2019
DOI: 10.1007/s11356-019-05676-z
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Differential growth, nutrition, physiology, and gene expression in Melissa officinalis mediated by zinc oxide and elemental selenium nanoparticles

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Cited by 92 publications
(53 citation statements)
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“…The incorporation of nSe as a supplement in the culture medium influenced morphology, growth, anatomy, and development in a manner dependent on the applied dose and the Se form. Responses to the nSe exposure were partly distinct from that of BSe, in line with the findings of Babajani et al, [6] in Melissa officinalis and Sotoodehnia-Korani et al, in Capsicum annuum [7]. The nano-type Se (nSe) exhibited a higher efficiency to stimulate plant growth and organogenesis than the bulk form.…”
Section: Discussionsupporting
confidence: 86%
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“…The incorporation of nSe as a supplement in the culture medium influenced morphology, growth, anatomy, and development in a manner dependent on the applied dose and the Se form. Responses to the nSe exposure were partly distinct from that of BSe, in line with the findings of Babajani et al, [6] in Melissa officinalis and Sotoodehnia-Korani et al, in Capsicum annuum [7]. The nano-type Se (nSe) exhibited a higher efficiency to stimulate plant growth and organogenesis than the bulk form.…”
Section: Discussionsupporting
confidence: 86%
“…On the other hand, several lines of evidence highlighted risks associated with high concentrations of Se [6,7,11,12]. Moreover, recent reports point out the plant cell may differentially respond to the nano-based materials relative to the bulk counterparts [6,7,13]. The elemental red Se nano-substance (nSe) exhibits efficient antimicrobial properties, great bioactivity, considerable antioxidant capacity, and anti-proliferative effects [14].…”
Section: Introductionmentioning
confidence: 99%
“…To prepare enzyme extracts, the well‐powdered leaves in liquid nitrogen were homogenized using a phosphate buffer (0.1 M, pH 7.3) supplemented by ascorbate and Na 2 EDTA . Peroxidase activity was spectrophotometrically measured based on absorbance variations at 470 nm per min in the enzyme reaction mixture . In addition, the activity of catalase enzyme was determined according to the protocol of Dhindsa et al…”
Section: Methodsmentioning
confidence: 99%
“…DAT transcriptions in the plasma‐treated seedlings were quantified using the real‐time quantitative reverse transcription polymerase chain reaction (RT‐PCR) method and a related kit (qPCR BIOSyGreen Mix Lo‐ROX). According to the ΔΔCT method, the expression rate of the DAT gene was calculated and expressed as a fold difference …”
Section: Methodsmentioning
confidence: 99%
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