| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 101 | Biological production of acetic acid from the waste gas | JP50406498 | 1996-07-01 | JP4101295B2 | 2008-06-18 | ジエイムズ・エル ギヤデイ，; グアングジヨング チェン， |
| A method and apparatus are designed for converting waste gases from industrial processes such as oil refining, and carbon black, coke, ammonia, and methanol production, into useful products. The method includes introducing the waste gases into a bioreactor where they are fermented to various products, such as organic acids, alcohols, hydrogen, single cell protein, and salts of organic acids by anaerobic bacteria within the bioreactor. These valuable end products are then recovered, separated and purified. | ||||||
| 102 | New ethanol-producing bacteria and method for producing ethanol | JP2002155085 | 2002-05-29 | JP2003339371A | 2003-12-02 | NISHIO NAOMICHI; NAKASHIMADA YUTAKA; WATANABE SHIGEYUKI; OTSUKA HIROAKI; CHIYODA OSAMU; TANAKA TORU |
| PROBLEM TO BE SOLVED: To provide a bacterial strain effective for continuously producing ethanol in high efficiency at a low cost at a temperature as high as ≥40°C by using a gas causing global warming such as carbon dioxide gas without cooling the gas. SOLUTION: The bacterial strain belongs to the genus Clostridium or its derivative strain capable of producing ethanol at ≥40°C from a carbon compound exhibiting gaseous state at normal temperature and pressure condition. The invention further provides a method for the production of ethanol by using the strain. COPYRIGHT: (C)2004,JPO | ||||||
| 103 | Clostridium strains to produce ethanol from a gas substrate contains | JP2000616373 | 1999-05-07 | JP2002543793A | 2002-12-24 | ガツデイ，ジエイムズ・エル |
| (57)【要約】 クロストリジウム・リュングダーリイの２種の新規な嫌気性菌株が、自然において共存している混在菌から単離され、そして工業的工程からのある種の廃ガスを有用な生産物、例えばエタノールへ変換するための方法において有用である。 | ||||||
| 104 | Biological production of acetic acid from the waste gas | JP50406498 | 1996-07-01 | JP2000513233A | 2000-10-10 | ギヤデイ，ジエイムズ・エル |
| A method and apparatus are designed for converting waste gases from industrial processes such as oil refining, and carbon black, coke, ammonia, and methanol production, into useful products. The method includes introducing the waste gases into a bioreactor where they are fermented to various products, such as organic acids, alcohols, hydrogen, single cell protein, and salts of organic acids by anaerobic bacteria within the bioreactor. These valuable end products are then recovered, separated and purified. | ||||||
| 105 | Method for improving soil | JP31583592 | 1992-10-30 | JPH06141672A | 1994-05-24 | KUME HIDE |
| PURPOSE:To provide the soil-improving method for fertilizing and improving the soil of a greening.agricultural and forestry field by rapidly decomposing and utilizing a slightly decomposable fibrous substance or hard protein material with a new strain which has an ability of solubilizing lignin whose solubilization has been difficult and which can vigorously ferment cellulose and protein. CONSTITUTION:A mixed culture product or an organic material-fermentation- decomposing agent containing the mixed culture product as an effective main ingredient is directly applied to the soil of a greening.agricultural and forestry field. The mixed culture product is produced by subjecting a thermophilic cellulose-decomposing bacteria: Clostridium thermocellumbiovar SK522 (FERM P-3459) and Thermus aquaticusbiovar SK542 (FERM P-3382) to a symbiotic mixed culture under a thermophilic environment at >=60 deg.C. | ||||||
