Literature DB >> 15621446

The nagA gene of Penicillium chrysogenum encoding beta-N-acetylglucosaminidase.

Bruno Díez1, Marta Rodríguez-Sáiz, Juan Luis de la Fuente, Miguel Angel Moreno, José Luis Barredo.   

Abstract

We purified the beta-N-acetylglucosaminidase from the filamentous fungus Penicillium chrysogenum and its N-terminal sequence was determined, showing the presence of a mixture of two proteins (P1 and P2). A genomic DNA fragment was cloned by using degenerated oligonucleotides from the Nt sequences. The nucleotide sequence showed the presence of an ORF (nagA gene) lacking introns, with a length of 1791 bp, and coding for a protein of 66.5 kDa showing similarity to acetylglucosaminidases. The NagA deduced protein includes P1 and P2 as incomplete forms of the mature protein, and contains putative features for protein maturation: an 18-amino acid signal peptide, a KEX2 processing site, and four glycosylation motifs. The sequence just after the signal peptide corresponds to P2 and that after the KEX2 site to P1. The nagA transcript has a size of about 2.1 kb and is present until the end of the fermentation process for penicillin production. NagA is one of the most largely represented proteins in P. chrysogenum, increasing along the fermentation process. The suitability of the nagA promoter (PnagA) for gene expression in fungi was demonstrated by expressing the bleomycin resistance gene (ble(R)) from Streptoalloteichus hindustanus in P. chrysogenum.

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Year:  2005        PMID: 15621446     DOI: 10.1016/j.femsle.2004.11.017

Source DB:  PubMed          Journal:  FEMS Microbiol Lett        ISSN: 0378-1097            Impact factor:   2.742


  6 in total

Review 1.  Review of fungal chitinases.

Authors:  Li Duo-Chuan
Journal:  Mycopathologia       Date:  2006-06       Impact factor: 2.574

2.  The design of oligonucleotide primers for the universal amplification of the N-acetylglucosaminidase gene (nag1) in Chytridiomycetes with emphasis on the anaerobic Neocallimastigales.

Authors:  K Fliegerová; K Hoffmann; J Mrázek; K Voigt
Journal:  Folia Microbiol (Praha)       Date:  2008-07-27       Impact factor: 2.099

3.  The Penicillium chrysogenum extracellular proteome. Conversion from a food-rotting strain to a versatile cell factory for white biotechnology.

Authors:  Mohammad-Saeid Jami; Carlos García-Estrada; Carlos Barreiro; Abel-Alberto Cuadrado; Zahra Salehi-Najafabadi; Juan-Francisco Martín
Journal:  Mol Cell Proteomics       Date:  2010-09-07       Impact factor: 5.911

4.  β-N-Acetylglucosaminidase MthNAG from Myceliophthora thermophila C1, a thermostable enzyme for production of N-acetylglucosamine from chitin.

Authors:  Malgorzata Krolicka; Sandra W A Hinz; Martijn J Koetsier; Gerrit Eggink; Lambertus A M van den Broek; Carmen G Boeriu
Journal:  Appl Microbiol Biotechnol       Date:  2018-06-25       Impact factor: 4.813

5.  Biosynthesis of truncated N-linked oligosaccharides results from non-orthologous hexosaminidase-mediated mechanisms in nematodes, plants, and insects.

Authors:  Martin Gutternigg; Dorothea Kretschmer-Lubich; Katharina Paschinger; Dubravko Rendić; Josef Hader; Petra Geier; Ramona Ranftl; Verena Jantsch; Günter Lochnit; Iain B H Wilson
Journal:  J Biol Chem       Date:  2007-07-18       Impact factor: 5.157

6.  Enzymatic properties and subtle differences in the substrate specificity of phylogenetically distinct invertebrate N-glycan processing hexosaminidases.

Authors:  Martin Dragosits; Shi Yan; Ebrahim Razzazi-Fazeli; Iain B H Wilson; Dubravko Rendic
Journal:  Glycobiology       Date:  2014-12-08       Impact factor: 4.313

  6 in total

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