Scale up of fermentation of recombinant Escherichia coli for efficient production of spider drag silk protein MaSp1s and its dimers

Abstract Background Spider dragline silk exhibits ultrahigh tensile strength and excellent ductility, making it one of the best-performing natural biomaterials. The major ampullate spidroin (MaSp1) has promising applications in the biomedical, chemical, and military industries owing to its good bioc...

Full description

Saved in:
Bibliographic Details
Main Authors: Yufan Huang, Bixia Zhou, Ziyang Chen, Yongqin Su, Cheng Cheng, Bingfang He
Format: Article
Language:English
Published: BMC 2025-05-01
Series:Microbial Cell Factories
Subjects:
Online Access:https://doi.org/10.1186/s12934-025-02734-9
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850272790231384064
author Yufan Huang
Bixia Zhou
Ziyang Chen
Yongqin Su
Cheng Cheng
Bingfang He
author_facet Yufan Huang
Bixia Zhou
Ziyang Chen
Yongqin Su
Cheng Cheng
Bingfang He
author_sort Yufan Huang
collection DOAJ
description Abstract Background Spider dragline silk exhibits ultrahigh tensile strength and excellent ductility, making it one of the best-performing natural biomaterials. The major ampullate spidroin (MaSp1) has promising applications in the biomedical, chemical, and military industries owing to its good biocompatibility, biodegradability, and low immunogenicity. The generation of recombinant spidroin can significantly facilitate its scaled production but has several challenges, including the high cost of the downstream spidroin solubilization process and the resulting toxicity due to the use of organic solvents. Unlike common MaSp, MaSp short (MaSp1s) from Cyrtophoramoluccensis is a low-molecular-weight spidroin, lacking the typical repetitive sequences and long poly(A) motif. These features enable the heterologous production of soluble spidroin. Results In this study, rMaSp1 and its dimer rMaSp1s-2Core were expressed in soluble form by introducing the SUMO fusion tag and the self-shearing peptide intein. To improve the yield of recombinant spidroin using shake-flask fermentation, response surface analysis was used to optimize the conditions. The yields of rMaSp1 and rMaSp1s-2Core were 218.9 and 95.76 mg/L, respectively. Subsequently, fermentation was scaled up in a 5 L fermenter after adding metal ions and other growth factors to the medium. The optimal inoculation amount, induction temperature, loaded liquid, and feeding strategy were explored. Finally, the yields of rMaSp1 and rMaSp1s-2Core reached 1,112.2 and 297.8 mg/L, respectively. Furthermore, the dimerization of rMaSp1 monomers was achieved by introducing disulfide bonds via exogenous cysteine residues in the C-terminal domain. The secondary structure and self-assembly of rMaSp1 were also analyzed. Conclusion This study successfully addressed key challenges in recombinant spidroin production by employing fusion tags (SUMO and self-shearing peptide intein) to enable the soluble expression of rMaSp1 and its dimer rMaSp1s-2Core. The secondary structure and self-assembly analyses further contributed to our understanding of recombinant spidroin. These findings enable the large-scale production of spidroin and its potential applications in the biomedical, chemical, and military industries, overcoming previous hurdles related to the solubility and toxicity associated with downstream processing.
format Article
id doaj-art-d80b04fcde294636b3501210c959f095
institution OA Journals
issn 1475-2859
language English
publishDate 2025-05-01
publisher BMC
record_format Article
series Microbial Cell Factories
spelling doaj-art-d80b04fcde294636b3501210c959f0952025-08-20T01:51:41ZengBMCMicrobial Cell Factories1475-28592025-05-0124111310.1186/s12934-025-02734-9Scale up of fermentation of recombinant Escherichia coli for efficient production of spider drag silk protein MaSp1s and its dimersYufan Huang0Bixia Zhou1Ziyang Chen2Yongqin Su3Cheng Cheng4Bingfang He5College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech UniversityCollege of Biotechnology and Pharmaceutical Engineering, Nanjing Tech UniversityCollege of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University2011 College, Nanjing Tech UniversitySchool of Pharmaceutical Sciences, Nanjing Tech UniversitySchool of Pharmaceutical Sciences, Nanjing Tech UniversityAbstract Background Spider dragline silk exhibits ultrahigh tensile strength and excellent ductility, making it one of