ライフサイエンスコーパス: Pisum sativum

1 ontrol pathways in the long-day legume, pea (Pisum sativum).

2 the patterns he observed in the garden pea (Pisum sativum).

3 ed or regulated during bud outgrowth in pea (Pisum sativum).

4 nd Tha4 and disulfide bond formation in pea (Pisum sativum).

5 s for their hormonal activity in garden pea (Pisum sativum).

6 coordinately regulate bud outgrowth in pea (Pisum sativum).

7 Arabidopsis (Arabidopsis thaliana) and pea (Pisum sativum).

8 d in the supernodulating nod3 mutant of pea (Pisum sativum).

9 shoot tip removal (decapitation) in the pea (Pisum sativum).

10 lar, is phytotoxic to etiolated seedlings of Pisum sativum.

11 syltransferase, was cloned from root tips of Pisum sativum.

12 -hydroxymaackiain 3-O-methyltransferase from Pisum sativum.

13 s type of learning occurs in the garden pea, Pisum sativum.

14 part of the chloroplast import machinery in Pisum sativum.

15 r oligosaccharide distribution, highlighting Pisum sativum (9.22 g/100 g) as the richest source of th

16 istatic isoflavonoid produced by garden pea (Pisum sativum), a host for this fungus.

17 al phenolic compounds (TPC) from green peas (Pisum sativum), a matrix not previously explored with th

18 lectins Galanthus nivalis agglutinin (GNA), Pisum sativum agglutinin (PSA), and Lens culinaris agglu

19 ously selected for resistance to pea lectin (Pisum sativum agglutinin) and shown to behave dominantly

20 phage galactose-type lectin, a plant lectin, Pisum sativum agglutinin, and the bacterial Gal-/Glc-bin

21 ectin, Griffonia simplicifolia lectin I, and Pisum sativum agglutinin.

22 In leguminous plants such as pea (Pisum sativum), alfalfa (Medicago sativa), barrel medic

23 against equine plasma amine oxidase (EPAO), Pisum sativum amine oxidase (PSAO), Pichia pastoris lysy

24 n of leaf complexity to different degrees in Pisum sativum and Lotus japonicus.

25 um meliloti, required for nodulation of pea (Pisum sativum) and alfalfa (Medicago sativum), respectiv

26 ng of endogenous Toc75 POTRA domains in pea (Pisum sativum) and Arabidopsis (Arabidopsis thaliana) co

27 Pea (Pisum sativum) and Arabidopsis contain similar, if not i

28 l proteins OEP21, OEP24, and OEP37 from pea (Pisum sativum) and Arabidopsis thaliana contain informat

29 We characterized the class II smHSPs of pea (Pisum sativum) and compared them with class I smHSPs.

30 originally studied by Gregor Mendel in pea (Pisum sativum) and involved in the degradation of photos

31 ologs from other legume species, namely pea (Pisum sativum) and Lotus japonicus, we show that this mo

32 rminal in some legume species, such as peas (Pisum sativum) and peanuts (Arachis hypogaea), likely du

33 enhancer sequences from a plant virus, pea (Pisum sativum) and wheat (Triticum aestivum), was just u

34 cotyledon phenotypes, has been identified in Pisum sativum, Arabidopsis thaliana, and Festuca pratens

35 ke cells." Whereas root border cells of pea (Pisum sativum) are clearly involved in defense against f

36 The Tic20 protein was identified in pea (Pisum sativum) as a component of the chloroplast protein

37 hese complexes by the embryo, using the pea (Pisum sativum) as a model species.

38 Here we use in vitro pea (Pisum sativum) chloroplast import assays and transient e

39 ein fusions, and import assays with purified Pisum sativum chloroplasts, indicated chloroplastic loca

40 nd alpha-CT were imported into isolated pea (Pisum sativum) chloroplasts and became integrated into A

41 Dual import assays with purified pea (Pisum sativum) chloroplasts and mitochondria, and subcel

42 d AtBCCP2 was competent for import into pea (Pisum sativum) chloroplasts and processed to a 25-kD pol

43 Import assays with pea (Pisum sativum) chloroplasts showed that PyrR and PyrD ar

44 An in vitro assay with pea (Pisum sativum) chloroplasts was developed to conduct mut

45 vement across the thylakoid membrane of pea (Pisum sativum) chloroplasts was directly measured by sto

46 t across the inner envelope membrane of pea (Pisum sativum) chloroplasts was directly measured by sto

47 Upon incubation of the precursor with pea (Pisum sativum) chloroplasts, it was imported and process

48 been studied extensively using isolated pea (Pisum sativum) chloroplasts.

