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利用乳清超滤物强化 Grace 培养基以提高 Sf9 细胞和杆状病毒的产量。

Enhancement of Sf9 Cells and Baculovirus Production Employing Grace's Medium Supplemented with Milk Whey Ultrafiltrate.

机构信息

Departamento de Processos Biotecnológicos, Faculdade de Engenharia Químca, Universidade Estadual de Campinas, P.O. Box 6066, 13083-852, Campinas, SP, Brazil.

出版信息

Cytotechnology. 2005 Sep;49(1):1-9. doi: 10.1007/s10616-005-4206-0.

Abstract

Animal cells can be cultured both in basal media supplemented with fetal bovine serum (FBS) and in serum-free media. In this work, the supplementation of Grace's medium with a set of nutrients to reduce FBS requirements in Spodoptera frugiperda (Sf9) cell culture was evaluated, aiming the production of Anticarsia gemmatalis nucleopolyhedrovirus (AgMNPV) at a cost lower than those for the production using Sf900 II medium. In Grace's medium supplemented with glucose, Pluronic F68 (PF68) and yeast extract (YE), the effects of FBS and milk whey ultrafiltrate (MWU) on cell concentration and viability during midexponential and stationary growth phase were evaluated. In spite of the fact that FBS presented higher statistical effects than MWU on all dependent variables in the first cell passage studies, after cell adaptation, AgMNPV polyhedra production was comparable to that in Sf900 II. Batch cultivation in Grace's medium with 2.7 g l(-1) glucose, 8 g l(-1) YE and 0.1% (w/v) PF68 supplemented with 1% (w/v) MWU and 3% (v/v) FBS increased viable cell concentration to about 5-fold (4.7x10(6) cells ml(-1)) when compared to Grace's containing 10% (v/v) FBS (9.5x10(5) cells ml(-1)). AgMNPV polyhedra (PIBs) production was around 3-fold higher in the MWU supplemented medium (1.6x10(7) PIBs ml(-1)) than in Grace's medium with 10% FBS (0.6x10(7) PIBs ml(-1)). This study therefore shows a promising achievement to significantly reduce FBS concentration in Sf9 insect cell media, keeping high productivity in terms of cell concentration and final virus production at a cost almost 50% lower than that observed for Sf900 II medium.

摘要

动物细胞可以在基础培养基中培养,该培养基添加了胎牛血清(FBS),也可以在无血清培养基中培养。在这项工作中,评估了 Grace 培养基中添加一组营养物质以减少 Spodoptera frugiperda(Sf9)细胞培养中 FBS 需求的效果,目的是生产 Anticarsia gemmatalis 核多角体病毒(AgMNPV),成本低于使用 Sf900 II 培养基的生产成本。在添加葡萄糖、Pluronic F68(PF68)和酵母提取物(YE)的 Grace 培养基中,评估了 FBS 和乳清超滤物(MWU)对指数生长期和静止生长期细胞浓度和活力的影响。尽管在第一细胞传代研究中,FBS 对所有依赖变量的影响均高于 MWU,但在细胞适应后,AgMNPV 多角体的产生与 Sf900 II 相当。在 Grace 培养基中进行批培养,其中含有 2.7 g l(-1)葡萄糖、8 g l(-1)YE 和 0.1%(w/v)PF68,并添加 1%(w/v)MWU 和 3%(v/v)FBS,与含有 10%(v/v)FBS 的 Grace 培养基相比,可将活细胞浓度提高约 5 倍(4.7x10(6)细胞 ml(-1))。在添加 MWU 的培养基中,AgMNPV 多角体(PIBs)的产量约为 3 倍(1.6x10(7) PIBs ml(-1)),高于含有 10% FBS 的 Grace 培养基中的产量(0.6x10(7) PIBs ml(-1))。因此,这项研究表明,在 Sf9 昆虫细胞培养基中显著降低 FBS 浓度是一项有前途的成就,可以保持高细胞浓度和最终病毒产量,成本比 Sf900 II 培养基低近 50%。

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本文引用的文献

2
Medium design for insect cell culture.
Cytotechnology. 1996 Jan;20(1-3):57-70. doi: 10.1007/BF00350389.
3
Modeling and optimization of the baculovirus expression vector system in batch suspension culture.
Biotechnol Bioeng. 1994 Sep 5;44(6):710-9. doi: 10.1002/bit.260440607.
4
Bovine colostrum or milk as a serum substitute for the cultivation of a mouse hybridoma.
Biotechnol Bioeng. 1990 Apr 15;35(9):882-9. doi: 10.1002/bit.260350905.
5
Insect cell culture for industrial production of recombinant proteins.
Appl Microbiol Biotechnol. 2003 Jul;62(1):1-20. doi: 10.1007/s00253-003-1223-9. Epub 2003 May 6.
7
Optimization of a feed medium for fed-batch culture of insect cells using a genetic algorithm.
Biotechnol Bioeng. 2003 Feb 5;81(3):269-78. doi: 10.1002/bit.10465.
8
Design of an efficient medium for insect cell growth and recombinant protein production.
In Vitro Cell Dev Biol Anim. 2001 Oct;37(9):549-59. doi: 10.1290/1071-2690(2001)037<0549:doaemf>2.0.co;2.
10
Differential requirements of two insect cell lines for growth in serum-free medium.
In Vitro Cell Dev Biol Anim. 1997 Jun;33(6):479-82. doi: 10.1007/s11626-997-0067-5.

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