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Substantial overproduction of antibodies by applying osmotic pressure and sodium butyrate

Publication ,  Journal Article
Oh, SKW; Vig, P; Chua, F; Teo, WK; Yap, MGS
Published in: Biotechnology and Bioengineering
January 1, 1993

Much of the current cell technology has enabled increased antibody production levels due to judicious nutrient feeding to raise cell densities and design better bioreactors. This study demonstrates that hybridomas can be hyperstimulated to produce higher immunoglobulin (lg) levels by suppressing cell growth and increasing culture longevity through adaptation to higher osmolarity media and addition of sodium butyrate. Prior to adaptation, cells placed in higher osmotic pressures (350 and 400 mOsm) were severely suppressed in growth down to 25% of the control (300 mOsm), although total lg titers achieved were similar to the control, approximately 140 mg/L. After a week of adaptation to 350 and 400 mOsm media, cell growth was not as dramatically suppressed, but considerably higher lg levels were attained at these elevated osmolarities. The highest yield of 265 mg/L was obtained at 350 mOsm compared to 140 mg/L at 300 mOsm, while maximum viable cell numbers dropped from 35 × 105 cells/mL to 31 × 105 cells/mL and culture longevity was extended by 20 h more than the control. Sodium butyrate, known to enhance protein production in other cell types, was then supplemented at a range of concentrations between 0.01 and 0.4 mM to the 350 mOsm culture to further enhance the lg levels. Butyrate at a concentration of 0.1 mM, in combination with osmotic pressure at 350 mOsm, further elevated the lg levels to 350 mg/L. Concomitantly, maximum viable cell numbers were reduced to 22 × 105 cells/mL, but culture longevity was extended by 40 h in the 0.1 mM butyrate supplemented culture compared to the control condition. Specific antibody productivity, qMab, continued to stay high during the stationary phase and was further elevated during the decline phase: thus, overall lg levels can be increased by 2.3 times by combining osmotic pressure and butyrate treatment. © 1993 John Wiley & Sons, Inc. Copyright © 1993 John Wiley & Sons, Inc.

Duke Scholars

Published In

Biotechnology and Bioengineering

DOI

EISSN

1097-0290

ISSN

0006-3592

Publication Date

January 1, 1993

Volume

42

Issue

5

Start / End Page

601 / 610

Related Subject Headings

  • Biotechnology
 

Citation

APA
Chicago
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Oh, S. K. W., Vig, P., Chua, F., Teo, W. K., & Yap, M. G. S. (1993). Substantial overproduction of antibodies by applying osmotic pressure and sodium butyrate. Biotechnology and Bioengineering, 42(5), 601–610. https://doi.org/10.1002/bit.260420508
Oh, S. K. W., P. Vig, F. Chua, W. K. Teo, and M. G. S. Yap. “Substantial overproduction of antibodies by applying osmotic pressure and sodium butyrate.” Biotechnology and Bioengineering 42, no. 5 (January 1, 1993): 601–10. https://doi.org/10.1002/bit.260420508.
Oh SKW, Vig P, Chua F, Teo WK, Yap MGS. Substantial overproduction of antibodies by applying osmotic pressure and sodium butyrate. Biotechnology and Bioengineering. 1993 Jan 1;42(5):601–10.
Oh, S. K. W., et al. “Substantial overproduction of antibodies by applying osmotic pressure and sodium butyrate.” Biotechnology and Bioengineering, vol. 42, no. 5, Jan. 1993, pp. 601–10. Scopus, doi:10.1002/bit.260420508.
Oh SKW, Vig P, Chua F, Teo WK, Yap MGS. Substantial overproduction of antibodies by applying osmotic pressure and sodium butyrate. Biotechnology and Bioengineering. 1993 Jan 1;42(5):601–610.
Journal cover image

Published In

Biotechnology and Bioengineering

DOI

EISSN

1097-0290

ISSN

0006-3592

Publication Date

January 1, 1993

Volume

42

Issue

5

Start / End Page

601 / 610

Related Subject Headings

  • Biotechnology