2012
DOI: 10.2503/jjshs1.81.337
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Methyl Jasmonate Treatment Enhanced Protodioscin Biosynthesis in White Asparagus (Asparagus officinalis L.) Spears

Abstract: The objective of this study was to clarify the factors that influence saponin biosynthesis, with an emphasis on protodioscin, a major saponin compound in white asparagus spears. We investigated the effects of methyl jasmonate (MeJM) treatment on protodioscin content in white spears harvested by spring semi-forced and winterforced cultivation. Protodioscin content was determined using high performance liquid chromatography equipped with an evaporative light scattering detector. Protodioscin was mainly localized… Show more

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Cited by 8 publications
(9 citation statements)
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References 30 publications
(54 reference statements)
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“…The samples of 18 different plant parts were pulverized for analysis. Rutin and protodioscin were extracted from 50 mg of freeze-dried powder with 1 mL of 70% ethanol according to the modification method of Maeda et al (2010Maeda et al ( , 2012 and Nikaido et al (2014). A highperformance liquid chromatography system (HPLC; Laboratory Solutions system; Shimadzu, Kyoto, Japan) equipped with an evaporative light scattering detector (ELSD-LTII detector; Shimadzu) and a photodiode array detector (SPD-M20A; Shimadzu) were used for quantification.…”
Section: Methodsmentioning
confidence: 99%
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“…The samples of 18 different plant parts were pulverized for analysis. Rutin and protodioscin were extracted from 50 mg of freeze-dried powder with 1 mL of 70% ethanol according to the modification method of Maeda et al (2010Maeda et al ( , 2012 and Nikaido et al (2014). A highperformance liquid chromatography system (HPLC; Laboratory Solutions system; Shimadzu, Kyoto, Japan) equipped with an evaporative light scattering detector (ELSD-LTII detector; Shimadzu) and a photodiode array detector (SPD-M20A; Shimadzu) were used for quantification.…”
Section: Methodsmentioning
confidence: 99%
“…A highperformance liquid chromatography system (HPLC; Laboratory Solutions system; Shimadzu, Kyoto, Japan) equipped with an evaporative light scattering detector (ELSD-LTII detector; Shimadzu) and a photodiode array detector (SPD-M20A; Shimadzu) were used for quantification. HPLC conditions were as follows: 1.0 mL · min -1 flow rate, 40°C column temperature, a Waters Symmetry C18 column (4.6 · 250 mm; Nihon Waters K. K., Tokyo, Japan) with a security guard cartridge (3.0 · 4.6 mm), 0.1% trifluoroacetic acid: acetonitrile-water (by volume) mobile phase with a gradient condition, 354-nm wavelength of a photodiode array detector (Maeda et al, 2010(Maeda et al, , 2012Nikaido et al, 2014). A calibration curve was prepared using external standard rutin solution (Wako Pure Chemical Industries, Osaka, Japan) and protodioscin solution (Chroma-Dex Inc., Los Angeles, CA), and the rutin and protodioscin content were calculated from the peak area, respectively.…”
Section: Methodsmentioning
confidence: 99%
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