首页> 外国专利> A method of colonizing a carrier comprising a layer of polyamide nanofibres by a population of bacteria of the Rhodococcus erythropolis strain

A method of colonizing a carrier comprising a layer of polyamide nanofibres by a population of bacteria of the Rhodococcus erythropolis strain

机译:一种通过红球红球菌菌株的细菌群体定殖包括聚酰胺纳米纤维层的载体的方法

摘要

A method of colonizing a carrier comprising a layer of polyamide nanofibres by a population of bacteria of the Rhodococcus erythropolis CCM 2595ad strain in which the bacterial population is transferred to a sterile culture medium containing NaNO3 at a concentration of 3 g/l, K2HPO4 at a concentration of 1 g/l, MgSO4.7H2O at a concentration of 0.5 g/l, KCl at a concentration of 0.5 g/l, FeSO4.7H2O at a concentration of 0.01 g/l, and phenol at a concentration of 0.3 g/l, with pH 7.0, and is cultured, wherein, upon reaching the exponential or stationary growth phase, this bacterial population is separated from the culture medium, washed with physiological saline and resuspended to a cell concentration corresponding to an optical density of 0.5. It is then separated from the physiological saline and inoculated into a fresh sterile culture medium of the same composition as in the first step, and, with this culture medium and carrier comprising a layer of polyamide nanofibres, it is placed in a reaction vessel of the biological reactor, where it is maintained in a movement relative to the carrier, wherein a natural bond between the cells of the bacterial or yeast population and the polyamide nanofibres of the carrier is formed. During this procedure, the layer of polyamide nanofibres of the carrier is colonized in 48 hours by a bacterial population capable of further reproduction in an amount of at least 0.05 mg/cm2 of the carrier.
机译:一种通过红细菌红球菌CCM 2595ad菌株的细菌群体定殖包括聚酰胺纳米纤维层的载体的方法,其中细菌群体​​被转移到含有NaNO 3 < / Sub>浓度为3 g / l,K 2 HPO 4 浓度为1 g / l,MgSO 4 .7H浓度为0.5 g / l的 2 O,浓度为0.5 g / l的KCl,FeSO 4 .7H 2 O培养浓度为0.01 g / l的苯酚和浓度为0.3 g / l的苯酚(pH值为7.0)并进行培养,其中,在达到指数生长期或固定生长期时,将该细菌群体从培养基中分离出来,用生理盐水洗涤盐水,并重悬至对应的光密度为0.5的细胞浓度。然后将其从生理盐水中分离出来,并接种到与第一步相同组成的新鲜无菌培养基中,然后在这种培养基和包含聚酰胺纳米纤维层的载体中,将其置于培养皿的反应容器中。生物反应器,其相对于载体保持运动,其中在细菌或酵母群体的细胞与载体的聚酰胺纳米纤维之间形成天然键。在此过程中,载体的聚酰胺纳米纤维层在48小时内被细菌种群定殖,该细菌种群能够以至少0.05 mg / cm 2 的量进一步繁殖。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号