Array comparative genomic hybridization analysis of Trichoderma reesei strains with enhanced cellulase production propertiesReport as inadecuate




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BMC Genomics

, 11:441

First Online: 19 July 2010Received: 15 February 2010Accepted: 19 July 2010

Abstract

BackgroundTrichoderma reesei is the main industrial producer of cellulases and hemicellulases that are used to depolymerize biomass in a variety of biotechnical applications. Many of the production strains currently in use have been generated by classical mutagenesis. In this study we characterized genomic alterations in high-producing mutants of T. reesei by high-resolution array comparative genomic hybridization aCGH. Our aim was to obtain genome-wide information which could be utilized for better understanding of the mechanisms underlying efficient cellulase production, and would enable targeted genetic engineering for improved production of proteins in general.

ResultsWe carried out an aCGH analysis of four high-producing strains QM9123, QM9414, NG14 and Rut-C30 using the natural isolate QM6a as a reference. In QM9123 and QM9414 we detected a total of 44 previously undocumented mutation sites including deletions, chromosomal translocation breakpoints and single nucleotide mutations. In NG14 and Rut-C30 we detected 126 mutations of which 17 were new mutations not documented previously. Among these new mutations are the first chromosomal translocation breakpoints identified in NG14 and Rut-C30. We studied the effects of two deletions identified in Rut-C30 a deletion of 85 kb in the scaffold 15 and a deletion in a gene encoding a transcription factor on cellulase production by constructing knock-out strains in the QM6a background. Neither the 85 kb deletion nor the deletion of the transcription factor affected cellulase production.

ConclusionsaCGH analysis identified dozens of mutations in each strain analyzed. The resolution was at the level of single nucleotide mutation. High-density aCGH is a powerful tool for genome-wide analysis of organisms with small genomes e.g. fungi, especially in studies where a large set of interesting strains is analyzed.

Electronic supplementary materialThe online version of this article doi:10.1186-1471-2164-11-441 contains supplementary material, which is available to authorized users.

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Author: Marika Vitikainen - Mikko Arvas - Tiina Pakula - Merja Oja - Merja Penttilä - Markku Saloheimo

Source: https://link.springer.com/article/10.1186/1471-2164-11-441







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