| 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 | 沙化土壤微生物改良剂 | CN201310639822.X | 2013-11-29 | CN104673320A | 2015-06-03 | 崔国臣; 顾艳丽; 崔昌娜; 周悦 |
| 本发明提供一种沙化土壤微生物改良剂，采用巨大芽孢杆菌(Bacillus megaterium)ACCC No.11011、大豆根瘤菌(Bacillus elkanii)ACCC No.15067、地衣芽孢杆菌(Bacillus licheniformis)ATCC No.11946、沼泽红假单胞菌(Rhodopseudom onas Palustris)和圆褐固氮菌(Azotobacter chroococcum)ACCC No.10096制备菌种；所述菌种的质量百分比如下：巨大芽孢杆菌5～45%，大豆根瘤菌15～40%，地衣芽孢杆菌5～30%，沼泽红假单胞菌10～30%，圆褐固氮菌20～35%。 | ||||||
| 2 | 利用抗氨固氮菌生产富硒单细胞蛋白，维生素E和菌肥的方法 | CN86100490 | 1986-04-08 | CN86100490B | 1987-09-30 | 相振华 |
| 应用人工诱变技术培育出一组抗氨固氮菌８５１黄菌株。该组菌具有明显抗氨固氮能力，能强力固定大气氮，在有化合态氮的培养基中，仍保持相当高的固氮酶活性，用该组菌作为生产菌株，在本发明所设计的培养基（甘露醇－酵母膏培养基，甘露醇培养基，淀粉培养基和废糖蜜培养基）中培养、可分别生产富硒、锌、钙及多种维生素的单细胞蛋白，维生素Ｅ和菌肥，该菌培养液对人类防癌延寿具有进一步的开发利用价值。 | ||||||
| 3 | 一种猪促生长冷制粒发酵饲料的生产工艺 | CN201710872788.9 | 2017-09-25 | CN107373157A | 2017-11-24 | 严国萍 |
| 本发明公开了一种猪促生长冷制粒发酵饲料的生产工艺，包括如下步骤：将需要发酵的原材料首先进行粉碎，之后浸水浸泡软化，选取培养基成分，并向培养基中加入足量的蜂蜜和多肽，并且将其溶解在葡萄糖溶液中，搅拌均匀后进行乳化处理，经过恒温培养形成发酵液，将发酵基质和发酵液搅拌混合均匀后加入生物质发酵酶后，再进行密闭恒温的发酵，进行过滤，过滤掉其中的发酵液后进行烘干干燥得到发酵饲料,单独的配置和活化，可以根据不同的需求进行差异性的变化，能够使得发酵基质得到更好差异性的处理，能够促进分解，有利于形成便于动物吸收的蛋白等，而且整个工艺简单、可操作性强，而且对于设备要求不高，能够被广泛推广使用。 | ||||||
| 4 | 利用抗氨固氮菌生产富硒单细胞蛋白，维生素E和菌肥的方法 | CN86100490 | 1986-04-08 | CN86100490A | 1987-09-23 | 相振华 |
| 应用人工诱变技术培育出一组抗氨固氮菌851黄(包括01，02和03三个菌株)。该组菌具有明显抗氨固氮能力，能强力固定大气氮，在有化合态氮的培养基中，仍保持相当高的固氮酶活性，用该组菌作为生产菌株，在本发明所设计的培养基(甘露醇—酵母膏培养基，甘露醇培养基，淀粉培养基和废糖蜜培养基)中培养，可分别生产富硒、锌、钙及多种维生素的单细胞蛋白，维生素E和菌肥，该菌培养液对人类防癌延寿具有进一步的开发利用价值。 | ||||||
| 5 | Polysaccharides, process for producing polysaccharides, uses of polysaccharides and Azotobacter beijerinckii TNM1 | US201698 | 1994-02-25 | US5527904A | 1996-06-18 | Osamu Nakanishi; Yoichi Ooiso; Takeshi Okumiya; Ryosuke Sugihara; Akira Misaki; Masahira Nakagawa |
| Disclosed are novel polysaccharides having the following physicochemical properties: (1) a molecular weight determined by gel filtration chromatography is about 5.times.10.sup.3 to 10.times.10.sup.6, (2) the constituent glycoses are D-galacturonic acid, L-rhamnose and D-glucose, (3) the constituent glycoses are joined substantially by 1,3-linkages, and (4) a configuration of D-galacturonic acid is .alpha., that of L-rhamnose is .beta. and that of D-glucose is .alpha.. A process for producing polysaccharides composed of D-galacturonic acid, L-rhamnose and D-glucose, use of the polysaccharides and a strain for producing the polysaccharides are also disclosed. | ||||||
| 6 | JPH06504664A - | JP50051690 | 1989-11-06 | JPH06504664A | 1994-06-02 | |
| 7 | JPS5530360B2 - | JP6268977 | 1977-05-28 | JPS5530360B2 | 1980-08-09 | |
| 8 | JPH0457318B2 - | JP24725886 | 1986-10-17 | JPH0457318B2 | 1992-09-11 | YAN CHENFUA |
| This invention related to a group of autogenic antiamonia azotobacter represented by 851 yellow. It can utilize low price starch medium. This culture fluid of azotobacter can be used for manufacturing single cell proteins riched in Se, Zn, VE, VB, VK, anticancer and antiaging tonic medicines. It also can be used for manufacturing bacteria manure, eel and animal forage, additive, antiseptic and binder. | ||||||
| 9 | Non-ammonia azotobacter and its production | JP24725886 | 1986-10-17 | JPS62239987A | 1987-10-20 | YAN CHIENFUA |
