scholarly journals The role of PKAc1 in gene regulation and trichodimerol production in Trichoderma reesei

2019 ◽  
Vol 6 (1) ◽  
Author(s):  
Wolfgang Hinterdobler ◽  
André Schuster ◽  
Doris Tisch ◽  
Ezgi Özkan ◽  
Hoda Bazafkan ◽  
...  

Abstract Background Trichoderma reesei represents a model system for investigation of plant cell wall degradation and its connection to light response. The cyclic adenosine monophosphate pathway (cAMP pathway) plays an important role in both physiological outputs, being crucial for regulation of photoreceptor function as well as for cellulase regulation on different carbon sources. Phosphorylation of photoreceptors and of the carbon catabolite repressor CRE1 was shown in ascomycetes, indicating a relevance of protein kinase A in regulation of the target genes of these transcription factors as well as an impact on regulation of induction specific genes. Moreover, the cAMP pathway impacts growth and development. Results Here, we investigated gene regulation by the catalytic subunit of protein kinase A (PKAc1) upon growth on cellulose. We found distinct gene sets for regulation upon growth in light and darkness with an overlap of only 13 genes. PKAc1 regulates metabolic genes as well as transport and defense functions. The overlap of gene regulation by PKAc1 with the genes representing the cAMP dependent regulatory output of the photoreceptor ENV1 indicates an involvement of PKA in this pathway, which counteracts its effects by contrasting regulation. Moreover, we found considerable overlap with the gene sets regulated under cellulase inducing conditions and by the carbon catabolite repressor CRE1. Our analysis also showed that PKAc1 regulates the genes of the SOR cluster associated with the biosynthesis of sorbicillinoids. The homologue of gin4, encoding a CAMK type kinase, which is regulated by PKAc1, CRE1 and YPR2 showed a moderate impact on trichodimerol production. We isolated trichodimerol as representative sorbicillin compound and established a method for its quantification in large sample sets using high performance thin layer chromatography (HPTLC), which can be broadly applied for secondary metabolite screening of mutants or different growth conditions. Due to the high expression levels of the SOR cluster under conditions of sexual development we crosschecked the relevance of PKAc1 under these conditions. We could show that PKAc1 impacts biosynthesis of trichodimerol in axenic growth and upon mating. Conclusions We conclude that PKAc1 is involved in light dependent regulation of plant cell wall degradation, including carbon catabolite repression as well as secondary metabolism and development in T. reesei.

2014 ◽  
Vol 111 (17) ◽  
pp. 6287-6292 ◽  
Author(s):  
J. W. Agger ◽  
T. Isaksen ◽  
A. Varnai ◽  
S. Vidal-Melgosa ◽  
W. G. T. Willats ◽  
...  

2010 ◽  
Vol 76 (13) ◽  
pp. 4546-4549 ◽  
Author(s):  
Jean-Charles Blouzard ◽  
Odile Valette ◽  
Chantal Tardif ◽  
Pascale de Philip

ABSTRACT Further understanding of the plant cell wall degradation system of Clostridium cellulolyticum and the possibility of metabolic engineering in this species highlight the need for a means of random mutagenesis. Here, we report the construction of a Tn1545-derived delivery tool which allows monocopy random insertion within the genome.


1990 ◽  
Vol 33 (3) ◽  
pp. 345-351 ◽  
Author(s):  
William S. Borneman ◽  
Roy D. Hartley ◽  
W. Herbert Morrison ◽  
Danny E. Akin ◽  
Lars G. Ljungdahl

2009 ◽  
Vol 20 (3) ◽  
pp. 330-338 ◽  
Author(s):  
Hui Wei ◽  
Qi Xu ◽  
Larry E Taylor ◽  
John O Baker ◽  
Melvin P Tucker ◽  
...  

2007 ◽  
Vol 20 (4) ◽  
pp. 411-419 ◽  
Author(s):  
M. Caroline Roper ◽  
L. Carl Greve ◽  
Jeremy G. Warren ◽  
John M. Labavitch ◽  
Bruce C. Kirkpatrick

Xylella fastidiosa is the causal agent of Pierce's disease of grape, an economically significant disease for the grape industry. X. fastidiosa systemically colonizes the xylem elements of grapevines and is able to breach the pit pore membranes separating xylem vessels by unknown mechanisms. We hypothesized that X. fastidiosa utilizes cell wall degrading enzymes to break down pit membranes, based on the presence of genes involved in plant cell wall degradation in the X. fastidiosa genome. These genes include several β-1,4 endoglucanases, several xylanases, several xylosidases, and one polygalacturonase (PG). In this study, we demonstrated that the pglA gene encodes a functional PG. A mutant in pglA lost pathogenicity and was compromised in its ability to systemically colonize Vitis vinifera grapevines. The results indicate that PG is required for X. fastidiosa to successfully infect grapevines and is a critical virulence factor for X. fastidiosa pathogenesis in grapevine.


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