会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 84. 发明授权
    • Microbial culture system
    • US4559305A
    • 1985-12-17
    • US270013
    • 1981-06-03
    • James E. ZajicMartha A. HillDonald F. ManchesterKarel Muzika
    • James E. ZajicMartha A. HillDonald F. ManchesterKarel Muzika
    • C02F1/24C02F3/34C12N1/00
    • C02F1/24C02F3/34Y10S435/911Y10S435/924
    • The specification discloses making a mixed fungal (yeast and yeast-like) system culture adapted to biodegradation of spent sulfite liquor (SSL) comprising the steps of exposing a mixed culture system (being a sludge from a sewage treatment plant) to increasing concentration of SSL until the fungus becomes acclimatized to SSL of the desired concentration. The resulting biotic population comprises a fungal mixture, of yeast and yeast-like cultures. It was based on an autolytic culture system: Phialophora jeanselmei, Phialophora richardsiae, Hyalodendron lignicola, Trichosporon infestans and Candida tropicalis. A method and apparatus are disclosed for biodegrading both the soluble substrates in a spent sulfite liquor and the biological solids produced therefrom by a potentially autolytic culture system. The method comprises the steps of adding a nutrient medium, adjusting the pH to mildly acid or neutral condition, feeding the mixture to a fungal culture inoculated fermentor with agitation and with aeration, resulting in foaming of the mixture, said foam carrying with it the fungi and sludge resulting from the fermentation, the suspended solids content of the foam when collapsed being generally not more than half the suspended solids content of the fermentor broth, said foam being processed so as to separate the components into a sludge and a clarified effluent, said sludge being recycled to the fermentor vessel and the clarified effluent prepared for discharge or additional processing. The recycling of sludge to the fermentor vessel is controlled where necessary to maintain the suspended solids in the fermentor vessel at not greater than 60,000 parts per million. The degree of recycling and retention time are held at a level at which autolysis of the suspended solids may be maintained. The process differs from other extended aeration processes in the high MLSS level in the reactor (.about.30,000-55,000 ppm); low sludge return rate (.about.43% of fresh feed rate); high BOD loading (1400 lb BOD/1000 cu. ft.); long mean cell residence time (up to 95 days). The system may be maintained at full sludge recycle thus obviating the need for an external sludge handling and disposal system. Under optimum operating conditions as much as 85 to 90% BOD removal from spent sulfite liquor is accomplished.
    • 85. 发明授权
    • Microbiological process for the preparation of unsaturated dicarboxylic
acids
    • 用于制备不饱和二羧酸的微生物过程
    • US4474882A
    • 1984-10-02
    • US304284
    • 1981-09-21
    • Etsumi KunishigeTsuyoshi Morinaga
    • Etsumi KunishigeTsuyoshi Morinaga
    • C12P7/46C12P7/44C12R1/74C12P7/64
    • C12P7/44Y10S435/924
    • A process for the preparation of an unsaturated dicarboxylic acid which comprises cultivating under aerobic conditions a yeast belonging to Candida tropicalis which is capable of producing an unsaturated dicarboxylic acid from an unsaturated fatty acid or its ester, such as Candida tropicalis 104-04 strain, in a medium containing an unsaturated fatty acid having 14 to 22 carbon atoms or its ester, to produce an unsaturated dicarboxylic acid having 14 to 22 carbon atoms; or effecting oxidation of said fatty acid or its ester in the presence of microorganisms of said yeast produced in advance by cultivation in an assimilable carbon source to produce an unsaturated dicarboxylic acid having 14 to 22 carbon atoms; and then recovering the thus-produced unsaturated dicarboxylic acid.
