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    Microbial consortium useful as seeding material for BOD analysis of pulp and paper industrial wastewater
    1.
    发明授权
    Microbial consortium useful as seeding material for BOD analysis of pulp and paper industrial wastewater 有权
    微生物联盟可用作纸浆和造纸工业废水BOD分析的播种材料

    公开(公告)号：US07429478B2

    公开(公告)日：2008-09-30

    申请号：US11024028

    申请日：2004-12-28

    申请人： Rita Kumar ,  Shikha Rastogi ,  Anil Kumar

    发明人： Rita Kumar ,  Shikha Rastogi ,  Anil Kumar

    IPC分类号： C12N1/20

    CPC分类号： C12R1/05 ,  C12N1/20 ,  C12R1/01 ,  C12R1/265 ,  C12R1/385 ,  C12R1/44

    摘要： The present invention provides a seeding material for accurate and reproducible monitoring of BOD load of pulp and paper wastewater, wherein the bacteria are isolated from various locations in India and comprise Micrococcus sp., Staphylococcus sp., Kurthia zopfii, Alcaligenes faecalis, and Pseudomonas aeruginosa, the microbial composition being capable of exerting an appropriate BOD for pulp and paper industrial wastewater due to the specificity of bacterial strains present therein towards the refractory organic compounds found in these effluents.

    摘要翻译： 本发明提供了用于准确和可重复地监测纸浆和纸浆废水的BOD负荷的播种材料，其中细菌是从印度的不同位置分离出来的，包括微球菌属，葡萄球菌属，肉毒杆菌属，粪产碱杆菌和铜绿假单胞菌 由于其中存在的细菌菌株对这些流出物中发现的难熔有机化合物的特异性，微生物组合物能够对纸浆和造纸工业废水施加适当的BOD。

    Process for preparing microbial consortium useful as seeding material for BOD analysis of pulp and paper industrial wastewater
    2.
    发明申请
    Process for preparing microbial consortium useful as seeding material for BOD analysis of pulp and paper industrial wastewater 有权
    制备用于纸浆和造纸工业废水BOD分析的种子材料的微生物联合体的方法

    公开(公告)号：US20060141553A1

    公开(公告)日：2006-06-29

    申请号：US11024028

    申请日：2004-12-28

    申请人： Rita Kumar ,  Shikha Rastogi ,  Anil Kumar

    发明人： Rita Kumar ,  Shikha Rastogi ,  Anil Kumar

    IPC分类号： C12Q1/04 ,  C12N1/20

    CPC分类号： C12R1/05 ,  C12N1/20 ,  C12R1/01 ,  C12R1/265 ,  C12R1/385 ,  C12R1/44

    摘要： The present invention provides a seeding material for accurate and reproducible monitoring of BOD load of pulp and paper wastewater, wherein the bacteria are isolated from various locations in India and comprise Micrococcus sp., Staphylococcus sp., Kurthia zopfii, Alcaligenes faecalis, and Pseudomonas aeruginosa, the microbial composition being capable of exerting an appropriate BOD for pulp and paper industrial wastewater due to the specificity of bacterial stows present therein towards the refractory organic compounds found in these effluents.

    摘要翻译： 本发明提供了用于准确和可重复地监测纸浆和纸浆废水的BOD负荷的播种材料，其中细菌是从印度的不同位置分离出来的，包括微球菌属，葡萄球菌属，肉毒杆菌属，粪产碱杆菌和铜绿假单胞菌 ，微生物组合物由于其中存在的细菌储存器的特异性而在这些流出物中发现的难熔有机化合物，因此能够为纸浆和造纸工业废水施加适当的BOD。

    Micro-organisms for the treatment of soil and process for obtaining them
    4.
    发明授权
    Micro-organisms for the treatment of soil and process for obtaining them 有权
    用于处理土壤的微生物和获得土壤的过程

    公开(公告)号：US07842494B2

    公开(公告)日：2010-11-30

    申请号：US10486747

    申请日：2002-08-12

    申请人： Gyorgy Botond Kiss ,  Istvan Ott

    发明人： Gyorgy Botond Kiss ,  Istvan Ott

    IPC分类号： A01N63/00 ,  C12N1/20

    CPC分类号： C12R1/11 ,  A01N63/00 ,  C05F11/08 ,  C12N1/20 ,  C12R1/01 ,  C12R1/12 ,  C12R1/265 ,  C12R1/39 ,  C12R1/47

    摘要： The present invention relates to product(s) containing living microorganism(s) suitable for soil treatment, microorganisms multiplying under different climatic and natural circumstances, as well as procedures for the production of the products, and procedures for the treatment of the soil and plants with the products. More particularly, the invention relates to a procedure for preparing the products from any of the microorganisms specified below, or from the mixture thereof. Furthermore, the invention relates to a procedure for the creation of the cultures of the microorganisms to be used. The subject invention also pertains to the microorganisms themselves. More particularly, the invention relates to a procedure for the treatment of the soil and the plants with a product containing at least one of the microorganisms selected from Azospirillum brasilense ssp. SW51 (NCAIM /P/ B 001293), Azotobacter vinelandii ssp. M657 (NCAIM /P/B 001292), Pseudomonas fluorescens var. SW11 (NCAIM /P/ B 001296), Bacillus polymyxa var. SW17 (NCAIM /P/ B 001295), Bacillus megaterium var. M326 (NCAIM /P/ B 001291), Micrococcus roseus ssp. A21 (NCAIM /P/B 001294), Bradyrhizobium japonicum var. PH25 (NCAIM /P/ B 001302), and Streptomyces albus var. 0003 LP (NCAIM /P/ B 001301), and furthermore the products multiplying and existing in the environment of the plant in question, containing the listed microorganisms and their production.

