2020
DOI: 10.1002/jobm.202000067
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Supplementation of Aspergillus glaucus with gfdB gene encoding a glycerol 3‐phosphate dehydrogenase in Aspergillus nidulans

Abstract: In Aspergillus nidulans, there are two putative glycerol 3‐phosphate dehydrogenases encoded by the genes gfdA and gfdB, while the genome of the osmophilic Aspergillus glaucus harbors only the ortholog of the A. nidulans gfdA gene. Our aim was to insert the gfdB gene into the genome of A. glaucus, and we reached this goal with the adaptation of the Agrobacterium tumefaciens‐mediated transformation method. We tested the growth of the gfdB‐complemented A. glaucus strains on a medium containing 2 mol l‒1 sorbitol … Show more

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Cited by 4 publications
(15 citation statements)
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“…The copy number of the gfdB gene incorporated in the A. wentii genome was quantified as previously described {(Király et al 2020a , b ; Szabó et al 2020a , b ); using the equation of (Herrera et al 2009 )}. …”
Section: Methodsmentioning
confidence: 99%
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“…The copy number of the gfdB gene incorporated in the A. wentii genome was quantified as previously described {(Király et al 2020a , b ; Szabó et al 2020a , b ); using the equation of (Herrera et al 2009 )}. …”
Section: Methodsmentioning
confidence: 99%
“…The following stress-eliciting agents were employed at the concentrations indicated in parentheses: cell wall integrity stress: Congo Red (54, 81, and 108 μM); oxidative stress: tert -butyl hydroperoxide ( t BOOH; 0.4, 1.6, and 2.4 mM), hydrogen peroxide (9 and 18 mM), menadione sodium bisulphite (MSB; 0.096, 0.19, 0.38, 0.62 mM), diamide (1.5 mM); heavy metal stress: CdCl 2 (0.1, 0.15, 0.2, and 0.5 mM); hyperosmotic stress (when this tearm is applicable)): sorbitol (2 M), NaCl (0.5, 1, and 1.5 mM). Following stress treatments, the stress sensitivity of the strains was characterized by the diameters of the colonies (Balázs et al 2010 ; de Vries et al 2017 ; Orosz et al 2018 ; Király et al 2020a , b ).…”
Section: Methodsmentioning
confidence: 99%
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“…The amplicons were digested with restriction enzymes as indicated in Supplementary Table S2, and ligated between the niiA promoter and the trpC terminator in pHS11 (Leiter et al, 2016). Overexpression of the strains was confirmed by rRT-PCR method (Supplementary Figure S1; Király et al, 2020b).…”
Section: Construction Of Gene Deletion and Overexpression Strainsmentioning
confidence: 99%