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 schachtii causes major yield losses in sugar beet.

4 bstituents were detected in the roots of red beet.

5 orphisms linked to bolting tendency in sugar beet.

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

7 the regulation of bolting tendency in sugar beet.

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

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

10 ed to produce the red betacyanin pigments in beets.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

71 The beet cyst nematode Heterodera schachtii causes major yie

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

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

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

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

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

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

78 this putative sugar transporter in the sugar beet genome.

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

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

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

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

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

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

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

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

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

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

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

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

91 Sugar beet leaves were extracted with two proteomic protocols:

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

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

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

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

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

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

98 Sugar beet pectin improved anthocyanin stability only to a lim

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

117 industry feed materials such as molasses and beet pulp.

118 Beet roots also expressed CMO, most strongly when salini

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

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

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

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

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

124 tered organization of these retroelements in beet species.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

147 1-2'-OH interaction in the related mRNA from beet western yellows virus (BWYV); however, the ScYLV an

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

164 and have slightly increased maize and sugar beet yields.