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Radishes

This enzyme Is widely distributed, more particularly in plants. Three important sources of the enzyme are horse-radish, turnips and milk. Peroxidase is capable of activating both hydrogen peroxide and a suitable substrate so that the latter is oxidised, although hydrogen peroxide alone may be incapable of affecting this change. It sometimes happens that hydrogen pcr-... [Pg.521]

Foam separation Foam stability FoamulaR Focused ion beams Fodder radish Fog... [Pg.417]

B. Dunlap, In FuHerenes Recent Advances in the Chemistry and Physics of FuHerenes and Related Materials, (Edited by K. Radish and R. S. Ruoff), p. 226. The Electrochemical Society, Pennington, NJ (1994). [Pg.148]

Horse radish peroxidase, H2O2 or Laccase, pH 4, 2% DMSO or DMF. Cleavage occurs by the formation of a phenyldiimide, which decomposes to the acid, nitrogen, and benzene. The laccase method is compatible with the readily oxidized tryptophan and methionine because it does not use peroxide. ... [Pg.450]

Sulfur compounds first detected in plants hy N. Deyeux (root.s of the dock, horse-radish, and cochlearia). [Pg.646]

The [resb roots of this plant yiirbl from Cl to 04 per ceac. of aa uii-pleasaDtly-smellicig oil reealliug ibe odonr of radishes. This oil contains phenyl-etbyl-thiocarbimide, 0.,H,(QH iNSC, and is a liquid of specific gravity lOI to 109 and optical roiaiion about + T to + 2°. [Pg.528]

Fig. 6.2.3 Luminescence spectra of pholasin in the presence of horse radish peroxidase (solid line from Henry et al, 1973 with permission from Elsevier), and in the presence of FeSC>4 in 10 mM phosphate buffer, pH 7.0, containing 0.1 M NaCl (dashed line Shimomura, 1980, unpublished). Fig. 6.2.3 Luminescence spectra of pholasin in the presence of horse radish peroxidase (solid line from Henry et al, 1973 with permission from Elsevier), and in the presence of FeSC>4 in 10 mM phosphate buffer, pH 7.0, containing 0.1 M NaCl (dashed line Shimomura, 1980, unpublished).
Cabbage Cavli- Brussels Broc- Kohlrabi Cress Radish flower Sprouts coli... [Pg.41]

The wide distribution of this insecticide in other cruciferous crops was investigated later, and the stability and occurrence of this compound were studied. Two cabbage varieties, cauliflower, brussels sprouts, broccoli, kale, mustard, and kohlrabi contained 2-phenylethyl isothiocyanate in various amounts as evidenced by gas-liquid chromatography and bioassay (houseflies and vinegar flies) (Table VII). Insecticidal activities were encountered only with root tissues. Compounds of insecticidal activity, not attributable to 2-phenylethyl isothiocyanate, were found in the edible parts of radish and leaves of turnip, rutabaga, and garden cress. [Pg.42]

Vegetables Carrots Lima beans Fbtatoes Radishes oinach Sweet potatoes Tomatoes... [Pg.453]

Radish KM, Smith KM, Guilard R (2000) (eds) In The Porphyrin Handbook, vol. 4 Academic Press, London... [Pg.113]

Pepper (red), pea, carrot, radish, potato, cucumber Moderately tolerant (2.0. 0 ppm)... [Pg.166]

Rodriguez-Saona, L.E. et al., Color and pigment stability of red radish and red-fleshed potato anthocyanins in juice model systems, J. Food Set, 64, 451, 1999. [Pg.83]

Most of the anthocyanins acylated with caffeic acid have this cinnamyl moiety linked to a glucosyl position 6, as in gooseberries, some grape cultivars, ° " ° black carrots, red cabbage,red radishes," and sweet potatoes. Some anthocyanins isolated from species of potatoes have a caffeyl group located at position 4 of the rhamnosyl unit of the rutinose disaccharide. " ... [Pg.259]

FIGURE 6.3.3 Fragment patterns of anthocyanins A, dephinidin 3-xyl-glc from Roselle (Hibiscus sabdariffa L.) B, pelargonidin-3-(feruloyl-sophoroside)-5-(malonyl-glucose) from radish (Raphanus sativus). (Source Giusti, M.M. et ah, J. Agric. Food Chem., 47,4657, 1999.)... [Pg.495]

Many recent stndies of NMR spectroscopy have been reported for structure elucidation of anthocyanins from many plant materials such as carrot, tart berries, boysenberries, " flowers, black soybeans, and anthocyanin and flavonol derivatives in red wine. Ginsti et al. (1998) structurally elucidated two novel diacylated anthocyanins and two monoacylated anthocyanins from radish Raphanus sativus) by one- and two-dimensional NMR. Anderson et al. (2006) applied two-dimensional NMR to characterize carboxypyranoanthocyanins. Two 3-deoxyantho-cyanins, lnteolinidin-5-glncoside, and apigeninidin-5-glucoside were identified by Swinny et al. nsing H and C NMR. [Pg.496]

Giusti, M.M., Ghanadan, H., and Wrolstad, R.E., Elucidation of the structure and conformation of red radish Raphanus sativus) anthocyanins using one- and two-dimensional nuclear magnetic resonance techniques, J. Agric. Food Chem., 46, 4858, 1998. [Pg.505]


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Experiments on Efficiency in the Forced Oscillatory Horse-Radish Peroxidase Reaction

Horse radish

Horse radish peroxidase

Horse radish peroxidase hydrogen peroxide

Horse radish peroxidase inhibition

Horse radish peroxidase properties

Horse radish peroxidase reaction

Japanese radish seed germination

Japanese radishes

Mevinolin radish seedlings

Peroxidase Japanese radish

Radish leaves

Radish oil

Radish seedlings

Radish seeds

Radish, Raphanus

Radish, vegetable

Radish, wild

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