ライフサイエンスコーパス: bean

1 in inhibitor (KTI) gene family within winged bean.

2 was the more dominant species in the edible bean.

3 he root-length density of maize but not faba bean.

4 hment of root nodule symbiosis in the common bean.

5 75.17-green pea, 83.18-lentil and 89.87-mung bean.

6 on of macrosynteny between cowpea and common bean.

7 rabica beans and 31.0+/-10.0mg/kg in Robusta beans.

8 her total fiber content compared with coffee beans.

9 lled red lentils to 1630.5mg/kg for ruviotto beans.

10 of useful genes and intercrossing among the beans.

11 cooked by water immersion, except for green beans.

12 e constituents of two "ready to eat" Spanish beans.

13 etic improvement programs in Nigerian common beans.

14 sphate ratio than barley bran and red kidney beans.

15 ence of aflatoxins were determined in edible beans.

16 theobromine and individual phenols in cocoa beans.

17 d CaCl2 on the physicochemical properties of beans.

18 er (1.06mugL(-1)), roots (2.065mugg(-1)) and bean (0.133mugg(-1)).

19 .50 mg 100 mg(-1)) compared with raw Almonga beans (0.6 mg 100 mg(-1)).

20 higher content was found in raw Curruquilla beans (16.50 mg 100 mg(-1)) compared with raw Almonga be

21 In this issue of Neuron, Gantz and Bean (2017) show that the endocannabinoid 2-arachidonoyl

22 polymorphisms to investigate 417 wild common bean accessions and a representative sample of 160 domes

23 Cowpea and common bean added 4.6-5.2 g protein/d and 4-5 g indigestible ca

24 previously reported growth angle response of bean adventitious roots.

25 production processes of single origin coffee beans affects the particle size distribution upon grindi

26 ined are useful for quality control of cocoa beans allowing their differentiation according to cocoa

27 solated fractions and extract made from faba bean and in faba bean suspension.

28 to soybean such as pigeonpea, cowpea, common bean and others could provide a valuable and diverse poo

29 so offers an opportunity to integrate French bean and soybean into genetic improvement programs in Ni

30 hree different lipoxygenases, soybean, horse bean and wheat and compared to the values obtained at pH

31 oat and barley) and bean samples (red kidney bean and white bean) were treated with phytase.

32 ydrine content was 1.5+/-0.5mg/kg in Arabica beans and 31.0+/-10.0mg/kg in Robusta beans.

33 recooked vegetables (cabbage, carrots, green beans and bell peppers).

34 Cocoa butter was the major nutrient in cocoa beans and carbohydrates were the most important in choco

35 residues of imidacloprid and oxamyl in green beans and chili peppers after treatment via irrigation s

36 issipation rates of both pesticides in green beans and chili peppers were studied and the pre-harvest

37 midacloprid were 0.47 and 2.6mug/kg in green beans and chili peppers, respectively, while for oxamyl

38 protein was isolated from the raw and cooked beans and digested to simulate human digestion.

39 , cyprodinil and phosmet) from spinach, snap beans and grapes, and the effect on produce quality.

40 of phosmet; were removed from spinach, snap beans and grapes, respectively, after 15min EO water tre

41 tter is the pure butter extracted from cocoa beans and is a major ingredient in the chocolate industr

42 nd 270% (whole grains) while underestimating beans and legumes (-50%) and nuts and seeds (-29%) (P <

43 30 y of data (1980-2009): fruit, vegetables, beans and legumes, nuts and seeds, whole grains, red and

44 e analysis of azoxystrobin residues in green beans and peas using HPLC-UV and the results confirmed b

45 9% to 94.56% and 80.77% to 100.91% for green beans and peas, respectively.

46 ermination of azoxystrobin residues in green beans and peas.

47 the ethanolic extracts from both pretreated beans and the control were 1.3-1.6 times higher than tho

48 atted cowpea flour was prepared from cow pea beans and the protein isolate was prepared (CPI) and the

49 ) ) double mutant was completely impaired on bean, and bacterial growth was significantly reduced, su

50 - 0.21, and 0.26 +/- 0.31 for cowpea, common bean, and control, respectively), nor did the change in

51 oid-like fibrils from whey, kidney bean, soy bean, and egg white to partially address this concern.

