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Efficient production of single-chain Fv antibody possessing rare codon linkers in fed-batch fermentation

Authors
Kumada, YoichiSakan, YoshinobuKajihara, HideyukiKihara, ManaKikuchi, YasufumiYamaji, HidekiSeong, Gi HunKatoh, Shigeo
Issue Date
Jan-2009
Publisher
SOC BIOSCIENCE BIOENGINEERING JAPAN
Keywords
scFv; Rare codon linker; Specific production rate; Fed-batch fermentation; Exponential feeding system
Citation
JOURNAL OF BIOSCIENCE AND BIOENGINEERING, v.107, no.1, pp 73 - 77
Pages
5
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF BIOSCIENCE AND BIOENGINEERING
Volume
107
Number
1
Start Page
73
End Page
77
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/41455
DOI
10.1016/j.jbiosc.2008.09.001
ISSN
1389-1723
1347-4421
Abstract
Single-chain Fv antibody (scFv) having 2 types of polypeptide linkers with or without rare codons, namely scFv (G(4)S)(3)(R) and scFv No.10 (with rare codons) and scFv (G(4)S)(3) and scFv No.10(NR) (without rare codon), were expressed under controllable conditions in batch and fed-batch fermentation, in order to compare volumetric productivity and specific productivity levels of scFvs as a soluble form. In batch fermentation, volumetric productivity levels of scFv (G(4)S)(3)(R) and scFv No.10, namely scFvs having the rare coclon linkers were 3-5 times higher than those of scFvs that had linkers without the rare codon. In fed-batch fermentation controlled by an exponential feeding system, the cell concentrations of the transformants increased with similar specific growth rates (0.1 h(-1)), while the specific productivity levels of scFvs with the rare codon linkers were 1.6 times higher than those of scFvs without the rare codon linkers. These results indicate that the presence of several rare codons in the gene of a polypeptide linker increases soluble amount of scFvs. This might be caused by a temporary decrease in translation speed at the position of the polypeptide linker allowing time for the folding of the V(H) domain and avoiding unfavorable interactions between amino acid residues at the unfolded V(H) and V(L) domains. Higher specific productivity levels of both scFv No. 10 and scFv No. 10(NR) than those of scFv (G(4)S)(3)(R) and (G(4)S)(3) might be caused by difference in stability of the polypeptide linkers on the basis of amino acid sequences. Thus, the rare codon linkers tested in this study will be considerably useful for large-scale production of soluble and active scFvs in fed-batch or continuous fermentations, in which high cell activity can be maintained. (C) 2008, The Society for Biotechnology, Japan. All rights reserved.
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ERICA 공학대학 (DEPARTMENT OF BIONANO ENGINEERING)
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