Comparison of the cultivation of wild and transfected Drosophila melanogaster S2 cells in different media

被引:2
|
作者
Swiech, K. [1 ]
Galesi, A. L. L. [2 ]
Moraes, A. M. [2 ]
Mendonca, R. Z. [3 ]
Pereira, C. A. [3 ]
Suazo, C. A. T. [1 ]
机构
[1] Univ Fed Sao Carlos, Dept Chem Engn, Sao Carlos, SP, Brazil
[2] Univ Estadual Campinas, Sch Chem Engn, Dept Biotechnol Proc, BR-13083970 Campinas, SP, Brazil
[3] Butantan Inst, Lab Viral Immunol, BR-05503900 Sao Paulo, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
S2 insect cells; G glycoprotein; TNM-FH; TC100; SF900II;
D O I
10.1007/978-1-4020-5476-1_68
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Insect cells have been increasingly employed for the production of recombinant proteins. One of the most widely used dipteran cells in transfection studies is the Schneider 2 (S2) cell line, established from Drosophila melanogaster embryonic tissue. In this work, the growth and proliferation of wild and transfected S2 cells expressing the G glycoprotein from rabies virus (GPV) were compared employing different culture media. For the transfected (S2AcGPV2) cell contruction, the plasmid pGPV encoding the sequence of interest and the vectors pAc 5.1/V5-His A under the control of the Drosophila actin promoter were utilized. The selection vector pCoHygro carrying genes coding for hygromicin-inactivating enzymes was also employed and the cells were transfected using lipofectin. Due to wide utilization of TNM-FH and TC100 media (both requiring supplementation with fetal bovine serum) for insect cells, their low cost and the low protein content of SF900II medium, the,se three media and the mixture TNM-FH-SF900II (1:1) were evaluated for the choice of a suitable media for S2 cells. The results indicated that the wild and the transfected cells presented different growth characteristics in the distinct media. In SF900II medium, larger accumulation and consumption of lactate were observed for the wild cell culture. In TC100, however, S2AcGPV2 cells did not produce lactate. In TNM-FH, the S2 cells presented lower growth rate (mu(max)=4.0078 h(-1)) when compared to the other media (mu(max)=0.0375 h(-1) and mu(max)=0.0112 h(-1) for SF900II and TC100, respectively), with an accentuated viability drop during the first days of culture. The mixture of TNM-FH and SF900II at a 1:1 volume ratio resulted in cell growth (mu(max)=0.0377 h(-1)) similar to that observed in SF900II medium only, allowing significant culture media cost reduction. Transfected cells could not be adapted to TNM-FH medium. Cell growth of S2AcGPV2 cells in TC 100 medium (mu(max)=0.0151 h(-1)) was lower than in SF900II medium (mu(max)=0.0407 h(-1)).
引用
收藏
页码:415 / +
页数:4
相关论文
共 50 条
  • [1] Behavior of Wild-type and Transfected S2 Cells Cultured in Two Different Media
    Batista, Fabiana R. X.
    Greco, Katia N.
    Astray, Renato M.
    Jorge, Soraia A. C.
    Augusto, Elisabeth F. P.
    Pereira, Carlos A.
    Mendonca, Ronaldo Z.
    Moraes, Angela M.
    APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 2011, 163 (01) : 1 - 13
  • [2] Behavior of Wild-type and Transfected S2 Cells Cultured in Two Different Media
    Fabiana R. X. Batista
    Kátia N. Greco
    Renato M. Astray
    Soraia A. C. Jorge
    Elisabeth F. P. Augusto
    Carlos A. Pereira
    Ronaldo Z. Mendonça
    Ângela M. Moraes
    Applied Biochemistry and Biotechnology, 2011, 163 : 1 - 13
  • [3] Copper homoeostasis in Drosophila melanogaster S2 cells
    Southon, A
    Burke, R
    Norgate, M
    Batterham, P
    Camakaris, J
    BIOCHEMICAL JOURNAL, 2004, 383 (02) : 303 - 309
  • [4] Growth of Rickettsia felis in Drosophila melanogaster S2 Cells
    Luce-Fedrow, Alison
    Macaluso, Kevin R.
    Richards, Allen L.
    VECTOR-BORNE AND ZOONOTIC DISEASES, 2014, 14 (02) : 101 - 110
  • [5] RNA Immunoprecipitation Technique for Drosophila melanogaster S2 Cells
    Kachaev, Z. M.
    Gilmutdinov, R. A.
    Kopytova, D. V.
    Zheludkevich, A. A.
    Shidlovskii, Y. V.
    Kurbidaeva, A. S.
    MOLECULAR BIOLOGY, 2017, 51 (01) : 72 - 79
  • [6] RNA immunoprecipitation technique for Drosophila melanogaster S2 cells
    Z. M. Kachaev
    R. A. Gilmutdinov
    D. V. Kopytova
    A. A. Zheludkevich
    Y. V. Shidlovskii
    A. S. Kurbidaeva
    Molecular Biology, 2017, 51 : 72 - 79
  • [7] Efficient expression of functional human coagulation factor IX in stably-transfected Drosophila melanogaster S2 cells; comparison with the mammalian CHO system
    Vatandoost, Jafar
    Bos, Mettine H. A.
    BIOTECHNOLOGY LETTERS, 2016, 38 (10) : 1691 - 1698
  • [8] Efficient expression of functional human coagulation factor IX in stably-transfected Drosophila melanogaster S2 cells; comparison with the mammalian CHO system
    Jafar Vatandoost
    Mettine H. A. Bos
    Biotechnology Letters, 2016, 38 : 1691 - 1698
  • [9] Culturing Drosophila melanogaster (S2) in a chemostat
    Paula Bruzadelle Vieira
    Bruno Labate Vale da Costa
    Elisabeth de Fatima Pires Augusto
    Aldo Tonso
    Biotechnology Letters, 2015, 37 : 533 - 538
  • [10] Culturing Drosophila melanogaster (S2) in a chemostat
    Vieira, Paula Bruzadelle
    Vale da Costa, Bruno Labate
    Pires Augusto, Elisabeth de Fatima
    Tonso, Aldo
    BIOTECHNOLOGY LETTERS, 2015, 37 (03) : 533 - 538