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Isolation and expression of two polyketide synthase genes from Trichoderma harzianum 88 during mycoparasitism.

Authors :
Yao L
Tan C
Song J
Yang Q
Yu L
Li X
Source :
Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] [Braz J Microbiol] 2016 Apr-Jun; Vol. 47 (2), pp. 468-79. Date of Electronic Publication: 2016 Mar 02.
Publication Year :
2016

Abstract

Metabolites of mycoparasitic fungal species such as Trichoderma harzianum 88 have important biological roles. In this study, two new ketoacyl synthase (KS) fragments were isolated from cultured Trichoderma harzianum 88 mycelia using degenerate primers and analysed using a phylogenetic tree. The gene fragments were determined to be present as single copies in Trichoderma harzianum 88 through southern blot analysis using digoxigenin-labelled KS gene fragments as probes. The complete sequence analysis in formation of pksT-1 (5669bp) and pksT-2 (7901bp) suggests that pksT-1 exhibited features of a non-reducing type I fungal PKS, whereas pksT-2 exhibited features of a highly reducing type I fungal PKS. Reverse transcription polymerase chain reaction indicated that the isolated genes are differentially regulated in Trichoderma harzianum 88 during challenge with three fungal plant pathogens, which suggests that they participate in the response of Trichoderma harzianum 88 to fungal plant pathogens. Furthermore, disruption of the pksT-2 encoding ketosynthase-acyltransferase domains through Agrobacterium-mediated gene transformation indicated that pksT-2 is a key factor for conidial pigmentation in Trichoderma harzianum 88.<br /> (Copyright © 2016 Sociedade Brasileira de Microbiologia. Published by Elsevier Editora Ltda. All rights reserved.)

Details

Language :
English
ISSN :
1678-4405
Volume :
47
Issue :
2
Database :
MEDLINE
Journal :
Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]
Publication Type :
Academic Journal
Accession number :
26991299
Full Text :
https://doi.org/10.1016/j.bjm.2016.01.004