Identification of a trypsin-like serine protease from Trichoderma reesei QM9414

Dóra Dienes, Johan Börjesson, Per Hägglund, Folke Tjerneld, Gunnar Lidén, K. Réczey, Henrik Stålbrand

Research output: Contribution to journalArticle

19 Citations (Scopus)

Abstract

In the present work the genetically modified Trichoderma reesei strain QM9414 was used to produce full-length Cel7B (endoglucanase I, EGI) under the control of the constitutive Aspergillus nidulans gpdA promoter in the presence of glucose. However, the full-length Cel7B enzyme was found to be truncated to lower molecular weight components in the culture broth. Truncation of recombinant proteins produced in fungi may be due to protease activity. In order to identify major sectreted proteases, protease activity was assessed in culture filtrate of the T. reesei QM9414 recombinant. Zymogram analysis revealed the presence of proteolytic activity corresponding to one protein, which was subsequently purified by a combination of ion exchange and size exclusion chromatography. The protein has a molecular mass of 25 kDa, and an isoelectric point of 7.3. By matching tryptic peptide fragments analyzed by tandem mass spectrometry to fungal proteins available in databases as well as to expressed sequence tag (EST) sequences, and comparing the coded amino acids to full-length amino acid sequences, the purified protein was found to be homologous to several trypsin-like fungal serine proteases, with the highest homology to the protease P27 from Trichoderma harzianum. The purified protein was further characterized using benzoyl-arginyl-p-nitroanilide (BApNA) as substrate. It was found to have maximum activity at pH 8 and 50 °C, with a km-value of 0.3 mM.

Original languageEnglish
Pages (from-to)1087-1094
Number of pages8
JournalEnzyme and Microbial Technology
Volume40
Issue number5
DOIs
Publication statusPublished - Apr 3 2007

Fingerprint

Trichoderma
Peptide Hydrolases
Proteins
Amino acids
Amino Acids
Cellulases
Aspergillus nidulans
Peptide Fragments
Fungal Proteins
Size exclusion chromatography
Aspergillus
Ion Exchange
Expressed Sequence Tags
Isoelectric Point
Molecular mass
Serine Proteases
Tandem Mass Spectrometry
Recombinant proteins
Fungi
Recombinant Proteins

Keywords

  • Cel7B (endoglucanase I)
  • Serine protease
  • Trichoderma reesei
  • Trypsin

ASJC Scopus subject areas

  • Biochemistry
  • Biotechnology
  • Applied Microbiology and Biotechnology

Cite this

Dienes, D., Börjesson, J., Hägglund, P., Tjerneld, F., Lidén, G., Réczey, K., & Stålbrand, H. (2007). Identification of a trypsin-like serine protease from Trichoderma reesei QM9414. Enzyme and Microbial Technology, 40(5), 1087-1094. https://doi.org/10.1016/j.enzmictec.2006.08.013

Identification of a trypsin-like serine protease from Trichoderma reesei QM9414. / Dienes, Dóra; Börjesson, Johan; Hägglund, Per; Tjerneld, Folke; Lidén, Gunnar; Réczey, K.; Stålbrand, Henrik.

In: Enzyme and Microbial Technology, Vol. 40, No. 5, 03.04.2007, p. 1087-1094.

Research output: Contribution to journalArticle

Dienes, D, Börjesson, J, Hägglund, P, Tjerneld, F, Lidén, G, Réczey, K & Stålbrand, H 2007, 'Identification of a trypsin-like serine protease from Trichoderma reesei QM9414', Enzyme and Microbial Technology, vol. 40, no. 5, pp. 1087-1094. https://doi.org/10.1016/j.enzmictec.2006.08.013
Dienes, Dóra ; Börjesson, Johan ; Hägglund, Per ; Tjerneld, Folke ; Lidén, Gunnar ; Réczey, K. ; Stålbrand, Henrik. / Identification of a trypsin-like serine protease from Trichoderma reesei QM9414. In: Enzyme and Microbial Technology. 2007 ; Vol. 40, No. 5. pp. 1087-1094.
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