Literature DB >> 25248702

Bi-functional cellulases complexes displayed on the cell surface of Corynebacterium glutamicum increase hydrolysis of lignocelluloses at elevated temperature.

Su Jung Kim1, Jeong Eun Hyeon1, Sang Duck Jeon1, Gi-wook Choi2, Sung Ok Han3.   

Abstract

Introducing cellulases into Corynebacterium glutamicum leads to the direct degradation of lignocellulosic materials for energy sources. In this study, a cellulase complex containing two cellulolytic enzymes, endoglucanase E (CelE) and β-glucosidase A (BglA), was established to completely degrade cellulose to glucose. The cellulases complexes were displayed on the cell surface of C. glutamicum by using the mechanosensitive channel (Msc) to anchor enzymes in the cytoplasmic membrane. As confirmed by comparison enzyme activities in the cell pellet fraction and supernatant and dual color based immunofluorescence microscopy, the cellulolytic enzymes was successfully associated with the cell surface of C. glutamicum. The displayed cellulases complexes had a synergic effect on the direct conversion of biomass to reducing sugars leading to 3.1- to 6.0-fold increase compared to the conversion by the secreted cellulases complexes. In addition, the displayed cellulases complexes increased the residual activities of cCelE and cBglA at 70°C from 28.3% and 24.3% in the secreted form to 65.1% and 82.8%, respectively. The display of cellulases complexes on the cell surface of C. glutamicum enhances the polysaccharide equivalent and the direct saccharification of low cost biomass via the action of multi-thermostable enzyme complexes.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Anchoring protein; Cellulases complex; Consolidated bioprocess; Corynebacterium glutamicum; Lignocelluloses degradation; Thermostability

Mesh:

Substances:

Year:  2014        PMID: 25248702     DOI: 10.1016/j.enzmictec.2014.08.010

Source DB:  PubMed          Journal:  Enzyme Microb Technol        ISSN: 0141-0229            Impact factor:   3.493


  7 in total

1.  Corynebacterium glutamicum possesses β-N-acetylglucosaminidase.

Authors:  Christian Matano; Stephan Kolkenbrock; Stefanie N Hamer; Elvira Sgobba; Bruno M Moerschbacher; Volker F Wendisch
Journal:  BMC Microbiol       Date:  2016-08-05       Impact factor: 3.605

Review 2.  Design of nanoscale enzyme complexes based on various scaffolding materials for biomass conversion and immobilization.

Authors:  Jeong Eun Hyeon; Sang Kyu Shin; Sung Ok Han
Journal:  Biotechnol J       Date:  2016-10-26       Impact factor: 4.677

3.  Biosynthesis of organic photosensitizer Zn-porphyrin by diphtheria toxin repressor (DtxR)-mediated global upregulation of engineered heme biosynthesis pathway in Corynebacterium glutamicum.

Authors:  Young Jin Ko; Young-Chul Joo; Jeong Eun Hyeon; Eunhye Lee; Myeong-Eun Lee; Jiho Seok; Seung Wook Kim; Chulhwan Park; Sung Ok Han
Journal:  Sci Rep       Date:  2018-09-27       Impact factor: 4.379

4.  Genome-Scale Mining of Novel Anchor Proteins of Corynebacterium glutamicum.

Authors:  Kerui Lin; Nannan Zhao; Youhua Cai; Ying Lin; Shuangyan Han; Suiping Zheng
Journal:  Front Microbiol       Date:  2022-02-04       Impact factor: 5.640

Review 5.  Metabolic Engineering for Valorization of Agri- and Aqua-Culture Sidestreams for Production of Nitrogenous Compounds by Corynebacterium glutamicum.

Authors:  Volker F Wendisch; K Madhavan Nampoothiri; Jin-Ho Lee
Journal:  Front Microbiol       Date:  2022-02-08       Impact factor: 5.640

Review 6.  Application of Corynebacterium glutamicum engineering display system in three generations of biorefinery.

Authors:  Kerui Lin; Shuangyan Han; Suiping Zheng
Journal:  Microb Cell Fact       Date:  2022-01-28       Impact factor: 5.328

7.  Construction of a trifunctional cellulase and expression in Saccharomyces cerevisiae using a fusion protein.

Authors:  Zi-Lu Liu; Hua-Nan Li; Hui-Ting Song; Wen-Jing Xiao; Wu-Cheng Xia; Xiao-Peng Liu; Zheng-Bing Jiang
Journal:  BMC Biotechnol       Date:  2018-07-13       Impact factor: 2.563

  7 in total

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