ライフサイエンスコーパス: beet

1 ch as squash, papaya, plum, grape, and sugar beet.

2 ically important soil-borne disease of sugar beet.

3 traction efficiency from by-product of sugar beet.

4 metabolism such as grain, potato, and sugar beet.

5 to the long-term sustainability of GR sugar beet.

6 traction efficiency from by-product of sugar beet.

7 ure of B. scoparia to glyphosate in GR sugar beet.

8 cospora species causing CLS in Iranian sugar beet.

9 ioxidant capacity of minimally processed red beet.

10 schachtii causes major yield losses in sugar beet.

11 bstituents were detected in the roots of red beet.

12 orphisms linked to bolting tendency in sugar beet.

13 rops such as potato, oilseed rape, and sugar beet.

14 the regulation of bolting tendency in sugar beet.

15 ed to produce the red betacyanin pigments in beets.

16 (BvMYB1), regulates the betalain pathway in beets.

17 atterning locus, Y, required for red-fleshed beets.

18 increase at 10-days of storage for both red beet (+1.3-fold) and amaranth (+1.1-fold).

19 raw materials was recorded in roasted sugar beet (2.26 mug/g), while roasting the chicory caused a 2

20 f barley, a hemibiotrophic pathogen of sugar beet and a saprotroph, to evaluate the role of SnTox1 in

21 phylogenetic analysis with B-box genes from beet and A. thaliana but only BvCOL1 clustered with CO.

22 e other hand, in vitro digestion of both red beet and amaranth microgreens produced a significant inc

23 the plants, such as high arabinan levels in beet and high galactan levels in carrot, appear to be ma

24 large naturally occurring populations of sea beet and subsequently in sugar beet breeding genotypes u

25 er, the same protein was identified in sugar beet and transgenic tobacco (Nicotaina tobacum L.) membr

26 been detected previously in the root of red beets and 27 saponins were tentatively identified as pot

27 beets are readily crossable with cultivated beets and are thus available for crop improvement.

28 ht into the phylogeny of wild and cultivated beets and establishes a framework for classification of

29 centromere loading of CENH3 in barley, sugar beet, and Arabidopsis thaliana.

30 r relationships in grain-potato, grain-sugar beet, and beet-potato mixtures enabled composition deter

31 er time, mothers liked the tastes of carrot, beet, and celery juices more, but no changes in dietary

32 duct, beta1,2-arabinobiose (Ara2) from sugar beet arabinan (SBA), and beta1,2-Ara2 and alpha-1,2-gala

33 antibodies binds strongly to isolated sugar beet arabinan samples in ELISAs.

34 s, versus unfractionated pea fiber and sugar beet arabinan, on a human gut bacterial strain consortiu

35 Species and subspecies of wild beets are readily crossable with cultivated beets and ar

36 instead of the blade, and not in response to beet army worm feeding.

37 plants infested with two agricultural pests, beet army worm or two-spotted spider mites; pesticidal e

38 sured in response to larval herbivory by the beet army worm, Spodoptera exigua.

39 seedling blades in response to herbivory by beet army worm.

40 r terpene emission and the reduced growth of beet armyworm (Spodoptera exigua) herbivores, respective

41 lon), fall armyworm (Spodoptera frugiperda), beet armyworm (Spodoptera exigua), tobacco budworm (Heli

42 ersicum) defenses against the chewing insect beet armyworm (Spodoptera exigua; BAW).

43 ent in the regurgitant of Spodoptera exigua (beet armyworm caterpillars) activates the emission of vo

44 glutamine, named volicitin and isolated from beet armyworm caterpillars, is a key component in plant

45 For example, maize seedlings attacked by beet armyworm larvae (Spodoptera exigua) produce a mixtu

46 is induced 15- to 30-fold in maize leaves by beet armyworm larvae feeding or by application of purifi

47 cotton plants subjected to feeding damage by beet armyworm larvae in situ.

