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1 heterologous transgenes from Arabidopsis and Nasturtium and examined lipid profiles and changes in ge
2                                     Rose and nasturtium are common ornamental edible flowers rich in
3  monosaccharide components when treated with nasturtium beta-D-galactosidase, followed by alternation
4                                          The nasturtium beta-glucosidase is ascribed a role in xylogl
5  with the highest sequence similarity to the nasturtium CSL gene, is coordinately expressed with othe
6 on ranging from 52.25 to 54.72%was found for nasturtium extracts, correlated to the behavior of some
7 gastrointestinal digestion (SGD) on rose and nasturtium flower extracts.
8  and myricitrin and dicaffeoylquinic acid in nasturtium flowers.
9  characterize underwater growth in the dicot Nasturtium officinale (watercress), a wild species of th
10 total folates or vitamin B(9) in watercress (Nasturtium officinale R.
11  quality parameters of fresh-cut watercress (Nasturtium officinale R.
12 radish (Armoracia rusticana) and watercress (Nasturtium officinale) are economically important crucif
13 transient expression in mature Eruca sativa, Nasturtium officinale, Nicotiana tabacum and Spinacia ol
14  properties in a microshoot culture model of Nasturtium officinale.
15                    During the last stages of nasturtium seed maturation, a large amount of XyG is dep
16 different sidechains of pea cell wall XG and nasturtium seed storage XG affect their binding to cellu
17 he enhanced ability of pea cell wall XG over nasturtium seed storage XG to associate with cellulose i
18 nalyses of SlXTH2, a Group 2 tomato XTH, and nasturtium seed TmXTH1 revealed a spectrum of modes of a
19  xyloglucan endo transglycosylase (tXET) and nasturtium seed xyloglucanase (nXGase) were produced het
20                                              Nasturtium shows the greatest radical scavenging activit
21 ween this and another now-extinct tetraploid Nasturtium species.
22 nly one member of Group 3 has been reported: nasturtium TmXH1, which has a highly specialized functio
23 omogeneity from the cotyledons of germinated nasturtium (Tropaeolum majus L.) seedlings during the mo
24 .), hibiscus (Hibiscus rosa-sinensis L.) and nasturtium (Tropaeolum majus L.), are common edible flow
25 sglycosylase (XET) homolog was isolated from nasturtium (Tropaeolum majus) epicotyl RNA.
26  backbone of XyG, we exploited a property of nasturtium (Tropaeolum majus) seed development.
27 DNA sequences were generated from developing nasturtium (Tropaeolum majus) seeds, which produce large
28 zyme had similar catalytic properties to the nasturtium (Tropaeolum majus) xyloglucanase1 responsible
29 ntially divergent from a previously isolated nasturtium XET (NXG1) expressed in germinating seed coty
30 r oligosaccharides representative of pea and nasturtium XG can adopt a hypothesized cellulose-binding
31   In contrast, the relatively low ability of nasturtium XG to bind cellulose is consistent with the n
32 s indeed occur at a twofold higher rate than nasturtium XG-avicel binding.
33 isaccharide sidechain, which is not found in nasturtium XG.
34 e of the cellulose binding conformation than nasturtium XG.
35 ould bind to cellulose at a higher rate than nasturtium XG.
36 D-galactosidase, followed by alternations of nasturtium xyloglucan-specific alpha-xylosidase and this