1.
    发明专利
    未知

    公开(公告)号:DK561687D0

    公开(公告)日:1987-10-27

    申请号:DK561687

    申请日:1987-10-27

    Applicant: KAO CORP

    Abstract: Novel alkaline cellulase K, CMCase I and CMCase II are obtained by isolation from a culture product of Bacillus sp KSM-635. These enzymes stably work in a wide range including an alkaline side, and their activity is shown even at low temperatures. Further, they have a strong resistance to surfce active agents, chelating agents and proteinases. Therefore, they can be effectively utilized not only as an additive for clothing detergents, but also as a biomass and in other fields.

    3.
    发明专利
    未知

    公开(公告)号:DE3787866T2

    公开(公告)日:1994-05-19

    申请号:DE3787866

    申请日:1987-10-21

    Applicant: KAO CORP

    Abstract: Novel alkaline cellulase K, CMCase I and CMCase II are obtained by isolation from a culture product of Bacillus sp KSM-635. These enzymes stably work in a wide range including an alkaline side, and their activity is shown even at low temperatures. Further, they have a strong resistance to surfce active agents, chelating agents and proteinases. Therefore, they can be effectively utilized not only as an additive for clothing detergents, but also as a biomass and in other fields.

    6.
    发明专利
    未知

    公开(公告)号:ES2060590T3

    公开(公告)日:1994-12-01

    申请号:ES87115430

    申请日:1987-10-21

    Applicant: KAO CORP

    Abstract: Novel alkaline cellulase K, CMCase I and CMCase II are obtained by isolation from a culture product of Bacillus sp KSM-635. These enzymes stably work in a wide range including an alkaline side, and their activity is shown even at low temperatures. Further, they have a strong resistance to surfce active agents, chelating agents and proteinases. Therefore, they can be effectively utilized not only as an additive for clothing detergents, but also as a biomass and in other fields.

    7.
    发明专利
    未知

    公开(公告)号:DE3787866D1

    公开(公告)日:1993-11-25

    申请号:DE3787866

    申请日:1987-10-21

    Applicant: KAO CORP

    Abstract: Novel alkaline cellulase K, CMCase I and CMCase II are obtained by isolation from a culture product of Bacillus sp KSM-635. These enzymes stably work in a wide range including an alkaline side, and their activity is shown even at low temperatures. Further, they have a strong resistance to surfce active agents, chelating agents and proteinases. Therefore, they can be effectively utilized not only as an additive for clothing detergents, but also as a biomass and in other fields.

    8.
    发明专利
    未知

    公开(公告)号:DK561687A

    公开(公告)日:1988-04-29

    申请号:DK561687

    申请日:1987-10-27

    Applicant: KAO CORP

    Abstract: Novel alkaline cellulase K, CMCase I and CMCase II are obtained by isolation from a culture product of Bacillus sp KSM-635. These enzymes stably work in a wide range including an alkaline side, and their activity is shown even at low temperatures. Further, they have a strong resistance to surfce active agents, chelating agents and proteinases. Therefore, they can be effectively utilized not only as an additive for clothing detergents, but also as a biomass and in other fields.

    PRODUCTION OF ALKALINE AMYLASE
    10.
    发明专利

    公开(公告)号:JPS61209588A

    公开(公告)日:1986-09-17

    申请号:JP5149285

    申请日:1985-03-14

    Applicant: KAO CORP

    Abstract: PURPOSE:To obtain an alkaline amylase by a novel method comprising the use of actinomycetes, by inoculating a microbial strain (actinomycets) belonging to Streptomyces genus and capable of producing an alkaline amylase in a medium and culturing the strain. CONSTITUTION:The above microbial strain, e.g. Streptomyces sp. KSM-9 (FERM P-2620) (separated from the soil of Haga Country, Tochigi Prefecture, Japan) is inoculated in a proper medium, and cultured. The medium is composed of a proper C source, N source or organic nutrients, inorganic salts, etc., to enable the sound proliferation of the strain and the smooth production of the alkaline amylase. The cultivation can be carried out by sterilizing the medium e.g. by heating, incoulating the strain to the medium and culturing at 25-35 deg.C and about 8-11pH for 2-4 days under shaking or aeration and agitation. The objective alkaline amylase can be separated from the medium and purified, according to the conventional method for the separation and purification of yeasts.

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