48 Caterpillar larvae of the beet armyworm Spodoptera exigua Hubner show a clear feed

49 ns, cotton bollworm Helicoverpa zea, and the beet armyworm Spodoptera exigua, 100% mortality was obse

50 Spodoptera exigua (beet armyworm) larvae show improved growth on igps1 muta

51 cult to control (10-day old cotton bollworm, beet armyworm) were killed 100% after consuming transgen

52 Beet armyworm, Spodoptera exigua, is a major pest of cot

53 insect defense, opr7 opr8 is susceptible to beet armyworm.

54 Chemical analysis of the oral secretion from beet armyworms that have fed on 13C-labeled corn seedlin

55 tobacco and edible plants (spinach and leafy beets) at costs that will allow commercialization.

56 the hAT transposon superfamily of the sugar beet (B. vulgaris) genome, using molecular, bioinformati

57 6 beet genomes, encompassing sugar beet, sea beet, B. v.

58 The wild ancestor of beet crops is the sea beet Beta vulgaris ssp.

59 Plasma membrane vesicles from red beet (Beta vulgaris L.) storage tissue contain two promi

60 ation of one of these porters found in sugar beet (Beta vulgaris L.).

61 a causes Cercospora Leaf Spot (CLS) of sugar beet (Beta vulgaris L.).

62 obe was used to isolate CMO cDNAs from sugar beet (Beta vulgaris L., Chenopodiaceae), a salt- and dro

63 igestion on the phytochemical profile of red beet (Beta vulgaris) and amaranth (Amaranthus sp.) micro

64 nalysis of the betalain-producing plants red beet (Beta vulgaris) and four o'clocks (Mirabilis jalapa

65 y in releasing the acetate moiety from sugar beet (Beta vulgaris) and potato (Solanum tuberosum) pect

66 syrups produced from C3 plants such as sugar beet (Beta vulgaris) and wheat (Triticium vulgare).

67 Sugar beet (Beta vulgaris) is a biennial root crop that grows

68 During vegetative growth, biennial sugar beet (Beta vulgaris) maintains a steep Suc concentration

69 ), Miscanthus x giganteus, and notably sugar beet (Beta vulgaris) roots where phloem identification i

70 This study develops the beet (Beta vulgaris) rust (Uromyces beticola) system to

71 vacuolar membrane vesicles purified from red beet (Beta vulgaris) storage root approximates Michaelis

72 cuoles of pea (Pisum sativum) leaves and red beet (Beta vulgaris) storage root are major sites for th

73 characterized a novel Vma6p homolog from red beet (Beta vulgaris) tonoplast membranes.

74 minating CLS-symptomatic and symptomless sea beets (Beta vulgaris L.ssp.

75 Cultivated beets (Beta vulgaris ssp.

76 r plant species (Arabidopsis thaliana, sugar beet [Beta vulgaris], tobacco [Nicotiana tabacum], and m

77 Red beet betalains, grape anthocyanins, and their mixtures w

78 port here the biogenesis and topology of the Beet black scorch virus (BBSV) replication complex.

79 e, we used a positive-strand RNA necrovirus, beet black scorch virus (BBSV), as a model to investigat

80 Beet black scorch virus, a necrovirus in the family Tomb

81 ables (broccoli, collard greens, carrots and beets), both raw and cooked.

82 eders, this is an untapped resource in sugar beet breeding efforts.

