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allium_tuberosum_rottler_ex_spreng [2016/11/01 00:29]
andreas 		allium_tuberosum_rottler_ex_spreng [2022/04/03 10:08] (aktuell)
andreas
Zeile 9: Zeile 9:
 "The flavor components of Nira (Allium tuberosum Rottl.) have been studied by a combination of gas chromatography and mass-spectrometry. Twenty-nine compounds were identified in the oil obtained from extraction of the steam distillate of Nira. The identified compounds include 7 sulfides, 2 ketones, 18 alcohols and 2 esters. The main volatile components were dimethyl disulfide and dimethyl trisulfide." \\ "The flavor components of Nira (Allium tuberosum Rottl.) have been studied by a combination of gas chromatography and mass-spectrometry. Twenty-nine compounds were identified in the oil obtained from extraction of the steam distillate of Nira. The identified compounds include 7 sulfides, 2 ketones, 18 alcohols and 2 esters. The main volatile components were dimethyl disulfide and dimethyl trisulfide." \\
 [Volatile flavor components of nira (Allium tuberosum Rottl.), Iida, Hiroshi, et al. Journal of Food Science Vol.48 (2), 1983, 660-661] [Volatile flavor components of nira (Allium tuberosum Rottl.), Iida, Hiroshi, et al. Journal of Food Science Vol.48 (2), 1983, 660-661]
 +
 +In the headspace of A. tuberosum, diallyl disulphide was detected as the main component (58%). \\
 +[Hori, Masatoshi. "Onion aphid (Neotoxoptera formosana) attractants, in the headspace of Allium fistulosum and A. tuberosum leaves." Journal of Applied Entomology 131.1 (2007): 8-12]
 +
 +The volatiles spectrum of Chinese chive was basically consistent with the volatiles surface enhanced Raman scattering spectrum of the mixture of liquid allyl methyl sulfide and diallyl disulfide. \\
 +[Zhang, Chuan-yun, et al. "Research on volatiles of rakkyo (Allium Chinense G. Don) and Chinese chive (Allium Tuberosum rottl. ex sprengel) based on headspace and the molecular recognition of SERS." Spectroscopy and Spectral Analysis 35.2 (2015): 394-398]
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 +{{:allicin.jpg|}} allicin
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 +Mean concentrations of individual thiosulphinates found in different A.tuberosum cultivars were (dry weight basis): [[https://en.wikipedia.org/wiki/Allicin|Allicin]] 183-330 ppm, allyl methyl thiosulphinate 2190-3550 ppm, and allyl trans-1-propenyl thiosulphinate 30-75ppm. \\
 +[Singh, Pritee, et al. "Comparative evaluation of different Allium accessions for allicin and other allyl thiosulphinates." Industrial Crops and Products 147 (2020): 112215]
  
 {{allium_tuberosum.jpg?600}} \\ {{allium_tuberosum.jpg?600}} \\
 Allium tuberosum leaves and inflorescences, Botanical Garden Berlin 2006; Author: BotBln \\ [[https://commons.wikimedia.org/wiki/File:Allium_tuberosum_HabitusInflorescences_BotGardBln0906.JPG]] \\ Allium tuberosum leaves and inflorescences, Botanical Garden Berlin 2006; Author: BotBln \\ [[https://commons.wikimedia.org/wiki/File:Allium_tuberosum_HabitusInflorescences_BotGardBln0906.JPG]] \\
 [[https://creativecommons.org/licenses/by-sa/3.0/de/|CC BY-SA 3.0]] [[https://creativecommons.org/licenses/by-sa/3.0/de/|CC BY-SA 3.0]]
allium_tuberosum_rottler_ex_spreng.1477956587.txt.gz · Zuletzt geändert: 2016/11/01 00:29 von andreas

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