52 ssed the past and recent evolution of common bean, and traced the diversification of patterns of gene

53 n, navy bean, rice bean, tepary bean, velvet bean, and wrinkled pea) and hylon VII starches towards i

54 st abundant chlorogenic acid in green coffee beans, and (alpha1 --> 5)-L-arabinotriose, structurally

55 me water losses) in row-crop monocultures of bean (annual herb) and cotton (woody shrub) would be glo

56 Bean anthocyanins were stable at pH 2.5 and low-temperat

57 Cocoa beans are a well-known source of antioxidant polyphenols

58 t traditional and classic nixtamalization of beans are alternatives to obtaining mineral fortified fl

59 Yeasts associated with cocoa and coffee beans are genetically distinct.

60 Cocoa beans are rich in bioactive phytochemicals such as alkal

61 Brown beans are the preferred varieties over the white beans i

62 Cultivated common beans are the primary protein source for millions of peo

63 ariety is the most demanded, since its cocoa beans are used to produce the finest chocolates.

64 erbation occur when oxidant foods (e.g. fava beans) are consumed.

65 risulfide, in contributing to 'cooked kidney bean' aroma, while dimethyl sulfoxide, dimethyl sulfone

66 maize (maize/maize) or faba bean (maize/faba bean) as competitors under five levels of phosphorus (P)

67 as lentils, with the value of 4.0, and Azuki beans, at 3.2.

68 heir relatives, including, for example, pea, bean, barley, oat, rye, rice and maize.

69 atial sorting in replicated invasions of the bean beetle Callosobruchus maculatus across homogeneous

70 00 mg/kg bulk-CeO2 were presented to Mexican bean beetles (Epilachna varivestis), which were then con

71 weet potato, purple carrot, black and purple bean, black lentil (BL), black peanut, sorghum (SH), bla

72 ivity were investigated in artichokes, green beans, broccoli and carrots cooked under different condi

73 the vicilin-class(7S) globulin of the cocoa beans by acid-induced proteolysis during cocoa fermentat

74 are formed during fermentation of the cocoa beans by acid-induced proteolysis.

75 precursor extract from well-fermented cocoa beans by ligand-exchange and subsequent Sephadex-LH20 ch

76 The determination of the origin of coffee beans by NMR fingerprinting has been shown promising and

77 , caffeine, and gas-producing foods, such as beans, cabbage, and onions), with greater emphasis on ho

78 Walp (cowpea beans), Cajanus cajan L.

79 y requires small aliquots of unroasted cocoa beans, can be automatated, requires no sample preparatio

80 s) aggregates of commercial urease from jack beans (Canavalia ensiformis) were prepared by desolvatio

81 The raw black eye bean, cheese and fish showed high Zn content up to 8.85

82 Pulses, which include lentils, beans, chickpeas, peas, and soybeans, provide an importa

83 We provide spatial models of the bean chloroplast biogenesis that allow such reconstructi

84 Lotus japonicus, Phaseolus vulgaris (common bean), Cicer arietinum (chickpea) and Cajanus cajan (pig

85 All bean coat anthocyanins combined with betaCD showed exten

86 These black bean coat aqueous extracts and powders might represent n

87 Ethanolic extract from black beans coat is a source of flavonoids, saponins and antoc

88 optimize anthocyanins extraction from black bean coats and evaluate their physicochemical stability

89 Black bean coats are a good source of anthocyanins and other p

90 Idaho and Otomi bean coats were extracted in water-citric acid 2% (1/50,

91 roasted blends of Arabica and Robusta coffee beans, commercial samples of roasted ground coffee blend

92 in legume seeds (chickpeas, field peas, faba beans, common vetch and lupins) produced in Europe were

93 ing of solid-state mixtures mimicking coffee beans composition allowed the conclusion that proteins p

94 Black beans contain anthocyanins that could be used as coloran

95 canned samples (cardoon, tuna, green and red beans, corn, and fungi) by Electrothermal Atomic Absorpt

96 The foremost difference in the raw beans corresponded to the lectin: a higher content was f

97 ysate obtained from one day germinated black bean cotyledons.

98 low phytic acid and lectin free (ws+lpa+lf) bean cultivar.

99 rint of bioactive compounds present in cocoa beans depending on genotype and origin.

100 We also located putative areas of common bean domestication in Mesoamerica, in the Oaxaca Valley,

101 The scavenging capacity of cocoa beans during fermentation correlated with total phenolic

102 rmidine and spermine) were detected in cocoa beans during fermentation.

103 bioactive amines and their changes in cocoa beans during seven days of traditional fermentation was

104 to environmental factors affecting the cocoa beans during the fermentation and drying processes.

