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[利用大孔NaCS-PDMDAAC胶囊固定化细胞及在摇瓶和鼓泡生物反应器中的培养]

[Immobilization of cells by macro-porous NaCS-PDMDAAC capsules and cultivation in shaking flask and bubble bioreactor].

作者信息

Zhang Jun, Yao Shan-Jing, Ying Xiao-Jiao, Guan Yi-Xin, Lin Dong-Qiang

机构信息

Department of Chemical and Biochemical Engineering, Zhejiang University, Hangzhou 310027, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2005 Jul;21(4):633-7.

Abstract

The membrane of sodium cellulose sulphate ( NaCS)-poly dimethyldiallylammonium chloride (PDMDAAC) microcapsule is compact and has low molecular weight cut-off, which would delay the mass transfer and affect the cell growth immobilized in the capsule. Macroporous NaCS-PDMDAAC microcapsules were prepared using the degradation of the starch by amylase in the membrane of the capsules. The pore size and the permeability in the membrane were improved obviously. As model cells, the Candida krusei CK1 and E. coli EC1 immobilized in the capsules were cultured in the shake flask and bubble column respectively. It was shown that the cell density immobilized in the microcapsules cultured in the bubble column was higher than that cultured in the shaking flask. It implied that the limiting factor of the cell growth in the capsule lied in the diffusion of the oxygen. Since the rate of the oxygen transporting across the membrane was greatly enhanced due to the enlarged pore size, the maximum cell density in the macroporous capsules was 20%-110% over than that in the standard capsules in the bubble column. However, the extent of E. coli cell density increasing was higher than that of the yeast, which may be due to the difference of the oxygen requirement between the two microbes.

摘要

硫酸纤维素钠(NaCS)-聚二甲基二烯丙基氯化铵(PDMDAAC)微胶囊的膜致密且截留分子量低,这会延迟传质并影响固定在胶囊中的细胞生长。通过淀粉酶降解胶囊膜中的淀粉制备了大孔NaCS-PDMDAAC微胶囊。膜的孔径和渗透率明显提高。以克鲁斯假丝酵母CK1和大肠杆菌EC1作为模型细胞,分别将固定在胶囊中的细胞在摇瓶和鼓泡塔中培养。结果表明,在鼓泡塔中培养的固定在微胶囊中的细胞密度高于在摇瓶中培养的细胞密度。这意味着胶囊中细胞生长的限制因素在于氧气的扩散。由于孔径增大,氧气跨膜运输速率大大提高,大孔胶囊中的最大细胞密度比鼓泡塔中标准胶囊中的最大细胞密度高20%-110%。然而,大肠杆菌细胞密度增加的程度高于酵母,这可能是由于两种微生物对氧气需求的差异。

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