| 106 | Mutant of bacterium clostridium histolyticum, its production and its use | JP20570491 | 1991-07-23 | JPH05219942A | 1993-08-31 | MIRAN HORUJIEBUATSUKU; IWAN YUDOBUISHITSUKU; SONJIYA SHIZUMETSUKU; BURASUTA SOYATSUKUUDERUKOSU; SUTEPAN GAMURIN; BURADEIMIIRU DERITSUKU |
| PURPOSE: To obtain a new mutant useful for producing clostripain-free collagenase. CONSTITUTION: This mutant Clostridium histolyticum K-26 clo 88 has characteristics comprising the lack of a motility system which is a fundamental characteristic of the parental strain Clostridium histolyticum K-26 and the inability to biosynthesize the accompanying enzyme clostripain. The mutant is deposited with the accession number NCAIMB (P) 001145 and the accession number 4043 in the Institute of Biochemical Engineering (Yugoslavia). The mutant is obtained by treating the Clostridium histolyticum K-26 with a mutagenic agent, N-methyl-N'-nitro-N-nitrosoguanidine. COPYRIGHT: (C)1993,JPO | ||||||
| 107 | JPH0526460B2 - | JP3812583 | 1983-03-08 | JPH0526460B2 | 1993-04-16 | MONITSUKU ERUMAN; FURANSOWAAZU FUAIYOORU; REMII MARUSHARU |
| The Clostridium acetobutylicum mutant IFP 904 (ATCC 39058) is obtained by spreading a culture of a strain of Clostridium acetobutylicum at the surface of a solid culture medium containing n-butanol at a specified concentration, growing the strain in the presence of a mutagenic agent and recovering a strain of increased resistance to n-butanol. The resultant mutant can be used to produce a mixture of butanol and acetone of increased concentration. | ||||||
| 108 | JPS638756B2 - | JP12945281 | 1981-08-20 | JPS638756B2 | 1988-02-24 | HAYASHIDA SHINSAKU; OGATA YASUYA; YOSHINO TEIZO |
| 109 | Toxin a and manufacture thereof | JP6053284 | 1984-03-28 | JPS60207060A | 1985-10-18 | TOREISHII DEERU UIRUKINSU; NEIJIN MAIKERU SARIBAN |
| Purified toxin A of C. difficile is produced. | ||||||
| 110 | New mutant variant of chrostolidium telmoacectium and use thereof in acetic acid production | JP4413584 | 1984-03-09 | JPS59173087A | 1984-09-29 | FUREDERITSUKU EI KERAA JIYUNIA; JIEFUERII ESU GANANGU; SUZAN JIEI RUENZAA |
| 111 | Preparation of butanol | JP12945281 | 1981-08-20 | JPS5831993A | 1983-02-24 | HAYASHIDA SHINSAKU; OGATA YASUCHIKA; YOSHINO TEIZOU |
| PURPOSE: To prepare butanol from cellulose, by cultivating a microorganism belonging to the genus Clostridium, having cellulose assimilating properties, capable of producing butanol in a medium comprising cellulose as a carbon source. CONSTITUTION: A new microorganism Clostridium sp. AH-1 (FERM-P 6093) separated from compost is used as a strain to be used. The microorganism has an ability to assimilate cellulose, starch, and sugar and an ability to assimilate them and to produce butanol. The microorganism is inoculated into a medium comprising 0.5W5wt% cellulose such as wood, straw of rice plant, bagasse, etc., a nitrogen source, an inorganic salt, etc., it is cultivated at 50W60°C for 2W7 days, to give butanol. Ethanol, acetic acid and n-butyric acid are prepared besides butanol. COPYRIGHT: (C)1983,JPO&Japio | ||||||
| 112 | 수소 생산이 억제된 클로스트리디움 타이로부티쿰 균주 및 이의 용도 | KR1020160047227 | 2016-04-18 | KR1020170119264A | 2017-10-26 | 엄영순; 김기연; 김연제; 우한민; 이선미; 공경택; 윤성훈; 이경민 |
| 본명세서에는수소화효소유전자발현을억제하기위한안티센스 RNA 분자, 그를포함하는조성물, 그를암호화하는 DNA 서열을포함하는벡터, 상기안티센스 RNA 분자또는그를암호화하는 DNA 서열을포함하거나또는상기벡터로형질전환된숙주세포, 및그 숙주세포를이용한물질생산방법이개시된다. 이를이용하면수소화효소발현을억제시킬수 있고그에따라수소생산이감소하여부티르산과같이유용한물질생산을증가시키면서아세트산과같은부산물을감소시킬수 있고, 목당을효과적으로활용하여부티르산과같은유용물질을생산할수 있다. | ||||||
