期刊文献+

大孔型NaCS-PDMDAAC微胶囊固定化细胞在摇床和鼓泡塔中的培养研究 被引量:1

Immobilization of Cells by Macro-porous NaCS-PDMDAAC Capsules and Cultivation in Shaking Flask and Bubble Bioreactor
下载PDF
导出
摘要 NaCS-PDMDAAC生物微胶囊囊膜较为致密,影响胶囊内外物质的交换,从而影响胶囊内细胞的生长.利用淀粉酶对致孔剂淀粉的降解作用制备了一种大孔型的纤维素硫酸钠-聚二甲基二烯丙基氯化铵(NaCS-PDMDAAC)生物微胶囊,实验表明胶囊的孔径和通透性能都有了很大的提高.将酵母和大肠杆菌作为模型细胞包埋于胶囊中分别通过摇瓶和鼓泡塔半连续培养,在鼓泡塔中胶囊内细胞的密度要高于摇床,表明氧气的传递是胶囊内好氧细胞生长的限制因素,大孔胶囊由于囊膜孔径变大,氧气的传递更为快速,在鼓泡塔中大孔型胶囊内的最大细胞密度比常规胶囊要高出20%~110%.由于对氧气的需求量的不同,大肠杆菌菌浓提高的程度要高于酵母. 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.
出处 《生物工程学报》 CAS CSCD 北大核心 2005年第4期633-637,共5页 Chinese Journal of Biotechnology
基金 国家自然科学基金资助项目(No.20276065)~~
关键词 大孔型胶囊 NaCS-PDMDAAC 扩散 固定化 macro-porous capsules, NaCS-PDMDAAC, diffusion, immobilization
  • 相关文献

参考文献8

二级参考文献40

  • 1吴军,于公义,冯尔玲.乙酸积累对基因工程菌培养的影响及与培养基pH的关系[J].微生物学报,1996,36(6):433-437. 被引量:13
  • 2陈因良 陈志宏.细菌培养工程[M].上海:华东化工学院出版社,1992.109-112.
  • 3刘国诠.生物工程下游技术-细胞培养、分离纯化、分析控制[M].北京:化学工业出版社,1993.58-64.
  • 4陈鹏.NaCS-PDADMAC生物微胶囊扩散与截留性能的研究:学位论文[M].杭州:浙江大学,1998..
  • 5陈鹏 姚善烃.小分子溶质在NaCS-PDADMAC生物微胶囊中的扩散性能研究.全国第二次发酵工程学术讨论会论文集[M].无锡,1998.433-436.
  • 6沈或.NaCS合成、动力学行为及NaCS-PDADMAC生物微胶囊生物相容性的初步考察:学位论文[M].杭州:浙江大学,1998..
  • 7梅乐和 林东强 等.用NaCS-PDMDAAC生物微胶囊固定化培养苏云金杆菌的初步研究.全国第二次发酵工程学术讨论会论文集[M].无锡,1998.59-60.
  • 8沈或 张惠勇 等.NaCS-PDMDAAC生物微胶囊微生物培养初探.全国第二次发酵工程学术讨论会论文集[M].无锡,1998.195-198.
  • 9Yao S J,Verfahrenstechniche Auslegung Einer Anlage Fuer NaCS-herstellung zur Immobiliserung von Biokatalysatoren,1996年
  • 10Yao S J,Chem Ing Tech,1993年,65卷,9期,1124页

共引文献100

同被引文献11

  • 1ZENG A P, BIEBL H. Bulk chemicals from biotechnology: The case of 1,3-propanediol production and the new trends[J]. Advances in Biochemical Engineering/Biotechnology, 2002,74:239-259.
  • 2SAINT-AMANS S, PERLIT P, GPMA G, et al. High production of 1,3-propanediol from glycerol by Clostridium butyricum VPI 3266 in a simply controlled fed-batch system[J]. Biotechnology Letters, 1994,16: 832-836.
  • 3MENZEL K, ZENG A P, DECKWER W D. High concentration and productivity of 1,3-propanediol from continuous fermentation of glycerol by Klebsiella pneumoniae[J]. Enzyme and Microbial Technology, 1997,20: 82-86.
  • 4CHEN X, ZHANG D J, QI W T, et al. Microbial fed-batch production of 1,3-propanediol by Klebsiella pneurnoniae under micro-aerobic conditions[J]. Applied Microbiology and Biotechnology,2003,63: 143-146.
  • 5BIEBL H, MARTEN S. Fermentation of glycerol to 1,3-propanediol: Use of cosubstrates[J]. Applied Microbiology and Biotechnology, 1995,44: 15-19.
  • 6MENZEL K,ZENG A P,BIEBL H, et al. Kinetic, dynamic, and pathway studies of glycerol metabolism by Klebsiella pneumoniae in anaerobic continuous culture: Ⅰ. The phenomena and characterization of oscillation and hystere- sis[J]. Biotechnology and Bioengineering, 1996,52: 549-560.
  • 7HOMANN T,TAG C, BIEBL H, et al. Fermentation of glycerol to 1,3-propanediol by Klebsiella and Citrobacter strains[J]. Applied Microbiology and Biotechnology, 1990,33 : 121-126.
  • 8ZENG A P, ROSS A, BIEBL H, et al. Multiple product inhibition and growth modeling of Clostridium butyricum and Klebsiella pneumoniae in glycerol fermentation[J]. Biotechnology and Bioengineering, 1994,44: 901-911.
  • 9姚善泾.新型生物微胶囊体系的生物相容性研究[J].生物工程学报,1998,14(2):193-197. 被引量:28
  • 10王剑锋,修志龙,范圣第.甘油转化生产1,3-丙二醇发酵液中甘油含量的测定[J].工业微生物,2001,31(2):33-35. 被引量:63

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部