83 ations of sea beet and subsequently in sugar beet breeding genotypes under either CLS symptomless or

84 bolters and non-bolters, to be used in sugar beet breeding programs for the development of improved g

85 These findings suggest that the sugar beet BvSTI gene may prove useful for effective control o

86 encapsulated polyphenols from a concentrated beet by-product extract (CEB) with linseed oil using W(1

87 Lactating mothers drank vegetable, beet, celery, and carrot juices for 1 mo beginning at 0.

88 The deduced beet CMO amino acid sequence comprised a transit peptide

89 proach to extracting and stabilizing the red beet compounds for application in food, nutraceutical, a

90 e extraction efficiency and stability of red beet compounds has gained the attention of researchers d

91 Organic beets contain lower NO3(-) compared with its conventiona

92 Tubers of carrots and beets contain the highest levels of Put.

93 nt cause of postharvest losses for the sugar beet crop, however, intrinsic physiological and genetic

94 The wild ancestor of beet crops is the sea beet Beta vulgaris ssp.

95 S) is a major disease impacting global sugar beet cultivation and yield.

96 infectious clones corresponding to CaLCuV or Beet curly top virus (BCTV), which are classified in dif

97 non-viruliferous and viruliferous [carrying beet curly top virus (BCTV)] beet leafhoppers [Circulife

98 nd to determine if the related L2 protein of Beet curly top virus (BCTV, genus Curtovirus) also has s

99 The related L2 protein of Beet curly top virus (genus Curtovirus) lacks transcript

100 The related L2 protein of Beet curly top virus (genus Curtovirus) shares the patho

101 Finally, we demonstrate that Beet curly top virus L2- mutant DNA present in tissues t

102 onas syringae pv tomato DC3000 bacterium and Beet curly top virus.

103 alysis of cytokinin genes in response to the beet cyst nematode (BCN), Heterodera schachtii, and the

104 Here, we describe its ortholog in the beet cyst nematode (Heterodera schachtii), Hs19C07.

105 cines), 10A06 gene was cloned from the sugar beet cyst nematode (Heterodera schachtii), which is able

106 mRNA levels following infection by the sugar beet cyst nematode (Heterodera schachtii; BCN), in contr

107 r to understand the relationship between the beet cyst nematode H. schachtii and its host, identifica

108 uring the compatible interaction between the beet cyst nematode Heterodera schachtii and Arabidopsis

109 The beet cyst nematode Heterodera schachtii causes major yie

110 A clone (Hs CBP) was isolated from the sugar beet cyst nematode Heterodera schachtii, which is able t

111 4E02 is an effector of the sugar beet cyst nematode Heterodera schachtii.

112 but opposite to that suggested for the sugar beet cyst nematode Heterodera schachtii.

113 ene in mediating plant susceptibility to the beet cyst nematode Heterodera schachtii.

114 protein is the 10A07 effector from the sugar beet cyst nematode, Heterodera schachtii, which is exclu

115 Beet cyst nematodes depend on a set of secretory protein

116 ach and the Arabidopsis-Beta vulgaris (sugar beet) cyst nematode (Heterodera schachtii) pathosystem,

117 ty of females for both Heterodera schachtii (beet-cyst nematode) and Meloidogyne incognita (root-knot

118 In red beet, cysteine did not inhibit PPO activity but enhanced

119 palm pollen with cowpea (D1), chickpea (D2), beet (D3), mung bean (D4), or maize (D5) seed powders.

120 In this issue of Neuron, Beets et al.

121 Betanin, the red pigment in red beet extract (RBE), is susceptible to degradation under

122 xtraction was used for the extraction of red beet extract, and lyophilized extracts were characterize

123 onditions, commercial brown sugars and sugar beet extracts were analyzed by (1)H NMR spectroscopy app

124 f hydroxypropylmethylcellulose (HPMC), sugar beet fibre (SBF) and apple fibre (AF) incorporation coup

125 to be the dominant species in Iranian sugar beet fields.

126 cally removed before flowering from GR sugar beet fields.

127 mic comparisons based on k-mers identify sea beets from Greece as the closest wild relatives of sugar

128 this putative sugar transporter in the sugar beet genome.

129 the genus Beta, we sequence and analyse 606 beet genomes, encompassing sugar beet, sea beet, B. v.

130 spheres, roots, and leaves of corn and sugar beet grown under irrigated and water deficit conditions.

131 ting that photosynthetic metabolism in sugar beet has not acclimated to increasing CO2 over >100 y.

