ライフサイエンスコーパス: papaya

1 fruit, pineapple, melon, coconut, banana and papaya).

2 bbage, garden cress, radish, horseradish and papaya.

3 integration of genetic and physical maps of papaya.

4 also slightly higher than that in poplar and papaya.

5 tis (Vitis vinifera; 156) and Carica (Carica papaya; 139) is similar to that in Populus, supporting t

6 ene was found for mango (10.1%), followed by papaya (5.3%), tomato (3.1%), and carrot (0.5%).

7 Papaya, a fruit crop cultivated in tropical and subtropi

8 Sequence analysis of wild and cultivated papaya accessions showed the presence of this frame-shif

9 eposited in globular and tubular elements in papaya and mango chromoplasts, where carotenoids accumul

10 Sex chromosomes have been found in papaya and originated approximately 2-3 million years ag

11 route to enhancing anti-cancer properties in papaya and other climacteric fruits.

12 hod, after validating on known strata on the papaya and S. latifolia X chromosome, was applied to the

13 To examine this food synergism, papaya and strawberry nectars and their respective blend

14 , differences between total lycopene BA from papaya and tomato were insignificant, possibly since bot

15 noids from edible portions of carrot, mango, papaya, and tomato was compared using an in vitro digest

16 by colinearity of two to four genes between papaya, Arabidopsis (Arabidopsis thaliana), grape (Vitis

17 tive compounds and contribute to the typical papaya aroma, from which ethyl butanoate, benzyl isothio

18 to the papaya X-specific region, and 1 to a papaya autosomal region.

19 nes had functional homologs elsewhere in the papaya autosomal regions, suggesting movement of genes o

20 sequence content of the X compared with the papaya autosomal sequence.

21 me of the studied pesticides in lime, melon, papaya, banana, tomato, and lettuce.

22 Moreover, the development of transgenic papaya by other laboratories and employment of a mechani

23 er with noni (Morinda citrifolia L.) (LN) or papaya (Carica papaya L.) (LP), were characterized by HP

24 Papaya (Carica papaya L.) is a fleshy fruit with a rapid

25 apaya ringspot virus (PRSV) seriously limits papaya (Carica papaya L.) production in tropical and sub

26 A high-density genetic map of papaya (Carica papaya L.) was constructed using 54 F(2)

27 A high-density genetic map of papaya (Carica papaya L.) was constructed using microsat

28 ality and sensory acceptability of fresh-cut papaya (Carica papaya L.).

29 The Y chromosome of papaya (Carica papaya) diverged from the X chromosome ap

30 Papaya (Carica papaya) fruit flesh color is caused by th

31 and other papain-like enzymes isolated from papaya (Carica papaya) laticifers when compared with all

32 genome sequences, grape (Vitis vinifera) and papaya (Carica papaya), have been recently released.

33 edonous plant species (Arabidopsis thaliana, papaya [Carica papaya], poplar [Populus trichocarpa], an

34 s and to assign genome sequence scaffolds to papaya chromosomes.

35 which 19 were detected for the first time as papaya constituents.

36 early visible by light microscopy, mango and papaya contained different types of carotenoid-bearing s

37 itoring for GMOs in food in the Netherlands, papaya-containing food supplements were found positive f

38 Here we show that papaya contains a primitive Y chromosome, with a male-sp

39 entation test in bacteria confirmed that the papaya CpCYC-b is the gene controlling fruit flesh color

40 The papaya crop is severely affected by papaya ringspot viru

41 The Y chromosome of papaya (Carica papaya) diverged from the X chromosome approximately 2-3

42 Further analyses showed that both papaya event 16-0-1 and event 18-2-4 were transformed wi

43 identify the unknown and EU unauthorised GM papaya event(s).

44 d novel sequence data to identify unknown GM papaya events.

45 parasite-derived resistance with transgenic papaya expressing the PSRV coat protein gene.

46 phenolic content and antioxidant activity of papaya extracts.

47 ncentration and increased the maintenance of papaya firmness.

48 he determination of tartrazine in lemon, and papaya-flavoured gelatin, candy, and in fruit syrup.

49 Our results enhanced our understanding of papaya flesh color inheritance and generated new tools f

50 To uncover the molecular basis of papaya flesh color, we took map-based cloning and candid

51 s compounds present in isooctane extracts of papaya fractions detected via gas chromatography (GC/ITD

52 cs and antioxidant activity of ozone-treated papaya fruit and untreated fruit.

