| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 1 | 一株防治棉花黄萎病的木霉菌及应用 | CN201410743008.7 | 2014-12-05 | CN104480023A | 2015-04-01 | 李梅; 蒋细良; 刘政; 孙艳 |
| 本发明提供了一种木霉菌，该木霉菌(Trichoderma longibrachiatum)的保藏编号为CGMCC No.9727。本发明还提供了一种复合微生物菌剂，所述的复合微生物菌剂的活性成分包含如上所述的木霉菌、蜡状芽胞杆菌(Bacillus cereus)和摩加夫芽胞杆菌(Bacillus mojavensis)。本发明还提供了如上所述的木霉菌或如上所述的微生物菌剂在棉花黄萎病防治中的应用。通过上述技术方案，本发明能够有效地防治棉花黄萎病的发生。 | ||||||
| 2 | 杀虫黄杆菌菌株和生物活性组合物、代谢物和用途 | CN201380014385.0 | 2013-03-13 | CN104508116A | 2015-04-08 | 安娜·露西娅·科尔多瓦-科雷洛斯; 拉特纳卡·阿索尔卡; 玛丽亚·科伊武宁; 玛格丽特·罗德里格斯; 邢丽娟; 帕梅拉·马罗内 |
| 本发明提供杀虫黄杆菌(Flavobacterium)菌株和自其衍生的生物活性组合物和代谢物，以及其用于控制害虫的使用方法。 | ||||||
| 3 | 黄杆菌属菌株与内切褐藻胶裂解酶编码基因及制备与应用 | CN201110424529.2 | 2011-12-16 | CN102994407A | 2013-03-27 | 杜昱光; 黄李淑馨; 李曙光; 赵小明; 曹海龙; 刘航 |
| 本发明公开了一种内切褐藻胶裂解酶Alg2A的基因序列及其制备方法与应用。本发明所涉及的褐藻胶裂解酶Alg2A来源土壤新分离菌株Flavobacterium sp.S20。本发明还提供了一种制备该新型褐藻胶裂解酶的方法，即利用基因工程的技术方法，将该新褐藻胶裂解酶的基因克隆到大肠杆菌表达载体上，获得可异源表达该酶的大肠杆菌重组菌株，用该菌株异源表达制备的褐藻胶裂解酶Alg2A，具有降解褐藻酸钠制备褐藻酸钠寡糖的功能。本发明提供的褐藻胶裂解酶Alg2A可广泛应用于化工、农业、食品、饲料添加、医药及海藻遗传工程等领域。 | ||||||
| 4 | 杀虫黄杆菌菌株和生物活性组合物、代谢物和用途 | CN201380014385.0 | 2013-03-13 | CN104508116B | 2017-05-24 | 安娜·露西娅·科尔多瓦-科雷洛斯; 拉特纳卡·阿索尔卡; 玛丽亚·科伊武宁; 玛格丽特·罗德里格斯; 邢丽娟; 帕梅拉·马罗内 |
| 本发明提供杀虫黄杆菌(Flavobacterium)菌株和自其衍生的生物活性组合物和代谢物，以及其用于控制害虫的使用方法。 | ||||||
| 5 | 一株降解纤维素和淀粉双功能菌株及其分离筛选方法和应用 | CN201510056059.7 | 2015-02-03 | CN104611266A | 2015-05-13 | 李大鹏; 李春艳; 成小松; 侯宁; 冯露; 成毅; 柳宏原; 刘科然; 曹会鸣; 黄馨凝 |
| 一株降解纤维素和淀粉双功能菌株及其分离筛选方法和应用，它涉及一株双功能菌株及其分离筛选方法和应用。本发明要解决由于低温限制造成生活垃圾降解速度慢的问题。本发明的菌株为黄杆菌(Flavobacterium sp.)FL-1，保藏在中国普通微生物菌种保藏管理中心，保藏日期为2015年01月04日，保藏号为CGMCC No.10272。分离方法：一、制备不同浓度的倍比稀释液；二、使平板中有菌落出现；三、低温恒温培养；四、分理纯化至有纯菌株。本发明的菌株能同时纤维素酶和淀粉酶，具有降解纤维素和淀粉效率高的特点。筛选用的培养基针对性强。本发明的方法具有工艺时间短、节约资源、费用小、设备简单的有点。 | ||||||
| 6 | 黄杆菌属菌株与内切褐藻胶裂解酶编码基因及制备与应用 | CN201110424529.2 | 2011-12-16 | CN102994407B | 2014-10-29 | 杜昱光; 黄李淑馨; 李曙光; 赵小明; 曹海龙; 刘航 |
| 本发明公开了一种内切褐藻胶裂解酶Alg2A的基因序列及其制备方法与应用。本发明所涉及的褐藻胶裂解酶Alg2A来源土壤新分离菌株Flavobacterium sp.S20。本发明还提供了一种制备该新型褐藻胶裂解酶的方法，即利用基因工程的技术方法，将该新褐藻胶裂解酶的基因克隆到大肠杆菌表达载体上，获得可异源表达该酶的大肠杆菌重组菌株，用该菌株异源表达制备的褐藻胶裂解酶Alg2A，具有降解褐藻酸钠制备褐藻酸钠寡糖的功能。本发明提供的褐藻胶裂解酶Alg2A可广泛应用于化工、农业、食品、饲料添加、医药及海藻遗传工程等领域。 | ||||||
| 7 | Microbial-derived zeaxanthin-containing composition and use thereof | JP30020498 | 1998-10-21 | JP3361064B2 | 2003-01-07 | エル． ギアハート、デニス |
| Zeaxanthin is produced using Flavobacterium multivorum. The process and the nutrient medium used in the process provide greater zeaxanthin and cell yields per liter, at a lower cost, and more rapidly than known methods and microorganisms. Biomass compositions containing the microorganism of this invention are also disclosed. | ||||||
| 8 | JPS6214272B2 - | JP15572480 | 1980-11-05 | JPS6214272B2 | 1987-04-01 | CHAARUZU TOOMASU GUTSUDOHYUU; SEODOORU UORUTAA ESUDAASU; PURAKASHU SHARACHANDORA MASUREKARU |
