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 通过胃肠道中生物的营养物温度诱导递送 CN200980126070.9 2009-07-01 CN102123615A 2011-07-13 C·吉斯勒; P·尼德尔伯格; N·帕日; C·沙费尔-勒卡特
发明大体上涉及健康和安宁领域。特别地,本发明涉及温度敏感生物以及其用作制备递送化合物例如营养物到身体特定区域的组合物之载体的用途。
2 用于治疗疾病的新细菌 CN03818675.6 2003-06-03 CN1674932A 2005-09-28 罗伯特·E·克利克
发明涉及包含用于治疗反刍动物的副结核的迪茨氏菌属细菌的组合物以及培养所述细菌的方法。本发明还涉及通过对哺乳动物施用本发明的组合物来治疗副结核病的方法。
3 将二甲酸中间体转化为脂肪族羧酸生物 CN201280044331.4 2012-07-13 CN103797109B 2016-12-07 艾琳·芬尼根
发明涉及一种生物,所述微生物包含能够将二转化为甲酸的氢化酶系统和能够将甲酸转化为具有五个以上碳原子的链长度的脂肪族羧酸的第二酶系统。还描述了用于产生油的各种方法、以及本发明的其它方面。
4 一种热带醋杆菌全细胞催化生产甘油酸的方法 CN201410552593.2 2014-10-17 CN104312952A 2015-01-28 卢英华; 蒲洋; 陈慧敏; 王宝贝; 敬科举; 陈翠雪
一种热带醋杆菌全细胞催化生产甘油酸的方法,涉及一种甘油酸的生产方法。1)一级摇瓶种子培养:将甘油酸生产菌热带醋杆菌(Acetobacter tropicalis)CHM061701接种于装有一级种子培养基的摇瓶中培养;2)二级摇瓶种子:将步骤1)的一级摇瓶种子培养的种子接种于装有二级种子培养基的摇瓶中培养;3)菌体富集培养:将步骤2)的二级摇瓶种子培养的种子接种于装有菌体富集培养基的摇瓶中培养;4)菌体收集:取步骤3)培养所得菌液离心,洗涤,收集菌体,再加入甘油溶液,调节初始pH为5~8;5)全细胞催化转化:将步骤4)所得的含有菌体的甘油水溶液于摇瓶中进行催化转化,得甘油酸。
5 益生菌双歧杆菌菌株 CN02818577.3 2002-07-26 CN1561387A 2005-01-05 约翰·凯文·柯林斯; 杰拉尔德·克里斯托弗·奥沙利文; 利亚姆·奥马霍尼; 弗格斯·沙纳汉; 巴里·基利
一种双歧杆菌(Bifidobacterium)菌株AH208,AH209,AH210,AH211,AH212或AH214或其突变体或变体,其用于预防和/或治疗炎性,尤其非所希望的胃肠道炎性,如炎症性肠病或过敏性肠综合征。
6 生产2-基-L-古洛糖酸或其盐的方法 CN92104573.5 1992-06-12 CN1052512C 2000-05-17 立夫星埜; 节子尾岛; 昭秀杉泽
发明涉及一种利用发酵法以高产率转化D-山梨糖醇而生产2-基-L-古洛糖酸的方法。2-酮基-L-古洛糖酸是制备L-抗坏血酸的重要中间体,它可用已知的赖希斯坦法进行转化。
7 一种蔬菜发酵用复合菌剂产品 CN201410492275.1 2014-09-23 CN104312941A 2015-01-28 李建树; 李政
发明公开了一种用于泡菜生产的蔬菜发酵用复合菌剂产品,属于生物制剂生产领域;所述蔬菜发酵用复合菌剂产品由如下菌剂组成:植物乳杆菌CGMCC No.9405、鼠李糖乳杆菌、醋酸杆菌和酵母菌,本发明首先对植物乳杆菌,醋酸杆菌、鼠李糖乳杆菌、酿酒酵母菌种进行单独培养,培养到预定时间后经离心后收集菌体,利用常规微生物制剂的生产方法制备各菌的粉状微生物菌粉;将制备的菌种粉剂根据配比进行混和调配,本发明中各种菌种组成比例也是经过精心试验研究得到,上述菌种的选择和配比保障了泡菜产品的生产速度、泡菜产品良好味和泡菜产品的良好质量
8 一种用于生产甘油酸的热带醋杆菌的驯化方法 CN201410553955.X 2014-10-17 CN104263689A 2015-01-07 卢英华; 陈慧敏; 蒲洋; 王宝贝; 敬科举; 陈翠雪
一种用于生产甘油酸的热带醋杆菌的驯化方法,涉及一种菌株的驯化方法。热带醋杆菌CHM061701保藏号CGMCC NO.9417。将热带醋杆菌接种至葡萄糖琼脂培养基平板中培养;取较大的单菌落转接至氮源优化琼脂培养基平板中培养,反复转接培养,取较大的单菌落转接至甘油优化琼脂培养基平板中培养;在甘油优化琼脂培养基平板中反复转接培养,取较大的单菌落转接至一级种子葡萄糖液体培养基中培养,得一级种子液;将一级种子液转接至二级种子葡萄糖液体培养基中培养,得二级种子液;将二级种子液转接至发酵培养基中培养,发酵结束后测定发酵液中甘油酸的含量;将获得的甘油酸驯化菌株经连续传代稳定性考察,获得经驯化的菌株。
9 生物接种物以及包含其的肥料组合物 CN201280062624.5 2012-11-05 CN104254508A 2014-12-31 韦恩·芬利森; 凯伦·朱里
在此提供了用于提高植物生长、植物生产和/或土壤质量生物接种物,该微生物接种物包括选自帕氏乳酸杆菌、布氏乳酸杆菌、瑞氏乳酸杆菌以及玉米乳酸杆菌的一个或多个细菌物种的菌株。任选地该微生物接种物还包括醋酸菌的一种菌株和/或嗜酒假丝酵母的一种菌株。还提供了包含所述微生物接种物的肥料组合物。