132 ated in the intron of Bv_22330_orky, a sugar beet homolog of a matrix metalloproteinase (MMP) gene th

133 de tag matching the HSPRO (ORTHOLOG OF SUGAR BEET Hs1(pro)(-)(1)) gene was found to be strongly induc

134 ved in causing cercospora leaf spot of sugar beet in Iran from which C. beticola was the dominant spe

135 protocols to assist plant breeding of sugar beet in the pursuit of improved pathogen resistance.

136 to manage the spread of rhizomania on sugar beet in the U.K. by matching the scale of control with t

137 e effective for insect control because sugar beet is cropped in restricted geographical areas thus li

138 Sugar beet is next to sugar cane one of the most important sug

139 e inoculum sources to CLS epidemics on table beet is not well understood.

140 fore, a new model for flowering induction in beet is proposed in which BTC1 and BvBBX19 complement ea

141 on problem, especially in countries in which beet is used in manufacturing sugar.

142 intragastric administration of fermented red beet juice with various betacyanin doses.

143 henols, oligosaccharides, fiber and nitrate (beet juice), which may induce a prebiotic-like effect.

144 T and emissions embodied in bilateral trade (BEET) lead us to recommend the former methodology to eva

145 fferent plant organs showed that the leaves (beet leaf and kale) and roots (carrot and beetroot) did

146 steady-state mRNA levels of BvSUT1, a sugar beet leaf sucrose symporter, are negatively regulated sp

147 eas tomato plants cannot be used to maintain beet leafhopper colonies (unsuitable).

148 wort plantain plants can be used to maintain beet leafhopper colonies for multiple generations (suita

149 Results presented were based on the BCTV-beet leafhopper pathosystem, but the approach taken (com

150 erous [carrying beet curly top virus (BCTV)] beet leafhoppers [Circulifer tenellus (Baker)] on three

151 anipulate probing preference and behavior by beet leafhoppers, whereas there was no significant diffe

152 t on the total protein extraction from sugar beet leaves (Beta vulgaris L.) by a traditional thermal

153 Sugar beet leaves were extracted with two proteomic protocols:

154 different dicotyledon plant sources, apples, beet leaves, beetroots, carrots and kale, and compositio

155 In senescent sugar beet leaves, reduction of ptDNA per cell to approximatel

156 In cultivated sugar beet material under CLS infection, the comparison betwee

157 that domestication of the ancestors of sugar beet may be traced to this area.

158 After red beet minimal processing increasing cysteine concentratio

159 coat protein-read through protein (CP-RT) of beet necrotic yellow vein furovirus determines vector tr

160 serve two genetically distinct groups of sea beets, one from the Atlantic coast and the other from th

161 charose syrups (SS), which are produced from beet or canes, can be used for adulterating honey.

162 The sugar beet pathogen Cercospora beticola secretes the peryleneq

163 between pea protein isolate (PPI) and sugar beet pectin (SBP) at concentrated solutions (~2.0 wt%).

164 rified citrus and apple pectins, and a sugar beet pectin (SBP), respectively, were added to strawberr

165 trates, such as destarched wheat bran, sugar beet pectin and coffee pulp.

166 th a shell composed of whey protein microgel/beet pectin complexes.

167 Sugar beet pectin improved anthocyanin stability only to a lim

168 epared by electrostatically depositing sugar beet pectin on the gelatin-coated droplets.

169 model solutions containing commercial sugar beet pectin or an isolated pectic polysaccharide fractio

170 xylated citrus and apple pectins and a sugar beet pectin were added to a purified anthocyanin extract

171 itrus pectin, which was in contrast to sugar beet pectin, where values fell below those of the blank

172 ificity towards the conjugation of PPT/sugar beet pectin.

