A serum-free culture medium production system by co-culture combining growth factor-secreting cells and l-lactate-assimilating cyanobacteria for sustainable cultured meat production
Large-scale production of cultured meat requires bulk culture medium containing growth-promoting proteins from animal serum. However, animal serum for mammalian cell culture is associated with high costs, ethical concerns, and contamination risks. Owing to its growth factor content, conditioned medi...
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Published in | Scientific reports Vol. 14; no. 1; pp. 19578 - 10 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
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Nature Publishing Group UK
23.08.2024
Nature Publishing Group Nature Portfolio |
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Abstract | Large-scale production of cultured meat requires bulk culture medium containing growth-promoting proteins from animal serum. However, animal serum for mammalian cell culture is associated with high costs, ethical concerns, and contamination risks. Owing to its growth factor content, conditioned medium from rat liver epithelial RL34 cells can replace animal serum for myoblast proliferation. More seeded cells and longer culture periods are thought to yield higher growth factor levels, resulting in more effective muscle cell proliferation. However, RL34 cells can deplete nutrients and release harmful metabolites into the culture medium over time, potentially causing growth inhibition and apoptosis. This issue highlights the need for waste clearance during condition medium production. To address this issue, we introduced a lactate permease gene (
lldP
) and an
l
-lactate-to-pyruvate conversion enzyme gene (
lldD
) to generate a recombinant
l
-lactate-assimilating cyanobacterium
Synechococcus
sp. KC0110 strain. Transwell co-culture of this strain with RL34 cells exhibited a marked reduction in the levels of harmful metabolites, lactate and ammonium, while maintaining higher concentrations of glucose, pyruvate, and pyruvate-derived amino acids than those seen with RL34 cell monocultures. The co-culture medium supported myoblast proliferation without medium dilution or additional nutrients, which was attributed to the waste clearance and nutrient replenishment effects of the KC0110 strain. This culture system holds potential for the production of low-cost, and animal-free cultured meat. |
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AbstractList | Large-scale production of cultured meat requires bulk culture medium containing growth-promoting proteins from animal serum. However, animal serum for mammalian cell culture is associated with high costs, ethical concerns, and contamination risks. Owing to its growth factor content, conditioned medium from rat liver epithelial RL34 cells can replace animal serum for myoblast proliferation. More seeded cells and longer culture periods are thought to yield higher growth factor levels, resulting in more effective muscle cell proliferation. However, RL34 cells can deplete nutrients and release harmful metabolites into the culture medium over time, potentially causing growth inhibition and apoptosis. This issue highlights the need for waste clearance during condition medium production. To address this issue, we introduced a lactate permease gene (lldP) and an L-lactate-to-pyruvate conversion enzyme gene (lldD) to generate a recombinant L-lactate-assimilating cyanobacterium Synechococcus sp. KC0110 strain. Transwell co-culture of this strain with RL34 cells exhibited a marked reduction in the levels of harmful metabolites, lactate and ammonium, while maintaining higher concentrations of glucose, pyruvate, and pyruvate-derived amino acids than those seen with RL34 cell monocultures. The co-culture medium supported myoblast proliferation without medium dilution or additional nutrients, which was attributed to the waste clearance and nutrient replenishment effects of the KC0110 strain. This culture system holds potential for the production of low-cost, and animal-free cultured meat. Large-scale production of cultured meat requires bulk culture medium containing growth-promoting proteins from animal serum. However, animal serum for mammalian cell culture is associated with high costs, ethical concerns, and contamination risks. Owing to its growth factor content, conditioned medium from rat liver epithelial RL34 cells can replace animal serum for myoblast proliferation. More seeded cells and longer culture periods are thought to yield higher growth factor levels, resulting in more effective muscle cell proliferation. However, RL34 cells can deplete nutrients and release harmful metabolites into the culture medium over time, potentially causing growth inhibition and apoptosis. This issue highlights the need for waste clearance during condition medium production. To address this issue, we introduced a lactate permease gene (lldP) and an L-lactate-to-pyruvate conversion enzyme