105 showed that the maximum intensity of 'kidney bean', 'earthy' and 'smoky' odour was observed in Kashmi

106 lpha-amylase assays were assessed; among all bean ecotypes, the tight green seed colour of Verdolino

107 Overall, faba bean, especially its seed coat, has great potential as a

108 es was also demonstrated from a crude castor bean extract and complex matrices.

109 the highly lethal protein ricin from castor bean extract.

110 Coffee bean extracts are consumed all over the world as beverag

111 roperties and in vitro digestibility of rice-bean extrudates has been investigated.

112 zed P application or by the presence of faba bean exudation stimulated root morphological plasticity

113 tides and amino acids generated during cocoa bean fermentation are the most important precursors for

114 Brown rice: pinto bean flour (0%, 15%, 30%, and 45% bean flour) were extru

115 h rice flour and different concentrations of bean flour (included at levels of 0%, 20% and 40%, w/w)

116 aration method was employed to separate navy bean flour (NBF) into protein-rich (PR) and starch-rich

117 Increasing bean flour and processing moisture increased density and

118 The influence of pinto bean flour and processing moisture on the physical prope

119 Incorporating bean flour into extruded snacks can negatively affect ph

120 a positive effect on the FeDa% as did broad bean flour on ZnDa%.

121 tein digestibility increased with increasing bean flour or with decreasing processing moisture.

122 complementary feeding with cowpea or common bean flour would reduce growth faltering and EED in 6-mo

123 ice: pinto bean flour (0%, 15%, 30%, and 45% bean flour) were extruded under 5 moisture conditions (1

124 n of peak, final, and setback viscosities of bean flours in DC indicate the application in refrigerat

125 From coffee beans flowing in a chute to cells remodelling in a livin

126 Roasting of marama beans for more than 20 min resulted in negative properti

127 characterising some popular Nigerian common beans for their nutritive value based on seed coat colou

128 d, under fermented, and well-fermented cocoa beans from all of the main producing countries, with the

129 means to distinguish between fermented cocoa beans from different geographical and varietal origins.

130 metric statistical methods allowed the cocoa beans from different origins to be distinguished.

131 rences in the average Raman spectra of cocoa beans from different sites but within the same variety c

132 Coffee beans from the same origin were roasted using six time-t

133 hat increasing intake of grains, vegetables, beans, fruits and nuts may help reduce mortality from th

134 ovatus was no longer able to grow on locust bean galactomannan.

135 ase (XO) inhibitory activity of green coffee beans (GCB) and wholemeal wheat flour (WF).

136 MC, a recognized marker compound for robusta beans) gives rise to an isolated peak in the 60MHz spect

137 f the processing chain (green beans, roasted beans, ground coffee, brews).

138 Xanthan, locust bean, guar and carboxy methyl cellulose significantly en

139 ive quantification of xanthan gum and locust bean gum (LBG) in gelled food concentrates is presented.

140 The effects of xanthan gum (XG)-locust bean gum (LBG) mixtures (0.05, 0.1, 0.15, 0.2 and 0.5 wt

141 n isolate (WPI) and 0.1% xanthan (XG)-locust bean gum (LBG) mixtures was investigated.

142 Locust bean gum showed the greatest phase separation, followed

143 fied in gum arabic whereas cherry and locust bean gums showed respectively PentxHexy and Hexn profile

144 es of gums such as arabic, cherry and locust-bean gums were successfully identified.

145 r, xanthan, carboxy methyl cellulose, locust bean gums, potato fiber, milk, potato and soy proteins)

146 Wheat bran, oat bran and white bean had a lower calcium:phosphate ratio than barley bra

147 At each P supply rate, faba bean had a smaller root system than maize but greater ex

148 Raw beans had C-type starch, 10.10% resistant starch (RS), a

149 seed coat), namely black lentils and diavoli beans, had higher antioxidant activity than those with p

150 HS-SPME-GC-MS) on conventional roasted cocoa beans, ILR-CIS-GC-MS data on unroasted cocoa beans showe

151 s are the preferred varieties over the white beans in Nigeria due to their assumed richer nutrients.

152 d as an indicator of the presence of robusta beans in the sample.