    摘要翻译： 本发明涉及含有适于土壤处理的活微生物，不同气候和天然环境下的微生物繁殖的产品，以及产品的生产程序，以及土壤和植物的处理程序 与产品。 更具体地说，本发明涉及从以下指定的任何微生物或其混合物制备产物的方法。 此外，本发明涉及用于产生待使用的微生物培养物的方法。 本发明也涉及微生物本身。 更具体地说，本发明涉及一种用含有至少一种微生物处理土壤和植物的方法，所述微生物选自巴西喷虫（Azospirillum brasilense ssp） SW51（NCAIM / P / B 001293），Azotobacter vinelandii ssp。 M657（NCAIM / P / B 001292），荧光假单胞菌变种 SW11（NCAIM / P / B 001296），多粘芽孢杆菌变种 SW17（NCAIM / P / B 001295），巨大芽孢杆菌变种 M326（NCAIM / P / B 001291），Micrococcus roseus ssp。 A21（NCAIM / P / B 001294），日本的Bradyrhizobium japonicum var。 PH25（NCAIM / P / B 001302）和链霉菌（Streptomyces albus var。 0003 LP（NCAIM / P / B 001301），此外，产品在相关工厂的环境中繁殖和存在，包含列出的微生物及其生产。

    Process for degradation of keratin, keratinaceous material, collagen and collagenaceous material with enzyme material, cell-free culture or cell culture from micrococcus sedentarius
    6.
    发明授权
    Process for degradation of keratin, keratinaceous material, collagen and collagenaceous material with enzyme material, cell-free culture or cell culture from micrococcus sedentarius 失效
    用酶材料降解角蛋白，角质形成物质，胶原和胶原物质的方法，来自小球菌的无细胞培养物或细胞培养物

    公开(公告)号：US5395613A

    公开(公告)日：1995-03-07

    申请号：US27820

    申请日：1993-03-08

    申请人： Keith T. Holland

    发明人： Keith T. Holland

    IPC分类号： A61K38/00 ,  C12N9/52 ,  A61K37/54 ,  C12N1/00 ,  C12N9/50

    CPC分类号： C12R1/265 ,  C12N9/52 ,  A61K38/00 ,  Y10S435/859

    摘要： A process for the degradation of keratin, keratinaceous material, collagen or collagenaceous material comprising contacting keratin, keratinaceous material, collagen or collagenaceous material with an enzyme material isolated from a culture of Micrococcus sedentarius. The enzyme material comprises one or more proteases having the ability to degrade keratin, keratinaceous material, collagen or collagenaceous material. The enzyme material is water soluble, non-dialysable through a membrane having a molecular weight cut-off of 10 kDa, has an isoelectric point of 4.6 or 2.7, a molecular weight of 30.3 kDa or 50 kDa, an optimum pH for protease activity at about 8.2 or at about 10.2 and an optimum temperature for protease activity at about 40.degree. C. or 46.degree. C.

    摘要翻译： 包括使角蛋白，角质素材料，胶原或胶原物质降解的方法，包括将角蛋白，角质材料，胶原或胶原物质与从小球菌（Micrococcus sedentarius）的培养物分离的酶物质接触。 酶材料包含一种或多种具有降解角蛋白，角质物质，胶原或胶原物质的能力的蛋白酶。 酶材料是水溶性的，通过具有10kDa分子量截止值的膜不透水，具有4.6或2.7的等电点，分子量为30.3kDa或50kDa的蛋白酶活性的最佳pH， 约8.2或约10.2，在约40℃或46℃下具有蛋白酶活性的最适温度。

    Protease from Micrococcus sedentarius for degrading protein of human callus or corn tissue
    8.
    发明授权
    Protease from Micrococcus sedentarius for degrading protein of human callus or corn tissue 失效
    用于降解人牙垢或蛋白组织蛋白质的微生物筛选

    公开(公告)号：US5213978A

    公开(公告)日：1993-05-25

    申请号：US705090

    申请日：1991-05-24

    申请人： Keith T. Holland

    发明人： Keith T. Holland

    IPC分类号： A61K38/46 ,  A61K38/00 ,  A61P17/16 ,  C12N1/20 ,  C12N5/06 ,  C12N9/52 ,  C12R1/265 ,  C12R1/91

    CPC分类号： C12R1/265 ,  C12N9/52 ,  A61K38/00 ,  Y10S435/859

    摘要： An enzyme material isolated from a culture of Micrococcus sedentarius which comprises one or more proteases having an ability to degrade protein, including human callus. In one embodiment the enzyme material is water soluble, non-dialyzable through a membrane having a molecular weight cut-off of 10 kDa, has an isoelectric point of 4.6, a molecular weight of 30.3 kDa, an optimum pH for protease activity at about 8.2, and functions at an optimum temperature of about 40.degree. C. In another embodiment, the enzyme material is water-soluble, non-dialyzable through a membrane having a molecular weight cut off of 10 kDa, has an isoelectric point of 2.7, a molecular weight of 50 kDa, an optimum pH for protease activity at about pH 10.2, and functions at an optimum temperature of about 46.degree. C.