| A urease-free creatinine iminohydrolase enzyme preparation obtained from an aerobic soil microorganism. The enzyme of the preparation preferably has a molecular weight of from about 250,000 to 300,000; a maximum activity at a pH between 7 and 8 as measured at 37 DEG C.; a Km of about 3 to 5 mM for creatinine as measured at 37 DEG C., pH 7.5; and a specific activity for creatinine of at least about 1.0 unit per milligram of protein in the preparation as measured at 37 DEG C., pH 7.5. The preferred enzyme preparation is derived from the aerobic soil microorganism ATCC 31,546. Assay methods, compositions, and elements containing the aforementioned urease-free creatinine iminohydrolase for the determination of creatinine in an aqueous liquid are also disclosed. | ||||||
| 9 | JPS617201B2 - | JP17147380 | 1980-12-06 | JPS617201B2 | 1986-03-05 | |
| The present invention relates to: (1) a heteroglycan composed of (a) fucose, (b) mannose, and (c) glucose in the molar ratio of (a):(b):(c)= 0.15 +/- 0.05 : 0.31 +/- 0.05 : 1, and having an infrared absorption spectrum as shown in Figure 4 of the accompanying drawings; (2) a process for production of the above heteroglycan (1) which comprises cultivating a heteroglycan-producing microorgansm belonging to the genus Flavobacterium and recovering the heteroglycan produced and accumulated in the media; and (3) an immunopotentator containing the above heteroglycan (1) or its salt as an active component. | ||||||
| 10 | Microorganism belonging to the genus flavobacterium designated ferm BP-4010 | US950586 | 1992-09-25 | US5342778A | 1994-08-30 | Kazuhito Moriya; Koki Horikoshi |
| A microorganism belonging to the genus Flavobacterium possessing the capacity to decompose hydrocarbons, tolerance to sulfurous acids, tolerance to salinity, tolerance to organic solvents, and tolerance to pressure. The microorganism is a strain of the genus Flavobacterium DS-711 (FERM BP-4010). | ||||||
| 11 | Production of disease suppresive compost and container media, and microorganism culture for use therein | US11831 | 1987-02-06 | US4900348A | 1990-02-13 | Harry A. Hoitink |
| Compost, e.g. hardwood bark, is rendered suppressive to plant pathogens, such as Rhizoctonia solani, Pythium ultimum and Fusarium, and/or diseases caused thereby by adding to the compost, desirably after peak heating has been achieved but before substantial recolonization of the compost by mesophilic microorganisms has occurred, one or more microorganisms antagonistic to the plant pathogen. Container media also is rendered suppressive to plant pathogens and/or diseases caused thereby by amending the media with the just-described prepared suppressive compost or, alternatively, by amending separately with the compost and with Trichoderma fungus and antagonistic bacterium separately or mixed together. Desirably, the inoculated antagonistic microorganisms comprise Trichoderma hamatum species A.T.C.C. No. 20765 or 20764, together with Xanthomonas maltophilia bacterium species A.T.C.C. No. 53199 or a Flavobacterium balustinum isolate 299, A.T.C.C. No. 53198 species, A.T.C.C. No. 53198. | ||||||
| 12 | Preparation and use of glucose isomerase | US834073 | 1977-09-19 | US4283496A | 1981-08-11 | Chin K. Lee |