153 The ws+lpa+lf bean inclusion increases quadratically (P<0.05) the resi

154 to 0% spaghetti, the inclusion of ws+lpa+lf bean increased linearly (P<0.05) the optimal cooking tim

155 w that RabA2, a monomeric GTPase from common bean, is required for the progression of the infection c

156 ed fractions were compared to proteins (navy bean isolate (NBI) and 7S globulin) prepared using a wet

157 % ranged from 42.0% to 57.4%, while in Azuki beans it was 57.5%.

158 tary pulses (nonoil seeds of legumes such as beans, lentils, chickpeas, and dry peas) are well positi

159 obic reaction catalysed by soybean and horse bean lipoxygenases was observed with 2,6-di-tert-butyl-4

160 (maize) or with maize (maize/maize) or faba bean (maize/faba bean) as competitors under five levels

161 ased shoot growth in maize in the maize/faba bean mixture, suggesting that root interactions of neigh

162 of camelid specific nanobodies against Broad bean mottle virus (BBMV).

163 ure on the percentage of moldy and fermented beans, mycotoxins levels, phenolic acids content, pastin

164 derlying the susceptibility of pulse (lablab bean, navy bean, rice bean, tepary bean, velvet bean, an

165 which led to the acquisition by domesticated beans of adaptive traits from wild relatives.

166 detected for the first time in green coffee beans of Robusta and Arabica species.

167 was found at similar levels in green coffee beans of Robusta and Arabica, whereas a noticeable diffe

168 paragine and glutamine in palm olein and soy bean oils was heated up in modelling system at different

169 r quantities (418microg/g) compared to other beans or seeds (up to 132microg/g) roasted under the sam

170 icle size distribution is independent of the bean origin and processing method.

171 Five Pinto bean peptides with alpha-amylase and angiotensin convert

172 compound screening of all Fagioli di Sarconi beans performed by flow injection-electrospray ionizatio

173 double sitA mntH mutant was Fix(+) on common bean (Phaseoli vulgaris), a member of the phaseoloid cla

174 ed the upstream region of the Scarlet Runner Bean (Phaseolus coccineus) G564 gene in order to underst

175 tioplast-to-chloroplast transition in runner bean (Phaseolus coccineus).

176 Among cultivated plants, common bean (Phaseolus vulgaris L.) is the most important grain

177 g genes of a Mesoamerican genotype of common bean (Phaseolus vulgaris L., BAT93).

178 ies of leaf area and leaf mass in the common bean (Phaseolus vulgaris) grown in two contrasting envir

179 red among recombinant inbred lines of common bean (Phaseolus vulgaris) having four distinct root phen

180 anization of genetic variation of the common bean (Phaseolus vulgaris) in its centres of domesticatio

181 that RNAi-mediated down-regulation of common bean (Phaseolus vulgaris) PI3K severely impaired symbios

182 anoceria exposure (62.5-500 mg/kg) on kidney bean (Phaseolus vulgaris) productivity and seed quality

183 Soybean (Glycine max) and common bean (Phaseolus vulgaris) share a paleopolyploidy (whole

184 Common bean (Phaseolus vulgaris) symbiotically associates with

185 black soybean (Glycine max) and black turtle bean (Phaseolus vulgaris), belonging to two different ge

186 odeling in SimRoot indicates that, in common bean (Phaseolus vulgaris), reduced root secondary growth

187 ere, we uncovered the role of TOR during the bean (Phaseolus vulgaris)-Rhizobium tropici (Rhizobium)

188 abidopsis thaliana) and other plants such as bean (Phaseolus vulgaris).

189 a compounds of three varieties of red kidney beans (Phaseolus vulgaris) namely Kashmiri red, Sharmili

190 ntidiabetic activities of Fagioli di Sarconi beans (Phaseolus vulgaris), including 21 ecotypes protec

191 nce of bottom-up effects, with reductions in bean plant biomass being observed.

192 Samples of soil, the broad bean plant, Vicia faba and irrigation water were collect

193 Kidney bean plants (Phaseolus vulgaris var. red hawk) grown in

194 Phenotypic analysis of composite bean plants with transgenic roots overexpressing miR172c

195 e in the 5' untranslated region (UTR) of the bean pod mottle comovirus (BPMV) RNA2, and found it to b

196 mpared with corresponding non-extruded (raw) bean powders (particle size0.5mm), the extrusion treatme

197 hange the protein and starch contents of the bean powders and showed inconsistent effects on the sucr

198 latinization and protein denaturation of the bean powders and thus changed their pasting properties a

199 The extruded bean powders displayed functional properties similar to

200 cal composition and functional properties of bean powders from four common bean varieties was investi

201 the cooked non-extruded and cooked extruded bean powders were comparable.