    • 一种制备不饱和二羧酸的方法,其包括在好氧条件下培养属于热带假丝酵母的酵母,其能够从不饱和脂肪酸或其酯生产不饱和二羧酸,例如热带假丝酵母104-04菌株, 含有14-22个碳原子的不饱和脂肪酸或其酯的介质,以制备具有14-22个碳原子的不饱和二羧酸; 或者在可同化碳源中预先通过培养生成的所述酵母的微生物存在下进行所述脂肪酸或其酯的氧化,生成具有14-22个碳原子的不饱和二羧酸; 然后回收由此产生的不饱和二羧酸。
    • 86. 发明授权
    • Suppressing method of iso-citric acid formation in producing citric acid
from hydrocarbons by fermentation
    • 通过发酵从碳氢化合物生产柠檬酸中抑制异柠檬酸形成的方法
    • US4411998A
    • 1983-10-25
    • US359773
    • 1982-03-19
    • Takao MatsumotoAtsushi FujimakiTakeo Nagata
    • Takao MatsumotoAtsushi FujimakiTakeo Nagata
    • C12P7/48
    • C12P7/48Y10S435/923Y10S435/924
    • The present invention relates to a suppressing method of iso-citric acid formation in producing citric acid from hydrocarbons by fermentation.This process is carried out by culturing the microorganisms selected from the group belonging to Candida tropicalis, Candida lipolytica, Candida intermedia and Candida brumptii and their mutants and variants in the culture medium containing paraffinic and olefinic hydrocarbons and their mixture as carbon source under aerobic conditions, wherein specific non-ionic surface active agent is added to said culture medium.The specific non-ionic surface active agent added to said culture medium is selected from the group of sorbitan fatty acid esters and polyoxy-ethylene sorbitan fatty acid esters. The amount of specific surface active agent added to said culture medium is enough from 0.005 to 0.5 percent by weight, preferably from 0.02 to 0.2 percent on the weight basis of said culture medium.
    • 本发明涉及通过发酵从烃生产柠檬酸中异柠檬酸形成的抑制方法。 该方法通过在需氧条件下培养选自属于热带假丝酵母,解脂假丝酵母,中间假丝酵母和布氏假丝酵母的组的微生物及其在含有链烷烃和烯烃的培养基及其混合物中的突变体和变体, 其中将特定的非离子表面活性剂加入到所述培养基中。 添加到所述培养基中的特定非离子表面活性剂选自脱水山梨糖醇脂肪酸酯和聚氧乙烯脱水山梨糖醇脂肪酸酯。 添加到所述培养基中的比表面积活性剂的量足以按所述培养基的重量计0.005至0.5重量%,优选0.02至0.2重量%。
    • 88. 发明授权
    • Cholesterol assay
    • 胆固醇测定
    • US3907645A
    • 1975-09-23
    • US43589274
    • 1974-01-23
    • NAT RES DEV
    • RICHMOND WILLIAM
    • C12N9/04C12Q1/26C12Q1/60G01N31/14
    • C12N9/0006C12Q1/26C12Q1/60Y10S210/922Y10S435/815Y10S435/866Y10S435/872Y10S435/911Y10S435/913Y10S435/923Y10S435/924Y10S435/942
    • Enzyme preparations which will convert cholesterol to Delta 4cholestenone and hydrogen peroxide are obtained from certain Nocardia species belonging to the Mycobacterium rhodocrous group. The preparations have a cholesterol oxidase specific activity of at least 1 unit per 5 mg of protein nitrogen and, when in liquid form, a potency of at least 10 2 units/ml. They are prepared by growing the organism and recovering the enzyme preparation, preferably by extracting the harvested cells with a surface active agent such as Triton X-100. The enzyme preparations are used to assay for cholesterol by measuring the amount in which one of the products of the cholesterol oxidase reaction, preferably hydrogen peroxide, is formed or the quantity in which oxygen is used.
    • 将胆固醇转化为DELTA4-胆甾烯酮和过氧化氢的酶制剂从属于分枝杆菌属的诺卡氏菌属获得。 该制剂具有每5mg蛋白质氮至少1单位的胆固醇氧化酶比活性,并且当以液体形式时,其效力为至少10 -3单位/ ml。 它们通过生长生物体并回收酶制剂,优选通过用表面活性剂如Triton X-100萃取收获的细胞来制备。 酶制剂用于通过测量胆固醇氧化酶反应的产物之一,优选过氧化氢的形成量或使用氧气的量来测定胆固醇。