gene (lldD) to generate a recombinant L-lactate-assimilating cyanobacterium Synechococcus sp. KC0110 strain. Transwell co-culture of this strain with RL34 cells exhibited a marked reduction in the levels of harmful metabolites, lactate and ammonium, while maintaining higher concentrations of glucose, pyruvate, and pyruvate-derived amino acids than those seen with RL34 cell monocultures. The co-culture medium supported myoblast proliferation without medium dilution or additional nutrients, which was attributed to the waste clearance and nutrient replenishment effects of the KC0110 strain. This culture system holds potential for the production of low-cost, and animal-free cultured meat.Large-scale production of cultured meat requires bulk culture medium containing growth-promoting proteins from animal serum. However, animal serum for mammalian cell culture is associated with high costs, ethical concerns, and contamination risks. Owing to its growth factor content, conditioned medium from rat liver epithelial RL34 cells can replace animal serum for myoblast proliferation. More seeded cells and longer culture periods are thought to yield higher growth factor levels, resulting in more effective muscle cell proliferation. However, RL34 cells can deplete nutrients and release harmful metabolites into the culture medium over time, potentially causing growth inhibition and apoptosis. This issue highlights the need for waste clearance during condition medium production. To address this issue, we introduced a lactate permease gene (lldP) and an L-lactate-to-pyruvate conversion enzyme gene (lldD) to generate a recombinant L-lactate-assimilating cyanobacterium Synechococcus sp. KC0110 strain. Transwell co-culture of this strain with RL34 cells exhibited a marked reduction in the levels of harmful metabolites, lactate and ammonium, while maintaining higher concentrations of glucose, pyruvate, and pyruvate-derived amino acids than those seen with RL34 cell monocultures. The co-culture medium supported myoblast proliferation without medium dilution or additional nutrients, which was attributed to the waste clearance and nutrient replenishment effects of the KC0110 strain. This culture system holds potential for the production of low-cost, and animal-free cultured meat. Large-scale production of cultured meat requires bulk culture medium containing growth-promoting proteins from animal serum. However, animal serum for mammalian cell culture is associated with high costs, ethical concerns, and contamination risks. Owing to its growth factor content, conditioned medium from rat liver epithelial RL34 cells can replace animal serum for myoblast proliferation. More seeded cells and longer culture periods are thought to yield higher growth factor levels, resulting in more effective muscle cell proliferation. However, RL34 cells can deplete nutrients and release harmful metabolites into the culture medium over time, potentially causing growth inhibition and apoptosis. This issue highlights the need for waste clearance during condition medium production. To address this issue, we introduced a lactate permease gene ( lldP ) and an l -lactate-to-pyruvate conversion enzyme gene ( lldD ) to generate a recombinant l -lactate-assimilating cyanobacterium Synechococcus sp. KC0110 strain. Transwell co-culture of this strain with RL34 cells exhibited a marked reduction in the levels of harmful metabolites, lactate and ammonium, while maintaining higher concentrations of glucose, pyruvate, and pyruvate-derived amino acids than those seen with RL34 cell monocultures. The co-culture medium supported myoblast proliferation without medium dilution or additional nutrients, which was attributed to the waste clearance and nutrient replenishment effects of the KC0110 strain. This culture system holds potential for the production of low-cost, and animal-free cultured meat. Abstract Large-scale production of cultured meat requires bulk culture medium containing growth-promoting proteins from animal serum. However, animal serum for mammalian cell culture is associated with high costs, ethical concerns, and contamination risks. Owing to its growth factor content, conditioned medium from rat liver epithelial RL34 cells can replace animal serum for myoblast proliferation. More seeded cells and longer culture periods are thought to yield higher growth factor levels, resulting in more effective muscle cell proliferation. However, RL34 cells can deplete nutrients and release harmful metabolites into the culture medium over time, potentially causing growth inhibition and apoptosis. This issue highlights the need for waste clearance during condition medium production. To address this issue, we introduced a lactate permease gene (lldP) and an l-lactate-to-pyruvate conversion enzyme gene (lldD) to generate a recombinant l-lactate-assimilating cyanobacterium Synechococcus sp. KC0110 strain. Transwell co-culture of this strain with RL34 cells exhibited a marked reduction in the levels of harmful metabolites, lactate and ammonium, while maintaining higher concentrations of glucose, pyruvate, and pyruvate-derived amino acids than those seen with RL34 cell monocultures. The co-culture medium supported myoblast proliferation without medium dilution or additional nutrients, which was attributed to the waste clearance and nutrient replenishment effects of the KC0110 strain. This culture system holds potential for the production of low-cost, and animal-free cultured meat. |