202 The raw bean powders were extruded under eight different conditi

203 roperties similar to those of two commercial bean powders.

204 The red and carioca beans presented the highest total phenolic content (1.8

205 Transglutaminase crosslinked faba bean protein extensively already with 10nkat/g enzyme do

206 Black bean protein hydrolysates obtained from pepsin and alcal

207 The pepsin-treated bean protein hydrolysates presented higher degree of hyd

208 The alcalase-treated bean protein hydrolysates showed higher surface hydropho

209 The emulsion stability of the bean protein hydrolysates were evaluated during 30days o

210 tides were successfully extracted from Pinto bean protein isolate (PBPI) using Protamex.

211 Oat and faba bean protein isolates were treated with transglutaminase

212 d ashes and Ca(OH)2 produced denaturation of bean proteins, decreasing the second transition enthalpy

213 ng" effect of cooking with NaCl and CaCl2 on bean proteins.

214 Winged bean, Psophocarpus tetragonolobus (L.) DC., is similar t

215 Actually, with the exception of green beans, PTR-ToF-MS technique was able to correctly recogn

216 ermine the DPPH-RSA of cinnamon, clove, mung bean, red bean, red rice, brown rice, black rice and tea

217 DPPH-RSA of cinnamon, clove, mung bean, red bean, red rice, brown rice, black rice and tea extract a

218 latory role of the miR172 node in the common bean-rhizobia symbiosis.

219 e susceptibility of pulse (lablab bean, navy bean, rice bean, tepary bean, velvet bean, and wrinkled

220 iva, and Camelina sativa expressing a castor bean (Ricinus communis) hydroxylase were analyzed.

221 in each step of the processing chain (green beans, roasted beans, ground coffee, brews).

222 content was found to be unaffected by coffee bean roasting treatment because of a noticeable heat sta

223 lot, multiple Rhizobium species can nodulate bean roots, but it is unclear how genetically isolated t

224 te, bran samples (wheat, oat and barley) and bean samples (red kidney bean and white bean) were treat

225 sor was used to quantify OTA in spiked cocoa bean samples and the results were compared with those re

226 tion (P<0.05) in soluble oxalate compared to bean samples.

227 otein, lipids) obtained from fermented cocoa bean samples.

228 articular nutritional benefits of whole faba bean seed (WFB) and fava bean seed coat (FBSC).

229 efits of whole faba bean seed (WFB) and fava bean seed coat (FBSC).

230 onoids, saponins and anthocyanins from black bean seed coat in NF used for the production of tortilla

231 oxidant activities, were obtained from black bean seed coats and applied to colour a sport beverage.

232 Ethanolic extracts of black bean seed coats were added (3g/kg or 7 g/kg) to NF in or

233 The application of elicitors in bean seed during sprouting enhances their nutraceutical

234 ring the range of v-c concentrations in faba bean seeds across all genotypes tested.

235 pes suggests that v-c concentrations in faba bean seeds may be independent quantitative traits.

236 The effect of germinating black bean seeds on the production of cotyledon protein hydrol

237 medium assumed dendritic morphologies, with bean-shaped condensed nuclei, absence of alpha-smooth mu

238 on of some nitrogenous compounds towards the bean shell during fermentation was demonstrated.

239 beans, ILR-CIS-GC-MS data on unroasted cocoa beans showed similar formation trends of important cocoa

240 arious components isolated from green coffee beans showed that CO2 was generated from various green c

241 The 18-h-germinated rice beans showed the highest crude protein content, as deter

242 ers to meeting recommendations for meats and beans; solid fats, alcohol, and added sugars; and physic

243 Coffee bean source and roasting conditions significantly (p<0.0

244 dy of amyloid-like fibrils from whey, kidney bean, soy bean, and egg white to partially address this

245 nt was observed between the two green coffee bean species.

246 Our results also suggest that most bean-specific gene family expansions, including resistan

247 tent, as well as the antioxidant capacity of bean sprouts (cv Dalia).

248 crease of several nutraceutical compounds in bean sprouts treated with SA such as coumaric (8.5-fold)

249 lics and antioxidant capacity of stored mung bean sprouts.

250 composition and antioxidant activity of rice bean sprouts.

251 al properties of protein isolates from black beans stored for 12months.