| Glucose is converted to fructose in the presence of an enzyme produced by Flavobacterium arborescens. | ||||||
| 13 | Flavobacterium strain | US194662 | 1994-02-14 | US5529923A | 1996-06-25 | Richard C. Honour; John J. Majnarich |
| The present invention includes a substantially pure bacterium, Flavobacterium spp., which produces compositions having unique anti-tumor and anti-inflammatory properties. The present invention includes methods for treating tumors in mammals comprising administering to such mammals a therapeutically effective amount of a composition of the invention. | ||||||
| 14 | Hydrocarbon emulsifier or solubilizer composition produced by Flavobacterium FERM BP-4010 | US242853 | 1994-05-16 | US5518726A | 1996-05-21 | Kazuhito Moriya; Koki Horikoshi |
| A microorganism belonging to the genus Flavobacterium posessing the capacity to decompose hydrocarbons, tolerance to sulfurous acids, tolerance to salinity, tolerance to organic solvents, and tolerance to pressure. The microorganism is of a strain of the genus Flavobacterium DS-711 (FERM BP-4010). A hydrocarbon emulsifier or solubilizer having as an active component thereof a water soluble and acetone insoluble fraction obtained by culturing DS-711 strain. In addition the emulsifier or solubilizer obtained by culturing the strain DS-711 contains 18.4% protein, 18.8% carbohydrates and 28.6% lipids. A separation method for an organic-solvent tolerant microorganism, wherein a sample is mixed with water and an organic solvent, shaking culturing is conducted, a cultured mixture is allowed to stand, separation into an aqueous phase and an organic solvent phase is conducted, an appropriate amount of said organic solvent phase is added to a culture medium and cultured, and microorganisms which grow therein are isolated. | ||||||
| 15 | Biodegradation of pentachlorophenol | US620231 | 1984-06-13 | US4713340A | 1987-12-15 | Ronald L. Crawford |
| A bacterium of the genus Flavobacterium which utilizes pentachlorophenol (PCP) as its sole carbon and energy source, which tolerates media PCP concentrations over about 250 mg/l, and which may be used in methods of detoxifying PCP-contaminated material. | ||||||
| 16 | Composition containing zeaxanthin derived from microorganism and its use | JP30020498 | 1998-10-21 | JPH11206339A | 1999-08-03 | GIERHART DENNIS L |
| PROBLEM TO BE SOLVED: To obtain a composition excellent in coloring rate and stability and usable for coloring a food, a fodder or a cosmetic at a low cost by treating cells of microorganisms belonging to Flavobacterium multivorum capable of producing zeaxanthin, under a specific condition. SOLUTION: Cells of microorganisms belonging to Flavobacterium multivorum capable of producing zeaxanthin are fermented in a nutrient medium containing a carbon source to be assimilated and absorbed, to provide a fermented liquid, and the cells are separated from the fermented liquid to provide a cell paste. The cell paste is formed into a slurry, and the paste formed into the slurry is homogenized. The homogenized paste is dried to provide the objective composition for coloring a food, a fodder or a cosmetic. The paste is preferably formed in the presence of an antioxidant, a chelating agent or a mixture thereof, and an emulsifying agent. | ||||||
