Optimization of bioprocess conditions improves production of a CHO cell-derived, bioengineered heparin

Heparin is the most widely used anticoagulant drug in the world today. Heparin is currently produced from animal tissues, primarily porcine intestines. A recent contamination crisis motivated development of a non‐animal‐derived source of this critical drug. We hypothesized that Chinese hamster ovary...

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Veröffentlicht in:Biotechnology journal 2015-07, Vol.10 (7), p.1067-1081
Hauptverfasser: Baik, Jong Youn, Dahodwala, Hussain, Oduah, Eziafa, Talman, Lee, Gemmill, Trent R., Gasimli, Leyla, Datta, Payel, Yang, Bo, Li, Guoyun, Zhang, Fuming, Li, Lingyun, Linhardt, Robert J., Campbell, Andrew M., Gorfien, Stephen F., Sharfstein, Susan T.
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container_end_page 1081
container_issue 7
container_start_page 1067
container_title Biotechnology journal
container_volume 10
creator Baik, Jong Youn
Dahodwala, Hussain
Oduah, Eziafa
Talman, Lee
Gemmill, Trent R.
Gasimli, Leyla
Datta, Payel
Yang, Bo
Li, Guoyun
Zhang, Fuming
Li, Lingyun
Linhardt, Robert J.
Campbell, Andrew M.
Gorfien, Stephen F.
Sharfstein, Susan T.
description Heparin is the most widely used anticoagulant drug in the world today. Heparin is currently produced from animal tissues, primarily porcine intestines. A recent contamination crisis motivated development of a non‐animal‐derived source of this critical drug. We hypothesized that Chinese hamster ovary (CHO) cells could be metabolically engineered to produce a bioengineered heparin, equivalent to current pharmaceutical heparin. We previously engineered CHO‐S® cells to overexpress two exogenous enzymes from the heparin/heparan sulfate biosynthetic pathway, increasing the anticoagulant activity ∼100‐fold and the heparin/heparan sulfate yield ∼10‐fold. Here, we explored the effects of bioprocess parameters on the yield and anticoagulant activity of the bioengineered GAGs. Fed‐batch shaker‐flask studies using a proprietary, chemically‐defined feed, resulted in ∼two‐fold increase in integrated viable cell density and a 70% increase in specific productivity, resulting in nearly three‐fold increase in product titer. Transferring the process to a stirred‐tank bioreactor increased the productivity further, yielding a final product concentration of ∼90 μg/mL. Unfortunately, the product composition still differs from pharmaceutical heparin, suggesting that additional metabolic engineering will be required. However, these studies clearly demonstrate bioprocess optimization, in parallel with metabolic engineering refinements, will play a substantial role in developing a bioengineered heparin to replace the current animal‐derived drug. Bioprocess engineering can be used to enhance the culture performance of mammalian cells that produce pharmaceutical biomolecules. Nutrient feeding to Chinese hamster ovary cell cultures results in 3∼4‐fold increase in heparin/heparan sulfate titers. This bioprocessing approach may contribute to replacing the current animal‐derived drug with a safer bioengineered heparin, manufactured under cGMP conditions. Bioreactor image by Miropiro, www.bioreactors.eu, www.bioreactor.ch (Own work) [CC BY‐SA 3.0 (http://creativecommons.org/licenses/by‐sa/3.0)], via Wikimedia Commons.
doi_str_mv 10.1002/biot.201400665
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Heparin is currently produced from animal tissues, primarily porcine intestines. A recent contamination crisis motivated development of a non‐animal‐derived source of this critical drug. We hypothesized that Chinese hamster ovary (CHO) cells could be metabolically engineered to produce a bioengineered heparin, equivalent to current pharmaceutical heparin. We previously engineered CHO‐S® cells to overexpress two exogenous enzymes from the heparin/heparan sulfate biosynthetic pathway, increasing the anticoagulant activity ∼100‐fold and the heparin/heparan sulfate yield ∼10‐fold. Here, we explored the effects of bioprocess parameters on the yield and anticoagulant activity of the bioengineered GAGs. Fed‐batch shaker‐flask studies using a proprietary, chemically‐defined feed, resulted in ∼two‐fold increase in integrated viable cell density and a 70% increase in specific productivity, resulting in nearly three‐fold increase in product titer. Transferring the process to a stirred‐tank bioreactor increased the productivity further, yielding a final product concentration of ∼90 μg/mL. Unfortunately, the product composition still differs from pharmaceutical heparin, suggesting that additional metabolic engineering will be required. However, these studies clearly demonstrate bioprocess optimization, in parallel with metabolic engineering refinements, will play a substantial role in developing a bioengineered heparin to replace the current animal‐derived drug. Bioprocess engineering can be used to enhance the culture performance of mammalian cells that produce pharmaceutical biomolecules. Nutrient feeding to Chinese hamster ovary cell cultures results in 3∼4‐fold increase in heparin/heparan sulfate titers. This bioprocessing approach may contribute to replacing the current animal‐derived drug with a safer bioengineered heparin, manufactured under cGMP conditions. 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Heparin is currently produced from animal tissues, primarily porcine intestines. A recent contamination crisis motivated development of a non‐animal‐derived source of this critical drug. We hypothesized that Chinese hamster ovary (CHO) cells could be metabolically engineered to produce a bioengineered heparin, equivalent to current pharmaceutical heparin. We previously engineered CHO‐S® cells to overexpress two exogenous enzymes from the heparin/heparan sulfate biosynthetic pathway, increasing the anticoagulant activity ∼100‐fold and the heparin/heparan sulfate yield ∼10‐fold. Here, we explored the effects of bioprocess parameters on the yield and anticoagulant activity of the bioengineered GAGs. Fed‐batch shaker‐flask studies using a proprietary, chemically‐defined feed, resulted in ∼two‐fold increase in integrated viable cell density and a 70% increase in specific productivity, resulting in nearly three‐fold increase in product titer. Transferring the process to a stirred‐tank bioreactor increased the productivity further, yielding a final product concentration of ∼90 μg/mL. Unfortunately, the product composition still differs from pharmaceutical heparin, suggesting that additional metabolic engineering will be required. However, these studies clearly demonstrate bioprocess optimization, in parallel with metabolic engineering refinements, will play a substantial role in developing a bioengineered heparin to replace the current animal‐derived drug. Bioprocess engineering can be used to enhance the culture performance of mammalian cells that produce pharmaceutical biomolecules. Nutrient feeding to Chinese hamster ovary cell cultures results in 3∼4‐fold increase in heparin/heparan sulfate titers. This bioprocessing approach may contribute to replacing the current animal‐derived drug with a safer bioengineered heparin, manufactured under cGMP conditions. Bioreactor image by Miropiro, www.bioreactors.eu, www.bioreactor.ch (Own work) [CC BY‐SA 3.0 (http://creativecommons.org/licenses/by‐sa/3.0)], via Wikimedia Commons.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><pmid>26037948</pmid><doi>10.1002/biot.201400665</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Anticoagulants
Bioreactors
Biosynthetic Pathways
CHO Cells
Cricetinae
Cricetulus
Disaccharide analysis
Fed-batch cultures
Glycosaminoglycans
Heparin - biosynthesis
Heparin - metabolism
Metabolic Engineering
title Optimization of bioprocess conditions improves production of a CHO cell-derived, bioengineered heparin
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