252 Beans stored under 14%/32 degrees C exhibited 16% of fer

253 introgression events occurring among common bean subpopulations in Mesoamerica and across hemisphere

254 decreased and resistant starch increased as bean substitution and processing moisture increased.

255 and extract made from faba bean and in faba bean suspension.

256 Blue rubber bleb nevus syndrome (Bean syndrome) is a rare, severe disorder of unknown cau

257 Furthermore, we elucidate the influence of bean temperature on particle size distribution, concludi

258 ility of pulse (lablab bean, navy bean, rice bean, tepary bean, velvet bean, and wrinkled pea) and hy

259 t biomass and P content when grown with faba bean than with maize.

260 g(-1), respectively); the fradinho and white beans the lowest (0.18 and 0.19mg.g(-1), respectively).

261 ent of symbiotic nitrogen fixation in common bean, the most important grain legume for human consumpt

262 yanidins, were isolated from unroasted cocoa beans (Theobroma cacao L.) using various techniques of c

263 TOR was expressed in all tested bean tissues, with higher transcript levels in the root

264 r gram non-fat dry matter in raw fresh cocoa beans to 4mg/g in the final chocolate product.

265 r gram non-fat dry matter in raw fresh cocoa beans to 6mg epicatechin equivalents per gram in the fin

266 Several characteristics of African Yam Bean tuber starch (AYB) were studied and compared with t

267 We expressed a common bean UPS1 transporter in cortex and endodermis cells of

268 The results obtained with jack bean urease as a model urease, may contribute to the und

269 ent in manuka honey, were identified as jack bean urease inhibitors with IC50 values of 2.8 and 5.0mM

270 sitive Ochratoxin A (OTA) detection in cocoa beans using competitive aptasensor by differential pulse

271 properties of bean powders from four common bean varieties was investigated.

272 henolic acid profiles were determined in ten bean varieties.

273 rhizosphere and root nodules of a particular bean variety grown in the same agricultural plot.

274 e (lablab bean, navy bean, rice bean, tepary bean, velvet bean, and wrinkled pea) and hylon VII starc

275 tine analysis of pesticide residues in cocoa beans via a monitoring study where 10% of them was found

276 Faba bean (Vicia faba L.) provides environmental and health b

277 tween the roots of maize (Zea mays) and faba bean (Vicia faba) are characterized.

278 orn (Zea mays) flour enriched with 30% broad bean (Vicia faba) flour and 20% of quinoa (Chenopodium q

279 Here, we show that BeAn virus RNA replication, translation, polyprotein pro

280 ple, 25 cocoa beans were considered and each bean was measured at 4 different spots.

281 alpha-amylase; Fraction V from black turtle bean was the most potent (IC50: 0.25mug/mL) against alph

282 a-glucosidase; Fraction IV from black turtle bean was the most powerful (IC50: 76mug/mL) against lipa

283 ins and on the antioxidant activity of cocoa beans was investigated.

284 uction of water soluble extracts from kidney beans was investigated.

285 (ORAC) of CPH obtained from germinated black beans was lower than that observed for raw cotyledons.

286 genetic spatial patterns of the wild common bean, we documented the existence of several genetic gro

287 rence methylomes for both soybean and common bean were constructed, providing resources for investiga

288 of certified pure Arabica and Robusta green beans were analyzed for their homostachydrine content.

289 s found in both 0-h and 18-h-germinated rice beans were catechin and rutin.

290 For each sample, 25 cocoa beans were considered and each bean was measured at 4 di

291 ments of fermented, dried and unpeeled cocoa beans were performed using a handheld spectrometer.

292 Marama beans were roasted at 150 degrees C for 20, 25 or 30 min

293 Cocoa beans were roasted at three temperatures (125, 135 and 1

294 pared from ricin toxin extracted from castor beans were the most effective in killing HIV-infected ce

295 and bean samples (red kidney bean and white bean) were treated with phytase.

296 and SPS-WW1 Batch 114) and spiked chickpea, bean, wheat, lentil, cherry juice, mineral water, well w

297 array of organic molecules from the roasted bean, which has been ground into fine particulates.

298 to obtain bioactive ingredients from kidney beans, which could encourage their utilisation in the fo

299 The movement protein VP37 of broad bean wilt virus 2 (BBWV 2) forms tubules in the plasmode

300 The peptides from the protein isolate of raw bean with molecular mass lower than 3kDa reduced 89% of

301 e derived percentages of Arabica and Robusta beans with those declared on packages by manufacturers w