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author:

Niu, Dandan (Niu, Dandan.) [1] | Li, Congying (Li, Congying.) [2] | Wang, Peng (Wang, Peng.) [3] | Huang, Lei (Huang, Lei.) [4] | Mchunu, Nokuthula Peace (Mchunu, Nokuthula Peace.) [5] | Singh, Suren (Singh, Suren.) [6] | Prior, Bernard A. (Prior, Bernard A..) [7] | Ye, Xiuyun (Ye, Xiuyun.) [8]

Indexed by:

EI

Abstract:

Background: Protein glutaminase specifically deamidates glutamine residue in protein and therefore significantly improves protein solubility and colloidal stability of protein solution. In order to improve its preparation efficiency, we exploited the possibility for its secretory expression mediated by twin-arginine translocation (Tat) pathway in Bacillus licheniformis. Results: The B. licheniformis genome-wide twin-arginine signal peptides were analyzed. Of which, eleven candidates were cloned for construction of expression vectors to mediate the expression of Chryseobacterium proteolyticum protein glutaminase (PGA). The signal peptide of GlmU was confirmed that it significantly mediated PGA secretion into media with the maximum activity of 0.16 U/ml in Bacillus subtilis WB600. A mutant GlmU-R, being replaced the third residue aspartic acid of GlmU twin-arginine signal peptide with arginine by site-directed mutagenesis, mediated the improved secretion of PGA with about 40% increased (0.23 U/ml). In B. licheniformis CBBD302, GlmU-R mediated PGA expression in active form with the maximum yield of 6.8 U/ml in a 25-l bioreactor. Conclusions: PGA can be produced and secreted efficiently in active form via Tat pathway of B. licheniformis, an alternative expression system for the industrial-scale production of PGA. How to cite: Niu D, Li C, Wang P, et al. Twin-arginine signal peptide of Bacillus licheniformis GlmU efficiently mediated secretory expression of protein glutaminase. Electron J Biotechnol 2019;42. https://doi.org/10.1016/j.ejbt.2019.10.006 © 2019

Keyword:

Arginine Bacteriology Cloning Escherichia coli Peptides Sols

Community:

  • [ 1 ] [Niu, Dandan]Fujian Provincial Key Laboratory of Marine Enzyme Engineering, College of Biological Science and Engineering, Fuzhou University, Fuzhou; 350108, China
  • [ 2 ] [Niu, Dandan]College of Chemical Engineering and Material Sciences, Tianjin University of Science and Technology, Tianjin; 300457, China
  • [ 3 ] [Li, Congying]Fujian Provincial Key Laboratory of Marine Enzyme Engineering, College of Biological Science and Engineering, Fuzhou University, Fuzhou; 350108, China
  • [ 4 ] [Wang, Peng]Fujian Provincial Key Laboratory of Marine Enzyme Engineering, College of Biological Science and Engineering, Fuzhou University, Fuzhou; 350108, China
  • [ 5 ] [Huang, Lei]College of Biotechnology, Tianjin University of Science and Technology, Tianjin; 300457, China
  • [ 6 ] [Mchunu, Nokuthula Peace]Department of Biotechnology and Food Technology, Faculty of Applied Sciences, Durban University of Technology, Durban, South Africa
  • [ 7 ] [Singh, Suren]Department of Biotechnology and Food Technology, Faculty of Applied Sciences, Durban University of Technology, Durban, South Africa
  • [ 8 ] [Prior, Bernard A.]Department of Microbiology, Stellenbosch University, Matieland, South Africa
  • [ 9 ] [Ye, Xiuyun]Fujian Provincial Key Laboratory of Marine Enzyme Engineering, College of Biological Science and Engineering, Fuzhou University, Fuzhou; 350108, China

Reprint 's Address:

  • [niu, dandan]fujian provincial key laboratory of marine enzyme engineering, college of biological science and engineering, fuzhou university, fuzhou; 350108, china;;[niu, dandan]college of chemical engineering and material sciences, tianjin university of science and technology, tianjin; 300457, china

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Source :

Electronic Journal of Biotechnology

Year: 2019

Volume: 42

Page: 49-55

2 . 8 9 4

JCR@2019

2 . 3 0 0

JCR@2023

ESI HC Threshold:189

JCR Journal Grade:2

CAS Journal Grade:4

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count: 10

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 2

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