| 17 | A novel microorganism belonging to the genus Flavobacterium | JP25219591 | 1991-09-30 | JPH07100026B2 | 1995-11-01 | 弘毅 掘越; 和仁 森屋 |
| 18 | New microorganism belonging to genus flavobacterium | JP25219591 | 1991-09-30 | JPH0680A | 1994-01-11 | MORIYA KAZUHITO; HORIKOSHI KOKI |
| PURPOSE: To provide a new microorganism belonging to the genus Flavobacterium, having excellent hydrocarbon decomposing activity, sulfurous acid resistance, salt resistance, organic solvent resistance and pressure resistance, exhibiting excellent hydrocarbon decomposition action and useful e.g. for the treatment of oil spilled on the surface of the sea. CONSTITUTION: The new microorganism Flavobacterium DS-711 strain (FERM P-12449) belonging to the genus Flavobacterium and having hydrocarbon decomposing activity, sulfurous acid resistance, salt resistance, organic solvent resistance and pressure resistance is produced by adding n-hexane to a sedimentary soil collected from the bottom of deep sea and suspended in seawater, gently shaking at 4°C for 1 week, adding kerosine to the mixture, culturing at room temperature for 2 days under vigorous shaking, leaving standing the cultured product to separate the kerosine layer from the water layer, smearing the kerosine layer on an agar medium, subjecting to standing culture at 20-30°C for 5 days, fishing a number of grown colonies, separating into each colony, inoculating on a medium and culturing at 30°C for 2 days under shaking. COPYRIGHT: (C)1994,JPO&Japio | ||||||
| 19 | Heteroglycan, its preparation and immune activator containing the same as an active ingredient | JP17147380 | 1980-12-06 | JPS5796001A | 1982-06-15 | UMEZAWA HAMAO; OKAMI YOSHIROU; KURASAWA SHIYOUGO; OONUKI TAKASHI |
| NEW MATERIAL:A heteroglycan having following properties: this compound is composed of (A) fucose, (B) mannose and (C) glucose where the molar ratio of these constituents A:B:C is 0.15±0.05: 0.31±0.05:1. USE: It shows strong immune activation activity and is use as a preventive against and remedy for infections diseases. It also develops carcinostatic activity through the immunological function of the host. PREPARATION: For example, a microorganism in Flavobacterium such as Flavobacterium uliginosum MP-55 strain (FERM-P5793) is cultured in a liquid medium containing sea water under aeration at 24W30°C for 15W100hr with stirring. COPYRIGHT: (C)1982,JPO&Japio | ||||||
| 20 | Plant growth-promoting rhizobacteria for agronomic, nonroot crops | US438739 | 1995-01-31 | US5503651A | 1996-04-02 | Joseph Kloepper; Fran Scher |
| Bacterial strains can be reproducibly isolated from the rhizosphere that enhance yield in nonroot crops under field conditions. | ||||||
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