Literature DB >> 28409820

Identification and control of novel growth inhibitors in fed-batch cultures of Chinese hamster ovary cells.

Bhanu Chandra Mulukutla1, Jaitashree Kale1, Taylor Kalomeris1, Michaela Jacobs1, Gregory W Hiller1.   

Abstract

Chinese hamster ovary (CHO) cells in culture are known to consume large amounts of nutrients and divert most of them toward byproducts, some of which, including lactate and ammonia, are known to be toxic in nature. Glucose limitation strategies can successfully control lactate accumulation in fed-batch cultures yielding higher peak cell densities and titers. Interestingly, even in such optimized cultures, cell growth slows and eventually stops, indicating the emergence of other factors that negatively affect cell growth. In this study, we employed omics techniques to identify and quantify nine compounds that are intermediates or byproducts of amino acid metabolism, and accumulate in fed-batch cultures. Treatment with these compounds either individually or in a combined fashion resulted in partial or complete cell growth inhibition. Careful control of selected amino acid concentrations between one-half and one millimolar during the growth phase of fed-batch cultures reduced accumulation of the inhibitory metabolites and allowed for higher peak cell densities and increased productivity. Biotechnol. Bioeng. 2017;114: 1779-1790.
© 2017 Wiley Periodicals, Inc. © 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  CHO cells; HiPDOG; amino acid metabolism; growth inhibitors

Mesh:

Substances:

Year:  2017        PMID: 28409820     DOI: 10.1002/bit.26313

Source DB:  PubMed          Journal:  Biotechnol Bioeng        ISSN: 0006-3592            Impact factor:   4.530


  8 in total

1.  Biological Filtering and Substrate Promiscuity Prediction for Annotating Untargeted Metabolomics.

Authors:  Neda Hassanpour; Nicholas Alden; Rani Menon; Arul Jayaraman; Kyongbum Lee; Soha Hassoun
Journal:  Metabolites       Date:  2020-04-21

2.  Using Metabolomics to Identify Cell Line-Independent Indicators of Growth Inhibition for Chinese Hamster Ovary Cell-based Bioprocesses.

Authors:  Nicholas Alden; Ravali Raju; Kyle McElearney; James Lambropoulos; Rashmi Kshirsagar; Alan Gilbert; Kyongbum Lee
Journal:  Metabolites       Date:  2020-05-15

Review 3.  Oxidative stress-alleviating strategies to improve recombinant protein production in CHO cells.

Authors:  Valentine Chevallier; Mikael Rørdam Andersen; Laetitia Malphettes
Journal:  Biotechnol Bioeng       Date:  2019-12-20       Impact factor: 4.530

4.  Caspase-7 deficiency in Chinese hamster ovary cells reduces cell proliferation and viability.

Authors:  Fatemeh Safari; Safar Farajnia; Abbas Behzad Behbahani; Habib Zarredar; Mazyar Barekati-Mowahed; Hesam Dehghani
Journal:  Biol Res       Date:  2020-11-13       Impact factor: 5.612

5.  Untargeted proteomics reveals upregulation of stress response pathways during CHO-based monoclonal antibody manufacturing process leading to disulfide bond reduction.

Authors:  Seo-Young Park; Susan Egan; Anthony J Cura; Kathryn L Aron; Xuankuo Xu; Mengyuan Zheng; Michael Borys; Sanchayita Ghose; Zhengjian Li; Kyongbum Lee
Journal:  MAbs       Date:  2021 Jan-Dec       Impact factor: 5.857

Review 6.  Metabolic Profiling of CHO Cells during the Production of Biotherapeutics.

Authors:  Mathilde Coulet; Oliver Kepp; Guido Kroemer; Stéphane Basmaciogullari
Journal:  Cells       Date:  2022-06-15       Impact factor: 7.666

7.  Application of metabolic modeling for targeted optimization of high seeding density processes.

Authors:  Matthias Brunner; Klara Kolb; Alena Keitel; Fabian Stiefel; Thomas Wucherpfennig; Jan Bechmann; Andreas Unsoeld; Jochen Schaub
Journal:  Biotechnol Bioeng       Date:  2021-03-01       Impact factor: 4.530

8.  A Metabolomics Approach to Increasing Chinese Hamster Ovary (CHO) Cell Productivity.

Authors:  Grace Yao; Kathryn Aron; Michael Borys; Zhengjian Li; Girish Pendse; Kyongbum Lee
Journal:  Metabolites       Date:  2021-11-30
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.