49 I integral membrane protein abundant in pea (Pisum sativum) clathrin-coated vesicles (CCVs) that bind

50 fected region of soybean (Glycine max), pea (Pisum sativum), clover (Trifolium pratense), and common

51 uncatula nodule root (noot) mutants and pea (Pisum sativum) cochleata (coch) mutants, which are chara

52 An apyrase from pea (Pisum sativum) complements a yeast (Saccharomyces cerevi

53 bi5 mutants in a second legume species, pea (Pisum sativum), confirmed a role for ABI5 in the regulat

54 A protein of 80 kD from developing pea (Pisum sativum) cotyledons has previously been shown to e

55 r chaperones, Escherichia coli DnaK and pea (Pisum sativum) CSS1, was investigated in detail.

56 of aggregated proteins from tobacco and pea (Pisum sativum cv "Little Marvel") chloroplasts showed th

57 is localized to developing vacuoles in pea (Pisum sativum cv Extra Early Alaska).

58 romoter fragment of the Blec4 gene from pea (Pisum sativum cv. Alaska) and demonstrate that it is cap

59 t phenotype was introgressed into a standard Pisum sativum cv. Birte to provide near-isogenic lines w

60 full-length CPCT cDNA (designated PCT2) from Pisum sativum cv. Feltham First using an Arabidopsis pro

61 sponds to a native protein of 159 kD in pea (Pisum sativum), designated Toc159.

62 il seven pairs of contrasting traits in pea (Pisum sativum), establishing the foundational principles

63 ha and beta subunits of the ch-cpn60 of pea (Pisum sativum), expressed them individually in Escherich

64 ansport chain, we overexpressed a minor pea (Pisum sativum) Fd isoform (PsFd1) in tobacco (Nicotiana

65 sgenic tobacco (Nicotiana tabacum), the pea (Pisum sativum) Ferredoxin 1 (Fed-1) mRNA dissociates fro

66 ther t-loops exist in the higher order plant Pisum sativum (garden pea).

67 -1,4-D-glucanase (EGase, EC 3.2.1.4) of pea (Pisum sativum) has been cloned and characterized.

68 The inheritance of flower color in pea (Pisum sativum) has been studied for more than a century,

69 Pea (Pisum sativum) has served as a model for development of

70 olymorphic PDR1 retrotransposon insertion in Pisum sativum have been developed.

71 eral ramosus (rms) branching mutants in pea (Pisum sativum) have SL defects, perturbed xylem CK level

72 The function of PsBRC1, the pea (Pisum sativum) homolog of the maize (Zea mays) TEOSINTE

73 tured firefly luciferase (Luc) bound to pea (Pisum sativum) Hsp18.1 as a model to define the minimum

74 t Aux/IAA proteins from Arabidopsis and pea (Pisum sativum) interact in vitro with recombinant phytoc

75 Pisum sativum is of great economic and nutritional inter

76 Here, we show that this dwarfism in pea (Pisum sativum) is not attributable to the strong branchi

77 eversibly glycosylated polypeptide from pea (Pisum sativum) is thought to have a role in the biosynth

78 solated a class 1 knox cDNA from pea, Pskn1 (Pisum sativum knotted1) and examined its expression patt

79 ndisturbed grassland (GP), winter wheat-pea (Pisum sativum L) rotations under conventional tillage (W

80 of tendrils in the compound leaves of pea - Pisum sativum L.

81 ravitropic curvature response of intact pea (Pisum sativum L. cv Alaska) epicotyls was examined by ge

82 were extracted from 7 day old etiolated pea (Pisum sativum L. cv Alaska) epicotyls with 3 molar LiCl.

83 Pea (Pisum sativum L. cv Alcan) endocarp tissue challenged wi

84 cDNA has been cloned and sequenced from pea (Pisum sativum L. cv. Birte).

85 was imported and processed by isolated pea (Pisum sativum L. Laxton's Progress No. 9) chloroplasts a

86 was investigated in etiolated pea seedlings (Pisum sativum L. var Alaska) by excising the cotyledons.

87 ation zone of the epicotyl of etiolated pea (Pisum sativum L. var Alaska) seedlings, there is little

88 When pea (Pisum sativum L. var Onward) seedlings are treated with

89 GalAT activity in homogenates from pea (Pisum sativum L. var. Alaska) stem internodes co-localiz

90 at (Triticum aestivum L.) (WW) - spring pea (Pisum sativum L.) (SP) rotation (WW-SP) under both CT an

91 , WF with different tillage (WT), wheat-pea (Pisum sativum L.) (WP), WF under different crop residue

92 5% of the SMM was extrachloroplastic in pea (Pisum sativum L.) and spinach (Spinacia oleracea L.), wh

93 A cDNA fragment coding for the pea (Pisum sativum L.) chloroplastic glyceraldehyde-3-P dehyd

94 phatase was purified from the stroma of Pea (Pisum sativum L.) chloroplasts that is capable of dephos

95 t across the inner-envelope membrane of pea (Pisum sativum L.) chloroplasts was directly measured by

96 We show for pea (Pisum sativum L.) epicotyl sections that this hypothesis

97 The lip1 mutant of pea (Pisum sativum L.) exhibits a de-etiolated phenotype.

98 tely 80% identical with Arabidopsis and pea (Pisum sativum L.) homologs.