10 将二甲酸中间体转化为脂肪族羧酸生物 CN201280044331.4 2012-07-13 CN103797109A 2014-05-14 艾琳·芬尼根
发明涉及一种生物,所述微生物包含能够将二转化为甲酸的氢化酶系统和能够将甲酸转化为具有五个以上碳原子的链长度的脂肪族羧酸的第二酶系统。还描述了用于产生油的各种方法、以及本发明的其它方面。
11 生产2-基-L-古洛糖酸或其盐的方法 CN97110732.7 1992-06-12 CN1181423A 1998-05-13 立夫星埜; 节子尾岛; 昭秀杉泽
发明涉及一种利用发酵法以高产率转化D-山梨糖醇而生产2-基-L-古洛糖酸的方法。2-酮基-L-古洛糖酸是制备L-抗坏血酸的重要中间体,它可用已知的赖希斯坦法进行转化。
12 发酵 CN92104573.5 1992-06-12 CN1067681A 1993-01-06 立夫星埜; 节子尾岛; 昭秀杉泽
发明涉及一种利用发酵法以高产率转化D-山梨糖醇而生产2-基-L-古洛糖酸的方法。2-酮基-L-古洛糖酸是制备L-抗坏血酸的重要中间体,它可用已知的赖希斯坦法进行转化。
13 Cellulose-producing bacteria US274470 1999-03-23 US6110712A 2000-08-29 Takayasu Tsuchida; Naoto Tonouchi; Akira Seto; Yukiko Kojima; Masanobu Matsuoka; Fumihiro Yoshinaga
This invention relates to a microorganism that is capable of producing a cellulosic product (referred to hereinafter as a "cellulose-producing bacterium") and belongs to a novel subspecies which is substantialy negative or very slightly positive in oxidation of acetates and lactates. This invention also relates to novel saccharide analog-resistant strains, amino acid analog-resistant strains and levan sucrase-defective strains. Further, this invention relates to a method for the production of cellulosic material (bacterial cellulose:"BC"), which comprises culturing these novel bactria and to bacterial cellulose which may be thus obtained. A larger amount of bacterial cellulose may be produced by culturing Acetobacter xylinum subsp. nonacetoxidans, the present resistant strains and the levan sucrase-defective strains, which have been derived and bred from the cellulose-producing bacteria, than by culturing the BPR 2001 strain in the medium containing especially sucrose or glucose as carbon sources.
14 Methods and nucleic acid sequences for the expression of the cellulose synthase operon US689008 1991-04-22 US5268274A 1993-12-07 Arie Ben-Bassat; Roger D. Calhoon; Anna L. Fear; David H. Gelfand; James H. Meade; Rony Tal; Hing Wong; Moshe Benziman
Nucleic acid sequences encoding the bacterial cellulose synthase operon derived from Acetobacter are disclosed. Methods for isolating the genes, vectors containing the genes, and transformed hosts useful for the expression of recombinant bacterial cellulose synthase or production of cellulose are also described.