173 PPS, including sugar beet pectin/arabinan, apple/citrus pectin and potato gal

174 ompared the extraction of betalains from red beet peel (RBP) using ultrasound-, high pressure-, and p

175 These findings highlight red beet peel as a sustainable source of natural pigments, d

176 rot pulp, white- and red-grape peels and red-beet peels and pulp) for the purpose of increasing the w

177 BvMYB1 resides at the historic beet pigment-patterning locus, Y, required for red-flesh

178 cotiana sylvestris and the distantly-related beet plant (Beta vulgaris).

179 symptoms occurring in a worker at the sugar-beet plant on or after 31 July 2000.

180 hogen and is based on the infection of sugar beet plants by the endoparasitic slime-mold vector Polym

181 Pseudomonas sp. SH-C52, which protects sugar beet plants from infections by specific soil-borne fungi

182 hat is expressed in the rhizosphere of sugar beet plants.

183 ships in grain-potato, grain-sugar beet, and beet-potato mixtures enabled composition determination.

184 h sprouted fava bean flour, wheat gluten and beet powder.

185 respiratory illness among workers at a sugar-beet processing plant.

186 s approach to 5S rDNA sequence data from sea beet produced a pruned network within which genetic isol

187 llage on soil bacterial communities in sugar beet production across two locations in the United State

188 tly impact soil health and function in sugar beet production.

189 imiting the exposure of the insects to sugar beet proteinase inhibitors and build up of non-sensitive

190 The effect of including sugar beet pulp (SBP) in laying hen diets on performance, egg

191 The results showed that in many samples of beet pulp and molasses the content of "undesirable subst

192 rved as crude protein (CP) sources while the beet pulp and timothy hay represented neutral detergent

193 t of the colony exposed to pectin-rich sugar beet pulp and to xylan-rich wheat bran showed high pecti

194 zones of 5-day-old colonies utilizing sugar beet pulp as a complex carbon source.

195 ungus Penicillium funiculosum grown on sugar beet pulp as the sole carbon source.

196 stimulated by growth of the fungus on sugar beet pulp but inhibited by free glucose.

197 oybean meal or heat-treated soybean meal and beet pulp or timothy hay) were delivered to 10 wethers.

198 synthesis and absorption were greater on the beet pulp treatment whereas synthesis and absorption of

199 industry feed materials such as molasses and beet pulp.

200 vulgaris), including sugar beet, rank among the most important crops.

201 Beet roots also expressed CMO, most strongly when salini

202 to evaluate the disease development in sugar beet roots caused by two common storage pathogens as a f

203 nsight into transcriptional changes in sugar beet roots during storage resulting in the characterizat

204 subcellular fractions of pea leaves and red beet roots established that GGH activity is confined to

205 ods by which storage rot resistance in sugar beet roots may be improved in the future.

206 sing is increasingly centralized, storage of beet roots over an extended time has become necessary.

207 In beet roots, 16-60% of the folate was vacuolar and was ag

208 tting and tissue damage in postharvest sugar beet roots.

209 quenced, assembled, and annotated the 588 Mb beet rust genome, developed a novel leaf peel pathogen D

210 Calibration using beet samples was more accurate than with Trolox.

211 Twenty-three beet samples were analyzed using both the conventional D

212 analyse 606 beet genomes, encompassing sugar beet, sea beet, B. v.

213 lerant hybrids is a major goal for the sugar beet sector.

214 me activity, likely aiding detoxification of beet seed phenolics.

215 itive colonization of the root tips of sugar beet seedlings but also caused a marked increase in the

216 The sugar beet serine proteinase inhibitor may be more effective f

217 AZP) targeting the replication origin of the Beet severe curly top virus (BSCTV), a model DNA virus,

218 We studied sugar beet sink-source dynamics upon vernalization and showed

219 tered organization of these retroelements in beet species.

220 vacuolar membrane vesicles purified from red beet storage root were studied.

221 We used internal cane and beet sugar industry documents from 1959 to 1971 to analy

222 as detected in the isotopomer trends between beet sugar samples covering the 20th century and CO2 man

223 epared with the addition of HFCS, GS and SS (beet sugar) at a ratio of 0%, 10%, 20%, 40% and 50% by w

224 ulteration of honey using C(3) sugar syrups (beet sugar) could not be detected.

