Literature DB >> 31786296

Efficient expression of chondroitinase ABC I for specific disaccharides detection of chondroitin sulfate.

Xingyu Lu1, Qian Zhong1, Jian Liu1, Fulin Yang1, Chenghui Lu1, Huan Xiong1, Sha Li2, Yibo Zhu1, Lingtian Wu3.   

Abstract

Chondroitinase ABC I (ChSase ABC I) is a key enzyme of chondroitin sulfate (CS) degradation and widely used for CS detection in the medicine filed. However, the recombinant ChSase ABC I was weakly expressed in Escherichia coli because the forms of it were mostly inclusion bodies. In this study, a signal peptide (pelB) was used for the soluble form expression of ChSase ABC I in E. coli. Then the culture condition for ChSase ABC I expression was optimized through response surface methodology. Results revealed that the expression level of ChSase ABC I in a 7.5 L fermentor (29.03 mL-1) was approximately 1.65-fold higher than that of the shake flask level (17.55 mL-1). The enzymatic properties and kinetic constants of recombinant ChSase ABC I were also studied. Recombinant ChSase ABC I was also used to detect the specific disaccharides content of CS from different sources. This study not only eliminates the problem of the enzyme expressed as an inclusion body, but also solves the current problem of expensive ChSase ABC. In a word, it would be an ideal strategy for ChSase ABC high-efficiency expression and a great method to detect specific disaccharides of CS in biomedical field.
Copyright © 2019 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Chondroitin sulfate; Chondroitinase ABC I; Signal peptide; Soluble expression

Mesh:

Substances:

Year:  2019        PMID: 31786296     DOI: 10.1016/j.ijbiomac.2019.11.215

Source DB:  PubMed          Journal:  Int J Biol Macromol        ISSN: 0141-8130            Impact factor:   6.953


  3 in total

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