敏度污染物分析成本高。解决方案：该方法包括从含微生物的污染物质中除去微生物未消化的有机物质的预处理步骤，从预处理的污染物质构建仅提供有机物质的污染物培养系统作为污染源的步骤呼吸基质和具有不含上述有机物的活体有机物的通用培养体系，以及测定上述培养体系中的微生物的呼吸活性的步骤。通过比较污染物培养系统的呼吸活性与通用培养系统的呼吸活性，测量被污染物质中的微生物降解污染源的能力。版权所有（C）2007，JPO＆INPIT

9. 发明专利

JP2011200177A Culturing device and culturing method 审中-公开
标题翻译：文化设备和文化方法
公开(公告)号：JP2011200177A
公开(公告)日：2011-10-13
申请号：JP2010071194
申请日：2010-03-26
申请人： Mitsui Eng & Shipbuild Co Ltd , 三井造船株式会社
发明人： ISHII TAKEO , TOYAMA MASAYUKI
IPC分类号： C12M1/02 , B01F3/08 , B01F5/00 , C12M1/00 , C12N1/00
CPC分类号： C12M23/06 , C12M21/02 , C12M23/20 , C12M27/06 , C12M29/06 , C12M29/22 , C12M31/08 , C12M41/06 , C12M41/26
摘要： PROBLEM TO BE SOLVED: To provide a culturing device and a culturing method which are capable of achieving the improvement of culturing efficiency, the scale up of culturing volume, and cost saving.SOLUTION: This culturing device 1 including a culturing vessel (a tube-shaped culturing vessel) 2 for making a culturing liquid for culturing microorganisms flow, culturing liquid-supplying means 3 for supplying the culturing liquid into the culturing vessel 2, gas-supplying means 4 for supplying a gas containing carbon dioxide to the culturing vessel 2, and an expansion tank 5 for absorbing the volume change of the culturing liquid in the culturing vessel 2, is formed with a mixing blade member 21 on the inside of the culturing vessel 2 for inducing the culturing liquid so as to flow around the axis of the culturing vessel.
摘要翻译：要解决的问题：提供能够实现培养效率的提高，培养体积的增加和成本节约的培养装置和培养方法。解决方案：该培养装置1包括培养容器（管 - 培养用于培养微生物的培养液的培养容器2用于培养培养液2的培养液培养用的供液装置3，向培养容器2供给含有二氧化碳的气体的气体供给装置4，和用于吸收培养容器2中的培养液体积变化的膨胀罐5，在培养容器2的内侧形成有用于诱导培养液体的混合叶片构件21，以便围绕培养容器2的轴线流动培养血管。

10. 发明专利

JP2009201387A New microorganism 有权
标题翻译：新型微生物
公开(公告)号：JP2009201387A
公开(公告)日：2009-09-10
申请号：JP2008045183
申请日：2008-02-26
申请人： Kyushu Univ , Mitsui Eng & Shipbuild Co Ltd , 三井造船株式会社 , 国立大学法人九州大学
发明人： TOYAMA MASAYUKI , TAKAOKA KAZUE , YOSHINO SADAZO
IPC分类号： C12N1/20 , C12R1/01
摘要： PROBLEM TO BE SOLVED: To provide a new microorganism having ability for producing ethanol.
SOLUTION: The new microorganism belonging to Veillonella has ability for producing ethanol in an anaerobic environment into which carbon monoxide, or a synthetic gas comprising carbon dioxide and hydrogen is introduced as a substrate, and is deposited as Veillonella sp. Strain G11 (Accession number NITE P-471) in Patent Organisms Depositary in National Institute of Technology and Evaluation.
COPYRIGHT: (C)2009,JPO&INPIT

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