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How to enter the state of dormancy? A suggestion by Trichoderma atroviride conidia. | LitMetric

How to enter the state of dormancy? A suggestion by Trichoderma atroviride conidia.

Fungal Biol

Institute of Biochemistry and Microbiology, Faculty of Chemical and Food Technology, Slovak University of Technology, Radlinského 9, 812 37, Bratislava, Slovakia.

Published: November 2021

AI Article Synopsis

  • Conidia, the dormant spores of filamentous fungi, have uncertain metabolic states, raising questions about whether they remain open or closed thermodynamic systems during dormancy.
  • Research on Trichoderma atroviride and Aspergillus niger indicates that conidia significantly inhibit calcium uptake and show a notable decline in the activity of key metabolic enzymes like α-ketoglutarate dehydrogenase after three weeks.
  • Despite these changes, conidia actively take up bicarbonate and convert it into stable compounds, suggesting metabolic activity during the first ten weeks of maturation, akin to chemoautotrophic microorganisms.

Article Abstract

It is generally accepted that conidia, propagules of filamentous fungi, exist in the state of dormancy. This state is defined mostly phenomenologically, e.g., by germination requirements. Its molecular characteristics are scarce and are concentrated on the water or osmolyte content, and/or respiration. However, a question of whether conidia are metabolic or ametabolic forms of life cannot be answered on the basis of available experimental data. In other words, are mature conidia open thermodynamic systems as are mycelia, or do they become closed upon the transition to the dormant state? In this article, we present observations which may help to define the transition of freshly formed conidia to the putative dormant forms using measurements of selected enzyme activities, H- and C-NMR and LC-MS-metabolomes, and C-bicarbonate or Ca inward transport. We have found that Trichoderma atroviride and Aspergillus niger conidia arrest the Ca uptake during the development stopping thereby the cyclic (i.e., bidirectional) Ca flow existing in vegetative mycelia and conidia of T. atroviride across the cytoplasmic membrane. Furthermore, we have found that the activity of α-ketoglutarate dehydrogenase was rendered completely inactive after 3 weeks from the conidia formation unlike of other central carbon metabolism enzymes. This may explain the loss of conidial respiration. Finally, we found that conidia take up the HCO and convert it into few stable compounds within 80 d of maturation, with minor quantitative differences in the extent of this process. The uptake of HCO confirmed these observation and demonstrated the incorporation of HCO even in the absence of exogenous substrates. These results suggest that T. atroviride conidia remain metabolically active during first ten weeks of maturation. Under these circumstances, their metabolism displays features similar to those of chemoautotrophic microorganisms. However, the Ca homeostasis changed from the open to the closed thermodynamic state during the early period of conidial maturation. These results may be helpful for studying the conidial ageing and/or maturation, and for defining the conidial dormant state in biochemical terms.

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Source
http://dx.doi.org/10.1016/j.funbio.2021.07.001DOI Listing

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