Literature DB >> 11270576

Regulation of chitinase 33 (chit33) gene expression in Trichoderma harzianum.

M de las Mercedes Dana1, M C Limón, R Mejías, R L Mach, T Benítez, J A Pintor-Toro, C P Kubicek.   

Abstract

We investigated the regulation of chit33 expression in Trichoderma harzianum CECT 2413. This gene encodes the Chit33 endochitinase, which is a major component of the fungus' chitinolytic enzyme system and is important for biocontrol. To this end, both Northern analysis and reporter gene fusions of a 1.4-kb fragment of the 5'-upstream sequences of chit33 to the Aspergillus niger goxA gene (encoding glucose oxidase) and the Aquorea victoria green fluorescent protein were used. Northern analysis and data obtained with the reporter systems were compatible, thus showing that the 1.4-kb fragment bears all necessary information for the regulation of chit33 gene expression. chit33 is weakly expressed during growth on chitin and Rhizoctonia solani cell walls. The addition of N-acetylglucosamine transiently induced chit33 expression in resting cells of the fungus. The addition of either glucose or glycerol prevented induction of chit33 gene expression by chitin or cell walls. Incubation of T. harzianum in the presence of low concentrations (0.1%, w/v) of glucose and high concentrations (38 mM) of ammonium sulfate, or in the presence of high concentrations (1%, w/v) of glucose and low concentrations (0.38 mM) of ammonium sulfate also stimulated chit33-mRNA accumulation, although to a lower degree than induction by N-acetylglucosamine. Transfer of T. harzianum cultures to either 40 degrees C or 4 degrees C initiated a very rapid expression of chit33 in the absence of an inducer, yet only at very low levels (5%) of the induced control. Confrontation experiments, using the gfp gene as a reporter and R. solani as a host, showed that chit33 is expressed only during but not before the stage of overgrowth on R. solani. These data show that Chit33 is an enzyme involved in mycoparasitism; and its formation is controlled by induction, by either carbon or nitrogen starvation and, to a low degree, also under conditions of temperature stress.

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Year:  2001        PMID: 11270576     DOI: 10.1007/s002940000169

Source DB:  PubMed          Journal:  Curr Genet        ISSN: 0172-8083            Impact factor:   3.886


  21 in total

1.  The Nag1 N-acetylglucosaminidase of Trichoderma atroviride is essential for chitinase induction by chitin and of major relevance to biocontrol.

Authors:  Kurt Brunner; Clemens K Peterbauer; Robert L Mach; Matteo Lorito; Susanne Zeilinger; Christian P Kubicek
Journal:  Curr Genet       Date:  2003-05-14       Impact factor: 3.886

Review 2.  Fungal chitinases: function, regulation, and potential roles in plant/pathogen interactions.

Authors:  Thorsten Langner; Vera Göhre
Journal:  Curr Genet       Date:  2015-11-02       Impact factor: 3.886

Review 3.  Review of fungal chitinases.

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

4.  Transgenic tobacco plants overexpressing chitinases of fungal origin show enhanced resistance to biotic and abiotic stress agents.

Authors:  María de las Mercedes Dana; José A Pintor-Toro; Beatriz Cubero
Journal:  Plant Physiol       Date:  2006-08-04       Impact factor: 8.340

5.  Interaction of ammonium, glucose, and chitin regulates the expression of cell wall-degrading enzymes in Trichoderma atroviride strain P1.

Authors:  B G Donzelli; G E Harman
Journal:  Appl Environ Microbiol       Date:  2001-12       Impact factor: 4.792

Review 6.  The Genomes of Three Uneven Siblings: Footprints of the Lifestyles of Three Trichoderma Species.

Authors:  Monika Schmoll; Christoph Dattenböck; Nohemí Carreras-Villaseñor; Artemio Mendoza-Mendoza; Doris Tisch; Mario Ivan Alemán; Scott E Baker; Christopher Brown; Mayte Guadalupe Cervantes-Badillo; José Cetz-Chel; Gema Rosa Cristobal-Mondragon; Luis Delaye; Edgardo Ulises Esquivel-Naranjo; Alexa Frischmann; Jose de Jesus Gallardo-Negrete; Monica García-Esquivel; Elida Yazmin Gomez-Rodriguez; David R Greenwood; Miguel Hernández-Oñate; Joanna S Kruszewska; Robert Lawry; Hector M Mora-Montes; Tania Muñoz-Centeno; Maria Fernanda Nieto-Jacobo; Guillermo Nogueira Lopez; Vianey Olmedo-Monfil; Macario Osorio-Concepcion; Sebastian Piłsyk; Kyle R Pomraning; Aroa Rodriguez-Iglesias; Maria Teresa Rosales-Saavedra; J Alejandro Sánchez-Arreguín; Verena Seidl-Seiboth; Alison Stewart; Edith Elena Uresti-Rivera; Chih-Li Wang; Ting-Fang Wang; Susanne Zeilinger; Sergio Casas-Flores; Alfredo Herrera-Estrella
Journal:  Microbiol Mol Biol Rev       Date:  2016-02-10       Impact factor: 11.056

7.  Regulation of two homodimer hexosaminidases in the mycoparasitic fungus Trichoderma asperellum by glucosamine.

Authors:  Ofir Ramot; Ada Viterbo; Dana Friesem; Amos Oppenheim; Ilan Chet
Journal:  Curr Genet       Date:  2003-12-19       Impact factor: 3.886

8.  Saprotrophic and mycoparasitic components of aggressiveness of Trichoderma harzianum groups toward the commercial mushroom Agaricus bisporus.

Authors:  Josie Williams; John M Clarkson; Peter R Mills; Richard M Cooper
Journal:  Appl Environ Microbiol       Date:  2003-07       Impact factor: 4.792

9.  Comparative molecular evolution of trichoderma chitinases in response to mycoparasitic interactions.

Authors:  Katarina Ihrmark; Nashwan Asmail; Wimal Ubhayasekera; Petter Melin; Jan Stenlid; Magnus Karlsson
Journal:  Evol Bioinform Online       Date:  2010-03-15       Impact factor: 1.625

10.  Mycotoxigenic Fusarium and deoxynivalenol production repress chitinase gene expression in the biocontrol agent Trichoderma atroviride P1.

Authors:  Matthias P Lutz; Georg Feichtinger; Geneviève Défago; Brion Duffy
Journal:  Appl Environ Microbiol       Date:  2003-06       Impact factor: 4.792

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