53 were used to analyse volatile compounds from papaya fruit cv. Red Maradol and to estimate the most od

54 Freshly harvested papaya fruit were exposed continuously to ozone fumigati

55 se constructs, which conceptually resemble a papaya fruit, are chemically stable, remain monodisperse

56 Papaya (Carica papaya) fruit flesh color is caused by the accumulation

57 equenced so far, may account for the smaller papaya gene number in most functional groups.

58 s region is nevertheless a small part of the papaya genome compared with other male-specific genome r

59 The papaya genome is three times the size of the Arabidopsis

60 V. vinifera, Arabidopsis thaliana and Carica papaya genomes are similar, despite the huge difference

61 antioxidant properties of Sel-42 and Tainung papayas grown in Turkey.

62 Consumption of papaya > or =1 time/week was inversely associated with p

63 Papaya has been identified as a valuable source of nutri

64 Only two plants Silene latifolia and papaya have been studied until now for the presence of e

65 s, grape (Vitis vinifera) and papaya (Carica papaya), have been recently released.

66 The papaya HSY differs from the X region by two large-scale

67 olor inheritance and generated new tools for papaya improvement.

68 igate the quality and stability of air-dried papaya in terms of quality dynamics and behavior of bio-

69 e supports the hypothesis that hermaphrodite papaya is a product of human domestication.

70 Sex in papaya is controlled by a pair of nascent sex chromosome

71 Sex determination in papaya is controlled by a recently evolved XY chromosome

72 proximately 90 and 81%, respectively, with a papaya isolate of MCLCuV from Costa Rica.

73 everage based on exotic fruits (mango juice, papaya juice and acai) mixed with orange juice and oat,

74 orinda citrifolia L.) (LN) or papaya (Carica papaya L.) (LP), were characterized by HPLC-DAD-ESI/MS(n

75 Papaya (Carica papaya L.) is a fleshy fruit with a rapid pulp softening

76 virus (PRSV) seriously limits papaya (Carica papaya L.) production in tropical and subtropical areas

77 A high-density genetic map of papaya (Carica papaya L.) was constructed using 54 F(2) plants derived

78 A high-density genetic map of papaya (Carica papaya L.) was constructed using microsatellite markers

79 ry acceptability of fresh-cut papaya (Carica papaya L.).

80 atography was used to enrich the caricain in papaya latex and an enzyme-linked immunosorbent assay te

81 ates from blacktip shark skin prepared using papaya latex enzyme with different degrees of hydrolysis

82 to fractionate glycyl endopeptidase from the papaya latex of Red Lady and Khack Dum cultivars.

83 ess the ability of the enzyme caricain (from papaya latex) to detoxify gliadin in whole wheat flour a

84 n isoelectric point of 3.5 was purified from papaya latex.

85 in-like enzymes isolated from papaya (Carica papaya) laticifers when compared with all other reported

86 Our results indicated that this transgenic papaya line has a useful application against PRSV in the

87 Coat protein (CP)- transgenic papaya lines resistant to PRSV isolates in the sequence-

88 also accumulated in PRSV infected transgenic papaya lines.

89 rmation system to produce RNAi-CP-transgenic papaya lines.

90 t quality of dehydrated fruits (apple, pear, papaya, mango) using combined drying techniques.

91 erola, monbin, cashew apple, guava, soursop, papaya, mango, passion fruit, surinam cherry, sapodilla,

92 plant species: Arabidopsis thaliana, Carica papaya, Medicago truncatula, Oryza sativa and Populus tr

93 Papaya mosaic virus (PapMV) is a filamentous plant virus

94 ate immunity through engagement of TLR7 with papaya mosaic virus (PapMV)-like nanoparticles.

95 uses potato virus X, narcissus mosaic virus, papaya mosaic virus and tobacco rattle virus, all of whi

96 We recently showed that papaya mosaic virus nanoparticles (PapMV), self-assemble

97 Papaya offers numerous advantages as a system for fruit-

98 fold higher fluorescence intensity with the "papaya particles" compared to current "best-in-class" co

99 oxidant properties of banana, litchi, mango, papaya, passion fruit and pineapple from Reunion French

100 cids) were identified in cherimoyas, lemons, papayas, passion-fruits and strawberries for the first t

101 The anticancer activity of papaya pectin is dependent on the presence and the branc

102 We purified a Carica papaya pectin methylesterase (CpL-PME; EC 3.1.1.11) from

103 e explanation for these observations is that papaya pectins extracted from the third day after harves

104 eports of an in vitro biological activity of papaya pectins that were modified by natural action of r

105 Control samples were obtained from papaya plantations cultivated in experimental areas, in

106 ensively tested in the field such as squash, papaya, plum, grape, and sugar beet.