99 lin (GA) controlling stem elongation in pea (Pisum sativum L.) is GA1, which is formed from GA20 by 3

100 Stem elongation in peas (Pisum sativum L.) is under partial control by gibberelli

101 P21 complex purified from heat-stressed pea (Pisum sativum L.) leaves contained no proteins other tha

102 ase (ACCase) have been characterized in pea (Pisum sativum L.) leaves; a heteromeric chloroplast enzy

103 Field pea (Pisum sativum L.) needs improvement to increase producti

104 A pea (Pisum sativum L.) nuclear enzyme with protein tyrosine p

105 op genetics and processing in two pea lines (Pisum sativum L.) on starch digestion kinetics.

106 Pea (Pisum sativum L.) ornithine transcarbamylase (OTC) antis

107 A cDNA of pea (Pisum sativum L.) RbcS 3A, encoding a small subunit prot

108 e), T(o) (optimal), T(m) (maximum)] for pea (Pisum sativum L.) seed germination and seedling growth t

109 lene biosynthesis in stems of etiolated pea (Pisum sativum L.) seedlings by rapidly increasing the ex

110 Treatment of 5- to 6-day-old etiolated pea (Pisum sativum L.) seedlings with indole-3-acetic acid (I

111 In pea (Pisum sativum L.) seeds, GA 2-oxidation is controlled by

112 on on pods of specific genetic lines of pea (Pisum sativum L.) stimulates cell division at the sites

113 zation and N fertilizer supply in maize/pea (Pisum sativum L.) strip intercropping was evaluated in a

114 Among a set of genes in pea (Pisum sativum L.) that were induced under drought-stress

115 ed how mixed-cropping between two field pea (Pisum sativum L.) varieties (Winfreda and Ambassador) in

116 An artificial gene encoding PBGS of pea (Pisum sativum L.) was designed to overcome previous prob

117 ntil (Lens culinaris Merr.), and yellow pea (Pisum sativum L.) were investigated over a 6-day germina

118 tivum L.), barley (Hordeum vulgare L.), pea (Pisum sativum L.), and fallow with or without N fertiliz

119 In this study, we used vegetable peas (Pisum sativum L.), harvested for human consumption as im

120 In pea (Pisum sativum L.), source to sink partitioning of amino

121 ox and GA 3beta-hy transcript levels in pea (Pisum sativum L.).

122 them to the introduced cash crop, green pea (Pisum sativum L.).

123 Yellow pea (Pisum sativum L., YP) grain is generally milled into flo

124 ivity in nuclei purified from etiolated pea (Pisum sativum, L.) plumules is present in a single enzym

125 ariations were then cross-compared with pea (Pisum sativum), leading to the identification of candida

126 quantified protein import into isolated pea (Pisum sativum) leaf chloroplasts and root leucoplasts an

127 Subcellular fractionation of pea (Pisum sativum) leaf protoplasts indicated that 30% of ly

128 The vacuoles of pea (Pisum sativum) leaves and red beet (Beta vulgaris) stora

129 Herein, we show that Pisum sativum LecRLK (PsLecRLK) localized in plasma memb

130 Three pea (Pisum sativum) loci controlling photoperiod sensitivity,

131 Dual-import assays with purified pea (Pisum sativum) mitochondria and chloroplasts, and subcel

132 hread formation, as a null SL-deficient pea (Pisum sativum) mutant forms significantly fewer infectio

133 ula ortholog of the Lotus japonicus and pea (Pisum sativum) NIN gene.

134 to Arabidopsis (Arabidopsis thaliana), pea (Pisum sativum), or tomato (Lycopersicon esculentum) tiss

135 rries a nonsense mutation in the single pea (Pisum sativum) ortholog of the ethylene signaling gene E

136 Two pea (Pisum sativum) P450 cDNAs (CYP73A9v1, encoding trans-cin

137 phenylpropanoid biosynthetic pathway of pea (Pisum sativum), partial cDNAs representing four distinct

138 ave isolated a DESD-box containing cDNA from Pisum sativum (Pea) and named it as PDH45.

139 The complex was purified from Pisum sativum (pea) chloroplast envelopes by native gel

140 The Pisum sativum (pea) mutants degenerate leaves (dgl) and

141 bacteriophages were isolated from leaves of Pisum sativum, Phaseolus vulgaris, Lycopersicon esculent

142 rmation of individual transcription units in Pisum sativum plant nucleoli using a novel labelling tec

143 ify the role of GA3ox expression during pea (Pisum sativum) plant growth and development, we generate

144 In this study, pea (Pisum sativum) plants overexpressing AMINO ACID PERMEASE

145 ortant for the metabolism and growth of pea (Pisum sativum) plants.