| This invention related to a group of autogenic antiamonia azotobacter represented by 851 yellow. It can utilize low price starch medium. This culture fluid of azotobacter can be used for manufacturing single cell proteins riched in Se, Zn, VE, VB, VK, anticancer and antiaging tonic medicines. It also can be used for manufacturing bacteria manure, eel and animal forage, additive, antiseptic and binder. | ||||||
| 10 | Indican and its use | JP2856680 | 1980-03-06 | JPS55123601A | 1980-09-24 | KURISUTOFUAA JIYON ROOSON; KENESU CHIYAARUZU SHIIMESU |
| Indican, a polysaccharide comprising (1->3) glucose, (1->4) mannose, (1->4) rhamnose and (1->3 or 4) -0-(1-carboxyethyl)-rhamnose units in a molar ratio of about 2:1:1-2:1 respectively; containing 12-15% by weight acetyl units; [ alpha ]D20 about -61 DEG ; having principle absorption bands in the infra red band at 3390, 1735, 1615, 1375, 1250 and 1050 cm-1; a solubility of at least 1% by weight in methanol and in ethylene glycol, and an inherent viscosity of about 33.5 dl/g. has useful thixotropic properties and provides a method of modifying the viscosity of a liquid by incorporating indican therein. The liquid may be aqueous or organic solvent-based. Thickened and stabilized products and a method of preparing indican by culture of an indican-producing microorganism are also provided. | ||||||
| 11 | New polysaccharide, its production, use of new polysaccharide and azotobacter beijerinckii tnm1 strain | JP30862093 | 1993-11-15 | JPH0790003A | 1995-04-04 | NAKANISHI OSAMU; OISO YOICHI; OKUMIYA TAKESHI; SUGIHARA RYOSUKE; MISAKI AKIRA; NAKAGAWA SHOHEI |
| PURPOSE:To obtain a polysaccharide collected from a cultured material of a microorganism belonging to Azotobacter, having a structure in which three kinds of specified constituent saccharides are mutually bonded through a 1, 3-bond, gentle for global environment and useful as a humectant, a film-forming agent, etc. CONSTITUTION:This polysaccharide has about 5X10<3> to 10X10<6> molecular weight measured by the gel filtration chromatography method and a configuration composed of three kinds of constituent saccharides, i.e., an alpha-D-galacturonic acid, a beta-L-rhamnose and an alpha-D-glucose mutually bonded through a 1,3-bond. This polysaccharide can be obtained by culturing a microorganism belonging to Azotobacter and capable of producing this polysaccharide, preferably Azotobacter beijerinckii TNM1 strain (FERM BP-4194) and collecting it from the cultured material. In addition, this polysaccharide has following physicochemical properties; Appearance: white cotton-like material (freeze dried material); solubility: soluble in water, dilute acid, dilute alkali and DMSO and insoluble in MeOH, EtOH and acetone; color reaction: positive, e.g. to phenol sulfuric acid method, etc. | ||||||
| 12 | JPH07501201A - | JP50555292 | 1992-03-02 | JPH07501201A | 1995-02-09 | |
| 13 | Production of polysaccharide substance | JP6268977 | 1977-05-28 | JPS52145595A | 1977-12-03 | RENTON KURAIBU RIGERATO; RINDA DEIIBUIN |
| 14 | 미생물을 이용한 수목 생리활성 영양제 조성물 및 그 사용방법 | KR1020090027735 | 2009-03-31 | KR100976445B1 | 2010-08-17 | 정용교; 방승준 |
