Evidence map›Paper›PMID 36166052›Full record

ArticleApplied microbiology and biotechnology2022

Identification of polyketide synthase genes required for aspinolide biosynthesis in Trichoderma arundinaceum.

Rosa E Cardoza, Susan P McCormick, Inmaculada Izquierdo-Bueno, Natalia Martínez-Reyes, Laura Lindo, Daren W Brown, Isidro G Collado, Robert H Proctor, Santiago Gutiérrez

Open access · hybridAbstract read
In one paragraph

Article in Applied microbiology and biotechnology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.1field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Journal of fungi (Basel, Switzerland) · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Effects of trichothecene production byFrontiers in plant science · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Rosa E CardozaUniversity Group for Research in Engineering and Sustainable Agriculture (GUIIAS), Area of Microbiology, University of León, 24400, Ponferrada, Spain.ORCID http://orcid.org/0000-0002-6589-0062
Susan P McCormickUSDA, Agricultural Research Service, National Center for Agricultural Utilization Research, Mycotoxin Prevention and Applied Microbiology Research Unit, 1815 N University St., Peoria, IL, 61604, USA.ORCID http://orcid.org/0000-0002-7824-6372
Inmaculada Izquierdo-Bueno *Departamento de Química Orgánica, Facultad de Ciencias, Universidad de Cádiz, Campus Universitario Río San Pedro s/n, Torre Sur, 4ª planta, 11510, Puerto Real, Cádiz, Spain.ORCID http://orcid.org/0000-0001-8861-408X
Natalia Martínez-ReyesUniversity Group for Research in Engineering and Sustainable Agriculture (GUIIAS), Area of Microbiology, University of León, 24400, Ponferrada, Spain.ORCID http://orcid.org/0000-0001-6560-417X
Laura LindoUniversity Group for Research in Engineering and Sustainable Agriculture (GUIIAS), Area of Microbiology, University of León, 24400, Ponferrada, Spain.ORCID http://orcid.org/0000-0003-1312-3360
Daren W BrownUSDA, Agricultural Research Service, National Center for Agricultural Utilization Research, Mycotoxin Prevention and Applied Microbiology Research Unit, 1815 N University St., Peoria, IL, 61604, USA.ORCID http://orcid.org/0000-0002-4754-8036
Isidro G ColladoDepartamento de Química Orgánica, Facultad de Ciencias, Universidad de Cádiz, Campus Universitario Río San Pedro s/n, Torre Sur, 4ª planta, 11510, Puerto Real, Cádiz, Spain.ORCID http://orcid.org/0000-0002-8612-0593
Robert H ProctorUSDA, Agricultural Research Service, National Center for Agricultural Utilization Research, Mycotoxin Prevention and Applied Microbiology Research Unit, 1815 N University St., Peoria, IL, 61604, USA. robert.proctor@ars.usda.gov.ORCID http://orcid.org/0000-0001-5400-1680
Santiago GutiérrezUniversity Group for Research in Engineering and Sustainable Agriculture (GUIIAS), Area of Microbiology, University of León, 24400, Ponferrada, Spain. s.gutierrez@unileon.es.ORCID http://orcid.org/0000-0001-6659-1390
Universidad de León · ESAgricultural Research Service · USUniversidad de Cádiz · ES

Funding

Agricultural Research ServiceMinisterio de Ciencia e Innovación PID2021-123874OB-I00Ministerio de Ciencia e Innovación RTI2018-099600-B-100
6 · The paper itself

Abstract

The fungus Trichoderma arundinaceum exhibits biological control activity against crop diseases caused by other fungi. Two mechanisms that likely contribute to this activity are upregulation of plant defenses and production of two types of antifungal secondary metabolites: the sesquiterpenoid harzianum A (HA) and the polyketide-derived aspinolides. The goal of the current study was to identify aspinolide biosynthetic genes as part of an effort to understand how these metabolites contribute to the biological control activity of T. arundinaceum. Comparative genomics identified two polyketide synthase genes (asp1 and asp2) that occur in T. arundinaceum and Aspergillus ochraceus, which also produces aspinolides. Gene deletion and biochemical analyses in T. arundinaceum indicated that both genes are required for aspinolide production: asp2 for formation of a 10-member lactone ring and asp1 for formation of a butenoyl subsituent at position 8 of the lactone ring. Gene expression and comparative genomics analyses indicated that asp1 and asp2 are located within a gene cluster that occurs in both T. arundinaceum and A. ochraceus. A survey of genome sequences representing 35 phylogenetically diverse Trichoderma species revealed that intact homologs of the cluster occurred in only two other species, which also produced aspinolides. An asp2 mutant inhibited fungal growth more than the wild type, but an asp1 mutant did not, and the greater inhibition by the asp2 mutant coincided with increased HA production. These findings indicate that asp1 and asp2 are aspinolide biosynthetic genes and that loss of either aspinolide or HA production in T. arundinaceum can be accompanied by increased production of the other metabolite(s). KEY POINTS: • Two polyketide synthase genes are required for aspinolide biosynthesis. • Blocking aspinolide production increases production of the terpenoid harzianum A. • Aspinolides and harzianum A act redundantly in antibiosis of T. arundinaceum.

Indexed as

PolyketidesSesquiterpenesTrichodermaAntifungal AgentsGene Expression Regulation, FungalHypocrealesLactonesPolyketide SynthasesTerpenesTrichothecenesAntifungal Agentsharzianum ALactonesPolyketidesPolyketide SynthasesSesquiterpenesTerpenesTrichothecenesAspinolidesComparative genomicsGene clustersMetabolomicsTrichodermaTrichothecenes

Identifiers

PMID36166052
PMCPMC9592644
OpenAlexW4297251486

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.