107 ored using the sequenced rosids Arabidopsis, papaya, poplar, and grape.

108 pecies (Arabidopsis thaliana, papaya [Carica papaya], poplar [Populus trichocarpa], and grape [Vitis

109 ent of commercial virus-resistant transgenic papaya provides a tangible approach to control PSRV in H

110 These are first reports of AGII in papaya pulp and the first reports of an in vitro biologi

111 Consumer acceptance of the papaya purees differed significantly.

112 Volatiles of papaya purees from four Costa Rican cultivars were analy

113 uch shorter (1.10 Mb) than the corresponding papaya region (2.56 Mb).

114 a dominant monogenic locus, Prs, conferring Papaya ring-spot virus (PRSV) resistance in bottle gourd

115 Papaya ringspot virus (PRSV) seriously limits papaya (Ca

116 The papaya crop is severely affected by papaya ringspot virus (PSRV) worldwide.

117 ment length polymorphism (AFLP) markers, the papaya ringspot virus coat protein marker, morphological

118 Pectin extracted from intermediate phases of papaya ripening markedly decreased cell viability, induc

119 During intermediate phases of papaya ripening, partial depolymerization of pectin to s

120 The nine major LGs of our map represent papaya's haploid nine chromosomes with LG 1 of the sex c

121 od recipes or the so-called "Som Tam" (green papaya salad) prior to determination by inductively coup

122 th true dithiocarbamate residues measured in papaya samples from the field trials following applicati

123 condition providing the highest recovery of papaya seed oil with the most desirable antioxidant acti

124 high oil recovery ( approximately 73%) from papaya seed.

125 idant activity and stability of the oil from papaya seed.

126 oncellea split therefore occurred before the papaya sex chromosomes stopped recombining, making V. mo

127 We compared the recently evolved papaya sex chromosomes with a homologous autosome of a c

128 ion years, supporting a recent origin of the papaya sex chromosomes.

129 nges since recombination stopped between the papaya sex chromosomes.

130 a suitable outgroup for inferring changes in papaya sex chromosomes.

131 The homomorphic sex chromosomes of papaya show features of incipient sex chromosome evoluti

132 ed genes < X-linked genes < autosomal genes; papaya shows an unprecedented pattern of X-linked genes

133 Papaya slices were packed and covered with polypropylene

134 human side of biotechnology; the transgenic papaya story; and my leadership time at USDA in Hawaii.

135 report a 3x draft genome sequence of 'SunUp' papaya, the first commercial virus-resistant transgenic

136 However, for papaya, the lowest colour change exhibited by samples dr

137 The new data show that, in papaya, these genes lie in a quite extensive non-recombi

138 V. monoica genome is 41% larger than that of papaya, this finding suggests considerable expansion of

139 the siRNAs products in virus-free transgenic papaya tissue culture seedlings.

140 The sensory attributes of papaya treated with 2.5ppm ozone was superior in sweetne

141 hods gave positive CS2 results for all three papaya varieties.

142 Aroma composition of papaya was analysed by gas chromatography-mass spectrome

143 olden, Sunrise Solo and Tainung cultivars of papaya were found to release CS2 when submitted to exper

144 e population that domesticated hermaphrodite papayas were selected from.

145 mal and safe food preservation technique for papaya which can benefit both the producers and consumer

146 The papaya X and the hermaphrodite-specific region of the Y(

147 V. monoica orthologs is almost identical for papaya X and Y alleles; the Carica-Vasconcellea split th

148 In application to gene sequences on the papaya X chromosome and protein-coding sequences on the

149 The extreme low nucleotide diversity in the papaya X-linked region is much greater than observed in

150 The extremely low diversity in the papaya X-linked region was probably caused by a recent,

151 ificial chromosomes, 11 corresponding to the papaya X-specific region, and 1 to a papaya autosomal re

152 nding suggests considerable expansion of the papaya X; expansion is supported by a higher repetitive

153 omosome (MSY) spans approximately 13% of the papaya Y chromosome.

154 The papaya Y-linked region showed clear population structure