Process for the purification of amylases
    1.
    发明授权
    Process for the purification of amylases 失效
    酰胺的纯化方法

    公开(公告)号:US3769168A

    公开(公告)日:1973-10-30

    申请号:US3769168D

    申请日:1971-06-11

    Applicant: HAYASHIBARA CO

    Inventor: MASUDA K

    CPC classification number: C12N9/2425 Y10S435/815

    Abstract: The present procedure concerns a process for the purification of beta-amylases comprising treating a crude beta-amylase solution derived from wheat bran, soy bean or fresh sweet potato with an adsorbent such as bentonite, acidic clay, kaolinite and activated clay at a pH lower than 5.0 to adsorb the beta-amylases, washing out the adsorbent with water, and then eluting the adsorbed betaamylases with a solution with an ionic strength over 0.5 Mu and a pH exceeding 5.0.

    Abstract translation: 本方法涉及纯化β-淀粉酶的方法,包括用pH低的吸附剂如膨润土,酸性粘土,高岭土和活性粘土处理来自麦麸,大豆或新鲜甘薯的粗β-淀粉酶溶液 超过5.0以吸附β-淀粉酶,用水洗涤吸附剂,然后用离子强度超过0.5μm并且pH超过5.0的溶液洗脱吸附的β-淀粉酶。

    Production of alpha-1,6-glucosidases
    3.
    发明授权
    Production of alpha-1,6-glucosidases 失效
    ALPHA-1,6-GLUCOSIDASASAS的生产

    公开(公告)号:US3766014A

    公开(公告)日:1973-10-16

    申请号:US3766014D

    申请日:1971-04-23

    Applicant: HAYASHIBARA CO

    Inventor: MASUDA K SUGIMOTO K

    CPC classification number: C12N9/2451 C12Y302/01033 Y10S435/816 Y10S435/852

    Abstract: The production of alpha-1,6-glucosidase by the cultivation of a strain of Klebsiella pneumoniae ATCC 13883, Klebsiella rhinoscleromatis ATCC 13884, Klebsiella ozaenae ATCC 13885, Klebsiella edwardsii ATCC 13886 or Klebsiella rubiacearum ATCC 15574 on media consisting of carbon sources, nitrogen sources, inorganic salts and others under aerating and agitating conditions thereby resulting in accumulation of alpha-1,6glucosidase on the media and the separation of the alpha-1,6glucosidase from the media following the purification of the alpha-1,6-glucosidase.

    Abstract translation: 通过在由碳源,氮源组成的培养基上培养肺炎克雷伯氏杆菌ATCC 13883,克雷伯杆菌ATCC 13884,克雷伯杆菌ATCC 13885,克雷伯氏菌ATCC 13886或克雷伯氏菌(Krebsiella rubiacearum)ATCC 15574的菌株生产α-1,6-糖苷酶 ,无机盐和其它物质,从而导致在介质上积累α-1,6-葡糖苷酶并且在纯化α-1,6之后从培养基中分离α-1,6-糖苷酶 葡萄糖苷酶。

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