146 Our data indicate that moss and pea (Pisum sativum) plastid transport systems are functionall

147 a nucleolar protein was selected from a pea (Pisum sativum) plumule library, cloned, and sequenced.

148 t) DC3000 hrcC(-) and to the nonadapted pea (Pisum sativum) powdery mildew Erysiphe pisi However, PLC

149 r a pea seed nuclear DNA-binding protein (of Pisum sativum) present at the cell expansion phase.

150 us analysis of the MAP kinase homologue from Pisum sativum (PsMAPK) revealed a potential MAP kinase m

151 and characterization of recombinant p68 from Pisum sativum (Psp68) is presented.

152 e required for plant life in that a UGT from Pisum sativum (PsUGT1) controls plant development by opp

153 curonosyltransferase-encoding gene from pea (Pisum sativum; PsUGT1).

154 d IV of the AUX/IAA protein PsIAA4 from pea (Pisum sativum) revealed a globular ubiquitin-like beta-g

155 iptomic and metabolomic analyses of the pea (Pisum sativum) rhizosphere, a suite of bioreporters has

156 took a systematic, detailed analysis of pea (Pisum sativum) root tip cell walls.

157 Pea (Pisum sativum) root tips incubated with [(32)P]dCTP duri

158 the production of root border cells by pea (Pisum sativum) root tips.

159 Yet, when pea (Pisum sativum) roots are inoculated with the pea pathoge

160 rrying genes encoding soybean lectin or pea (Pisum sativum) seed lectin (PSL) were inoculated with Br

161 c activity found within the germinating pea (Pisum sativum) seed, 4 days from the initiation of imbib

162 complex (mt-PDC) by using intact green pea (Pisum sativum) seedlings.

163 eolin mRNA using plumules of dark-grown pea (Pisum sativum) seedlings.

164 Thermal profiles of viable, aged, and dead Pisum sativum seeds were recorded, and image analysis of

165 Here, we show that in pea (Pisum sativum) seeds, 4-chloroindole-3-acetic acid is sy

166 However, in maturing pea (Pisum sativum) seeds, the level of the chlorinated auxin

167 from endoplasmic reticula of developing pea (Pisum sativum) seeds.

168 eat (Triticum aestivum); but the dicots pea (Pisum sativum), soybean (Glycine max Merr.), and spinach

169 ids, Percoll-isolated chloroplasts from pea (Pisum sativum) synthesized FAD from imported riboflavin.

170 n nodulation in Medicago truncatula and pea (Pisum sativum) that form indeterminate nodules.

171 t at the LATE BLOOMER2 (LATE2) locus in pea (Pisum sativum) that is late-flowering with a reduced res

172 In pea (Pisum sativum), the protein-lysine methyltransferase (Ps

173 In pea (Pisum sativum), the reverse reaction, phenylpyruvate to

174 tematic cells exist within root tips of pea (Pisum sativum): the root apical meristem, which gives ri

175 m of 45Ca2+ transport into the lumen of pea (Pisum sativum) thylakoid membranes using silicone-oil ce

176 We purified from pea (Pisum sativum) tissue an approximately 40 kDa reversibly

177 dopsis thaliana, Lycopersicon esculentum and Pisum sativum tissues.

178 s trend is found in the Fabaceae, where pea (Pisum sativum) uses UNIFOLIATA, an ortholog of the flora

179 n the Toc159 GTPase domain (Toc159G) of pea (Pisum sativum) using cleavage by bound preproteins conju

180 Rhizobium leguminosarum 3841, a symbiont of Pisum sativum, using chemical methods, mass spectrometry

181 opersicon lycopersicum), and sugar snap pea (Pisum sativum var. macrocarpon) from an industrially imp

182 profile from the oil of harvested field pea (Pisum sativum) varieties as part of a research project t

183 ith legumes belonging to the galegoid clade (Pisum sativum, Vicia faba and Vicia hirsuta).

184 The STERILE NODES (SN) locus in pea (Pisum sativum) was one of the first photoperiod response

185 Nectria haematococca infection of pea (Pisum sativum) was used as a model to explore possible m

186 In contrast to peas (Pisum sativum), where mitochondrial lipoamide dehydrogen

187 We describe here the FRO1 gene from pea (Pisum sativum), which encodes an Fe(III)-chelate reducta

188 mutants at the Crispoid (Crd) locus in pea (Pisum sativum), which have altered auxin homeostasis and

189 ll wall of the root cap in two species: pea (Pisum sativum), which makes border cells, and Brassica n

190 nt steps of ABA biosynthesis as well as pea (Pisum sativum) wilty and tomato (Solanum lycopersicum) f