the best-performing natural biomaterials. The major ampullate spidroin (MaSp1) has promising applications in the biomedical, chemical, and military industries owing to its good biocompatibility, biodegradability, and low immunogenicity. The generation of recombinant spidroin can significantly facilitate its scaled production but has several challenges, including the high cost of the downstream spidroin solubilization process and the resulting toxicity due to the use of organic solvents. Unlike common MaSp, MaSp short (MaSp1s) from Cyrtophoramoluccensis is a low-molecular-weight spidroin, lacking the typical repetitive sequences and long poly(A) motif. These features enable the heterologous production of soluble spidroin. Results In this study, rMaSp1 and its dimer rMaSp1s-2Core were expressed in soluble form by introducing the SUMO fusion tag and the self-shearing peptide intein. To improve the yield of recombinant spidroin using shake-flask fermentation, response surface analysis was used to optimize the conditions. The yields of rMaSp1 and rMaSp1s-2Core were 218.9 and 95.76 mg/L, respectively. Subsequently, fermentation was scaled up in a 5 L fermenter after adding metal ions and other growth factors to the medium. The optimal inoculation amount, induction temperature, loaded liquid, and feeding strategy were explored. Finally, the yields of rMaSp1 and rMaSp1s-2Core reached 1,112.2 and 297.8 mg/L, respectively. Furthermore, the dimerization of rMaSp1 monomers was achieved by introducing disulfide bonds via exogenous cysteine residues in the C-terminal domain. The secondary structure and self-assembly of rMaSp1 were also analyzed. Conclusion This study successfully addressed key challenges in recombinant spidroin production by employing fusion tags (SUMO and self-shearing peptide intein) to enable the soluble expression of rMaSp1 and its dimer rMaSp1s-2Core. The secondary structure and self-assembly analyses further contributed to our understanding of recombinant spidroin. These findings enable the large-scale production of spidroin and its potential applications in the biomedical, chemical, and military industries, overcoming previous hurdles related to the solubility and toxicity associated with downstream processing.https://doi.org/10.1186/s12934-025-02734-9MaSp1sFermentation optimizationEscherichia coliHeterologous expression
spellingShingle Yufan Huang
Bixia Zhou
Ziyang Chen
Yongqin Su
Cheng Cheng
Bingfang He
Scale up of fermentation of recombinant Escherichia coli for efficient production of spider drag silk protein MaSp1s and its dimers
Microbial Cell Factories
MaSp1s
Fermentation optimization
Escherichia coli
Heterologous expression
title Scale up of fermentation of recombinant Escherichia coli for efficient production of spider drag silk protein MaSp1s and its dimers
title_full Scale up of fermentation of recombinant Escherichia coli for efficient production of spider drag silk protein MaSp1s and its dimers
title_fullStr Scale up of fermentation of recombinant Escherichia coli for efficient production of spider drag silk protein MaSp1s and its dimers
title_full_unstemmed Scale up of fermentation of recombinant Escherichia coli for efficient production of spider drag silk protein MaSp1s and its dimers
title_short Scale up of fermentation of recombinant Escherichia coli for efficient production of spider drag silk protein MaSp1s and its dimers
title_sort scale up of fermentation of recombinant escherichia coli for efficient production of spider drag silk protein masp1s and its dimers
topic MaSp1s
Fermentation optimization
Escherichia coli
Heterologous expression
url https://doi.org/10.1186/s12934-025-02734-9
work_keys_str_mv AT yufanhuang scaleupoffermentationofrecombinantescherichiacoliforefficientproductionofspiderdragsilkproteinmasp1sanditsdimers
AT bixiazhou scaleupoffermentationofrecombinantescherichiacoliforefficientproductionofspiderdragsilkproteinmasp1sanditsdimers
AT ziyangchen scaleupoffermentationofrecombinantescherichiacoliforefficientproductionofspiderdragsilkproteinmasp1sanditsdimers
AT yongqinsu scaleupoffermentationofrecombinantescherichiacoliforefficientproductionofspiderdragsilkproteinmasp1sanditsdimers
AT chengcheng scaleupoffermentationofrecombinantescherichiacoliforefficientproductionofspiderdragsilkproteinmasp1sanditsdimers
AT bingfanghe scaleupoffermentationofrecombinantescherichiacoliforefficientproductionofspiderdragsilkproteinmasp1sanditsdimers