2022
DOI: 10.1016/j.indcrop.2022.115488
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Growth and flavonol accumulation of Ginkgo biloba leaves affected by red and blue light

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Cited by 14 publications
(4 citation statements)
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“…The presence of five G-box elements in the FtUFGT163 promoter (Figure A) further supported the potential interaction with G subfamily FtbZIPs. Under various lighting conditions, particularly under blue light, bZIP transcription factors have been shown to effectively enhance the accumulation of flavonoid compounds, , aligning with the biological function of FtUFGT163 . Therefore, we performed a correlation analysis between the expression of FtbZIPs and the FtUFGT163 gene based on the blue light transcriptome (Figure S7 of the Supporting Information).…”
Section: Resultsmentioning
confidence: 99%
“…The presence of five G-box elements in the FtUFGT163 promoter (Figure A) further supported the potential interaction with G subfamily FtbZIPs. Under various lighting conditions, particularly under blue light, bZIP transcription factors have been shown to effectively enhance the accumulation of flavonoid compounds, , aligning with the biological function of FtUFGT163 . Therefore, we performed a correlation analysis between the expression of FtbZIPs and the FtUFGT163 gene based on the blue light transcriptome (Figure S7 of the Supporting Information).…”
Section: Resultsmentioning
confidence: 99%
“…For example, the use of LED lights to apply red, mixed (red:blue = 1:1), and blue light to treat annual ginkgo seedlings showed that mixed and blue light significantly increased the flavonoid content. In particular, blue light significantly increased the flavonoid yield (0.76-fold increase) and antioxidant capacity, which laid a foundation for the exploitation of light quality in the cultivation of ginkgo leaf utilization forests [73]. The expression of the PAL, CHS, F3H, and FLS genes related to ginkgo flavonoid biosynthesis decreases with an increasing degree of shading [74].…”
Section: Ecological Factors 621 Lightmentioning
confidence: 98%
“…The quercetin, kaempferol, and isorhamnetin contents were determined using high-performance liquid chromatography (HPLC) (Alliance e2695, Waters, Milford, MA, USA), following the method outlined by Zhang et al [27]. The contents of quercetin, kaempferol, and isorhamnetin were calculated based on the peak areas in the liquid chromatograms.…”
Section: Determination Of the Flavonol Contentmentioning
confidence: 99%