| PURPOSE: A physiologically active nutrition composition using microorganism is provided to reduce environmental stress of plants and to enhance plant growth. CONSTITUTION: A physiologically active nutrition composition contains: a microorganism extract which is isolated from indigenous microorganism and activates plant growth; a plant extract of salt resistance, which enhance resistance to salt stress and contains proline and betaine; an inorganic nutrition of potassium nitrate, magnesium sulfate, calcium nitrate, first potassium phosphate or ferric chloride; a growth regulator which contains niacin, pyridoxine, thiamine, and kinetin or indole butyric acid; and vitamin containing tocopherol or choline. | ||||||
| 15 | 아조토박터 비네란디에서 유래한 돌연변이 알긴산 분해효소 | KR1020120019933 | 2012-02-27 | KR1020130098093A | 2013-09-04 | 조훈; 최철희; 장철호; 박옥란 |
| 본발명은에서유래한알긴산분해효소의돌연변이단백질들에관한것이다. 구체적으로본 발명은돌연변이알긴산분해효소, 이의생산방법, 및이들을함유한약학적조성물에관한것이다. 본발명의돌연변이알긴산분해효소들은야생형효소보다분해활성이높은것을확인하였으므로알긴산을저분자화또는소멸시키기위한목적으로이용될수 있다. 특히세균이감염을위하여형성하는생물막의알긴산을제거하는역할을수행할수 있으므로기존의항생제와함께사용할경우효과적으로세균의감염을억제시킬수 있을것이다. | ||||||
| 16 | Azotobacter beijerinckii TNM1 | US404642 | 1995-03-15 | US5508190A | 1996-04-16 | Osamu Nakanishi; Yoichi Ooiso; Takeshi Okumiya; Ryosuke Sugihara; Akira Misaki; Masahira Nakagawa |
| Disclosed are novel polysaccharides having the following physicochemical properties: (1) a molecular weight determined by gel filtration chromatography is about 5.times.10.sup.3 to 10.times.10.sup.6 (2) the constituent glycoses are D-galacturonic acid, L-rhamnose and D-glucose, (3) the constituent glycoses are joined substantially by 1,3-linkages, and (4) a configuration of D-galacturonic acid is .alpha., that of L-rhamnose is .beta. and that of D-glucose is .alpha.. A process for producing polysaccharides composed of D-galacturonic acid, L-rhamnose and D-glucose, use of the polysaccharides and a strain for producing the polysaccharides are also disclosed. | ||||||
| 17 | Hyperproduction of poly-.beta.-hydroxybutyrate during exponential growth by mutant strains of Azotobacter vinelandii | US528214 | 1990-05-25 | US5096819A | 1992-03-17 | William J. Page; Olga Knosp |
| A mutant strain of Azotobacter vinelandii exhibits hyperproduction of poly-.beta.-hydroxybutyrates during its growth. Poly-.beta.-hydroxybutyrate yield is further enhanced when sugar beet molasses is used as carbon source. | ||||||
| 18 | Mutant strains of azotobacter vinelandii used for the hyperproduction of poly-.beta.-hydroxybutyrate during exponential growth | US631211 | 1990-12-21 | US5059536A | 1991-10-22 | William J. Page; Olga Knosp |
| A mutant strain of Azotobacter vinelandii exhibits hyper-production of poly-.beta.-hydroxybutyrate during its growth. | ||||||
| 19 | Continuous process for the production of polysaccharide under phosphate limiting conditions | US798762 | 1977-05-20 | US4130461A | 1978-12-19 | Renton C. Righelato; Lynda Deavin |
| Polysaccharide is produced in high yields by continuous culture of a polysaccharide-producing strain of Azotobacter vinelandii under phosphate-limited conditions, preferably with restricted oxygen uptake. | ||||||
| 20 | Method of fixing nitrogen utilizing azotobacter oleovorans | US40056864 | 1964-09-30 | US3393063A | 1968-07-16 | COTY VERNON F; DAVIS JOHN B |
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