| 113 | 관절염 예방 및 치료 효과를 갖는 아이디-씨비티5101(ID-CBT5101) 및 이의 용도 | KR1020150062300 | 2015-05-01 | KR101688224B1 | 2016-12-20 | 이승훈; 김민구; 강대중; 강재훈 |
| 본발명은관절염예방및 치료효과를갖는틴달화클로스트리디움부티리쿰및 이의용도에관한발명으로, 보다상세하게는관절염증의바이오마커인 COX-2 및염증성싸이토카인인 tumor necrosis factor-α (TNF-α)의수치를낮춰관절염을예방하고증상을완화시키는데기여하는틴달화된클로스트리디움부티리쿰 IDCC 5101 사균체및 이를유효성분으로포함하는관절염예방및 치료용조성물에관한것이다. 본발명에따른클로스트리디움부티리쿰 IDCC 5101 사균체는관절염동물모델에서농도의존적으로관절염증상을완화시켜관절염예방및 치료효과가있음을확인하였다. | ||||||
| 114 | 재조합 미생물에 의한 일산화탄소로부터 부탄올의 제조 | KR1020147000771 | 2011-09-29 | KR101640325B1 | 2016-07-15 | 퀩케미카엘; 류풍민; 심슨션 |
| 본발명은특히, CO를사용하여 1-부탄올및/또는이의전구체를생성할수 있는유전적으로변형된신규미생물, 신규메틸전달효소및 이를코딩하는핵산, 상기신규메틸전달효소를사용하여유전적으로변형된미생물을제조하는방법, 및미생물발효를통해 1-부탄올및/또는이의전구체를제조하는방법에관한것이다. | ||||||
| 115 | 미생물 배양액으로부터 1,3-프로판디올과 2,3-부탄디올의 분리 및 정제방법 | KR1020140088851 | 2014-07-15 | KR1020160008756A | 2016-01-25 | 박정호; 임용배 |
| 본발명은 1,3-프로판디올및 2,3-부탄디올을생산하는미생물배양액으로부터 1,3-프로판디올과 2,3-부탄디올을분리및 정제하는방법에관한것으로, 상세하게는 1,3-프로판디올및 2,3-부탄디올을생산하는미생물배양액을증발시킨후 콘덴서를순차적으로통과시켜탈수및 제염을동시에진행하며분리및 정제하는단계를포함하는 1,3-프로판디올및 2,3-부탄디올의분리및 정제방법에관한것이다. 본발명따른분리방법을사용함으로써, 1,3-프로판디올(1,3-propanediol) 및 2,3-부탄디올(2,3-butanediol)을생산하는미생물의배양액으로부터고순도의 1,3-프로판디올및 2,3-부탄디올을고효율, 저비용으로분리및 정제할수 있다. | ||||||
| 116 | 산으로 전처리한 바이오매스를 이용한 부탄올 발효 | KR1020147005604 | 2012-08-01 | KR1020140147798A | 2014-12-30 | 랑가스와미,비드야; 이사,재스민; 조시,하슈바르단 |
| 본 발명은 클로스트리듐 아세토부틸리쿰 MTCC587 돌연변이 균주에 의한 부탄올 생산에 사용되는 재생가능한 원료로 자트로파 씨앗 깻묵, 퐁가미아 씨앗 깻묵, 바나나 줄기와 같은 산으로 전처리한 바이오매스를 사용하는 것을 제시한다. 균주를 개선하여 보다 나은 부탄올 내성과 생산성을 얻기 위해 화학적 돌연변이를 유발시킨다. 본 발명은 최초로 산으로 전처리한 자트로파 씨앗 깻묵을 사용하여 단일 비연속 발효에서 수율이 높은 부탄올을 생산하는 효과적인 공정을 보고했다.
|
||||||
| 117 | 신규 세균 및 이의 이용 방법 | KR1020107013119 | 2008-11-13 | KR101375029B1 | 2014-03-14 | 심슨숀데니스; 포스터리처드르웰린시드니; 트랑프엉론; 로우매튜제임스; 워너이안린드스트랜드 |
| 일산화탄소를 포함하는 기질의 혐기성 발효에 의하여 에탄올 생성 효율이 개선된 신규한 세균을 기술하였다.
|
||||||
| 118 | 재조합 미생물에 의한 일산화탄소로부터 부탄올의 제조 | KR1020147000771 | 2011-09-29 | KR1020140012212A | 2014-01-29 | 퀩케미카엘; 류풍민; 심슨션 |
| 본 발명은 특히, CO를 사용하여 1-부탄올 및/또는 이의 전구체를 생성할 수 있는 유전적으로 변형된 신규 미생물, 신규 메틸전달효소 및 이를 코딩하는 핵산, 상기 신규 메틸전달효소를 사용하여 유전적으로 변형된 미생물을 제조하는 방법, 및 미생물 발효를 통해 1-부탄올 및/또는 이의 전구체를 제조하는 방법에 관한 것이다.
|
||||||
| 119 | 클로스트리디움 디피실리 균주 검출용 조성물과 키트 및 이를 이용한 검출 방법 | KR1020120061671 | 2012-06-08 | KR1020130137952A | 2013-12-18 | 정선옥; 김준호; 이수관; 황규연; 엄태희 |
| Disclosed are a composition for detecting Clostridium difficile including a primer set for detecting Clostridium difficile strains, a kit, and a Clostridium difficile detection method. The detection method is capable of rapidly detecting the Clostridium difficile strains from a sample with high sensitivity and accuracy. [Reference numerals] (AA,CC) Response Unit;(BB,DD) Cycle number (BAA-1382) | ||||||
| 120 | 식중독 세균 Clostridium perfringens 탐지용 탐침자 및 그를 포함한 DNA 칩 | KR1020110111448 | 2011-10-27 | KR1020130046323A | 2013-05-07 | 조재창; 김혜진 |
| PURPOSE: A probe for detecting bacteria causing food poisoning, and a DNA chip containing the same are provided to quickly and accurately detect Clostridium perfringens. CONSTITUTION: A probe for detecting bacteria causing food poisoning, Clostridium perfringens, contains one or more among sequence lists 13-50. A DNA chip for detecting Clostridium perfringens contains the probe. The DNA chip quickly and accurately detects Clostridium perfringens. Clostridium perfringens is prepared from ATCC(American Type Culture Collection). | ||||||
QQ群二维码
意见反馈
意见反馈