Evidence map›Paper›PMID 33993368›Full record

ArticleBiotechnology letters2021

A temperature-induced chitosanase bacterial cell-surface display system for the efficient production of chitooligosaccharides.

Qianqian Li, Tuantuan Wang, Yangzhi Ye, Shimin Guan, Baoguo Cai, Shuo Zhang, Shaofeng Rong

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Article in Biotechnology letters, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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3 · Its place in the literature

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3 citing papers in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Qianqian LiDepartment of Bioengineering, Shanghai Institute of Technology, 100 Haiquan Road, Shanghai, 201418, People's Republic of China.
Tuantuan WangDepartment of Bioengineering, Shanghai Institute of Technology, 100 Haiquan Road, Shanghai, 201418, People's Republic of China.
Yangzhi YeDepartment of Bioengineering, Shanghai Institute of Technology, 100 Haiquan Road, Shanghai, 201418, People's Republic of China.
Shimin GuanDepartment of Bioengineering, Shanghai Institute of Technology, 100 Haiquan Road, Shanghai, 201418, People's Republic of China.
Baoguo CaiDepartment of Bioengineering, Shanghai Institute of Technology, 100 Haiquan Road, Shanghai, 201418, People's Republic of China.
Shuo ZhangDepartment of Bioengineering, Shanghai Institute of Technology, 100 Haiquan Road, Shanghai, 201418, People's Republic of China.
Shaofeng RongDepartment of Bioengineering, Shanghai Institute of Technology, 100 Haiquan Road, Shanghai, 201418, People's Republic of China. rongshaofeng@163.com.ORCID http://orcid.org/0000-0003-1747-0263

Funding

Science and Technology Commission of Shanghai Municipality Grant no. 17441905400
6 · The paper itself

Abstract

objectiveTo establish a temperature-induced chitosanase bacterial cell-surface display system to produce chitooligosaccharides (COSs) efficiently for industrial applications.

resultsTemperature-inducible chitosanase CSN46A bacterial surface display systems containing one or two copies of ice nucleation protein (InaQ-N) as anchoring motifs were successfully constructed on the basis of Escherichia coli and named as InaQ-N-CSN46A (1 copy) and 2InaQ-N-CSN46A (2 copies). The specific enzyme activity of 2InaQ-N-CSN46A reached 761.34 ± 0.78 U/g cell dry weight, which was 45.6% higher than that of InaQ-N-CSN46A. However, few proteins were detected in the 2InaQ-N-CSN46A hydrolysis system. Therefore, 2InaQ-N-CSN46A had higher hydrolysis efficiency and stability than InaQ-N-CSN46A. Gel permeation chromatography revealed that under the optimum enzymatic hydrolysis temperature, the final products were mainly chitobiose and chitotriose. Chitopentaose accumulated (77.62%) when the hydrolysis temperature reached 60 °C. FTIR and NMR analysis demonstrated that the structures of the two hydrolysis products were consistent with those of COSs.

conclusionsIn this study, chitosanase was expressed on the surfaces of E. coli by increasing the induction temperature, and chitosan was hydrolysed directly without enzyme purification steps. This study provides a novel strategy for industrial COS production.

Indexed as

Escherichia coliGlycoside HydrolasesRecombinant Fusion ProteinsBacterial Outer Membrane ProteinsBacterial ProteinsCell Surface Display TechniquesChitosanHydrolysisOligosaccharidesTemperatureBacterial Outer Membrane ProteinsBacterial ProteinsChitosanchitosanaseGlycoside Hydrolasesice nucleation proteinoligochitosanOligosaccharidesRecombinant Fusion ProteinsCell-surface displayChitooligosaccharidesChitosanasesEscherichia coliTemperature-inducible

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.