15 Novel bacterium, Acetobacter altoacetigenes MH-24, useful for the fermentation production of vinegar US703705 1985-02-21 US4654306A 1987-03-31 Etsuzo Entani; Seiichi Fujiyama; Shoji Ohmori; Hiroshi Masai
A novel species of acetic acid bacteria belonging to the genus of Acetobacter, to which a scientific name of Acetobacter altoacetigenes MH-24 (FERM BP-491) is given. The bacteria can grow in a culture medium containing at least 4 w/v % of acetic acid with a pH of 3.5 at the highest. Pure samples of species have been isolated and used for the fermentation production of vinegar without undertaking the conventional inoculation process using the prior art seed vinegar to provide a high-quality vinegar of high acetic acid concentration such as white vinegar, with high production efficiency.
16 Acidic heteropolysaccharide AM-2 US545270 1983-10-25 US4575551A 1986-03-11 Seiichi Fujiyama; Hiroyuki Minakami; Kenji Tayama; Hiroshi Masai
Novel highly viscous acidic heterpolysaccharide AM-2 is produced from a strain of genus Acetobacter isolated from vinegar mash, and is useful as an adhesive, coating agent, drilling mud additive, enhanced oil recovering agent, etc., as well as a material useful for the production of foods, drugs and cosmetics because of its safety and high viscosity.
17 Thermotolerant and high acetic acid-producing Acetobacter bacterium US370784 1999-08-05 US6096528A 2000-08-01 Shu-Fen Lu; Fwu-Ling Lee; Han-Ken Chen
The present invention relates to a thermotolerant bacterium, designated as Acetobacter sp. I14-2, with high production of acetic acid which was isolated from spoiled banana in Taiwan. The present invention also relates to compositions containing the new species and methods for acetic acid production.
18 Cellulose-producing bacteria US930587 1998-01-09 US5962277A 1999-10-05 Kunihiko Watanabe; Hiroshi Takemura; Mari Tabuchi; Naoki Tahara; Hiroshi Toyosaki; Yasushi Morinaga; Takayasu Tsuchida; Hisato Yano; Fumihiro Yoshinaga
Novel cellulose-producing bacteria including one capable of producing of a bacterial cellulose having a weight-average degree of polymerization in terms of polystyrene of 1.6.times.10.sup.4 or above, one capable of producing a bacterial cellulose containing a small amount of the fraction with low degrees of polymerization, one producing a Bingham polysaccharide as a by-product, and one producing a small amount of water-soluble polysaccharide; a method for the production of bacterial cellulose, which comprises culturing these cellulose-producing bacteria; and bacterial cellulose thus obtained.
19 Method of producing reticulated cellulose having type II crystalline cellulose US442595 1995-05-17 US5871978A 1999-02-16 Arie Ben-Bassat; Robert Bruner; Sharon Shoemaker; Yehoshua Aloni; Harry Wong; Donald C. Johnson; Amar N. Neogi
A method and media are provided for producing bacterial cellulose under agitated culture conditions resulting in sustained production over an average of 70 hours of at least 0.1 g/liter per hour are achieved. A unique reticulated cellulose product is produced using the methods and conditions claimed, and may be in the form of a sheet characterized by substantial resistance to densification and great tensile strength when produced by sheet forming means. Strains of Acetobacter that are stable under agitated culture conditions and that exhibit substantially reduced gluconic and keto-gluconic acids production are described.
20 Reticulated cellulose and methods and microorganisms for the production thereof US442597 1995-05-17 US5821109A 1998-10-13 Arie Ben-Bassat; Robert Bruner; Sharon Shoemaker; Yehoshua Aloni; Harry Wong; Donald C. Johnson; Amar N. Neogi
A method and media for producing bacterial cellulose under agitated culture conditions resulting in sustained production over an average of 70 hours of at least 0.1 g/liter per hour are achieved. A unique reticulated cellulose II product is produced using the methods and conditions claimed, and may be in the form of a sheet characterized by resistance to densification and great tensile strength when produced by sheet forming means. Also strains of Acetobacter that are stable under agitated culture conditions and that exhibit substantially reduced gluconic and keto-gluconic acids production are described.
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