Literature DB >> 24084004

Recombinant expression of Laceyella sacchari thermitase in Lactococcus lactis.

Casper M Jørgensen1, Søren M Madsen, Astrid Vrang, Ole C Hansen, Mads G Johnsen.   

Abstract

Thermitase (EC 3.4.21.66) is a thermostable endo-protease with the ability to convert various food relevant substrates into low-molecular weight peptides. A thermitase produced by Laceyella sacchari strain DSM43353 was found to have a mature amino acid sequence nearly identical to that of the original thermitase isolated from Thermoactinomyces vulgaris. The DSM43353 thermitase gene sequence contains a pro-peptide including parts of an I9 inhibitor motif. Expression of the thermitase gene in the Lactococcus lactis P170 expression system allowed secretion of stable thermitase in an auto-induced fermentation setup at 30°C. Thermitase accumulated in the culture supernatant during batch fermentations and was easily activated at 50°C or by prolonged dialysis. The activation step resulted in an almost complete degradation of endogenous L. lactis host proteins present in the supernatant. Mature activated product was stable at 50°C and functional at pH values between pH 6 and pH 11, suggesting that substrate hydrolysis can be performed over a broad range of pH values. The L. lactis based P170 expression system is a simple and safe system for obtaining food compatible thermitase in the range of 100 mg/L. Crown
Copyright © 2013. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Heterologous expression; Laceyella sacchari; Lactococcus lactis; P170 Expression System; Protease; Thermitase

Mesh:

Substances:

Year:  2013        PMID: 24084004     DOI: 10.1016/j.pep.2013.09.009

Source DB:  PubMed          Journal:  Protein Expr Purif        ISSN: 1046-5928            Impact factor:   1.650


  2 in total

1.  Expanding the recombinant protein quality in Lactococcus lactis.

Authors:  Olivia Cano-Garrido; Fabian L Rueda; Laura Sànchez-García; Luis Ruiz-Ávila; Ramon Bosser; Antonio Villaverde; Elena García-Fruitós
Journal:  Microb Cell Fact       Date:  2014-12-04       Impact factor: 5.328

2.  The complete genome sequence of the thermophilic bacterium Laceyella sacchari FBKL4.010 reveals the basis for tetramethylpyrazine biosynthesis in Moutai-flavor Daqu.

Authors:  Dounan Li; Wei Huang; Chunxiao Wang; Shuyi Qiu
Journal:  Microbiologyopen       Date:  2019-09-04       Impact factor: 3.139

  2 in total

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