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Method for obtaining exopolygalacturonase at the time of growing the culture of Penicillium chrysogenum mould

机译:产黄青霉菌培养时获得胞外半乳糖醛酸酶的方法

摘要

the subject of the invention is a method for egzo - polygalacturonase during husbandry of penicillium chrysogenum, whereby, in the first stage, preparing culture medium, in order to material containing pectic substances undergo sterilization at 121 oc for 20 minutes.then the sounds to a sterile saline solution (nh4) so4 and mgso4 - 7h2o concentration of 10 g / l, in the proportion of solution mixture of mass substrate 1 ml to 3 g substrate.in the second stage strain penicillium chrysogenum activated previously by transfer to a substrate agarowe and incubation at 21 - 24u00b0c by 10 - 14 days in sterile culture medium in a quantity of 1,0 ml 15 gram substrate breeding and production is periodic in 21 - 24u00b0c temperature for at least 5 dayswith between 45 and 55 hour breeding the following concentrated inorganic buffer: buffer fosforanowo - citrate or phosphate at ambient temperature of 0.5 - 1.0 ml for 3 g substrate, so that the culture ph ranging from 3.4 to 5.6, followed after 3 consecutive days isolated product in after staci proteins showing activity egzo - polygalacturonase.
机译:本发明的主题是一种在青霉青霉菌的饲养期间用于偶氮-聚半乳糖醛酸酶的方法,由此,在第一阶段,制备培养基,以使含有果胶的物质在121℃下灭菌20分钟,然后发出声音。无菌盐溶液(nh4)so4和mgso4-7h2o浓度为10 g / l,在质量底物1 ml与3 g底物的混合溶液中所占的比例。在第二阶段的产黄青霉菌株中,先前通过转移到底物agarowe中而活化并在无菌培养基中以1,0 ml 15克底物在21-24 u00b0c下孵育10-14天,繁殖和生产在21-24 u00b0c温度下定期进行至少5天,持续45至55小时繁殖以下浓缩的无机缓冲液:3 g底物在环境温度为0.5-1.0 ml的情况下将磷草铵-柠檬酸盐或磷酸盐缓冲液制成,使培养液的pH在3.4至5.6范围内,随后3 staci蛋白连续分离后的产物显示出活性,例如偶氮-聚半乳糖醛酸酶。

著录项

  • 公开/公告号PL411702A1

    专利类型

  • 公开/公告日2016-01-18

    原文格式PDF

  • 申请/专利权人 POLITECHNIKA WROCŁAWSKA;

    申请/专利号PL20150411702

  • 发明设计人 ANNA TRUSEK-HOŁOWNIA;HALINA ZASŁONA;

    申请日2015-03-26

  • 分类号C12P21/00;C12Q1/34;C12N9/26;C12R1/82;

  • 国家 PL

  • 入库时间 2022-08-21 14:23:30

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