Sesquiterpenyl epoxy-cyclohexenoids (SECs) that depend on a polyketide synthase-terpenoid synthase (PKS-TPS) pathway are widely distributed in plant pathogenic fungi. However, the biosynthesis and function of the acetylated SECs still remained cryptic. Here, we identified that 00215 273 (273) was responsible for the acetylation of SECs in via the construction of Δ273, in which the acetylated SECs were absent and major antibacterial nonacetylated SECs accumulated. Mutant Δ273 displayed increased trap formation, and nematicidal and antibacterial activities but decreased fungal growth and soil colonization. Glutamine, a key precursor for NH as a trap inducer, was highly accumulated, and biologically active phenylpropanoids and antibiotics were highly enriched in Δ273. The decreased endocytosis and increased autophagosomes, with the most upregulated genes involved in maintaining DNA and transcriptional stability and pathways related to coronavirus disease and exosome, suggested that lack of 273 might result in increased virus infection and the acetylation of SECs played a key role in fungal diverse antagonistic ability.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.jafc.2c01914 | DOI Listing |
J Fungi (Basel)
November 2022
State Key Laboratory for Conservation and Utilization of Bio-Resources & Key Laboratory for Microbial Resources of the Ministry of Education, School of life Sciences, Yunnan University, Kunming 650091, China.
The predominant nematode-trapping fungus harbors a unique polyketide synthase-prenyltransferase (PKS-PTS) gene cluster responsible for the biosynthesis of sesquiterpenyl epoxy-cyclohexenoids (SECs) that are involved in the regulation of fungal growth, adhesive trap formation, antibacterial activity, and soil colonization. However, the function of one rare gene ( ()) embedded in the cluster has remained cryptic. Here, we constructed two mutants with the disruption of and the overexpression of , respectively, and compared their fungal growth, morphology, resistance to chemical stress, nematicidal activity, transcriptomic and metabolic profiles, and infrastructures, together with binding affinity analysis.
View Article and Find Full Text PDFJ Agric Food Chem
May 2022
State Key Laboratory for Conservation and Utilization of Bio-Resources & Key Laboratory for Microbial Resources of the Ministry of Education, School of Life Sciences, Yunnan University, Kunming 650091, People's Republic of China.
Sesquiterpenyl epoxy-cyclohexenoids (SECs) that depend on a polyketide synthase-terpenoid synthase (PKS-TPS) pathway are widely distributed in plant pathogenic fungi. However, the biosynthesis and function of the acetylated SECs still remained cryptic. Here, we identified that 00215 273 (273) was responsible for the acetylation of SECs in via the construction of Δ273, in which the acetylated SECs were absent and major antibacterial nonacetylated SECs accumulated.
View Article and Find Full Text PDFJ Agric Food Chem
April 2021
State Key Laboratory for Conservation and Utilization of Bio-Resources & Key Laboratory for Microbial Resources of the Ministry of Education, School of life Sciences, Yunnan University, Kunming, 650091, People's Republic of China.
Polyketide synthase-terpenoid synthase (PKS-TPS) hybrid pathways for biosynthesis of unique sesquiterpenyl epoxy-cyclohexenoids (SECs) have been found to be widely distributed in plant pathogenic fungi. However, the natural and ecological functions of these pathways and their metabolites still remain cryptic. In this study, the whole PKS-TPS hybrid pathway in the predominant nematode-trapping fungus was first proposed according to all the intermediates and their derivatives from all the mutants with a deficiency in each gene involved in SEC biosynthesis.
View Article and Find Full Text PDFJ Agric Food Chem
October 2020
State Key Laboratory for Conservation and Utilization of Bio-Resources & Key Laboratory for Microbial Resources of the Ministry of Education, School of Life Science, Yunnan University, Kunming 650091, People's Republic of China.
Here, we reported that detailed investigation on trace targeted metabolites from nematode-trapping fungus mutant with deletion of P450 gene led to isolation of 9 new polyketide-terpenoid hybrid derivatives, including four new glycosides of the key precursor farnesyl hydrotoluquinol () and, surprisingly, four new sesquiterpenyl epoxy-cyclohexenoids (SECs) analogues. Among them, two major target metabolites and displayed moderate nematode inhibitory ability. Moreover, the mutant lacking could form far more nematode-capturing traps within 6 h in contact with nematodes and show rapid potent nematicidal activity with killing 93.
View Article and Find Full Text PDFJ Agric Food Chem
July 2020
State Key Laboratory for Conservation and Utilization of Bio-Resources and Key Laboratory for Microbial Resources of the Ministry of Education, School of life Sciences, Yunnan University, Kunming 650091, People's Republic of China.
Nematode-trapping fungus can produce a type of sesquiterpenyl epoxy-cyclohexenoid (SEC) metabolites that are regarded as characteristic chemtaxonomic markers. Here, we reported investigation on the functions of a putatively cupin-like family gene and a dehydrogenase gene by gene engineering, chemical metabolite profiling and phenotype analysis. Ten targeted metabolites were isolated from two mutants Δ and Δ and four novel metabolites including three polyketide-terpenoid (PK-TP) hybrid ones were characterized.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!