225 Adulteration by using SS (beet sugar) still has a serious detection problem, espec

226 with the saccharose, which is obtained from beet sugar, or invert sugar syrups.

227 reece as the closest wild relatives of sugar beet, suggesting that domestication of the ancestors of

228 syntenic analysis between spinach and sugar beet suggests substantial inter- and intra-chromosome re

229 Pathogen isolates collected from table beet, Swiss chard and common lambsquarters in mixed-crop

230 Phylogeny of these wild beet taxa was inferred from the sequence data using phen

231 the continued use of glyphosate in GR sugar beet, the effect of increasing glyphosate rates (applied

232 ptomic and functional reprogramming of sugar beet tissue, resulting in a reversal of flux direction i

233 expressed AtMRP1 and its equivalents in red beet vacuolar membranes are not only competent in the tr

234 vated VCL currents were also observed in red beet vacuoles suggesting that these channels may provide

235 arative transcriptomic approach on six sugar beet varieties showing different amount of sucrose loss

236 l-DOPA formation in red beet was found to be redundantly catalyzed by CYP76AD6 t

237 pe waste followed by thermally processed red-beet waste.

238 beticola derived from Swiss chard and table beet were not genetically differentiated.

239 uctures of the RNA pseudoknots from PLRV and beet western yellow virus (BWYV) are similar, nucleotide

240 ole of Mg(2+) ions for the resistance of the Beet Western Yellow Virus (BWYV) pseudoknot (PK) to unfo

241 rms of the frameshifting RNA pseudoknot from beet western yellow virus at resolutions of 1.25 and 2.8

242 ent high-resolution crystal structure of the beet western yellow virus pseudoknot, a systematic mutat

243 ytidine in a tertiary structure element from beet western yellows virus (BWYV) RNA.

244 hese findings with previous results from the beet western yellows virus (BWYV) RNA.

245 The RNA genomes of plant luteovirids beet western yellows virus (BWYV), potato leaf roll viru

246 1-2'-OH interaction in the related mRNA from beet western yellows virus (BWYV); however, the ScYLV an

247 ations of the frame-shifting pseudoknot from beet western yellows virus (BWYV, NDB file UR0004) were

248 roove base quadruple, like that found in the beet western yellows virus pseudoknot and the hepatitis

249 on of the thermodynamics of unfolding of the beet western yellows virus pseudoknot reveals strongly p

250 ture of the -1 frameshifting pseudoknot from beet western yellows virus reveals, in addition to Watso

251 (p < 0.05) more abundant in symptomatic sea beets with respect to symptomless.

252 A full-length cDNA clone of beet yellows closterovirus (BYV) was engineered and used

253 P70 homolog (HSP70h) in viral infection, the beet yellows closterovirus (BYV) was modified to express

254 was utilized for tagging individual genes of beet yellows closterovirus (BYV).

255 The beet yellows closterovirus leader proteinase (L-Pro) pos

256 Cell-to-cell movement of beet yellows closterovirus requires four structural prot

257 The filamentous virion of the closterovirus Beet yellows virus (BYV) consists of a long body formed

258 The Hsp70 homolog (Hsp70h) of Beet yellows virus (BYV) functions in virion assembly an

259 The cell-to-cell movement of the Beet yellows virus (BYV) is mediated by a movement prote

260 The 66-kDa leader proteinase (L-Pro) of the Beet yellows virus (BYV) possesses a nonconserved N-term

261 The leader proteinase (L-Pro) of Beet yellows virus (BYV; a closterovirus) was replaced w

262 e have shown previously, the movement of the Beet yellows virus requires the concerted action of five

263 composition and architecture of particles of beet yellows virus, a closterovirus.

264 and have slightly increased maize and sugar beet yields.