ArticleNumber | 19578 |
Author | Kondo, Akihiko Haraguchi, Yuji Asahi, Toru Hasunuma, Tomohisa Chu, Shanga Kato, Yuichi Shimizu, Tatsuya |
Author_xml | – sequence: 1 givenname: Shanga surname: Chu fullname: Chu, Shanga organization: Department of Advanced Science and Engineering, Graduate School of Advanced Science and Engineering, Waseda University, TWIns, Institute of Advanced Biomedical Engineering and Science, TWIns, Tokyo Women’s Medical University – sequence: 2 givenname: Yuji surname: Haraguchi fullname: Haraguchi, Yuji organization: Institute of Advanced Biomedical Engineering and Science, TWIns, Tokyo Women’s Medical University – sequence: 3 givenname: Toru surname: Asahi fullname: Asahi, Toru organization: Department of Advanced Science and Engineering, Graduate School of Advanced Science and Engineering, Waseda University, TWIns, Department of Life Science and Medical Bioscience, School of Advanced Science and Engineering, Waseda University, TWIns, Faculty of Science and Engineering, Waseda University – sequence: 4 givenname: Yuichi surname: Kato fullname: Kato, Yuichi organization: Engineering Biology Research Center, Kobe University, Graduate School of Science, Technology and Innovation, Kobe University – sequence: 5 givenname: Akihiko surname: Kondo fullname: Kondo, Akihiko organization: Engineering Biology Research Center, Kobe University, Graduate School of Science, Technology and Innovation, Kobe University, Research Center for Sustainable Resource Science, RIKEN – sequence: 6 givenname: Tomohisa surname: Hasunuma fullname: Hasunuma, Tomohisa organization: Engineering Biology Research Center, Kobe University, Graduate School of Science, Technology and Innovation, Kobe University, Research Center for Sustainable Resource Science, RIKEN – sequence: 7 givenname: Tatsuya surname: Shimizu fullname: Shimizu, Tatsuya email: shimizu.tatsuya@twmu.ac.jp organization: Institute of Advanced Biomedical Engineering and Science, TWIns, Tokyo Women’s Medical University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/39179636$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_susmat_2025_e01368 crossref_primary_10_1007_s00203_024_04149_3 crossref_primary_10_1016_j_tjnut_2025_01_010 crossref_primary_10_3390_fermentation10120612 |
Cites_doi | 10.1111/padr.12508 10.1038/s41598-023-34289-3 10.1126/sciadv.1603078 10.1038/s43016-021-00322-9 10.3390/su13020956 10.1016/S0041-0101(98)00128-7 10.1016/j.scr.2014.03.004 10.7150/thno.31884 10.1007/s00203-022-03234-9 10.1016/0168-1656(95)00196-4 10.1038/s41598-023-27629-w 10.1007/s00203-023-03607-8 10.1007/s00449-008-0202-z 10.1016/j.actbio.2014.12.012 10.1007/s00204-002-0330-1 10.1080/00139157.2015.1025644 10.1126/science.1239402 10.1016/j.bbrc.2023.10.018 10.14573/altex.1705101 |
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Keywords | RL34 cells lactate-assimilating cyanobacterium Co-culture Serum replacement Cultured meat Mammalian cell cultures l-lactate-assimilating cyanobacterium |
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Snippet | Large-scale production of cultured meat requires bulk culture medium containing growth-promoting proteins from animal serum. However, animal serum for... Abstract Large-scale production of cultured meat requires bulk culture medium containing growth-promoting proteins from animal serum. However, animal serum for... |
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SubjectTerms | 631/1647/2234 631/61 631/61/168 631/80 Amino acids Ammonium Animals Apoptosis Cell culture Cell Line Cell Proliferation Co-culture Coculture Techniques - methods Culture media Culture Media, Serum-Free Cultured meat Growth factors Hepatocytes Humanities and Social Sciences In Vitro Meat Intercellular Signaling Peptides and Proteins - genetics Intercellular Signaling Peptides and Proteins - metabolism l-lactate-assimilating cyanobacterium Lactate permease Lactic acid Lactic Acid - metabolism Mammalian cell cultures Meat Meat production Metabolites Monoculture multidisciplinary Myoblasts Myoblasts - cytology Myoblasts - metabolism Nutrients Permease Pyruvic acid Rats RL34 cells Science Science (multidisciplinary) Serum replacement Synechococcus - genetics Synechococcus - growth & development Synechococcus - metabolism |
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Title | A serum-free culture medium production system by co-culture combining growth factor-secreting cells and l-lactate-assimilating cyanobacteria for sustainable cultured meat production |
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